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鞘氨醇对线粒体功能的影响。

Effect of psychosine on mitochondrial function.

作者信息

Tapasi S, Padma P, Setty O H

机构信息

Department of Biochemistry, School of Life Sciences, University of Hyderabad, India.

出版信息

Indian J Biochem Biophys. 1998 Jun;35(3):161-5.

PMID:9803665
Abstract

The effect of psychosine on the rate of respiration at different segments of the electron transport chain, respiratory control ratio and the efficiency of phosphorylation was studied. The transfer of electrons through site I, site II and site III was studied independently. The transfer through site I and site III was inhibited by psychosine, whereas the transfer through site II was not inhibited. Cardiolipin, which is essential for the electron transfer through site I and III, was implicated to be responsible for the inhibition of electron transfer by psychosine. Electron carriers of site II are not sensitive to cardiolipin, so psychosine could not inhibit the electron transfer through this site. The ADP/O ratio and respiratory control ratio were inhibited by psychosine showing that it has an uncoupler like effect. Mitochondria isolated from rat liver, kidney and brain behaved essentially the same way in their response to psychosine. Cytochrome c oxidase was significantly inhibited by psychosine and the degree of inhibition was almost same in mitochondria and sub mitochondrial particles. The preence of outer membrane in mitochondria did not make any difference with respect to the action of psychosine on electron transport chain. Psychosine interacts at site I and site III and a change in the lipid environment of the membrane is responsible for the mitochondrial dysfunctions induced by psychosine. This represents a possible mechanism for the destruction of cells in Gaucher's and Krabbe's disease.

摘要

研究了神经鞘氨醇对电子传递链不同区段呼吸速率、呼吸控制率和磷酸化效率的影响。分别研究了电子通过位点I、位点II和位点III的传递情况。神经鞘氨醇抑制电子通过位点I和位点III的传递,而不抑制通过位点II的传递。对通过位点I和III的电子传递至关重要的心磷脂被认为是神经鞘氨醇抑制电子传递的原因。位点II的电子载体对心磷脂不敏感,因此神经鞘氨醇不能抑制通过该位点的电子传递。神经鞘氨醇抑制了ADP/O比和呼吸控制率,表明它具有解偶联剂样作用。从大鼠肝脏、肾脏和大脑分离的线粒体对神经鞘氨醇的反应基本相同。细胞色素c氧化酶被神经鞘氨醇显著抑制,线粒体和亚线粒体颗粒中的抑制程度几乎相同。线粒体中外膜的存在对神经鞘氨醇对电子传递链的作用没有任何影响。神经鞘氨醇在位点I和位点III相互作用,膜脂质环境的变化是神经鞘氨醇诱导线粒体功能障碍的原因。这代表了戈谢病和克拉伯病中细胞破坏的一种可能机制。

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