Yamamoto M, Shimizu M, Iwai A
Department of Pharmacology, Yamanouchi Pharmaceutical Co. Ltd., Tokyo, Japan.
Psychopharmacology (Berl). 1988;95(2):162-6. doi: 10.1007/BF00174502.
Effects of YM-14673 (N alpha-[[S)-4-oxo-2-azetidinyl)-carbonyl]-L-histidyl-L-prolinamide dihydrate), a new TRH derivative, on reserpine-induced behavioural and electroencephalographic changes were observed in comparison with those of TRH. YM-14673 antagonized reserpine-induced hypothermia and decrease in convulsion threshold in mice. The number of PGO waves recorded from the lateral geniculate body was decreased by administration of YM-14673 in reserpinized cats. The anti-reserpine activity of intravenous YM-14673 was about 8-20 times more potent than that of TRH. In inhibiting reserpine-induced hypothermia, the oral ED2 degrees C relative to IV ED2 degrees C as an indirect indication of absorption rate of the drugs was 15 for both YM-14673 and TRH. These results suggest that YM-14673 possesses more potent facilitatory effects on the central monoamine systems than TRH.
与促甲状腺激素释放激素(TRH)相比,观察了新型TRH衍生物YM-14673(Nα-[[S)-4-氧代-2-氮杂环丁烷基)-羰基]-L-组氨酰-L-脯氨酰胺二水合物)对利血平诱导的行为和脑电图变化的影响。YM-14673可对抗利血平诱导的小鼠体温过低和惊厥阈值降低。在利血平化的猫中,给予YM-14673可减少从外侧膝状体记录到的PGO波数量。静脉注射YM-14673的抗利血平活性比TRH强约8至20倍。在抑制利血平诱导的体温过低方面,相对于静脉注射ED2℃,口服ED2℃作为药物吸收率的间接指标,YM-14673和TRH均为15。这些结果表明,YM-14673对中枢单胺系统的促进作用比TRH更强。