Vinogradov V A, Polonskiĭ V M
Biull Eksp Biol Med. 1985 May;99(5):548-9.
A study was made of the effects of some endogenous opioids (beta-endorphin, gamma-endorphin, met-enkephalin, leu-enkephalin and dinorphin) formed in the body from different high-molecular precursors (pro-opiomelanocortin, proenkephalins A and B) on the development in rats of the cysteamine-induced duodenal ulcers. All the peptides under study, gamma-endorphin, in particular, had an anti-ulcerous activity which was mediated by specific opiate receptors. The majority of the opioids was characterized by reduction of the anti-ulcerous effect as the dose was raised. It is assumed that protection of the duodenal mucosa under ulcerogenic exposures is an essential property of endogenous peptides. It is concluded that opioid peptides derived from different precursors are arranged in a complex synergic system responsible for cytoprotection of the duodenum.
研究了体内由不同高分子前体(阿片-促黑素原、脑啡肽原A和B)形成的一些内源性阿片样物质(β-内啡肽、γ-内啡肽、甲硫氨酸脑啡肽、亮氨酸脑啡肽和强啡肽)对大鼠半胱胺诱导的十二指肠溃疡发展的影响。所有研究的肽,特别是γ-内啡肽,都具有由特定阿片受体介导的抗溃疡活性。大多数阿片样物质的特点是随着剂量增加抗溃疡作用减弱。推测在致溃疡暴露情况下十二指肠黏膜的保护是内源性肽的一项基本特性。得出的结论是,源自不同前体的阿片肽排列在一个负责十二指肠细胞保护的复杂协同系统中。