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Excerpts from:
The Psychedelic Model of Schizophrenia:
The Case of N,N-Dimethyltryptamine

by Gillin, Kaplan, Stillman & Wyatt
American Journal of Psychiatry 133;2 pp.203-208, February 1976

Abstract: The authors review the research on N,N-dimethyltryptamine (DMT) as a possible "schizotoxin". DMT produces psychedelic effects when administered to normal subjects, the means are present to synthesize it in man, it has occasionally been found in man, and tolerance to its behavioral effects is incomplete. However, DMT concentrations have not been proven to differ significantly in schizophrenics and normal controls. Also, in vivo synthesis of DMT has not been convincingly demonstrated, and the psychological changes it produces do not closely mimic the symptoms of schizophrenia. The authors conclude that more data are necessary before the validity of this theory can be determined.

Does DMT produce significant schizophrenic-like symptoms?

In 1956 Szara (9) found that the effects of DMT on 20 normal volunteer subjects were similar to those of LSD and mescaline: visual illusions and hallucinations, distortions of spatial perception and body image, speech disturbances, and euphoria. A striking finding was that the effects of DMT began within 5 minutes and ended within 1 hour after injection. Similar results have since been reported by Rosenberg and associates (10) and Turner and Merlis (5).

In order to reexamine the psychological effects of DMT and to correlate them with pharmacokinetic aspects, we administered .7mg/kg of DMT intramuscularly to 15 make volunteers. Each subject was an experienced user of LSD, mescaline, or other psychedelic substances who expressed an intention to continue using these agents in the future. All subjects were intereviewed by two psychiatrists and were given a complete medical history and examination prior to testing in order to ensure the absence of psychiatric and physical impairment.

Like previous investigators, we found that DMT was a hallucinogen with rapid action and a short duration of effect. Psychological changes were evident within 5 minutes of injection, peaked at about 10 to 15 minutes, and ended within 45 to 120 minutes. The major psychological effects are shown in table 1. The subjects became so uncommunicative and withdrawn during the drug experience that we were forced to inquire about the subjective effects with simple "yes-no" questions. Although all subjects reported visual distortions and illusions, these were color or spatial distortions rather than formed visual hallucinations. Only 1 subject reported an auditory hallucination, a "buzzing bee" in his ear. We did not observe formal loosening of associations, although several subjects seemed to have thought blocking. Two subjects had paranoid symptoms that lasted less than an hour.

These psychological changes were accompanied by mydriasis, tachycardia, and increased blood pressure. Blood levels of DMT (see figure 2), assayed by a gas chromatographic-mass spectrometric (GC-MS) isotopic dilution technique, closely paralleled the psychological and autonomic changes (11). Peak concentrations of DMT, which averaged approximately 100 ng/ml, were reached about 10 to 15 minutes after injection; the concentration then fell rapidly to baseline, undetectable levels within about 45 to 120 minutes after administration.

TABLE 1.
Subjective Effects of DMT Experienced by 15 Normal Volunteer Subjects


 %  - Subjective Effects
-------------------------------------------
100 - Visual hallucinations
100 - Hallucinations with eyes closed
 93 - Movement of surroundings
 93 - Difficulty talking
 93 - Difficulty describing feelings
 93 - Relaxation
 93 - Difficulty concentrating
 87 - Colors seem brighter
 87 - Excitation
 87 - Thinking faster 
 87 - Dry mouth
 80 - Tenseness
 75 - People look different
 60 - Depersonalization
 60 - Nausea
 53 - People have orange-red hue
 27 - Hallucinating "real things"
 20 - Paranoia
  7 - Auditory hallucinations
-------------------------------------------

FIGURE 2.
Mean DMT Concentrations in Whole Blood Following Injection of DMT in 15 Normal Volunteers.

140+
   |
   |
   |         +
120+         |        Blood DMT Concentrations (ng/ml)
   |         |
   |         |
   |         |
100+         *
   |        .|.
   |       ..|.
   |       . | .
 80+       . | .
   |    + .  +  .
   |    | .     . +
   |    | .      .|
 60+    |.        |
   |    |.        *
   |    *         |.
   |   .|         | .
 40+   .|         +  .
   |  . |              .           
   |  . |                . .    +
   |  . +                    . .* . . . . .
 20+ .                          +            . . . .          +
   | .                                               . . . . .*.
   | .                                                        +  .
   |.                                                               .
  0*---------+--------+---------+---------+---------+---------+--//--*----
   0        10       20        30        40       50        60 //  120

                     Time After Injection (minutes)

Does tolerance to DMT develop?

Tolerance to LSD, mescaline and psilocybin develops rapidly in man and animals, for some if not all behavioral effects.

In our initial efforts, we found that tolerance did not develop to unconditioned behavioral and EEG effects of DMT in cats administered DMT twice daily for 15 days or every 2 hours for 24 hours (34). Also, lack of behavioral tolerance has been reported in squirrel monkeys given DMT once daily for 38 days (35).

More recently, we studied the issue of tolerance in normal male volunteers who received 0.7 mg/kg of DMT intramuscularly twice daily for 5 days. Repeated administration did not consistently alter the peak blood concentration of DMT; autonomic changes in pupil size, pulse, or heart rate; the number of psychological items changed in a psychological scale; or the frequency of errors in a test requiring the subject to cross out a specific number in a list of random numbers. Three of the 4 subjects reported diminished subjective "highs" on a scale of 0 to 10 after two to four injections of DMT, but their subjective responses were variable from trial to trial and did not indicate a general loss of responsiveness to DMT. Rather, these subjects exhibited a variable or aperiodic partial tolerance to DMT. This pattern is reminiscent of Koella and associates' report of a cyclic change in ambulation produced by LSD in goats (36). Further studies, including longer or more frequent trials with DMT, are neccesary to fully evaluate this phenomenon.

This type of variable tolerance has also been reported recently by Kovacic and Domino (37), who studied the supressive effects of DMT on the operant behavior of appetitively conditioned rats who were given DMT every 2 hours for periods of up to 21 days.

Bszrmnyi and Szara (38) reported that schizophrenics do show diminished responsiveness to DMT, this may result from increased metabolism or variable tolerance resulting from long-term endogenous synthesis of DMT.

Next: Psychedelic Bodily Fluids?

Bibliographic Items

(5) Turner WJ, Merlis S: Effect of some indolealkylamines in man. Arch Neurol Psychiatry 81:121-129, 1959

(9) Szara S; Dimethyltryptamine: its metabolism in man: the relation of its psychotic effect to serotonin metabolism. Experientia 12:441-442, 1956

(10) Rosenberg DE, Isbell H, Miner EJ; Comparison of placebo, N,N-dimethyltryptamine, and 6-hydroxy-N-methyltryptamine in man. Psychopharmacol 4;39-42, 1963

(11) Kaplan J, Mandel LR, Stillman R, et al; Blood and urine levels of N,N-dimethyltryptamine following administration of psychoactive doses to human subjects. Psychopharmacologia 38;239-245, 1956

(34) Gillin JC, Cannon E, Magyar R, et al; Failure of N,N-dimethyltryptamine to evoke tolerance in cats. Biol Psychiatry 7;213-220, 1973

(35) Cole JM, Pieper WA; The effects of N,N-dimethyltryptamine on operant behavior in squirrel monkeys. Psychopharmacologia 29;107-112, 1973

(36) Koella WP, Beaulieu RF, Bergen JR; Stereotyped behavior and cyclic changes in response produced by LSD in goats. Int J Neuropharmacol 3;398-403, 1964

(37) Kovacic B, Domio EF; Tolerance to behavioral effects of dimethyltryptamine (DMT) in the rat (abstract). Fed Proc 33;549, 1974

(38) Bszrmnyi A, Szara S; Dimethyltryptamine experiments with psychotics. J Mental Sci 104;445-453, 1958

Next: Psychedelic Bodily Fluids?