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肝脏溶酶体对内源性和外源性阳离子化合物的体外反应。

In vitro response of hepatic lysosomes to endogenous and exogenous cationic compounds.

作者信息

Powell J H, Reidenberg M M

出版信息

Proc Soc Exp Biol Med. 1984 Sep;176(4):346-9. doi: 10.3181/00379727-176-41881.

Abstract

An investigation of the effect of four cationic compounds on rat liver lysosomes was carried out. Lysosomes from homogenized rat liver were isolated by differential centrifugation at 0-5 degrees C in 0.3 M sucrose. These lysosomes were then incubated for 1 hr at 37 degrees C in 0.25 M glycine solution containing widely varied concentrations of the test agent. The lysosomes were resedimented and the N-acetyl-beta-glucosaminidase (NAG) activity was measured in the supernatant and in the remaining pellet after disruption. Spermine, ferric ion, mepacrine, and gentamicin all produced dose-dependent effects on these lysosomes. Low concentrations of these compounds inhibited the release of NAG into the supernatant while high concentrations enhanced the release of NAG. This effect of these cationic compounds on the lysosomal membrane may be a mechanism by which they produce cellular toxicity with the organ or tissue selectivity being related to the distribution of the cation.

摘要

对四种阳离子化合物对大鼠肝脏溶酶体的影响进行了研究。通过在0-5摄氏度下于0.3M蔗糖中进行差速离心,从匀浆的大鼠肝脏中分离出溶酶体。然后将这些溶酶体在含有浓度差异很大的受试剂的0.25M甘氨酸溶液中于37摄氏度孵育1小时。溶酶体重新沉淀后,测定上清液和破碎后剩余沉淀中的N-乙酰-β-氨基葡萄糖苷酶(NAG)活性。精胺、铁离子、米帕林和庆大霉素对这些溶酶体均产生剂量依赖性效应。这些化合物的低浓度抑制NAG释放到上清液中,而高浓度则增强NAG的释放。这些阳离子化合物对溶酶体膜的这种作用可能是它们产生细胞毒性的一种机制,其器官或组织选择性与阳离子的分布有关。

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