首页> 外文期刊>Hypertension research: Official journal of the Japanese Society of Hypertension >Tacrolimus-induced hypertension and nephrotoxicity in Fawn-Hooded rats are attenuated by dual inhibition of renin-angiotensin system
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Tacrolimus-induced hypertension and nephrotoxicity in Fawn-Hooded rats are attenuated by dual inhibition of renin-angiotensin system

机译:他克莫司引起的高血压和肾毒性在双黄连的大鼠中被肾素-血管紧张素系统的双重抑制所减弱

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Chronic immunosuppressive therapy is often complicated by the development of both arterial hypertension and renal dysfunction. The principal aim of this study was to assess the effects of dual inhibition of renin-angiotensin system (RAS) and other antihypertensive treatment on blood pressure and renal function in normotensive and hypertensive Fawn-Hooded (FH) strains during chronic calcineurin inhibitor (CNI) administration. Combinations of perindopril (5mgkg~-1 per day) and losartan (50mgkg~-1 per day) or amlodipine (6mgkg~~-1per day) and metoprolol (80mgkg~-1 per day) were administered to normotensive (FHL) and hypertensive (FHH) rats, fed with diet containing tacrolimus (Tac; 12mgkg~-1 per day). Tac-induced arterial hypertension in both animal strains (FHL 151 +-4; FHH: 198 +-6 mm Hg) was prevented by dual RAS inhibition (FHL: 132 +- 3 mm Hg, P<0.05; FHH: 153 +- 3 mm Hg, P<0.05) as well as by a combination of amlodipine and metoprolol (FHL: 136 +-3 mm Hg, P<0.05; FHH: 166 +-4 mm Hg, P<0.05). However, significant nephroprotection was observed only in animals on dual RAS inhibition where albuminuria was reduced in both FHL (51.1 +-3.9 vs. 68.3+-4.5fig per day; P<0.05) and FHH rats (13.1 +-0.3 vs. 18.8+-0.7mg per day; P<0.05). We also found Tac-induced enhancement in renal angiotensin II activity that was significantly reduced by dual RAS inhibition in both FHL (63.5+-3.2 vs. 23.1 +-3.0fmolg1) and FHH (79.8+-8.5 vs. 32.2 +- 5.8fmolg~-1). In addition, histological analysis revealed that RAS inhibition noticeably diminished glomerulosclerosis and tubulo-interstitial injury. This study indicates that dual blockade of RAS significantly attenuates Tac-induced arterial hypertension and nephrotoxicity in FH rats and further supports the notion that RAS inhibitors display efficient renoprotective properties during CNI treatment.
机译:慢性免疫抑制疗法通常由于动脉高血压和肾功能障碍的发展而变得复杂。这项研究的主要目的是评估在长期钙调神经磷酸酶抑制剂(CNI)期间,双重抑制肾素-血管紧张素系统(RAS)和其他降压治疗对血压和肾功能正常和淡黄褐色(FH)菌株的影响行政。给予降血压(FHL)和高血压的培哚普利(每天5mgkg〜-1)和氯沙坦(每天50mgkg〜-1)或氨氯地平(每天6mgkg〜-1)和美托洛尔(每天80mgkg〜-1)的组合(FHH)大鼠,饲喂含有他克莫司(Tac;每天12mgkg〜-1)的饮食。通过双重RAS抑制(FHL:132 +-3 mm Hg,P <0.05; FHH:153 +-)来预防两种动物品系中Tac诱导的动脉高血压(FHL 151 + -4; FHH:198 + -6 mm Hg) 3 mm Hg,P <0.05)以及氨氯地平和美托洛尔的组合(FHL:136 + -3 mm Hg,P <0.05; FHH:166 + -4 mm Hg,P <0.05)。但是,只有在双重RAS抑制作用下的动物中才观察到明显的肾保护作用,FHL(每天51.1 + -3.9 vs. 68.3 + -4.5fig; P <0.05)和FHH大鼠(13.1 + -0.3 vs. 18.8)均降低了蛋白尿每天+ -0.7mg; P <0.05)。我们还发现,Fac(63.5 + -3.2 vs. 23.1 + -3.0fmolg1)和FHH(79.8 + -8.5 vs. 32.2 +-5.8fmolg)的双重RAS抑制作用显着降低了Tac诱导的肾血管紧张素II活性增强。 〜-1)。此外,组织学分析表明,RAS抑制作用明显降低了肾小球硬化和肾小管间质损伤。这项研究表明,双重阻断RAS可以显着减轻TH诱导的FH大鼠动脉高压和肾毒性,并进一步支持RAS抑制剂在CNI治疗期间显示出有效的肾脏保护特性。

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