
FOLLOWUS
1. 1Department of Cardiology, the Fifth Hospital of Wuhan & Institute of Cardiovascular Sciences of Jianghan University, Wuhan 430050, China;
2. 2Department of Cardiology, the First Hospital of Yangtze University,Jingzhou, Hubei 434000, China
* Corresponding author Tel: 86-27-84812640, E-mail: leefenghong@gmail.com
收稿日期:2014-02-12,
网络出版日期:2015-04-20,
纸质出版日期:2015-04
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Impact of 1, 25-(OH)2D3 on Left Ventricular Hypertrophy in Type 2 Diabetic Rats△[J]. 中国医学科学杂志(英文版), 2015,30(2):114-120.
Fan Ying, Zhang Shan-xiao, Ren Meng, et al. Impact of 1, 25-(OH)2D3 on Left Ventricular Hypertrophy in Type 2 Diabetic Rats△[J]. Chinese medical sciences journal, 2015, 30(2): 114-120.
Impact of 1, 25-(OH)2D3 on Left Ventricular Hypertrophy in Type 2 Diabetic Rats△[J]. 中国医学科学杂志(英文版), 2015,30(2):114-120. DOI:
Fan Ying, Zhang Shan-xiao, Ren Meng, et al. Impact of 1, 25-(OH)2D3 on Left Ventricular Hypertrophy in Type 2 Diabetic Rats△[J]. Chinese medical sciences journal, 2015, 30(2): 114-120. DOI:
Objective
To investigate the impact of 1
25-(OH)
2
D
3
on left ventricular hypertrophy (LVH) in type 2 diabetic rats.
Methods
Type 2 diabetic mellitus (DM) model rats were established by intraperitoneally injecting with 30 mg/kg streptozotocin. After 8 weeks
19 male rats were identified as diabetic with left ventricular hypertrophy (LVH) by ultrasound examination
and randomly assigned into three groups: untreated (DM-LVH
n
=7)
treated with insulin (DM-LVH+INS
n
=6)
and treated with 1
25-(OH)
2
D
3
(DM-LVH+VD
n
=6). Healthy male rats were used as the controls group (
n
=6). The fasting blood glucose and the insulin level were determined weekly. The left ventricular mass index
myocardial collagen content
collagen volume fraction
and 1
25-(OH)
2
D
3
-receptor level were determined by 4 weeks later.
Results
In the DM-LVH model group
the insulin level was significantly decreased compared with the non-diabetic control group (
P
<
0.05)
whereas the blood glucose
left ventricular mass index
myocardial collagen content
collagen volume fraction
and 1
25-(OH)
2
D
3
-receptor expression were significantly increased (all
P
<
0.05). In the DM-LVH+INS and DM-LVH+VD groups
the insulin levels were significantly increased compared with the DM-LVH model group (
P
<
0.05)
whereas the other parameters were significantly decreased (all
P
<
0.05).
Conclusion
1
25-(OH)
2
D
3
could reverse LVH in diabetic rats and that the mechanism may involve stimulating insulin secretion and reducing blood glucose
via
direct up-regulation of 1
25-(OH)
2
D
3
-receptor expression.
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