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Granulocyte-Colony Stimulating Factor Reduces Cardiomyocyte Apoptosis and Ameliorates Diastolic Dysfunction in Otsuka Long-Evans Tokushima Fatty Rats
Authors:Jeong Hun Shin  Young-Hyo Lim  Yi-Sun Song  Byung-Im So  Jun-Young Park  Cheng-Hu Fang  Yonggu Lee  Hyuck Kim  Kyung-Soo Kim
Affiliation:1. Cardiology division, Department of Internal Medicine, Hanyang University College of Medicine, 222 Wangsipri Street, Sungdong-gu, Seoul, 133-792, Republic of Korea
2. Graduate School of Biomedical Science and Engineering, Hanyang University, Seoul, Republic of Korea
3. Department of Internal Medicine, College of Medicine, Yanbian University, Yanji, 133000, China
4. Department of Thoracic and Cardiovascular Surgery, Hanyang University College of Medicine, Seoul, Republic of Korea
Abstract:

Background

In recent studies, granulocyte-colony stimulating factor (G-CSF) was shown to improve cardiac function in myocardial infarction and non-ischemic cardiomyopathies. The mechanisms of these beneficial effects of G-CSF in diabetic cardiomyopathy are not yet fully understood. Therefore, we investigated the mechanisms of action of G-CSF on diabetic cardiomyopathy in a rat model of type 2 diabetes.

Methods

Seventeen-week-old OLETF (Otsuka Long Evans Tokushima Fatty) diabetic rats and LETO (Long Evans Tokushima Otuska) rats were randomized to treatment with 5 days of G-CSF (100 μg/kg/day) or with saline. Cardiac function was evaluated by serial echocardiography performed before and 4 weeks after treatment. We measured expression of the G-CSF receptor (GCSFR) and Bcl-2, as well as the extent of apoptosis in the myocardium.

Results

G-CSF treatment significantly improved cardiac diastolic function in the serial echocardiography assessments. Expression of G-CSFR was down-regulated in the diabetic myocardium (0.03?±?0.12 % vs. 1?±?0.15 %, p?p?p?p?Conclusions Our results suggest that G-CSF might have a cardioprotective effect in diabetic cardiomyopathy through up-regulation of G-CSFR, attenuation of apoptosis by up-regulation of Bcl-2 expression, and glucose-lowering effect. Our findings support the therapeutic potential of G-CSF in diabetic cardiomyopathy.
Keywords:
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