Jope R S
Brain Res. 1979 Dec;180(3):313-44. doi: 10.1016/0165-0173(79)90009-2.
This review describes recent advances made in the understanding of the regulation of acetylcholine synthesis in brain with regard to the availability of its two precursors, choline and acetylCoA. Choline availability appears to be regulated by the high affinity choline transport system. Investigations of the localization and inhibition of this system are reviewed. Procedures for measuring high affinity choline transport and their shortcomings are described. The kinetics and effects of previous in vivo and in vitro treatments on high affinity choline transport are reviewed. Kinetic and direct coupling of the transport and acetylation of choline are discussed. Recent investigations of the source of acetylCoA used for the synthesis of acetylcholine are reviewed. Three sources of acetylCoA have recently received support: citrate conversion catalyzed by citrate lyase, direct release of acetylCoA from mitochondria following its synthesis from pyruvate catalyzed by pyruvate dehydrogenase, and production of acetylCoA by cytoplasmic pyruvate dehydrogenase. Investigations indicating that acetylCoA availability may limit acetylcholine synthesis are reviewed. A model for the regulation of acetylcholine synthesis which incorporates most of the reviewed material is presented.
本综述描述了在理解脑内乙酰胆碱合成调节方面的最新进展,涉及到其两种前体物质胆碱和乙酰辅酶A的可利用性。胆碱的可利用性似乎受高亲和力胆碱转运系统的调节。本文综述了对该系统定位和抑制的研究。描述了测量高亲和力胆碱转运的方法及其缺点。综述了先前体内和体外处理对高亲和力胆碱转运的动力学和影响。讨论了胆碱转运与乙酰化的动力学及直接偶联。综述了近期对用于乙酰胆碱合成的乙酰辅酶A来源的研究。乙酰辅酶A的三个来源最近得到了支持:由柠檬酸裂解酶催化的柠檬酸转化、由丙酮酸脱氢酶催化丙酮酸合成后线粒体直接释放乙酰辅酶A以及细胞质丙酮酸脱氢酶产生乙酰辅酶A。综述了表明乙酰辅酶A可利用性可能限制乙酰胆碱合成的研究。提出了一个整合了大部分综述内容的乙酰胆碱合成调节模型。