Mazzocchi G, Rossi G P, Rebuffat P, Malendowicz L K, Markowska A, Nussdorfer G G
Department of Anatomy, University of Padua, Italy.
Endocrinology. 1997 Jun;138(6):2333-7. doi: 10.1210/endo.138.6.5191.
The effects of endothelins (ET) on the proliferative activity of the rat adrenal cortex have been investigated in vivo, using an in situ perfusion technique of the intact left gland. The chemicals were dissolved in the perfusion medium, and the perfusion continued for 120 min. ET-1 concentration dependently increased the mitotic index and [3H]thymidine incorporation into DNA in the zona glomerulosa (ZG; 6- and 3-fold increases, respectively, at a 10(-8) M concentration), but not in the inner adrenocortical layers, where the basal proliferative activity was negligible. The effect of 10(-8) M ET-1 was blocked by the ETA receptor antagonist BQ-123, whereas the ETB receptor antagonist BQ-788 was ineffective. ET-2 and ET-3 (10(-8) M) enhanced DNA synthesis in the ZG, but their effects were less intense than that of 10(-8) M ET-1 and were directly related to their binding potency for the ETA receptor subtype (ET-1 > ET-2 >> ET-3). The selective ETB receptor agonists BQ-3020, IRL-1620, and sarafotoxin-6B were ineffective. The ZG proliferogenic action of 10(-8) M ET-1 was reversed by both the protein kinase C inhibitor Ro31-8220 and the tyrosine kinase inhibitor tyrphostin-23; a complete blockade was obtained at a 10(-6)-M concentration of each inhibitor. In contrast, neither the protein kinase A inhibitor H-89 (10(-5) M) nor the cyclooxygenase and lipoxygenase inhibitors indomethacin and phenidone (10(-5) M) affected ET-1 action. Collectively, our findings indicate that ETs stimulate the proliferation of rat adrenal ZG cells, acting through ETA receptors coupled with protein kinase C- and tyrosine kinase-dependent signaling pathways. The results of the present study are in keeping with the view that in mammals, ZG is the proliferative layer involved in the maintenance of growth of the entire adrenal cortex and with the previous autoradiographic demonstration that ZG is the only adrenocortical layer provided with ETA receptors.
采用完整左肾上腺原位灌注技术,在体内研究了内皮素(ET)对大鼠肾上腺皮质增殖活性的影响。将化学物质溶解于灌注培养基中,灌注持续120分钟。ET-1浓度依赖性地增加了肾小球带(ZG)的有丝分裂指数以及[3H]胸腺嘧啶核苷掺入DNA的量(在10^(-8) M浓度时分别增加6倍和3倍),但在内层肾上腺皮质层中未出现这种情况,因为内层的基础增殖活性可忽略不计。10^(-8) M的ET-1的作用被ETA受体拮抗剂BQ-123阻断,而ETB受体拮抗剂BQ-788则无效。ET-2和ET-3(10^(-8) M)增强了ZG中的DNA合成,但其作用强度低于10^(-8) M的ET-1,且与它们对ETA受体亚型的结合能力直接相关(ET-1 > ET-2 >> ET-3)。选择性ETB受体激动剂BQ-3020、IRL-1620和铃蟾毒素-6B无效。10^(-8) M的ET-1对ZG的促增殖作用被蛋白激酶C抑制剂Ro31-8220和酪氨酸激酶抑制剂 tyrphostin-23逆转;在每种抑制剂浓度为10^(-6) M时可完全阻断。相反,蛋白激酶A抑制剂H-89(10^(-5) M)以及环氧化酶和脂氧化酶抑制剂吲哚美辛和非那吡啶(10^(-5) M)均不影响ET-1的作用。总体而言,我们的研究结果表明,ET通过与蛋白激酶C和酪氨酸激酶依赖性信号通路偶联的ETA受体刺激大鼠肾上腺ZG细胞的增殖。本研究结果与以下观点一致,即在哺乳动物中,ZG是参与维持整个肾上腺皮质生长的增殖层,并且与先前的放射自显影证明一致,即ZG是唯一具有ETA受体的肾上腺皮质层。