Manhiani M M, Quigley J E, Socha M J, Motamed K, Imig J D
Department of Vascular Biology, Medical College of Georgia, Augusta, GA, USA.
Kidney Blood Press Res. 2007;30(4):195-202. doi: 10.1159/000104094. Epub 2007 Jun 15.
Impaired cytochrome P450 epoxygenase enzyme (Cyp2c) regulation contributes to renal damage in angiotensin salt-sensitive hypertension (ANG/HS). We hypothesized that interleukin-6 null mice (IL6-/-) would improve Cyp2c regulation and reduce renal damage in hypertensive mice fed a high salt diet. Systolic blood pressure increased to a greater extent in ANG/HS hypertension as compared to angiotensin (ANG) hypertension but blood pressure did not differ between WT and IL6-/- hypertensive groups. Albuminuria, a marker for renal injury, increased significantly in ANG/HS hypertension in WT mice (5,113 +/- 1,050 mug/day) and was attenuated in the ANG/HS IL6-/- group (1,306 +/- 385 mug/day). Renal Cyp2c protein expression significantly decreased with ANG/HS hypertension in WT mice as compared to high salt alone. However, the ability to upregulate Cyp2c expression in response to a high salt diet was restored in the ANG/HS IL6 deficient hypertensive mice. Renal expression of soluble epoxide hydrolase, which inactivates protective epoxygenase metabolites, was significantly reduced in ANG/HS IL6-/- hypertensive mice compared to the ANG/HS WT group. These data suggest that IL6, while having no effect on blood pressure, impairs regulation of epoxygenase producing Cyp2c, which could contribute to the development of renal injury in angiotensin salt-sensitive hypertension.
细胞色素P450环氧合酶(Cyp2c)调节受损会导致血管紧张素盐敏感性高血压(ANG/HS)中的肾损伤。我们推测,白细胞介素-6基因敲除小鼠(IL6-/-)在喂食高盐饮食的高血压小鼠中会改善Cyp2c调节并减少肾损伤。与血管紧张素(ANG)高血压相比,ANG/HS高血压中收缩压升高幅度更大,但野生型(WT)和IL6-/-高血压组之间的血压没有差异。蛋白尿是肾损伤的一个指标,在WT小鼠的ANG/HS高血压中显著增加(5,113±1,050微克/天),而在ANG/HS IL6-/-组中则有所减轻(1,306±385微克/天)。与单独高盐饮食相比,WT小鼠中ANG/HS高血压导致肾Cyp2c蛋白表达显著降低。然而,在ANG/HS IL6缺陷型高血压小鼠中,对高盐饮食上调Cyp2c表达的能力得以恢复。与ANG/HS WT组相比,ANG/HS IL6-/-高血压小鼠中使保护性环氧合酶代谢产物失活的可溶性环氧化物水解酶的肾表达显著降低。这些数据表明,IL6虽然对血压没有影响,但会损害产生Cyp2c的环氧合酶的调节,这可能导致血管紧张素盐敏感性高血压中肾损伤的发展。