Comparative Clinical Efficiency of Resveratrol, Allopurinol, and Resveratrol Plus Allopurinol in Canine Visceral Leishmaniasis

dc.contributor.author Erdogan, Songul
dc.contributor.author Erdogan, Hasan
dc.contributor.author Ural, Kerem
dc.contributor.author Pasa, Serdar
dc.contributor.author Gultekin, Mehmet
dc.contributor.author Balikci, Canberk
dc.contributor.author Gunal, Ismail
dc.date.accessioned 2025-06-30T15:25:52Z
dc.date.available 2025-06-30T15:25:52Z
dc.date.issued 2025
dc.description.abstract Objective To assess the clinical and immunological effectiveness of resveratrol alone or combined with allopurinol for treating canine visceral leishmaniasis (CVL). Methods This study included 50 dogs, 30 diagnosed with CVL and 20 healthy controls. Dogs were classified based on their treatment regime (receiving resveratrol [200 mg/dog/d] and/or allopurinol [10 mg/kg/d]). Clinical scores, antileishmanial antibody titers, and routine blood parameters were evaluated on days 0, 15, and 30 after treatment. Results Dogs treated with the combination therapy showed the most substantial improvements, with a 75.77% reduction in clinical scores and an 81.25% reduction in antibody titers. Dogs receiving allopurinol exhibited a 56.25% reduction in clinical scores, while those treated with resveratrol showed a 42.82% reduction. Antibody titers were less signifi-cantly reduced in the resveratrol group (67.5%) compared to the allopurinol group (45%). Conclusions Combining resveratrol with allopurinol enhances the therapeutic efficacy for CVL, leading to significant clinical im-provements and reductions in antibody titers. Resveratrol alone also demonstrates promising anti-leishmanial effects. Clinical Relevance Resveratrol, either alone or in combination with allopurinol, offers a feasible and effective alternative for improving clinical outcomes in CVL. Its incorporation into standard protocols may enhance treatment strategies in veterinary medicine. en_US
dc.description.sponsorship Scientific and Technological Research Council of Turkey (TUBITAK) [121O192] en_US
dc.description.sponsorship This research was supported by The Scientific and Technological Research Council of Turkey (TUBITAK) under the 1002 program with project No. 121O192. en_US
dc.identifier.doi 10.2460/javma.24.11.0738
dc.identifier.issn 0003-1488
dc.identifier.issn 1943-569X
dc.identifier.scopus 2-s2.0-105005749121
dc.identifier.uri https://doi.org/10.2460/javma.24.11.0738
dc.language.iso en en_US
dc.publisher Amer veterinary Medical Assoc en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.title Comparative Clinical Efficiency of Resveratrol, Allopurinol, and Resveratrol Plus Allopurinol in Canine Visceral Leishmaniasis en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.scopusid 57205310406
gdc.author.scopusid 56276427100
gdc.author.scopusid 56045626500
gdc.author.scopusid 56038680600
gdc.author.scopusid 39361395500
gdc.author.scopusid 57188928984
gdc.author.scopusid 59020760200
gdc.author.wosid Günal, İsmail/Aad-4413-2021
gdc.author.wosid Ayan, Adnan/Aac-5226-2020
gdc.author.wosid Erdogan, Hasan/Abc-1640-2020
gdc.author.wosid Balıkçı, Canberk/Abg-8719-2020
gdc.author.wosid Gultekin, Mehmet/D-5771-2017
gdc.coar.access metadata only access
gdc.coar.type text::journal::journal article
gdc.description.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
gdc.description.departmenttemp [Erdogan, Songul; Erdogan, Hasan; Ural, Kerem; Pasa, Serdar; Gultekin, Mehmet; Ozalp, Tahir] Aydin Adnan Menderes Univ, Fac Vet Med, Dept Internal Med, Aydin, Turkiye; [Balikci, Canberk; Gunal, Ismail] Harran Univ, Fac Vet Med, Dept Internal Med, Sanliurfa, Turkiye; [Ayan, Adnan] Van Yuzuncu Yil Univ, Fac Vet Med, Dept Genet, Van, Turkiye en_US
gdc.description.endpage 767 en_US
gdc.description.issue 6 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q2
gdc.description.startpage 762 en_US
gdc.description.volume 263 en_US
gdc.description.woscitationindex Science Citation Index Expanded
gdc.description.wosquality Q2
gdc.identifier.pmid 39938209
gdc.identifier.wos WOS:001515633200001
gdc.index.type WoS
gdc.index.type Scopus
gdc.index.type PubMed

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