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Updated: Jun 18, 2026

Modeling and Evaluation of Murine Diabetic Cardiomyopathy Model
Published on: November 29, 2024
[Effect of BMSCs transplantation on cardiac function of diabetes mellitus rats]
Qinan Wu1, Wuquan Deng, Bing Chen
1Department of Endocrine, the First Affiliated Hospital of the Third Military Medical University, Chongqing, 400038, P.R. China.
Objective:
To observe the effect of BMSCs on the cardiac function in diabetes mellitus (DM) rats through injecting BMSCs into the ventricular wall of the diabetic rats and investigate its mechanism.
Methods:
BMSCs isolated from male SD rats (3-4 months old) were cultured in vitro, and the cells at passage 5 underwent DAPI labeling. Thirty clean grade SD inbred strain male rats weighing about 250 g were randomized into the normal control group (group A), the DM group (group B), and the cell transplantation group (group C). The rats in groups B and C received high fat forage for 4 weeks and the intraperitoneal injection of 30 mg/kg streptozotocin to made the experimental model of type II DM. PBS and DAPI-labeled passage 5 BMSCs (1 x 10(5)/microL, 160 microL) were injected into the ventricular wall of the rats in groups B and C, respectively. After feeding those rats with high fat forage for another 8 weeks, the apoptosis of myocardial cells was detected by TUNEL, the cardiac function was evaluated with multi-channel physiology recorder, the myocardium APPL1 protein expression was detected by Western blot and immunohistochemistry test, and the NO content was detected by nitrate reductase method. Group C underwent all those tests 16 weeks after taking basic forage.
Results:
In group A, the apoptosis rate was 6.14% +/- 0.02%, the AAPL1 level was 2.79 +/- 0.32, left ventricular -dP/dt (LV-dP/dt) was (613.27 +/- 125.36) mm Hg/s (1 mm Hg = 0.133 kPa), the left ventricular end-diastolic pressure (LVEDP) was (10.06 +/- 3.24) mm Hg, and the NO content was (91.54 +/- 6.15) nmol/mL. In group B, the apoptosis rate was 45.71% +/- 0.04%, the AAPL1 level 1.08 +/- 0.24 decreased significantly when compared with group A, the LV-dP/dt was (437.58 +/- 117.58) mm Hg/s, the LVEDP was (17.89 +/- 2.35) mm Hg, and the NO content was (38.91+/-8.67) nmol/mL. In group C, the apoptosis rate was 27.43% +/- 0.03%, the APPL1 expression level was 2.03 +/- 0.22, the LV -dP/dt was (559.38 +/- 97.37) mm Hg/s, the LVEDP was (12.55 +/- 2.87) mm Hg, and the NO content was (138.79 +/- 7.23) nmol/mL. For the above mentioned parameters, there was significant difference between group A and group B (P < 0.05), and between group B and group C (P < 0.05).
Conclusion:
BMSCs transplantation can improve the cardiac function of diabetic rats. Its possible mechanism may be related to the activation of APPL1 signaling pathway and the increase of NO content.
