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作 者:武哲丽[1] 陈群[1] 刘梅[1] 莫传伟[1] 王剑[1] 路艳[1]
机构地区:[1]广州中医药大学,广州510006
出 处:《中华中医药杂志》2011年第8期1878-1880,共3页China Journal of Traditional Chinese Medicine and Pharmacy
基 金:国家"十一五"科技支撑计划课题(No.2006BAI08B01-3);广东省科技计划项目(No.2009B060700121)~~
摘 要:目的:从分子水平探讨肝病患者不同血瘀证及其形成的病理机制。方法:采用前瞻性研究的方法进行肝病瘀血舌患者血液血栓素B2(TXB2)、6-酮-前列腺素F1α(6-keto-PGF1α)的测定。结果:肝病各组的TXB2显著增高(P<0.01),6-keto-PGF1α显著降低(P<0.05,P<0.01)。TXB2/6-keto-PGF1α显著增高(P<0.01);不同肝病血瘀证组与正常组的TXB2、6-keto-PGF1α、TXB2/6-keto-PGF1α的比较有显著性差异(P<0.01),湿热瘀滞、肝瘀痰阻、气滞血瘀的TXB2、6-keto-PGF1α、TXB2/6-keto-PGF1α与气虚血瘀组比较有显著差异(P<0.01)。结论:肝病及不同血瘀证组的TXB2与TXB2/6-keto-PGF1α显著增高,6-keto-PGF1α显著降低,说明血浆TXA2-PGI2平衡失调与血瘀证发生发展密切相关,通过测定TXB2、6-keto-PGF1α的含量可以反映肝病瘀血舌象及其不同血瘀证的发生机制。Objective:To explore the pathology mechanism of hepatopathy tongue of blood stasis(TBS)on molecule level.Methods:Tongue of blood stasis of hepatopathy TBS and blood stasis syndrome and mechanism of their formation were probed by means of the test of molecular and prospective study.Results:TXB2 and TXB2 /6-keto-PGF1α of all the hepatopathy group were risen significantly compared with normal group(P0.01),6-keto-PGF1α of all the hepatopathy group were sharp dropped compared with normal group(P0.01);On the indexes of TXB2 and TXB2 /6-keto-PGF1α,there was significant difference between BSS group and normal group(P0.01),there was very marked difference between Qi deficiency and blood stasis syndrome(QDBSS)and the others(P0.01).Conclusion:TXB2 and TXB2 /6-keto-PGF1α of all the hepatopathy group and BSS group are risen significantly compared with normal group,6-keto-PGF1α was dropped significantly,the balance inorder of TXA2 and PGI2 blood plasma is closely bound up with development and consequences of BSS,the content of TXB2 and 6-keto-PGF1α may reflect the mechanism of their formation between tongue of blood stasis of hepatopathy and blood stasis syndrome.
关 键 词:治未病 瘀血舌象 血栓素B2/6-酮-前列腺素F1α 实验研究
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