dc.contributor.author | Arda-Pirincci, Pelin | |
dc.contributor.author | Aykol-Celik, Guliz | |
dc.date.accessioned | 2021-03-05T17:37:06Z | |
dc.date.available | 2021-03-05T17:37:06Z | |
dc.date.issued | 2020 | |
dc.identifier.citation | Arda-Pirincci P., Aykol-Celik G., "Galectin-1 reduces the severity of dextran sulfate sodium (DSS)-induced ulcerative colitis by suppressing inflammatory and oxidative stress response", BOSNIAN JOURNAL OF BASIC MEDICAL SCIENCES, cilt.20, ss.319-328, 2020 | |
dc.identifier.issn | 1512-8601 | |
dc.identifier.other | av_c66d3973-47dc-4fb1-9b65-66c25c55566a | |
dc.identifier.other | vv_1032021 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/131555 | |
dc.identifier.uri | https://doi.org/10.17305/bjbms.2019.4539 | |
dc.description.abstract | Ulcerative colitis is an inflammatory bowel disease that affects a large number of people around the world. Galectin-1 is a beta-galactoside-binding lectin with a broad range of biological activities. The effects of galectin-1 on dextran sulfate sodium (DSS)-induced ulcerative colitis in vivo is not clear. We investigated the effect of galectin-1 on colon morphology, cell proliferation, oxidative stress, antioxidant system, and proinflammatory/antiinflammatory cytokines in a DSS-induced mouse model of ulcerative colitis. Thirty-two C57BL/6 mice were randomly assigned to one of the four groups: control, acute colitis, galectin-1, and DSS+galectin-1. Controls were treated with phosphate-buttered saline (PBS) for seven days. Acute colitis was induced by 3% DSS in drinking water administered orally for five days. Mice in galectin-1 groups were treated with 1 mg/kg recombinant human galectin-1 in PBS for seven consecutive days. Oral DSS administration resulted in acute colitis by causing histopathological changes; an increase in disease activity index (DAI), lipid peroxidation (malondialdehyde MDA]), myeloperoxidase (MPO), and tumor necrosis factor (TNF)-alpha levels; a decrease in body weight, colon length, cell proliferation index, catalase, glutathione peroxidase (GSH-Px) and superoxide dismutase (SOD) activities, and GSH and interleukin (IL)-10 levels. The treatment with galectin-1 attenuated DSSinduced acute colitis by reducing DAI, MDA, MPO, and TNF-alpha levels and by increasing body weight, colon length, cell proliferation, antioxidant enzyme activity, GSH, and IL-10 levels. These findings suggest that galectin-1 has proliferative, antioxidant, antiinflammatory, and cytoprotective effects against DSS-induced ulcerative colitis in mice. Due to its antiinflammatory and antioxidant activity galectin-1 may be effective in preventing and treating ulcerative colitis. | |
dc.language.iso | eng | |
dc.subject | Tıbbi Ekoloji ve Hidroklimatoloji | |
dc.subject | Dahili Tıp Bilimleri | |
dc.subject | Sağlık Bilimleri | |
dc.subject | Tıp | |
dc.subject | Klinik Tıp (MED) | |
dc.subject | Klinik Tıp | |
dc.subject | TIP, ARAŞTIRMA VE DENEYSEL | |
dc.title | Galectin-1 reduces the severity of dextran sulfate sodium (DSS)-induced ulcerative colitis by suppressing inflammatory and oxidative stress response | |
dc.type | Makale | |
dc.relation.journal | BOSNIAN JOURNAL OF BASIC MEDICAL SCIENCES | |
dc.contributor.department | İstanbul Üniversitesi , Fen Fakültesi , Biyoloji Bölümü | |
dc.identifier.volume | 20 | |
dc.identifier.issue | 3 | |
dc.identifier.startpage | 319 | |
dc.identifier.endpage | 328 | |
dc.contributor.firstauthorID | 2275648 | |