نمایش مختصر رکورد

dc.contributor.authorSoudkhah, Sevilen_US
dc.contributor.authorKeyghobadi, Saharen_US
dc.contributor.authorShadboorestan, Amiren_US
dc.contributor.authorGholami, Mahdien_US
dc.contributor.authorOmidi Sarajar, Behnamen_US
dc.contributor.authorSalek Maghsoudi, Arminen_US
dc.contributor.authorOmidi, Mahmouden_US
dc.contributor.authorMohammadi Motamed, Saeeden_US
dc.contributor.authorAkbarzadeh Kolahi, Saeiden_US
dc.contributor.authorRastegar-Pouyani, Nimaen_US
dc.contributor.authorHassani, Shokoufehen_US
dc.date.accessioned1404-02-11T08:50:29Zfa_IR
dc.date.accessioned2025-05-01T08:50:30Z
dc.date.available1404-02-11T08:50:29Zfa_IR
dc.date.available2025-05-01T08:50:30Z
dc.date.issued2025-05-01en_US
dc.date.issued1404-02-11fa_IR
dc.date.submitted2024-05-18en_US
dc.date.submitted1403-02-29fa_IR
dc.identifier.citationSoudkhah, Sevil, Keyghobadi, Sahar, Shadboorestan, Amir, Gholami, Mahdi, Omidi Sarajar, Behnam, Salek Maghsoudi, Armin, Omidi, Mahmoud, Mohammadi Motamed, Saeed, Akbarzadeh Kolahi, Saeid, Rastegar-Pouyani, Nima, Hassani, Shokoufeh. (2025). The hydroalcoholic extract of Nasturtium officinale protectively inhibits apoptotic and inflammatory pathways in hepato- and nephrotoxicity: An in vivo study. Avicenna Journal of Phytomedicine, 15(3), 1177-1192. doi: 10.22038/ajp.2024.25213en_US
dc.identifier.issn2228-7930
dc.identifier.issn2228-7949
dc.identifier.urihttps://dx.doi.org/10.22038/ajp.2024.25213
dc.identifier.urihttps://ajp.mums.ac.ir/article_25213.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/1163698
dc.description.abstractObjective: Nasturtium officinale (N. officinale (NO)) has been widely used in traditional medicine. This study investigates the protective effects of NO against hepatic and renal damage induced by CCl4 and gentamicin, respectively, in rats.Materials and Methods: Male Wistar rats were divided into two arms: A (CCl4-induced hepatotoxicity) and B (gentamicin-induced nephrotoxicity). Seventeen groups were formed by dividing arms A and B, with nine groups in arm A and eight groups in arm B (n=5). Rats were daily treated with various doses (50, 100, and 200 mg/kg BW) of N. officinale extract (NOE) (Total extract; Oral gavage) for 14 and 28 days in arm A and B, respectively. Biochemical and histopathological evaluations and gene expression analyses were conducted on blood, liver, and kidney tissues.Results: NOE treatment significantly modulated B-cell lymphoma protein 2 (Bcl-2)-associated X (Bax) and B-cell lymphoma protein 2 (Bcl-2) expression in kidney tissue, reducing Bax (p<0.01) and increasing Bcl-2 (p<0.05). In liver tissue, NOE inhibited tumor necrosis factor alpha (TNF-α) (p<0.01) and Interleukin-1 beta (IL-1β) (p<0.001), while reducing AST and ALT activity (p<0.001). Additionally, blood urea nitrogen (BUN) levels significantly decreased (p<0.05) in nephrotoxic rats.Conclusion: Our findings highlight the capability of NOE as a promising therapeutic against liver and kidney damage induced by CCl4 and gentamicin, respectively, in animal models.en_US
dc.format.extent1572
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherMashhad University of Medical Sciencesen_US
dc.relation.ispartofAvicenna Journal of Phytomedicineen_US
dc.relation.isversionofhttps://dx.doi.org/10.22038/ajp.2024.25213
dc.subjectNephrotoxicityen_US
dc.subjectHepatotoxicityen_US
dc.subjectNasturtium officinaleen_US
dc.subjectInflammationen_US
dc.subjectApoptosisen_US
dc.subjectToxicologyen_US
dc.titleThe hydroalcoholic extract of Nasturtium officinale protectively inhibits apoptotic and inflammatory pathways in hepato- and nephrotoxicity: An in vivo studyen_US
dc.typeTexten_US
dc.typeOriginal Research Articleen_US
dc.contributor.departmentDepartment of Pharmacology and Toxicology, Faculty of Pharmacy and Pharmaceutical Sciences, Tehran Medical Sciences, Islamic Azad University, Tehran, Iranen_US
dc.contributor.departmentDepartment of Pharmacology and Toxicology, Faculty of Pharmacy and Pharmaceutical Sciences, Tehran Medical Sciences, Islamic Azad University, Tehran, Iranen_US
dc.contributor.departmentDepartment of Toxicology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iranen_US
dc.contributor.departmentDepartment of Toxicology and Pharmacology, Faculty of Pharmacy, Tehran University of Medical Sciences (TUMS), Tehran, Iranen_US
dc.contributor.departmentDepartment of toxicology and pharmacology, faculty of pharmacy,Tehran university of medical sciences,Tehran,Iranen_US
dc.contributor.departmentDepartment of Toxicology and Pharmacology, Faculty of Pharmacy, Tehran University of Medical Sciences (TUMS), Tehran, Iranen_US
dc.contributor.departmentDepartment of Toxicology and Pharmacology, School of Pharmacy and Pharmaceutical Sciences, Hormozgan University of Medical Sciencesen_US
dc.contributor.departmentdepartment of Pharmacognosy, Pharmaceutical sciences Branch, islamic Azad University, Tehran, Iranen_US
dc.contributor.departmentDepartment of Pharmacology and Toxicology, Faculty of Pharmacy and Pharmaceutical Sciences, Tehran Medical Sciences, Islamic Azad University, Tehran, Iranen_US
dc.contributor.departmentDepartment of Toxicology and Pharmacology, Faculty of Pharmacy, Tehran University of Medical Sciences (TUMS), Tehran, Iranen_US
dc.contributor.departmentToxicology and Diseases Group (TDG), Pharmaceutical Sciences Research Center (PSRC), Tehran University of Medical Sciences (TUMS), Tehran, Iran.en_US
dc.citation.volume15
dc.citation.issue3
dc.citation.spage1177
dc.citation.epage1192
nlai.contributor.orcid0000-0001-7832-4724
nlai.contributor.orcid0000-0003-1266-2354
nlai.contributor.orcid0000-0003-0533-2170


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