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黄曲霉毒素对小鼠和大鼠肝脏中ATP酶活性的影响。

Effects of the aflatoxins on ATPase activities in mouse and rat liver.

作者信息

Desaiah D, Phillips T D, Hayes A W, Ho I K

出版信息

J Environ Sci Health B. 1979;14(3):265-78. doi: 10.1080/03601237909372127.

Abstract

The effects of the aflatoxins on ATPase activities in mouse and rat tissues were investigated in vitro. The hepatic oligomycin-sensitive (O.S.) Mg++ ATPase was inhibited significantly. The order of inhibition was G1 greater than B1 greater than G2 greater than B2. Mouse O.S. Mg++ ATPase was more sensitive than the corresponding rat enzyme. The oligomycin-insensitive (O.I.) Mg++ ATPase activities in rat and mouse liver were not altered. Although aflatoxins G1 and B1 were more potent inhibitors of hepatic O.S. Mg++ ATPase, no concentration-response was observed, whereas aflatoxins G2 and B2 inhibited enzyme activity in a concentration-dependent manner. Spectral analysis of aflatoxin G1 solutions suggested that solubility was not related to the observed effects. In addition, the effects of aflatoxin B1 and G1 on mouse brain microsomal Na+-K+ ATPase were examined. Although aflatoxin B1 was more potent that G1, both mycotoxins significantly inhibited enzyme activity in a concentration-dependent fashion.

摘要

在体外研究了黄曲霉毒素对小鼠和大鼠组织中ATP酶活性的影响。肝寡霉素敏感(O.S.)的Mg++ATP酶受到显著抑制。抑制顺序为G1>B1>G2>B2。小鼠的O.S.Mg++ATP酶比相应的大鼠酶更敏感。大鼠和小鼠肝脏中寡霉素不敏感(O.I.)的Mg++ATP酶活性未改变。虽然黄曲霉毒素G1和B1是肝O.S.Mg++ATP酶更有效的抑制剂,但未观察到浓度-反应关系,而黄曲霉毒素G2和B2以浓度依赖的方式抑制酶活性。黄曲霉毒素G1溶液的光谱分析表明,溶解度与观察到的效应无关。此外,还研究了黄曲霉毒素B1和G1对小鼠脑微粒体Na+-K+ATP酶的影响。虽然黄曲霉毒素B1比G1更有效,但两种霉菌毒素均以浓度依赖的方式显著抑制酶活性。

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