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特拉唑嗪可保护大鼠的肝脏免受肾缺血/再灌注损伤。

Prazosin Protects the Liver Against Renal Ischemia/Reperfusion Injury in Rats.

机构信息

Faculty of Veterinary Medicine, Tabriz Branch, Islamic Azad University, Tabriz, Iran.

Kidney Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.

出版信息

Drug Res (Stuttg). 2023 Jun;73(5):289-295. doi: 10.1055/a-2015-7976. Epub 2023 Mar 20.

Abstract

Acute kidney injury (AKI) is a common subsequent problem after many medical conditions. AKI is associated with distant organ dysfunction where systemic inflammation and oxidative stress play major roles. In this study, the effect of Prazosin, an α1-Adrenergic receptor antagonist, was investigated on the liver injury induced by kidney ischemia-reperfusion (I/R) in rats. Male adult Wistar rats (n=21) were divided into three groups: sham, kidney I/R, and kidney I/R pre-treated with Prazosin (1 mg/kg). Kidney I/R was induced by vascular clamping of the left kidney for 45 min to reduce the blood flow. Oxidative and antioxidant factors along with apoptotic (Bax, Bcl-2, caspase3), and inflammatory (NF-κβ, IL-1β, and IL-6) factors were measured in the liver at protein levels. Prazosin could reserve liver function (p<0.01) and increase glutathione level (p<0.05) after kidney I/R significantly. Malonil dialdehyde (MDA), a lipid peroxidation marker, was diminished more significantly in Prazosin-treated rats compared to the kidney I/R group (p<0.001). Inflammatory and apoptotic factors were diminished by Prazosin pre-treatment in the liver tissue (p<0.05). Pre-administration of Prazosin could preserve liver function and decrease its inflammatory and apoptotic factors under kidney I/R conditions.

摘要

急性肾损伤(AKI)是许多医学病症后的常见后续问题。AKI 与远处器官功能障碍相关,其中系统性炎症和氧化应激起着主要作用。在这项研究中,研究了 α1-肾上腺素能受体拮抗剂普萘洛尔对肾缺血再灌注(I/R)诱导的大鼠肝损伤的影响。雄性成年 Wistar 大鼠(n=21)分为三组:假手术组、肾 I/R 组和肾 I/R 预先用普萘洛尔(1mg/kg)处理组。通过夹闭左肾 45 分钟来减少血流以诱导肾 I/R。在蛋白质水平上测量肝中氧化和抗氧化因子以及凋亡(Bax、Bcl-2、caspase3)和炎症(NF-κβ、IL-1β 和 IL-6)因子。普萘洛尔能显著保留肾 I/R 后大鼠的肝功能(p<0.01)并增加谷胱甘肽水平(p<0.05)。与肾 I/R 组相比,普萘洛尔治疗组丙二醛(MDA),一种脂质过氧化标志物,明显减少(p<0.001)。肝组织中炎症和凋亡因子通过普萘洛尔预处理减少(p<0.05)。普萘洛尔预先给药可在肾 I/R 条件下保护肝功能并降低其炎症和凋亡因子。

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