Takagi H, Shiomi H, Ueda H, Amano H
Nature. 1979 Nov 22;282(5737):410-2. doi: 10.1038/282410a0.
It is generally accepted that morphine exerts its analgesic effect by binding to specific opiate receptors in the brain and spinal cord. Since Hughes et al. isolated and identified two endogenous pentapeptides, Met- and Leu-enkephalin, from the brain and found that they acted as agonists at opiate receptors, alpha-, beta- and gamma-endorphins, larger peptides than enkephalins and having morphine-like activity, have been identified in either the brain or pituitary of various species. Several studies have demonstrated that enkephalins possess analgesic properties and that they are distributed in the pain-mediated pathways in the central nervous system. These findings suggest that enkephalins are important neurotransmitters or neuromodulators regulating pain transmission. We now report the isolation of a novel substance which has a Met-enkephalin releasing action. Our findings suggest the possibility of a regulating mechanism for the release of endogenous opioid peptides, especially Met-enkephalin.
人们普遍认为,吗啡通过与大脑和脊髓中的特定阿片受体结合来发挥其镇痛作用。自从休斯等人从大脑中分离并鉴定出两种内源性五肽,即甲硫氨酸脑啡肽和亮氨酸脑啡肽,并发现它们作为阿片受体的激动剂以来,在各种物种的大脑或垂体中已经鉴定出了α-、β-和γ-内啡肽,这些肽比脑啡肽更大,具有类似吗啡的活性。多项研究表明,脑啡肽具有镇痛特性,并且它们分布在中枢神经系统中疼痛介导的通路中。这些发现表明,脑啡肽是调节疼痛传递的重要神经递质或神经调节剂。我们现在报告一种具有释放甲硫氨酸脑啡肽作用的新物质的分离。我们的发现提示了内源性阿片肽,尤其是甲硫氨酸脑啡肽释放调节机制的可能性。