Carr D B, Bergland R, Hamilton A, Blume H, Kasting N, Arnold M, Martin J B, Rosenblatt M
Science. 1982 Aug 27;217(4562):845-8. doi: 10.1126/science.6285473.
Small doses of endotoxin evoked a dramatic biphasic response of opioid peptide secretion into blood in sheep. The first phase began within minutes and coincided with a brief hypertensive response to endotoxin well before the appearance of fever or hypotension. The ratio of beta-endorphin to beta-lipotropin fell abruptly at the onset of the second phase of release, suggesting early depletion of a pool rich in beta-endorphin and subsequent emergence of a pool rich in unprocessed precursor. The concentration of cerebrospinal fluid opioids increased tenfold during the second phase. Naloxone administration augmented endotoxin-induced opioid secretion in both early and late phases, suggesting a short-loop feedback regulation of stress-induced endorphin secretion.
小剂量内毒素可引起绵羊血液中阿片肽分泌显著的双相反应。第一阶段在数分钟内开始,与内毒素引起的短暂高血压反应同时出现,远早于发热或低血压的出现。在释放的第二阶段开始时,β-内啡肽与β-促脂素的比例突然下降,这表明富含β-内啡肽的池早期耗竭,随后出现富含未加工前体的池。在第二阶段,脑脊液中阿片类物质的浓度增加了10倍。纳洛酮给药在早期和晚期均增强了内毒素诱导的阿片肽分泌,提示应激诱导的内啡肽分泌存在短反馈调节。