Chen Chung-Yu, Chen Chien-Rung, Chen Chiao-Nan, Wang Paulus S, Mündel Toby, Liao Yi-Hung, Tsai Shiow-Chwen
Department of Exercise and Health Sciences, University of Taipei, Taipei City 111, Taiwan.
Department of Nursing, Cardinal Tien Junior College of Healthcare and Management, New Taipei City 231, Taiwan.
Biomedicines. 2021 Apr 29;9(5):493. doi: 10.3390/biomedicines9050493.
The purpose of this study is to evaluate the amphetamine effects on progesterone and estradiol production in rat granulosa cells and the underlying cellular regulatory mechanisms. Freshly dispersed rat granulosa cells were cultured with various test drugs in the presence of amphetamine, and the estradiol/progesterone production and the cytosolic cAMP level were measured. Additionally, the cytosolic-free Ca concentrations ([Ca]i) were measured to examine the role of Ca influx in the presence of amphetamine. Amphetamine in vitro inhibited both basal and porcine follicle-stimulating hormone-stimulated estradiol/progesterone release, and amphetamine significantly decreased steroidogenic enzyme activities. Adding 8-Bromo-cAMP did not recover the inhibitory effects of amphetamine on progesterone and estradiol release. H89 significantly decreased progesterone and estradiol basal release but failed to enhance a further amphetamine inhibitory effect. Amphetamine was capable of further suppressing the release of estradiol release under the presence of nifedipine. Pretreatment with the amphetamine for 2 h decreased the basal [Ca]i and prostaglandin F2α-stimulated increase of [Ca]i. Amphetamine inhibits progesterone and estradiol secretion in rat granulosa cells through a mechanism involving decreased PKA-downstream steroidogenic enzyme activity and L-type Ca channels. Our current findings show that it is necessary to study the possibility of amphetamine perturbing reproduction in females.
本研究的目的是评估苯丙胺对大鼠颗粒细胞中孕酮和雌二醇生成的影响以及潜在的细胞调节机制。将新鲜分离的大鼠颗粒细胞与各种测试药物在苯丙胺存在的情况下进行培养,并测量雌二醇/孕酮的生成以及胞质环磷酸腺苷(cAMP)水平。此外,测量胞质游离钙浓度([Ca]i)以研究在苯丙胺存在下钙内流的作用。体外实验中,苯丙胺抑制基础和猪促卵泡激素刺激的雌二醇/孕酮释放,且苯丙胺显著降低类固醇生成酶活性。添加8-溴-cAMP不能恢复苯丙胺对孕酮和雌二醇释放的抑制作用。H89显著降低孕酮和雌二醇的基础释放,但未能增强苯丙胺的进一步抑制作用。在硝苯地平存在的情况下,苯丙胺能够进一步抑制雌二醇的释放。用苯丙胺预处理2小时可降低基础[Ca]i以及前列腺素F2α刺激引起的[Ca]i升高。苯丙胺通过涉及降低蛋白激酶A下游类固醇生成酶活性和L型钙通道的机制抑制大鼠颗粒细胞中孕酮和雌二醇的分泌。我们目前的研究结果表明,有必要研究苯丙胺干扰雌性生殖的可能性。