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在假定的癌前病变以及由降血脂过氧化物酶体增殖剂Wy-14,643诱导的大鼠肝细胞癌中缺乏γ-谷氨酰转肽酶活性。

The absence of gamma-glutamyl transpeptidase activity in putative preneoplastic lesions and in hepatocellular carcinomas induced in rats by the hypolipidemic peroxisome proliferator Wy-14,643.

作者信息

Rao M S, Lalwani N D, Scarpelli D G, Reddy J K

出版信息

Carcinogenesis. 1982;3(10):1231-3. doi: 10.1093/carcin/3.10.1231.

Abstract

Administration of Wy-14,643, a hypolipidemic agent which induces peroxisome proliferation, at a concentration of 0.1% (w/w) in the diet, leads to the development of altered foci, neoplastic nodules and hepatocellular carcinomas (HCC) in the liver of rats between 21 and 70 weeks. These various lesions in liver were analyzed histochemically for gamma-glutamyl transpeptidase (GGT) activity. The presence of lipofuscin, a putative indicator of lipid peroxidation was evaluated by autofluorescence. All the altered foci, neoplastic nodules and HCC were consistently negative for GGT, and had small amounts of lipofuscin contrasted to large deposits of this pigment in the surrounding normal liver. These results indicate that GGT is not a phenotypic marker in Wy-14,643 induced hepatic carcinogenesis. Whether the neoplastic alterations induced in liver by other peroxisome proliferators are similarly GGT negative remains to be determined.

摘要

在饮食中以0.1%(w/w)的浓度给予Wy-14,643(一种诱导过氧化物酶体增殖的降血脂剂),会导致21至70周龄大鼠肝脏中出现改变灶、肿瘤结节和肝细胞癌(HCC)。对肝脏中的这些不同病变进行了γ-谷氨酰转肽酶(GGT)活性的组织化学分析。通过自发荧光评估脂褐素(一种脂质过氧化的假定指标)的存在情况。所有改变灶、肿瘤结节和HCC的GGT均持续呈阴性,且与周围正常肝脏中大量的这种色素沉积相比,它们的脂褐素含量较少。这些结果表明,GGT不是Wy-14,643诱导的肝癌发生中的表型标志物。其他过氧化物酶体增殖剂在肝脏中诱导的肿瘤改变是否同样为GGT阴性仍有待确定。

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