» Articles » PMID: 30903350

Thymol Reduces Acetic Acid-induced Inflammatory Response Through Inhibition of NF-kB Signaling Pathway in Rat Colon Tissue

Overview
Specialty Pharmacology
Date 2019 Mar 24
PMID 30903350
Citations 26
Authors
Affiliations
Soon will be listed here.
Abstract

Aim: The aim of the present study was to evaluate the anti-inflammatory effect of thymol in acetic acid-induced rat colitis through inhibiting the NF-κB signaling pathway.

Methods: Colitis was induced by intra-rectal administration of 2 mL of diluted acetic acid (4%) solution using a flexible plastic rubber catheter in Wistar rats. Colitis was induced on the first day and all treatments were applied 5 days after the induction of colitis. Thymol was dissolved in 0.2% tween 80 in saline and administered orally at doses of 10, 30, and 100 mg/kg per day. Macroscopic and histopathologic investigations were done. The expression of myeloperoxidase (MPO) and tumor necrosis factor-α (TNF-α) was determined by immunohistochemistry (IHC) assay. The protein expression level of pNF-κB p65 was measured by the Western blot technique.

Results: Treatment with thymol reduced mucosal and histological damages compared to the acetic acid group. Our results showed that thymol markedly inhibited the production of MPO and TNF-α in the colon tissue of the acetic acid-induced group. In addition, thymol decreased acetic acid-induced up-regulation of pNFκB p65 protein.

Conclusions: The results of our study suggest that thymol exerts an anti-inflammatory effect in acetic acid-induced rat colitis by inhibiting the NF-κB signaling pathway and downregulating TNF-α and MPO expressions.

Citing Articles

Ability of short-chain fatty acids to reduce inflammation and attract leucocytes to the inflamed skin of gilthead seabream (Sparus aurata L.).

Albaladejo-Riad N, El Qendouci M, Cuesta A, Esteban M Sci Rep. 2024; 14(1):31404.

PMID: 39732927 PMC: 11682419. DOI: 10.1038/s41598-024-83033-y.


Antioxidant Therapy in Inflammatory Bowel Diseases: How Far Have We Come and How Close Are We?.

Xavier L, Reis T, da Paz Martins A, Santos J, Bueno N, Goulart M Antioxidants (Basel). 2024; 13(11).

PMID: 39594511 PMC: 11590966. DOI: 10.3390/antiox13111369.


Harnessing nature's pharmacy: investigating natural compounds as novel therapeutics for ulcerative colitis.

Huang Y, Wu Q, Li S, Lin X, Yang S, Zhu R Front Pharmacol. 2024; 15:1394124.

PMID: 39206263 PMC: 11349575. DOI: 10.3389/fphar.2024.1394124.


Thymol Protects against 5-Fluorouracil-Induced Hepatotoxicity via the Regulation of the Akt/GSK-3β Pathway in In Vivo and In Silico Experimental Models.

Mahran Y, Badr A, Al-Kharashi L, Alajami H, Aldamry N, Bayoumy N Pharmaceuticals (Basel). 2024; 17(8).

PMID: 39204199 PMC: 11357534. DOI: 10.3390/ph17081094.


Natural approaches for the management of ulcerative colitis: evidence of preclinical and clinical investigations.

Subudhi R, Poonia N, Singh D, Arora V Nat Prod Bioprospect. 2024; 14(1):42.

PMID: 39078427 PMC: 11289194. DOI: 10.1007/s13659-024-00463-x.


References
1.
Liang D, Li F, Fu Y, Cao Y, Song X, Wang T . Thymol inhibits LPS-stimulated inflammatory response via down-regulation of NF-κB and MAPK signaling pathways in mouse mammary epithelial cells. Inflammation. 2013; 37(1):214-22. DOI: 10.1007/s10753-013-9732-x. View

2.
Deng X, Li H, Chen J, Li R, Qu R, Fu Q . Thymol produces an antidepressant-like effect in a chronic unpredictable mild stress model of depression in mice. Behav Brain Res. 2015; 291:12-19. DOI: 10.1016/j.bbr.2015.04.052. View

3.
Klebanoff S . Myeloperoxidase: friend and foe. J Leukoc Biol. 2005; 77(5):598-625. DOI: 10.1189/jlb.1204697. View

4.
Arijs I, Li K, Toedter G, Quintens R, Van Lommel L, Van Steen K . Mucosal gene signatures to predict response to infliximab in patients with ulcerative colitis. Gut. 2009; 58(12):1612-9. DOI: 10.1136/gut.2009.178665. View

5.
Lv J, Zhang Y, Tian Z, Liu F, Shi Y, Liu Y . Astragalus polysaccharides protect against dextran sulfate sodium-induced colitis by inhibiting NF-κВ activation. Int J Biol Macromol. 2017; 98:723-729. DOI: 10.1016/j.ijbiomac.2017.02.024. View