Kaminski T
Department of Animal Physiology, University of Warmia and Mazury in Olsztyn, 10-719 Olsztyn-Kortowo 1A, Poland.
Domest Anim Endocrinol. 2004 Nov;27(4):379-96. doi: 10.1016/j.domaniend.2004.05.001.
Opioids were found as factors affecting porcine ovarian steroidogenesis. The mechanism of opioid action, however, on porcine theca interna cells is completely unknown. Therefore, the present study was designed to investigate the possible involvement of two intracellular pathways, phospholipase C/protein kinase C and adenylyl cyclase/protein kinase A, in opioid signal transduction in porcine theca cells treated with mu opioid receptor agonist, FK 33-824. Incubation of the cells for 4 h with FK 33-824 at the dose 1 nM resulted in decreases in inositol phosphate accumulation as well as androstenedione (A(4)), testosterone (T), and estradiol (E(2)) secretions. Protein kinase C (PKC) inhibitors, staurosporine (1-100 nM), D-sphingosine (10-500 nM), and PKCi (100-2000 nM), both added alone and together with the opioid agonist, depressed release of the steroid hormones. PKC activator, phorbol ester (PMA, 1-100 nM), used alone was without effect on theca cell steroidogenesis, but added in combination with FK 33-824 abolished inhibitory influence of the opioid on A(4), T, and E(2) output. The steroid hormone secretion by PKC-deficient theca cells was inhibited by the opioid agonist. FK 33-824 also suppressed PKC activity reducing [(3)H]PDBu specific binding to theca cells, whereas ionomycin (a positive control) increased labeled phorbol ester binding to the cells. In the next experiment, cAMP release from theca cells during 2 and 4 h incubations with FK 33-824 (1-100 nM), naloxone (10 microM; opioid receptor antagonist), and LH (100 ng/mL; a positive control) was examined. FK 33-824 at the dose 1 nM inhibited cAMP secretion during 2 h incubation, but had no effect during longer incubation. LH in a manner independent on incubation time multiplied cAMP release. Protein kinase A inhibitor, PKAi (100-2000 nM), alone and in combination with FK 33-824 (1 nM), inhibited A(4), T, and E(2) secretions by theca cells. PKA activator, 8BrcAMP (10-1000 microM), stimulated the steroid hormone release, but this stimulatory effect was diminished in the presence of FK 33-824. The results allow to suggest that opioid peptides affect porcine theca cell steroidogenesis and their acute action on the cells is connected with the inhibition of phospholipase C/protein kinase C and adenylyl cyclase/protein kinase A signal transduction systems.
阿片类物质被发现是影响猪卵巢类固醇生成的因素。然而,阿片类物质对猪卵泡内膜细胞的作用机制完全未知。因此,本研究旨在探讨两条细胞内信号通路,即磷脂酶C/蛋白激酶C和腺苷酸环化酶/蛋白激酶A,在经μ阿片受体激动剂FK 33-824处理的猪卵泡膜细胞阿片信号转导中可能发挥的作用。用1 nM剂量的FK 33-824孵育细胞4小时,导致肌醇磷酸积累以及雄烯二酮(A4)、睾酮(T)和雌二醇(E2)分泌减少。蛋白激酶C(PKC)抑制剂,星形孢菌素(1-100 nM)、D-鞘氨醇(10-500 nM)和PKCi(100-2000 nM),单独添加以及与阿片类激动剂一起添加时,都会抑制类固醇激素的释放。PKC激活剂佛波酯(PMA,1-100 nM)单独使用对卵泡膜细胞类固醇生成没有影响,但与FK 33-824联合添加时,可消除阿片类物质对A4、T和E2分泌的抑制作用。阿片类激动剂可抑制PKC缺陷型卵泡膜细胞的类固醇激素分泌。FK 33-824还抑制PKC活性,降低[3H]PDBu与卵泡膜细胞的特异性结合,而离子霉素(阳性对照)则增加标记佛波酯与细胞的结合。在接下来的实验中,检测了用FK 33-824(1-100 nM)、纳洛酮(10 μM;阿片受体拮抗剂)和促黄体生成素(LH,100 ng/mL;阳性对照)孵育2小时和4小时期间卵泡膜细胞中cAMP的释放。1 nM剂量的FK 33-824在孵育2小时期间抑制cAMP分泌,但在较长时间孵育时没有影响。LH以与孵育时间无关的方式增加cAMP释放。蛋白激酶A抑制剂PKAi(100-2000 nM)单独以及与FK 33-824(1 nM)联合使用时,均可抑制卵泡膜细胞分泌A4、T和E2。PKA激活剂8BrcAMP(10-1000 μM)刺激类固醇激素释放,但在FK 33-824存在的情况下,这种刺激作用减弱。这些结果表明,阿片肽影响猪卵泡膜细胞类固醇生成,它们对细胞的急性作用与抑制磷脂酶C/蛋白激酶C和腺苷酸环化酶/蛋白激酶A信号转导系统有关。