Comparison of the Protective Effects of Curcumin and Caffeic Acid Phenethyl Ester Against Doxorubicin-Induced Testicular Toxicity

dc.contributor.author Huyut, Zubeyir
dc.contributor.author Alp, Hamit Hakan
dc.contributor.author Yaman, Turan
dc.contributor.author Keles, Omer Faruk
dc.contributor.author Yener, Zabit
dc.contributor.author Turkan, Fikret
dc.contributor.author Ayengin, Kemal
dc.date.accessioned 2025-05-10T17:07:44Z
dc.date.available 2025-05-10T17:07:44Z
dc.date.issued 2021
dc.description Alp, Hamit Hakan/0000-0002-9202-4944; Keles, Omer Faruk/0000-0002-7869-5311; Ayengin, Kemal/0000-0002-1633-3200 en_US
dc.description.abstract Whether testicular toxicity is mediated by matrix metalloproteinases (MMPs) is an important question that has not been examined. This study investigated the suppressive effect of curcumin and caffeic acid phenethyl ester (CAPE) on oxidative stress, apoptosis, and whether MMPs mediate doxorubicin (DOX)-induced testicular injury. Male rats were randomly divided into eight groups (n = 8 per group). The groups were as follows: sham, dimethyl sulphoxide (100 mu L), DOX (3 mg/kg), CAPE (2.68 mg/kg), curcumin (30 mg/kg), DOX+CAPE (3 mg/kg DOX and 2.68 mg/kg CAPE), DOX+curcumin (3 mg/kg DOX and 30 mg/kg curcumin) and DOX+CAPE+curcumin (3 mg/kg DOX, 2.68 mg/kg CAPE and 30 mg/kg curcumin). Injections were administered daily for 21 days. The oxidative stress, MMPs, proinflammatory cytokines and apoptotic markers in the DOX group were higher than the sham group (p < .05); these measures were lower in the groups treated with CAPE and curcumin together with DOX compared with the DOX group (p < .05). The results showed that MMPs mediated DOX-induced testicular injury, but CAPE and especially curcumin suppressed testis injury and cell apoptosis by suppressing DOX-induced increases in MMPs, oxidative stress and proinflammatory cytokines. However, curcumin exhibited more pronounced effects than CAPE in terms of all studied parameters. en_US
dc.description.sponsorship Research Fund of the Yuzuncu Yil University [TSA-2018-7138] en_US
dc.description.sponsorship This work was supported by the Research Fund of the Yuzuncu Yil University (project number: TSA-2018-7138). en_US
dc.identifier.doi 10.1111/and.13919
dc.identifier.issn 0303-4569
dc.identifier.issn 1439-0272
dc.identifier.scopus 2-s2.0-85096999594
dc.identifier.uri https://doi.org/10.1111/and.13919
dc.identifier.uri https://hdl.handle.net/20.500.14720/6867
dc.language.iso en en_US
dc.publisher Wiley en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Apoptosis en_US
dc.subject Caffeic Acid Phenethyl Ester en_US
dc.subject Curcumin en_US
dc.subject Doxorubicin en_US
dc.subject Testicular Toxicity en_US
dc.title Comparison of the Protective Effects of Curcumin and Caffeic Acid Phenethyl Ester Against Doxorubicin-Induced Testicular Toxicity en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.id Alp, Hamit Hakan/0000-0002-9202-4944
gdc.author.id Keles, Omer Faruk/0000-0002-7869-5311
gdc.author.id Ayengin, Kemal/0000-0002-1633-3200
gdc.author.scopusid 55394375700
gdc.author.scopusid 24328770500
gdc.author.scopusid 18539360300
gdc.author.scopusid 57195562796
gdc.author.scopusid 56087055000
gdc.author.scopusid 57115336200
gdc.author.scopusid 57115336200
gdc.author.wosid Ayengin, Kemal/Abi-4555-2020
gdc.author.wosid Hakan, Hamit/U-2671-2018
gdc.coar.access open access
gdc.coar.type text::journal::journal article
gdc.description.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
gdc.description.departmenttemp [Huyut, Zubeyir; Alp, Hamit Hakan] Van Yuzuncu Yil Univ, Med Fac, Dept Biochem, Van, Turkey; [Yaman, Turan; Keles, Omer Faruk; Yener, Zabit] Van Yuzuncu Yil Univ, Dept Pathol, Fac Vet, Van, Turkey; [Turkan, Fikret] Igdir Univ, Hlth Serv Vocat Sch, Igdir, Turkey; [Ayengin, Kemal] Van Yuzuncu Yil Univ, Med Fac, Dept Pediat Surg, Van, Turkey en_US
gdc.description.issue 2 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q2
gdc.description.volume 53 en_US
gdc.description.woscitationindex Science Citation Index Expanded
gdc.description.wosquality Q2
gdc.identifier.pmid 33289171
gdc.identifier.wos WOS:000594537200001
gdc.index.type WoS
gdc.index.type Scopus
gdc.index.type PubMed

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