Key result
Xueshuan Xinmaining Tablet ameliorated blood stasis in rat models by reducing blood viscosity and inhibiting platelet aggregation through regulation of F13a1, Car1, and Tbxa2r expression.
Why the study?
Does Xueshuan Xinmaining Tablet ameliorate blood stasis in rat models of cold coagulation?
Does Xueshuan Xinmaining Tablet ameliorate blood stasis in rat models of cold coagulation?
Xueshuan Xinmaining Tablet improves blood stasis in rat models by modulating coagulation parameters and regulating F13a1, Car1, and Tbxa2r gene expression.
Should not change clinical practice; leaves open translation of Xueshuan Xinmaining Tablet effects to human blood stasis.
Xueshuan Xinmaining Tablet (XXT), the Chinese formula, has long been administered in clinical practice for the treatment of cerebral thrombosis and coronary heart disease. In this study, we aimed to study the effect and the molecular mechanism of activating blood circulation and removing blood stasis. Rat models of cold coagulation blood stasis were induced with ice-water bath and epinephrine to assess the amelioration of blood stasis by XXT. Microarray technique was used to identify gene expression from the model and XXT-treated rats. In addition, Quantitative Real-Time PCR (qPCR) was performed to verify the microarray results. The results showed that XXT had a good therapeutic effect on blood stasis by reducing the whole blood viscosity (WBV), plasma viscosity (PV), increasing PT, APTT and TT, and by inhibiting platelet aggregation. Genes were differentially expressed in rats among the model group and the XXT-pretreated groups. XXT ameliorated blood stasis by regulating the expressions of F13a1, Car1, and Tbxa2r.
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Zhang et al. (2015) studied blood stasis. Xueshuan Xinmaining Tablet (XXT) vs. model group was evaluated on blood stasis amelioration. Xueshuan Xinmaining Tablet ameliorated blood stasis in rat models by reducing blood viscosity and inhibiting platelet aggregation through regulation of F13a1, Car1, and Tbxa2r expression.
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