Mokuda O, Sakamoto Y, Ubukata E, Shimizu N
Third Department of Internal Medicine, Teikyo University School of Medicine, Chiba, Japan.
Horm Metab Res. 1996 May;28(5):227-9. doi: 10.1055/s-2007-979170.
To clearly understand the feedback mechanism of renin secretion by intrarenal angiotensin II synthesis, we studied the stimulatory effect of captopril, an angiotensin converting enzyme inhibitor, on renin release from the isolated perfused guinea pig kidneys. Captopril did not affect the basal renin secretion. Captopril increased on a dose dependent basis renin release induced by 0.1 mg/ml furosemide; 5.8 +/- 1.3 ng/ml/hr at 0 mg/ml of captopril vs. 8.8 +/- 1.6 ng/ml/hr at 0.01 mg/ml (p < 0.05) and 11.8 +/- 2.4 ng/ml/hr at 0.1 mg/ml (p < 0.01), 15-20 min after furosemide infusion. After lowering the flow rates from 10 to 5 ml/min, renin secretion was not altered during the first 12 minutes. However, after adding 0.1 mg/ml captopril, renin secretion was enhanced within the following 8 minutes (8.3 +/- 1.5 vs. 3.7 +/- 0.5 ng/ml/hr at the end of low flow rate period, p < 0.01). Lowering the perfusion flow of the guinea pig kidneys decreases the NaCl flux at the macula densa and also seems to have a similar effect to furosemide. Therefore, these effects of captopril suggest that intrarenal angiotensin II production has an important role in the regulation of renin secretion, probably via effects on the macula densa function.
为了清楚地了解肾内血管紧张素II合成对肾素分泌的反馈机制,我们研究了血管紧张素转换酶抑制剂卡托普利对离体灌注豚鼠肾脏肾素释放的刺激作用。卡托普利不影响基础肾素分泌。卡托普利能剂量依赖性地增加由0.1mg/ml速尿诱导的肾素释放;在0mg/ml卡托普利时为5.8±1.3ng/ml/小时,在0.01mg/ml时为8.8±1.6ng/ml/小时(p<0.05),在0.1mg/ml时为11.8±2.4ng/ml/小时(p<0.01),在速尿输注后15 - 20分钟。将流速从10ml/min降至5ml/min后,在最初12分钟内肾素分泌未改变。然而,在加入0.1mg/ml卡托普利后,在接下来的8分钟内肾素分泌增强(低流速期结束时分别为8.3±1.5与3.7±0.5ng/ml/小时,p<0.01)。降低豚鼠肾脏的灌注流量会降低致密斑处的NaCl通量,并且似乎与速尿有类似作用。因此,卡托普利的这些作用表明肾内血管紧张素II的产生在肾素分泌的调节中起重要作用,可能是通过对致密斑功能的影响。