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胆红素对大鼠脑突触体膜电位的影响。

Effect of bilirubin on the membrane potential of rat brain synaptosomes.

作者信息

Mayor F, Díez-Guerra J, Valdivieso F, Mayor F

出版信息

J Neurochem. 1986 Aug;47(2):363-9. doi: 10.1111/j.1471-4159.1986.tb04510.x.

Abstract

The effect of the neurotoxic pigment bilirubin on the membrane potential of rat brain synaptosomes was studied by using the tetraphenylphosphonium ion (TTP+) technique. Bilirubin induces a rapid depolarization of synaptosomes, as reflected by an efflux of previously accumulated [3H]TTP+. This phenomenon persisted when the membrane potential across either the plasma membrane of the synaptosome or the inner membrane of the entrapped mitochondria was selectively depressed, thus indicating that both components of the synaptosomal membrane potential were affected by bilirubin. Bovine serum albumin, used at a albumin/bilirubin molar ratio of 1:1, had the capacity to completely prevent and reverse the effect of bilirubin. This fact demonstrates that the bilirubin-induced TPP+ release from synaptosomes is a reversible process that requires the presence of bilirubin interacting with the synaptosomal membranes. These results, together with the inhibition by bilirubin of [3H]TPP+ and [2-14C]acetate uptake by synaptosomal plasma membrane vesicles isolated from rat brain, suggest that bilirubin depresses the membrane potential across the synaptosomal plasma membrane by a mechanism involving alterations in ion permeability. This effect could be of relevance in the pathogenesis of bilirubin encephalopathy.

摘要

采用四苯基鏻离子(TTP⁺)技术研究了神经毒性色素胆红素对大鼠脑突触体膜电位的影响。胆红素可诱导突触体快速去极化,这可通过先前积累的[³H]TTP⁺外流来反映。当突触体的质膜或被困线粒体的内膜上的膜电位被选择性降低时,这种现象仍然存在,这表明突触体膜电位的两个组成部分均受胆红素影响。以白蛋白/胆红素摩尔比为1:1使用的牛血清白蛋白能够完全预防和逆转胆红素的作用。这一事实表明,胆红素诱导的TPP⁺从突触体释放是一个可逆过程,需要胆红素与突触体膜相互作用。这些结果,连同胆红素对从大鼠脑分离的突触体质膜囊泡摄取[³H]TPP⁺和[2-¹⁴C]乙酸盐的抑制作用,提示胆红素通过涉及离子通透性改变的机制降低突触体质膜上的膜电位。这种效应可能与胆红素脑病的发病机制有关。

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