Suppr超能文献

糖尿病肥胖沙鼠中的高胰岛素原血症和胰岛素缺乏

Hyperproinsulinemia and insulin deficiency in the diabetic Psammomys obesus.

作者信息

Gadot M, Leibowitz G, Shafrir E, Cerasi E, Gross D J, Kaiser N

机构信息

Department of Endocrinology and Metabolism, Hebrew University-Hadassah Medical Center, Jerusalem, Israel.

出版信息

Endocrinology. 1994 Aug;135(2):610-6. doi: 10.1210/endo.135.2.8033810.

Abstract

Patients with noninsulin-dependent diabetes mellitus exhibit increased proportions of plasma proinsulin and proinsulin conversion intermediates. We used hyperinsulinemic diabetic and nondiabetic Psammomys obesus to study the possible relationship between steady state pancreatic insulin stores and the proportion of proinsulin-related peptides in the plasma and pancreas. Insulin-like peptides were separated by reverse phase HPLC and identified by pulse-chase experiments. A marked increase in the proportions of proinsulin and proinsulin conversion intermediates in the plasma and pancreas of diabetic nonfasted Psammomys was associated with 90% reduction in insulin stores of the pancreas. After a 16- to 20-h fast, the depletion of pancreatic insulin in the diabetic animals was partially corrected, and the proinsulin/insulin ratio was normalized. In contrast, nondiabetic Psammomys showed only 50% reduction in pancreatic insulin stores under nonfasting conditions, with no change in the proinsulin/insulin ratio. These findings suggest that in the diabetic Psammomys obesus, the pancreatic capacity for storage of insulin may be limited; the metabolic consequences of this limitation are amplified by increased secretory demand secondary to insulin resistance, thus facilitating the establishment of hyperglycemia, which may in itself further exacerbate pancreatic dysfunction.

摘要

非胰岛素依赖型糖尿病患者血浆中胰岛素原和胰岛素原转化中间产物的比例增加。我们使用高胰岛素血症的糖尿病和非糖尿病肥胖沙鼠来研究胰腺胰岛素稳态储备与血浆和胰腺中胰岛素原相关肽比例之间的可能关系。胰岛素样肽通过反相高效液相色谱法分离,并通过脉冲追踪实验进行鉴定。糖尿病非禁食肥胖沙鼠血浆和胰腺中胰岛素原和胰岛素原转化中间产物的比例显著增加,同时胰腺胰岛素储备减少了90%。禁食16至20小时后,糖尿病动物胰腺胰岛素的消耗得到部分纠正,胰岛素原/胰岛素比值恢复正常。相比之下,非糖尿病肥胖沙鼠在非禁食条件下胰腺胰岛素储备仅减少50%,胰岛素原/胰岛素比值无变化。这些发现表明,在糖尿病肥胖沙鼠中,胰腺储存胰岛素的能力可能有限;这种限制的代谢后果因胰岛素抵抗继发的分泌需求增加而放大,从而促进高血糖的形成,而高血糖本身可能进一步加剧胰腺功能障碍。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验