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链脲佐菌素诱导的糖尿病和胰岛素瘤大鼠胃中的生长抑素、胃泌素释放肽和胃泌素

Somatostatin, gastrin-releasing peptide and gastrin in the stomach of rats with streptozotocin-induced diabetes and insulinoma.

作者信息

Flatt P R, Bailey C J, Conlon J M

机构信息

Biomedical Sciences Research Centre, University of Ulster, Coleraine, Northern Ireland, U.K.

出版信息

J Nutr. 1991 Sep;121(9):1414-7. doi: 10.1093/jn/121.9.1414.

Abstract

Somatostatin, gastrin-releasing peptide (GRP) and gastrin were measured in the stomach of rats with streptozotocin-induced diabetes, insulinoma-bearing rats and their respective controls. Rats injected with streptozotocin exhibited hyperphagia, insulinopenia and severe hyperglycemia. Stomach weights, and the concentrations and total amounts of GRP and gastrin in the stomach, were similar to nondiabetic control rats. The concentration of somatostatin in the stomach of diabetic rats was 25% greater, but the total stomach content of somatostatin was similar to that of control rats. Insulinoma-bearing rats exhibited hyperphagia, hyperinsulinemia and hypoglycemia. Concentrations of GRP and gastrin in the stomach were 72% and 19% lower, respectively, than in control rats. Despite 45% greater stomach weight, the total stomach content of GRP was 61% lower. Stomach concentrations of somatostatin, and total stomach contents of somatostatin and gastrin, were similar in insulinoma-bearing and control rats. The results demonstrate abnormalities in the stomach concentrations of regulatory peptides in rats with diabetes and insulinoma. These abnormalities are not attributable to changes in food intake alone, suggesting specific effects of these metabolic diseases on gastric regulatory peptides and gastric function.

摘要

在链脲佐菌素诱导的糖尿病大鼠、携带胰岛素瘤的大鼠及其各自的对照大鼠的胃中,检测了生长抑素、胃泌素释放肽(GRP)和胃泌素。注射链脲佐菌素的大鼠表现出食欲亢进、胰岛素缺乏和严重高血糖。胃重量以及胃中GRP和胃泌素的浓度及总量与非糖尿病对照大鼠相似。糖尿病大鼠胃中生长抑素的浓度高25%,但胃中生长抑素的总含量与对照大鼠相似。携带胰岛素瘤的大鼠表现出食欲亢进、高胰岛素血症和低血糖。胃中GRP和胃泌素的浓度分别比对照大鼠低72%和19%。尽管胃重量增加了45%,但胃中GRP的总量却低61%。携带胰岛素瘤的大鼠和对照大鼠胃中生长抑素的浓度以及胃中生长抑素和胃泌素的总含量相似。结果表明糖尿病和胰岛素瘤大鼠胃中调节肽的浓度存在异常。这些异常并非仅由食物摄入量的变化引起,提示这些代谢性疾病对胃调节肽和胃功能有特定影响。

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