Busch Lucila, Borda Enri
Pharmacology Unit, School of Dentistry, University of Buenos Aires, Argentina.
Exp Physiol. 2002 Jul;87(4):447-52. doi: 10.1111/j.1469-445x.2002.tb00057.x.
The purpose of this study was to determine the influence of testosterone, the male sex hormone, on beta-adrenergic agonist-induced amylase secretion from rat parotid glands. Isoprenaline (isoproterenol)-induced amylase secretion was measured in vitro from the parotid glands of control and castrated rats with and without testosterone replacement. The isoprenaline-induced amylase release was reduced in parotid glands from castrated rats compared to controls. The reduction of amylase release by isoprenaline in parotid glands of castrated rats, could be reversed by administration of testosterone. Furthermore, beta-adrenergic receptor density and the level of isoprenaline-evoked cAMP in parotid glands from castrated rats was lower compared to intact rats. Using SQ-22536 (an adenylyl cyclase inhibitor), dibutyryl cAMP (a cAMP analogue) and verapamil (a calcium channel blocker), we conclude that the impairment of amylase release from parotid glands after castration was not related to either adenylyl cyclase activity or cAMP accumulation. Amylase release from the parotid glands of castrated rats appears to be mediated by an increase in calcium ion influx.
本研究的目的是确定男性性激素睾酮对β-肾上腺素能激动剂诱导的大鼠腮腺淀粉酶分泌的影响。在体外测量了给予和未给予睾酮替代的对照大鼠和去势大鼠腮腺中异丙肾上腺素诱导的淀粉酶分泌。与对照相比,去势大鼠腮腺中异丙肾上腺素诱导的淀粉酶释放减少。睾酮给药可逆转去势大鼠腮腺中异丙肾上腺素引起的淀粉酶释放减少。此外,与完整大鼠相比,去势大鼠腮腺中β-肾上腺素能受体密度和异丙肾上腺素诱发的cAMP水平较低。使用SQ-22536(一种腺苷酸环化酶抑制剂)、二丁酰cAMP(一种cAMP类似物)和维拉帕米(一种钙通道阻滞剂),我们得出结论,去势后腮腺淀粉酶释放受损与腺苷酸环化酶活性或cAMP积累均无关。去势大鼠腮腺中的淀粉酶释放似乎是由钙离子内流增加介导的。