Abstract: Cannabis, or marijuana, has been used for centuries for both symptomatic and prophylactic treatment of migraine. It was highly esteemed as a headache remedy by the most prominent physicians of the age between 1874 and 1942, remaining part of the Western pharmacopoeia for this indication even into the mid twentieth century. Current ethnobotanical and anecdotal references continue to refer to its efficacy for this malady, while biochemical studies of THC and anandamide have provided a scientific basis for such treatment.
The author believes that controlled clinical trials of Cannabis in acute migraine treatment are warranted.
One of the basic tenets of medical history is that remedies fall in and out of favor. Once supplanted, most pharmaceuticals fail to re-attain a position of prominence. Very few are popular for many decades. Not many physicians today are aware of the prominence that Cannabis drugs once held in medical practice. Problems with quality control and an association with perceived dangerous effects sounded the death knell for Cannabis as a recognized Western therapy. Other medicines that are far more potentially damaging than Cannabis remain in our pharmocopeias because of recognized medical indications: opiates for pain control, amphetamines for narcolepsy and attention deficit hyperactivity disorder, etc. Thalidomide, which was banned due to its role in birth defects, may be effecting a therapeutic revival. Even the lowly leech is once again the object of serious medical investigation. This study will examine the history of Cannabis use for one indication, that of headache treatment, its scientific rationale, and possible future as an alternative therapeutic agent.
Historical and Ethnobotanical Usage of Cannabis in Migraine Treatment:
Headaches have likely afflicted man throughout history. Archeological records substantiate an ancient association between man and the plant genus Cannabis, plant family, Cannabaceae. Its botanical origin has been debated to be as far east as China, but most experts suspect it to be in Central Asia, possibly in the Pamir Plains (Camp, 1936). Some botanists have maintained Cannabis as monotypic genus, while others (Schultes et al., 1974) have provided convincing documentation of three Cannabis species: sativa, indica, and ruderalis. All contain the psychoactive chemical delta-9-tetrahydrocannabinol (THC) in varying degree.
Use of Cannabis fibers to make hemp has been documented as early as 4000 BC by Carbon-14 dating (Li, 1974), and that use has been maintained continuously up to the present day. Its seed grain was an ancient human foodstuff, which may have lead to an early recognition of its medicinal use. The first records of the latter seem to be in the Pên-tsao Ching, a traditional herbal written down in the first two centuries AD, but said to be based on the oral traditions passed down from the Emperor Shên-nung in the third millenium BC. The text noted that the plant fruits "if taken in excess will produce hallucinations (literally "seeing devils")(Li, 1974).
The Zend-Avesta, the holy book of Zoroastrianism, which survives only in fragments, dating from around 600 BC in Persia, alludes to the use of Banga in a medical context, and it is identified as hemp by the translator (Darmesteter, 1895).
The classical Greek literature also documents knowledge of the inebriating actions of Cannabis. Herodotus, circa 450 BC, described how the Scythians set up tents, heated stones and threw Cannabis seeds or flowering tops upon them to create a vapor, and "the Scythians, delighted, shout for joy." The Greek physicians Dioscorides and Galen expounded on medical indications, mainly gastrointestinal (Brunner, 1977).
The Atharva Veda of India, dated to between 1400 and 2000 BC referred to a sacred grass, bhang, and medicinal references to Cannabis were cited by Susrata in the sixth to seventh centuries AD (Chopra and Chopra, 1957) and included indication for its use for headache (Dwarakanath, 1965). O'Shaughnessy introduced the medical use of Cannabis indica, or "Indian hemp," to the West in 1839 (Walton, 1938; Mikuriya, 1969). His treatise on the subject supported the utility of an extract in patients suffering from rabies, cholera, tetanus, and infantile convulsions.
Throughout the latter half of the nineteenth century, many prominent physicians in Europe and North America advocated the use of extracts of Cannabis indica for the symptomatic and preventive treatment of headache.
Proponents included Weir Mitchell in 1874, E.J. Waring in 1874, Hobart Hare in 1887, Sir William Gowers in 1888, J.R. Reynolds in 1890, J.B. Mattison in 1891, et al., (Walton, 1938; Mikuriya, 1969). Cannabis was included in the mainstream pharmacopeias in Britain and America for this indication. As late as 1915, Sir William Osler, the acknowledged father of modern medicine, stated of migraine treatment (Osler, 1915), "Cannabis indica is probably the most satisfactory remedy. Seguin recommends a prolonged course." This statement supports its use for both acute and prophylactic treatment of migraine.
In 1916, in a quotation attributed to Dr. Dixon, Professor of Pharmacology, Kings' College, and the University of Cambridge (Ratnam, 1916), reference is specifically made to the therapeutic effects of smoked Cannabis for headache treatment. He stated, "In cases where immediate effect is desired, the drug should be smoked, the fumes being drawn through water. In fits of depression, mental fatigue, nervous headache, feelings of fatigue disappear and the subject is able to continue his work refreshed and soothed."
In the years that followed, Cannabis came to be perceived as a drug of abuse, smoked by certain classes of people as "marijuana" or "marihuana." Nevertheless, it retained adherents for a variety of medical indications, throughout the early decades of the twentieth century. In 1938 Robert Walton published a comprehensive review of Cannabis, with botanical, historical, chemical and political discussions (Walton, 1938). After discussing the abuse issue, he stated his belief that the political action that had rendered marijuana illegal in the U.S.A. in 1937 (and which the American Medical Association vigorously opposed), should not serve to prohibit further medical use and scientific investigation of Cannabis' possible applications. Walton referred to twelve major authorities on its efficacy for migraine, and only one detractor.
In 1941, Cannabis preparations were dropped from the United States Pharmacopeia (U.S.P.), but the following year, the editor of the Journal of the American Medical Association still advocated oral preparations of Cannabis in treatment of menstrual (catamenial) migraine (Fishbein, 1942). This practitioner seemed to prefer Cannabis to ergotamine tartrate, which remains in the migraine armamentarium, some fifty-five years later. Thus, Cannabis was touted in eight consecutive decades in the mainstream Western medical literature as a, or the, primary treatment for migraine. As late as 1957, despite governmental controls in that country, Cannabis drugs retained a role in the indigenous medicine of India (Chopra and Chopra, 1957), and other countries.
In the 1960's marijuana moved to center stage of Western consciousness, and attained a degree of notoriety sufficient to render medical usage inconceivable to most. Medical research has resumed only recently, spurred on by anecdotal reports of patients who serendipitously discovered its benefits on their maladies.
Modern Research Developments on Cannabis:
In 1974, the first of several studies appeared examining issues of pain relief with Cannabis (Noyes and Baram, 1974). This article examined five case studies of patients who volitionally experimented with the substance to treat painful conditions. Three had chronic headaches, and found relief by smoking Cannabis that was comparable, or superior to ergotamine tartrate and aspirin.
One subsequent study of Cannabis pertained to pain tolerance in an experimental protocol (Milstein et al., 1975). A statistically significant increase in pain threshold was observed after smoking Cannabis in both naïve (8% increase) and experienced subjects (16% increase). Another trial involved oral THC in cancer patients (Noyes et al., 1975a). They observed a trend toward pain relief with escalating doses significant to the P<0.001 level. The peak effect occurred at three hours with doses of 10 and 15 mg., but not until five hours after ingestion of 20 mg. Subsequently, the analgesic effect of THC was compared to codeine (Noyes et al., 1975b). In essence, 10 mg. of oral THC vs. 60 mg. of codeine, and 20 mg. of THC vs. 120 mg. of codeine relieved the subjective pain burden of patients by similar decrements. The effects of 10 mg. of THC were well tolerated, but at 20 mg., sedation, and psychic disturbances bothered many of the elderly Cannabis-naïve subjects.
In the 1980's more comprehensive data on pharmacological effects of Cannabis and its derivative, THC became available. In 1983, research with varying potencies of smoked Cannabis demonstrated some correlation between serum THC levels and subjective "high" (Chiang and Barnett, 1983). Additionally, experimental subjects were able to distinguish the potency of the various samples with accuracy.
In a forensic review (Mason et al., 1985), the issue of marijuana's effect on driving was addressed, and it was indicated that isolated reports of adverse outcomes secondary to impairment by Cannabis as a sole inebriant were rare. The authors concluded that there was no suitable correlation between plasma or blood levels of THC and the degree of apparent impairment a human might exhibit.
In 1986 the journal Pharmacological Reviews devoted an entire issue to Cannabis and cannabinoids. In "Cellular Effects of Cannabinoids" (Martin, 1986), the author noted their analgesic properties, but reported that the mode of action was not blocked by naloxone, and seemed to work independently of opioid mechanisms.
Another article examined pharmacokinetics (Agurell et al., 1986). Many facets were presented, including their findings that smoking a standard marijuana cigarette destroyed 30% of available THC.
The final article of the issue was entitled "Health Aspects of Cannabis" (Hollister, 1986). Pertinent points made included dose delivery efficiency of THC by inhalation of 10% in marijuana-naïve vs. 23% in experience smokers. Oral bioavailability for THC was only about 6%, and onset of effects was not seen for 30-120 minutes.
Smoking of massive Cannabis doses daily for a prolonged period produced lower intraocular pressure, serum testosterone levels, and airway narrowing, but no chromosomal aberrations, or impairment of immune responses were noted (Cohen, 1976). Other "marijuana myths" were unsupported by careful review of the literature. While aggravation of pre-existing psychotic conditions by marijuana use was documented, no cause and effect relationship was noted.
Similarly, chronic use studies in Jamaica (Comitas et al., 1976), revealed no deficits in worker motivation or production. Two studies of brain computerized tomography (CT scan) refuted prior claims of heavy use producing cerebral atrophy (Co et al, 1977; Kuehnle et al., 1977). With respect to behavior, Hollister refuted the tenet that depicted Cannabis as a contributor to violent and aggressive behavior. Concerning addiction, he noted minimal withdrawal symptoms of nausea, vomiting, diarrhea, and tremors in some experimental subjects after very heavy chronic usage. Such effects were brief and self-limited.
The next year, an article entitled "Marijuana and Migraine" (El-Mallakh, 1987), presented three cases in which abrupt cessation of frequent, prolonged, daily marijuana smoking were followed by migraine attacks. One patient noted subsequent remission of headaches with episodic marijuana use, while conventional drugs successfully treated the others. The author hypothesized that THC's peripheral vasoconstrictive actions in rats, or its action to minimize serotonin release from the platelets of human migraineurs (Volfe et al., 1985), might explain its actions.
In 1988 action was initiated through the DEA to reclassify marijuana to Schedule 2, potentially making it available for prescription to patients. The DEA administrative law judge, Francis Young, reviewed a tremendous amount of testimony from patients, scientists, and politicians in rendering his ruling. Although a medical indication of marijuana for migraine was not considered, its use was approved as an anti-emetic, an anti-spasticity drug in multiple sclerosis and paraplegia, while its utilization in glaucoma was considered reasonable. He stated, "By any measure of rational analysis marijuana can be safely used within a supervised routine of medical care."
In 1992, a study examined subjective preferences of experimental subjects smoking Cannabis, or ingesting oral THC (Chait and Zacny, 1992). Ten subjects in two trials preferred smoking active Cannabis over placebo, while ten of eleven preferred oral THC to placebo. These results call into serious question the plausibility of true blinding with placebo preparations in prospective therapeutic drug studies of marijuana, especially when smoked.
A more profound understanding of Cannabis, THC, and their actions in the brain has occurred with the discovery of an endogenous cannabinoid in the human brain, arachidonylethanolamide, named anandamide, from the Sanskrit word ananda, or "bliss" (Devane et al., 1992). This ligand inhibits cyclic AMP in its target cells, which are widespread throughout the brain, but demonstrate a predilection for areas involved with nociception (Herkenham, 1993). The exact physiological role of anandamide is unclear, but preliminary tests of its behavioral effects reveal actions similar to those of THC (Fride and Mechoulam, 1993).
Additional research sheds light on possible mechanisms of therapeutic action of the cannabinoids on migraine. An inhibitory effect of anandamide and other cannabinoid agonists on rat serotonin type 3 (5-HT3) receptors was demonstrated (Fan, 1995). This receptor has been implicated as a mediator of emetic and pain responses. In 1996, a study in rats demonstrated antinociceptive effects of delta-9-THC and other cannabinoids in the periaqueductal gray matter (Lichtman et al., 1996). The PAG has been frequently cited as a likely anatomic area for migraine generation (Goadsby and Gundlach, 1991).
The understanding that Cannabis and THC effect their actions through natural cerebral biochemical processes has intensified the public debate on medical benefits of marijuana. In 1993, a book entitled Marihuana: The Forbidden Medicine (Grinspoon and Bakalar, 1993) examined a variety of claims for ailments treated by marijuana, and included an entire section on migraine. One clinical vignette discussed at length the medical odyssey of a migraineur through failures with standard pharmaceuticals, and ultimate preference for small doses of smoked marijuana for symptom control.
The editor of the British Medical Journal (Smith, 1995) recently wrote an editorial espousing moderation in the drug war. The Journal of the American Medical Association published a supportive commentary in 1995 (Grinspoon, 1995). The author rated the respiratory risks potent medical marijuana as low, and pointed out the contradiction of the Schedule 2 status of synthetic THC, dronabinol, while its natural source, marijuana remained a Schedule 1 product, and thus unavailable for legal use to patients who might prefer its easier dose titration. Grinspoon raised as a theoretical possibility the synergistic effects of the whole plant and its components as compared to pure THC.
The American Journal of Public Health issued its plea (AJPH, 1996), to allow access to medical marijuana as an Investigational New Drug (IND). The Australian government (Hall et al., 1995) recently compiled a recent exhaustive review of sequelae of Cannabis use. In the summary, it states:
anxiety, dysphoria, panic and paranoia, especially in naïve users;
cognitive impairment, especially of attention and memory, for the duration of intoxication;
psychomotor impairment, and probably an increased risk of accident if an intoxicated person attempts to drive a motor vehicle, or operate machinery;
an increased risk of experiencing psychotic symptoms among those who are vulnerable because of personal or family history of psychosis;
an increased risk of low birth weight babies if cannabis is used during pregnancy.
In a current review of over 65,000 patient records in an HMO (Sidney et al., 1997), little effect of smoked Cannabis was seen on morbidity and mortality of non-AIDS patients.
Surely, not all in the medical establishment are convinced of the relative safety or benefit of Cannabis for medical usage. In a recent review (Voth and Schwartz, 1997) the authors concluded, "The evidence does not support the reclassification of crude marijuana as a prescribable medicine." However, their study was far from comprehensive, confining itself to the clinical issues of nausea, appetite stimulation, glaucoma, and spasticity.
Methodologically, it was flawed in that only the medical literature from 1975-1996 was screened, an era during which it was quite difficult to initiate research seeking to support medical indications for Cannabis. These authors did not examine migraine as an indication for Cannabis usage, nor did they review the extensive literature of the past. The debate on the subject of "medical marijuana" has extended to the World Wide Web, and includes myriad postings with anecdotal attestations of efficacy for a variety of indications.
Various investigators have examined the roles of different smoke delivery systems (Gieringer, 1996). From these studies, it is clear that vaporization of marijuana makes it possible to deliver even high doses of THC to the lungs of a prospective patient far below the flash point of the Cannabis leaf, eliminating a fair amount of smoke, containing tar and other possible carcinogens. However, the marijuana joint was about as effective as any examined smoking device, including waterpipes, in providing a favorable ratio of THC to tar and other by-products of smoking. A standardized smoking procedure for use of Cannabis in medical research has been developed (Foltin et al., 1988).
Suppository preparations of Cannabis have been used to advantage in the past, and may be an acceptable form of administration for the migraineur, although dose titration would be less available.
Despite the development of serotonin 1D-agonist medications, migraine remains a serious public health issue. An estimated 23 million Americans suffer severe migraine. Of these, 25% have four or more episodes per month, and 35% have one to three severe headaches each month (Stewart et al., 1992). In economic terms, the impact of migraine is enormous: an estimated 14% of females, and 8% of males missed a portion of, or an entire day of work or school in one month (Linet et al., 1989). Migraine has been estimated to account for an economic impact of $1.2 to $17.2 billion annually in the U.S.A. in terms of lost productivity (Lipton et al., 1993). In 1990 studies were published outlining the biochemical basis of migraine treatment in serotonin receptor pharmacology (Peroutka, 1990). It was this research that led to the development of the first drugs active on serotonin receptor subtypes, sumatriptan, and ondansetron.
However, despite the justifiable success of sumatriptan in treating acute migraine, problems remain. Although rapidly active subcutaneously, its oral absorption is relatively slow, and often unreliable in the migraineur. Sumatriptan and its analogues are ineffective when administered in the "aura phase" of classic migraine (Ferrari and Saxena, 1995). Additionally, headache recurrence after "triptan" 5-HT1D agonist agents is a not infrequent occurrence. Unfortunately, repetitive dosing, and development of agents with longer half-lives does not seem to avert the issue (Ferrari and Saxena, 1995).
Another curiosity in the development of sumatriptan is its relative inability to pass the blood-brain barrier. Once more, the development of newer agents with improved central nervous system penetration has not necessarily improved efficacy, but does increase the likelihood of side effects, such as chest and throat tightness, numbness, tingling, anxiety, etc. (Ferrari and Saxena, 1995; Mathew, 1997).
Ultimately disappointing, none of the triptan drugs seems to exert any benefit on the frequency of migraine incidence, unlike dihydroergotamine, which has degree of prophylactic benefit.
Thus, it is the author's contention that this group of agents, though impressive, may represent somewhat of a "therapeutic dead end." Especially considering the large percentages of migraineurs who either fail to respond to the triptans, or can not tolerate them, there seems to be definite need for alternative treatment agents.
The author believes that the issue of medical marijuana, and its possible role in migraine treatment deserves proper scientific examination, both biochemically and clinically.
Results of controlled clinical trials may be valuable for migraineurs and professionals who treat them because there is a strong need for additional medications that will effectively this condition in its acute state. At this time, the best available medication, injected sumatriptan (Imitrex) has been ineffective in up to 30% of patients, or has produced undesirable side effects for up to 66% when administered subcutaneously (Mathew, 1997). The available evidence seems to suggest that smoked Cannabis would be a far safer alternative than butorphanol nasal spray (Stadol-NS), which, heretofore, has been an unscheduled drug approved in the U.S.A. for migraine treatment despite its addictive potential and unfavorable side effect profile (Fisher and Glass, 1997).
In closing, a quotation seems pertinent (Schultes, 1973):
There can be no doubt that a plant that has been in partnership with man since the beginnings of agricultural efforts, that has served man in so many ways, and that, under the searchlight of modern chemical study, has yielded many new and interesting compounds will continue to be a part of man's economy. It would be a luxury that we could ill afford if we allowed prejudices, resulting from the abuse of Cannabis, to deter scientists from learning as much as possible about this ancient and mysterious plant.
The author would like to thank the following individuals:
Rick Doblin and Sylvia Thiessen of the Multidisciplinary Association for Psychedelic Studies (MAPS), for financial support, and continued advice and suggestions. Paulette Cote of Western Montana Clinic Library, and the Inter-Library Loan Department at the Mansfield Library of the University of Montana for wonderful service in locating obscure references. Drs. Tod Mikuriya and Lester Grinspoon for provision of books, suggestions and encouragement. Drs. Keith Parker and Vernon Grund of the Department of Pharmacy, University of Montana for their guidance and good sense. Drs. Varro Tyler and Dennis McKenna for their inspiration and the confidence they engendered. Dr. Donald Abrams for his continuing efforts in pursuit of
medical indications for Cannabis. The Herbal Research Foundation and NAPRALERT for assistance on ethnobotanical information. Dr. Samir Ross for his initial guidance on my inquiries about experimental research on Cannabis. Marie-Josée Thibault, Deborah Somerville, and Penny King for their faithfulness and "morale support." Ultimately, to Dr. Mark Russo, for reasons he alone will understand.
Agurell, S., Halldin, M., Lindgren, J-E, Ohlsson, A., Widman, M., Gillespie, H. and Hollister, L., Pharmacokinetics and Metabolism of Delta-1-Tetrahydrocannabinol and Other Cannabinoids with Emphasis on Man, Pharmacol. Rev., 38 (1986) 21-43.
AJPH, Access to Therapeutic Marijuana/Cannabis, Amer. J. Pub. Health, 86 (1996) 441-442.
Brunner, T.F., Marijuana in Ancient Greece and Rome?: the Literary Evidence, J. Psychedel. Drugs, 9 (1977) 221-225.
Camp, W.H., The Antiquity of Hemp as an Economic Plant, J. N.Y, Bot. Gard., 37 (1936) 110-114.
Chait, L.D., and Zacny, J.P., Reinforcing and Subjective Effects of oral Delta-9-THC and Smoked Marijuana in Humans, Psychopharmacol., 107 (1992) 255-262.
Chiang, C.N. and Barnett, G., Marijuana Effect and Delta-9-Tetrahydrocannabinol Plasma Level, Clin. Pharm. Therap., 36 (1984) 234-238.
Chopra, I.C. and Chopra, R.W., The Use of Cannabis Drugs in India, Bull. on Narcotics, 9 (1957) 4-29.
Co, B.T., Goodwin, D.W., Gado, M., Mikhael, M. and Hill, S.Y., Absence of Cerebral Atrophy in Chronic Cannabis Users by Computerized Transaxial Tomography, JAMA, 237 (1977) 1229-1230.
Cohen, S., The 94-Day Cannabis Study, Ann. NY Acad. Sci., 282 (1976) 211-220.
Comitas, L., Cannabis and Work in Jamaica: A Refutation of the Amotivational Syndrome, Ann. NY Acad. Sci., 282 (1976) 211-220.
Darmsteter, J. (trans.), The Zend-Avesta, Part I, The Vendîdâd, Oxford, London, 1895, 389 pp.
Devane, W.A., Hanus, L., Breuer, A., Pertwee, R.G., Stevenson, L.A., Griffin, G., Gibson, D., Mandelbaum, A., Etinger, A. and Mechoulam, R., Isolation and Structure of a Brain Constituent That Binds to the
Cannabinoid Receptor, Science, 258 (1992) 1946-1949.
El-Mallakh, R.F., Marijuana and Migraine, Headache, 27 (1987) 442-443.
Fan, P., Cannabinoid Agonists Inhibit the Activation of 5-HT3 Receptors in Rat Nodose Ganglion Neurons, J. Neurophys., 73 (1995) 907-910.
Ferrari, M.D., and Saxena, P.R., 5-HT1 Receptors in Migraine Pathophysiology and Treatment, Europ. J. Neurol., 2 (1995) 5-21.
Fishbein, M., Migraine Associated with Menstruation, JAMA, 237 (1942) 326.
Fisher, M.A., and Glass, S., Butorphanol (Stadol): A Study in Problems of Current Drug Information and Control, Neurol., 48 (1997) 1156-1160.
Foltin, R.W., Fischman, M.W. and Byrne, M.F., Effects of Smoked Marijuana on Food Intake and Body Weight of Humans Living in a Residential Laboratory, Appetite, 11 (1988) 1-14.
Fride, E. and Mechoulam, R., Pharmacological Activity of the Cannabinoid Receptor Agonist, Anandamide, a Brain Constituent, Europ. J. Pharmacol., 231 (1993) 313-314.
Gieringer, D., Waterpipe Study, Bull. of Multidisc. Assoc. For Psychedel. Stud., 6 (1996) 59-63.
Goadsby, P.J. and Gundlach, A. L., Localization of [3H]-Dihydroergotamine Binding Sites in the Cat Central Nervous System: Relevance to Migraine, Ann. Neurol., 29 (1991) 91-94.
Grinspoon, L. and Bakalar, J.B., Marihuana: The Forbidden Medicine, Yale Univ., New Haven, 1993, 184 pp.
Grinspoon, L. and Bakalar, J.B., Marihuana as Medicine: A Plea for Reconsideration, JAMA, 273 (1995) 1875.
Hall, W., Solowij, N. and Lemon, J., The Health and Psychological Consequences of Cannabis Use, National Drug Strategy Monograph Series No. 25, National Drug and Alcohol Research Centre, Australia, 1995.
Herkenham, M.A., Localization of Cannabinoid Receptors in Brain: Relationship to Motor and Reward Systems. In: Biological Basis of Substance Abuse, Oxford Univ. Press, New York and London, 1993, pp. 187-200.
Hollister, L.E., Health Aspects of Cannabis, Pharmacol. Rev., 38 (1986) 1-20.
Kuehnle, J., Mendelson, J.H., Davis, K.R. and New, P.F.J., Computed Tomographic Examination of Heavy Marihuana Smokers, JAMA, 237 (1977) 1231-1232.
Li, Hui-Lin, An Archaeological and Historical Account of Cannabis in China, Econ. Bot., 28 (1974) 437-448.
Lichtman, A.H., Cook, S.A., and Martin, B.R., Investigation of Brain Sites Mediating Cannabinoid-Induced Antinociception in Rats: Evidence Supporting Periaqueductal Gray Involvement, J. Pharmacol. Exper. Therap., 276 (1996) 585-593.
Linet, M.S., Stewart, W.F., Celentano, D.D., An Epidemiological Study of Headache Among Adolescents and Young Adults, JAMA, 261 (1989) 2211-2216.
Lipton, R.B., Stewart, W.F., Migraine in the United States: Epidemiology and Health Care Use, Neurol., 43(suppl.) (1993) 6-10.
Martin, B.R., Cellular Effects of Cannabinoids, Pharmacol. Rev., 38 (1986) 45-74.
Mason, A.P. et al., Cannabis: Pharmacology and Interpretation of Effects, J. Forens. Sci., 30 (1985) 615-631.
Mathew, N.T., Serotonin 1D (5-HT 1D) Agonists and Other Agents in Acute Migraine, Neurol. Clinics, 15 (1997) 61-83.
Mikuriya, T.H. (ed.), Marijuana: Medical Papers 1839-1972, Medi-Comp Press, Oakland, CA, 1973, 465 pp.
Milstein, S.L., MacCannell, K., Karr, G. and Clark, S., Marijuana-Produced Changes in Pain Tolerance: Experienced and Non-Experienced Subjects, Int. Neuropsychiatr., 10 (1975) 177-182.
Noyes, R. and Baram, D.A., Cannabis Analgesia, Compr. Psychiatr. 15 (1974) 531-535.
Noyes, R., Brunk, F., Baram, D.A. and Canter, A., Analgesic Effect of Delta-9-Tetrahydrocannabinol, J. Clin. Pharmacol., 15 (1975) 134-143.
Noyes, R., Brunk, F., Avery, D.H. and Canter, A., The Analgesic Properties of Delta-9-Tetrahydrocannabinol and Codeine, Clin. Pharmacol. Ther., 18 (1975) 84-89.
Osler, W. and McCrae, T., The Principles and Practice of Medicine, Appleton and Co., New York and London, 1915, 1225 pp.
Peroutka, S.J., Developments in 5-Hydroxytryptamine Receptor Pharmacology in Migraine, Neurol. Clinics 8 (1990) 829-839.
Russo, E.B., Medora, R., Parker, K. and Thompson, C., Schedule 1 Research Protocol: An Investigation of Psychedelic Plants and Compounds for Activity in Serotonin Receptor Assays for Headache Treatment and Prophylaxis, Bull. Multidisc. Assoc. Psychedel. Stud. 7 (1997) 4-8.
Schultes, R.E., Man and Marijuana, Nat. Hist. 82 (1973) 59-63, 80, 82.
Schultes, R.E., Klein, W.M., Plowman, T. and Lockwood, T.E., Cannabis: An Example of Taxonomic Neglect, Bot. Mus. Leafl. Harv. Univ., 23 (1974) 337-367.
Sidney, S., Beck, J.E., Tekawa, I.S., Quesenberry, C.P., and Friedman, G.D., Marijuana Use and Mortalilty, Am. J. Publ. Health, 87 (1997) 585-590.
Smith, R., Editorial: The War on Drugs, Brit. Med. J., 311 (1995) 23-30.
Stewart, W.F., Lipton, R.B., Celantano, D.D., Prevalence of Migraine Headache in the United States, JAMA, 267 (1992) 64-69.
Volfe, Z., Dvilansky, A., and Nathan, I., Cannabinoids Block Release of Serotonin from Platelets by Plasma from Migraine Patients, Int. J. Clin. Pharm. Res., 4 (1985) 243-246.
Voth, E.A., and Schwartz, R.H., Medical Applications of Delta-9-Tetrahydrocannabinol and Marijuana, Ann. Int. Med., 126 (1997) 791-798.
Walton, R.P., Marihuana: Americas's New Drug Problem: A Sociologic Question with its Basic Explanation Dependent on Biologic and Medical Principles, J.B. Lippincott, Philadelphia, 1938, 223 pp.
Weber, J.T., O'Connor, M-F, Hayakataka, K., Colson, N., Medora, R., Russo, E.B., and Parker, K.K., Activity of Parthenolide at 5HT2A Receptors, J. Natl. Prod., 60 (1997)in press.
Young, F.L., In the Matter of Marijuana Rescheduling Petition, Dept. of Justice, Drug Enforcement Administration. Docket 86-22. Washington, D.C.: Drug Enforcement Administration, September 6, 1988.
Clinical Child and Adult Neurologist
Clinical Assistant Professor of Medicine, University of Washington
Adjunct Associate Professor of Pharmacy, University of Montana