Camargo L A, Saad W A, Netto C R, Gentil C G, Antunes-Rodrigues J, Covian M R
Can J Physiol Pharmacol. 1976 Jun;54(3):219-28. doi: 10.1139/y76-034.
Urinary output of Na+ and K+, and volume of urine have been studied in conscious, unrestrained, water-loaded male rats following the intraseptal injection of catecholamines. Natriuresis and kaliuresis increased after injecting noradrenaline (NA), the intensity being dose related. The dose-response curve suggests that a monomolecular interacting takes place between NA and pharmacological receptors present in the septal area. No change was observed in diuresis. Systematic mapping of the septal area yielded about the same results for all sites except a zone located in the lateral nucleus that was more sensitive. An alpha blocker (dibenamine), injected intraseptally before NA, showed an inhibitory effect while a beta blocker (propranolol) yielded a potentiation effect. These same effects of the blocking agents were observed when adrenaline was used instead of NA. Lidocaine, which inhibits the re-uptake of NA, showed an enhancement of the natriuretic and kaliuretic effect of NA, and the same effect was observed when the enzymatic destruction of NA was prevented by nialamide, an inhibitor of monoaminoxidase. Dopamine showed a natriuretic effect, but no effect was observed on K+ and urine output. Serotonin had no action on natriuresis, kaliuresis and diuresis.
在对清醒、不受限制且水负荷的雄性大鼠进行中隔内注射儿茶酚胺后,研究了其尿中钠(Na⁺)和钾(K⁺)的排出量以及尿量。注射去甲肾上腺素(NA)后,钠利尿和钾利尿增加,其强度与剂量相关。剂量反应曲线表明,NA与中隔区域存在的药理受体之间发生了单分子相互作用。未观察到利尿作用的变化。对中隔区域进行系统定位后发现,除位于外侧核的一个更敏感的区域外,所有部位的结果大致相同。在注射NA前经中隔内注射α受体阻滞剂(双苄胺)显示出抑制作用,而β受体阻滞剂(普萘洛尔)则产生增强作用。当使用肾上腺素代替NA时,观察到阻滞剂的这些相同作用。抑制NA再摄取的利多卡因显示出NA的利钠和利钾作用增强,并且当用单胺氧化酶抑制剂尼亚酰胺防止NA的酶促破坏时,也观察到了相同的作用。多巴胺显示出利钠作用,但对K⁺和尿量无影响。5-羟色胺对钠利尿、钾利尿和利尿均无作用。