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焦亚硫酸钠对大鼠血管的舒张作用及其机制

The vasodilator effect and its mechanisms of sodium metabisulfite on rat artery

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【作者】 杨振华冯燕张月霞张全喜孟紫强董川

【Author】 YANG Zhenhua;FEN Yan;ZHANG Yuexia;ZHANG Quanxi;MENG Ziqiang;DONG Chuan;Institute of Environmental Science, Shanxi University;

【机构】 山西大学环境科学研究所

【摘要】 <正>焦亚硫酸钠(SMB)作为一种常见的食品添加剂,在食品行业应用广泛。本文研究了SMB对去甲肾上腺素(NE)预激的离体大鼠血管环的舒张效应,同时对其可能涉及的K离子通道舒张机制进行了研究。结果表明:(1)SMB可以浓度依赖性的舒张NE预激的大鼠血管环(未去内皮,EC50为830±97μmol·L-1;去内皮,EC50为1087±139μmol·L-1)。(2)在低浓度下SMB诱导的舒张效应是内皮依赖性的,且其最大舒张率约为20%,然而高浓度下SMB诱导的舒张效应与内皮无关,且其舒张率可达90%以上。(3)四乙基氯化铵(TEA,非特异性钾离子通道阻断

【Abstract】 Sodium metabisulfite(SMB) is most commonly used as a food additives. In the present paper, the vasodilator effects of SMB and roles of K+ channels on isolated rat aortic rings were studied. The results show that:(1) SMB could relax isolated aortic rings precontracted by norepinephrine in a concentration-dependent manner for both endothelium-intact(EC50, 830 ± 97 μmol·L-1) and endothelium-denuded aortic rings(EC50, 1087 ± 139 μmol·L-1).(2)The maximal endotheliumdependent vasorelaxation was approximately 20% whereas that not depending on the presence of the endothelium was more than 90%.(3) The SMB induced vasorelaxation was partically inhibited by tetraethylammonium(TEA, the inhibitor of non-specific K+ channel).(4) The vasorelaxation of 1000 μM SMB was partially inhibited by glibenclamide(the inhibitor of ATP-sensitive K+(KATP)channel).(5) The vasorelaxant effects induced by 50 or 200 μmol·L-1 SMB were partially inhibited by iberiotoxin(Ib Tx, the inhibitor of big-conductance Ca2+-activated K+ channel(BKCa). These results led to the conclusions that the vasorelaxation of SMB at low concentrations(<400 μmol·L-1) was endothelium-dependent and mediated by BKCa channel, but at high concentrations(>500 μmol·L-1) was endothelium-independent and mediated by KATP channel.

  • 【会议录名称】 2015年第十四届全国应用化学年会论文集(下)
  • 【会议名称】2015年第十四届全国应用化学年会
  • 【会议时间】2015-07-21
  • 【会议地点】中国江西南昌
  • 【分类号】TS202.3;TS201.4
  • 【主办单位】中国化学会应用化学学科委员会
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