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链脲佐菌素诱导的糖尿病对大鼠肾脏超氧化物歧化酶的影响。一项放射免疫分析和免疫组织化学研究。

Effect of diabetes mellitus induced by streptozotocin on renal superoxide dismutases in the rat. A radioimmunoassay and immunohistochemical study.

作者信息

Dobashi K, Asayama K, Hayashibe H, Uchida N, Kobayashi M, Kawaoi A, Kato K

机构信息

Department of Pediatrics, Yamanashi Medical College, Japan.

出版信息

Virchows Arch B Cell Pathol Incl Mol Pathol. 1991;60(1):67-72. doi: 10.1007/BF02899529.

Abstract

Two forms of superoxide dismutase, CuZn-SOD and MnSOD, have been investigated in the kidneys of streptozotocin-induced diabetic rats using both radio-immunoassay and immunoenzyme staining. The rats were killed 2, 8 and 12 weeks after the induction of diabetes mellitus and the kidneys excised. Two weeks after the induction of diabetes, the kidneys were hypertrophied because of the proliferation of renal tubular epithelium. However, the total CuZnSOD content of the kidneys did not increase and, because of the epithelial proliferation, the CuZnSOD concentration in each proximal tubular cell was decreased. Armanni-Ebstein lesions were found in the distal tubules 8 and 12 weeks after the induction of diabetes. The cells in these lesions were intensely stained for CuZnSOD, suggesting an adaptive response to the enhanced oxidative stress. The MnSOD staining in the thick ascending limbs of Henle's loops was enhanced in the diabetic kidneys, while that in the cortical tubules was unaltered. MnSOD was assumed to increase in response to hypermetabolism associated with the proliferation of renal tubules. This was most marked in the cells which were rich in mitochondria, again suggesting an adaptive response to enhanced oxidative stress induced by diabetes mellitus. The glomeruli of both the diabetic and control groups were not stained for SODs, and no significant microscopic change was found even 12 weeks after the induction of diabetes mellitus.

摘要

利用放射免疫分析法和免疫酶染色法,对链脲佐菌素诱导的糖尿病大鼠肾脏中的两种超氧化物歧化酶,即铜锌超氧化物歧化酶(CuZn-SOD)和锰超氧化物歧化酶(MnSOD)进行了研究。在诱导糖尿病后2周、8周和12周处死大鼠并切除肾脏。糖尿病诱导后2周,由于肾小管上皮细胞增殖,肾脏出现肥大。然而,肾脏中铜锌超氧化物歧化酶的总量并未增加,且由于上皮细胞增殖,每个近端肾小管细胞中的铜锌超氧化物歧化酶浓度降低。糖尿病诱导后8周和12周,在远端小管中发现了阿马氏小体病变。这些病变中的细胞铜锌超氧化物歧化酶染色强烈,提示对增强的氧化应激有适应性反应。糖尿病肾脏中亨利袢升支粗段的锰超氧化物歧化酶染色增强,而皮质小管中的染色未改变。推测锰超氧化物歧化酶的增加是对肾小管增殖相关的高代谢的反应。这在富含线粒体的细胞中最为明显,再次提示对糖尿病诱导的增强氧化应激有适应性反应。糖尿病组和对照组的肾小球均未显示超氧化物歧化酶染色,即使在糖尿病诱导12周后也未发现明显的微观变化。

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