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首页> 外文期刊>Iranian Journal of Basic Medical Sciences >Protective effects of celecoxib on ischemia reperfusion–induced acute kidney injury: comparing between male and female rats
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Protective effects of celecoxib on ischemia reperfusion–induced acute kidney injury: comparing between male and female rats

机译:Celecoxib对缺血再灌注诱导的急性肾损伤的保护作用:雄性和女性大鼠的比较

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Objective(s): There is increasing evidence for the importance of gender in different diseases; however, the role of gender in response to treatments is still unknown. Therefore, this study investigated the impact of gender on the protective effects of celecoxib in ischemia reperfusion (IR)-induced acute kidney injury. Materials and Methods: In this experimental study, rats were randomly divided into 6 groups (n=6): IR, sham and celecoxib groups of males and females. In IR groups, after orally receiving saline for 5 days, renal pedicles were clamped for 55 min and then kidneys were reperfused for 24 hr. In the sham groups, clamping of renal pedicles was not performed. In the celecoxib groups, 30 mg/kg celecoxib was given orally for 5 days before induction of ischemia. Plasma was collected to determine creatinine (Cr) and blood urea nitrogen (BUN). Kidney tissue samples were also stored for examining the histopathology and measuring malondialdehyde (MDA) levels and superoxide dismutase (SOD) activities. Results: IR caused significant increases in plasma Cr ( P 0.05), BUN ( P 0.05) and renal histopathological damages in both genders. Also, induction of IR resulted in significant increase of MDA levels ( P 0.05) and decrease of SOD activities ( P 0.05) in the kidney in both genders. Celecoxib administration prevented the IR-induced functional, histopathological and oxidative changes in both genders by similar degrees. Conclusion: This study suggested that in similar pathological conditions, celecoxib improves renal function and histopathological damages and attenuates oxidative stress in both genders by the same degrees. These protective effects of celecoxib on IR-induced kidney injury are gender-independent.
机译:目标:在不同疾病中,性别的重要性越来越多;然而,性别对治疗的反应的作用仍然未知。因此,本研究调查了性别对塞克西布在缺血再灌注(IR)的保护作用的影响 - 诱导急性肾损伤。材料和方法:在该实验研究中,大鼠随机分为6组(n = 6):IR,Sham和Celecoxib的男性和女性。在IR组中,在口服接受盐水5天后,将肾椎弓夹夹持55分钟,然后再灌注肾脏24小时。在假群中,未进行肾椎弓根的夹紧。在Celecoxib组中,在诱导缺血前口服5天给出30mg / kg Celecoxib。收集血浆以确定肌酐(Cr)和血尿尿素氮(BUN)。还储存肾组织样品以检查组织病理学和测量丙二醛(MDA)水平和超氧化物歧化酶(SOD)活性。结果:IR引起两种性别血浆Cr(P <0.05),面包(P <0.05)和肾组织病理学损害的显着增加。此外,IR的诱导导致MDA水平的显着增加(P <0.05)和两种性别肾脏中的SOD活性(P <0.05)降低。 Celecoxib管理通过类似的程度预防了两种性别的IR诱导的功能,组织病理学和氧化变化。结论:本研究表明,在类似的病理条件下,Celecoxib改善了肾功能和组织病理学损伤,并通过相同程度抑制了两种性别的氧化应激。 Celecoxib对IR诱发的肾损伤的这些保护作用是性别无关的。

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