丙烯醛对雄性大鼠皮质酮分泌的下调作用

J. Chou, Ting-Chun Weng, C. Soong, Sindy Hu, F. Lieu, G. Idova, Paulus S. Wang, Shyi-Wu Wang
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引用次数: 0

摘要

丙烯醛是一种小的不饱和醛,可以在广泛的资源中找到,包括所有类型的烟雾和汽油发动机的废气。虽然丙烯醛的毒性和损伤性已被认识,但其作用机制,特别是对应激激素的作用机制尚不清楚。本研究假设丙烯醛通过调节大鼠束状网状带(ZFR)细胞的类固醇生物合成途径改变促肾上腺皮质激素(ACTH)和皮质酮的分泌。采用了体内和体外两种方法。在体内研究中,每日一次腹腔注射丙烯醛(2mg /ml/kg),持续1或3天,可降低血浆ACTH和皮质酮水平,以及细胞内cAMP和ACTH诱导的皮质酮分泌。丙烯醛处理1天和3天后,大鼠ZFR细胞中ACTH受体(ACTHR)的蛋白表达也分别降低了40-60%。在体外实验中,制备大鼠ZFR细胞,用ACTH (10 -9 M)、forskolin(腺苷酸环化酶活性,10 -5 M)、8-Br-cAMP(可渗透合成cAMP, 5 × 10 -5 M)、25- oh -胆固醇(10 -5 M)±trilostane (3β-羟基类固醇脱氢酶抑制剂,3β-HSD, 10 -5 M)刺激。ACTH、forskolin、8-Br-cAMP诱导皮质酮释放量和25- oh -胆固醇+三olostane诱导孕烯醇酮释放量均降低。由于三叶烷阻断3β-HSD后孕烯醇酮的积累代表了P450 scc的活性,P450 scc是类固醇生物合成的限速步骤,我们认为丙烯醛不仅抑制了cAMP途径,而且降低了P450 scc的酶活性。体内丙烯醛处理后,ZFR细胞中类固醇急性调节蛋白(StAR)的表达降低了40%。丙烯醛(10 -9 ~10 -7 M)对ZFR细胞的体外释放也有抑制作用。这些结果表明,丙烯醛通过抑制cAMP通路、StAR蛋白表达和P450 scc酶活性来抑制皮质酮的产生。ACTHR(又称黑素皮质素2受体,MC2R)蛋白表达的减弱和ACTH分泌的减少表明丙烯醛也下调了下丘脑-垂体-肾上腺(H-P-A)轴。
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Down regulation of acrolein on corticosterone secretion in male rats
Acrolein is a small unsaturated aldehyde and can be found in a wide range of resources including all types of smoke and exhaust gases from gasoline engines. Although the toxicity and damage of acrolein have been recognized, the action mechanisms of acrolein, especially that of acrolein on the response of stresshormones are still unclear. The present study hypothesized that administration of acrolein altered the secretion of both adrenocorticotropin (ACTH) and corticosterone via the regulation of steroid biosynthetic pathway in rat zona fasciculata-reticularis (ZFR) cells. Both in vivo and in vitro approaches were uased. In the in vivo study, intraperitonal injection of acrolein (2 mg/ml/kg) once daily for 1 or 3 days resulted in a reduction of plasma levels of ACTH and corticosterone as well as the intracellular cAMP and ACTH-induced secretion of corticosterone. The protein expression of ACTH receptor (ACTHR) in rat ZFR cells was also reduced by 40-60% after treatment of acrolein for 1 day and 3 days, respectively. In the in vitro study, rat ZFR cells were prepared and chanllenged with ACTH (10 -9 M), forskolin (an adenylyl cyclase activitior, 10 -5 M), 8-Br-cAMP (a permeable synthetic cAMP, 5x10 -5 M), 25-OH-cholesterol (10 -5 M) ± trilostane (an inhibitor of 3β-hydroxysteroid dehydrogenase, 3β-HSD, 10 -5 M). The evoked release of corticosterone by ACTH, forskolin, 8-Br-cAMP and the induced release of pregnenolone in response to 25-OH-cholesterol plus triolostane were decreased. Since the accumulation of pregnenolone after blocking 3β-HSD by trilostane represents the activity of P450 scc, therate-limiting step of steroid biosynthesis, we suggest that not only the cAMP pathway was inhibited, but also the enzyme activity of P450 scc was attenuated following administration of acrolein. Although insignificant, the protein expression of steroidogenic acute regulatory protein (StAR) was decreased by 40% in ZFR cells after treatment of acrolein in vivo . Incubation of ZFR cells with acrolein (10 -9 ~10 -7 M) also decreased the in vitro release of corticosterone. These results suggest that administration of acrolein inhibited corticosterone production via the attenuation of cAMP pathway, StAR protein expression, and the enzyme activity of P450 scc. The attenuation of protein expression of ACTHR (also named melanocortin 2 receptor, MC2R) and reduced secrection of ACTH indicated that the hypothalamus-pituitary-adrenal (H-P-A) axis was also down- regulated by the administration of acrolein.
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