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菊三七多糖可调节链脲佐菌素诱导的糖尿病大鼠肠道双糖酶的活性。

Polysaccharide from Gynura divaricata modulates the activities of intestinal disaccharidases in streptozotocin-induced diabetic rats.

机构信息

Department of Pharmaceutical Science, Medical College of Hunan Normal University, Changsha, People's Republic of China.

出版信息

Br J Nutr. 2011 Nov;106(9):1323-9. doi: 10.1017/S0007114511001693. Epub 2011 May 31.

Abstract

During diabetes, structural and functional changes in the alimentary tract are known to take place resulting in an increased absorption of intestinal glucose and alterations in the activities of brush-border disaccharidases. To elucidate the effect of administrating polysaccharide from Gynura divaricata (PGD) on disaccharidase activities, the specific activities of intestinal disaccharidases, namely sucrase, maltase and lactase, were measured in streptozotocin-induced diabetic rats. Normal control and diabetic rats were treated by oral administration with PGD. Specific activities of intestinal disaccharidases were increased significantly during diabetes, and amelioration of the activities of sucrase and maltase during diabetes was clearly visible by the treatment with PGD. However, the increased activity of lactase during diabetes mellitus was remarkably alleviated by the administration of PGD only in the duodenum. Meanwhile, oral sucrose tolerance tests demonstrated that PGD alleviated the hyperglycaemia during diabetes mellitus, resulting from the amelioration in the activities of intestinal disaccharidases. The present investigation suggests that PGD exerted an anti-diabetic effect partly via inhibiting the increased intestinal disaccharidase activities of diabetic rats. This beneficial influence of administration of PGD on intestinal disaccharidases clearly indicates their helpful role in the management of diabetes.

摘要

在糖尿病期间,已知消化道会发生结构和功能变化,导致肠道葡萄糖吸收增加和刷状缘二糖酶活性改变。为了阐明菊三七多糖(PGD)对二糖酶活性的影响,我们测量了链脲佐菌素诱导的糖尿病大鼠的肠二糖酶(蔗糖酶、麦芽糖酶和乳糖酶)的比活性。正常对照组和糖尿病组大鼠通过口服给予 PGD 进行治疗。糖尿病期间,肠二糖酶的比活性显著增加,PGD 治疗明显改善了蔗糖酶和麦芽糖酶的活性。然而,只有在十二指肠中,PGD 对糖尿病期间乳糖酶活性的增加有明显的缓解作用。同时,口服蔗糖耐量试验表明,PGD 通过改善肠二糖酶的活性缓解了糖尿病期间的高血糖。本研究表明,PGD 通过抑制糖尿病大鼠肠道二糖酶活性发挥抗糖尿病作用。PGD 对肠二糖酶的这种有益影响清楚地表明它们在糖尿病管理中的有益作用。

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