Wang P S, Tsai S C, Hwang G S, Wang S W, Lu C C, Chen J J, Liu S R, Lee K Y, Chien E J, Chien C H
Department of Physiology, National Yang-Ming University, Taipei, Taiwan, Republic of China.
J Bone Miner Res. 1994 Oct;9(10):1583-90. doi: 10.1002/jbmr.5650091011.
Effects of calcitonin peptides, including human calcitonin (hCT), salmon calcitonin (sCT), and calcitonin gene-related peptide (CGRP), on the secretion of testosterone and luteinizing hormone (LH) in male rats were studied. Male rats were injected intravenously with human chorionic gonadotropin (hCG), calcitonin peptides, or hCG plus calcitonin peptides. Blood samples were collected at several intervals following hormone challenge. In an in vitro experiment, testis blocks were incubated with hCG (0, 0.05, 0.5, or 5 IU/ml) or hCG (0.5 IU/ml) plus calcitonin peptides (0-10(-9) or 10(-6) M) at 34 degrees C for 30 minutes. Both medium and plasma samples were extracted by ether and analyzed for testosterone by radioimmunoassay (RIA). The concentration of calcium in each plasma sample was measured by an automatic calcium analyzer. The anterior pituitary gland (AP) was incubated with or without calcitonin peptides (0-10 nM) at 37 degrees C for 30 minutes. They were then incubated with gonadotropin releasing hormone (GnRH, 10 nM) for a further 30 minutes. The concentration of LH in AP medium was measured by RIA. The accumulation of cyclic adenosine monophosphate (cAMP) and cyclic guanosine monophosphate (cGMP) in both testicular tissues and APs were measured by RIA. A single intravenous injection of calcitonin peptides decreased the basal and hCG-stimulated levels of plasma testosterone gradually from 60 to 180 or 360 minutes after challenge. The plasma calcium was not altered by the injection of calcitonin peptides and/or hCG. Administration of calcitonin peptides in vitro resulted in a dose-dependent inhibition of both basal and hCG-stimulated release of testosterone.(ABSTRACT TRUNCATED AT 250 WORDS)
研究了降钙素肽,包括人降钙素(hCT)、鲑鱼降钙素(sCT)和降钙素基因相关肽(CGRP)对雄性大鼠睾酮和促黄体生成素(LH)分泌的影响。给雄性大鼠静脉注射人绒毛膜促性腺激素(hCG)、降钙素肽或hCG加降钙素肽。在激素刺激后的几个时间间隔采集血样。在体外实验中,将睾丸组织块在34℃下与hCG(0、0.05、0.5或5IU/ml)或hCG(0.5IU/ml)加降钙素肽(0 - 10⁻⁹或10⁻⁶M)孵育30分钟。培养基和血浆样品均用乙醚提取,并用放射免疫分析法(RIA)检测睾酮。用自动钙分析仪测量每个血浆样品中的钙浓度。将垂体前叶(AP)在37℃下与或不与降钙素肽(0 - 10nM)孵育30分钟。然后再与促性腺激素释放激素(GnRH,10nM)孵育30分钟。用RIA测量AP培养基中LH的浓度。用RIA测量睾丸组织和AP中环状单磷酸腺苷(cAMP)和环状单磷酸鸟苷(cGMP)的积累。单次静脉注射降钙素肽可使刺激后60至180或360分钟时血浆睾酮的基础水平和hCG刺激水平逐渐降低。注射降钙素肽和/或hCG后血浆钙未发生改变。体外给予降钙素肽导致基础和hCG刺激的睾酮释放均呈剂量依赖性抑制。(摘要截短于250字)