Division of Endocrinology, Department of Medicine, Université de Sherbrooke, Sherbrooke, Québec, Canada J1H 5N4.
Steroids. 2012 Mar 10;77(4):347-53. doi: 10.1016/j.steroids.2011.12.017. Epub 2012 Jan 9.
Polycystic ovary syndrome (PCOS) is mainly defined by hyperandrogenemia, from ovarian and adrenal origin, and is characterized by insulin resistance (IR). Studies found that raising in vivo non-esterified fatty acid (NEFA) levels, which induces lipotoxicity, increases androgen levels and IR. The aim of this study was therefore to determine the effects of in vitro over-exposure to NEFA on androgen synthesis in a bovine adrenocortical cell model.
Bovine fasciculata/reticularis cells were cultured for 2days in the absence or presence of ACTH (10nmol/L) or Forskolin (fsk, 10μmol/L), alone or in combination with the saturated fatty acid (FA) palmitate (100μmol/L). Steroid production was measured in medium and corrected for initial cell seeding count. CYP17 protein expression and ERK1/2 phosphorylation were assessed by Western blotting.
Under unstimulated conditions, dehydroepiandrosterone (DHEA) levels were barely detected and no difference was observed after palmitate exposure, which was also the case for CYP17 expression and ERK1/2 phosphorylation. Under stimulation, palmitate exposure increased DHEA production by 38% and 69%, for ACTH and fsk, respectively, as compared to untreated conditions (Ps⩽0.05). In palmitate-treated vs untreated cells, fsk-stimulated ERK1/2 phosphorylation was reduced by 46% (P=0.0047), but stimulated CYP17 expression was not significantly affected.
In a model of androgen-producing cells, under stimulated conditions, overexposure to saturated FAs significantly increases androgen production and reduces MEK/ERK activation. Therefore, this study is the first to demonstrate that lipotoxicity can directly trigger androgen overproduction in vitro, in addition to its well-described impact on IR, which strongly supports a central role of lipotoxicity in PCOS pathophysiology.
多囊卵巢综合征(PCOS)主要表现为来源于卵巢和肾上腺的高雄激素血症,并伴有胰岛素抵抗(IR)。研究发现,体内非酯化脂肪酸(NEFA)水平升高,导致脂毒性,增加雄激素水平和 IR。因此,本研究旨在确定体外过度暴露于 NEFA 对牛肾上腺皮质细胞模型中雄激素合成的影响。
牛束状带/网状带细胞在无或有 ACTH(10nmol/L)或 Forskolin(fsk,10μmol/L)存在的情况下培养 2 天,单独或与饱和脂肪酸(FA)棕榈酸(100μmol/L)联合培养。通过 Western 印迹法评估 CYP17 蛋白表达和 ERK1/2 磷酸化。
在未刺激条件下,脱氢表雄酮(DHEA)水平几乎检测不到,棕榈酸暴露后也没有差异,CYP17 表达和 ERK1/2 磷酸化也是如此。在刺激条件下,与未处理条件相比,棕榈酸暴露分别使 ACTH 和 fsk 刺激的 DHEA 产生增加了 38%和 69%(Ps ⩽0.05)。与未处理细胞相比,在棕榈酸处理的细胞中,fsk 刺激的 ERK1/2 磷酸化减少了 46%(P=0.0047),但刺激的 CYP17 表达没有明显影响。
在雄激素产生细胞模型中,在刺激条件下,过度暴露于饱和 FA 可显著增加雄激素的产生并降低 MEK/ERK 激活。因此,本研究首次证明,脂毒性除了对 IR 具有明显影响外,还可以直接导致体外雄激素过度产生,这强烈支持脂毒性在 PCOS 发病机制中的核心作用。