磺胺吡啶
肾
体内
血尿素氮
急性肾损伤
败血症
医学
肌酐
药理学
炎症
结扎
转铁蛋白
坏死
免疫学
肿瘤坏死因子α
胃肠病学
口服
腹膜炎
体外
毒性
动物模型
精氨酸
头孢菌素
脾脏
巨噬细胞
泌尿系统
内科学
热疗
作者
Zeynep Çiçek,Murat Çakır,Ali Aydın,Burak Bircan,Semanur Fırat,Suat Tekin
摘要
Sepsis is a medical condition that occurs when a harmful inflammatory response damages tissues and organs. The kidneys are among the organs most frequently affected by sepsis. Anti-inflammatory strategies are crucial in treating sepsis. The anti-inflammatory properties of sulphasalazine (SFZ) have been demonstrated in various in vitro and in vivo studies. This study investigates the effect of SFZ on kidney damage in a rat model of sepsis induced by the cecal ligation and puncture (CLP) method. Animals were divided into control, CLP, CLP + SFZ50, and CLP + SFZ250. Two doses of SFZ (50 and 250 mg/kg) were applied in two different treatment groups after CLP. The administration of SFZ reduced the CLP-induced increase in serum blood urea nitrogen (BUN), tumor necrosis factor-alpha (TNF-α), interleukin-1 beta (IL-1β), neutrophil gelatinase-associated lipocalin (NGAL), interleukin-18 (IL-18), kidney injury molecule-1 (KIM-1), and creatinine (Cre) levels for both doses (p < 0.05). Additionally, SFZ treatment significantly decreased histopathological damage, phosphorylated NF-κB, toll-like receptor-4 (TLR-4), IL-1β, phosphorylated IκB-α, interleukin-6 (IL-6), TNF-α, caspase-3, and caspase-8 levels (p < 0.05). In this study, we found that two different doses of SFZ (50 and 250 mg/kg) showed protective effects by decreasing inflammation and kidney damage in a CLP-induced experimental sepsis model.
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