SENATE SELECT COMMITTEE REQUEST (ARTICHOKE(Sanitized))

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CIA-RDP83-01042R000800010006-8
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RIPPUB
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S
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41
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December 15, 2016
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September 8, 2003
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6
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August 20, 1975
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Approved For Release 2004/03/11 : ,; 9a3-01042R0Q0800010006-8 2 0 AUG 1975 25X1 25X1 EORAI)U VIA CT The Review Staff Deputy Director for Adninistratioa Senate Select Committee M T1C EImmG T) Reference is a e to the 7 August 17 verbal _ 's Ellif -r.ot i. we Senate Select Committee of the office of Security certain u en s ro* the Office of Securi.tw una tiered rile eut It e 3 which 4r. "axwe sa.uitizad by the Office of Security is view of the need for additional coordination within the Agency prior to in an uusa.a.1tltei form. Thusc ocu eats were not Z. Three copies of 4 portion of those docu nts requested by A r. Maxwell are being ferwarde,I herewith their reiease to taxer Senate select committee. 'forwardee to the Review Staff via a separate memorandum. Further, two of those documents requested dir. } axwoli are Third Agency atoriai an l1 he 25X1A Robert . Gaabia Director of Secur 25X1 Distribu rig i 2 - Adres D/A w/o at 1 - D/Security w/o att 1 - OS Registry w/o att I - SAG w/att I - DD/PSI w/att OS/PSI/SAG/ by (19 August 1975) CL 3Y 0 Approved For Release 2004/03/11 : CIA-RDP83-01042R0008000100 SECRET J'00 0.4 25X1A Approved For Release 2004/03/11 : CIA-RDP83-01042 Q00800010006-8 Approved For Release 2004/03/11 : CIA-RDP83-01042R000800010006-8 Approved Fpj Release 2004/03/11: CIA-RDP83-01 Q4R000800010006-8 Of ;t')(~ U, h t- 6-4- -,e S- I , G ~ C- .., 25X1A STATINTL Approved For Release 2004/03/11 : CIA-RDP83-01042R000800010006-8 Approved For Release 2004/03/11 : CIA-RDP83-01042M00800010006-8 STATINTL FOR : Circulation Action Coordination Information Filing v 0( Carding fj FORM NO. 59-93 AUG 1953 Approved For Release 2004/03/11 : CIA-RDP83-01042R000800010006-8 25X6 Approved For Release 2004/03/11 : CIA-RDP83-01042R000800010006-8 Next 5 Page(s) In Document Exempt Approved For Release 2004/03/11 : CIA-RDP83-01042R000800010006-8 Approved For Release 2004/SKGREIDP83-0104 09080001000 It SUBJECT I Transmittal of Scientific Intelligence ) e noranthn CENTRAL INTELLIGENCE AGENCY t-f ,CRIt? W TDs lir. Frank 0. Wisner Deputy Director/Plane 1. Our studies of unconventional warfare have included for acme time the potential, agent, Iyeergio Acid Diethylamids (LSD), which appears to be bettor adapted than known drugs to both interrogation of prisoners and use against troops or civilians, The Soviet Bloo has the necessary vqppliea of or; pt from which to a ntheaiss this drug. moreover, the Bloc is prosumably in full possesion of the pertinent information on it since it is oozmseraially available and open literature carries full accounts of experimental use. 2. Bo cruse we feel that the matter may be of concern to you, we are forwarding the attached Scientific Intelligence arandump which discusses briefly the intelligence implications of LSD. 0/sI has in production a detailed study on this drug that summa Izop the literature on the subject,, recounts the results of medical exporimontation with it, and deals with its possible synthesis and production. This study, ";trat?io I edical Significance of X raergio Acid Diet' ylaraido (LSD)", will soon bo available to those who have a paramount interest in the subject. ILLEGIB Aaaistant Director' xcientifie Intelligence Copies attacheds 1 - Cornelius Roosevelt, TSS 1 - W s Gibbons, Approved For Release 2004/03/ -V 11 LT3-01042R000800010006-8 25X1 C pp qd For Releas 2004/03/11 : CIA-RDP83-01042R000800010006-8 C.3' SCIENTIFIC INTELLIGENCE ME/VIORANDUM POTENTIAL NEW AGENT FOR UNCONVENTIONAL WARFARE' Lysergic Acid Diethylamide(LSD) (N, N - Diethyllysergamid .CIA/SI 101-54 5 August 1954 CENTRAL INTELLIGENCE: AGENCY OFFICE OF SCIENTIFIC INTELLIGENCE Approved-For Release 2004/03/11 C1A-RDP83-01 2 X1 Approved For Relea004/03 - - 10006-8 SECRET Scientific Intelligence Memorandum POTENTIAL NEW AGENT FOR UNCONVENTIONAL WARFARE Lysergic Acid Diethylamide (LSD) (N, N-Diethyllysergamide) This memorandum is based on intelligence ' available as of 1 August 1954 Office of Scientific Intelligence 44OA SECRET Approved For Release 2004/ - - 0800010006-8 CIA/SI 101-54 5 August 1954 25X1 25X1 4 a Approved For Rele 2004/03/11 : CIA-RDP83-01042R000r1010006-8 SECRE'T' Allen W. Dulles, DCI, 1- Charles P. Cabell, DDCI, 1 Robert Amory, Jr.;, DDI, 1 Frank G. Wisner. , 1 C/FI, 1 FI, 1 Willys Gibbons, C/TSS, 1 Cornelius Roosevelt, TSS, 1 Sheffield Edwards. Dir. Security, 1 AD 7 SECRET~ Approved For Release 2004/03/11 - CIA-RD P83-01042R000800010006-8 25X1 Approved For R ON . 200 - - 00010006-8 POTENTIAL NEW AGENT FOR UNCONVENTIONAL WARFARE Lysergic Acid Diethylamide (LSD) (N, N-Diethyllysergamide) Lysergic acid dietbylamide (LSD) (N, N-diethyllysergamide), a drug derived from ergot, is of great strategic significance as a potential agent in unconventional warfare and in interrogatioiis.* In effective doses, LSD is not lethal, nor does it have color, odor-or taste. Since the effect of this drug is temporary in'contrast to the fatal nerve, agents, there are important strategic advantages for its use in certain operations. Possessing both a wide margin of safety and the requisite physiological properties, it is capable of rendering whole groups of people, including military forces, indifferent to their surroundings and situations, interfering with planning and judgment, and even creating apprehension, uncontrollable confusion and terror. Of all substances now known to affect the mind, such as mescaline, harmine and others,' LSD is by far the most potent. Very minute quantities (upwards of 30 millionths of a gram) create serious mental confusion and sensual disturbances, or render the mind temporarily susceptible to many types of influences. Administration of the drug produces in an individual such mental characteristics of schizophrenia as visual or auditory halluci- nations and physiological reactions of dizziness, nausea, dilation of the pupils, and lachrymation. These reactions, however, are not necessarily obvious and only a trained observer, after giving pe.ychological tests, may definitely ascertain that a psychogenic drug has been administered. Data, although still very limited, are available which indicate its usefulness for eliciting trues and accurate statements from subjects under its influence during interrogation. It also revives memories of past experiences. In at least one case there was complete amnesia of events during the effective period. To date, no antidote nor specific counteragent is available. The effect of LSD may, however, be shortened in duration by the use of chlorpromazine, barbiturates, or the intravenous injection of glucose. Very limited methods of detection and identification are known, such as fluorescence, staining and spectrophotometry. Although the mechanism of action of this drug in the human body is not fully understood, it is nevertheless known to interfere with=the carbohydrate metabolism and to affect the ent`ral nervous system, certain of---the'.brain, hormones,..and other body funetiots. 4 *06I is - now completing, a detailed study of : LSD that gill- deal with the composition of the drug, its psychogenic properties,--its development, experimental use, and distribution. This study entitled "Strategic Medical Significance of Lysergic Acid Diethylamide (LSD)" will be made available to those with a paramount interest in the subject. Approved For Releas 2 00E/ - - 00010006-8 Approved For Rell--- 2(1041d 010006-8 25X1 LSD is a partially synthesized drug and was first prepared by Sandoz Ltd., of Switzerland in 1943. The unusually complex synthesis of the lysergic acid fraction of the drug, attempted by many workers during the past 20 years, has apparently not yet been accomplished by any country, progress in the synthesis of the drug in the United States is reported to have reached the last and most difficult stage. Completion of the syn- thesis will facilitate the rapid solution of many problems, such as that of an effective antidote, stability, more effective derivatives andJo=_ combinations, more accurate dosage ranges, adequate methods of specific detection, dissemination and complete control, for which there are still urgent strategic needs. The basic material from which LSD is prepared is ergot and the Soviet Bloc has an abundant supply of it. The preparation of LSD has been pub- lished openly in considerable detail. Further, Sandoz Ltd., has made available free samples of it for clinical testing both in this country and in Europe. It is therefore assumed that this material is available to the Bloc inasmuch as no effective geographic limitation is known. 25X1 Approved For Release/11 : CIA-RDP83-01042R000100010006-8 Approved For Release 2004/03/11 : CIA-RDP83-01042R000800010006-8 Approved For Release 2004/03/11 : CIA-RDP83-01042R000800010006-8 Approved For Release 2604/03/11 : CIA-RDP83-01042R000860010006-8 (SCE- ~~ P ~ v" _` C (A- O ILLEGIB t TRANSMITTAL SLIP STAT kawm,r5.~ BUILDING 11 REMARKS: FROM= -_._ BUILOI G ROOM NO;--' 1946 36-8 la a i N1L 2X1 A Approved For Release 2004/03/11 : CIA-RDP83-01042R000800010006-8 25X6 Approved For Release 2004/03/11 : CIA-RDP83-01042R000800010006-8 Next 3 Page(s) In Document Exempt Approved For Release 2004/03/11 : CIA-RDP83-01042R000800010006-8 25X1 SECURITY INFORMATION CENTRAL INTELLIGENCE AGENCY INFORMATION REPORT SUBJECT Review and Preliminary Report of Experimental Wank on the Pharmacology of Lysergic Acid Dieth,rlamide (LSD-25 ) - PLACE ACQUIRED (BY SOURCE)- DATE . ACQUIRED (BY SOURCE) DATE (OF INFO.) (a) diethylamine (LSD`-25) upon an.i.mal& and poisibl y` huffs. doing extensive-. research on the phys..ological effects. of,--lysergic acid OF THE UNITED STATES. WITHIN THE MEANING OF TITLE 10, SECTIONS 79% AND 714, or THE U.S. CODE. AS AMENDED. ITS TRANSMISSION OR REVE- LATION OF ITS CONTENTS TO OR RECEIPT BY AN UNAUTHORIZED PERSON IS TED. OF TH1) REPORT IS PROHIS I RODUCTION EREP PROHIBITED WY LAW. TH Oat 53 Oct 53 CD NO. 00/C N0. DAS N0. OCI NO.` DATE DISTR. i" NDV V NO. OF PAGES 6 NO. OF ENCLS. I SUPP. T 107- THIS Is UNEVALUATED INFORMATION REPORT US citizen, professor of pharmaeognosy at a major US university. He is well known in the field of pharmacognosy through many publications appearing in US scientific journals. ? His present- duti es include supervision of all development thid. research connected with the medi.ciralplant gardens maintained by his university. His work with the production of ergot and its alkaloids through natural means and by 6yn.thessis is recognized throughout the scientific world, (b) . US citizen, professor of pharmacology and executive officer of the School of Pharmacology at the Medical School of a major US university. He holds, a PhD in pharmacology and a degree of Doctor of Medicine. He, is pharmacognosy and pharmacology have worked together on this project which is about two thirds completed. Following is our combined preliminary report on the Swiss* controlled material; conduct-extensive experiments. In addition to the LSD-25 we were given a cash grant by Sandoz to partially support our research work. Our departments of (LSD-25-) by. Sandoz Pharmaceuticals, a diviiion-of Sandoz Chemical Works Ltd, to On 23 Jan 53 we 'were furnished an amplequantity of d-lysergic aaid diethyl.emide '-Lysergic acid diethylamide is a partially synthetic derivative of the ergot alkaloids obtained from the fungus Claviceps purpurea 'which grows ' as a contaminate on the fruit of rye.. Lysergic acid diethylamide belongs to the ergonovine group of these alkaloids and is obtained as a condensation product of d-lysergic acid .. with diethylamide.. It has the following structural formula: ' S-T PAGE FOR SLjlr~' T & ARIA CODES 25X1 SECURITY INFORMATION kIARMY NAVY AIR r 3-01 04 QOO80DO10006-8 This report is for the use within the USA of the Intelligence components of the ments or Agencies indicated above. It is not to be transmitted overseas without the eonr rrenee of the originating office through the Assistant Director of the Office of Collection and Dissemination, CIA. Approved For Release 2004/03/11 : CIA-RDP83-01042R000800010006-8 Approved Fo ele 25X1 ? ' , . sEC C "3 25X1A1 Lysergic acid diethylamide was fi'rst synthesized in 1938 by Stoll and Hoffman (1). Lysergic acid diethylamide is known by the code number LSD-25. It is soluble in., distilled water but dissolves best when four parts by weight of tartaric acid to one part of LSD are used. The material used in these experiments consisted of lea ampules each cc containing x.10 milligrams of LSD-25. This preparation was indicated for oral administration but in the animal experimentation the solution was administered parenterally, usually intravenously. "Description of the Action of LSD-25 on Humans 'Rinkel et al (2) described four effects of LSD-25 on humans. These are as follows: Phase 1, prodomal phase,- the period between the administration of the drug and the height of the reaction, lasting about 1 hour. Phase 2, the height of the reaction occurring 1 to 5 hours-after the drug has been given. Phase 3, the period from the height of the reaction for several hours a. Those referrable to the autonomic nervous system and comprising slightly increased blood pressure and heart rate, slight ' vasodilatation, nausea and occasional vomiting, slightly increased salivation, perspiration and lacrimation, dilatation of pupils, mydriasis,a slight increase in blood sugar, a slight and temporary increase in total white count. All of these symptoms were variable and all were not observed in any one subject. Indeed, some individuals responded in opposite and unpredictable ways. In general it may be considered that LSD-25 produces autonomic instability(3).. a _. b. Motor symptoms were those oaf- ataxia which was general]l y= slight)_ lack of precision in movements, slight incoordination and unsteadiness and occasional faulty speech in articulation. There was occasional facial clonism with clamping of the jaws, trismus and forced laughter. In some cases with high doses there was produced catatonia 25X1 observable after-the administration' of.. the drug'may be. divided' into',-t r Phase'.#,:- the after-effects lasting from one to . several days Signs Approved For Release 2004/03/11 : CIA-RDP83-01042R000800010006-8 roved For Release 2004/03/11 : CIA-RDP83-01042R 0 - 25X1 A 25X1 For Release 2004/03/11 : CIA-RDP83-01042R000 -3- The majority of Sensory perceptions are disturbed. Either by distortion or by hallucinations. Colors seem brighter and shadows more intense. In the dark there are hallucinations which generally consists of flashes of light, line patches of color or complex geometrical figures. There. is false. interpretation of noises, taste is usually lost, although some- times there is a metallic or bitter taste experienced. There is a feeling of strangeness and distortion of certain parts of the body. There is a feeling of depersonalization, and there is the impression of looking at one's self from a distance, of having lost control of one's real self, as if having changed and become more or less unreal and out off from the rest of the world. The acute effects generally.wear off in six to eight hours but in most cases there'is a more or less unusual-mental - condition persisting for the following day or for the following week. Sometimes the euphoria lasts for several days and there are periods of dreaminess alternated, with depression. Beaker (4) and Rinkel et al (2) state that there are two main types of psychiatric effects of LSD-25 Mania, expansive reaction with psychomotor excitement, euphoria. and less frequently depression. -conditions with lack of-facial expression and preservation of body -Posture, (3 )._ In human subjects the- mental effects are generally marked. Consciousness is maintained although occasionally disturbed:. There is a feeling of- intoxication. Judgment and memory are not usually- impaired:- The.' subject' to usually aware of his condition iud the fact-that-_be:is- eXperiencing effects due to- the administration-of the drug. Spatial orientation remains good. There is disturbance at time judgment., Attention and'concentration are reduced. There is some incoherence of ideas and the faculty of expression is decreased. Euphoria is evident by disordered activity. Occasionally shown by manic behavior with unmotivated attacks of laughter. Occasionally the euphoria is passive, apathetic and hebephrenia.. There may be tears, resentment, aggressiveness or passive withdrawal into indifference. Sometimes there are suicidal ideas. There is sometimes associated anxiety and paranoid trends. A schizophrenic reaction with slowing of mental processes, inhibitions, autism, depersonalization and hallucinations. subjects present a mixture of these two extreme types. "Pharmacological. Effects on -Animals- = s. Original'; observations on_I,SD2j were made iI miTe. These aanimals showei xditatory_ei 'ect5 of the drug and are most marked, in-'wa].tzing`_`mice ( ). n the dog there'--are evidences J of autonomic effects as..seen..in salivation Higher,doses produeecl motor, rigidity. in rabbits there is evidence of motor excitement in medium doses. It has been reported,--- that LSD-25 resembles ergonovine in that it produces contraction of the rabbit uterus It has been reported to have no blocking action to adrenalin in contrast to ergotamine. "EXPERIMENTAL PROCEDURES AND RESULTS ."Description of Effects'of LSD-25 'in Animals Rabbit administered 60 gamma per. kilogram intravenously showed after the lapse of three' to five minutes augmented placing reflexes and a slightly increased vigor of the righting reflex. This effect lasted from 10 to 15 minutes after which there was loss of the placing reflexes and loss of the righting reflex.-. There was dilatation of the pupil and loss of the response to light._ Cats administered 50 to 100 gamma per kilogram showed----=? increased alertness and appeared,to-freeze in attention-to-small movements of objects.:;.-. Later there was a, tendency for the animal to retire into dark corners where it remaIned immobile.. There was dilatation of the pupil and absence of reaction to light. The entire duration of. the effect was'about one hour after which the animal appeared to be normal. Dogs administered 50 to 100 gamma per kilogram showed incoordination in walking and evidence of excitement. This was followed by paralysis and dragging of the hind-limbs on Approved For Release 2004/03/11 CIA-RDP83-01042R000800010006-8 25X1A 25X1 walking but the animal preferred to remain immobile string at some object or corner of the room. These effects lasted one half; to one hour after which there was complete 'recovery of walking and running movements., "Action of- -25 0n Spinal Reflex Paavays transected at the level of.the medulla by means of a sharp scalpel. The wound was packed with a pledget of cotton to control bleeding. The frog was suspended from a stand by means of a hook through the lower jaw and allowed to hang free. Stimulation was applied to one or the other of the lower limbs by means of an electrode consisting of two parallel brass rods, 3 mm, in diameter separated 5 mm apart. The frog?s foot was placed between the electrodes and stimulated for one second with varying voltages from a Harvard inductorium. The endpoint, or threshold voltage, was recorded as a point at which a reflexing response occurred in the leg efficient to withdraw it from between the electrodes. This was recorded in 'stimulation units' each unit representing a 1 cm gap between the primary and secondary cause of the inductorium. The higher the nu irieal value of the stimulation units (SU) the lower the actual voltage. Between the application of test stimuli the.frog's foot-and leg was immersed in a 'beaker of normal saline. After a control period.of 30 to 60 minutes during which the threshold-voltage as measured by- the stimulating units was determi4ed. ':ze solution of LSD-25 was introduced into the anterior lymph sac. Results of these experiments are given in Table 1. N "Ipsilatoral Responses in Frogs. Large Rana'Pipien frogs verb used. The spinal cord was "Table 1. Ipsilateral flexion response of frogs with cord tray-section belCW the medulla. Dose Duration of Mean. threshold Mean threshold 8. "Experiment 1 2 3 4 5 6 .7 8 9 10 11 .12 13 1- 15 100.... . =30 100 = 75 : 75 100 90 90 200 4+5 60 200 105:-- - 105:;. 200- 120 120 11 11 11.5 11.5 13 15 12 15 12 11 13 13 15.5 13.5 R 9 11 1.1 13.5 1.2 11.5 10 12.5 9 10.5 12 12 15 - 1.1.5 12 16'. +5 +2 +2 +0.5 .$.1 -0.5 ...2.0 .-0.5 i.1.0 -0.5 45.0 +3.5 +2.0 0 42.5 -1.0 .13 . 10 x.2.0 -2.0 10 10 1.? .~1.0 .. 31.5 10 .) ..3.5.`43.0 1.2 10 2.4 +3.0__ 1. . 10.5 = 2 0; 12 18.5 `41.0 -3.0' 17 11 . 4 .2.5 0 . 'Threshold voltages are recorded in 'stimulation units' (SU) **Positive number are indicative of a higher threshold; negative figures indicate lowered threshold. "The general results may be summarized as follows s The threshold voltage required for evoking ipsilateral flexion--- responses was in most cases higher after instillation of.L LSD-25-., In some cases with higher doses there was complete abolition of, response=to the stimulus.-,regardlessof the increase in voltage b. The preparation studied represents essentially a three-neuron reflex pathway.. LSD-25 appears to act directly upon the neurons at the synapse. Its effect is characteristic of blocking or retarding conduction at this point. 25X1 in gammas eax. in minutes before LSD* After LSD* R L R_~ D 5 15 30 5 45 60 5 15 15 5 60 60 25 120 135 25 ? 120 120. 25 30 30 25 90 , 90 50 180 180 Approved For Release 2004/03/11: CIA-RDP83-01042R000800010006-8 Threshold Difference Approved 1t fem -5- This indicates that the quantity of LSD-25,requi.red to produce equivalent effects of ergotoxin is approximately six to seven times greater. approximately comparable- to that produced by' 3 gsmara of ergotoxin ethanosulfate -; one-strip; 20 gamma of LSD-25 produced.a depression of the'6pineph4ne contraction' emooth muscle was depressed in -the same -way .asit is depressed by, ergotoxin On and?20 gamma or LSD-25 were added `td. the--50-ml. bath -the :epinephrine 'response of the uniform response to :.standard. :amiount--of.epinephrih.e quantitips -of 4, 5, 10, 15, the LSD-25 epinephrine antagonism' vas studied. After the determination of a "Using isolated rabbit uterus strips maintained in a standard smooth muscle bath "SU 4MARY a. Lysergic acid diethylemide produces evidences of autonomic effects and motor effects in intact rabbits, cats, and dogs. b. It produces blocking of spinal synaptic transmission in frogs and cats. There is no effect at the' myoneural juncture. a. It is capable of diminishing the epinephf?ine effect on isolated rabbit ? uterus . a. These experiments in frogs leave the possibility. of inaction at the myoneural juncture which will be experiment. "Effect of LSD-92 on the Spinal Cat-Flexor Response. considered in the following 25X1A 5X1 "A decapitate cat preparation was used in the following experiments. The eat was anesthetized with ether. The trachea was. cannulated, the common carotid arteries were isolated and ligated anteriorly and posteriorly and sectioned between the ligations. Using a 30 amp cautery the muscle structures and other tissues were divided exposing the spinal column at level C2 or C3, A heavy cord or wire was then tied around the exposed bony spinal column and wouni tightly to reduce hemorrhage by compressing the vertebral arteries. The spinal column and cord was then out through anterior to the ligature. As soon as possible after this cord section artifice.1 respiration was begun. A blood pressure was recorded from one of the common carotid arteries. A venous crnnula for the administration of the drug was introduced into the right femoral vein. The left femoral nerve was exposed and sectioned and the tendenous insertion of the left tibialis anterior muscle was isolated and connected to a recording lever. The left sciatic nerve was exposed. The nerve to the ham string muscles was sectioned and arranged for satimulatio.. The muscle twitch was recorded after the bone of the left leg was exposed and pinned securely. Warm saline packs were used to protect the exposed nerve structures. between the application of stimulations. Ii this preparation it is possible to.. elicit muscle contractions as the result'.of stimulation at two points. The stimulation may be applied to the nerve leading directly to the muscle in which case the effect of the agent on the myondural Juncture may be tested; or the stimulation may be applied to the sciatic nerve in which case the pathway traverses the spinal cord. It was possible to show that the LSD-25 did not affect transmission to the muscle through the myoneural jungture, the threshold stimulils remaining constant after the administration of the drug. The LSD-25 did affect transmission through the spinal cord synaptic junctures, diminishing the conduction and eventually blocking this pathway entirely. It was not possible to secure recovery of the preparation and restoration of the pathways and it is believed that the effect of the agent extendr beyond the life of 'the decapitate preparation. 10. "Symphatholytic Effects of LW..25 SECRET 25X1 Approved For Release 2004/03/11 CIA-RDP83-01042R000800010006-8 Approved r r Release CIA-Rut-83-0 1 T -6_ 25X1A; I X1 Rinkel, M De Short, H J Hyde, H W and Solomonr, H 0, Amer Jr Psyehiat, 108 572, 1952 De Shone; H J Rinkel, M and Solomon, H C Psychiat. Quart-26: Becker, A M Wien Z Nervenhk, 2: 402, 191+9. Rothlin, E and Cerletti, A Rely Physiol, 10: 319, 1952." - end 614.4 29M 644.oi 29M SECRET/ 25X1 Approved For Release 2004/03/11 : CIA-RDP83-01042R000800010006-8 DEC 1951 a a-'" 25X1 Approved SECRET SECURITY INFORMATION CENTRAL INTELLIGENCE AGENCY. INFORMATION REPORT COUNTRY UKfSw.tzerland SUBJECT Experimental Psychoses and Other Mental Abnormalities Produced by Drugs PLACE ACQUIRED (BY SOURCE) DATE ACQUIRED (BY SOURCE) 11 Aug 51 to Sep 53 DATE (OF INFO.) Sep 53 THIS DOCUMENT CONTAINS INFORMATION AFFECTING THE NATIONAL DEFENSE OF THE UNITED STATES. WITHIN THE MEANING OF TITLE 10. SECTIONS 793 AND 194. OF THE U.S. CODE. AS AMENDED. ITS TRANSMISSION DR REVE. LATION OF ITS CONTENTS TO OR RECEIPT BY AN UNAUTHORIZED PERSON IS PROHIBITED BY LAW. THE REPR D CTION OF THIS REPORT IS PROHIBITED. THIS IS UNEVALUATED INFORMATION RES PONSIVE TO i t CD NO. OO/C NO. ORR NO. DAS NO. 3o OCI NO. 25X1A DATE DISTR. jV s 3 NO. OF PAGES NO. OF ENCLS.- SUPP. TO REPORT NO. SOURCE US citizen who is on the faculty of the medical school at a. major US university. He is a professor of psychiatry who has done considerable research on the effects of various drugs on the oentral:'nervous_ .system : : Oe:.of'his.,,najor fields of interest is research on the psychic changes brought about by dosages, of d-lysergic acid diethylamide. 1. I have read with interest the extract from the British Medical Journal dated 11'Aug 51 and titled."Experimental Psychoses and Other Mental Abnormalities Produced by Drugs." The author, W Mayer-Gross, MD, FRCP, director of Clinical Research, Crichton Royal, Dumfries, is well qualified to discuss this subject. Our university is conducting clinical studies on d-lysergic acid diethyl- amide (LSD 25 ) 41ii-cDi" l w an exc.Tve product of Sandoz Ltd, a Swiss pharma eeutieal company 1e:purpose of='=these investigations is to determin the 'human and animal pYi'rsia-logical' and psychic reactions Ito this substance LSD-25 is a synthetic amide` prepared' from natural d-lysergic acid and diethyl-' amide. D-lysergic acid is the basic component of the alkaloids of ergot. Dr Mayer-Gross describes the mental reactions following dosages of mescaline, a substance which has been.described in medical journals for many ars. It is his opinion that the symptoms produded~b. ,5D 25. appear to }~t3 c ps~e tQ those II , produaed^bIcm si alihe dedpit cthe; .wid9 'chem :aelidif-fo eiao@ betwe@oi#> @Stwo products, LSD-25 is many times stronger than mescaline or than any other known sub- stance similar in nature. Dr Mayer-Gross sees value in the self use of LSD-25 or mescaline by psychi- atrists as they provide a safe means for them to be temporarily transformed into the strange'vorld of. some of the mental patients they are trying to treat. Our research on LSD-25 has not been thorough enough to make this same statement -- we have not used the material on human subjects. We do feel, however, that psychic reactions from mescaline and LSD-25 are somewhat the same. available on loan from the CIA Library is the text of W Mayer-Gross, MD, FRCP, article entitled. "Experimental Psychoses and Other Mental Abnormalities Produced by Drugs," dated.'ll Aug 51J LIBRARY SU 3J ? 'T APEA (ZO ;ES 25X1 SECRET . SECURITY INFORMATION X Approved For Release,;2004/03/11: CIA=RDP83-01042R000800010006-8 VW 1951 -r'"N' _ 25'1 SECURITY-INFORMATION SECRET. CENTRAL INTELLIGENCE AGENCY INFORMATION REPORT COUNTRY. USSR SUBJECT Soviet Organic Chemist: I Rapoport PLACE ACQUIRED (BY SOURCE) DATE ACQUIRED Aug 53 and earlier (BY SOURCE) DATE (OF INFO.) Aug 53 THIS DOCUMENT CONTAINS INFORMATION AFFECTING THE NATIONAL DEFENSE OF THE UNITED STATES. WITHIN THE MEANING DF TITLE 18. SECTIONS 793 AND 794. OF THE U.S. CODE. AS AMENDED. ITS TRANSMISSION OR REVE- LATION OF ITS CONTENTS TO OR RECEIPT BY AN UNAUTHORIZED PERSON IS PROHIBITED BY LAW. THE REPRODUCTION OF THIS REPORT 15 PROHIBITED, THIS IS UNEVALUATED INFORMATION RES PONSIVE TO 1 2 CD NO. 41-13400 OOIC NO. ORR NO. DAS NO. ? 7 OCI NO. 25X1A DATE D I STR ;Llt S'e,pr f $ NO. OF PAGES 2 SUPP,. TO REPORT NO. SOURCE Naturalized US citizen of Russian birth, a chemist and fluent. in the Russian language. He holds BS, MS and SoD degrees in chemistry from US universities of high stand- ing and is currently teaching chemistry and doing original research in organic chemistry at a US polytechnic-institute, He was formerly a research chemist for two large US industrial corporations-. For the past several years he has been translating and digesting articles of scientific interest appearing in Soviet publications. He is a long-time source whose great number of reports have been, practically without exception, of intelligence interest and have received high evaluations. Interest has been expressed in your comments on the work of I Rapoport dealing with mutations. Can you sup y a, p l name, a list of his publications and his present position? - I am not surprised at, the ? interest mdhifested ' in: Rapopcrt'w! woA... As I. have stated; his'work:on mutatio s may beextremely significant from a BW standpoint.? . Unfortunately, my knowledge of Rapoport is confined_.tothemeagre information, given in Soviet scientific journals.-- Such Journals rarely give the full names of an author but merely list a patronymic and one or more initials. Moreover, the listings are not always uniform or consistent. In the following list of publications the patronymic "Rapoport" is sometimes preceded merely by the initial "I". At other times, it is preceded by the initials "I A". I am unable to state whether "I Rapoport" and "I A Rapoport" are one and the same individual. The following is a list of all publications attributed to "Rapoport" which I have seen in Soviet scientific literature: L Shtern and I Rapoport, Compt rend sec biol USSR, 97,366-8 (1927) Concerning-the_mechanism'of passage of various substances from the blood into the "OerebrnBpii nal, fluid,I i r3 L Shtern, I Rapoport and L Kremlev, Compt, rend sec biol USSR, 97.,61+4-5 (1927) Effect of thyroidectomy and castration on the function of the hemato- encephalic barrier. $EE LAST PAGE FOR, w UBJECT Se AREA. CODES ww 11 25X1 .OISTRIBUTION ? STATE i IARMY NAVY x AIR X I FBI OSi B This report is for the use within the USA. of the Intelligence components of the departments or Agencies indicated above. It is not to be transmitted overseas without the concurrence of the originating office through the Assistant Director of the Office of Collection and Dissemination, CIA. Approved For Release 2004/03/11 : CIA-RDP83-01042R000800.010006-8 ((r.1 i j~(1tiI~,+ -01042*6080001004r 2...~ 25X1A Approved Fc JgjtaRg 4/03/11 : CIA-RDP83- 104cR 080 Security 2 - I A Rapoport, Bull biol med exptl, URSS?7,415-17 (1939) - Specific morphoses Chemistry of the Academy of Sciences of the USSR in Moscow. in Drosophila induced by chemical compounds. I A Rapoport, Bumazhnaya Prom 18, No 7, 34-8 (1940) iontan wax, its I A Rapoport, Compt rend acad sci, URSS 27, 1033-6 (1940) - Effect of thy- monucleic and nucleic acids and of some of their compopents on mutations. disturb the symtnetry,in the organism. I A Rapoport, Compt reridacad sci, URSS,.27, 369-72 (1940) -xSubstances'which properties and use in the paper industry. I A Rapoport, Sbornik Dikhloretan, 92-5 (1939) 1 1 Regeneration of oils from I A Rapoport, Sbornik Dikhloretan, 96-9 (1939)- Degreasing metallic shavings. wiping materials. I A Rapoport, Sbornik Dikhloretan, 52-91 (1939) - Use of dichloroethane in .extraction processes. . Extracting wool-spinning waste with dichloroethane. I A Rapoport, J Chem Ind USSR, 18 No 22, 8-10 (1941) - Extraction of, Ukrainian brown coal. I A Rapoport, Sherstnyanoe Delo, 19, No 5, 12-13 (1939); also 18, 20-2 (1939). action, of mutational factors, I A Rapoport, J Gen tiol USSR,.1+., 65-72 (1943) Oxidation and mechanism of I A Rapoport, J Gen Biol USSR 8, 359-79 (1947)- Chemical reactions with the protein amino groups in gene structure. I A Rapoport, Compt rend acad?sci URSS'54, 65-7 (1946) - Carbonyl compounds and the chemical mechanism of mutations., I A Rapoport, Byull, eksptl Biol Med 23, 198-201 (1947) - Derivatives of of, diethyl sulfate and dimethyl sulfate. ..I A Rapoport, Doklady Vsesoyuz, Akad Sel'sko-Khoz, Nauk in V I Lenina, 12, No 10, 12-15 (1947) - Inheritance changes taking place under the influence carbaminic,acid and mutation.. I A Rapoport, Dokiady`Akad Nauk. SSSR, 60, .469-72 (1948)-- Action "of, ethylene; oxide,. glycidol ;and glycols on gene, mutations molecules. 25X1A I A Rapoport, ~ Dokiady Akad Nauk SSSR, - 59, _1183w;6 ~194:8) ' - Alkylation of gene:: . I A Rapoport,.Doklady .rkad Nauk SSSR, 61,?713-15 (1948) - Mutations under. the influence of unsaturated aldehydes. I A Rapoport, Am Naturalist, 81, 30-7_(1947).- Synthesis of gene products in equimolar quantities. I have no information concerning Rapoport's present connection or position. I know only that, he was, at one time, connected with the Institute of Organic LIBRARY SUBJECT & AREA CODES CI/.O'7' /' ApproAN' 25X1 25X6 Approved For Release 2004/03/11 : CIA-RDP83-01042R000800010006-8 Approved For Release 2004/03/11 : CIA-RDP83-01042R000800010006-8 25X1. SECRET, Approve or Release 004/03/11 : - - 0010 SECRET 'LSD-25 has the potential of being an aid in the treatment of mental patients. -c. LSD-25, if improperly used is a dangerous material--- it creates serious mental confusion. and makes the human mind temporarily susceptible to suggestions. No research has been done to determine what permanent damage could be done to the human mind.if the material was administered over extended periods., d. LSD-25 could be used in the interrogations.of`unwilling subjects for the purpose of getting them to "confess" as the material stimulates subjects- to talk more freely'. LSD-25, because of- its potency., could possibly be used in the-contamino- tibn of food and water for the purpose of rendering whole groups of and situation. Our investigations thus far substantiate the findings of other investigators but we have carried our research on animals much further than others working on LSD-25. We can take no serious exception to the printed material furnished us by Sandoz Ltd which gives a summary of extensive research on ISD-25 as of November 1952 and "CHEMICAL CONSTITUTION: D-lysergic acid diethylamice isa partially synthetic der.vative obtained_by condensing D-lysergic acid, extracted from ergot of` rye, with a secondary amino.,. diethylamine. Thus LSD-25, first prepared in 1938 by A Stoll and A Hofmann , L5ee notes at end of report belongs to the ergonovine group. LSD-25 is. soluble in distilled water, a process. facilitated by adding crystalline tartaric- acid "D-LYSERGIC ACID DIETHYLAMIDE (LSD-25) In certain `respects:LSD_ resembles`ergonoyine to that of ergonovine and ergotamine (the IUD 50 in mice of intravenous LSD-25 is 65 mg/Kg, of intravenous ergotamine 84 mg/K; and of intravenous ergonovine 25 in+ro the anaesthetized rabbit produces motor excitation. In the dog the first apparent effects of LSD-25 'are of a vegetative nature, e g copious Approved For Release 2004/03/11 : CIA-RDP83-01042R000800010006-8 25)K (the'` uterotonic effect` of LSD s n-'the rabbit uterus in situ is 7/lO` of:.that of '?- ergonovine).. LSD exerts-no adrenosympq,thicolytic action (a contrast to the alkaloids of the ergotamine and ergotoxine groups) and its toxicity is similar, 125 mg/Kg.) However, LSD-25 may be clearly distinguished from all the other ergot alkaloids. so far investigated in' other respects,.- The injection of,-.a small :dose :of LSD-..-- 25X1 -3- salivation, without any significant change in affective behavior. High doses of LSD."25, like bbulbocapnine, cause-motor rigidity in the dog and cats a condition On the normal mouse, LSD has a subtoxic dosage level. Mice with hereditary waltzing anomaly are more' sensitive. to this drug. state, but with simultaneous suppression of waltzing movements (ROTHLIN, CERLETTI 25). Subcutaneous doses of no,more than three percent of.the LD 50 increase the general excitatory DELAY et al studied the effect of LSD on the electrocorticogram of the rabbit, 15 Doses of 40 mgJKg (average) injected intravenously or into the carotid artery caused marked or even complete flattening of the tracing. The effect was .progressive, setting in after approximately one minute and lasting one - two hours. The effect was clear-cut even after dose8 as small as-18-2O mg/Kg. An identical effect was noted'after massive doses (300-600 mg/Kg). There was simultaneous marked motor hiyperexcitability. LSD inhibited the spontaneous rhythmic activity; it did not prevent the response to electrical stimulation, the epileptic'$pikes, the bursts of rapid spikes produced by barbiturates or cortical trauma. Of the. vasodilator substances investigated, nicotinic acid, dibenamine; bexamethonium,'priscol and alcohol did not modify ;tl effect of' ISD Acetylcholine,givep intravenously,indoses_ of 20-k0 mg/K c.,"caused the reaiTearaiice of. burs.ts of_ basal. rhythm. `? Urethane' and chloralose'did not modify the effect of ISD "EFFECTS OF LSD ON HUMAN BEINGS: the mental effects exerted by LSD in human beings. Hofmann discovered' these The above mentioned animal experiments do not give any hint whatsoever as to effects by accident and then carried out investigations on himself which were yet been published. reported by W Stoll Studies on the- effects of LSD 25 in normal subjects have 2 6 8 10 been carried out by W Stoll ;,_Condrau , Becker , Georgi et al , Rinkel et al 3 11 17 1; Matkfi 3 dyer -Gross. s_.Weil'-and other; research_.workers-, whose reports have not 25X1 SECRET/ Approved For Release 2004/03/11 : CIA-RDP83-01042R000800010006-8 25X1P The effects-of LSD have been investigated in psychotic patients by Stoll 25X1A 25 X1 21+ De Giacono , Forrer and Goldner , Condrau , Busch and Johnson , Hoch it al Savage 27 9 and Belsanti. Rostafineki has made' some experiments with LSD in epileptic, grouv. However, this'is not the case with the mental effects, and therefore respond in almost the same manner to ISD and may, 'therefore, be considered as?one As far as systemic effects are concerned, both normal and psychopathic subjects normal and psychopathic patients have to be considered separately in this respect. Active and maximum dosess Up, to the present, LSD has always been admin istered orally,-generally in the morning on an. empty stomach. LSD is active in very small doses. In certain subjects the characteristic effects are observed. after the administration of a dose as small as 20jttg (microgram dose of .l+0-100 / g (about -lpg/Kg body weight) is active in most cases Doses as In general psychopathic patients show greater resistance to the systemic and psychopathic patients high as 500 fig (= 0.5 mg) or 6 pg,/Kg body weight, have been well. tolerated by mental effects of LSD than do normal subjects. Onset and duration of actiona The first, effects of an active dose of LSD generally appear within one-half - one hour (maximum three hours), Maximum effectiveness is reached, on :an average, after two hours and the effects persist Delayed_effects may be. observed for`. one one. week; .' Rinkel et all-" recognize four--phases - in reaction- to LSD. Phase. I: the prodromal phase;-represents the period- between f one hour. Phase II represents-the height of the reaction, occurring one-five hours after the drug had been given. Phase III was the period from the end of the administration of the drug and the height of the reaction. It lasts about the height of the reaction until evening. Phase IV comprised after-effects last-. c. Systemic effectst Distinction. may be drawn between vegetative - symptoms,. fairly slight effects on metabolism and motor symptoms. 25X1 SECRET/~ Approved For Release 2004/03/11 :. CIA-RDP83-01042R000800010006-8 7, 19. Vegetative symptoms:' 2,5,7 5,10 Giddiness. ;."empty-headedness," 2 isolated,.cases general-malaise.._ feelin 10 shaking. ,f Effects of LSD on: (1)'- Cardiovascular system: occasionally headaches .5,1? 5 of._weakness , fatigue tremor and 25X1 Approved SECRET -daily Blood pressure8 Slightly increased, within physiological limits 10 2,5 or not modified ; less frequently slightly decreased In.exceptional cases danger of collapse '. Two patients developed profound circulatory depression . x,7,8,11 10 Heart rates increased or not modified 2,3,5 decreased Vasomotor functions: flushes of 5. 25X1 SECRET Subjective impressional sometimes 5 discomfort ) Digestive system: 2),5,6,7,10,19 Anorexia, sometimes nausea occasionally vomiting 5,7,1 5 and. in isolated cases lyocrexia 2,5 palpitations - or precordial tests such as" .the Takata-Ara and ? the Hi jmaA ? -.v d Borg' reactions:- the quick test (excretion of bippuric acid following ingestion-of .In isolated cases sodium benzoate) or the caphalin-cholesterol flocculation test 3)+,8,27 show no,change , the Snapper test (determination of glucoronic acid in the urine after administration of cinnamic acid). reveal's slight, temporary disturbance of hepatic function . It should_be noted that the Quick.-,test-and the Snapper test"are positive in schizophrenia and mescaline intoxication . Subjects in whom even only, a slight modification of hepatic function is present (e g cases where there are protracted'sequelae of infectious hepatitis) make-a very marked response-to LSD Approved. For Release 2004/03/11': CIA-RDP83-01042R000800010006-8 25X1 25X1 2, 3, I,.5 Usually not changed ; respiration sometimes dee:Rer and 2,3,5 25X1 SECRET/ No changes in composition of urine iiuresis"sometimes increased In isolated cases.retentIon of.i 6 the effects of LSD had worn off 2,5,6,19 2,5,6,7,1 10,19 warmth or cold , sometimes periods of shivering No.change, in exceptional cases increased by 1?F . Feeling of Temperature: (8) Saliva secretion:' (9)? Sweat secretion: k,5,6,5,10- Often increased 2 Often increased (10) Lacrimal se'cretiont' Sometimes increased (11) Pupils: 2 Generally dilatation reaction to ;light mydriasis less modifications in the differential count or relative neutrophilia Slight increase in potassium blood values, no change in calcium 3, 27 2 blood values Savage observed some tendency for anaemia to appear during prolonged treatment (20-100 ug_daily for one month). Blood sugars3 In 24 subjects Mayer-Gross et al found that LSD caused a slight, Slight- risey-within physiological limits ; less1 frequently a fall :It J: Approved For Release 2004/03/11 :,CIA-RDP83-01042R000800010006-8 25X1 Approved 1~ or- Iease 2004/03/11: IA-RDP83-01 42Rd60800 SECRET transitory increase in the glucose and hexosemen-ophosphate levels n the blood.; Otherwise: carbohydrate 'metabolism? was riot affected. LSD interrupts the break down of glycogen at the hexosemenophosphate state. "The'intravenous injection of 33% glucose solution modified'. LSD tends to produce amphotonia. The rate and the dilatation of the pupils suggest The nausea and the"periods of vasodilation suggest parasympathetic hyperactivity. However,, it should be noted that there are great differences from indi- vidual to individual. Some subjects respond. to LSD.with a fall in blood pressure, 3,13 bradycardia and other symptoms suggestive of sympathetic inhibition. In general, LSD produces vegetative instability which may tend sympathicotonia or to vagotoi(ia, depending on the individual subject. Motor symptoms:- LSD causes disturbances of voluntary motor functions (which are generally incoordination. LOA i SECRET/ Ataxia: generally not pronounced, lack of precision in intentional movements,. slight degree of.incoordination, occasionally unsteadiness of- 2 4 s 6 , gait, ,=_ Aij. Occasionally faulty speech articulation ?, ::: :n`:_:, r: 2, 5, 2 { -,.2 slightly positive-.?_--2. Sometime s'tremor.of the hand and twitching of the eyelids Often facial clonism, 2,5,6,7,8,10 - ` cramps of the jaws, trismus and forced laughter .. Sometimes 2,4,5 3,5,7,10 of tendon reflexes . Sometimes motor excitement in exceptional cases athetoxic movements In certain cases high doses- 3 and perservation of body posture-. Aggregate-of. motor: ; symptoms t.; The most frequent motor effect of ISD may an increase in sympathetic tenus. (300-500 mg) produce catatonic conditions with a lack of facial expression of muscular hyperexcitability accompanied by more or less pronounced signs of The catatonic effect of high doses has increase in blood pressure and heart Approved For Release 2004/03/11: CIA-RDP~ as_yet, only been studied be described as aslight degree 3-01042 R000800010006-8 25X1 (2) Depression.whichmay bey; demonstrative' with. teers, resentment-,!"r.'10,14': aggressiveness or passive with negative withdrawal into't -even complete indifference ._-_ , some- ?5X in five cases. 25X1 SECRET/I Approl SECRE'ij e or Release - Mental effects in normal subjects: Consciousness, orientation*.", Consciousness generally maintained but" occasionally slightly clouded- ; a feeling of intoxication j, often occurring in a wave.- 6 2 pattern of outbursts . In exceptional cases short periods of confusion As a rule,. judgment and memory are not unpaired: -The subject is conscious of his condition and does not lose sight of the-fact, that what he.is experiencing is due to the drug ingested Certain subjects, notice that their - 6 of self-observation and introspection are increased Spatial orientation remains'good.' The notion of duration of time is .2,5,6,8,10,11 .often disturbed, time seeming to pass too quickly or-too slowly Ideation: may be accelerated, accompanied sometimes by incoherence, and "running away" of,ideas in other cases ideation is slowed down and the faculty of 2,8;16: expression inhibited . Often a tendency to preoccupation with one idea. 2,5,6,8,11 Attention and,concentration are reduced Approved For Release 2004/03/11: CIA-RDP81 a1 -Affectivity and behavior: Several types of reactions may be.observed: (1)' Marked euphoria made evident by disordered activity, manic behavior, more or less unmotivated attack of laughter, or even involuntary 2,5,6,10,1+,17 Less frequently the euphoria rs 8,10,17, passive, apathic and,hebephrenio self, autism, apathyand 2,6 times suicidal ideas 2;5,17 "(3) Alternate phases of euphoria and depression 2k In addition to these effects, there is sometimes associated anxiety paranoid trends , or the fear that the abnormal state will persist,or will be 2,5,6 noted'by a third party In general,--under the effect of LSD en enhancement of the previous -.._.. C affective state whether constitutional or temporary may be , observed . The 2,8,10-. euphoric reaction seems, however, most.frequent -01 042R000800010006-8 25X1A Behavior is controlled by affectivity.,In cases -of hypomanic euphoria, the. disordered activity is often accompanied by logorrhoea nd loss of inhibition; the, subject cannot prevent hiinsel#' from'-saying what he thinks affective'contacts. On the other hand., often all affective contact is suppressed and the apathy may even develop into- 6,1c a state of stupor 2 - Sedative effects on sexuality Sensory perceptions2 Disturbances of. perception are frequent and sometimes very pronounced. Either the object perceived is distorted or there are hallucinations 'generally of an elementary nature: Vision: Often the objects appear distorted,'perspective is incorrect, distances are overestimated, colors seem brighter, shadows very intense and contours very 2, 5,'6, 8,11,11+ - clear-cut_ Less frequently the`outline of the object seen is less 6 distinct and colors are dull Certain subjects qxperience hallucinations especially if they are in the dark and their eyee are closed.. These hallucinations generally consist of flashes of light, lines, patches of color, sometimes more complex geometrical figures, objects, flowers and animals In exceptional cases the visual hallucinations-are provoked by auditory stimuli affected. Food?--and cigarettes 2,58,10_,}- --- Sometimes metallic or bitter taste In rare cases olfactory 11 hallucinations, e g garlic odor seem_,tastelese 2,5,6,8,10,11,19 Hearings Often hyperacusia and false_ interpretationof noises. -, Less frequently - .true`..s,uditory hallucination-A- e g sound- of a bell:y Frequently distortion, hypoesthesia and paresthesia: things feel -206 different . In isolated cases true tactile hallucinations, e g sensation of Touchy 10 being wet from urine 25X1 SECRET) . General bodily feelings! Feeling of,strangeness or distortion of--certain parts 2,5, ,8,10,14 of the bodyQdT - - ! the sub jeet?has the impression that his head is, enormous, that, one limb is excessively long or separated from the body, that his nose is not in its right place, that his arm "no longer belongs to him" or that his body weight has decreased or increased. 8000100 Approved For Release 2004/03/11 CIA-RDP83-01042R000800010006-8 25X1- SECRET/ - 10 - Personality: In certain subjects LSD produces a-feeling of depersonalization or of 2,5,6,10 split personality of a clearly schizophrenic-nature , Impression of looking at one's self from a distance, g of, havin lost control'of. one's real self, of having changed and become more or less unreal and cut off from the rest of,the world. _s_.R These phenomena are generally associated with the cenestheticdisorders 'as well as with autism, withdrawal and indifference. These personality disorders are less frequent in subjects who make a manic euphoric or depressive response to LSD. 10,13 - Psychological tests: Rinkel ' ` carried out Rorschach's test on five subjects under the influence of LSD. The results of the test confirmed the clinical observations` of the effect of LSD in each of the five individuals:. autism, negativism, weakening of powers of logical reasoning, anxiety, depression, and aggressiveness. Another test ("concrete-abstract thinking") consisting of noting reminiscent of those of schizophrenic patients, (predominance of-concrete re- sponses; abstract responsescduld.be obtained with effort but were characterized by overgeneralized and tangential thinking). Rimmel did'not employ these. tests in persons who made a manic depressive response to LSD. In an alcoholic, a Rorschach's test carried out just after the subsidence of the LSD effects showed profound changes over the previous tests . 13 Matkfi studied the effects of LSD on himself*He made a series of drawings supposed to - represent the -same person _eiphentest' =).- chile' under -the th influence of 'LSD and found -that- his strokei the drawing became larger, and even went- off the paper 'In"spite of all his efforts, he could not coordinate his drawing with what he saw, whether it was. normal or not. When the height of the LSD effect was reached, he made a drawing Electroencophalogram: EEG tracings have been taken, as yet.. in only about 15 10,13 4 10,13 cases. - There- have been slightor no changes:.. Rinkel:....v. found,, in.general-,_-.-_ an increase in alpha rhythm of one-three waves per second, but in one very . relaxed subject the alpha rhythm was slowed by two waves per second. - In eight--. - cases out of nine he noted a pronounced increase in muscle activity. 25XAECRETJ 25X1 Approved For Release 2004/03/11 : CIA-RDP83-011042R000800010006-8 Approve - - 0 SECRET every case a more or less unusual mental status persists In the evening. after 'the"experiment, euphoria, logorrioea, difficulty of concentration and sometimes great fatigue are noted. The'subjects generally- sleep well, but'the following morning certain of them complain of a "hangover," similar to that produced by excessive amounts of alcohol. However, by this time 2 most subjects have returned to their normal status . Sometimes the euphoria lasts several days .Less frequently.a depressive state is observed.. This may last several 6,8 days One subject exhibited periods of dreaminess (with feelings of strange- . ness, of "deja vu" and'disturbed general bodily-feelings), alternating with phases 6 -- - of depression -,after a single dose' of 18D. These delayed effects often occurred 13 Aggregate. of psychic effects Fin normal subjects: .The symptoms-produced by LSD` have been considered by W Stoll as the expression of"anacute exogenic psychosis, analogous to those produced-by alcohol; opium, cocaine, hashish, mescaline and the, 23 amphetamines (however, all these substances are only active in far higher doses ). There is'no uniform reaction .to ISD. Two main types may be distinguished a schizophrenic reaction with slowing of mental processes, inhibitions; autism, depersonalization and hallucinations: The majority-of subjects present a mixture of these.two extreme types. 6 Becker attributes the manic response to,the action of LSD on the sphere of intention and the schizophrenic reaction to the action of LSD on the sphere of, affect. In general,. #: feuds-to-reinforce pre-existing: tendencies,. producing a,r4 caricature of the subject : the cyclothymic patient often becomes euphoric and 5 6- expansive while the schizoid becomes a true schizophrene . Thus LSD reveals latent 25X1 SECRET P83-01042R000800010006-8 25X1A 25X1 Appro a or Release - - SECRET) tendencies-and its effect may be considered,'to a certain degree, as.a personality '2,5,6 LSD makes it possible for the psychiatrist to study in himself some of the mental symptoms which he is called upon to analyze and. treat in his patients. This experience is often instructive -. 2,6 LSD 25 and Mescaline: The first workers to carry, out research were struck by the. analogy between the 'intoxication' produced.by LSD and mescaline delirium, although the active doses of these two products are quite different (mescaline at least 0.2 Various that of LSD 8' g a c. LSD generally less been found when comparing animals. The lethal dose ., ?u_ ..._---~- ------- -- -- - _.-_ ____ _--_-- -- _ - 8,11 comparative studies carried out on the same subjects have shown L'S'D produces, above fall else, manic depressive or hebephrenic symptoms In other words,-an expansive or foolish euphoria of periodic depression predominates lessness, stupor, personality, disturbances or hallucinationsare predominant. With'mescaline; on the other Land, catatonic symptoms such as rest- while the hallucinations and depersonalization are fairly slight. LSD and mescaline do not exert.the'same actions on nervous centers in lower animals. According-to-Witt' -these two substances have opposite effects. on the behavior of spiders "(as ' determined. by web' pattern _and purposefu1ndso: oft--the 19 Mescaline produces fairly important changes in hepatic function demonstrable increase in anxiety occurred frequently with- mescaline-1 usual laboratory than 0.0001 g 100 mg). An analogous relationship has the toxicity of the two substances 'in cold-blooded of mescaline, in tadpoles, is 100-1000 times greater than tests, whereas LSD produces'a much slighter change which is only made evident.by an ultrasensitive test 8 e. Effects of LSD,25 on psychopathic patients: Generally psychopathic 2,3,5 patients are much less sensitive to LSD than normal subjects . The vegetative and motor effects often appear only after the administration,of very high doses, e g tvo-three mg/Kg. Mental effects- are generally less marked and difficult to evaluate in patients who have, in any case, similar symptoms before treatment 25X1 SECRET 83 a1042R000800010006-8 25X1 25X1 under the effect. of iSD. '. Approve - - 00 SECRET13--- and in whom there may be very great spontaneous variations in effect . It is also possible that-the negative attitude and the tendency towards dissimulation- However, in 'practically every case there are certain behavior changes - which are generally accentuated if the dosage of ISD is increased With regard to psychomotor affects, LSD generally produces, sometimes even in stuporous schizophrenics, an increase in activity and verbal expression 4, 5, ? which may, especially in manic patients, develop as far as pronounced After very high doses (30p-500 mg) De'Giacomo observed in five cases out of 12 (3-schizophrenics, 2.olig?phrenics) a preliminary phase of excitement followed-,by typical catatonia,' during which the, patient's face remained in- expressive while he-maintained the same posture for several minutes. This phase lasted up to two hours. As far as affect is concerned, the previous status depressive patiento become still more depressed, manic patients 5,27 euphoric . In the majority of cases, however, the'euphoric 2,11.,9,27 19 Of the 21 schizophrenic patients reported by Hoch a predominantly=- anxious reaction: (totsl of `22 : patients) The improvement in verbal activity and in-. affect often-facilitate $.a 2,', 7 contact with the patient". Patients become more accessible , and memories hidden in the subconscious may be brought to the surface, particularly- still more' effect predominates seven exhibited 7 in cases of psychoneurosis The hallucinatory phenomena due to LSD seem to be less frequent and much 2,x+,5,7 less varied in psychopathic patients than in normal subjects, . The 5' patient's spontaneous hallucinations may be. activated In one case of chronic alcohol. 1ntoxieationfrith previous ~ episodes of hallucinosis l0O/ng LSD produced =spa extremely vivid hallucinations resembling the alcoholic delirium that the patient had experienced in the past In this case, the shock'effect produced by this SECRET 83-01042 R000800010006-8 25X1 Approve SECRET/ experience seemed to exert a favorable action on the later evolution. 'In'other 2,.9. and those provoked by the drug- intensified in some schizophrenic patients .. distinction between the-usual hallucinations Depersonalization in psychopathic 5,9 only been mentioned in a few cases Catatonic 19 and paranoid features'were Possibilities of using LSD-25 in psychiatry: The effects described-above make it `? possible to visualize, the diagnostic and therapeutic use of-LSD. Personality test: Subjects response to LSD with euphoria manifestations, etc dependson their latent tendency. In psychopathic patients patient. The intoxication of LSD thus makes it possible in many cases to deter- LSD enhances the pre-existing conditions and inclines to give 'a caricature of the - mine the deep-seated tendencies of the subject and may be used, in'this respect,- 2,5,6 as a personality test and Johnson-have confirmed that analysis under the influence of LSD is not hampered by speech difficulties, such as frequently occur during barbiturate 7 analysis by improving contact.and facilitating the recall of memories. Busch Psychoanalysis; In many cases.L$D makes the patient more accessible to psycho- narco-analysis nor by the confusion which hampers analysis. during insulin shock or immediately after electroshock. In patients reacting to LSD with heightened' anxietyj--tpntact`was rendered more difficutt_ 'Effect oft- 'shock'.:.. The sometimes extremely --pronounced_ mental :effects--of LSD,` usual dosage, is generally too slight to produce a useful shock effect . As an 26 of the patient . In psychopathic patients the action of LSD, at least in the 5 6 particularly in-normal individuals,-may produce-a-feelinglof hiatus- in -the life : exception, one case of alcoholic' psychosis described by Benedetti must be mentioned, in which the extremely vivid hallucinations produced by the LSD seemed to exert a favorable psychic effect. Treatment of depression: The euphoric effect of LSD may be of use in the ment of certain depressive states. However, one should not be too optimistic since, as a general rule, LSD tends rather to reinforce a pre-existing depression. - - 5 Condrau carried out trial treatment with daily-doses of. LSD in five depressive 25X1 SECRET/ Approve'd. For Release. 200410311 1 - P83=01042R000800010006-8 25X1A Approved SECRET, 010 06-8 or Release - - patients. Only in two; of them did he observe a slight improvement in"affect. This result is not sufficient to be considered atherapeu:tic success. 'Savage gave 25X1 A five schizoid patients with severe depressive reaction became free of depression, and four patients suffering from schizophrenic reaction with depression showed no change or became worse. The improvement obtained with LSD treatment. was not greater than that obtained without LSD in comparable cases.. f "REFERENCES Hely. Chim Acta 26: 94+4, 1943- a) Lysergsaure-diathylamid, einPhantastikum aus der Mutterkorngruppe, Schweis, Arch Neurol Psych. 60: 279, 1947. rAvailable on loan from CIA L ibrari b) Psychischo Wirkung eines Mutterkornstoffee in ungewohnlichschwacher Dosierung Schweiz med Wschr 9: 110,:l9k9 Stoll, A Partialsynthese von Alkaloiden vom Typus Hofmann, A . des Ergobasins "De Giacomo, .t1;: Catatonie toxique `.experimentale? Congres._international.de Psychiatric Acta Neurol (Ital) 6: No 1, 1953 Goldner, R D acid die'thylamide.(LSD 25) Forrer, G R Experimental physiological'studies with lysergic Becker, A M Arch Neurol (Am)_ L: 581, 1951 LAvailable on loan from CIA Library) Klinische E.rfahrungen an Geisteskranken mit Lysergsaurs-Diathylamid Acts psych _neurol scand 24t 9, 1949. [Available on loan from CIA Library Zur Psychopathologie der Lysergsaurediathylamid Wien, Z Nerveahk.. 2: 11.02, 1949. LAvailable on loan in CIA Library is English translation of summary] 25X1. SECRETII Experimental studies of the pathogenesis of psychosis: Theoretical interest in A detailed study-of its mechanism of action may enlighten us as to the patho- 2,5,8,10 genesis-of psychoses - The possibility of a 'psychiatrist studying in a substance such'as,ISD-25 which in infinitesimal doses is capable of reproducing a whole series of symptoms characteristic of e-ndogenic psychoses may, be noted. himself some mental symptoms is also of interest:_ Approved or a ease DP83-01042R000800010006-8 Busch, A K Johnson, W.C #""' SECRET Rostafinski, M 10. Rinkel, M De Shcn , H J Hyde, K W Solomon, H C 12. Witt, P N 13. De Shon, H J Rinkel, M. Solomon, H C 14. Delay, J Pichot,:P 15. Delay, J Lhermitte, F Verdeaux, G_ . VerdLau t, J -.., 17. Mayer-Gross, W McAdam, W Walker, J W 18. Buscaino, G A 19. Hoch, P H .Cattell ., J P Penns, H H 20. Hoch,.PS__._ Cattell, J P Pennes, H, H 00100 23 - 16 LSD-25 as an, aid in psychotherapy`(Preliminary report. of a ,new drug) Die Nw System llt_ _2k1, 1950. Psychophysische Korrelationen- VIII Modell ver ruche zum Schizophrenieproblem Lysergsaure diathylamid and Mezcali'n .. Schweiz med Wschr 81z 817.& 837, 1951. Comamach doswiadezalnych'u chorych na padaczke-: (Experimentally produced hallucinations in epileptic patients) Reczu psychjatr (pol) 38: 109, 1950. - Experimental Schizophrenia-like Symptoms, abstract of Read before the American Psychiatric Association Amer J Psychiat 108:- 572, 1952. Lvailable on loan from CIA Library] Mezcalin- and Lysergsaurediathylamid-Rausch. Selbat_versuche'mit besonderer_Berucksichtigung Dissertation Basle 1951. -. , LAvailable on loan from CIA Library) d-lysergsaure-diathylamid (LSD-25)*in' Spinnentest, Experientia 1a 310, 1951?__ Mental changes experimentally produced by LSD (d-lysergic acid'diethylamide Tartrate). Psychiatric Quart 26Z 33, 1952. Diethylamide de_1'acide'd-lysergique et psychiques de,l'ergotisme C R Soc Biol 145: 1609, 1951. troubles Modifications de 1'electrocortisogramme du lapin par=la diethylamide de-1'acide d-lysergique ( LSD,-25 ) Revue Neurelogique 862 i'81,, 1952.:-5 Versich einer pzycho-pathologischen Analyse der ISD-Wirkung Dies Freiburg .i Br 1951. Psychological and biological effects of lysergic acid-diethylamide Nature 168: 827, 1951.. Studio quantitativo dell apettro di flu-orescenza - dell dietilamide dell'acido lisergico Ricerca scientifica-21t 519, 1951. Effects of mescaline and-lysergic acid (d-LSD-25) Am J. Psychiat 1081 ?-579, 1952 Effects of drugs- Am J Psychiat 1082 585, 1952. Approved For Release 2004/03/11 : CIA-RDP83-01042R000800010006-8 25X1A paper " X11 25X1 Influence of organic phosphates_ on tuberculin ,sensitivity in B C G infected guinea pigs.. Relation to. Cortisone, desensitizption ` Lancet 262: 950, 1952' SECRET a or Release - - 80001 -17- 21. Mayer-Gross, W Lysergsaure-Diathylamid und. Kohlehydratstoff- McAdam, W wechsel Walker, J. Norvenarst 2 t' 30, 1952 23. Blickenstorfer, E 24. Savage, C Zum atiologischen Problem der Psychosen vom akuten exogenen Reaktionstypus Lysergsaure diathylr'riid, ein psychisch.wirkeamer toxischer. Spurenstoff Arch f Psychiatrie;b Etschr Neuroi 188: 226, 1952. available on loan from CIA Libra Lysergic acid diethylamide (LSD-2 - A clinical- psychological study, Ad J Psychiat. 108t 896, 1952. 25. Rothlin, E Gerletti, A Uber einige pharmakologieche Untersuchungen an Mausen mit congenitalar Drehsucht' elv Physiol. Acts 10: 319, 1952. Available on loan from CIA Library] Beispiel einer, etrukturanalytiachen and pharmakodynamischen Untersuchung an einem ' Fall-von Alkoholhalluzinoso, Charakterneurose` and Psychoreaktiver Halluzinose Z f Psychotherapic u: med Psychol. 1: 176, 1951 ELAvailable on loan from CIA Library] dalla dietilamido dell-'acido lisergico in schizofrenici a frenastenici Acta. Neurol (ltal) 1: 310, 1952." 27. Deleanti, R. Modificiazioni Neuro-psico-biochi miche indotte RDP83-01?.042R000800010006-8 25X1A A 3 ED CONFIDENTIAL OFFICIAL ROUTING SLIP TO I NAME AND ADDRESS Remarks: Review Staff RETURN Attached are three copies of the 20 August 1975 memorandum with attach- ments. Note that the documents required additional coordination and because of this were not fully classified or stamped IMPDET. FOLD HERE TO RETURN TO SENDER FROM: NAME, ADDRESS AND PHONE NO. ...~.e a~ gW&%g ele FONM No, 237 Use previous editions 1-67 G I CONFIDENTIAL Amsifoo7( SECRET