Schmid G, Geiger H, Bahner U, Heidland A
Medical Clinic, University of Würzburg, F.R.G.
Eur J Pharmacol. 1988 Mar 15;147(3):397-402. doi: 10.1016/0014-2999(88)90174-4.
The parotid excretion of cAMP was measured in normotensive Wistar-Kyoto rats (WKY) and spontaneously hypertensive rats (SHR) in this study. In addition, adenylate cyclase activity in parotid gland tissue was determined. The cAMP excretion rate was increased immediately after isoproterenol infusion. This elevation was more pronounced in young (6-8 weeks) than in older (16-18 weeks) animals, both in WKY and in SHR. These data demonstrate a diminished cAMP response to isoproterenol application with respect to the age of the animals. This could indicate that there is an age-dependent functional alteration of the beta-adrenoceptor-adenylate cyclase complex. In agreement with the results of these in vivo studies, the stimulation of adenylate cyclase activity of the parotid gland by isoproterenol or fluoride was enhanced in young SHR and lowered in old SHR when compared to their normotensive controls of the same age. One may conclude that the sympathetic activity is enhanced in young SHR, and that the beta-adrenoceptor system is hypersensitive to adrenoceptor agonists. This might contribute to the development of hypertension in SHR. Sixteen to eighteen weeks old SHR showed a diminished cAMP output following isoproterenol application when compared to normotensive control rats of the same age. The reduction of the response to isoproterenol stimulation in old SHR seems to be related to a reduced sensitivity to catecholamine stimulation.
在本研究中,测量了正常血压的Wistar-Kyoto大鼠(WKY)和自发性高血压大鼠(SHR)腮腺中cAMP的排泄量。此外,还测定了腮腺组织中的腺苷酸环化酶活性。异丙肾上腺素输注后,cAMP排泄率立即升高。无论是在WKY还是SHR中,这种升高在年轻(6 - 8周)动物中比在年长(16 - 18周)动物中更为明显。这些数据表明,随着动物年龄的增长,对异丙肾上腺素应用的cAMP反应减弱。这可能表明β-肾上腺素能受体-腺苷酸环化酶复合物存在年龄依赖性功能改变。与这些体内研究结果一致,与同龄正常血压对照相比,异丙肾上腺素或氟化物对年轻SHR腮腺腺苷酸环化酶活性的刺激增强,而对老年SHR则降低。可以得出结论,年轻SHR的交感神经活动增强,且β-肾上腺素能受体系统对肾上腺素能受体激动剂高度敏感。这可能有助于SHR高血压的发展。与同龄正常血压对照大鼠相比,16至18周龄的SHR在应用异丙肾上腺素后cAMP输出减少。老年SHR对异丙肾上腺素刺激反应的降低似乎与对儿茶酚胺刺激的敏感性降低有关。