An investigation of the anti-inflammatory effects of gabapentin on acetic acid-induced colitis in rats

被引:10
作者
Motavallian, Azadeh [1 ,2 ]
Bouzari, Saba [3 ]
Zamani, Ehsan [1 ]
Karimian, Paridokht [4 ]
Dabirian, Sara [5 ]
Molavi, Mehdi [6 ]
Torshkooh, Forough Aghajani [1 ]
机构
[1] Guilan Univ Med Sci, Sch Pharm, Dept Pharmacol & Toxicol, Rasht, Iran
[2] Guilan Univ Med Sci, Amiralmomenin Hosp, Rhinosinus Ear & Skull Base Dis Res Ctr, Dept Otolaryngol & Head & Neck Surg,Sch Med, Rasht, Iran
[3] Guilan Univ Med Sci, Sch Pharm, Student Res Comm, Rasht, Iran
[4] Guilan Univ Med Sci, Sch Med, Dept Pathol & Histol, Rasht, Iran
[5] Guilan Univ Med Sci, Sch Pharm, Dept Pharmaceut Biotechnol, Rasht, Iran
[6] Sabzevar Univ Med Sci, Sch Med, Dept Internal Med, Sabzevar, Iran
关键词
Experimental colitis; Gabapentin; Pro-inflammatory cytokines; Rat; INFLAMMATORY-BOWEL-DISEASE; GAMMA-AMINOBUTYRIC-ACID; TNBS-INDUCED COLITIS; RECEPTORS; ACTIVATION; EXPRESSION;
D O I
10.1007/s11033-021-06357-2
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
Inflammatory bowel disease (IBD) is considered a chronic inflammatory gastrointestinal disease with treatment options which exhibit low efficacies and lead to considerable side effects. Hence, the challenge to alleviate IBD complications is remained to be resolved. The purpose of this study is evaluating anti-inflammatory impacts of gabapentin on acetic acid-induced colitis in rats. Colitis was induced by the instillation of 2 mL of 3% acetic acid solution into rat's colons. Rats were randomly allocated into six groups including normal group, colitis control group, gabapentin-treated groups (25, 50, and 100 mg/kg; i.p.), and dexamethasone-treated group (1 mg/kg; i.p.). Based on the macroscopic assessment besides histological and biochemical findings [myeloperoxidase (MPO), pro-inflammatory cytokines], the efficacy of gabapentin was investigated. Gabapentin (50 and 100 mg/kg), and dexamethasone considerably reduced macroscopic and microscopic colonic lesions induced by acetic acid in rats in comparison with colitis control group. These results were confirmed by reduced levels of MPO activity and colonic concentrations of interleukin-6, interleukin-1 beta, and tumor necrosis factor-alpha, in inflamed colon tissue. Our data demonstrated that gabapentin exerts profitable impacts in experimental colitis that might be ascribed to its anti-inflammatory features and thus can be a potential therapeutic agent for IBD treatment.
引用
收藏
页码:3423 / 3430
页数:8
相关论文
共 44 条
[1]  
Abdel-Salam OME, 2009, DRUG DISCOV THER, V3, P18
[2]  
Abramoff D. M. D., 2004, Biophotonics Int, P36
[3]   Attenuated GABAergic Signaling in Intestinal Epithelium Contributes to Pathogenesis of Ulcerative Colitis [J].
Aggarwal, Surbhi ;
Ahuja, Vineet ;
Paul, Jaishree .
DIGESTIVE DISEASES AND SCIENCES, 2017, 62 (10) :2768-2779
[4]  
[Anonymous], 2013, NIH PUBLIC ACCESS, DOI DOI 10.1111/J.1747-0285.2012.01428.X.IDENTIFICATION
[5]   Gabapentin for the symptomatic treatment of painful neuropathy in patients with diabetes mellitus - A randomized controlled trial [J].
Backonja, M ;
Beydoun, A ;
Edwards, KR ;
Schwartz, SL ;
Fonseca, V ;
Hes, M ;
LaMoreaux, L ;
Garofalo, E .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1998, 280 (21) :1831-1836
[6]   Effect of gabapentin on fetal rat brain and its amelioration by ginger [J].
Badawy, Gamal M. ;
Atallah, Marwa N. ;
Sakr, Saber A. .
HELIYON, 2019, 5 (09)
[7]   GABAergic signalling in the immune system [J].
Barragan, A. ;
Weidner, J. M. ;
Jin, Z. ;
Korpi, E. R. ;
Birnir, B. .
ACTA PHYSIOLOGICA, 2015, 213 (04) :819-827
[8]   Gastroenterology 2 - Inflammatory bowel disease: clinical aspects and established and evolving therapies [J].
Baumgart, Daniel C. ;
Sandborn, William J. .
LANCET, 2007, 369 (9573) :1641-1657
[9]   MEASUREMENT OF CUTANEOUS INFLAMMATION - ESTIMATION OF NEUTROPHIL CONTENT WITH AN ENZYME MARKER [J].
BRADLEY, PP ;
PRIEBAT, DA ;
CHRISTENSEN, RD ;
ROTHSTEIN, G .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1982, 78 (03) :206-209
[10]   Advances in the pathogenesis and treatment of IBD [J].
Braus, Nicholas A. ;
Elliott, David E. .
CLINICAL IMMUNOLOGY, 2009, 132 (01) :1-9