中国药理学通报
中國藥理學通報
중국약이학통보
CHINESE PHARMACOLOGICAL BULLETIN
2014年
7期
956-960
,共5页
王政%蒋嘉烨%可燕%江永波%魏莉%王佑华
王政%蔣嘉燁%可燕%江永波%魏莉%王祐華
왕정%장가엽%가연%강영파%위리%왕우화
三七花%总皂苷%血管舒张%抑制剂%一氧化氮合酶%环氧合酶
三七花%總皂苷%血管舒張%抑製劑%一氧化氮閤酶%環氧閤酶
삼칠화%총조감%혈관서장%억제제%일양화담합매%배양합매
flower of Panax notoginseng%saponins%vasodilation%inhibitors%nitric oxide synthase%cyclooxy-genase
目的:研究三七花总皂苷对大鼠离体胸主动脉的舒张作用,探讨其可能机制。方法提取分离得到三七花总皂苷,利用指纹图谱说明其成分;分离SD大鼠胸主动脉,采用离体血管环实验,观察三七花总皂苷对血管环基础状态,高浓度K+溶液预收缩及苯肾上腺素(phenylephrine,PE)预收缩引起的舒缩功能的反应,并结合不同抑制剂处理,探讨三七花总皂苷作用血管环的可能机制。结果累计浓度的三七花总皂苷对基础状态血管无明显影响;对高浓度K+预收缩的血管环对内皮完整最大舒张率可达23.6%;对PE预收缩的血管环在有无内皮完整差异有统计学意义,三七花总皂苷内皮完整的情况下最大舒张率可达55.51%;无钙液与皂苷培育的血管环对PE预收缩有明显的收缩抑制作用;对一氧化氮合酶抑制剂L-NAME孵育血管环后能明显抑制三七花总皂苷扩血管的作用;对环氧合酶抑制剂吲哚美辛孵育血管环后能明显抑制三七花总皂苷扩血管的作用。结论三七花总皂苷引起离体大鼠胸主动脉的舒张作用途径:内皮依耐性舒张主要与激活氧化氮合酶途径与激活环氧合酶途径有关。
目的:研究三七花總皂苷對大鼠離體胸主動脈的舒張作用,探討其可能機製。方法提取分離得到三七花總皂苷,利用指紋圖譜說明其成分;分離SD大鼠胸主動脈,採用離體血管環實驗,觀察三七花總皂苷對血管環基礎狀態,高濃度K+溶液預收縮及苯腎上腺素(phenylephrine,PE)預收縮引起的舒縮功能的反應,併結閤不同抑製劑處理,探討三七花總皂苷作用血管環的可能機製。結果纍計濃度的三七花總皂苷對基礎狀態血管無明顯影響;對高濃度K+預收縮的血管環對內皮完整最大舒張率可達23.6%;對PE預收縮的血管環在有無內皮完整差異有統計學意義,三七花總皂苷內皮完整的情況下最大舒張率可達55.51%;無鈣液與皂苷培育的血管環對PE預收縮有明顯的收縮抑製作用;對一氧化氮閤酶抑製劑L-NAME孵育血管環後能明顯抑製三七花總皂苷擴血管的作用;對環氧閤酶抑製劑吲哚美辛孵育血管環後能明顯抑製三七花總皂苷擴血管的作用。結論三七花總皂苷引起離體大鼠胸主動脈的舒張作用途徑:內皮依耐性舒張主要與激活氧化氮閤酶途徑與激活環氧閤酶途徑有關。
목적:연구삼칠화총조감대대서리체흉주동맥적서장작용,탐토기가능궤제。방법제취분리득도삼칠화총조감,이용지문도보설명기성분;분리SD대서흉주동맥,채용리체혈관배실험,관찰삼칠화총조감대혈관배기출상태,고농도K+용액예수축급분신상선소(phenylephrine,PE)예수축인기적서축공능적반응,병결합불동억제제처리,탐토삼칠화총조감작용혈관배적가능궤제。결과루계농도적삼칠화총조감대기출상태혈관무명현영향;대고농도K+예수축적혈관배대내피완정최대서장솔가체23.6%;대PE예수축적혈관배재유무내피완정차이유통계학의의,삼칠화총조감내피완정적정황하최대서장솔가체55.51%;무개액여조감배육적혈관배대PE예수축유명현적수축억제작용;대일양화담합매억제제L-NAME부육혈관배후능명현억제삼칠화총조감확혈관적작용;대배양합매억제제신타미신부육혈관배후능명현억제삼칠화총조감확혈관적작용。결론삼칠화총조감인기리체대서흉주동맥적서장작용도경:내피의내성서장주요여격활양화담합매도경여격활배양합매도경유관。
Aim To investigate the vasorelaxation effects of saponins from flower of Panax notoginsen on the isolated thoracica aorta ,and to explore its possible mechanism.Methods Total saponins were extracted and high phase liquid chromatography was utilized to describe saponins ingredients;SD rat thoracic aortas were isolated.In vitro vascular ring experiment was used to observe,basal state of saponins on vascular ring,and high concentrations of K+solution pre-con-traction and phenylephrine (PE ) pre-contraction caused by systolic and diastolic function of the re-sponse.And different inhibitors were combined to ex-amine the possible mechanism of notoginsenoside in vascular ring.Results Cumulative concentration of saponins had no significant effect on the basis of state vessels,but had significant effect on endothelium-in-tact aortic (MAX Relaxation 23.6%) rings pre-con-tracted by high concentrations of K+;endothelium and endothelial aortia had significant effect on PE pre-con-traction, and endothelium MAX relaxation was 55.5 1%.Calcium-free solution and saponin cultivated aortic rings significantly inhibited pre-contraction.Af-ter nitric oxide synthase inhibitor L-NAME and indom-ethacin incubating vascular ring ,it could significantly inhibited vasodilatory effect of saponin.Conclusion Saponins have concentration dependent diastolic func-tion on rat thoracic aorta,and its main ways cause vas-odilation.Endothelial dependent diastolic function is related to activation of nitric oxide synthase and cy-clooxygenase pathway.