Horita A, Carino M A, Chesnut R M
Psychopharmacology (Berl). 1976 Aug 26;49(1):57-62. doi: 10.1007/BF00427471.
Thyrotropin releasing hormone (TRH) administered via the intracerebroventricular (icv) route in doses ranging between 0.1 and 100 mug decreased the duration of pentobarbital-induced narcosis in rabbits. Antagonism of narcosis occurred whether TRH was administered before or after the barbiturate. TRH doses above 10 mug produced, in addition, behavioral excitation and hyperthermia. The antagonism of phenobarbital-induced narcosis was not as profound; animals were aroused only for a short period of time, after which the narcotized state returned. However, TRH exerted a prolonged antagonism or reversal of the phenobarbital-induced hypothermia. The central nervous system depression and analgesia produced by morphine were unaffected by TRH, but hypothermia and respiratory depression were reversed. TRH may represent an arousal factor in mammalian brain.
通过脑室内(icv)途径给予剂量在0.1至100微克之间的促甲状腺激素释放激素(TRH)可缩短戊巴比妥诱导的家兔麻醉持续时间。无论TRH是在巴比妥酸盐之前还是之后给药,均可产生麻醉拮抗作用。此外,剂量高于10微克的TRH会引起行为兴奋和体温过高。TRH对苯巴比妥诱导的麻醉的拮抗作用不那么显著;动物仅在短时间内被唤醒,之后麻醉状态恢复。然而,TRH对苯巴比妥诱导的体温过低具有延长的拮抗或逆转作用。吗啡产生的中枢神经系统抑制和镇痛作用不受TRH影响,但体温过低和呼吸抑制被逆转。TRH可能是哺乳动物脑中的一种唤醒因子。