机构地区:[1]河北北方学院微循环研究所基础医学院病理生理学教研室,河北张家口075029
出 处:《中国病理生理杂志》2012年第1期29-34,共6页Chinese Journal of Pathophysiology
基 金:国家自然科学基金资助项目(No.30770845);河北省自然科学基金资助项目(No.C2008000503);河北省教育厅科学研究重点项目(No.ZH2007101)
摘 要:目的:应用离体淋巴管灌流技术,观察一氧化氮(NO)在失血性休克(HS)大鼠离体淋巴管对P物质(SP)反应性双相变化中的作用。方法:Wistar雄性大鼠随机分为对照组(仅手术)和休克组(复制HS模型后分为shock 0.5 h、shock 2 h组)。在相应时点分离胸导管,制备淋巴管条,3 cmH2O跨壁压下行离体灌流,应用一氧化氮合酶(NOS)工具药分别孵育shock 0.5 h和shock 2 h的淋巴管。分别给予从低到高浓度的SP,测量淋巴管收缩末期口径、舒张末期口径、收缩频率(CF)和被动管径,计算收缩幅度(CA)、泵流分数(FPF)和紧张指数(TI),以给予SP前后淋巴管的CF、TI、CA和FPF的差值ΔCF、ΔTI、ΔCA和ΔFPF评价淋巴管对SP的反应性。结果:NO供体L-Arg可显著降低shock 0.5 h淋巴管对多个SP浓度点的ΔCF、ΔTI与ΔFPF;可溶性鸟苷酸环化酶抑制剂ODQ可显著抑制L-Arg的作用,在某些SP浓度点上,使ΔCF、ΔTI和ΔFPF显著高于shock 0.5 h+L-Arg组,ΔCF和ΔFPF高于对照组水平。NOS抑制剂L-NAME可提高shock 2 h淋巴管对多个SP浓度点的ΔCF、ΔTI与ΔFPF,且高于对照组水平;shock 2 h淋巴管与L-NAME和磷酸二酯酶抑制剂氨茶碱(AP)同时孵育后,在SP为1×10-8mol/L和3×10-8mol/L时,AP显著抑制了L-NAME的作用,使ΔCF、ΔTI与ΔFPF明显降低。结论:NO参与了休克淋巴管反应性的双相调节,其机制可能是通过环鸟苷酸实现的。AIM: To observe the role of nitric oxide(NO) in the reactivity of isolated lymphatics to substance P(SP),which presents a biphasic change,in the hemorrhagic shock(HS) rats with the technique of lymphatic perfusion in vitro.METHODS: Male Wistar rats were randomly divided into control group(surgical procedure only) and shock group(the rats were further divided into shock 0.5 h and shock 2 h groups after the HS model was established).A segment of lymphatics was pressed and perfused in vitro at transmural pressure of 3 cmH2O after thoracic ducts were separated from the rats at the corresponding time points in each group.The lymphatics of shock 0.5 h and shock 2 h were incubated with different drugs for changing the activity of No and nitric oxide synthase(NOS),respectively.The end-systolic diameter,end-diastolic diameter,contraction frequency(CF) and passive diameter of isolated lymphatics were measured,while the contraction amplitude(CA),tonic index(TI) and fractional pump flow(FPF) were calculated after stimulated with gradient SP.Different values between pre-and post-administration of SP in CF,CA,TI and FPF were calculated and expressed as ΔCF,ΔTI,ΔCA and ΔFPF for further assessing the reactivity of lymphatics.RESULTS: NO donor L-Arg reduced ΔCF,ΔTI and ΔFPF of 0.5 h-shocked lymphatics treated with different concentrations of SP.The effect of L-Arg was obviously suppressed by a soluble guanylate cyclase inhibitor ODQ.ΔCF,ΔTI and ΔFPF increased strikingly compared with shock 0.5 h+L-Arg group in the presence of SP at certain concentration,and ΔCF and ΔFPF increased remarkably compared with control group.NOS inhibitor L-NAME elevated ΔCF,ΔTI and ΔFPF of 2 h-shocked lymphatics treated with different concentrations of SP and the manifestation of lymphatics exceeded the values of control levels.In the experiment of 2 h-shocked lymphatics treated with L-NAME+phosphodiesterase inhibitor aminophylline(AP),the effect of L-NAME was suppressed significantly
分 类 号:R331.4[医药卫生—人体生理学] R322.26[医药卫生—基础医学]
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