Key result
Treatment with Yiqi Tongyang increased HCN4 protein expression, phosphorylation, and PKA activity in rabbit sinoatrial node cells damaged by ischemia-reperfusion compared to the model group.
Why the study?
Does Yiqi Tongyang increase HCN4 protein expression and phosphorylation in rabbit sinoatrial node cells damaged by ischemia-reperfusion?
Does Yiqi Tongyang increase HCN4 protein expression and phosphorylation in rabbit sinoatrial node cells damaged by ischemia-reperfusion?
Yiqi Tongyang increases HCN4 protein expression and phosphorylation in damaged rabbit sinoatrial node cells, suggesting a potential molecular mechanism for its use in treating sick sinus syndrome.
Answers are grounded in this paper and cite their sources.
May guide preclinical development of Yiqi Tongyang for sick sinus syndrome; leaves open human translation from this rabbit model.
The hyperpolarization-activated cyclic nucleotide-gated cation channel (I f ) is closely associated with sinoatrial node pacing function. The present study aimed to investigate the molecular mechanisms involved in pacing function improvements of damaged sinoatrial node cells and the consequent treatment effects on sick sinus syndrome (SSS) after the use of Yiqi Tongyang. HCN4 channel protein expression and phosphorylation were measured by immunoblotting and fluorescent quantitation. After ischemia-reperfusion injury (model group), the HCN4 protein and the optical density (OD) of the phosphorylated HCN4 protein as well as intracellular PKA activity in the sinoatrial node cells decreased significantly. However, the OD values and PKA activity increased to different degrees after treatment with serum containing different doses of Yiqi Tongyang; in contrast, no significant improvement was seen in the control group compared to the model group. These findings demonstrated that the use of the traditional Chinese medicine Yiqi Tongyang could increase HCN4 protein expression and phosphorylation as well as PKA activity within sinoatrial node cells damaged by ischemia-reperfusion. The HCN4 protein is involved in the I f -related ion channel. Here, we speculated that these effects could be associated with upregulation of HCN4 protein phosphorylation, which consequently improved cell automaticity, increased heart rate, and had treatment effects on SSS.
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Liu et al. (2016) studied Ischemia-reperfusion injury / Sick sinus syndrome. Yiqi Tongyang vs. Model group (ischemia-reperfusion injury without treatment) was evaluated on HCN4 protein expression, phosphorylation, and intracellular PKA activity. Treatment with Yiqi Tongyang increased HCN4 protein expression, phosphorylation, and PKA activity in rabbit sinoatrial node cells damaged by ischemia-reperfusion compared to the model group.
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