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胰岛素给药对链脲佐菌素诱导的大鼠糖尿病性高血压的影响。

Effect of administration of insulin on streptozotocin-induced diabetic hypertension in rat.

作者信息

Chen S, Yuan C M, Haddy F J, Pamnani M B

机构信息

Department of Physiology, Uniformed Services University of Health Sciences, Bethesda, MD 20814-4799.

出版信息

Hypertension. 1994 Jun;23(6 Pt 2):1046-50. doi: 10.1161/01.hyp.23.6.1046.

Abstract

We have reported that streptozotocin-induced insulin-dependent diabetes mellitus in 25% reduced renal mass rats is associated with low-renin, volume-expanded hypertension and that the development of the hypertension can be prevented with insulin. In this study we examined the effect of insulin after the animals had developed sustained hypertension. Normotensive 25% reduced renal mass rats were treated with streptozotocin and, as expected, developed insulin-dependent diabetes mellitus and hypertension. After 4 weeks of sustained hypertension, neutral protamine Hagedorn insulin (6 to 8 IU/d) was administered subcutaneously for 4 weeks. As expected, insulin treatment decreased plasma glucose and increased body weight gain relative to untreated diabetic rats. On the other hand, insulin treatment did not reverse the hypertension and albuminuria. It also did not normalize extracellular fluid volume and plasma renin activity. Furthermore, insulin treatment did not reverse the increase in plasma Na+,K(+)-ATPase inhibitory activity (determined by both radioimmunoassay and bioassay) and the inhibition of myocardial microsomal Na+,K(+)-ATPase activity observed in the untreated diabetic hypertensive rats. 5'-Nucleotidase, a membrane marker, was not different between insulin-treated and untreated diabetic rats. These results show that insulin, given as here described, does not reverse the insulin-dependent diabetes mellitus hypertension in 25% reduced renal mass rats once it is established, perhaps because it does not reverse the albuminuria, volume expansion, increase in endogenous digitalis-like substance, and inhibition of cardiovascular muscle cell Na+,K(+)-ATPase activity.

摘要

我们曾报道,在肾质量减少25%的大鼠中,链脲佐菌素诱导的胰岛素依赖型糖尿病与低肾素、容量扩张性高血压有关,且胰岛素可预防高血压的发生。在本研究中,我们在动物出现持续性高血压后检测了胰岛素的作用。将血压正常、肾质量减少25%的大鼠用链脲佐菌素处理,不出所料,这些大鼠发生了胰岛素依赖型糖尿病和高血压。在出现持续性高血压4周后,给大鼠皮下注射中性鱼精蛋白锌胰岛素(6至8 IU/天),持续4周。不出所料,与未治疗的糖尿病大鼠相比,胰岛素治疗降低了血糖水平并增加了体重增加。另一方面,胰岛素治疗并未逆转高血压和蛋白尿。它也未使细胞外液容量和血浆肾素活性恢复正常。此外,胰岛素治疗并未逆转在未治疗的糖尿病高血压大鼠中观察到的血浆Na⁺,K⁺-ATP酶抑制活性增加(通过放射免疫测定和生物测定确定)以及心肌微粒体Na⁺,K⁺-ATP酶活性的抑制。膜标志物5'-核苷酸酶在胰岛素治疗组和未治疗的糖尿病大鼠之间没有差异。这些结果表明,如此处所述给予胰岛素,一旦胰岛素依赖型糖尿病高血压在肾质量减少25%的大鼠中确立,就无法逆转,这可能是因为它无法逆转蛋白尿、容量扩张、内源性类洋地黄物质增加以及心血管肌细胞Na⁺,K⁺-ATP酶活性的抑制。

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