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小鼠多次妊娠后子宫肌层复旧主要机制的形态学研究

Morphological study of the main mechanisms of myometrium involution after repeated pregnancies in mice.

作者信息

Shkurupiy V A, Obedinskaya K S, Nadeev A P

机构信息

Institute of Clinical and Experimental Medicine, Siberian Division of the Russian Academy of Medical Sciences, Novosibirsk, Russia.

出版信息

Bull Exp Biol Med. 2011 Jan;150(3):378-82. doi: 10.1007/s10517-011-1147-9.

DOI:10.1007/s10517-011-1147-9
PMID:21240359
Abstract

Elimination of "excessive" myocytes and their structures during involution of the myometrium after the first and third pregnancies was realized by clasmocytosis (eliminating the greatest volume of myocyte cytoplasm fragments), apoptosis, and necrosis (equal percentage by volume). In contrast to the first pregnancy, involution after the third one was not over by day 10 because of inhibited elimination of functionally lost myocytes by necrosis and apoptosis mechanisms. Presumably, this was caused by slower hydrolysis of apoptotic bodies by macrophages. The concentration of macrophages in the myometrium on day 10 of the involution period in females after the third delivery was 4-fold higher than in intact mice and in females after the first delivery during the same period.

摘要

在第一次和第三次妊娠后子宫肌层复旧过程中,通过胞质溶解(消除最大体积的肌细胞胞质片段)、凋亡和坏死(体积百分比相等)实现了“多余”肌细胞及其结构的清除。与第一次妊娠不同,第三次妊娠后的复旧到第10天时并未完成,原因是坏死和凋亡机制对功能丧失的肌细胞的清除受到抑制。据推测,这是由于巨噬细胞对凋亡小体的水解较慢所致。在第三次分娩后雌性动物复旧期第10天时,子宫肌层中巨噬细胞的浓度比同期未孕小鼠和第一次分娩后雌性动物高4倍。

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引用本文的文献

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Postpartum Involution of Mouse Myometrium in Acute CCl-Induced Hepatosis and Its Correction with Immobilized Hyaluronidase.急性 CCl 诱导肝损伤时小鼠子宫肌的产后退化及其与固定化透明质酸酶的关系。
Bull Exp Biol Med. 2022 Jun;173(2):265-269. doi: 10.1007/s10517-022-05531-1. Epub 2022 Jun 23.
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Improvement in post-partum uterine involution in rats treated with Apios americana.用美洲菜豆治疗后大鼠产后子宫复旧的改善。
J Zhejiang Univ Sci B. 2019 Jul;20(7):576-587. doi: 10.1631/jzus.B1800475.
3
Apoptosis in Living Animals Is Assisted by Scavenger Cells and Thus May Not Mainly Go through the Cytochrome C-Caspase Pathway.
活体内细胞凋亡受吞噬细胞辅助,因此可能并不主要通过细胞色素 C-半胱氨酸蛋白酶途径。
J Cancer. 2013 Nov 15;4(9):716-23. doi: 10.7150/jca.7577. eCollection 2013.