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作 者:任俊杰[1,2] 王科科[1] 许慧玉[2] 黄婷娟 吕怡[1] 武冬梅[2] 张轩萍[2] 郑晓俊[3]
机构地区:[1]山西医科大学第一医院内科学教研室,山西太原030001 [2]山西医科大学药理学教研室,山西太原030001 [3]山西医科大学第一医院药学部,山西太原030001
出 处:《中国药理学通报》2017年第8期1131-1135,共5页Chinese Pharmacological Bulletin
基 金:山西省研究生教育创新项目(No 2016BY077);山西医科大学青年基金(No 02201514)
摘 要:目的本实验观察咪达唑仑(midazolam)对离体猪冠状动脉环的作用,并探讨其作用机制。方法采用离体血管张力测定实验方法,记录咪达唑仑对KCl(30 mmol·L^(-1))预收缩猪冠状动脉环张力的变化及不同工具药的影响。结果各浓度组咪达唑仑(3×10^(-6)~1×10^(-4)mol·L^(-1))对预收缩猪冠脉环产生浓度依赖性舒张作用,内皮完整组舒张作用强于去内皮组(P<0.05);在KCl预收缩基础上,加入NOS抑制剂L-NAME、L-NAME+L-Arg后,咪达唑仑舒血管作用明显减弱(P<0.05),而加入外源性的NO合成底物L-Arg、i NOS抑制剂1400W、环氧合酶抑制剂Indo均不能抑制咪达唑仑的舒血管作用;Na^+/Ca^(2+)交换体特异性阻断剂KBR7943亦不能抑制咪达唑仑的舒血管作用;钾通道阻断剂K_(ATP)阻断剂Gli可以抑制咪达唑仑的舒张冠脉作用(P<0.05),BKCa阻断剂TEA、Kir阻断剂Ba Cl2、KV阻断剂4-AP则不能改变咪达唑仑的舒张冠脉作用。结论咪达唑仑可浓度和内皮依赖性地舒张KCl预收缩的猪冠脉环,内皮分泌的NO参与了其舒血管作用,外源性NO、i NOS以及PGI2的合成与其舒血管作用无关,咪达唑仑对猪冠脉的舒张可能与K_(ATP)通道有关,与Na^+/Ca^(2+)交换体、K_V通道、BK_(Ca)通道、K_(ir)通道无关。Aim To investigate the effects of midazolam on porcine isolated coronary artery rings pre-contracted by potassium chloride( KCl) and the possible mechanism. Methods The vessel tension recorder system was used. Isotonic tension of porcine isolated coronary artery rings precontracted by KCl( 30 mmol·L-1) was recorded. The vasorelaxing action of midazolam and effects of various drugs were observed in the rings. Results Midazolam( 3 × 10(-6) 1 × 10(-4)mol·L-1) respectively concentration-dependently reduced the contraction induced by KCl,and there was significant difference between the rings with intact and denude endothelium( P〈0. 05). On KCl-induced precontraction,midazolam's relaxation was depressed by LNAME and the blend of L-NAME and L-Arg( P〈0. 05), but was not affected by Indo,L-Arg and1400 W. The contraction was not prevented by pretreatment with the inhibitor of Na+/Ca2+exchanger( KBR7943). The inhibitor of K(ATP)( Gli) restrained the diastolic function of midazolam( P〈0. 05),while the inhibitor of BKCa( TEA),Kir( Ba Cl2),KV( 4-AP) had no obvious effect. Conclusions Midazolam produces remarkable vasodilatation on KCl pre-contracted porcine isolated coronary artery rings. Its relaxtion effect is via concentration-dependent and endothelium-dependent mechanisms and relevant to the production of NO. Na+/Ca2+exchanger is not involved midazolam's vasodilatation on KCl pre-contracted porcine coronary artery rings. The relaxant mechanism of midazolam may be concerned with K(ATP). The K(ir),BK(Ca) and KV may be not involved.
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