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新生大鼠肝细胞中胰岛素诱导的超微结构变化的定量描述。

A quantitative description of the insulin-induced ultrastructural changes in newborn rat hepatocytes.

作者信息

Maintas D B, Kotoulas O B, Kotoulas A O

机构信息

Department of Anatomy, Histology and Embryology, Medical School, University of Ioannina, Greece.

出版信息

Histol Histopathol. 1993 Apr;8(2):235-42.

PMID:8490249
Abstract

The effects of insulin on the ultrastructure of newborn rat hepatocytes were systematically quantified at satisfactory statistical significance. Insulin prevented the normal postnatal increase in the total volume of lysosomes and the breakdown of glycogen inside these organelles. The lysosomal glycogen-hydrolysing enzyme, acid alpha 1,4 glucosidase was inhibited by the hormone. Insulin also prevented the normal postnatal increase in the total volume of peroxisomes, especially of the crystalloid core-devoid type. The hormone produced an increase in the area of cell membrane, due to the formation of many irregular folds of the cell surface. These results constitute good evidence for participation of lysosomes and peroxisomes in the overall glycogen degradation and or gluconeogenesis in the newborn rat hepatocytes.

摘要

胰岛素对新生大鼠肝细胞超微结构的影响得到了系统定量,具有令人满意的统计学意义。胰岛素阻止了出生后溶酶体总体积的正常增加以及这些细胞器内糖原的分解。溶酶体糖原水解酶酸性α-1,4-葡萄糖苷酶受到该激素的抑制。胰岛素还阻止了出生后过氧化物酶体总体积的正常增加,尤其是无晶体核心类型的过氧化物酶体。由于细胞表面形成许多不规则褶皱,该激素使细胞膜面积增加。这些结果充分证明了溶酶体和过氧化物酶体参与新生大鼠肝细胞的整体糖原降解和/或糖异生过程。

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