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苏拉明在体内外诱导大鼠肾溶酶体膜损伤。

Rat kidney lysosomal membrane damage induced by suramin in vitro and in vivo.

作者信息

Akanji M A

机构信息

Biochemistry Department, Nigerian Institute for Trypanosomiasis Research, Vom, Plateau State.

出版信息

Pharmacol Toxicol. 1988 May;62(5):318-21. doi: 10.1111/j.1600-0773.1988.tb01895.x.

Abstract

The effect of suramin, an acid naphthylamine, on rat kidney lysosomal membrane integrity was studied. Lysosomal particles were incubated with suramin (0.1-0.4 mM) and light scattering behaviour of the mixtures were subsequently measured. There was a significant decrease (P less than 0.005) in the amount of light absorbed in the presence of suramin compared to lysosomal particle suspension alone. This was accompanied by release of acid phosphatase, a lysosomal 'marker' enzyme, into the suspending medium. These effects were reduced in the presence of acetylsalicylic acid, a known lysosomal membrane stabilizer. Administration of suramin to rats resulted in loss of kidney acid phosphatase and lysozyme activities from the tissue. These results indicate labilization of rat kidney lysosomal membrane by suramin molecules both in vitro and in vivo.

摘要

研究了酸性萘胺苏拉明对大鼠肾脏溶酶体膜完整性的影响。将溶酶体颗粒与苏拉明(0.1 - 0.4 mM)一起孵育,随后测量混合物的光散射行为。与单独的溶酶体颗粒悬浮液相比,在苏拉明存在下吸收的光量显著减少(P < 0.005)。这伴随着溶酶体“标记”酶酸性磷酸酶释放到悬浮介质中。在已知的溶酶体膜稳定剂乙酰水杨酸存在下,这些作用减弱。给大鼠施用苏拉明导致组织中肾脏酸性磷酸酶和溶菌酶活性丧失。这些结果表明,苏拉明分子在体外和体内均可使大鼠肾脏溶酶体膜不稳定。

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