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叔丁基过氧化氢对分离的大鼠肝细胞中Ca(2+) ATP酶活性的影响及其抗氧化剂的逆转作用。

Effects of tert-butyl hydroperoxide on Ca(2+) ATPase activity in isolated rat hepatocytes and its reversal by antioxidants.

作者信息

Singh Sangram, Agarwal Richa, Jamal Farrukh, Mehrotra Sudhir, Singh Rakesh

机构信息

Department of Biochemistry, Dr. R. M. L. Avadh University, Faizabad-224001, India.

出版信息

J Environ Biol. 2012 Sep;33(5):867-70.

Abstract

Calcium ions play an importantrole in various physiological processes such as nerve impulse transmission, muscle contraction, hormone action, blood clotting. They ions act as an intracellular second messenger, relaying information within cells to regulate their activity. To understand the mechanism of hepatotoxicity of t-BHP, studies were carried out using freshly isolated rat hepatocytes. The effect of t-BHP on Ca(2+) accumulation and Ca(2+) uptake by rat hepatocytes was monitored using 45Ca(2+). It caused decrease in 15% accumulation of 45Ca(2+) in comparison to the control group. t-BHP also significantly decreased the Ca(2+) ATPase activity in isolated hepatocytes .This decrease in Ca(2+) ATPase activity by t-BHP was reversed 40% by naturally occurring antioxidant glutathione (GSH) and 20% by the synthetic antioxidant butylated hydroxy toluene (BHT). These results indicate that the hepatotoxic action of t-BHP involves oxidative stress as evident by the protection accorded by various antioxidants employed in the study as well as impairment of intracellular calcium homeostasis which can lead to liver cell injury.

摘要

钙离子在多种生理过程中发挥重要作用,如神经冲动传递、肌肉收缩、激素作用、血液凝固。这些离子作为细胞内的第二信使,在细胞内传递信息以调节其活性。为了解叔丁基过氧化氢(t-BHP)的肝毒性机制,使用新鲜分离的大鼠肝细胞进行了研究。用45Ca(2+)监测t-BHP对大鼠肝细胞Ca(2+)积累和Ca(2+)摄取的影响。与对照组相比,它导致45Ca(2+)积累减少了15%。t-BHP还显著降低了分离肝细胞中的Ca(2+)ATP酶活性。t-BHP导致的Ca(2+)ATP酶活性降低,被天然抗氧化剂谷胱甘肽(GSH)逆转了40%,被合成抗氧化剂丁基羟基甲苯(BHT)逆转了20%。这些结果表明,t-BHP的肝毒性作用涉及氧化应激,这在研究中使用的各种抗氧化剂所提供的保护以及细胞内钙稳态的损害中很明显,而细胞内钙稳态的损害可导致肝细胞损伤。

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