Sforzo G A
School of Health Sciences and Human Performance, Ithaca College, New York.
Sports Med. 1989 Feb;7(2):109-24. doi: 10.2165/00007256-198907020-00003.
A number of endogenously produced opioid peptides interact with centrally and peripherally located specific receptors to form a widespread neuroendocrine system with many implications for human function. It is becoming increasingly evident that moderately high and high intensity exercise stimulate the release of the opioid peptide beta-endorphin to the circulation and this event may be subject to considerable intra- and interindividual variation. Moreover, endorphin levels probably remain elevated for 15 to 60 minutes following exercise. The duration of exertion does not seem to be critical, and low or moderate (less than 75% VO2max) intensity efforts do not stimulate this response. It also appears (mostly from animal model research) that exercise might elicit central opioid effects, but there is conflicting evidence on this topic. Physical training may encourage adapted opioid system function (e.g. altered peptide response to exercise or receptor number), but these adaptations are not well elucidated by the few existing studies. The significance of peripherally released opioid peptides during exercise has frequently been questioned. Exercise-induced affective response (e.g. mood enhancement), analgesia, food intake suppression and reproductive dysfunction are often mentioned as potentially controlled by an opioid mediated mechanism. While most of these events are normally considered under central control, it is time we begin entertaining the notion of peripheral effects (e.g. altered catecholamine release) and afferent input affecting central function in some of these phenomena. Additionally, evidence exists to suggest peripherally released enkephalins may cross the blood-brain barrier, but this is probably not true for endorphins. A number of other reported exercise-related events could possibly involve an underlying opioid mechanism. Exercise-associated metabolic regulation, immunosuppression, and cardiovascular function are areas for future opioid research.
许多内源性产生的阿片肽与中枢和外周特定受体相互作用,形成一个对人类功能有诸多影响的广泛神经内分泌系统。越来越明显的是,中等强度和高强度运动刺激阿片肽β-内啡肽释放进入循环,并且这一事件可能存在相当大的个体内和个体间差异。此外,运动后内啡肽水平可能会在15至60分钟内持续升高。运动持续时间似乎并不关键,低强度或中等强度(低于最大摄氧量的75%)运动不会刺激这种反应。似乎(主要来自动物模型研究)运动可能引发中枢阿片样作用,但关于这一主题存在相互矛盾的证据。体育锻炼可能会促进阿片系统功能的适应性变化(例如肽对运动的反应改变或受体数量变化),但现有的少数研究并未很好地阐明这些适应性变化。运动过程中外周释放的阿片肽的意义经常受到质疑。运动诱导的情感反应(如情绪改善)、镇痛、食物摄入抑制和生殖功能障碍常被认为可能由阿片介导的机制控制。虽然这些事件大多通常被认为受中枢控制,但我们现在应该开始考虑外周效应(如儿茶酚胺释放改变)以及传入输入在其中一些现象中影响中枢功能的概念。此外,有证据表明外周释放的脑啡肽可能穿过血脑屏障,但内啡肽可能并非如此。其他一些报道的与运动相关的事件可能也涉及潜在的阿片机制。运动相关的代谢调节、免疫抑制和心血管功能是未来阿片研究的领域。