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Effects of naringin on oxidative stress, inflammation, some reproductive parameters, and apoptosis in acrylamide‐induced testis toxicity in rat

dc.contributor.authorSengul, Emin
dc.contributor.authorGelen, Volkan
dc.contributor.authorYildirim, Serkan
dc.contributor.authorCinar, İrfan
dc.contributor.authorAksu, Emrah Hicazi
dc.date.accessioned2026-01-04T18:19:54Z
dc.date.issued2023-01-04
dc.description.abstractAbstract Acrylamide (ACR) is used in many fields such as cosmetics, paper, and textile industries. It also occurs at very high temperatures in some foods. Gonadotoxic effects of ACR have been found in experimental animals. Many studies use flavonoids to prevent the reproductive side effects of ACR. Naringin (NA) is a flavonoid and it has been determined by studies that it has no toxic effect on tissues. In our study, we aimed to determine the protective effect of NA against the damage of ACR on testicular tissue and the reproductive system in rats. In our study, 50 Spraque Dawley male rats weighing 220‐250 grams were used. Control: Only intragastric saline was administered for 10 days. ACR: Animals received ACR (40 mg/kg, intraperitoneally) for 10 days. NA50+ACR: Animals were given NA for 10 days and each NA was one hour after the administration of ACR. NA100+ACR: Animals received NA for 10 days and one hour after each NA was given ACR. NA100: Animals were given NA for 10 days. At the end of the applications, the rats were euthanized by cervical dislocation under anesthesia. Serum FSH, LH, and Dihydrotestosterone levels were compared between the groups. In addition, oxidative stress, inflammation, expression of some reproductive enzymes, and apoptosis markers were determined in testicular tissues. When these parameters were compared between groups, ACR induced testicular dysfunction and tissue damage in rats. We determined that only the NA application did not cause tissue damage. and the administration of NA along with ACR significantly reduced ACR‐induced testis toxicity.
dc.description.urihttps://doi.org/10.1002/tox.23728
dc.description.urihttps://pubmed.ncbi.nlm.nih.gov/36598108
dc.description.urihttps://avesis.atauni.edu.tr/publication/details/915aeee2-c295-4b8f-af01-b45e163a1cf0/oai
dc.identifier.doi10.1002/tox.23728
dc.identifier.eissn1522-7278
dc.identifier.endpage808
dc.identifier.issn1520-4081
dc.identifier.openairedoi_dedup___::b54533fe81e4de72b89147661ccc4ad2
dc.identifier.orcid0000-0003-1566-1816
dc.identifier.orcid0000-0002-5091-1262
dc.identifier.pubmed36598108
dc.identifier.scopus2-s2.0-85145569729
dc.identifier.startpage798
dc.identifier.urihttps://hdl.handle.net/20.500.12597/40460
dc.identifier.volume38
dc.identifier.wos000907243900001
dc.language.isoeng
dc.publisherWiley
dc.relation.ispartofEnvironmental Toxicology
dc.rightsCLOSED
dc.subjectMale
dc.subjectFlavonoids
dc.subjectInflammation
dc.subjectAcrylamide
dc.subjectReproduction
dc.subjectApoptosis
dc.subjectAntioxidants
dc.subjectRats
dc.subjectOxidative Stress
dc.subjectTestis
dc.subjectAnimals
dc.subject.sdg3. Good health
dc.titleEffects of naringin on oxidative stress, inflammation, some reproductive parameters, and apoptosis in acrylamide‐induced testis toxicity in rat
dc.typeArticle
dspace.entity.typePublication
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In our study, we aimed to determine the protective effect of NA against the damage of ACR on testicular tissue and the reproductive system in rats. In our study, 50 Spraque Dawley male rats weighing 220‐250 grams were used. Control: Only intragastric saline was administered for 10 days. ACR: Animals received ACR (40 mg/kg, intraperitoneally) for 10 days. NA50+ACR: Animals were given NA for 10 days and each NA was one hour after the administration of ACR. NA100+ACR: Animals received NA for 10 days and one hour after each NA was given ACR. NA100: Animals were given NA for 10 days. At the end of the applications, the rats were euthanized by cervical dislocation under anesthesia. Serum FSH, LH, and Dihydrotestosterone levels were compared between the groups. In addition, oxidative stress, inflammation, expression of some reproductive enzymes, and apoptosis markers were determined in testicular tissues. 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