Lee N M, Friedman H J, Leybin L, Cho T M, Loh H H, Li C H
Proc Natl Acad Sci U S A. 1980 Sep;77(9):5525-6. doi: 10.1073/pnas.77.9.5525.
The synthetic beta-endorphin analogs with the omission of the NH2-terminal [Met]enkephalin segment [beta-endorphin-(6-31) and beta-endorphin-(20-31)] are shown to inhibit morphine- or beta-endorphin-induced analgesia in mice by the tail-flick test, whereas the synthetic NH2-terminal pentadecapeptide beta-endorphin-(1-15) has no inhibitory activity. This study raises the possibility that endogenous inhibiting peptides exist in the brain which play a role in the regulation of endorphin actions.
去除NH2末端[Met]脑啡肽片段的合成β-内啡肽类似物[β-内啡肽-(6 - 31)和β-内啡肽-(20 - 31)],通过甩尾试验显示可抑制小鼠体内吗啡或β-内啡肽诱导的镇痛作用,而合成的NH2末端十五肽β-内啡肽-(1 - 15)则无抑制活性。本研究提出了一种可能性,即大脑中存在内源性抑制肽,它们在调节内啡肽作用中发挥作用。