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[遗传性自发性高血压大鼠胰腺胰岛装置的特征]

[Characteristics of the islet apparatus of the pancreas in rats with genetic spontaneous hypertension].

作者信息

Postnov Iu V, Gor'kova S I, Petrunina L A

出版信息

Kardiologiia. 1975 May;15(5):89-94.

PMID:1097803
Abstract

In spontaneously hypertensive rats (SHR) at the age of 7-9 weeks a poor development of the beta-cellular part of the islet-cell tissue was found, as compared to normotensive Wistar rats of the same age (a lower number of beta-cellular islets, decreased mass of the islet-cell tissue). With glucose load in SHR hyperglycemia was more distinct and longer lasting, which indicates the development of insulin insufficiency in them, in a situation demanding forced insulin incretion. A histochemical examination proved a reduction of the insulin content in the islet-cells of these animals, as compared with the control ones. The above mentioned changes evidently do not pertain to the primary genetically-determined pathology of their pancreas, but are of a secondary nature of atrophy of the insulin-forming tissue, that is probably conditioned by the decreased tissue requirements (target) for insulin due to the increased permeability of the cell membranes.

摘要

在7 - 9周龄的自发性高血压大鼠(SHR)中,与同龄的正常血压Wistar大鼠相比,发现胰岛细胞组织的β细胞部分发育不良(β细胞胰岛数量减少,胰岛细胞组织质量降低)。给SHR注射葡萄糖后,高血糖更为明显且持续时间更长,这表明在需要强制分泌胰岛素的情况下,它们出现了胰岛素分泌不足。组织化学检查证明,与对照动物相比,这些动物胰岛细胞中的胰岛素含量减少。上述变化显然与它们胰腺的原发性基因决定的病理学无关,而是胰岛素形成组织萎缩的继发性变化,这可能是由于细胞膜通透性增加导致组织对胰岛素的需求(靶点)减少所致。

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