龙民慧, 朱泽轶, 王园园, 武立昌, 白喜龙, 刁爱坡, 王嘉玺, 邹民吉, 徐东刚. 重组SRH蛋白抑制SHR大鼠动脉粥样硬化发展的研究[J]. 华南师范大学学报(自然科学版), 2013, 45(5).
引用本文: 龙民慧, 朱泽轶, 王园园, 武立昌, 白喜龙, 刁爱坡, 王嘉玺, 邹民吉, 徐东刚. 重组SRH蛋白抑制SHR大鼠动脉粥样硬化发展的研究[J]. 华南师范大学学报(自然科学版), 2013, 45(5).
Inhibition effect of staphylokinase mutant SRH on the development of SHR rat's Atherosclerosis[J]. Journal of South China Normal University (Natural Science Edition), 2013, 45(5).
Citation: Inhibition effect of staphylokinase mutant SRH on the development of SHR rat's Atherosclerosis[J]. Journal of South China Normal University (Natural Science Edition), 2013, 45(5).

重组SRH蛋白抑制SHR大鼠动脉粥样硬化发展的研究

Inhibition effect of staphylokinase mutant SRH on the development of SHR rat's Atherosclerosis

  • 摘要: 利用SHR大鼠和正常WKY大鼠评价SRH,研究探讨融合蛋白SRH对高脂喂养诱导的自发性高血压症大鼠(Spontaneously hypertensive rat, SHR)动脉粥样硬化发展的影响.结果发现,正常大鼠和高脂喂养的SHR大鼠体外和体内均未见出血现象,重组SRH能够降低高脂喂养的SHR大鼠的血液凝血指标,减少血液中总胆固醇量,降低血压,减弱主动脉弓病变程度,对正常WKY大鼠则无任何影响.

     

    Abstract: The effect of SRH on development of atherosclerosis in SHR rats fed on high fat diet was investigated, in order to obtain reliable evidence for the possibility of further clinical application. SRH was taken intravenously by healthy rats and high fat diet SHR rats in the same dosage (0.5 mg/kg) for 20 days (once two days). The clinical hemorrhagic manifestations were observed and a set of hemostatic tests ( ATPP, PT, TT, Fg) , blood fat (TG, TC, LDL-C, HDL), and fibrinolytic systems tests (PLG, PI, FDP, D-D), electrocardiogram and blood pressure were monitored before and after injection. None of them showed visceral bleeding and gingival bleeding. There were no significant changes in WKY fibrinolytic and coagulative phases. It was supported that SRH was a highly selective fibrirolytic agent without significant influence on rat hemostatic and coagulatic systems. While, SRH can decrease the high thromboxane states of high diet fat SHR rats and the blood fat levels of high diet fat SHR rats, and it can release the blood pressure and weaken vessel wall lesion. The SRH is a relatively safe and well tolerated agent for healthy and atherosclerosis rats, and it contributes to inhibit the progression of SHR's atherosclerosis.

     

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