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CHANGES IN BODY TEMPERATURE AND OXYGEN CONSUMPTION RATE OF CONSCIOUS MICE PRODUCED BY INTRAHYPOTHALAMIC AND INTRACEREBROVENTRICULAR INJECTIONS OF Δ 9 ‐TETRAHYDROCANNABINOL
Author(s) -
FITTON A.G.,
PERTWEE R.G.
Publication year - 1982
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1111/j.1476-5381.1982.tb08802.x
Subject(s) - tetrahydrocannabinol , δ9 tetrahydrocannabinol , oxygen , chemistry , metabolic rate , anesthesia , neuroscience , medicine , biology , biochemistry , cannabinoid , receptor , organic chemistry
1 Δ 9 ‐Tetrahydrocannabinol (Δ 9 ‐THC) was injected into the preoptic area of the anterior hypothalamus or into the third or fourth cerebral ventricle of the conscious mouse through a chronically implanted cannula and the effects on body temperature and oxygen consumption rate were measured. 2 At an ambient temperature of 22°C, injections of Δ 9 ‐THC into the fourth ventricle (5 and 10 μg) produced dose‐dependent falls in rectal temperature. Hypothermia was also observed after injections of the drug into the hypothalamus (5 and 10 μg) or into the third ventricle (10 μg). 3 The hypothermia produced by Δ 9 ‐THC was associated with a fall in oxygen consumption rate. Falls in rectal temperature and in oxygen consumption rate were significantly greater after injection of Δ 9 ‐THC than after injection of the drug vehicle, Tween 80. 4 The falls in rectal temperature and oxygen consumption rate produced by injection of Δ 9 ‐THC into the fourth ventricle were abolished by elevation of the ambient temperature from 22 to 32°C. 5 A pretreatment that consisted of subcutaneous injections of Δ 9 ‐THC (20 mg/kg) given once daily for three days produced tolerance to the hypothermic effect of the drug when injected on day 4 either into the fourth ventricle (10 μg) or into a lateral tail vein (2.0 mg/kg). 6 The results suggest that Δ 9 ‐THC acts centrally to alter thermoregulation in mice not only when it is injected directly into the hypothalamus or cerebral ventricles but also when it is given intravenously. After intraventricular or intravenous administration the drug may act at extrahypothalamic as well as at hypothalamic sites. The data also support the hypothesis that in mice, tolerance to the hypothermic effect of Δ 9 ‐THC is pharmacodynamic and does not depend on changes in metabolism or distribution of the drug.