Glucocorticoid receptor haploinsufficiency causes hypertension and attenuates hypothalamic-pituitary-adrenal axis and blood pressure adaptions to high-fat diet

被引:43
作者
Michailidou, Z.
Carter, R. N.
Marshall, E.
Sutherland, H. G. [2 ]
Brownstein, D. G.
Owen, E.
Cockett, K.
Kelly, V.
Ramage, L.
Al-Dujaili, E. A. S. [3 ]
Ross, M.
Maraki, I.
Newton, K. [2 ]
Holmes, M. C.
Seckl, J. R.
Morton, N. M.
Kenyon, C. J.
Chapman, K. E. [1 ]
机构
[1] Univ Edinburgh, Endocrinol Unit, Ctr Cardiovasc Sci, Queens Med Res Inst, Edinburgh EH16 4TJ, Midlothian, Scotland
[2] MRC, Human Genet Unit, Edinburgh, Midlothian, Scotland
[3] Queen Margaret Univ, Musselburgh, East Lothian, Scotland
基金
英国惠康基金; 英国医学研究理事会;
关键词
HPA axis; diet-induced obesity; NR3C1; glucose and lipid homeostasis;
D O I
10.1096/fj.08-111914
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Glucocorticoid hormones are critical to respond and adapt to stress. Genetic variations in the glucocorticoid receptor (GR) gene alter hypothalamic-pituitary-adrenal (HPA) axis activity and associate with hypertension and susceptibility to metabolic disease. Here we test the hypothesis that reduced GR density alters blood pressure and glucose and lipid homeostasis and limits adaption to obesogenic diet. Heterozygous GR(beta geo/+) mice were generated from embryonic stem (ES) cells with a gene trap integration of a beta-galactosidase-neomycin phosphotransferase (beta geo) cassette into the GR gene creating a transcriptionally inactive GR fusion protein. Although GR(beta geo/+) mice have 50% less functional GR, they have normal lipid and glucose homeostasis due to compensatory HPA axis activation but are hypertensive due to activation of the renin-angiotensin-aldosterone system (RAAS). When challenged with a high-fat diet, weight gain, adiposity, and glucose intolerance were similarly increased in control and GR(beta geo/+) mice, suggesting preserved control of intermediary metabolism and energy balance. However, whereas a high-fat diet caused HPA activation and increased blood pressure in control mice, these adaptions were attenuated or abolished in GR(beta geo/+) mice. Thus, reduced GR density balanced by HPA activation leaves glucocorticoid functions unaffected but mineralocorticoid functions increased, causing hypertension. Importantly, reduced GR limits HPA and blood pressure adaptions to obesogenic diet. -Michailidou, Z., Carter, R. N., Marshall, E., Sutherland, H. G., Brownstein, D. G., Owen, E., Cockett, K., Kelly, V., Ramage, L., Al-Dujaili, E. A. S., Ross, M., Maraki, I., Newton, K., Holmes, M. C., Seckl, J. R., Morton, N. M., Kenyon, C. J., Chapman, K. E. Glucocorticoid receptor haploinsufficiency causes hypertension and attenuates hypothalamic-pituitary-adrenal axis and blood pressure adaptions to high-fat diet. FASEB J. 22, 3896-3907 (2008)
引用
收藏
页码:3896 / 3907
页数:12
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