Shi Ya-Hong, Ren Jian-Xun, Liu Jian-Xun, Huang Ting-Ting, Hao Ting-Ting, Wang Min, Li Jun-Mei, Lin Cheng-Ren, Ren Jun-Guo
Beijing Key Laboratory of Pharmacology of Chinese Materia Medica, Institute of Basic Medical Sciences of Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing 100091, China.
Zhongguo Zhong Yao Za Zhi. 2018 Aug;43(16):3341-3345. doi: 10.19540/j.cnki.cjcmm.20180522.006.
Blood stasis syndrome is the pre-state of thrombotic disease. The model of blood stasis syndrome in rats was induced by sleep deprivation to study on effects of blood stasis syndrome on platelet activation. The weight, the color of tongue and hemorheology for the blood stasis syndrome of Chinese medicine were measured after modeling. The release of platelet granules and platelet activation factors in plasma were detected by ELISA kit related indicators to provide experimental basis for platelet function evaluation and related drug effects in syndrome research. The results showed that the weight of the model group rats was significantly lower than that of the normal group (<0.01). The tongue showed a dark purple blood stasis pattern, and the R, G and B values of the tongue surface in model group were significantly lower than those of the normal group (<0.01). The hemorheological parameters including high shear, middle shear and low shear viscosity in whole blood were significantly higher than those in the normal group (<0.01). But plasma viscosity did not change significantly. The release levels of platelet α particles (GMP-140, -TG, PF4) and dense particles (ADP, 5-HT) were significantly higher than those in the normal group (<0.01). The levels of TXB₂ and 6-keto-PGF₁α in plasma were significantly higher than those in the normal group (<0.01). The ratios of TXB₂ and 6-keto-PGF₂α were also significantly higher than those in the normal group (<0.01). The levels of PAF in plasma in model group were significantly higher than those in the normal group (<0.01). It was concluded that platelet functions could be changed induced by sleep deprivationin rats with blood stasis syndrome, and there might be inflammation and endothelial cell dysfunction.
血瘀证是血栓性疾病的前期状态。通过睡眠剥夺诱导大鼠血瘀证模型,以研究血瘀证对血小板活化的影响。造模后测量中医血瘀证大鼠的体重、舌色及血液流变学指标。采用ELISA试剂盒检测血浆中血小板颗粒及血小板活化因子相关指标的释放,为证候研究中血小板功能评价及相关药物疗效提供实验依据。结果显示,模型组大鼠体重显著低于正常组(<0.01)。舌象呈现暗紫色血瘀表现,模型组舌面R、G、B值显著低于正常组(<0.01)。全血高切、中切、低切黏度等血液流变学参数显著高于正常组(<0.01),但血浆黏度无明显变化。血小板α颗粒(GMP-140、-TG、PF4)及致密颗粒(ADP、5-HT)释放水平显著高于正常组(<0.01)。血浆TXB₂和6-keto-PGF₁α水平显著高于正常组(<0.01)。TXB₂与6-keto-PGF₂α比值也显著高于正常组(<0.01)。模型组血浆PAF水平显著高于正常组(<0.01)。结论为,睡眠剥夺可诱导血瘀证大鼠血小板功能发生改变,可能存在炎症及内皮细胞功能障碍。