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参附注射液对血栓闭塞性脉管炎模型大鼠的保护作用。

Protective effect of Shenfu injection on thromboangiitis obliterans model rats.

机构信息

Department of Physiology, College of Medicine, Nanchang University, Nanchang 310006, China.

出版信息

J Ethnopharmacol. 2011 Nov 18;138(2):458-62. doi: 10.1016/j.jep.2011.09.033. Epub 2011 Sep 29.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

Thromboangiitis obliterans (TAO) or Buerger's disease is a non atherosclerotic, segmentar inflammatory vasculitis that is incurable at present. Shenfu injection (SFI), a traditional Chinese formulation, have been confirmed to produce protective influences on several organs and limb during ischemia and reperfusion (IR) injury in rats. However, the effects of SFI on TAO remain unclear.

MATERIALS AND METHODS

Adult male Sprague Dawley rats were randomly divided into sham operated group, TAO model group, SFI 2.5mg/kg (low dose), 5mg/kg (medium dose) and 10mg/kg (high dose) groups (n=8). Rats were intravenously administered SFI 2.5, 5 and 10mg/kg or saline once per day for 15 days. TAO model was prepared by injecting sodium laurate into the femoral artery of rats. Then we examined the changes of pathological signs, pathologic grading of thrombus, the indexes of hematology, the contents of thromboxane B2 (TXB2), 6-keto-prostaglandin F(lα) (6-K-PGF(1α)) in plasma following SFI or saline treatment.

RESULTS

More pathological signs of lesions, higher grades of pathological thrombosis, increased blood platelet counts, the increase in the TXB2 and TXB2/6-K-PGF(1α) ratio, as well as the decrease of 6-K-PGF(1α) in TAO model group were shown in present experiments; SFI treatment significantly improved the pathological signs of lesions induced by sodium laurate injection, reduced the numbers of thrombus formation, blood platelet counts, the TXB2 and TXB2/6-K-PGF(1α) ratio but increased the 6-K-PGF(1α) compared with TAO model group. However, there were no significant alterations in the counts of red blood cell, leucocyte and neutrophil among these groups.

CONCLUSIONS

Our preliminary findings first indicated that SFI can produce significant therapeutic effects on experimental Buerger's disease model rats in a dose independent manner. The underlying mechanisms may be due to its modifying hematology, inhibiting platelet aggregation and enhancing anti-thrombotic function of vessel endothelia.

摘要

民族药理学相关性

血栓闭塞性脉管炎(TAO)或伯格氏病是一种非动脉粥样硬化、节段性炎症性血管炎,目前无法治愈。参附注射液(SFI)是一种传统的中药制剂,已被证实对大鼠缺血再灌注(IR)损伤时的几个器官和肢体具有保护作用。然而,SFI 对 TAO 的影响尚不清楚。

材料和方法

成年雄性 Sprague Dawley 大鼠随机分为假手术组、TAO 模型组、SFI 2.5mg/kg(低剂量)、5mg/kg(中剂量)和 10mg/kg(高剂量)组(n=8)。大鼠每天静脉注射 SFI 2.5、5 和 10mg/kg 或生理盐水一次,共 15 天。通过向大鼠股动脉注射月桂酸钠制备 TAO 模型。然后,我们检查了 SFI 或生理盐水处理后病理征象、血栓病理分级、血液学指标、血浆血栓素 B2(TXB2)、6-酮-前列腺素 F1α(6-K-PGF1α)含量的变化。

结果

本实验中,TAO 模型组病变的病理征象较多,血栓病理分级较高,血小板计数增加,TXB2 和 TXB2/6-K-PGF1α 比值增加,6-K-PGF1α 减少;SFI 治疗能显著改善月桂酸钠注射引起的病变病理征象,减少血栓形成、血小板计数、TXB2 和 TXB2/6-K-PGF1α 比值,但增加 6-K-PGF1α 与 TAO 模型组比较。然而,这些组之间的红细胞、白细胞和中性粒细胞计数没有明显变化。

结论

我们的初步研究结果首次表明,SFI 能以剂量依赖的方式对实验性伯格氏病大鼠模型产生显著的治疗作用。其作用机制可能与其改变血液学、抑制血小板聚集和增强血管内皮抗血栓功能有关。

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