Lecci A, Borsini F, Mancinelli A, D'Aranno V, Stasi M A, Volterra G, Meli A
A Menarini Pharmaceuticals, Pharmacological Research Department, Firenze, Italy.
J Neural Transm Gen Sect. 1990;82(3):219-30. doi: 10.1007/BF01272765.
8-OH-DPAT (2.5-10 mg/kg) and buspirone (10 mg/kg) but not 5,7-DHT (200 micrograms/mouse), pCPA (75 and 150 mg/kg, three times), ritanserin (0.1 and 0.2 mg/kg), LY 53857 (1.5 and 3 mg/kg), GR 38032 F (0.1-100 micrograms/kg), TFMPP (5 and 20 mg/kg) and mCPP (2.5 and 5 mg/kg) antagonized the rise in body temperature that occurs to the last mice removed from their group housing, which was termed as stress-induced hyperthermia (SIH). Ro 15-1788, at a dose which blocked the effect of diazepam on SIH, did not reverse the anxiolytic effect of buspirione. Instead, when cerebral 5-HT content was reduced to 50% by 5,7-DHT-induced lesion, the effect of buspirone on SIH was decreased. TFMPP 5 mg/kg did not shorten significantly the onset of SIH as could have been expected by an anxiogenic drug, while the dose of 20 mg/kg did not modify the pattern of SIH at all. The lower dose of TFMPP evoked a hyperthermic and the higher a hypothermic response.
8-羟基二苯丙氨酸(2.5 - 10毫克/千克)和丁螺环酮(10毫克/千克),但5,7-二氢睾酮(200微克/只小鼠)、对氯苯丙氨酸(75和150毫克/千克,三次)、利坦色林(0.1和0.2毫克/千克)、LY 53857(1.5和3毫克/千克)、GR 38032 F(0.1 - 100微克/千克)、三氟甲基苯哌嗪(5和20毫克/千克)和间氯苯哌嗪(2.5和5毫克/千克)不能对抗从群居笼中最后取出的小鼠所出现的体温升高,这种体温升高被称为应激性体温过高(SIH)。Ro 15 - 1788在能阻断地西泮对SIH作用的剂量下,并不能逆转丁螺环酮的抗焦虑作用。相反,当5,7-二氢睾酮诱导的损伤使脑5-羟色胺含量降低至50%时,丁螺环酮对SIH的作用减弱。三氟甲基苯哌嗪5毫克/千克并没有如促焦虑药物所预期的那样显著缩短SIH的发作时间,而20毫克/千克的剂量根本没有改变SIH的模式。三氟甲基苯哌嗪较低剂量引起体温升高,较高剂量引起体温降低反应。