Please use this identifier to cite or link to this item: http://hdl.handle.net/11189/10390
DC FieldValueLanguage
dc.contributor.authorAjibade, Temitayo Olabisien_US
dc.contributor.authorOliyide, Esther Oluwaseyien_US
dc.contributor.authorEsan, Oluwaseun Olanrewajuen_US
dc.contributor.authorAdetona, Moses Olusolaen_US
dc.contributor.authorAwoyomi, Omolola Victoriaen_US
dc.contributor.authorOyagbemi, Taiwo Olaideen_US
dc.contributor.authorAdeogun, Adewumi Victoriaen_US
dc.contributor.authorOyagbemi, Ademola Adetokunboen_US
dc.contributor.authorOmobowale, Temidayo Olutayoen_US
dc.contributor.authorSoetan, Kehinde Olugboyegaen_US
dc.contributor.authorNkadimeng, Sanah Malomileen_US
dc.contributor.authorMcGaw, Lyndy Joyen_US
dc.contributor.authorKayoka-Kabongo, Prudence Ngalulaen_US
dc.contributor.authorYakubu, Momoh Auduen_US
dc.contributor.authorNwulia, Evaristusen_US
dc.contributor.authorOguntibeju, Oluwafemi Omoniyien_US
dc.date.accessioned2025-11-24T10:28:46Z-
dc.date.available2025-11-24T10:28:46Z-
dc.date.issued2024-
dc.identifier.citationAjibade, T.O. et al. 2024. Protective effects of naringin on fipronil-induced cardiovascular and renal dysfunctions in rats. Clinical Traditional Medicine and Pharmacology, 5(2): 1-9. [https://doi.org/10.1016/j.ctmp.2024.200138]en_US
dc.identifier.issn2097-3829-
dc.identifier.issn2950-5771 (Online)-
dc.identifier.urihttp://hdl.handle.net/11189/10390-
dc.description.abstractBackground: Naringin as a bioflavanone glycoside is abundant in citrus fruits, which since ancient times have been utilized as natural herbal treatments in traditional medicine. Naringin has potent antioxidant effect that may mitigate oxidative stress mediated cardiovascular and renal dysfunctions in mammalian systems. Objective: To explore probable modulatory actions of naringin on fipronil-induced cardio-renal dysfunctions. Methods: Twenty-four Wistar rats weighing 140 ± 3.0 g were divided into four groups including normal control (saline), 10 mg/kg Fipronil (FIP), FIP+100 mg/kg naringin, and 100 mg/kg naringin. Administration of naringin and fipronil was by oral gavage for 28 consecutive days. Urinalysis, blood pressure monitoring, biochemical assays, histology, and immunohistochemical evaluations were performed. Results: Naringin significantly (P < 0.001) lessened blood pressure parameters, oxidative stress markers but significantly (P < 0.001) heightened the systemic antioxidants. Likewise, naringin prevented fipronil-induced histopathological lesions such as congestion and cellular infiltration in cardiac and renal tissues. Moreover, naringin attenuated the immunohistochemical expression of troponin 1 and matrix metalloperoxidase-2 in cardiac tissues, but heightened angiotensin converting enzyme 2 expression in contrast to that of fipronil group. Conclusion: The observation in this study shows potent attenuation of fipronil-induced toxicity by naringin, through inhibiting processes related to oxidation and inflammation.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.relation.ispartofClinical Traditional Medicine and Pharmacologyen_US
dc.subjectBiomarkers of cardiorenal dysfunctionen_US
dc.subjectFipronil toxicityen_US
dc.subjectNaringinen_US
dc.subjectImmunohistochemistryen_US
dc.titleProtective effects of naringin on fipronil-induced cardiovascular and renal dysfunctions in ratsen_US
dc.identifier.doihttps://doi.org/10.1016/j.ctmp.2024.200138-
dc.typeArticleen_US
Appears in Collections:HWSci - Journal Articles (DHET subsidised)
Files in This Item:
File Description SizeFormat 
Protective_effects_of_naringin.pdf3.09 MBAdobe PDFView/Open
Show simple item record

Page view(s)

98
Last Week
1
Last month
checked on Aug 15, 2026

Download(s)

40
checked on Aug 15, 2026

Google ScholarTM

Check

Altmetric


Items in Digital Knowledge are protected by copyright, with all rights reserved, unless otherwise indicated.