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High density lipoprotein as a source of cholesterol for adrenal steroidogenesis: a study in individuals with low plasma HDL-C

机译:高密度脂蛋白作为肾上腺类固醇生成的胆固醇来源:一项针对低血浆HDL-C患者的研究

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摘要

Few studies have addressed the delivery of lipoprotein-derived cholesterol to the adrenals for steroid production in humans. While there is evidence against a role for low-density lipoprotein (LDL), it is unresolved whether high density lipoprotein (HDL) contributes to adrenal steroidogenesis. To study this, steroid hormone profiles in urine were assessed in male subjects suffering from functional mutations in ATP binding cassette transporter A1 (ABCA1) (n = 24), lecithin:cholesterol acyltransferase (LCAT) (n = 40), as well as in 11 subjects with low HDL cholesterol (HDL-C) without ABCA1/LCAT mutations. HDL-C levels were 39% lower in the ABCA1, LCAT, and low HDL-C groups compared with controls (all P < 0.001). In all groups with low HDL-C levels, urinary excretion of 17-ketogenic steroids was reduced by 33%, 27%, and 32% compared with controls (all P < 0.04). In seven carriers of either type of mutation, adrenocorticotropic hormone (ACTH) stimulation did not reveal differences from normolipidemic controls. In conclusion, this study shows that basal but not stimulated corticosteroid metabolism is attenuated in subjects with low HDL-C, irrespective of its molecular origin. These findings lend support to a role for HDL as a cholesterol donor for basal adrenal steroidogenesis in humans.
机译:很少有研究讨论过将脂蛋白衍生的胆固醇输送到肾上腺以产生人类类固醇。虽然有证据表明低密度脂蛋白(LDL)的作用,但高密度脂蛋白(HDL)是否有助于肾上腺类固醇生成尚未得到解决。为了研究这一点,对患有ATP结合盒转运蛋白A1(ABCA1)(n = 24),卵磷脂:胆固醇酰基转移酶(LCAT)(n = 40)以及功能障碍的男性受试者的尿液中类固醇激素谱进行了评估。 11位HDL胆固醇低(HDL-C)没有ABCA1 / LCAT突变的受试者。与对照组相比,ABCA1,LCAT和低HDL-C组的HDL-C水平降低39%(所有P <0.001)。在所有HDL-C水平低的组中,与对照组相比,17-酮类固醇的尿排泄减少了33%,27%和32%(所有P <0.04)。在这两种突变类型的七个携带者中,促肾上腺皮质激素(ACTH)刺激均未显示与血脂正常对照组的差异。总之,这项研究表明,在低水平HDL-C患者中,无论其分子来源如何,基础皮质类固醇激素的代谢都会受到减弱,而皮质类固醇激素的刺激作用不会受到刺激。这些发现支持了HDL作为人类基础肾上腺类固醇生成的胆固醇供体的作用。

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