Schricker K, Hamann M, Kurtz A
Physiologisches Institut, Universität Regensburg, Germany.
Am J Physiol. 1995 Dec;269(6 Pt 2):F825-30. doi: 10.1152/ajprenal.1995.269.6.F825.
This study sought to examine the involvement of prostaglandins and of nitric oxide (NO) in the macula densa-dependent activation of the renin system in vivo. For this purpose, male Sprague-Dawley rats were chronically infused with furosemide (12 mg/day) for 6 days to inhibit macula densa salt transport. To inhibit the synthesis of prostaglandins and of NO, animals were injected with indomethacin (2 mg/kg twice daily) and with nitro-L-arginine methyl ester (L-NAME; 40 mg/kg twice daily) for the last 2 days of the experiment, respectively. Furosemide infusion increased plasma renin activity (PRA) from 8.8 +/- 1.4 to 41 +/- 5.2 ng angiotensin I (ANG I).h-1.ml-1 and renin mRNA levels from 112 +/- 8 of standard to 249 +/- 18% of standard. After treatment with indomethacin, the furosemide-induced increases in renin mRNA levels was attenuated to 190 +/- 11% of standard. After injections of L-NAME, both the furosemide-induced increases of renin mRNA levels and of PRA were reduced to 126 +/- 14% of standard and 22 +/- 5 ng ANG I.h-1.ml-1, respectively. These findings suggest that activation of renin gene expression by blockade of the macula densa function is dependent on intact NO and prostaglandin formation, whereas for stimulation of renin secretion mainly intact NO formation appears to be necessary.
本研究旨在探讨前列腺素和一氧化氮(NO)在体内致密斑依赖性肾素系统激活中的作用。为此,将雄性Sprague-Dawley大鼠连续6天慢性输注速尿(12毫克/天)以抑制致密斑盐转运。为了抑制前列腺素和NO的合成,在实验的最后2天分别给动物注射吲哚美辛(2毫克/千克,每日两次)和硝基-L-精氨酸甲酯(L-NAME;40毫克/千克,每日两次)。输注速尿使血浆肾素活性(PRA)从8.8±1.4增加到41±5.2纳克血管紧张素I(ANG I)·小时-1·毫升-1,肾素mRNA水平从标准的112±8%增加到249±18%。用吲哚美辛治疗后,速尿诱导的肾素mRNA水平升高减弱至标准的190±11%。注射L-NAME后,速尿诱导的肾素mRNA水平和PRA的升高分别降至标准的126±14%和22±5纳克ANG I·小时-1·毫升-1。这些发现表明,通过阻断致密斑功能激活肾素基因表达依赖于完整的NO和前列腺素形成,而刺激肾素分泌似乎主要需要完整的NO形成。