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1.
Diabetes & Metabolism Journal ; : 46-53, 2016.
Article in English | WPRIM | ID: wpr-90971

ABSTRACT

BACKGROUND: Diabetic cardiomyopathy is an important causal factor in morbidity and mortality among diabetic patients, and currently, no effective means are available to reverse its pathological progress. The purpose of the present study was to investigate the effect of ginger extract on apolipoproteins (apo) A and B, hyperhomocysteinemia, cathepsin G and leptin changes, as well as cardiac fibrosis and heart muscle cell proliferation under hyperglycemic conditions in vivo. METHODS: Twenty-four male Wistar rats were divided into three groups, namely: control, non-treated diabetic, and ginger extract-treated diabetic groups. The ginger extract-treated diabetic group received a 50 mg daily dose of ginger extract intragastrically for 6 weeks. RESULTS: The results revealed concurrent significant increases in plasma C-reactive protein (CRP), homocysteine (Hcy), cathepsin G and apoB levels and decreases in apoA and leptin levels in the non-treated diabetic group compared to the control group. Moreover, heart structural changes, including fibrosis and heart muscle cell proliferation, were observed in non-treated diabetic rats compared to the control rats. Significant amelioration of changes in the heart structure together with restoration of the elevated levels of Hcy and CRP, leptin, cathepsin G, and apoA and B were found in the ginger extract-treated diabetic group compared to the non-treated diabetic group. CONCLUSION: The findings indicated that ginger extract significantly reduces heart structural abnormalities in diabetic rats and that these effects might be associated with improvements in serum apo, leptin, cathepsin G, and Hcy levels and with the antioxidant properties of ginger extract.


Subject(s)
Animals , Humans , Male , Rats , Apolipoproteins A , Apolipoproteins B , C-Reactive Protein , Cathepsin G , Diabetic Cardiomyopathies , Fibrosis , Zingiber officinale , Heart Defects, Congenital , Heart , Homocysteine , Hyperhomocysteinemia , Leptin , Mortality , Myocytes, Cardiac , Plasma , Rats, Wistar
2.
IBJ-Iranian Biomedical Journal. 2015; 19 (2): 117-123
in English | IMEMR | ID: emr-161818

ABSTRACT

Hyperlipidemia and oxidized-low-density lipoproteins [Ox-LDL] are important independent cardiovascular risk factors that have been shown to stimulate vascular smooth muscle cell [VSMC] proliferation. The purpose of the present study was to investigate the effect of vitamin E on Ox-LDL, lipid profile, C-reactive protein [CRP], and VSMC proliferation of rat aorta. Male Wistar rats [n = 32] were divided into four groups namely: sham [SH], control [C], non-treated diabetic, and vitamin E-treated diabetic [VETD] groups. Ox-LDL, lipid profile, CRP and VSMC proliferation of aorta were measured after 42 days. The results revealed that along with a significant increase in VSMC proliferation, the amount of CRP, Ox-LDL, and lipid profiles in diabetic rats. VSMC proliferation was significantly ameliorated, and elevated CRP, Ox-LDL, and lipid profiles were also restored to those of shams in VETD. These findings strongly support the idea that diabetes induces Ox-LDL-mediated oxidative stress and VSMC proliferation in aorta of rat and imply that vitamin E has a strong protective effect as an antioxidant


Subject(s)
Diabetes Mellitus , Lipoproteins, LDL , Oxidation-Reduction , Aorta , Rats, Wistar , Lipids , C-Reactive Protein , Muscle, Smooth, Vascular , Cell Proliferation , Protective Agents
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