[自然低温和人工低温条件下异温和同温动物的红细胞]。

V V Lomako, A V Shilo, I F Kovalenko, G A Babiĭchuk
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引用次数: 0

摘要

利用低角度光散射技术揭示了异温(金仓鼠)和等温(白鼠)动物在自然冬眠和假死、颅脑低温和浸入式低温下红细胞转化动力学(渗透脆性、溶血水平和球形指数比值)的特点。在对照组中,仓鼠的渗透脆弱性和红细胞溶血水平高于大鼠,主要是改良形式(特别是气孔细胞)。在人工低温下,无论实现方式、深度和持续时间如何,我们观察到的变化方向相似,但表达不同:渗透脆性和溶血增加,椎间盘细胞比例减少(假死仓鼠尤其明显),红细胞形态改变数量增加。冬眠时渗透脆性、溶血和气孔细胞数量下降,盘状细胞比例增加,但溶血前形态(球细胞)数量也增加。24h渗透脆性下降(假死后的仓鼠更为明显),溶血水平下降(浸泡低温后尤为明显),椎间盘细胞部分恢复,假死后的仓鼠和浸泡低温后的大鼠甚至超过对照水平;仓鼠血液中的球细胞未被发现,大鼠血液中的球细胞升高。可能,观察到的低温24小时后球细胞群质变趋同,不仅取决于衰老和缺陷细胞的消除、红细胞生成的激活、高抗性红细胞的出现,还取决于时间膜稳定机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Erythrocytes of hetero- and homoiothermal animals in natural and artificial hypothermia].

By the low-angle light scattering technique there are revealed peculiarities of dynamics of transformation (osmotic fragility, level of hemolysis and ratio of forms by index of sphericity) of erythrocytes of hetero- (golden hamsters Mesocricetus auratus) and homoiothermal (white rats Rattus norbegicus) animals in natural hibernation and suspended animation, craniocerebral and immersion hypothermia. In control in hamsters the osmotic fragility and the level of hemolysis of erythrocytes were higher than in rats, predominant were modified forms (in particular stomatocytes). Under artificial hypothermia, regardless of the way of achievement, depth and duration, we observed changes similar in direction, but different in expression: the osmotic fragility and hemolysis increased, the portion of discocytes decreased (especially sharply in hamsters under suspended animation), the number of changed erythrocytic forms rose. In contrast, under hiberation the osmotic fragility, hemolysis and the amount of stomatocytes declined, the portion of discocytes increased, but at the same time the amount of prehemolytic forms (spherocytes) rose too. In 24 hs there occurred a decrease of osmotic fragility (after suspended animation more pronounced in hamsters) and the level of hemolysis (especially after immersion hypothermia), the portion of discocytes was restored, in hamsters after suspended animation and in rats after immersion hypothermia it even exceeded the control level; spherocytes in blood of hamsters were not revealed, in rats they were elevated. Possibly, the observed qualitative change of population of spherocytes 24 h after hypothermia toward its homogeneity is determined not only at the level of elimination of old and defected cells, activation of erythropoiesis, the appearance of highly resistant erythrocytes, but also at the level of time membrane-stabilizing mechanisms.

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