TY - JOUR
T1 - High calorie diet triggers hypothalamic angiopathy
AU - Yi, Chun-Xia
AU - Gericke, Martin
AU - Krüger, Martin
AU - Alkemade, Anneke
AU - Kabra, Dhiraj G.
AU - Hanske, Sophie
AU - Filosa, Jessica
AU - Pfluger, Paul
AU - Bingham, Nathan
AU - Woods, Stephen C.
AU - Herman, James
AU - Kalsbeek, Andries
AU - Baumann, Marcus
AU - Lang, Richard
AU - Stern, Javier E.
AU - Bechmann, Ingo
AU - Tschöp, Matthias H.
PY - 2012
Y1 - 2012
N2 - 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
AB - 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
U2 - https://doi.org/10.1016/j.molmet.2012.08.004
DO - https://doi.org/10.1016/j.molmet.2012.08.004
M3 - Article
C2 - 24024123
SN - 2212-8778
VL - 1
SP - 95
EP - 100
JO - Molecular metabolism
JF - Molecular metabolism
IS - 1-2
ER -