Abu-Salah K M
Department of Biochemistry, College of Science, King Saud University, Riyadh, Saudi Arabia.
Life Sci. 1996;58(3):187-93. doi: 10.1016/0024-3205(95)02276-7.
A study has been carried out into the effects of clinically important antisickling and anaesthetic substances and ionophoric antibiotics on the activities of (Na+, K+)- and (Ca+2, Mg2+)-ATPases of the human erythrocyte membrane. In general, these drugs, with the exception of nystatin, inhibit both types of enzymic activities but with varying degrees of efficacy. (Ca2+, Mg2+)-ATPases was more sensitive to the lipophilic anaesthetics and (Na+,K+)-ATPase to the ionophoric antibiotic, amphotericin B. These results are explained in the light of the partition coefficients of these drugs in erythrocyte membranes, their effects on the fluidity of the erythrocytes membranes, the changes they induce in the permeability properties of erythrocytes and the subsequent effect of procaine on sickling of erythrocytes, and their potential interaction with specific membrane components.
一项关于具有临床重要性的抗镰变和麻醉物质以及离子载体抗生素对人红细胞膜(Na⁺,K⁺)-和(Ca²⁺,Mg²⁺)-ATP酶活性影响的研究已经展开。总体而言,除制霉菌素外,这些药物均抑制这两种酶活性,但效力程度各异。(Ca²⁺,Mg²⁺)-ATP酶对亲脂性麻醉剂更敏感,而(Na⁺,K⁺)-ATP酶对离子载体抗生素两性霉素B更敏感。根据这些药物在红细胞膜中的分配系数、它们对红细胞膜流动性的影响、它们诱导红细胞通透性特性的变化以及随后普鲁卡因对红细胞镰变的影响,以及它们与特定膜成分的潜在相互作用,对这些结果进行了解释。