Campbell W B, Graham R M, Jackson E K
Arch Int Pharmacodyn Ther. 1980 Aug;246(2):315-23.
Renal prostaglandins (PG) appear to mediate the release of renin due to activation of the intrarenal baroreceptor and stimulation of the renal sympathetic nerves. Since the vasodilator hydralazine is thought to stimulate renin release by both of these mechanisms, we examined the effect of indomethacin, a PG synthetase inhibitor, on hydralazine-induced renin release. Hydralazine increased the serum renin levels from 3.3 +/- 0.5 to 13.7 +/- 3.1 and 41.9 +/- 2.4 ng/ml/hr at the 1 and 10 mg/kg doses, respectively. Indomethacin inhibited this hydralazine-induced renin release by 100% at the 1 mg/kg dose and 36% at the 10 mg/kg dose even though the hypotensive effect of the drug was unaltered. Indomethacin (5 mg/kg) also suppressed urinary PGE2 excretion by 60% (p < 0.001). The beta-blocker, propranolol, was as effective as indomethacin in attenuating hydralazine-induced renin release. Additionally, propranolol blocked the tachycardia associated with hydralazine and slightly enhanced the hypotensive action of the drug. When indomethacin and propranolol were combined, no further inhibition of hydralazine-induced renin release was observed. Thus, renal PG's appear to be important as mediators of hydralazine-stimulated renin release but no hydralazine-induced vasodilatation.
肾前列腺素(PG)似乎通过激活肾内压力感受器和刺激肾交感神经来介导肾素的释放。由于血管扩张剂肼屈嗪被认为通过这两种机制刺激肾素释放,我们研究了PG合成酶抑制剂吲哚美辛对肼屈嗪诱导的肾素释放的影响。肼屈嗪分别以1和10mg/kg的剂量使血清肾素水平从3.3±0.5升高至13.7±3.1和41.9±2.4ng/ml/hr。吲哚美辛在1mg/kg剂量时100%抑制了肼屈嗪诱导的肾素释放,在10mg/kg剂量时抑制了36%,尽管该药物的降压作用未改变。吲哚美辛(5mg/kg)也使尿PGE2排泄减少了60%(p<0.001)。β受体阻滞剂普萘洛尔在减弱肼屈嗪诱导的肾素释放方面与吲哚美辛同样有效。此外,普萘洛尔阻断了与肼屈嗪相关的心动过速,并略微增强了该药物的降压作用。当吲哚美辛和普萘洛尔联合使用时,未观察到对肼屈嗪诱导的肾素释放有进一步抑制作用。因此,肾PG作为肼屈嗪刺激肾素释放的介质似乎很重要,但对肼屈嗪诱导的血管扩张不重要。