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首页> 外文期刊>American Journal of Physiology >Immune suppression blocks sodium-sensitive hypertension following recovery from ischemic acute renal failure
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Immune suppression blocks sodium-sensitive hypertension following recovery from ischemic acute renal failure

机译:从缺血性急性肾功能衰竭恢复后,免疫抑制可阻止钠敏感性高血压

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The present study determined the effect of immune suppression with mycophenolate mofetil (MMF) on sodium-sensitive hypertension following recovery from ischemia reperfusion (I/R)-induced acute renal failure. Male Sprague-Dawley rats fed 0.4% NaCl chow were subjected to 40 min bilateral I/R or control sham surgery. After 35 days of recovery, when plasma creatinine levels had returned to normal, the rats were switched to 4.0% NaCl chow for 28 days and administered vehicle or MMF (20 mg centre dot kg~(-1) centre dot day~(-1) ip). High-salt mean arterial pressure was significantly higher in I/R rats (144 +- 16 mmHg) compared with vehicle-treated sham rats (122 +- 2 mmHg). Treatment of I/R rats with MMF during the period of high salt intake prevented the salt-induced increase in arterial pressure (114 +- 3 mmHg). Conscious creatinine clearance was lower in I/R rats (0.27 +- 0.07 ml centre dot min~(-1) centre dot 100 g body wt~(-1)) compared with vehicle-treated sham rats (0.58 +- 0.04 ml centre dot min~(-1) centre dot 100 g body wt~(-1)); MMF treatment prevented the decrease in creatinine clearance in I/R rats (0.64 +- 0.07 ml centre dot min~(-1) centre dot 100 g body wt~(-1)). I/R injury also significantly increased glomerular tissue damage and increased the presence of ED-1 positive (macrophages) and S100A4 positive cells (fibroblasts) in the renal interstitium. The I/R rats treated with MMF exhibited a significant reduction in infiltrating macrophages and fibroblasts and decreased histological damage. The present data indicate that infiltrating immune cells mediate or participate in the development of sodium-sensitive hypertension and renal damage in rats apparently recovered from renal I/R injury.
机译:本研究确定了从局部缺血再灌注(I / R)引起的急性肾衰竭恢复后,用霉酚酸酯(MMF)进行免疫抑制对钠敏感性高血压的影响。饲喂0.4%NaCl饲料的雄性Sprague-Dawley大鼠接受40分钟的双侧I / R或对照假手术。恢复35天后,当血浆肌酐水平恢复正常时,将大鼠换成4.0%NaCl食物28天,并给予媒介物或MMF(20 mg中心点kg〜(-1)中心点天〜(-1 )ip)。与载体治疗的假手术大鼠(122±2 mmHg)相比,I / R大鼠(144±16 mmHg)的高盐平均动脉压明显更高。在高盐摄入期间用MMF对I / R大鼠进行治疗可防止盐诱导的动脉压升高(114±3 mmHg)。 I / R大鼠的自觉肌酐清除率较低(0.27 +-0.07 ml中心点min〜(-1)中心点100 g体重(-1)),与媒介物处理的假手术大鼠(0.58 +-0.04 ml中心点最小〜(-1)中心点100 g体重(〜-1)); MMF处理阻止了I / R大鼠肌酐清除率的降低(0.64±0.07 ml中心点min〜(-1)中心点100 g体重(-1))。 I / R损伤也显着增加肾小球组织损伤,并增加肾间质中ED-1阳性(巨噬细胞)和S100A4阳性细胞(成纤维细胞)的存在。用MMF处理的I / R大鼠的巨噬细胞浸润和成纤维细胞浸润明显减少,组织学损伤减少。目前的数据表明,浸润的免疫细胞介导或参与了对钠敏感的高血压的发展以及明显从肾脏I / R损伤中恢复的大鼠的肾脏损害。

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