期刊
JOURNAL OF NEUROPHYSIOLOGY
卷 90, 期 2, 页码 613-621出版社
AMER PHYSIOLOGICAL SOC
DOI: 10.1152/jn.00042.2003
关键词
-
Metabotropic receptors modulate numerous cellular processes by intracellular Ca2+ signaling, but less is known about their role in regulating mitochondrial metabolic function within the CNS. In this study, we demonstrate in area CA3 of rat organotypic hippocampal slice cultures that glutamatergic, serotonergic, and muscarinic metabotropic receptor ligands, namely trans-azetidine-2,4-dicarboxylic acid, alpha-methyl-5-hydroxytryptamine, and carbachol, transiently increase mitochondrial Ca2+ concentration ([Ca2+](m)) as recorded by changes in Rhod- 2 fluorescence, stimulate mitochondrial oxidative metabolism as revealed by elevations in NAD( P) H fluorescence, and induce K+ outward currents as monitored by rapid increases in extracellular K+ concentration ([K+](o)). Carbachol (1-1,000 muM) elevated NAD(P) H fluorescence by less than or equal to 14% DeltaF/F-0 and increased [K+](o) by less than or equal to4.3 mM in a dose-dependent manner. Carbachol-induced responses persisted in Ca2+-free solution and blockade of ionotropic glutamatergic and nicotinic receptors. Under similar conditions caffeine, known to cause Ca2+-induced Ca2+ release (CICR), also evoked elevations in [Ca2+](m), NAD(P) H fluorescence and [K+](o) that, in contrast to carbachol-induced responses, displayed oscillations. After depletion of intracellular Ca2+ stores by carbachol in Ca2+-free solution, re-application of 1.6 mM Ca2+-containing solution triggered marked elevations in [Ca2+](m), NAD(P) H fluorescence and [K+](o). These data indicate that metabotropic transmission effectively regulates mitochondrial oxidative metabolism via diverse receptor types in hippocampal cells and that inonitol 1,4,5-trisphosphate-induced Ca2+ release (IICR) or CICR or capacitative Ca2+ entry might suffice in stimulating oxidative metabolism by elevating [Ca2+](m). Thus activation of metabotropic receptors might significantly contribute to generation of ATP within neurons and glial cells.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据