二十二碳六烯酸对低氧性肺血管收缩的影响及机制
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国家自然科学基金(81170279);江苏省自然科学基金(BK2010335;BK2011486);江苏省科教兴卫工程(LJ201116);镇江市心血管病重点实验室资助项目(SS2012002)


Effects of Doeosahexecnoic Acid on Hypoxic Pulmonary Vasoconstriction and Its Mechanism
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    目的 探讨二十二碳六烯酸(DHA)对大鼠低氧性肺血管收缩的影响及电生理机制。方法 12只雄性SD大鼠随机分为两组:低氧组和低氧+DHA组。将大鼠三级肺动脉制备成去除内皮的血管环,急性缺氧溶液诱导血管环收缩后用二十二碳六烯酸处理血管环,测定其舒张血管的作用。建立大鼠肺动脉平滑肌细胞全细胞膜片钳法并观察二十二碳六烯酸对肺动脉平滑肌细胞膜上钾离子通道的作用。结果 二十二碳六烯酸(1 μmol/L、10 μmol/L)可显著舒张急性缺氧诱发的血管收缩(P<0.05,n6),最大舒张率为48.63%±9.16%。二十二碳六烯酸可显著激活总钾离子电流(P<0.01)。在指令电位+60 mV时,细胞外给予10 μmol/L 二十二碳六烯酸后,该电流由121.52±17.43 pA/pF增加至209.81±12.57 pA/pF。该钾电流为混合电流,能被蝎毒素和4-氨基吡啶部分阻断。二十二碳六烯酸(10 μmol/L)对肺动脉平滑肌细胞大电导钙激活的钾离子通道可产生显著激活作用(P<0.05,n6),指令电压+60 mV时的增加率是125.21%±5.62%;对电压门控钾通道可产生显著抑制作用(P<0.05,n6),指令电压+60 mV时的抑制率是63.21%±7.32%。结论 二十二碳六烯酸可通过开放大电导钙激活的钾离子通道而舒张急性缺氧引起的肺血管收缩。

    Abstract:

    Aim To study the effects of doeosahexecnoic acid (DHA) on hypoxic pulmonary vasoconstriction (HPV) and its mechanism. Methods Pulmonary arteries were cut by 2 to 3 mm for vascular rings. Following the vascular constriction induced by acute hypoxia, DHA was administrated and the relaxing forces were measured without endothelia. Using the whole cell patch-clamp technique in freshly isolated pulmonary artery smooth muscle cells, the effects of DHA on total K currents, the large conductance Ca2+-activated K (BKCa) and voltage gated K currents were recorded. Results DHA relaxed vascular ring tone without endothelia (P<0.05). DHA could significantly activate total K currents in pulmonary artery smooth muscle cells (P<0.01). It also greatly enhanced BKCa currents (P<0.05) and at a testing potential of +60 mV, 125.21%±5.62%of BKCa currents were increased. In contrast, DHA inhibited K currents and at a testing potential of +60 mV, 63.21%±7.32% of K currents were decreased. Conclusion DHA can activate BKCa channels and relax the vascular constriction induced by acute hypoxia.

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刘培晶,陈 蕊,严金川,王中群.二十二碳六烯酸对低氧性肺血管收缩的影响及机制[J].中国动脉硬化杂志,2013,21(08):680~684.

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  • 收稿日期:2013-03-24
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