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钙可增强红细胞膜脂质的过氧化作用。

Calcium potentiates the peroxidation of erythrocyte membrane lipids.

作者信息

Jain S K, Shohet S B

出版信息

Biochim Biophys Acta. 1981 Mar 20;642(1):46-54. doi: 10.1016/0005-2736(81)90136-x.

Abstract

To explore the possible role of intracellular calcium in membrane lipid peroxidation, we subjected red cells to conditions designed to increase intracellular calcium levels and then measured lipid peroxidation after exposure to a peroxidant threat. Human erythrocytes were pretreated for 3 h with either very high levels of CaCl2, or with low levels in the presence of the ionophore A23187. The erythrocytes were subsequently exposed to a peroxide-generating system consisting of xanthine and xanthine oxidase, or H2O2 for 1 h at 37 degrees C. As measured by a malonyldialdehyde assay, the calcium-treated cell showed up to a 2-fold increase in lipid peroxidation in comparison to untreated cells. In experiments with the ionophore, calcium concentration-dependent effects were detected at levels as low as 10 microM and were maximal at 50 microM. A significant loss of phosphatidylserine and phosphatidylethanolamine was observed in calcium- and peroxide-treated erythrocytes. This potentiation of membrane lipid peroxidation and lipid loss could be prevented by either lipid antioxidants or EGTA. The present study shows that pretreatment of erythrocytes with calcium increases their sensitivity to lipid peroxidation. This suggests that increased calcium concentration may be a factor in the potentiation of membrane lipid peroxidation of erythrocytes known to have increased calcium levels such as sickled and senescent red cells.

摘要

为了探究细胞内钙在膜脂质过氧化中的可能作用,我们使红细胞处于旨在提高细胞内钙水平的条件下,然后在暴露于过氧化物威胁后测量脂质过氧化情况。人红细胞用非常高浓度的氯化钙预处理3小时,或在离子载体A23187存在的情况下用低浓度的氯化钙预处理。随后,红细胞在37℃下暴露于由黄嘌呤和黄嘌呤氧化酶组成的过氧化物生成系统或过氧化氢中1小时。通过丙二醛测定法测量,与未处理的细胞相比,经钙处理的细胞脂质过氧化增加了两倍。在使用离子载体的实验中,在低至10微摩尔的水平上检测到钙浓度依赖性效应,在50微摩尔时达到最大值。在经钙和过氧化物处理的红细胞中观察到磷脂酰丝氨酸和磷脂酰乙醇胺的显著损失。脂质抗氧化剂或乙二醇双四乙酸(EGTA)均可防止膜脂质过氧化和脂质损失的这种增强。本研究表明,用钙预处理红细胞会增加其对脂质过氧化的敏感性。这表明钙浓度升高可能是已知钙水平升高的红细胞(如镰状红细胞和衰老红细胞)膜脂质过氧化增强的一个因素。

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