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首页> 外文期刊>Japanese Journal of Pharmacology >Reversal of Antinociceptive Effect of Cholecystokinin by Benzodiazepines and a Benzodiazepine Antagonist, Ro 15-1788
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Reversal of Antinociceptive Effect of Cholecystokinin by Benzodiazepines and a Benzodiazepine Antagonist, Ro 15-1788

机译:苯二氮卓类和苯二氮卓类拮抗剂Ro 15-1788逆转胆囊收缩素的镇痛作用

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References(16) Cited-By(31) Intraperitoneally administered benzodiazepines, chlordiazepoxide (2-5 mg/kg), diazepam (1 mg/kg), flurazepam (1 mg/kg) and a benzodiazepine antagonist, Ro 15-1788 (0.5 mg/kg), reversed the antinociceptive effect in mice which was induced by intracisternal administration of 1 μg of sulfated cholecystokinin octapeptide. The antinociceptive effect of cholecystokinin was reversed by naloxone, suggesting that the antinociceptive action involves endogenous opioid peptides in its production. On the other hand, morphine-induced analgesia was not reversed by diazepam and Ro 15-1788. These facts rule out opioid receptors as the site of the antagonism between the benzodiazepines or Ro 15-1788 and cholecystokinin on the antinociceptive effect. Benzodiazepines and Bo 15-1788 seem to inhibit the release of opioid peptides induced by cholecystokinin.
机译:参考文献(16)Cited-By(31)腹膜内施用苯二氮卓类,氯二氮卓(2-5 mg / kg),地西epa(1 mg / kg),氟拉西m(1 mg / kg)和苯二氮卓拮抗剂Ro 15-1788(0.5 (mg / kg),逆转了由小鼠胸腔内给予1μg硫酸胆囊收缩素八肽诱导的镇痛作用。纳洛酮逆转了胆囊收缩素的抗伤害感受作用,表明该抗伤害感受作用涉及其生产中的内源性阿片肽。另一方面,地西epa和Ro 15-1788不能逆转吗啡引起的镇痛作用。这些事实排除了阿片受体作为苯二氮卓类或Ro 15-1788与胆囊收缩素之间在拮抗作用方面的拮抗作用的部位。苯二氮卓类药物和Bo 15-1788似乎抑制胆囊收缩素诱导的阿片肽释放。

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