Hypnotic And Antiepileptic Effects Of Cannabidiol


Journal of Clinical Pharmacology, 1981; 21: 417S-427S

By Elisaldo A. Carlini, M.D., and Jomar M. Cunha, M.D.
Department of Psychobiology, Escola Paulista de Medicina, Sao Paulo, Brazil.

Abstract: Clinical trials with cannabidiol (CBD) in healthy volunteers, insomniacs, and epileptic patients conducted in the authors’ laboratory from 1972 up to the present are reviewed. Acute doses of cannabidiol ranging from 10 to 600 mg and chronic administration of 10 mg. for 20 days or 3 mg/kg/day for 30 days did not induce psychologic or physical symptoms suggestive of psychotropic or toxic effects; however, several volunteers complained of somnolence. Complementary laboratory testsl (EKG, blood pressure, and blood and urine analysis) revealed no sign of toxicity. Doses of 40, 80s, and 160 mg cannabidiol were compared to placebo and 5 mg nitrazepam in 15 insomniac volunteers. Subjects receiving 160 mg cannabidiol reported having slept significantly more than those receiving placebo; the volunteers also reported significantly less dream recall with the three doses of cannabidiol than with placebo. Fifteen patients suffering from secondary generalized epilepsy refractory to known antiepileptic drugs received either 200 to 300 mg cannabidiol daily or placebo for as long as 4.5 months. Seven out of the eight epileptics receiving cannabidiol had improvement of their disease state, whereas only one placebo patient improved.

An advertisement published in 1905 by a Brazilian newspaper advised the use of “Cigarros Indios” prepared from Cannabis indica to treat insomnia, among other diseases. Anecdotal reports also claim that Queen Carlota Joaquina of Portugal, while living in Brazil at the beginning of the last century, used to drink a tea of “Maconha” (Brazilian name for marihuana) to calm herself. These uses of marihuana in the past were by no means restricted to Brazil. Its use for sedative, hypnotic, anesthetic, and antiepileptic effects goes back to ancient times and all continents. (1-3)

In our times, the unraveling of the chemistry of Cannabis sativa brought renewed interest in old reports concerning the therapeutic properties of marihuana, and much new research has been carried out. Quite expectedly, the attention has focused on delta-9-tetrahydrocannabinol (THC), considered the main active principle of marihuana, due to its remarkable psychotropic properties. Its hypnotic and anticonvulsive effects in animals and in man have been reported by several laboratories, (4-11) but eventual medical use of THC would be hindered by its hallucinogenic effects. Furthermore, THC also possesses convulsant activity. (12-14)

Cannabidiol (CBD), on the other hand, lacks hallucinogenic properties and is therefore a better candidate for therapeutic use. In fact, work carried out with laboratory animals has shown that cannabidiol has depressant effects on the central nervous system in such tests as potentiation of barbiturate sleeping time and decrease of spontaneous motor activity. (15, 16) It has been further demonstrated that cannabidiol possesses a rather potent protective effect against certain types of experimental convulsions in animals (17-20) and an hypnotic-like effect in the rat. (21)s Therefore, trial of cannabidiol in humans was in order.

This report reviews data obtained in our laboratory from 1972 up to the present dealing with the effects of acute and chronic administration of cannabidiol to healthy volunteers and to insomniacs and epileptic patients. More detailed information of these experiments can be found elsewhere. (22-25)


Three experiments were performed on different occasions.

Experiment 1 (performed November 1972). Four physicians, three psychologists, and three biologists, all staff members of the Department of Psychobiology, varying in age from 23 to 42 years (four females and six males) volunteered. On the first day of the experiment, they underwent a complete medical checkup, including clinical and neurologic examinations, EKG and EEG, blood tests (hematocrit, hemoglobin, leukocyte and erythrocyte counts, bilirubin, oxaloacetic and puruvic transaminases, and creatinine) and urine tests (osmolarity, pH, albumin, leukocyyte and erythrocyte counts, cylinders, and crystals). All volunteers were in good health, showing neither clinical nor laboratory evidence of cardiovascular, renal, hepatic, or other impairment.

On the morning of the seventh day, two volunteers were randomly assigned, in a blind procedure, to receive identical gelatin capsules containing either glucose or 10, 40, 80, or 160 mg cannabidiol. The sample of crystalline cannabidiol was kindly supplied by the National Institutes of Health, United States. At 30, 90, 240, and 480 minutes, EKGs were again performed. EEGs were also obtained 240 and 480 minutes after the dose, and so were blood and urine samples for laboratory procedures. These examinations were repeated in the morning of the following day.

All laboratory results obtained on days 7 and 8 were within normal limits and similar to the values obtained on the first day, without drug. Physical and neurologic examinations revealed no abnormalities, and the volunteers did not complain of untoward effects.

Experiment 2 (January 1976). Two male physicians, aged 37 and 47 years, from the staff of the Department of Psychobiology received 600 mg cannabidiol for two days, 300 mg in the morning and 300 mg in the evening. The drug was furnished by R. Mechoulam, Department of Natural Products, University of Jerusalem, Israel. The experimental protocol was identical to that of experiment 1, with the exception that EEG and blood and urine tests were not performed. With the exception that one volunteer reported having slept more heavily on the nights after taking the drug, no abnormal finding was detected.

Experiment 3 (February and June 1978). The overall design of this experiment included a study of the interaction between cannabidiol and alcohol on psychomotor and psychologic functions of healthy volunteers. In the present review only data concerning the effects of cannabidiol and placebo will be compared. Details concerning cannabidiol-alcohol interactions can be found elsewhere. (23)

Ten healthy postgraduate students volunteered (sic males and four females), 21 to 33 years of age and weighing 52 to 85 kg. Crystalline cannabidiol (supplied by R. Mechoulam, Israel) and glucose, 200 mg each, were formulated separately in opaque gelatin capsules. The experiment comprised four different drug administrations, at weekly intervals, one being with glucose and another with cannabidiol. The other two were alcohol and alcohol plus cannabidiol administration and will not be further referred to here. Inasmuch as drug administration was given randomly in a double-blind procedure, glucose and cannabidiol ingestions were from one to three weeks apart. The experiments began at 11:00 A.M. and continued until 4:00 P.M. The subjects were submitted to objective and subjective tests 1/2, 1, 2, and 4 hours after cannabidiol or glucose ingestion. The following battery of tests, taking about 25 minutes per session, was applied: cancellation test, differential aptitude test (Form A, the Psychological Corporation, New York, N.Y.), time production task, finger tap test, and a subjective drug reaction scale. Details of these tests are given elsewhere. (23)

Table I presents the results of the first four tests in a condensed form. For each test the data obtained at times 30, 60, 120, and 240 minutes after drug ingestion were similar and were therefore pooled. It is seen that in the cancellation test the volunteers reacher very close to the total of 40 possible correct responses, regardless of whether they were under placebo or cannabidiol. Also with both treatments they have a near-perfect performance in the differential aptitude test and reached above 300 presses per minute in the finger tap test. Finally, Table I shows that treatment did not influence the capacity of the volunteers to produce ddd1-minute time. The results obtained with the subjective drug reaction scale also confirmed the lack of effects of cannabidiol on the subjective functioning of the volunteers, as they felt equally sober, non-drugged, alert, and nondizzy under either cannabidiol or glucose.

Chronic Administration of Cannabidiol to Healthy Volunteers (Phase I Studies)

Two experiments were performed on different occasions.

Experiment 4 (December 1972 and January 1973). Due to the small amount of cannabidiol available (remaining NIH material from experiment 1 and a sample supplied by Prof. R. Mechoulam, Israel), only four male volunteers from the Department of Psychobiology staff were selected — two physicians, one biochemist, and one psychologist, age range 23 to 30 years. The experiment was run double-blind, and on day 1 complete medical checkups and complementary laboratory tests were done as in experiment 1. Two volunteers were randomly assigned to receive 10 mg cannabidiol daily for 20 days (two gelatin capsules containing 5 mg each, one to be ingested at 9:00 A.M. and the other at 5:00 P.M. every day). The third volunteer received two identical capsules with glucose for 20 days, and the fourth ingested cannabidiol during the first 10 days and was crossed over to placebo for the last 10 days. Drug ingestion began on day 7, extending to day 26, and medical and laboratory examinations were repeated in the morning of days 8, 15, 22, and 27 (corresponding to days 1, 8, 15, and 21 after the beginning drug ingestion).

The two volunteers receiving 10 mg cannabidiol for 20 days and the one who received it for the fist 10 days did not complain of any physical discomfort or psychologic disturbnance. However, two volunteers complained of somnolence with cannabidiol, one after day 3 and another after day 4; the symptom subsided by day 15s. Physical and neurologic examinations, EEG, EKG, and blood and urine tests were all within normal limits and did not differ in the same volunteer regardless of being performed before or at different times after the beginning of drug ingestion. Further details of these results can be found elsewhere. (25)

Experiment 5 (between February and April 1976). Sixteen adult volunteers (11 men and five women), aged 22 to 35 years, with an average weight of 65 kg. were chosen from the staff of Escola Paulista de Medicina. They were all in apparent good health, which was confirmed on day 1 when they were subjected to complete medical and laboratory examinations as described in experiment 1.

On day 7 (having given informed consent), they were randomly divided into two groups of eight. Each group received capsules containing either glucose or cannabidiol. Crystalline cannabidiol was supplied by R. Mechoulam, Israel. The experiment was performed on a double-blind basis, and the subjects were instructed to ingest the assigned capsules, one in the morning and one in the afternoon. Each capsule contained an amount of cannabidiol equivalent to 1.5 mg/kg, i.e., a daily dosage of 3.0 mg/kg. On days 3, 7, 31 and 37 after the beginning of drug ingestion, the volunteers returned to undergo the medical and laboratory examinations as described above.

The results confirmed the absence of toxic effects of cannabidiol Thus, of the eight volunteers receiving placebo, one withdrew on the 21st day for personal reasons; a second placebo subject complained of sudoresis and “palpitations” from days 7 to 10 in the veins of the feet. Clinical and laboratory examinations were normal, and the symptoms subsided after day 11 without intervention being required on the part of the investigators. On the other hand, none of the eight cannabidiol volunteers complained of any symptom suggestive of psychotropic effect during the entire period of the experiment. However, two of them reported somnolence–one during the first week and the other throughout the 30 days of drug ingestion. A third subject, with a history of mild insomnia, reported better sleep during the first week of medication.

For the 16 subjects (placebo and cannabidiol groups), neurologic and clinical examinations, EEG and EKG tracings, and blood and urine analysis were within normal limits before, during and after the experiment. Detailed accounts of these results have been published recently. (24)

Clinical Trial of Cannabidiol as an Hypnotic Drug

The lack of toxicity of cannabidiol observed in our Phase I studies (experiments 1, 2, 4, and 5) and the complaints of somnolence by several volunteers receiving the drug (experiments 2, 4, and 5), together with the reported hypnotic-like effect of cannabidiol in rats, (21) encouraged us to give a first trial of cannabidiol as an hypnotic agent in humans. This experiment was carried out during June–November 1977. A detailed account of the findings was previously published. (22)

A new sample crystalline cannabidiol, kindly supplied by NIH, was incorporated into gelatin capsules in amounts of 40, 80, and 160 mg. Pills containing 5 mg nitrazepam (Mogadon kindly supplied by Roche Laboratories) were crushed and encapsulated. As placebo, 200 mg glucose was encapsulated in identical gelatin capsules.

After physical examination and psychiatric interview, 15 relatives of staff members of Escola Paulista de Medicina were selected. They were chosen on the basis of (a) complaints of difficulty in falling asleep (at least 1 hour) and poor sleep throughout the night; (b) history of previous good physical and mental health; (c) no previous history of nonmedical use of drugs; and (d) no prescribed medicines for at least 15 days before.

In a double-blind procedure and in random order, once a week, the volunteers were instructed to ingest one assigned capsule. At dinner of the chosen days, they were requested to refrain from alcohol and coffee, and to ingest the capsule 30 minutes before going to bed, between 10:00 and 10:30 P.M. All volunteers received all treatments, that is, placebo, 5 mg nitrazepam, and the three dosages of cannabidiol Therefore, the experiment lasted five weeks. In the mornings of days after drug administration, the volunteers answered a ten-point questionnaire, adapted from Bloomfield et al., (26) and were briefly interviewed. The questions sought information on induction of sleep (questions 1 and 2), sleep quality (questions 3, 4, and 5), dream recall (questions 6 and 7), and reawakening (questions 8, 9, and 10). Answers to questions 1, 2, 3, 4, and 8 had five possibilities, scored from 0 to 4, score 4 indicting the best hypnotic effect. For example, the five possible answers to question 1, “How much time elapsed between going to bed and onset of sleep?” were: less than 15 minutes (grade 4), between 15 and 30 minutes (grade 3), between 30 and 45 minutes (grade 2), between 45 and 60 minutes (grade 1) and more than 60 minutes (grade 0). Answers to questions 5, 6, 7, 9, and 10 were not transformed into scores, as they had only two options, yes and no.

The results are condensed in Table II. The first noticeable finding was the placebo effect, which is rather common in this kind of research. Thus, before starting drug administration all patients took at least 1 hour to fall asleep (score 0). However, under placebo, six patients scored grades 3 and 4–five reported having slept within 15 to 30 minutes after going to bed (grade 3) and one in less than 15 minutes (grade 4). Cannabidiol, and also 5 mg. nitrazepam, did not produce a positive sleep induction effect in the volunteers. Thus, although eight subjects reported grades 3 and 4 for 160 mg cannabidiol and 5 mg nitrazepam, this number fell short of statistical significance when compared to the large value also found for placebo. The quality of sleep induction, assessed by the answers to question 2, “What was the effect o the medication before you fell asleep?” also was not influenced by the treatments. Thus, the majority of the volunteers answered “nil” to that question, and only a few volunteers (see second row of Table II) answered “pleasant” (grade 3). It is interesting that Bloomfield et al (26) also reported that secobarbital failed to influence sleep induction.

Sleep quality was significantly influenced by 160 mg cannabidiol, as two thirds of the subjects slept more than 7 hours, scoring 3 and 4 in answer to question 3. Furthermore, most subjects had few interruptions of sleep (question 4) and reported having a good night’s sleep (question 5).

The three doses of cannabidiol were effective in significantly reducing dream recall of the volunteers. This could have occurred because cannabidiol may decrease the capacity to dream in itself, that is, the volunteers dreamed less. Conversely, cannabidiol may also have reduced dream recall, that is, the volunteers dreamed as usual but could not remember. The latter possibility would indirectly indicate that cannabidiol may have decreased the frequency of small awakening periods during the night sleep which facilitates remembering the oneiric events.

Finally, the last four questions of Table II indicate that cannabidiol did not induce nightmares or symptoms that could indicate hangover the following morning.

Antiepileptic Effects of Cannabidiol

This experiment was done between May 1976 and March 1978, and the results were recently published. (24)

Fifteen epileptic patients (11 women and four men), aged 14 to 49 years (average 24 years) with a documented history of frequent convulsions for at least one year were selected. These patients were not responding satisfactorily to their prescribed antiepileptic drugs. The patients were diagnosed as cases of secondary generalized epilepsy; EEG tracings revealed irritative activity with temporal projections. They had at least one generalized convulsive crisis weekly. In the two weeks before cannabidiol or placebo administration, the number of focal and generalized convulsive crises was recorded and considered as the baseline to evaluate treatment.

On the first day of the experiment, the patients were submitted to the examinations described in experiment 1. They were randomly divided into one group of eight (control) and another group of seven )cannabidiol). One week later, each group began to receive placebo or cannabidiol capsules in a double-blind procedure in addition to the antiepileptic drugs they were already receiving. The patients were instructed to take two or three capsules daily (containing 100 mg cannabidiol or glucose) and to return to the hospital every week for clinical and/or laboratory examinations.

Clinical evaluation of drug treatment was made weekly using a score scale of 0 to 3, which took into consideration absence of convulsive crises or absence of generalization and self-reported subjective improvement. On this scale, a score of 3 meant no improvement, that is, no reduction in crises and no self-reported subjective improvement; a score of 2, small improvement or self-reported subjective improvement; a score of 1, partial improvement or absence of generalization of crisis and self-reported improvement; finally, a score of 0, complete improvement or total absence of convulsive crisis and self-reported subjective improvement. According to these criteria, all patients had a score of 3 during the pre drug phase (baseline).

The results are seen in Table III. At the end of placebo treatment, seven patients had a median score of 3 (i.e., no improvement), whereas one patient (patient 7) showed complete improvement (median score 0). Placebo patients 2 and 3, with no improvement, received the capsules for the fourth week of treatment but did not return. Three other placebo patients (1, 4, and 5) remained under treatment for 12, 12, and eight weeks, respectively, after which they were withdrawn from the experiment and underwent a change in the prescribed antiepileptic drugs in an attempt to improve their condition. Finally, patient 8 remained on placebo for four weeks with no improvement (median score 3) and wanted to give up, being transferred without her knowledge to cannabidiol with a small improvement (median score 2).

Of the eight patients receiving cannabidiol, four (patients 10, 11, 12, and 15) showed considerable improvement (median score 0); however, in one case (patient 15) this was achieved by increasing the dosage to 300 mg daily. Patient 11, who showed much improvement from the first week, moved to another city after completing six weeks of treatment. Patient 9 improved partially (median score 1) although he attained score 0 ( no convulsive crisis and subjective improvement) in seven out of the 16 weeks of treatment. Finally, two of the three remaining patients had a median score of 2 (only self-reported subjective improvement), whereas the last patient, 14, did not improve at all in spite of increasing cannabidiol to 300 mg daily for the last two weeks of treatment.

Clinical examination proved normal for all cannabidiol patients, and the pulse, cardiac, and respiratory rates remained constant during the course of the experiment. Also cannabidiol did not alter the creatinine, bilirubin, or transaminase values in the eight patients. However, four patients complained of somnolence during the experiment.

General Comments

The first relevant finding of these studies concerns the rather remarkable lack of toxicity from acute and chronic administration of cannabidiol Thus, in five experiments with healthy volunteers there was no subjective or physical symptom suggestive of toxic effect. The same conclusion was also reached after the laboratory examinations. Although in some experiments the number of subjects was low due to the limited availability of cannabidiol, taken all together the data strongly support our contention, regarding the excellent toleration of cannabidiol Furthermore, the acute administration of the drug to the insomniacs and the 3 to 4.5 months of treatment of the epileptics confirm the lack of toxicity.

Concerning the eventual hypnotic effect of cannabidiol, our preliminary data with 15 subjects tend to confirm that it has such potential use. In fact, 160 mg cannabidiol significantly increased the number of hours the subjects slept, and all three doses decreased dream recall, which could be the consequence of less sleep interruptions during the night’s sleep. It is significant in this respect that several healthy volunteers complained of somnolence when under cannabidiol, a fact also reported by four of the eight epileptic patients. It is interesting that 5 mg nitrazepam (the amount commercially available in sleeping pills in Brazil), did not differ in its effect from placebo. Other authors have reported clear hypnotic effects with 10 mg nitrazepam. (27,28)

A note is in order about the method used to measure hypnotic effect of cannabidiol The use of self-reported questionnaires to evaluate hypnotic effects is considered a subjective method, in opposition to the objective methods such as the inspection of the volunteers in inpatient-settings throughout the night or the obtention of continuous EEG recordings. Both methods have enthusiastic followers. (29,30)

The clinical trial of cannabidiol as an eventual antiepileptic agent was conducted with eight cases of severely ill patients, refractory to all known antiepileptic drugs. The results indicate that cannabidiol has a beneficial effect in patients suffering from secondary generalized epilepsy with temporal focus who do not benefit from known antiepileptic drugs. The mechanism by which cannabidiol benefited our epileptic patients is not known. One possibility is that cannabidiol potentiates the action of the other anticonvulsants since enhancement by cannabidiol of the anticonvulsant activity of phenobarbital and phenytoin in animals has been demonstrated. (18, 31,32) In man however, 50 to 500 mcg/kg cannabidiol given in cigarette form is not able to alter plasma concentrations of secobarbital. (33) The possibility that cannabidiol acts per se should also be taken into consideration, as shown by several reports describing its direct anticonvulsant effects in animals. In this respect it is important to note that Tamir et al. (34) have reported that cannabidiol and phenytoin both possess similar stereochemical requirements for anticonvulsant drug action.

Discussion of the Paper

Dr. Cornwell: Why did you use weekly doses of CBD for your insomnia study? Was there any differential effect in terms of improvement in sleep for the 7 nights between the doses?

Dr. Carlini: We used single doses of CBD 40, 80, and 160 mg at weekly intervals mainly because we had only a very small supply of CBD. I have no data on differential effects on sleep since the patients were interviewed only at weekly intervals.

Dr. Benowitz: We studied 10 patients receiving 600 mg of CBD per day for up to 12 days (Benowitz, NL, et al. Clin Pharmacol Therap. 1980; 28: 115-120) We found no psychophysiological, sedative hypnotic, nor EEG effects. Consistent with findings from experiments in animals, barbiturate metabolism was inhibited (35-40% reduction of hexobarbital clearance). Is it possible that some of the hypnotic and anticonvulsant effects of CBD might be due to inhibition of metabolism of co-administered anticonvulsant drugs?

Dr. Carlini: That is a real possibility, since all patients were also receiving phenobarbital, mehpobarbital, or phenytoin. The first hypothesis would be that CBD interferes with metabolism, potentiating the action of these drugs as you suggest. The second of course would be that CBD had an action by itself. We have no data to address these two possibilities.

Dr. Karler: The sedative effects appear to be real, because some normal volunteers were sedated by CBD in the absence of any coexisting drug therapy. Why is it, however, that Dr. Benowitz did not see sedative effects in his patients? Was that due to a dose-differential? Dr. Benowitz: In our study, 600 mg a day was administered in divided 100 mg doses.


1. Carlini EA. Maconha (Cannabis sativa): da erva do diabo a medicamento do establishment? Ciencia e Cultura. 1980; 32: 684-690.

2. Mechoulam R, Carlini EA. Toward drugs derived From Cannabis. Naturwissenschaften. 1978; 65: 174-179.

3. Winek CL. Some historical aspects of marihuana. Clin Toxicol. 1977; 10: 243-253.

4. Consroe PF, Man DP. Effects of Delta-8-and Delta-9-tetrahydrocannabinol on experimentally induced seizures. Life Sci. 1973; 13: 429-439.

5. Consroe PF, Man DP, Chin L, Piccioni AL. Reduction of audiogenic seizure by Delta-8-and-Delta-9-tetrahydrocannabinols. J Pharm Pharmacol. 1973; 25: 764-765.

6. Cousens K, Di Mascio A. Delta-9-THC as an hypnotic. An experimental study of 3 dose levels. Psychopharmacology. 1973; 33: 355-364.

7.Gildea ML, Bourn WM. The effect of delta-9-tetrahydrocannabinol on barbiturate withdrawal convulsions in the rat. Life Sci. 1977; 21: 829-832.

8. Karler R, Cely W, Turkanis SA. Anti-convulsant activity of delta-9-tetrahydrocannabinol and its 11-hydroxy and 8a, 11-hydroxy-metabolites in the frog. Res Commun Chem Pathol Pharmacol. 1974; 9: 441-452.

9. Sofia RD, Barry H III. Comparative activity of THC, diphenylhydantoin, phenobarbital and chlordiazepoxide on electroshock seizure threshold in mice. Arch Int Pharmacodyn Therap. 1977; 228: 73-78.

10. Sofia RD, Solomon TA, Barry H III. Anticonvulsant activity of delta-9-THC compared to three other drugs. Eur J Pharmacol. 1976; 35: 7-16.

11. Wada JA, Wake A, Sato M, Corcoran ME. Antiepileptic and prophylactic effects of tetrahydrocannabinols in amygdaloid kindled cats. Epilepsia. 1975; 16: 503-510.

12. Consroe P, Martin P, Eisenstein D. Anticonvulsant drug antagonism of delta-9-THC-induced seizures in rabbits. Res Commun Chem Pathol Pharmacol. 1977; 16: 1-13.

13. Craigmill AL. Cannabinoids and handling-induced convulstions. Res Commun Psychol Psychiat Behavior 1979; 4: 51-63.

14. Feeney DM. Marihuana and epilepsy: paradoxical anticonvulsant and convulsant effects. In: Nahas GG, Paton WDM, eds. Marihuana, Biological Effects. Advances in the Biosciences 22/23. Oxford: Pergamon Press; 1979: 643-657.

15. Carlini EA, Mechoulam R, Lander N. Anticonvulsant activity of four oxygenated cannabidiol derivatives. Res Commun Chem Pathol Pharmacol. 1975; 12: 1-15.

16. Savaki HE, Cunha J, Carlini EA, Kephalas TA. Pharmacological activity of three fractions obtained by smoking cannabis through a water pipe. Bull Narcotics. 1976; 28: 49-56.

17. Carlini EA, Leite JR, Tannhauser M, Berardi AC. Cannabidiol and Cannabis sativa extract protect mice and rats against convulsive agents. J Pharm Pharmacol. 1973; 25: 664-665.

18. Consroe P, Wolkin A. Cannabidiol–antiepileptic drug comparisons and interactions in experimentally induced seizures in rats. J Pharmacol Exp Therap. 1977; 201: 26-32.

19. Karler R, Cely W, Turkanis SA. The anticonvulsant activity of cannabidiol and cannabinol. Life Sci. 1973; 13: 1527-1531.

20. Karler R, Turkanis SA. Subacute cannabinoid treatment: anticonvulsant activity and withdrawal excitability in mice. Br J Pharmacol. 1980; 68: 479-484.

21. Monti JM. Hypnotic-like effect of cannabidiol in the rat. Psychopharmacology. 1977; 55: 263-265.

22. Carlini EA, Masur J, Magalhaes CCPB, Possivel efeito hipnotico do canabidiol no ser humano. Estudo preliminar. Ciencia e Cultura. 1979: 31: 315-322.

23. Consroe P, Carlini EA, Zweicker AP, Lacerda LA. Interaction of cannabidiol and alcohol in humans. Psychopharmacology. 1979: 45-50.

24. Cunha JM, Carlini EA, Pereira AE, Ramos OL, Pimentel C, Gagliardi R, Sanvito WL, Lander N, Mechoulam R. Chronic Administration of cannabidiol to healthy volunteers and epileptic patients. Pharmacology. 1980; 21: 175-185.

25. Mincis M, Pfeferman A, Guimaraes RX, Ramos OL, Zukerman E, Karniol IG, Carlini EA. Administracao cronica de canabidiol em seres humanos Rev Ass Med Bras. 1973; 19: 185-190.

26. Bloomfield SS, Tetreault L, Lafreniere B, Bordeleau JM. A method for the evaluation of hypnotic agents in man. Comparative hypnotic effects of secobarbital, methaqualone and placebo in normal subjects and in psychiatric patients. J Pharmacol Exp Therap. 1967; 156: 375-382.

27. Davis C, Levine S. A controlled comparison of nitrazepam (“Mogadon”) with sodium amylobarbitone as a sleep inducing agent. Br. J Psychiat. 1967; 113: 1005-1008.

28. Haider I. A double-blind controlled trial of an nonbarbiturate hypnotic–nitrazepam. Br J Psychiat. 1968; 114: 337-343.

29. Hartman E, Chung R, Chien CC. L-Tryptophane and sleep. Psychopharmacology. 1971; 19: 114-127.

30. Rickels K. Clinical evaluation of hypnotic agents in outpatients. In: Kagan F, Harwood T, Rickels K, Rudzik AD, Sorer H, eds. Hypnotics–Methods of Development and Evaluation. New York: Spectrum Publications; 1975.

31. Chesher GB, Jackson DM. Anticonvulsant-effects of cannabinoids in mice. Drug interactions with cannabinoids and cannabinoid interactions with phenytoin. Psychopharmacology. 1974; 37: 255-264.

32. Chesher GB, Jackson DM, Malor Rm. Interaction of Delta-9-tetrahydrocannabinol and cannabidiol in protecting mice from electrically induced convulsions. J Pharm Pharmacol. 1975; 27: 608-609.

33. Dalton WS, Martz R, Rodda BE, Lemberger L, Forney RB. Influence of cannabidiol on secobarbital effects and plasma kinetics. Clin Pharmacol Therap. 1976; 20: 695-700.

34. Tamir I, Mechoulam R, Meyer AY. Cannabidiol and phenytoin: a structural comparison. J Med Chem. 1980; 23: 220-223.