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蜂毒肽对离子跨细胞膜转运的影响。

Effect of melittin on ion transport across cell membranes.

作者信息

Yang S, Carrasquer G

机构信息

Department of Medicine, University of Louisville, KY 40292, USA.

出版信息

Zhongguo Yao Li Xue Bao. 1997 Jan;18(1):3-5.

Abstract

Extensive work with melittin has shown that the venom has multiple effects, probably, as a result of its interaction with negatively changed phospholipids. It inhibits well known transport pumps such as the Na(+)-K(+)-ATPase and the H(+)-K(+)-ATPase. Melittin increases the permeability of cell membranes to ions, particularly Na+ and indirectly Ca2+, because of the Na(+)-Ca(2+)-exchange. This effect results in marked morphological and functional changes, particularly in excitable tissues such as cardiac myocytes. In some other tissues, e.g., cornea, not only Na+ but Cl- permeability is also increased by melittin. Similar effects to melittin on H(+)-K(+)-ATPase have been found with the synthetic amphipathic polypeptide Trp-3.

摘要

对蜂毒肽的大量研究表明,该毒液具有多种作用,这可能是其与带负电荷的磷脂相互作用的结果。它能抑制诸如钠钾ATP酶和氢钾ATP酶等知名的转运泵。蜂毒肽可增加细胞膜对离子的通透性,尤其是钠离子,并由于钠钙交换而间接增加钙离子的通透性。这种作用会导致明显的形态和功能变化,特别是在诸如心肌细胞等可兴奋组织中。在其他一些组织中,例如角膜,蜂毒肽不仅会增加钠离子的通透性,还会增加氯离子的通透性。已发现合成的两亲性多肽Trp-3对氢钾ATP酶具有与蜂毒肽类似的作用。

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