El-Sisi Alaa E, Sokar Samia S, Abu-Risha Sally E, Ibrahim Hanaa A
Department of Pharmacology and Toxicology, Faculty of Pharmacy, Tanta University, Tanta, Egypt.
Department of Pharmacology and Toxicology, Faculty of Pharmacy, Tanta University, Tanta, Egypt.
Biomed Pharmacother. 2016 Dec;84:861-869. doi: 10.1016/j.biopha.2016.10.009. Epub 2016 Oct 11.
Life threatening conditions characterized by renal ischemia/reperfusion (RIR) such as kidney transplantation, partial nephrectomy, renal artery angioplasty, cardiopulmonary bypass and aortic bypass surgery, continue to be among the most frequent causes of acute renal failure. The current study investigated the possible protective effects of tadalafil alone and in combination with diltiazem in experimentally-induced renal ischemia/reperfusion injury in rats. Possible underlying mechanisms were also investigated such as oxidative stress and inflammation. Rats were divided into sham-operated and I/R-operated groups. Anesthetized rats (urethane 1.3g/kg) were subjected to bilateral ischemia for 30min by occlusion of renal pedicles, then reperfused for 6h. Rats in the vehicle I/R group showed a significant (p˂0.05) increase in kidney malondialdehyde (MDA) content; myeloperoxidase (MPO) activity; TNF-α and IL-1β contents. In addition significant (p˂0.05) increase in intercellular adhesion molecule-1(ICAM-1) content, BUN and creatinine levels, along with significant decrease in kidney superoxide dismutase (SOD) activity. In addition, marked diffuse histopathological damage and severe cytoplasmic staining of caspase-3 were detected. Pretreatment with combination of tadalafil (5mg/kg bdwt) and diltiazem (5mg/kg bdwt) resulted in reversal of the increased biochemical parameters investigated. Also, histopathological examination revealed partial return to normal cellular architecture. In conclusion, pretreatment with tadalafil and diltiazem combination protected against RIR injury.
以肾缺血/再灌注(RIR)为特征的危及生命的病症,如肾移植、部分肾切除术、肾动脉血管成形术、体外循环和主动脉搭桥手术,仍然是急性肾衰竭最常见的原因之一。本研究调查了他达拉非单独使用以及与地尔硫卓联合使用对实验性诱导的大鼠肾缺血/再灌注损伤可能的保护作用。还研究了可能的潜在机制,如氧化应激和炎症。将大鼠分为假手术组和缺血/再灌注手术组。麻醉的大鼠(乌拉坦1.3g/kg)通过阻断肾蒂进行双侧缺血30分钟,然后再灌注6小时。载体缺血/再灌注组大鼠的肾丙二醛(MDA)含量、髓过氧化物酶(MPO)活性、肿瘤坏死因子-α(TNF-α)和白细胞介素-1β(IL-1β)含量显著(p˂0.05)增加。此外,细胞间粘附分子-1(ICAM-1)含量、血尿素氮(BUN)和肌酐水平显著(p˂0.05)增加,同时肾超氧化物歧化酶(SOD)活性显著降低。此外,检测到明显的弥漫性组织病理学损伤和半胱天冬酶-3的严重细胞质染色。用他达拉非(5mg/kg体重,每日两次)和地尔硫卓(5mg/kg体重)联合预处理导致所研究的升高的生化参数逆转。此外,组织病理学检查显示细胞结构部分恢复正常。总之,他达拉非和地尔硫卓联合预处理可预防肾缺血/再灌注损伤。