نمایش مختصر رکورد

dc.contributor.authorEntezari Heravi, Nazaninen_US
dc.contributor.authorHosseinian, Saraen_US
dc.contributor.authorNaji Ebrahimi Yazd, Zohrehen_US
dc.contributor.authorShafei, Mohammad Naseren_US
dc.contributor.authorEbrahimzadeh, Alirezaen_US
dc.contributor.authorShahraki, Samiraen_US
dc.contributor.authorSamadi, Zahraen_US
dc.contributor.authorMotejadded, Fatemehen_US
dc.contributor.authorBeheshti, Farimahen_US
dc.contributor.authorMohebbati, Rezaen_US
dc.contributor.authorParhizgar, Soghraen_US
dc.contributor.authorKhajavirad, Abolfazlen_US
dc.date.accessioned1399-07-09T12:38:27Zfa_IR
dc.date.accessioned2020-09-30T12:38:27Z
dc.date.available1399-07-09T12:38:27Zfa_IR
dc.date.available2020-09-30T12:38:27Z
dc.date.issued2018-02-01en_US
dc.date.issued1396-11-12fa_IR
dc.date.submitted2017-12-13en_US
dc.date.submitted1396-09-22fa_IR
dc.identifier.citationEntezari Heravi, Nazanin, Hosseinian, Sara, Naji Ebrahimi Yazd, Zohreh, Shafei, Mohammad Naser, Ebrahimzadeh, Alireza, Shahraki, Samira, Samadi, Zahra, Motejadded, Fatemeh, Beheshti, Farimah, Mohebbati, Reza, Parhizgar, Soghra, Khajavirad, Abolfazl. (2018). Doxorubicin-induced renal inflammation in rats: Protective role of Plantago major. Avicenna Journal of Phytomedicine, 8(2), 179-187. doi: 10.22038/ajp.2018.10396en_US
dc.identifier.issn2228-7930
dc.identifier.issn2228-7949
dc.identifier.urihttps://dx.doi.org/10.22038/ajp.2018.10396
dc.identifier.urihttp://ajp.mums.ac.ir/article_10396.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/425514
dc.description.abstractObjective: The aim of the present study was to evaluate the possible protective effect of Plantago major (P. major) extract against doxorubicin (DXR)-induced renal inflammation in rats.<br /> Materials and Methods: 80 male albino rats were randomly divided into 8 groups as follows: control, DXR, Ext (extract) 600, Ext1200, dexamethasone+DXR, vitamin E+DXR, Ext600+DXR, and Ext1200+DXR. Duration of the study was 35 days and DXR was intravenously injected on the 7<sup>th</sup> day of the experiment. Tumor necrosis factor-alpha (TNF-α) production and monocyte chemoattractant protein-1 (MCP-1) expression levels were assessed in the left kidney. Serum creatinine concentration and osmolarity were determined on the 1<sup>st</sup>, 14<sup>th</sup>, 21<sup>st</sup>, 28<sup>th</sup> and 35<sup>th</sup> days of the experiment.<br /> Results: DXR caused a significant increase in renal expression of MCP-1 and TNF-α production compared to control animals. Administration of dexamethasone, vitamin E and P. major extract significantly improved the expression of these inflammatory mediators compared to DXR group. Compared to day 1 in DXR group, serum osmolarity showed a significant increase on days 21, 28 and 35. Also, on these days, serum osmolarity in DXR group was significantly higher than that on the same days in control group. In Vit E+DXR and Ext 1200+DXR groups, there was no significant changes in serum osmolarity among different days of the study. However, in these groups, serum osmolarity on days 21, 28 and 35 showed a significant decrease compared to the same days in DXR group.<br /> Conclusion: Present results suggest that hydroethanolic extract of P. major protected renal tissue against DXR–induced renal inflammation.en_US
dc.format.extent848
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.2018.10396
dc.subjectPlantago majoren_US
dc.subjectDoxorubicinen_US
dc.subjectVitamin Een_US
dc.subjectDexamethasoneen_US
dc.subjectInflammationen_US
dc.subjecturology-Kidneyen_US
dc.titleDoxorubicin-induced renal inflammation in rats: Protective role of Plantago majoren_US
dc.typeTexten_US
dc.typeOriginal Research Articleen_US
dc.contributor.departmentDepartment of Physiology, School of Medicine, Mashhad University of Medical Sciences Mashhad, Iranen_US
dc.contributor.departmentDepartment of physiology, School of medicine, Mashhad University of Medical Sciences, Mashhad, Iranen_US
dc.contributor.departmentDepartment of Physiology, School of Medicine, Mashhad University of Medical Sciences Mashhad, Iranen_US
dc.contributor.departmentDivision of Neurocognitive Sciences, Psychiatry and Behavioral Sciences Research Center, Mashhad University of Medical Sciences, Mashhad, Iranen_US
dc.contributor.departmentDepartment of Anatomy and Cell Biology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iranen_US
dc.contributor.departmentDepartment of Physiology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.en_US
dc.contributor.departmentDepartment of Physiology, School of Medicine, Mashhad University of Medical Sciences Mashhad, Iranen_US
dc.contributor.departmentDepartment of Anatomy and Cell Biology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iranen_US
dc.contributor.departmentDepartment of Physiology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iranen_US
dc.contributor.departmentDepartment of Physiology, School of Medicine, Mashhad University of Medical Sciences, Iranen_US
dc.contributor.departmentDepartment of Physiology, School of Medicine, Mashhad University of Medical Sciences Mashhad, Iranen_US
dc.contributor.departmentNeurogenic Inflammation Research Center, Mashhad University of Medical Sciences, Mashhad, Iranen_US
dc.citation.volume8
dc.citation.issue2
dc.citation.spage179
dc.citation.epage187
nlai.contributor.orcid0000-0001-5148-9895
nlai.contributor.orcid0000-0003-1524-2339
nlai.contributor.orcid0000-0002-1645-7094


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