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首页> 外文期刊>Circulation. Heart failure >Effects of chronic rosiglitazone treatment on renal handling of salt and water in rats with volume-overload congestive heart failure.
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Effects of chronic rosiglitazone treatment on renal handling of salt and water in rats with volume-overload congestive heart failure.

机译:慢性罗格列酮治疗对容量超负荷充血性心力衰竭大鼠肾脏盐和水处理的影响。

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摘要

BACKGROUND: The side effects of fluid retention and edema of the thiazolidinedione (TZD) class of peroxisome proliferator-activated receptor-gamma agonists limit their use in patients with congestive heart failure (CHF). The present study aims to explore whether chronic treatment with the TZD compound rosiglitazone (RGZ) is associated with worsening of salt and water retention in male Sprague-Dawley rats with aorto-caval fistula, an experimental model of volume-overload CHF. METHODS AND RESULTS: The effects of oral RGZ (30 mg/kg per day for 4 weeks) in CHF rats on plasma volume, cumulative sodium excretion, renal expression of Na(+) channels and transporters, and selected biomarkers of CHF were compared with those in CHF rats and sham-operated control rats treated with vehicle only (n=7 to 10). Additionally, the response to acute saline loading (3.5% of body weight) was evaluated after 2 weeks of treatment by renal clearance methodology. Chronic RGZ treatment caused no further increase in plasma volume compared with vehicle-treated CHF rats. Moreover, no increase in renal expression of Na(+) transport-linked channels/transporters was observed in response to RGZ. Cumulative sodium excretion was enhanced in CHF rats after RGZ and by another TZD compound, pioglitazone. In response to saline loading, RGZ-treated animals displayed a higher natriuretic/diuretic response than did vehicle-treated rats. Chronic RGZ treatment was not associated with any deterioration in selected biomarkers of CHF, whereas indices of cardiac hypertrophy and blood pressure were improved. CONCLUSIONS: Chronic RGZ treatment was not associated with worsening of fluid retention or cardiac status in rats with experimental volume-overload CHF. Rather, RGZ appeared to improve renal handling of salt and water in rats with CHF.
机译:背景:过氧化物酶体增殖物激活的受体-γ激动剂的噻唑烷二酮(TZD)类液体滞留和水肿的副作用限制了它们在充血性心力衰竭(CHF)患者中的使用。本研究旨在探讨TZD复合罗格列酮(RGZ)的长期治疗是否与雄性主动脉瘘瘘Sprague-Dawley大鼠(体内超负荷的CHF实验模型)的盐和水retention留恶化相关。方法和结果:比较了CHF大鼠口服RGZ(每天30 mg / kg,共4周)对血浆容量,累积钠排泄,Na(+)通道和转运蛋白的肾脏表达以及所选CHF生物标志物的影响。仅用赋形剂治疗的CHF大鼠和假手术对照大鼠中的那些(n = 7至10)。此外,在治疗2周后,通过肾脏清除方法评估了对急性盐水负荷(体重的3.5%)的反应。与载体治疗的CHF大鼠相比,慢性RGZ治疗不会导致血浆容量进一步增加。此外,没有观察到对RGZ有反应的Na(+)运输相关通道/转运蛋白的肾脏表达增加。 RGZ后,CHF大鼠和另一种TZD化合物吡格列酮可增加钠的累积排泄。响应于生理盐水负荷,RGZ处理的动物显示出的利尿钠/利尿剂的响应高于媒介物处理的大鼠。慢性RGZ治疗与所选的CHF生物标志物没有任何恶化相关,而心脏肥大和血压指数得到改善。结论:慢性RGZ治疗与实验性超负荷CHF大鼠的体液retention留或心脏状态恶化无关。 RGZ似乎可以改善CHF大鼠的肾脏对盐和水的处理。

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