Jin Fan-Mao, Wang Mei, Wu Xiu-Mei, Xiao Huai, Wang De-Xiao, Wang Guang-Ming, Zhang Cheng-Gui, Zhao Hai-Rong
Lishui City People's Hospital, Lishui, Zhejiang 323000, People's Republic of China.
These authors contributed equally to this work.
Iran J Basic Med Sci. 2022 Jul;25(7):822-826. doi: 10.22038/IJBMS.2022.63219.13962.
This study aimed to investigate the potential effects of wasp venom (WV) from on antithrombosis in rats with inferior vena cava (IVC) thrombosis.
The thrombosis rat model was established by improving the IVC stenosis, in which rats were subjected to IVC ligation for 75 min. Rats were administered argatroban (IP) or WV (s.c.) for 4 hr after IVC thrombosis. The weight, inhibition rate, and pathological morphology of the thrombosis induced by IVC ligation and the variation in four coagulation parameters, coagulation factors, and CD61+CD62P+ were simultaneously determined in IVC rats.
The thrombus formed as a result of IVC ligation was stable. Compared with the control group, the weight of the thrombus was significantly reduced in the argatroban group. Thrombus weight was reduced by treatment with 0.6, 0.2, and 0.05 mg/kg WV, with inhibition rates of 52.19%, 35.32%, and 28.98%, respectively. Inflammatory cells adhered to and infiltrated the vessel wall in the IVC group more than in the sham group. However, the pathological morphology and CD61+CD62P+ of the WV treatment groups tended to be normal.
We improved the model of IVC thrombosis to be suitable for evaluation of antithrombotic drugs. Our findings demonstrated that WV could inhibit IVC thrombosis associated with reducing coagulation factors V and CD61+CD62p expression in rats.
本研究旨在探讨黄蜂毒液(WV)对下腔静脉(IVC)血栓形成大鼠抗血栓形成的潜在作用。
通过改进IVC狭窄建立血栓形成大鼠模型,将大鼠的IVC结扎75分钟。IVC血栓形成后4小时,给大鼠腹腔注射阿加曲班(IP)或皮下注射WV。同时测定IVC结扎诱导的血栓形成的重量、抑制率和病理形态,以及IVC大鼠的四个凝血参数、凝血因子和CD61 + CD62P +的变化。
IVC结扎形成的血栓稳定。与对照组相比,阿加曲班组的血栓重量显著降低。用0.6、0.2和0.05mg/kg WV治疗可降低血栓重量,抑制率分别为52.19%、35.32%和28.98%。与假手术组相比,IVC组炎性细胞黏附并浸润血管壁的情况更严重。然而,WV治疗组的病理形态和CD61 + CD62P +趋于正常。
我们改进了IVC血栓形成模型以适用于抗血栓药物的评估。我们的研究结果表明,WV可通过降低大鼠凝血因子V和CD61 + CD62p表达来抑制IVC血栓形成。