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Journal of Pharmacology and Experimental Therapeutics

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Research ArticleNEUROPHARMACOLOGY

CB1 Receptors in the Preoptic Anterior Hypothalamus Regulate WIN 55212-2 [(4,5-Dihydro-2-methyl-4(4-morpholinylmethyl)-1-(1-naphthalenyl-carbonyl)-6H-pyrrolo[3,2,1ij]quinolin-6-one]-Induced Hypothermia

S. M. Rawls, Jose Cabassa, Ellen B. Geller and Martin W. Adler
Journal of Pharmacology and Experimental Therapeutics June 2002, 301 (3) 963-968; DOI: https://doi.org/10.1124/jpet.301.3.963
S. M. Rawls
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Jose Cabassa
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Ellen B. Geller
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Martin W. Adler
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Abstract

The present study investigated the effect of the selective cannabinoid agonist, WIN 55212-2 [(4,5-dihydro-2-methyl-4(4-morpholinylmethyl)-1-(1-naphthalenyl-carbonyl)-6H-pyrrolo[3,2,1ij]quinolin-6-one], on body temperature. WIN 55212-2 (1, 2.5, 5, and 10 mg/kg, i.m.) induced hypothermia in a dose-dependent manner. The peak hypothermia occurred 60 to 180 min postinjection. Body temperature was still suppressed 5 h after the injection of the highest dose of WIN 55212-2. The selective CB1 antagonist, SR141716A [N-(piperidin-1-yl)-5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxamide hydrochloride] (5 and 10 mg/kg, i.m.), blocked the WIN 55212-2-induced hypothermia, suggesting that CB1 receptor activation mediated the hypothermia. In contrast, the selective CB2antagonist, SR144528 [N-{(1S)-endo-1,3,3-trimethyl bicyclo heptan-2-yl]-5-(4-chloro-3-methylphenyl)-1-(4-methylbenzyl)-pyrazole-3-carboxamide}] (5 mg/kg, i.m.), did not alter the WIN 55212-2-induced hypothermia. Neither SR141716A nor SR144528 alone altered body temperature. WIN 55212-2 (1–30 μg/μl) injected directly into the preoptic anterior hypothalamic nucleus (POAH) induced hypothermia in an immediate and dose-dependent fashion. The hypothermia produced by intra-POAH injection of WIN 55212-2 was brief, with body temperature returning to baseline 60 min postinjection. SR141716A (5 mg/kg, i.m.) abolished the hypothermia induced by intra-POAH injection of WIN 55212-2 (30 μg/μl), indicating that CB1 receptors in the POAH mediated the hypothermia. The present results confirm the idea that CB1 receptors mediate the hypothermic response to cannabinoid agonists. Moreover, the present data suggest that 1) the POAH is the central locus for thermoregulation, and 2) CB1receptors within the POAH are the primary mediators of cannabinoid-induced hypothermia.

Footnotes

  • This study was supported by Grants DA 00376, DA 13429, and T32 DA 07237 from the National Institute on Drug Abuse.

  • Abbreviations:
    WIN 55212-2
    (4,5-dihydro-2-methyl-4(4-morpholinylmethyl)-1-(1-naphthalenyl-carbonyl)-6H-pyrrolo[3,2,1ij]quinolin-6-one
    SR141716A
    N-(piperidin-1-yl)-5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxamide hydrochloride
    SR144528
    N-{(1S)-endo-1,3,3-trimethyl bicyclo heptan-2-yl]-5-(4-chloro-3-methylphenyl)-1-(4-methylbenzyl)-pyrazole-3-carboxamide}
    POAH
    preoptic anterior hypothalamic nucleus
    Δ9-THC
    Δ9-tetrahydrocannabinol
    • Received December 19, 2001.
    • Accepted February 25, 2002.
  • The American Society for Pharmacology and Experimental Therapeutics
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Journal of Pharmacology and Experimental Therapeutics: 301 (3)
Journal of Pharmacology and Experimental Therapeutics
Vol. 301, Issue 3
1 Jun 2002
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Research ArticleNEUROPHARMACOLOGY

CB1 Receptors in the Preoptic Anterior Hypothalamus Regulate WIN 55212-2 [(4,5-Dihydro-2-methyl-4(4-morpholinylmethyl)-1-(1-naphthalenyl-carbonyl)-6H-pyrrolo[3,2,1ij]quinolin-6-one]-Induced Hypothermia

S. M. Rawls, Jose Cabassa, Ellen B. Geller and Martin W. Adler
Journal of Pharmacology and Experimental Therapeutics June 1, 2002, 301 (3) 963-968; DOI: https://doi.org/10.1124/jpet.301.3.963

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Research ArticleNEUROPHARMACOLOGY

CB1 Receptors in the Preoptic Anterior Hypothalamus Regulate WIN 55212-2 [(4,5-Dihydro-2-methyl-4(4-morpholinylmethyl)-1-(1-naphthalenyl-carbonyl)-6H-pyrrolo[3,2,1ij]quinolin-6-one]-Induced Hypothermia

S. M. Rawls, Jose Cabassa, Ellen B. Geller and Martin W. Adler
Journal of Pharmacology and Experimental Therapeutics June 1, 2002, 301 (3) 963-968; DOI: https://doi.org/10.1124/jpet.301.3.963
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