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锂和肌醇对原代培养的小脑颗粒细胞中磷酸肌醇代谢周转影响的表征。

Characterization of the effects of lithium and inositol on phosphoinositide turnover in cerebellar granule cells in primary culture.

作者信息

del Río E, Nicholls D G, Downes C P

机构信息

Pharmacology Department, Ninewells Medical School, Dundee, Scotland.

出版信息

J Neurochem. 1996 Feb;66(2):517-24. doi: 10.1046/j.1471-4159.1996.66020517.x.

Abstract

The effect of lithium on inositol phospholipid resynthesis in primary cultures of cerebellar granule cells was studied. During activation of phospholipase C by the combined action of a muscarinic agonist and mild depolarization, the levels of inositol phospholipids as well as the inositol phospholipid precursor CMP-phosphatidate appeared highly sensitive to lithium with half-maximal accumulation of CMP-phosphatidate attained at 0.5 mM LiCl, a concentration close to that in the plasma of patients subjected to lithium therapy. Under the same conditions, the effect of lithium on inositol phospholipid metabolism appeared to be mediated by depletion of cytoplasmic free inositol content. This was indicated by the observation that preincubation for 48 h in high extracellular inositol concentrations could decrease or delay the depletion of inositol phospholipids and the accumulation of CMP-phosphatidate induced by 10 mM LiCl. Because even relatively high concentrations of extracellular inositol (500 microM) only partially prevented inositol phospholipid depletion, cerebellar granule cells appear to have a comparatively low capacity to accumulate inositol intracellularly, in comparison with other brain cells in culture. The relationship between CMP-phosphatidate accumulation and phospholipase C activity has also been investigated using a range of agonists that have been reported to act on cerebellar granule cells.

摘要

研究了锂对小脑颗粒细胞原代培养物中肌醇磷脂再合成的影响。在毒蕈碱激动剂和轻度去极化的联合作用激活磷脂酶C的过程中,肌醇磷脂水平以及肌醇磷脂前体CMP - 磷脂酸对锂高度敏感,在0.5 mM LiCl时达到CMP - 磷脂酸积累的半数最大值,该浓度接近接受锂治疗患者血浆中的浓度。在相同条件下,锂对肌醇磷脂代谢的影响似乎是由细胞质游离肌醇含量的消耗介导的。这一点通过以下观察得以表明:在高细胞外肌醇浓度下预孵育48小时可减少或延迟由10 mM LiCl诱导的肌醇磷脂消耗和CMP - 磷脂酸积累。由于即使相对高浓度的细胞外肌醇(500 microM)也只能部分阻止肌醇磷脂消耗,与培养中的其他脑细胞相比,小脑颗粒细胞在细胞内积累肌醇的能力似乎相对较低。还使用一系列据报道作用于小脑颗粒细胞的激动剂研究了CMP - 磷脂酸积累与磷脂酶C活性之间的关系。

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