Shimizu T, Katsuura G, Nakamura M, Nakao K, Morii N, Itoh Y, Shiono S, Imura H
Life Sci. 1986 Oct 6;39(14):1263-70. doi: 10.1016/0024-3205(86)90187-6.
In order to clarify the role of atrial natriuretic polypeptide (ANP) in the brain on regulation of blood pressure and urine output, we examined the effects of intracerebroventricular (i.c.v.) administration of synthetic alpha-human ANP (alpha-hANP) to both anesthetized and conscious rats. In anesthetized rats, i.c.v. injection of angiotension II (A II) caused increases of blood pressure, urine flow and sodium excretion in a dose dependent manner. alpha-HANP alone had no effect on these two parameters. The hypertensive effect of A II was apparently attenuated by concurrent injection of alpha-hANP, while, the diuretic response to A II was not changed by alpha-hANP. In conscious spontaneously hypertensive rats, i.c.v. injection of saralasin (an A II antagonist) produced a decrease in blood pressure. The i.c.v. pretreatment with alpha-hANP significantly potentiated the central depressor effect of saralasin. These findings suggest that brain ANP may be involved in controlling blood pressure in the central renin-angiotensin system.
为了阐明脑钠尿肽(ANP)在调节血压和尿量方面的作用,我们研究了向麻醉和清醒大鼠脑室内(i.c.v.)注射合成α-人ANP(α-hANP)的效果。在麻醉大鼠中,脑室内注射血管紧张素II(A II)可使血压、尿流量和钠排泄量呈剂量依赖性增加。单独注射α-HANP对这两个参数无影响。同时注射α-hANP可明显减弱A II的升压作用,而α-hANP对A II的利尿反应无影响。在清醒的自发性高血压大鼠中,脑室内注射沙拉新(一种A II拮抗剂)可使血压降低。用α-hANP进行脑室内预处理可显著增强沙拉新的中枢降压作用。这些发现表明,脑ANP可能参与中枢肾素-血管紧张素系统对血压的控制。