4.7 Article

High calorie diet triggers hypothalamic angiopathy

期刊

MOLECULAR METABOLISM
卷 1, 期 1-2, 页码 95-100

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.molmet.2012.08.004

关键词

Obesity; Diabetes; Blood brain barrier; Capillary; Fluorescent angiography; Endothelial cell

资金

  1. Netherlands Organization for Scientific Research (NWO)-ALW-Rubicon
  2. [DFG-FOR1336]

向作者/读者索取更多资源

Obesity, type 2 diabetes, and related diseases represent major health threats to modem society. Related pathophysiology of impaired neuronal function in hypothalamic control centers regulating metabolism and body weight has been dissected extensively and recent studies have started focusing on potential roles of astrocytes and microglia. The hypothalamic vascular system, however, which maintains the microenvironment necessary for appropriate neuronal function, has been largely understudied. We recently discovered that high fat/high sucrose diet exposure leads to increased hypothalamic presence of immunoglobulin G (IgG1). Investigating this phenomenon further, we have discovered a significant increase in blood vessel length and density in the arcuate nucleus (ARC) of the hypothalamus in mice fed a high fat/high sucrose diet, compared to matched controls fed standard chow diet. We also found a clearly increased presence of cc -smooth muscle actin immunoreactive vessels, which are rarely present in the ARC and indicate an increase in the formation of new arterial vessels. Along the blood brain barrier, an increase of degenerated endothelial cells are observed. Moreover, such hypothalamic angiogenesis was not limited to rodent models. We also found an increase in the number of arterioles of the infundibular nucleus (the human equivalent of the mouse ARC) in patients with type 2 diabetes, suggesting angiogenesis occurs in the human hypothalamus of diabetics. Our discovery reveals novel hypothalamic pathophysiology, which is reminiscent of diabetic retinopathy and suggests a potential functional involvement of the hypothalamic vasculature in the later stage pathogenesis of metabolic syndrome. (C) 2012 Elsevier GmbH. Open access under CC-BY-NC-ND license.

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