Protective Effects Of<i> Rubus</I><i> Tereticaulis</I> Leaves Ethanol Extract on Rats With Ulcerative Colitis and Bio-Guided Isolation of Its Active Compounds: a Combined <i>in Silico</I>, <i>in Vitro</I> and <i>in Vivo</I> Study

dc.contributor.author Sen, Ali
dc.contributor.author Ozbeyli, Dilek
dc.contributor.author Terali, Kerem
dc.contributor.author Goger, Fatih
dc.contributor.author Yildirim, Aybeniz
dc.contributor.author Ertas, Busra
dc.contributor.author Sener, Goksel
dc.contributor.other Eczacılık Meslek Bilimleri Bölümü
dc.date.accessioned 2025-01-11T13:00:48Z
dc.date.available 2025-01-11T13:00:48Z
dc.date.issued 2023
dc.description dogan, ahmet/0000-0003-0603-5100; Yildirim, Aybeniz/0000-0002-5801-4726; Sen, Ali/0000-0002-2144-5741; Ozbeyli, Dilek/0000-0002-4141-6913; Terali, Kerem/0000-0002-9964-6383; ERTAS, BUSRA/0000-0001-8374-1098; Sener, Goksel/0000-0001-7444-6193; Goger, Fatih/0000-0002-9665-0256 en_US
dc.description.abstract The aim of this study was to evaluate the therapeutic effect of active ethanol extract obtained from the leaves of Rubus tereticaulis (RTME) against colitis, and to purify major compounds from this extract by bioassay-directed isolation. Rats with colitis induced via intra-rectal acetic acid administration (5%, v/v) received RTME or sulfasalazine for three consecutive days. On day four, all rats were decapitated, and the colonic tissue samples were collected for macroscopic score, colon weight, reduced glutathione (GSH), myeloperoxidase (MPO), and malondialdehyde (MDA) analyses. The active compounds and chemical composition of RTME were determined by bio-guided isolation and LC-MS/MS, respectively. Compared to the colitis group, the rats treated with RTME displayed significantly lowered macroscopic scores and colon wet weights (p < 0.001). These effects were confirmed biochemically by a decrease in colonic MPO activity (p < 0.001), MDA levels (p < 0.001), and an increase in GSH levels (p < 0.001). Kaempferol-3-O-beta-D-glucuronide (RT1) and quercetin-3-O-beta-D-glucuronide (RT2) were found to be the major compounds of RTME, as evidenced by in vitro anti-inflammatory and antioxidant activity-guided isolation. Their anti-inflammatory/antioxidant activities were also predicted by docking simulations. Additionally, quinic acid, 5-caffeoylquinic acid, quercetin pentoside, quercetin glucoside, quercetin3-O-beta-D-glucuronide, kaempferol-3-O-beta-D-glucuronide, and kaempferol rutinoside were identified in RTME via using LC-MS/MS. RT2, along with other compounds, may be responsible for the observed protective action of RTME against colitis. This study represents the first report on the beneficial effects of RTME in an experimental model of colitis and highlights the potential future use of RTME as a natural alternative to alleviate colitis. en_US
dc.description.sponsorship Marmara University Scientific Research Projects Coordination Unit [SAG -K- 110117-0001] en_US
dc.description.sponsorship This work has been supported by Marmara University Scientific Research Projects Coordination Unit under grant number SAG -K- 110117-0001. en_US
dc.identifier.citation 1
dc.identifier.doi 10.1016/j.cbi.2022.110263
dc.identifier.issn 0009-2797
dc.identifier.issn 1872-7786
dc.identifier.scopus 2-s2.0-85142319014
dc.identifier.uri https://doi.org/10.1016/j.cbi.2022.110263
dc.identifier.uri https://hdl.handle.net/20.500.14627/72
dc.language.iso en en_US
dc.publisher Elsevier Ireland Ltd en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Antioxidant Activity en_US
dc.subject Anti-Inflammatory Activity en_US
dc.subject Colitis en_US
dc.subject Flavonoids en_US
dc.subject Rubus Tereticaulis en_US
dc.title Protective Effects Of<i> Rubus</I><i> Tereticaulis</I> Leaves Ethanol Extract on Rats With Ulcerative Colitis and Bio-Guided Isolation of Its Active Compounds: a Combined <i>in Silico</I>, <i>in Vitro</I> and <i>in Vivo</I> Study en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.id dogan, ahmet/0000-0003-0603-5100
gdc.author.id Yildirim, Aybeniz/0000-0002-5801-4726
gdc.author.id Sen, Ali/0000-0002-2144-5741
gdc.author.id Ozbeyli, Dilek/0000-0002-4141-6913
gdc.author.id Terali, Kerem/0000-0002-9964-6383
gdc.author.id ERTAS, BUSRA/0000-0001-8374-1098
gdc.author.id Goger, Fatih/0000-0002-9665-0256
gdc.author.institutional Şener, Göksel
gdc.author.scopusid 55250649800
gdc.author.scopusid 6504603410
gdc.author.scopusid 55867022200
gdc.author.scopusid 8926845400
gdc.author.scopusid 57215874552
gdc.author.scopusid 57196052987
gdc.author.scopusid 23017859400
gdc.author.wosid yıldırım, aybeniz/GZG-3445-2022
gdc.author.wosid Gögel, Fatih/HTR-3454-2023
gdc.author.wosid Ozbeyli, Dilek/AAC-2498-2020
gdc.author.wosid Ertas, Busra/IQS-8337-2023
gdc.author.wosid dogan, ahmet/C-1547-2015
gdc.author.wosid Terali, Kerem/Q-3270-2016
gdc.description.department Fenerbahçe University en_US
gdc.description.departmenttemp [Sen, Ali; Yildirim, Aybeniz; Bitis, Leyla] Marmara Univ, Fac Pharm, Dept Pharmacognosy, TR-34854 Istanbul, Turkiye; [Ozbeyli, Dilek] Marmara Univ, Vocat Sch Hlth Serv, Dept Med Serv & Tech, Istanbul, Turkiye; [Terali, Kerem] Cyprus Int Univ, Fac Med, Dept Med Biochem, Nicosia 99258, Cyprus; [Goger, Fatih] Afyonkarahisar Hlth Sci Univ, Fac Pharm, Dept Pharmaceut Bot, Afyon, Turkiye; [Ertas, Busra] Marmara Univ, Fac Pharm, Dept Pharmacol, Istanbul, Turkiye; [Dogan, Ahmet] Marmara Univ, Fac Pharm, Dept Pharmaceut Bot, Istanbul, Turkiye; [Sener, Goksel] Fenerbahce Univ, Fac Pharm, Dept Pharmacol, TR-34758 Istanbul, Turkiye en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q1
gdc.description.volume 369 en_US
gdc.description.woscitationindex Science Citation Index Expanded
gdc.description.wosquality Q1
gdc.identifier.pmid 36375516
gdc.identifier.wos WOS:000967045500001
gdc.scopus.citedcount 4
gdc.wos.citedcount 2
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