Vidotti D B, Casarini D E, Cristovam P C, Leite C A, Schor N, Boim M A
Renal Div., UNIFESP, Rua Botucatu, 740, 04023-900 São Paulo, Brazil.
Am J Physiol Renal Physiol. 2004 Jun;286(6):F1039-45. doi: 10.1152/ajprenal.00371.2003. Epub 2004 Jan 13.
Increased intrarenal renin-angiotensin system activity contributes to diabetic nephropathy. ANG II generation in mesangial cells (MC) is increased by high-glucose (HG) exposure. This study assessed the mechanisms involved in the glucose-induced ANG II generation in rat MC. Under basal conditions, MC mainly secreted prorenin. HG decreased prorenin secretion and induced a striking 30-fold increase in intracellular renin activity. After 72 h of HG exposure, only the mRNA levels for angiotensinogen and angiotensin-converting enzyme (ACE) were significantly elevated. However, after shorter periods of 24 h of HG stimulation the mRNA levels of the enzymes prorenin and cathepsin B, besides that for ACE, were significantly increased. The results suggest that the HG-induced increase in ANG II generation in MC results from an increase in intracellular renin activity mediated by at least three factors: a time-dependent stimulation of (pro)renin gene transcription, a reduction in prorenin enzyme secretion, and an increased rate of conversion of prorenin to active renin, probably mediated by cathepsin B. The increase in angiotensinogen mRNA in parallel to increased renin activity indicates that HG also increased the availability of the renin substrate. The consistent upregulation of ACE mRNA suggests that, besides renin, ACE is directly involved in the increased mesangial ANG II generation induced by HG.
肾内肾素 - 血管紧张素系统活性增加会导致糖尿病肾病。高糖(HG)暴露会使系膜细胞(MC)中血管紧张素II(ANG II)的生成增加。本研究评估了大鼠MC中葡萄糖诱导ANG II生成所涉及的机制。在基础条件下,MC主要分泌肾素原。HG降低了肾素原的分泌,并使细胞内肾素活性显著增加了30倍。HG暴露72小时后,只有血管紧张素原和血管紧张素转换酶(ACE)的mRNA水平显著升高。然而,在HG刺激24小时的较短时间后,除了ACE的mRNA水平外,肾素原和组织蛋白酶B的mRNA水平也显著增加。结果表明,HG诱导的MC中ANG II生成增加是由至少三个因素介导的细胞内肾素活性增加所致:(前)肾素基因转录的时间依赖性刺激、肾素原酶分泌的减少以及肾素原向活性肾素转化速率的增加,可能由组织蛋白酶B介导。血管紧张素原mRNA与肾素活性增加同时升高表明HG也增加了肾素底物的可用性。ACE mRNA的持续上调表明,除了肾素外,ACE也直接参与了HG诱导的系膜ANG II生成增加。