Nifuroxazide, a STAT3 inhibitor, mitigates inflammatory burden and protects against diabetes-induced nephropathy in rats

被引:67
作者
Said, Eman [1 ]
Zaitone, Sawsan A. [2 ,3 ]
Eldosoky, Mohamed [4 ]
Elsherbiny, Nehal M. [5 ,6 ]
机构
[1] Mansoura Univ, Dept Pharmacol & Toxicol, Fac Pharm, Mansoura, Egypt
[2] Suez Canal Univ, Dept Pharmacol Toxicol, Fac Pharm, Ismailia, Egypt
[3] Univ Tabuk, Dept Pharmacol Toxicol, Fac Pharm, Tabuk, Saudi Arabia
[4] Mansoura Univ, Dept Med Physiol, Fac Med, Mansoura, Egypt
[5] Mansoura Univ, Dept Biochem, Fac Pharm, Mansoura, Egypt
[6] Univ Tabuk, Dept Pharmaceut Chem, Fac Pharm, Tabuk, Saudi Arabia
关键词
Nifuroxazide; STAT3; TNF-alpha; IL-18; Diabetes; JAK/STAT SIGNALING PATHWAY; OXIDATIVE STRESS; KAPPA-B; PREVENTS; TRANSDUCER; ACTIVATOR; DAMAGE; JANUS;
D O I
10.1016/j.cbi.2017.12.030
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Diabetic nephropathy (DN) is a serious complication of diabetes mellitus. Moreover, it is amongst the most common causes of end-stage renal failure. Inflammation is a crucial player in both development and progression of DN. JAK2/STA3 is a pleotropic cascade reported to regulate diverse inflammatory events. Previous studies reported involvement of JAK2/STA3 signal transduction pathway in diabetes-associated renal injury. In the current study, the inhibitory effect of nifuroxazide (25 mg/kg/day, orally) against inflammatory condition associating diabetic kidney progression in rats was evaluated. The underlying hypothesis is mainly via the inhibitory effect of nifuroxazide on STAT3 signaling. Results revealed that nifuroxazide effectively inhibited STAT3 activation in diabetic male rats, improved glomerular filtration function, protected against diabetes-induced histopathological and ultramicroscopic structural alterations. Further, nifuroxazide treatment significantly reduced renal macrophage infiltration and fibrosis and decreased mRNA and protein levels of TNF-alpha and IL-18 in diabetic renal tissue. The current findings shed the light on nifuroxazide's efficacy as an alternative anti-inflammatory therapy to hinder the development and progression of DN in diabetic patients mainly via STAT3 inhibition.
引用
收藏
页码:111 / 120
页数:10
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