Key result
Intramyocardial injection of rAAV-asPLB down-regulated PLB protein expression and improved left ventricular function compared to saline in rats with streptozotocin-induced diabetes.
Why the study?
Does phospholamban antisense RNA improve SR Ca2+-ATPase activity and left ventricular function in STZ-induced diabetic rats?
Does phospholamban antisense RNA improve SR Ca2+-ATPase activity and left ventricular function in STZ-induced diabetic rats?
In a diabetic rat model, gene therapy with phospholamban antisense RNA improved sarcoplasmic reticulum calcium handling and left ventricular function.
Answers are grounded in this paper and cite their sources.
Hypothesis-generating for PLB-targeted gene therapy in diabetic cardiomyopathy; leaves open clinical translation.
OBJECTIVE: To study the effect of phospholamban antisense RNA (asPLB) on sarcoplasmic reticulum Ca2+-ATPase activity and cardiac function in rats with diabetes mellitus (DM) mediated by recombinant adeno-associated virus (rAAV) vector. METHODS: Six weeks after the induction of DM by streptozotocin injected intraperitoneally, the rats were divided into three groups, namely: DM-rAAV-asPLB group, DM-saline group and DM group (control group). The rats in the DM-rAAV-asPLB group were intramyocardially injected with rAAV-asPLB, the rats in the DM-saline group were injected with saline, and those in the control group did not receive any treatment. Six weeks after gene transfer, the expressions of PLB protein and PLB phosphorylation were detected by Western-blot, while the activity of sarcoplasmic reticulum (SR) Ca2+-ATPase and left ventricular function were measured. RESULTS: The PLB protein expression level was significantly higher whereas the PLB phosphorylation, SR Ca2+-ATPase activity and left ventricular function were significantly lower in the DM-saline group than in the control group. No significant difference was found in PLB protein expression level, PLB phosphorylation or SR Ca2+-ATPase activity between the DM-rAAV-asPLB group and the control group. The left ventricular function in the DM-rAAV-asPLB group was poorer than in the control group and was better than in the DM-saline group. CONCLUSION: rAAV-asPLB can down-regulate PLB protein expression and up-regulate PLB phosphorylation and SR Ca2+-ATPase activity, thus contributing to the improvement of in vivo left ventricular function.
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Li et al. (2013) studied Diabetes mellitus. rAAV-asPLB vs. Saline and no treatment was evaluated on PLB protein expression, PLB phosphorylation, SR Ca2+-ATPase activity, and left ventricular function. Intramyocardial injection of rAAV-asPLB down-regulated PLB protein expression and improved left ventricular function compared to saline in rats with streptozotocin-induced diabetes.
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