Leptin Activates a Novel CNS Mechanism for Insulin-Independent Normalization of Severe Diabetic Hyperglycemia

被引:126
作者
German, Jonathan P. [1 ]
Thaler, Joshua P. [1 ]
Wisse, Brent E. [1 ]
Oh-I, Shinsuke [1 ]
Sarruf, David A. [1 ]
Matsen, Miles E. [1 ]
Fischer, Jonathan D. [1 ]
Taborsky, Gerald J., Jr. [2 ]
Schwartz, Michael W. [1 ]
Morton, Gregory J. [1 ]
机构
[1] Univ Washington, Diabet & Obes Ctr Excellence, Dept Med, Seattle, WA 98109 USA
[2] Dept Vet Affairs Med Ctr, Vet Affairs Puget Sound Hlth Care Syst, Seattle, WA 98108 USA
基金
美国国家卫生研究院;
关键词
PROTEIN-2; MESSENGER-RNA; GLUCOSE-PRODUCTION; PERIPHERAL-TISSUES; GENE-EXPRESSION; RESISTANCE; HYPERPHAGIA; SENSITIVITY; RATS; INFUSION; GLUCAGON;
D O I
10.1210/en.2010-0890
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The brain has emerged as a target for the insulin-sensitizing effects of several hormonal and nutrient-related signals. The current studies were undertaken to investigate mechanisms whereby leptin lowers circulating blood glucose levels independently of insulin. After extending previous evidence that leptin infusion directly into the lateral cerebral ventricle ameliorates hyperglycemia in rats with streptozotocin-induced uncontrolled diabetes mellitus, we showed that the underlying mechanism is independent of changes of food intake, urinary glucose excretion, or recovery of pancreatic beta-cells. Instead, leptin action in the brain potently suppresses hepatic glucose production while increasing tissue glucose uptake despite persistent, severe insulin deficiency. This leptin action is distinct from its previously reported effect to increase insulin sensitivity in the liver and offers compelling evidence that the brain has the capacity to normalize diabetic hyperglycemia in the presence of sufficient amounts of central nervous system leptin. (Endocrinology 152: 394-404, 2011)
引用
收藏
页码:394 / 404
页数:11
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