el-Dahr S S, Gomez R A, Khare G, Peach M J, Carey R M, Chevalier R L
Department of Pediatrics, University of Virginia Health Sciences Center, Charlottesville 22908.
Am J Kidney Dis. 1990 Jun;15(6):575-82. doi: 10.1016/s0272-6386(12)80529-4.
Angiotensin II has been implicated in mediating renal vasoconstriction resulting from chronic unilateral ureteral obstruction (UUO) in both mature and developing animals. We have previously shown that chronic neonatal UUO results in increased distribution of renin and its mRNA in the obstructed kidney, as well as of immunoreactive renin in the intact opposite kidney. The present study was designed to evaluate the effects of 24 hours versus 4 weeks of UUO on the distribution of renin mRNA and its protein in the adult rat kidney. Renin was detected by immunocytochemistry using a polyclonal anti-rat renin antibody. Renin mRNA was localized by in situ hybridization to an oligonucleotide complementary to renin mRNA. UUO of 24 hours' or 4 weeks' duration did not alter the distribution of renin and its mRNA in the obstructed kidneys as compared with sham-operated kidneys, although kidneys obstructed for 4 weeks had a significant increase in the percent of renin-containing juxtaglomerular apparatuses (JCA) when compared with the intact opposite kidneys (P less than 0.05). Compensatory hypertrophy was not present in the intact opposite kidneys after 24 hours of UUO and distribution of renin gene expression was not altered at that time. However, 4 weeks following contralateral UUO, the intact kidneys were hypertrophied and showed a decrease in renin gene expression relative to the obstructed and sham-operated kidneys. We conclude that unlike UUO during early development, chronic UUO in the mature animal does not activate renin gene expression nor alter renin distribution in the obstructed kidneys. Renin gene expression is suppressed in the hypertrophied kidney with prolonged contralateral UUO.(ABSTRACT TRUNCATED AT 250 WORDS)
血管紧张素II被认为在介导成熟和发育中动物慢性单侧输尿管梗阻(UUO)所致的肾血管收缩中起作用。我们之前已表明,慢性新生期UUO会导致梗阻肾脏中肾素及其mRNA分布增加,以及完整对侧肾脏中免疫反应性肾素增加。本研究旨在评估24小时与4周UUO对成年大鼠肾脏中肾素mRNA及其蛋白分布的影响。使用多克隆抗大鼠肾素抗体通过免疫细胞化学检测肾素。肾素mRNA通过原位杂交定位到与肾素mRNA互补的寡核苷酸上。与假手术组肾脏相比,持续24小时或4周的UUO并未改变梗阻肾脏中肾素及其mRNA的分布,尽管与完整对侧肾脏相比,梗阻4周的肾脏中含肾素的球旁器(JCA)百分比显著增加(P<0.05)。UUO 24小时后,完整对侧肾脏未出现代偿性肥大,此时肾素基因表达分布也未改变。然而,对侧UUO 4周后,完整肾脏出现肥大,相对于梗阻和假手术组肾脏,肾素基因表达降低。我们得出结论,与早期发育期间的UUO不同,成熟动物中的慢性UUO不会激活肾素基因表达,也不会改变梗阻肾脏中肾素的分布。随着对侧UUO时间延长,肥大肾脏中的肾素基因表达受到抑制。(摘要截短至250字)