نمایش مختصر رکورد

dc.contributor.authorGholami, Mahbobeen_US
dc.contributor.authorMoallem, Seyed Adelen_US
dc.contributor.authorAfshar, Mohammaden_US
dc.contributor.authorAmoueian, Sakinehen_US
dc.contributor.authorEtemad, Leilaen_US
dc.contributor.authorKarimi, Gholamrezaen_US
dc.date.accessioned1399-07-09T12:39:27Zfa_IR
dc.date.accessioned2020-09-30T12:39:27Z
dc.date.available1399-07-09T12:39:27Zfa_IR
dc.date.available2020-09-30T12:39:27Z
dc.date.issued2016-08-01en_US
dc.date.issued1395-05-11fa_IR
dc.date.submitted2015-10-10en_US
dc.date.submitted1394-07-18fa_IR
dc.identifier.citationGholami, Mahbobe, Moallem, Seyed Adel, Afshar, Mohammad, Amoueian, Sakineh, Etemad, Leila, Karimi, Gholamreza. (2016). Teratogenic effects of silymarin on mouse fetuses. Avicenna Journal of Phytomedicine, 6(5), 542-549. doi: 10.22038/ajp.2016.6679en_US
dc.identifier.issn2228-7930
dc.identifier.issn2228-7949
dc.identifier.urihttps://dx.doi.org/10.22038/ajp.2016.6679
dc.identifier.urihttp://ajp.mums.ac.ir/article_6679.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/425827
dc.description.abstract<br/><strong>Objective: </strong><em>Silybum marianum</em> has been used for centuries in herbal medicine for treatment of liver diseases. Currently, there is no data available on the possible effects of silymarin on fetal development. This study aimed to investigate the teratogenic effect of silymarin on BALB/c mice fetuses. <br/><strong>Materials and Methods</strong>: A total of 40 pregnant mice were divided into 4 groups of 10 mice each. Three groups received silymarin at three different doses of 50, 100 and 200 mg/kg/day during gestational days (GDs). The control group received normal saline and tween (solvent). Dams were sacrificed on GD 18 and all fetuses were examined for gross malformations, size and body weight. Malformed fetuses were double stained with alizarin red and alcian blue. <br/><strong>Results</strong>: Silymarin administration at all doses resulted in reduction of the mean fetal body weights. The abnormalities included limb, vertebral column and craniofacial malformations. Craniofacial malformations were the most common abnormalities, but they were not observed in a dose-dependent manner. The percentage of fetal resorption significantly increased (up to 15%) in all treatment groups. <br/><strong>Conclusion</strong>: Based on our results, silymarin, especially at high doses can lead to fetal resorption, intrauterine growth retardation and limb, vertebral column and craniofacial abnormalities. More precise studies should be conducted about the teratogenic effects of herbal medicine investigating the underlying mechanisms. Thus, caution should be taken when administering <em>S. marianum </em>to pregnant woman.en_US
dc.format.extent478
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.2016.6679
dc.subjectSilybum marianumen_US
dc.subjectSilymarinen_US
dc.subjectMouse fetusen_US
dc.subjectTeratogenicityen_US
dc.subjectToxicologyen_US
dc.titleTeratogenic effects of silymarin on mouse fetusesen_US
dc.typeTexten_US
dc.typeOriginal Research Articleen_US
dc.contributor.departmentDepartment of Pharmacodynamics and Toxicology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iranen_US
dc.contributor.departmentPharmaceutical Research Center, Mashhad University of Medical Sciences, Mashhad, Iranen_US
dc.contributor.departmentDepartment of Anatomy, Birjand University of Medical Sciences, Birjand, Iranen_US
dc.contributor.departmentDepartment of Pathology, Imam-Reza Hospital, Mashhad University of Medical Sciences, Mashhad, Iranen_US
dc.contributor.departmentPharmaceutical Research Center, Mashhad University of Medical Sciences, Mashhad, Iranen_US
dc.contributor.departmentPharmaceutical Research Center, Pharmacy school, Mashhad University of Medical Sciences, Mashhad, Iranen_US
dc.citation.volume6
dc.citation.issue5
dc.citation.spage542
dc.citation.epage549
nlai.contributor.orcid0000000212735448


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