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高脂饮食和链脲佐菌素处理的大鼠肠道、肝脏和肾脏中DPP-IV的增加。

Increase in DPP-IV in the intestine, liver and kidney of the rat treated with high fat diet and streptozotocin.

作者信息

Yang Jian, Campitelli Jack, Hu Gang, Lin Yanhe, Luo Jin, Xue Chun

机构信息

Department of Pharmacology, Nanjing Medical University, Nanjing 210029, China.

出版信息

Life Sci. 2007 Jul 4;81(4):272-9. doi: 10.1016/j.lfs.2007.04.040. Epub 2007 May 21.

Abstract

High fat diet or insulin deficiency is commonly seen in Type II diabetes, while the mechanism remains unclear. To test our hypothesis that DPP-IV contributes to Type II diabetes, we examined the expression and activity of DPP-IV in rats (n=8 to each group) treated for 12 weeks with 3 separate diets: a) normal control; b) a high fat diet; and c) a high fat diet plus streptozotocin, a chemical for induction of insulin-deficient diabetes. Compared to rats on the normal diet, the rats with a high fat diet significantly increased DPP-IV's expression and activity about 142-152% in the intestine (P<0.05) and 153-240% in kidneys (P<0.05), but there was no change in the liver. Administration of streptozotocin to the rats treated with the high fat diet showed an insufficient insulin secretion and higher blood glucose in response to glucose/insulin tolerance test, and an increase in expression of DPP-IV and activity by 188-242% in the intestine (P<0.01); 191-225% in liver (P<0.01); and 211-321% in the kidneys (P<0.01). Immunohistochemistry studies confirmed the above results, showing increased DPP-IV immunostaining localized primarily in intestinal epithelium, hepatocytes and renal tubular cells. This study, for the first time reports an increase in DPP-IV associated with a high fat diet, as well as in the combination of a high fat diet with an insulin deficiency. Since both high fat diet and insulin deficiency are closely linked with etiology of Type II diabetes, the evidence in this study suggests a role of DPP-IV in development of Type II diabetes.

摘要

高脂肪饮食或胰岛素缺乏在II型糖尿病中很常见,但其机制尚不清楚。为了验证我们的假设,即二肽基肽酶-IV(DPP-IV)与II型糖尿病有关,我们检测了用三种不同饮食处理12周的大鼠(每组n = 8)中DPP-IV的表达和活性:a)正常对照;b)高脂肪饮食;c)高脂肪饮食加链脲佐菌素,一种诱导胰岛素缺乏性糖尿病的化学物质。与正常饮食的大鼠相比,高脂肪饮食的大鼠肠道中DPP-IV的表达和活性显著增加,约为142 - 152%(P < 0.05),肾脏中为153 - 240%(P < 0.05),但肝脏中无变化。对高脂肪饮食处理的大鼠给予链脲佐菌素后,葡萄糖/胰岛素耐量试验显示胰岛素分泌不足和血糖升高,并且肠道中DPP-IV的表达和活性增加了188 - 242%(P < 0.01);肝脏中为191 - 225%(P < 0.01);肾脏中为211 - 321%(P < 0.01)。免疫组织化学研究证实了上述结果,显示DPP-IV免疫染色增加,主要定位于肠上皮、肝细胞和肾小管细胞。本研究首次报道了与高脂肪饮食相关的DPP-IV增加,以及高脂肪饮食与胰岛素缺乏共同作用时DPP-IV的增加。由于高脂肪饮食和胰岛素缺乏都与II型糖尿病的病因密切相关,本研究的证据表明DPP-IV在II型糖尿病的发生发展中起作用。

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