Involvement of Serotonergic Receptor Subtypes in the Production of Antinociception by Psychological Stress in Mice.
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概要
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Besides the important role of emotional factors in the production of psychological-stress-induced analgesia (PSY-SIA), recent attention to the participation of serotonergic (5-HTnergic)neurons in the fear and anxiety-evoking mechanism led us to examine the effects of 5-HTnergic ligands on PSY-SIA. Pretreatment of mice with 2.0 to 10 mg/kg of methysergide, a 5-HT receptor antagonist, or 1.0 to 10 mg/kg of buspirone, a 5-HT<SUB>1A</SUB> receptor partial agonist, dose-dependently suppressed the production of PSY-SIA. Ritanserin, a 5-HT<SUB>2</SUB> receptor antagonist, 1.0 to 5.0 mg/kg, or Y-25, 130, a 5-HT<SUB>3</SUB> receptor antagonist, 0.03 and 0.1 mg/kg, also inhibited PSY-SIA dose-dependently, while (±)pindolol, a 5-HT<SUB>1A/1B</SUB> receptor antagonist, was ineffective at doses up to 3.0 mg/kg. Furthermore, the suppressive effect of PSY-stress on the development of antinociceptive tolerance to morphine was also antagonized by methysergide, buspirone, ritanserin and Y-25, 130, but not by (±)pindolol. These results suggest that 5-HT receptor (5-HT<SUB>1A</SUB>, 5-HT<SUB>2</SUB> and 5-HT<SUB>3</SUB> but not 5-HT<SUB>1B</SUB>)-mediated mechanisms play an important role in the production of PSY-SIA.
- 公益社団法人 日本薬理学会の論文
著者
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Tokuyama Shogo
Department Of Clinical Pharmacy Kobe Gakuin University Faculty Of Pharmaceutical Sciences
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Kaneto Hiroshi
Department Of Pharmacology Faculty Of Pharmaceutical Science Nagasaki University
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Takahashi Masakatsu
Department of Analytical Research for Pharmacoinformatics, Graduate School of Pharmaceutical Sciences, Nagasaki University
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