Zahran Mohamed H, Barakat Nashwa, Khater Shery, Awadalla Amira, Mosbah Ahmed, Nabeeh Adel, Hussein Abdelaziz M, Shokeir Ahmed A
Urology and Nephrology Center, Mansoura University, Mansoura, Egypt.
Medical Physiology Department, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Arab J Urol. 2019 Apr 18;17(2):150-159. doi: 10.1080/2090598X.2019.1600995. eCollection 2019.
: To design a new canine model to assess the renoprotective effect of local sildenafil administration, as the renoprotective effect of systemic sildenafil administration in renal ischaemia-reperfusion (IR) injury in animal models has been shown but its local effects have not been established to date. : In all, 120 dogs were assigned to five groups: sham, oral control (OC) group (right nephrectomy + left renal ischaemia for 60 min), oral sildenafil (OS) group (oral sildenafil 1 mg/kg, 60 min before ischaemia), local control (LC) group (local renal perfusion with saline and heparin for 5 min) and local sildenafil (LS) group (perfusion with sildenafil 0.5 mg/kg). Renal functions, histopathological changes, expression of caspase-3, nuclear factor erythroid 2-related factor 2 (Nrf2), inflammatory cytokines (intracellular adhesion molecule 1, tumour necrosis factor α and interleukin 1β) and endothelial nitric oxide synthase (eNOS) in renal tissues were assessed in all groups at 1, 3, 7 and 14 days. : There were significant improvements in renal functions and cortical and medullary damage scores in the sildenafil-treated groups compared to their control groups ( < 0.05). Also, the LS group showed significantly better improvement of renal functions and cortical and medullary damage scores than the OS group ( < 0.05). Moreover, sildenafil significantly decreased the expression of caspase-3 and inflammatory cytokines and increased the expression of Nrf2 and eNOS in renal tissue, which were statistically significant in the LS group. : LS has a greater renoprotective effect against renal IR injury than systemic administration via anti-inflammatory, antioxidant and anti-apoptotic pathways. : BUN: blood urea nitrogen; Ct: cycle threshold; eNOS: endothelial nitric oxide synthase; GAPDH: glyceraldehyde 3-phosphate dehydrogenase; H&E: haematoxylin and eosin; IL-1β: interleukin 1β; NO: nitric oxide; Nrf2: nuclear factor erythroid 2-related factor 2; OC: oral control; OS: oral sildenafil; LC: local control; LS: local sildenafil.
为设计一种新的犬类模型以评估局部给予西地那非的肾脏保护作用,因为在动物模型中已显示全身给予西地那非对肾缺血再灌注(IR)损伤具有肾脏保护作用,但其局部作用迄今尚未明确。总共120只犬被分为五组:假手术组、口服对照组(OC组,右肾切除+左肾缺血60分钟)、口服西地那非组(OS组,缺血前60分钟口服西地那非1mg/kg)、局部对照组(LC组,用生理盐水和肝素进行局部肾脏灌注5分钟)和局部西地那非组(LS组,用0.5mg/kg西地那非灌注)。在第1、3、7和14天对所有组的肾功能、组织病理学变化、肾组织中半胱天冬酶-3、核因子红细胞2相关因子2(Nrf2)、炎性细胞因子(细胞间黏附分子1、肿瘤坏死因子α和白细胞介素1β)以及内皮型一氧化氮合酶(eNOS)的表达进行评估。与各自对照组相比,西地那非治疗组的肾功能以及皮质和髓质损伤评分有显著改善(P<0.05)。此外,LS组在肾功能以及皮质和髓质损伤评分方面的改善明显优于OS组(P<0.05)。而且,西地那非显著降低了肾组织中半胱天冬酶-3和炎性细胞因子的表达,并增加了Nrf2和eNOS的表达,这在LS组中具有统计学意义。与全身给药相比,LS通过抗炎、抗氧化和抗凋亡途径对肾IR损伤具有更大的肾脏保护作用。BUN:血尿素氮;Ct:循环阈值;eNOS:内皮型一氧化氮合酶;GAPDH:甘油醛-3-磷酸脱氢酶;H&E:苏木精和伊红;IL-1β:白细胞介素1β;NO:一氧化氮;Nrf2:核因子红细胞2相关因子2;OC:口服对照;OS:口服西地那非;LC:局部对照;LS:局部西地那非。