Arbutin ameliorated ulcerative colitis of mice induced by dextran sodium sulfate (DSS)

References

• Taha MM, Salga MS, Ali HM, et al. Abdelwahab SI and Hadi AH. Gastroprotective activities of Turnera diffusa Willd. ex Schult. revisited: role of arbutin. J Ethnopharmacol. 2012;141:273–281.
   PubMed Web of Science ®Google Scholar
• Ma F, Js T. Inflammatory Bowel Disease and Short Bowel Syndrome. Surg Clin North Am. 2019;99:1209–1221.
   PubMed Web of Science ®Google Scholar
• Fuller MK. Pediatric Inflammatory Bowel Disease: special Considerations. Surg Clin North Am. 2019;99:1177–1183.
   PubMed Web of Science ®Google Scholar
• Narula N, Peerani F, Meserve J, et al. Vedolizumab for Ulcerative Colitis: treatment Outcomes from the VICTORY Consortium. Am J Gastroenterol. 2018;113:1345.
   PubMed Web of Science ®Google Scholar
• Sandborn WJ, Peyrin-Biroulet L, Quirk D, et al. Efficacy and Safety of Extended Induction With Tofacitinib for the Treatment of Ulcerative Colitis. Clin Gastroenterol Hepatol. 2020;S1542-3565(20)31496-8.
   Web of Science ®Google Scholar
• Seyedian SS, Nokhostin F, Malami R. A review of the diagnosis, prevention, and treatment methods of inflammatory bowel disease. J Med Life. 2019;12:113–122.
   PubMedGoogle Scholar
• Neurath MF. Cytokines in inflammatory bowel disease. Nat Rev Immunol. 2014;14:329–342.
   PubMed Web of Science ®Google Scholar
• Sharma A, Tirpude NV, Kulurkar PM, et al. Berberis lycium fruit extract attenuates oxi-inflammatory stress and promotes mucosal healing by mitigating NF-κB/c-Jun/MAPKs signalling and augmenting splenic Treg proliferation in a murine model of dextran sulphate sodium-induced ulcerative colitis. Eur J Nutr. 2020;59:2663–2681.
   PubMed Web of Science ®Google Scholar
• Gao W, Wang C, Yu L, et al. Chlorogenic Acid Attenuates Dextran Sodium Sulfate-Induced Ulcerative Colitis in Mice through MAPK/ERK/JNK Pathway. Biomed Res Int. 2019;2019:6769789.
   PubMed Web of Science ®Google Scholar
• Shi L, Lin Q, Yang T, et al. Oral administration of Lentinus edodes β-glucans ameliorates DSS-induced ulcerative colitis in mice via MAPK-Elk-1 and MAPK-PPARγ pathways. Food Funct. 2016;7:4614–4627.
   PubMed Web of Science ®Google Scholar
• Zhou W, Chen K, Lu Q, et al. The Protective Effect of Rosavin from Rhodiola rosea on Radiation-Induced Intestinal Injury. Chem Biodivers. 2020;17:e2000652.
   PubMed Web of Science ®Google Scholar
• Wu LH, Li P, Zhao QL, et al. Arbutin, an intracellular hydroxyl radical scavenger, protects radiation-induced apoptosis in human lymphoma U937 cells. Apoptosis. 2014;19:1654–1663.
   PubMed Web of Science ®Google Scholar
• Kihara N, de La Fuente SG, Fujino K, et al. Vanilloid receptor-1 containing primary sensory neurones mediate dextran sulphate sodium induced colitis in rats. Gut. 2003;52:713–719.
   PubMed Web of Science ®Google Scholar
• Wang Q, Ch F, Hasselgren PO. Intestinal permeability is reduced and IL-10 levels are increased in septic IL-6 knockout mice. Am J Physiol Regul Integr Comp Physiol. 2001;281:R1013–1023.
   PubMed Web of Science ®Google Scholar
• Billmeier U, Dieterich W, Mf N, et al. Molecular mechanism of action of anti-tumor necrosis factor antibodies in inflammatory bowel diseases. World J Gastroenterol. 2016;22:9300–9313.
   PubMed Web of Science ®Google Scholar
• Ma TY, Iwamoto GK, Hoa NT, et al. TNF-alpha-induced increase in intestinal epithelial tight junction permeability requires NF-kappa B activation. Am J Physiol Gastrointest Liver Physiol. 2004;286:G367–376.
   PubMed Web of Science ®Google Scholar
• Kim JJ, Shajib MS, Manocha MM, et al. Investigating intestinal inflammation in DSS-induced model of IBD. J Vis Exp. 2012;(60):3678. Published 2012 Feb 1.
   Web of Science ®Google Scholar
• Turner JR. Molecular basis of epithelial barrier regulation: from basic mechanisms to clinical application. Am J Pathol. 2006;169:1901–1909.
   PubMed Web of Science ®Google Scholar
• Groschwitz KR, Hogan SP. Intestinal barrier function: molecular regulation and disease pathogenesis. J Allergy Clin Immunol. 2009;124(3–20):21–22. quiz.
   Google Scholar
• Capaldo CT, Nusrat A. Cytokine regulation of tight junctions. Biochim Biophys Acta. 2009;1788:864–871.
   PubMed Web of Science ®Google Scholar
• Clayburgh DR, Barrett TA, Tang Y, et al. Epithelial myosin light chain kinase-dependent barrier dysfunction mediates T cell activation-induced diarrhea in vivo. J Clin Invest. 2005;115:2702–2715.
   PubMed Web of Science ®Google Scholar
• Blair SA, Kane SV, Dr C, et al. Epithelial myosin light chain kinase expression and activity are upregulated in inflammatory bowel disease. Lab Invest. 2006;86:191–201.
   PubMed Web of Science ®Google Scholar
• Deramaudt TB, Ali M, Vinit S, et al. Sulforaphane reduces intracellular survival of Staphylococcus aureus in macrophages through inhibition of JNK and p38 MAPK‑induced inflammation. Int J Mol Med. 2020;45:1927–1941.
   PubMed Web of Science ®Google Scholar
• Kim EK, Choi EJ. Compromised MAPK signaling in human diseases: an update. Arch Toxicol. 2015;89:867–882.
   PubMed Web of Science ®Google Scholar
• Ren Q, Guo F, Tao S, et al. Flavonoid fisetin alleviates kidney inflammation and apoptosis via inhibiting Src-mediated NF-κB p65 and MAPK signaling pathways in septic AKI mice. Biomed Pharmacother. 2020;122:109772.
   PubMed Web of Science ®Google Scholar
• Singla DK, Ta J, Tavakoli DZ. Exosome Treatment Enhances Anti-Inflammatory M2 Macrophages and Reduces Inflammation-Induced Pyroptosis in Doxorubicin-Induced Cardiomyopathy. Cells. 2019;8(10):1224. Published 2019 Oct 9.
   Web of Science ®Google Scholar
• Huang FC. Upregulation of Salmonella-induced IL-6 production in Caco-2 cells by PJ-34, PARP-1 inhibitor: involvement of PI3K, p38 MAPK, ERK, JNK, and NF-kappaB. Mediators Inflamm. 2009;2009:103890.
   PubMed Web of Science ®Google Scholar
• Lian L, Zhang S, Yu Z, et al. The dietary freeze-dried fruit powder of Actinidia arguta ameliorates dextran sulphate sodium-induced ulcerative colitis in mice by inhibiting the activation of MAPKs. Food Funct. 2019;10:5768–5778.
   PubMed Web of Science ®Google Scholar
• Whitmarsh AJ, Yang SH, Su MS, et al. Role of p38 and JNK mitogen-activated protein kinases in the activation of ternary complex factors. Mol Cell Biol. 1997;17:2360–2371.
   PubMed Web of Science ®Google Scholar