Saria A, Troger J, Kirchmair R, Fischer-Colbrie R, Hogue-Angeletti R, Winkler H
Department of Psychiatry, University of Innsbruck, Austria.
Neuroscience. 1993 May;54(1):1-4. doi: 10.1016/0306-4522(93)90377-r.
Proteolytic processing of secretogranin II (chromogranin C) in brain leads to the formation of a 33-amino acid peptide which we have named secretoneurin. All the properties of secretoneurin are consistent with the concept that this peptide represents a neuropeptide. However, a biological function has not yet been demonstrated. Therefore, we have now investigated whether secretoneurin could alter transmitter release in brain. Slices of rat caudate-putamen were superfused in an in vitro system and dopamine was measured in the superfusate. Secretoneurin dose-dependently increased the outflow of dopamine. This response was abolished in Ca(2+)-free medium. The secretoneurin-response could also be blocked by preincubation of the peptide with a specific antiserum and was subject to rapid specific and reversible desensitization. This effect on dopamine release constitutes the first discovered biological effect found for a peptide derived from secretogranin II. Thus, secretoneurin can be added to the ever-growing number of neuropeptides.
脑内分泌粒蛋白II(嗜铬粒蛋白C)的蛋白水解加工会导致形成一种33个氨基酸的肽,我们将其命名为分泌神经素。分泌神经素的所有特性都与该肽代表一种神经肽的概念相一致。然而,其生物学功能尚未得到证实。因此,我们现在研究了分泌神经素是否会改变脑内神经递质的释放。在体外系统中对大鼠尾状核 - 壳核切片进行灌流,并测量灌流液中的多巴胺。分泌神经素以剂量依赖的方式增加多巴胺的流出量。这种反应在无钙培养基中消失。分泌神经素的反应也可通过将该肽与特异性抗血清预孵育来阻断,并且会经历快速的特异性和可逆脱敏。这种对多巴胺释放的影响是首次发现的源自分泌粒蛋白II的肽的生物学效应。因此,分泌神经素可以加入到不断增加的神经肽数量中。