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dc.contributor.authorHabibi, P
dc.contributor.authorAlihemmati, A
dc.contributor.authorNasirzadeh, M
dc.contributor.authorYousefi, H
dc.contributor.authorHabibi, M
dc.contributor.authorAhmadiasl, N
dc.date.accessioned2018-08-26T05:06:07Z
dc.date.available2018-08-26T05:06:07Z
dc.date.issued2016
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/39409
dc.description.abstractMenopause and diabetes obviously increase the risk of cardiovascular disease in women. The aims of the present study were to evaluate the effects of ovariectomy in type 2 diabetes on the histology and expression of miRNA-29, miRNA-133, IGF-1 and Bcl-2 genes and Bcl-2 protein and caspase 3 activity in the hearts of female rats.Forty Female Wistar rats were divided into four groups: control, sham, ovariectomized (OVX), and ovariectomized with type 2 diabetes (OVX.D). After the 8-week experiment, the histological evaluation of the heart tissue was performed using H&E staining and PAS analysis, and cardiac expression of miRNA-29, miRNA-133, IGF-1, and Bcl-2 were evaluated using real-time PCR, and Bcl-2 protein and caspase 3 activity were evaluated using Western blot and ELISA.Ovariectomy significantly decreased miRNA-29, miRNA-133, IGF-1, and BCL-2 expression and Bcl-2 protein and increased caspase 3 activity in the heart compared to sham animals group (P<0.05). Type 2 diabetes in ovariectomized rats markedly decreased expression of miRNA-29, miRNA-133, IGF-1, BCL-2 genes, and Bcl-2 protein, and increased caspase 3 activity and reduced collagen and fibroblast tissue and glycogen granule deposition in relation to OVX group (P<0.05).Our findings suggest that type 2 diabetes and menopause synergically could enhance the cardiac fibrosis through dysregulation of miRNA-29, miRNA-133, IGF-1, and Bcl-2 genes expression and Bcl-2 protein and upregulation of caspase 3 activity.
dc.language.isoEnglish
dc.relation.ispartofIranian journal of basic medical sciences
dc.titleInvolvement of microRNA-133 and -29 in cardiac disturbances in diabetic ovariectomized rats.
dc.typearticle
dc.citation.volume19
dc.citation.issue11
dc.citation.spage1177
dc.citation.epage1185
dc.citation.indexPubmed


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