中国药理学通报
中國藥理學通報
중국약이학통보
CHINESE PHARMACOLOGICAL BULLETIN
2010年
3期
367-371
,共5页
杨景靠%冯国清%于爽%胡香杰
楊景靠%馮國清%于爽%鬍香傑
양경고%풍국청%우상%호향걸
巴戟天糖链%血管生成%心肌梗死%大鼠%血管内皮细胞生长因子%碱性成纤维细胞生长因子
巴戟天糖鏈%血管生成%心肌梗死%大鼠%血管內皮細胞生長因子%堿性成纖維細胞生長因子
파극천당련%혈관생성%심기경사%대서%혈관내피세포생장인자%감성성섬유세포생장인자
Morinda officinalis how oligosaccharides(MOO)%angiogenesis%acute myocardial infarction(AMI)%rats%vascular endothelial growth factor(VEGF)%basic fibroblast growth factor(bFGF)
目的 探讨巴戟天糖链(MOO)对急性心肌梗死(AMI) 大鼠缺血心肌治疗性血管生成的影响及其机制.方法 ♂ Wistar大鼠,结扎冠状动脉左前降支,成功制成AMI模型40只,随机分为MOO小、中、大剂量组、麝香保心丸组及模型组,每组8只.另取10只建立假手术组.药物治疗组分别灌胃给予巴戟天醇提物水溶性部分(0.7、1.4、2.8 mg·kg~(-1) ·d~(-1))及麝香保心丸悬浊液(30 mg·kg~(-1) ·d~(-1)),其余两组灌胃给予等量蒸馏水.连续灌胃6 wk后处死大鼠,心肌取材,应用免疫组织化学法检测大鼠缺血心肌Ⅷ因子及血管内皮细胞生长因子(vascular endothelial growth factor,VEGF)、碱性成纤维细胞生长因子(basic fibroblast growth factor,bFGF)蛋白表达情况;计算微血管密度(microvessec density,MVD),用图像分析软件测定VEGF及bFGF表达灰度值,并进行半定量分析.结果 与模型组相比,MOO中、大剂量组能增加缺血心肌MVD及VEGF、bFGF灰度值(P <0.05),但作用弱于麝香保心丸组(P <0.05);MOO 3个剂量组之间MVD差异均有显著性(P <0.05); MOO 3个剂量组之间VEGF灰度值差异均有显著性(P <0.05);MOO中、大剂量组bFGF灰度值与小剂量组相比差异有显著性(P <0.05).结论 MOO可促进AMI后大鼠缺血心肌的血管生成,其机制可能与上调缺血心肌VEGF、bFGF蛋白的表达有关.
目的 探討巴戟天糖鏈(MOO)對急性心肌梗死(AMI) 大鼠缺血心肌治療性血管生成的影響及其機製.方法 ♂ Wistar大鼠,結扎冠狀動脈左前降支,成功製成AMI模型40隻,隨機分為MOO小、中、大劑量組、麝香保心汍組及模型組,每組8隻.另取10隻建立假手術組.藥物治療組分彆灌胃給予巴戟天醇提物水溶性部分(0.7、1.4、2.8 mg·kg~(-1) ·d~(-1))及麝香保心汍懸濁液(30 mg·kg~(-1) ·d~(-1)),其餘兩組灌胃給予等量蒸餾水.連續灌胃6 wk後處死大鼠,心肌取材,應用免疫組織化學法檢測大鼠缺血心肌Ⅷ因子及血管內皮細胞生長因子(vascular endothelial growth factor,VEGF)、堿性成纖維細胞生長因子(basic fibroblast growth factor,bFGF)蛋白錶達情況;計算微血管密度(microvessec density,MVD),用圖像分析軟件測定VEGF及bFGF錶達灰度值,併進行半定量分析.結果 與模型組相比,MOO中、大劑量組能增加缺血心肌MVD及VEGF、bFGF灰度值(P <0.05),但作用弱于麝香保心汍組(P <0.05);MOO 3箇劑量組之間MVD差異均有顯著性(P <0.05); MOO 3箇劑量組之間VEGF灰度值差異均有顯著性(P <0.05);MOO中、大劑量組bFGF灰度值與小劑量組相比差異有顯著性(P <0.05).結論 MOO可促進AMI後大鼠缺血心肌的血管生成,其機製可能與上調缺血心肌VEGF、bFGF蛋白的錶達有關.
목적 탐토파극천당련(MOO)대급성심기경사(AMI) 대서결혈심기치료성혈관생성적영향급기궤제.방법 ♂ Wistar대서,결찰관상동맥좌전강지,성공제성AMI모형40지,수궤분위MOO소、중、대제량조、사향보심환조급모형조,매조8지.령취10지건립가수술조.약물치료조분별관위급여파극천순제물수용성부분(0.7、1.4、2.8 mg·kg~(-1) ·d~(-1))급사향보심환현탁액(30 mg·kg~(-1) ·d~(-1)),기여량조관위급여등량증류수.련속관위6 wk후처사대서,심기취재,응용면역조직화학법검측대서결혈심기Ⅷ인자급혈관내피세포생장인자(vascular endothelial growth factor,VEGF)、감성성섬유세포생장인자(basic fibroblast growth factor,bFGF)단백표체정황;계산미혈관밀도(microvessec density,MVD),용도상분석연건측정VEGF급bFGF표체회도치,병진행반정량분석.결과 여모형조상비,MOO중、대제량조능증가결혈심기MVD급VEGF、bFGF회도치(P <0.05),단작용약우사향보심환조(P <0.05);MOO 3개제량조지간MVD차이균유현저성(P <0.05); MOO 3개제량조지간VEGF회도치차이균유현저성(P <0.05);MOO중、대제량조bFGF회도치여소제량조상비차이유현저성(P <0.05).결론 MOO가촉진AMI후대서결혈심기적혈관생성,기궤제가능여상조결혈심기VEGF、bFGF단백적표체유관.
Aim To investigate the angiogenic promoting effect of Morinda officinalis How oligosaccharides(MOO) in the ischemic myocardium of rats after acute myocardial infarction(AMI).Methods 40 male Wistar rats were established into AMI model successfully and were randomly divided into 5 groups equally, i. e. the low, medium and high doses of MOO groups, the Shexiangbaoxin group and the model group. They were treated with different doses of the water fraction of the ethanolic extract of Radix morinda officinalis (0.7, 1.4, 2.8 mg·kg~(-1) ·d~(-1)), suspension liquid of Shexiangbaoxin Pill(30 mg·kg~(-1) ·d~(-1)) and distilled water with the same volume respectively.Besides, a sham operated group with 10 rats was set up for control. All rats were sacrificed after 6-week-treatment.The Ⅷ coagulation factor, vascular endothelial growth factor(VEGF) and basic fibroblast growth factor(bFGF) protein in ischemic myocardium of rats in each group were detected by immunohistochemistry assay.The microvessel density(MVD) was calculated. Gray values of protein expression of VEGF and bFGF in ischemic myocardium were calculated and analyzed by image analysis system.Results The MVD, the gray values of VGF and bFGF were higher in the medium and high doses of MOO groups than those in the model group(P <0.05), but still lower than those in the Shexiangbaoxin group(P <0.05). The MVD and the gray values of VEGF among 3 doses of MOO groups showed significant differences (P <0.05).Significant differences of gray value of bFGF were observed between small and middle doses of MOO groups, also between small and large doses of groups(P <0.05).Conclusion MOO can obviously promote angiogenesis in the ischemic myocardium of the rats after AMI.And up-regulating expressions of VEGF and bFGF protein in the ischemic myocardium may act as one of its angiogenic promoting mechanisms.