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内质网某些酶系统活性的不同修饰因素对细胞器抵抗化学试剂损伤作用敏感性的影响。II. 氯丙嗪、2,4-二硝基苯酚、苯巴比妥和滴滴涕的研究

Effect of different factors modifying the activity of some enzyme systems of the endoplasmic reticulum on the sensitivity of cell organelles against the damaging action of chemical agents. II. Studies with chlorpromazine, 2,4-dinitrophenol, phenobarbital and DDT.

作者信息

Popov C S, Yantchev I, Popova M P, Vultcheva G M

出版信息

Br J Exp Pathol. 1979 Feb;60(1):85-95.

Abstract

Further investigations on the effect of different stress factors on the stability of intracellular membranes were carried out. Large granule fractions derived from livers of sleep-deprived and dehydrated rats and subjected to preincubation at 37 degrees and pH 5 were shown to release latent acid phosphatase with a delayed rate indicating an increased lysosomal stability towards acid media conditioning. Lysosomes of such animals, however, were found to be more sensitive to mechanical treatments (homogenization procedure in this case) than that of controls, a conclusion made on the basis of enhanced "free" and nonsedimentable phosphatase activities in liver homogenates. The stress factors which previously were included in the group of modifiers of the activity of the endoplasmic reticulum-located enzymes caused some changes in the action of certain chemicals on membranes. Earlier such changes were elicited for carbon tetrachloride and only on low-temperature-conditioned rats for chlorpromazine. The present results show that stress factors studied result in deviations (different in extent and in direction) from the usual effects of chlorpromazine, 2,4-dinitrophenol, phenobarbital and DDT on liver lysosomes and peroxisomes.

摘要

对不同应激因素对细胞内膜稳定性的影响进行了进一步研究。从睡眠剥夺和脱水大鼠肝脏中分离出大颗粒部分,在37℃和pH 5条件下进行预孵育,结果显示其释放潜伏性酸性磷酸酶的速率延迟,表明溶酶体对酸性介质条件的稳定性增加。然而,发现这类动物的溶酶体比对照组对机械处理(在这种情况下为匀浆过程)更敏感,这一结论是基于肝脏匀浆中“游离”和不可沉淀的磷酸酶活性增强得出的。先前被归入内质网定位酶活性调节剂组的应激因素,导致某些化学物质对膜的作用发生了一些变化。早期,四氯化碳引发了这种变化,而氯丙嗪仅在低温条件下的大鼠中引发了这种变化。目前的结果表明,所研究的应激因素导致氯丙嗪、2,4 -二硝基苯酚、苯巴比妥和滴滴涕对肝脏溶酶体和过氧化物酶体的通常作用出现偏差(程度和方向不同)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7dd3/2041429/45affdcae600/brjexppathol00121-0105-a.jpg

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