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作为脊髓中脑啡肽释放指标的三肽酪氨酸-甘氨酸-甘氨酸水平的变化:伤害性刺激和胃肠外活性肽酶抑制剂的作用。

Changes in levels of the tripeptide Tyr-Gly-Gly as an index of enkephalin release in the spinal cord: effects of noxious stimuli and parenterally-active peptidase inhibitors.

作者信息

Llorens-Cortes C, Gros C, Schwartz J C, Clot A M, Le Bars D

机构信息

Unité de Neurobiologie et Pharmacologie, l'INSERM Centre Paul Broca, Paris, France.

出版信息

Peptides. 1989 May-Jun;10(3):609-14. doi: 10.1016/0196-9781(89)90151-4.

Abstract

The tripeptide Tyr-Gly-Gly (YGG), representing the product of enkephalin hydrolysis by enkephalinase (EC 3.4.24.11), was characterized and its levels measured in spinal cord perfusates of halothane-anaesthetized rats. During noxious pinching of the muzzle, which is known to trigger enkephalin release, YGG levels were enhanced more markedly and for longer than were those of [Met5]enkephalin (YGGFM), in the same samples. By contrast, neither YGG nor YGGFM levels were affected by pinching the tail. Treatment with carbaphethiol, a parenterally-active aminopeptidase inhibitor, markedly increased YGG levels and lengthened the duration of the increase produced by pinching the muzzle. Treatment with acetorphan, a parenterally-active enkephalinase inhibitor, given alone or in combination with carbaphethiol, completely prevented the rise in YGG triggered by noxious stimulation. By contrast, [Met5]enkephalin levels in the perfusates were increased by the combined administration of the two peptidase inhibitors but these levels were not further enhanced by noxious stimulation. Thus, spinal cord YGG appears to be formed under the influence of enkephalinase and to constitute a sensitive index of enkephalin release.

摘要

三肽酪氨酸-甘氨酸-甘氨酸(YGG),代表脑啡肽酶(EC 3.4.24.11)水解脑啡肽的产物,已被鉴定,并在氟烷麻醉大鼠的脊髓灌注液中测量了其水平。在已知会触发脑啡肽释放的口鼻部有害夹捏过程中,在相同样本中,YGG水平的升高比[Met5]脑啡肽(YGGFM)更显著且持续时间更长。相比之下,夹捏尾巴对YGG和YGGFM水平均无影响。用卡巴硫醇(一种胃肠外活性氨肽酶抑制剂)处理,可显著提高YGG水平,并延长口鼻部夹捏所产生的升高持续时间。用阿塞托芬(一种胃肠外活性脑啡肽酶抑制剂)单独或与卡巴硫醇联合处理,可完全阻止有害刺激引发的YGG升高。相比之下,灌注液中[Met5]脑啡肽水平通过两种肽酶抑制剂联合给药而升高,但有害刺激并未进一步提高这些水平。因此,脊髓YGG似乎是在脑啡肽酶的影响下形成的,并构成脑啡肽释放的一个敏感指标。

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