Stolk J M, Hurst J H, Nisula B C
Behav Genet. 1982 Feb;12(1):37-52. doi: 10.1007/BF01065739.
Dopamine-beta-hydroxylase (DBH) is unique among the catecholamine biosynthetic enzymes in that release from sympathoadrenal cells during neurotransmission is an integral part of the enzyme's physiology. Because of this unique attribute, the metabolic pathways regulating DBH cannot depend solely upon intraneuronal processes. This manuscript summarizes evidence relating to the regulation of DBH metabolism in the rat. Levels of DBH in the circulation, which derive from release of sympathoadrenal cellular enzyme stores, are genetically determined; even though inherited, circulating DBH levels bear no apparent consistent relationship to cellular enzyme levels or to sympathoadrenal function. These findings suggest that processes regulating neuronal release of DBH are separate from other processes regulating disposal of the circulating enzyme. We have evaluated the circulating DBH disposal pathways by standard metabolic techniques. Our data strongly suggest that clearance of DBH from the circulatory compartment is a main, and perhaps the primary, disposal mechanism for cellular enzyme stores.
多巴胺-β-羟化酶(DBH)在儿茶酚胺生物合成酶中独具特色,即在神经传递过程中,交感肾上腺细胞释放该酶是其生理功能的一个组成部分。由于这一独特特性,调节DBH的代谢途径不能仅依赖于神经元内的过程。本手稿总结了与大鼠DBH代谢调节相关的证据。循环中DBH的水平源自交感肾上腺细胞酶储存的释放,由基因决定;尽管是遗传性的,但循环中DBH的水平与细胞酶水平或交感肾上腺功能并无明显一致的关系。这些发现表明,调节DBH神经元释放的过程与调节循环酶清除的其他过程是分开的。我们已通过标准代谢技术评估了循环中DBH的清除途径。我们的数据有力地表明,从循环系统中清除DBH是细胞酶储存的主要,甚至可能是首要的清除机制。