Guo Shunhua, Kowalewska Jolanta, Wietecha Tomasz A, Iyoda Masayuki, Wang Li, Yi Kenneth, Spencer Min, Banas Miriam, Alexandrescu Sanda, Hudkins Kelly L, Alpers Charles E
Department of Pathology, University of Washington, 1959 NE Pacific Avenue, Seattle, WA 98195, USA.
J Am Soc Nephrol. 2008 Jun;19(6):1168-76. doi: 10.1681/ASN.2007050607. Epub 2008 Mar 12.
Blockade of the renin-angiotensin system is renoprotective in a variety of chronic nephropathies, but the direct effect of such treatment in active, immune complex-mediated glomerulonephritis is unknown. This study investigated the short- and long-term effects of an angiotensin-converting enzyme inhibitor (enalapril) and an angiotensin II type 1 receptor blocker (losartan) in thymic stromal lymphopoietin transgenic (TSLPtg) mice, which develop mixed cryoglobulinemia and severe cryoglobulinemia-associated membranoproliferative glomerulonephritis. Enalapril and losartan each reduced hypertension, proteinuria, glomerular extracellular matrix deposition, and mesangial cell activation in TSLPtg mice. These renoprotective effects were not observed with hydralazine treatment, despite a similar antihypertensive effect. Treatment with enalapril or losartan also decreased renal plasminogen activator inhibitor-1 in TSLPtg mice, assessed by immunohistochemistry and quantitative real-time reverse transcriptase-PCR. None of the treatments affected immune complex deposition or macrophage infiltration. Overall, enalapril- and losartan-treated TSLPtg mice survived significantly longer than untreated TSLPtg mice. These studies demonstrate that angiotensin blockade may provide renoprotective benefits, independent of its BP-lowering effect, in the treatment of active immune complex-mediated glomerulonephritis.
肾素-血管紧张素系统的阻断在多种慢性肾病中具有肾脏保护作用,但这种治疗在活动性、免疫复合物介导的肾小球肾炎中的直接效果尚不清楚。本研究调查了血管紧张素转换酶抑制剂(依那普利)和血管紧张素II 1型受体阻滞剂(氯沙坦)对胸腺基质淋巴细胞生成素转基因(TSLPtg)小鼠的短期和长期影响,这些小鼠会发生混合性冷球蛋白血症和严重的冷球蛋白血症相关的膜增生性肾小球肾炎。依那普利和氯沙坦均可降低TSLPtg小鼠的高血压、蛋白尿、肾小球细胞外基质沉积和系膜细胞活化。尽管肼屈嗪治疗具有相似的降压效果,但未观察到这些肾脏保护作用。通过免疫组织化学和定量实时逆转录聚合酶链反应评估,依那普利或氯沙坦治疗还可降低TSLPtg小鼠的肾纤溶酶原激活物抑制剂-1。所有治疗均未影响免疫复合物沉积或巨噬细胞浸润。总体而言,接受依那普利和氯沙坦治疗的TSLPtg小鼠的存活时间明显长于未治疗的TSLPtg小鼠。这些研究表明,在治疗活动性免疫复合物介导的肾小球肾炎时,血管紧张素阻断可能提供肾脏保护益处,而与其降压作用无关。