کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2196277 | 1550913 | 2012 | 7 صفحه PDF | دانلود رایگان |
Since high expression of farnesoid X receptor (FXR) has been detected in glucocorticoid-producing adrenocortical cells, we evaluated the potential role of FXR in adrenal glucocorticoid production.FXR agonist GW4064 increased fasting plasma corticosterone levels (+45%; P < 0.01) in C57BL/6 mice, indicative of enhanced adrenal steroidogenesis. GW4064 treatment did not affect plasma ACTH levels, adrenal weight, or adrenal expression of steroidogenic genes. Scavenger receptor BI (SR-BI) mRNA and protein expression, respectively, increased 1.9-fold (P < 0.01) and 1.5-fold, which suggests a stimulated lipoprotein-associated cholesterol uptake into the adrenals upon GW4064 treatment. In line with an enhanced flux of cellular cholesterol into the steroidogenic pathway, adrenal unesterified and esterified cholesterol stores were 21–41% decreased (P < 0.01) upon GW4064 treatment.In conclusion, we have shown that the FXR agonist GW4064 stimulates plasma corticosterone levels in C57BL/6 mice. Our findings suggest a novel role for FXR in the modulation of adrenal cholesterol metabolism and glucocorticoid synthesis in mice.
► The FXR agonist GW4064 increases fasting plasma corticosterone levels.
► GW4064 activates FXR locally within the adrenals.
► GW4064 does not directly affect adrenal steroidogenic gene expression.
► GW4064 stimulates the adrenal gene expression of the HDL receptor SR-BI.
Journal: Molecular and Cellular Endocrinology - Volume 362, Issues 1–2, 15 October 2012, Pages 69–75