郑州大学学报(医学版)
鄭州大學學報(醫學版)
정주대학학보(의학판)
JOURNAL OF ZHENGZHOU UNIVERSITY(MEDICAL SCIENCES)
2013年
4期
459-462,463
,共5页
高秀艳%宋士军%崔同%王腾腾%李朝苹%田粟
高秀豔%宋士軍%崔同%王騰騰%李朝蘋%田粟
고수염%송사군%최동%왕등등%리조평%전속
阿魏酸%胸主动脉环%舒张作用%机制%大鼠
阿魏痠%胸主動脈環%舒張作用%機製%大鼠
아위산%흉주동맥배%서장작용%궤제%대서
ferulic acid%thoracic aortic ring%vasodilatation effect%mechanism%rat
目的:探讨阿魏酸( FA)对大鼠离体胸主动脉环的舒张作用。方法:采用离体血管灌流法,检测FA对去氧肾上腺素( PE )和KCl 预收缩大鼠离体胸主动脉环的舒张作用,观察去内皮或L-亚硝基精氨酸甲基酯( L-NAME)、亚甲蓝(MB)、吲哚美辛(Indo)、格列苯脲(Gli)、四乙基胺(TEA)孵育后舒张作用的变化;并观察在无钙K-H液中FA对PE诱发动脉环收缩作用的影响。结果:FA具有浓度依赖性地舒张PE和KCl预收缩的胸主动环的作用;完整内皮组和去内皮组的舒张作用的pD2分别为2.62±0.08和2.60±0.09(Z=0.447,P=0.655),与各种受体阻断剂孵育后FA的舒张作用间差异无统计学意义(P>0.05)。 FA可明显抑制PE诱发的依外Ca2+性收缩反应(FFA =134.517,P<0.001)和依内Ca2+性收缩反应(F=108.816,P<0.001)。结论:FA具有舒张动脉环作用,其机制与抑制平滑肌细胞内Ca2+的释放和外Ca2+内流有关,其中考虑以抑制细胞内Ca2+的释放为主。
目的:探討阿魏痠( FA)對大鼠離體胸主動脈環的舒張作用。方法:採用離體血管灌流法,檢測FA對去氧腎上腺素( PE )和KCl 預收縮大鼠離體胸主動脈環的舒張作用,觀察去內皮或L-亞硝基精氨痠甲基酯( L-NAME)、亞甲藍(MB)、吲哚美辛(Indo)、格列苯脲(Gli)、四乙基胺(TEA)孵育後舒張作用的變化;併觀察在無鈣K-H液中FA對PE誘髮動脈環收縮作用的影響。結果:FA具有濃度依賴性地舒張PE和KCl預收縮的胸主動環的作用;完整內皮組和去內皮組的舒張作用的pD2分彆為2.62±0.08和2.60±0.09(Z=0.447,P=0.655),與各種受體阻斷劑孵育後FA的舒張作用間差異無統計學意義(P>0.05)。 FA可明顯抑製PE誘髮的依外Ca2+性收縮反應(FFA =134.517,P<0.001)和依內Ca2+性收縮反應(F=108.816,P<0.001)。結論:FA具有舒張動脈環作用,其機製與抑製平滑肌細胞內Ca2+的釋放和外Ca2+內流有關,其中攷慮以抑製細胞內Ca2+的釋放為主。
목적:탐토아위산( FA)대대서리체흉주동맥배적서장작용。방법:채용리체혈관관류법,검측FA대거양신상선소( PE )화KCl 예수축대서리체흉주동맥배적서장작용,관찰거내피혹L-아초기정안산갑기지( L-NAME)、아갑람(MB)、신타미신(Indo)、격렬분뇨(Gli)、사을기알(TEA)부육후서장작용적변화;병관찰재무개K-H액중FA대PE유발동맥배수축작용적영향。결과:FA구유농도의뢰성지서장PE화KCl예수축적흉주동배적작용;완정내피조화거내피조적서장작용적pD2분별위2.62±0.08화2.60±0.09(Z=0.447,P=0.655),여각충수체조단제부육후FA적서장작용간차이무통계학의의(P>0.05)。 FA가명현억제PE유발적의외Ca2+성수축반응(FFA =134.517,P<0.001)화의내Ca2+성수축반응(F=108.816,P<0.001)。결론:FA구유서장동맥배작용,기궤제여억제평활기세포내Ca2+적석방화외Ca2+내류유관,기중고필이억제세포내Ca2+적석방위주。
Aim:To investigate the vasodilatation effects and mechanism of ferulic acid ( FA) on isolated thoracic aor-tic rings from rats .Methods: Using isolated vascular methods , the vasodilatation effects of accumulated FA on thoracic aortic rings preconstricted with L-phenylephrine hydrochloride (PE) and KCl were observed.After the isolated thoracic aortic rings were pretreated with removing the endothelium , or pretreated with the drugs , the changes of vasodilatation effects were observed .And in Ca2+-free K-H solution, the influence of FA on thoracic aortic rings proconstricted with PE was observed .Results:With the increasing concentration , FA increased the vasodilatation effects of vascular aortic rings in a dose-dependent manner .The values of pD2 of endothelial groups and the endothelial-denuded group were 2.62 ±0.08, 2.60 ±0.93, respectively (Z=0.447,P=0.655).Compared with them, there was no significant changes after incubation with the drugs of L-NAME, Indo, Gli, TEA, or MB ( P>0.05).In addition, FA inhibited PE-induced contraction in Ca2+-free K-H solution(FFA =134.517,P<0.001).In Ca2+-depleted, PE-treated aortic rings, FA inhibited the Ca2+-in-duced contraction in a concentration-dependent manner (F=108.816,P<0.001).Conclusion: These results indicate that FA relaxes the thoracic aortic rings of rats in an endothelium-indepedended manner , and the vasorelaxing effect of FA might be mediated mainly through inhibiting Ca 2+release from intracellular stores and extracellular Ca 2+influx into vascular smooth muscle cells .