Reny-Palasse Véronique, Rips Richard
Unité de Pharmacologie Chimique INSERM, 75005 Paris France.
Pain. 1987 Aug;30(2):259-269. doi: 10.1016/0304-3959(87)91081-5.
The antinociceptive action of the 2 main metabolites of thyrotropin-releasing hormone (TRH), pyroglutamyl-histidyl-proline (TRH-OH) and histidyl-proline-diketopiperazine or cyclo(His-Pro), were studied using mechanical (Haffner's test) and chemical (phenyl-p-benzoquinone writhing test) stimuli. TRH has previously been shown to be active against both these stimuli. TRH-OH showed an antinociceptive action against both stimuli, while cyclo(His-Pro) had a dose-dependent effect only against a mechanical stimulus. Both metabolites of TRH were less effective than TRH. The antinociception induced by TRH does not appear to depend on the biotransformation of TRH to its metabolites since they are less active than TRH itself.
利用机械刺激(哈夫纳试验)和化学刺激(苯对苯醌扭体试验),研究了促甲状腺激素释放激素(TRH)的2种主要代谢产物焦谷氨酰-组氨酰-脯氨酸(TRH-OH)和组氨酰-脯氨酸二酮哌嗪或环(组-脯)的抗伤害感受作用。此前已证明TRH对这两种刺激均有活性。TRH-OH对两种刺激均显示出抗伤害感受作用,而环(组-脯)仅对机械刺激有剂量依赖性效应。TRH的两种代谢产物的效力均低于TRH。TRH诱导的抗伤害感受似乎并不依赖于TRH向其代谢产物的生物转化,因为它们的活性低于TRH本身。