Ismail Basma, deKemp Rob A, Croteau Etienne, Hadizad Tayebeh, Burns Kevin D, Beanlands Rob S, DaSilva Jean N
Cardiac PET Centre, Department of Medicine (Division of Cardiology), University of Ottawa Heart Institute, Ottawa, ON, Canada.
Department of Cellular and Molecular Medicine, University of Ottawa, Ottawa, ON, Canada.
PLoS One. 2017 May 19;12(5):e0177451. doi: 10.1371/journal.pone.0177451. eCollection 2017.
ACE inhibitors are considered first line of treatment in patients with many forms of chronic kidney disease (CKD). Other antihypertensives such as calcium channel blockers achieve similar therapeutic effectiveness in attenuating hypertension-related renal damage progression. Our objective was to explore the value of positron emission tomography (PET) imaging of renal AT1 receptor (AT1R) to guide therapy in the 5/6 subtotal-nephrectomy (Nx) rat model of CKD. Ten weeks after Nx, Sprague-Dawley rats were administered 10mg/kg/d enalapril (NxE), 30mg/kg/d diltiazem (NxD) or left untreated (Nx) for an additional 8-10 weeks. Kidney AT1R expression was assessed using in vivo [18F]fluoropyridine-losartan PET and in vitro autoradiography. Compared to shams, Nx rats exhibited higher systolic blood pressure that was reduced by both enalapril and diltiazem. At 18-20 weeks, plasma creatinine and albuminuria were significantly increased in Nx, reduced to sham levels in NxE, but enhanced in NxD rats. Enalapril treatment decreased kidney angiotensin II whereas diltiazem induced significant elevations in plasma and kidney levels. Reduced PET renal AT1R levels in Nx were normalized by enalapril but not diltiazem, and results were supported by autoradiography. Reduction of renal blood flow in Nx was restored by enalapril, while no difference was observed in myocardial blood flow amongst groups. Enhanced left ventricle mass in Nx was not reversed by enalapril but was augmented with diltiazem. Stroke volume was diminished in untreated Nx compared to shams and restored with both therapies. [18F]Fluoropyridine-Losartan PET allowed in vivo quantification of kidney AT1R changes associated with progression of CKD and with various pharmacotherapies.
血管紧张素转换酶(ACE)抑制剂被认为是多种形式慢性肾脏病(CKD)患者的一线治疗药物。其他抗高血压药物,如钙通道阻滞剂,在减轻高血压相关的肾损害进展方面具有相似的治疗效果。我们的目的是探讨在CKD的5/6肾大部切除术(Nx)大鼠模型中,肾脏血管紧张素Ⅱ1型受体(AT1R)的正电子发射断层扫描(PET)成像对指导治疗的价值。Nx术后10周,将斯普拉格-道利大鼠再给予10mg/kg/d依那普利(NxE组)、30mg/kg/d地尔硫䓬(NxD组)或不进行治疗(Nx组),持续8 - 10周。使用体内[18F]氟吡啶-氯沙坦PET和体外放射自显影评估肾脏AT1R表达。与假手术组相比,Nx大鼠收缩压更高,依那普利和地尔硫䓬均可降低收缩压。在18 - 20周时,Nx组血浆肌酐和蛋白尿显著增加,NxE组降至假手术组水平,但NxD组升高。依那普利治疗可降低肾脏血管紧张素Ⅱ水平,而地尔硫䓬可导致血浆和肾脏水平显著升高。Nx组PET显示肾脏AT1R水平降低,依那普利可使其恢复正常,而地尔硫䓬则不能,放射自显影结果支持这一结论。依那普利可恢复Nx组减少的肾血流量,而各组心肌血流量无差异。Nx组左心室质量增加,依那普利不能使其恢复,但地尔硫䓬可使其进一步增加。与假手术组相比,未治疗的Nx组每搏输出量减少,两种治疗均可使其恢复。[18F]氟吡啶-氯沙坦PET可在体内定量评估与CKD进展及各种药物治疗相关的肾脏AT1R变化。