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ST-1抗豚鼠和兔心肌缺血再灌注损伤的血流动力学研究 被引量:1

Effects of ST-1 on myocardial dysfunction and hemodynamics induced by ischemia reperfusion
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摘要 目的 :拟证实双萜类化合物ST 1的抗心肌缺血再灌注损伤作用。方法 :(1)Langendorff装置逆向豚鼠心脏灌注 ,预先灌注ST 11.0、5 .0和 10 μmol·L- 1 5min ,停灌 3 0min ,再灌注 2 0min ,制成豚鼠心肌缺血再灌注损伤模型 ,观察药物对心脏舒缩功能、冠脉流出液量的影响 ;(2 )结扎麻醉兔冠脉左前降支 3 0min后再连续灌注 60min ,制成兔心肌缺血再灌注损伤模型 ,ST 12 5~ 10 0 μg·kg- 1 静脉注射 ,动态观察其对血流动力学指标的影响。结果 :ST 1预处理可有效减轻离体豚鼠缺血再灌注引起的左室舒缩功能下降 ;兔ST 1组左心室等容期压力最大变化速率、左心室收缩压、左心室发展压、左心室压峰值时间的变化值明显小于模型对照组 (P <0 .0 5 ) ,心率、舒张压、收缩压和平均动脉压变化不明显 (P >0 .0 5 )。结论 :ST 1预处理有抗离体豚鼠和在体家兔心肌缺血再灌注损伤的作用。 Objective To study the effects of ST-1,a diterpen e c ompound, on myocardial dysfunction induced by ischemia reperfusion.Meth ods The isolated guinea-pig heart was perfused with modified Tyrde bu ffer solution by Langendorff. ST-1 1,5,10-μmol·L -1 were perfused 10 min prior to ischemia, ischemia 30 min and reperfusion 20 min in vitro,respecti vely. The changes of hemodynamics were observed in rabbits with m yocardial ischemia reperfusion model induced by occluding the left anterior desc ending coronary artery(LAD) for 30 min followed by 60 min reperfusion.R esults The preconditioning with ST-1 could effectively preserve the ca rdiac function.The values of change in LVSP,LVDP',±dp/dt max,T-dp/dt m a x induced by ST-1 were significantly less than the respective value of vehi c le control inanesthetized and ischemia reperfused rabbits.There were no signifi can t changes of heart rate and blood pressure by administration of ST-1.Co n clusion Preconditioning with ST-1 could ameliorate cardiac dysfunction induced by ischemia and reperfusion significantly.
作者 赵蕾 许德义
出处 《南京铁道医学院学报》 2004年第6期384-387,共4页 Journal of Nanjing Railway Medical College
基金 铁道部科技基金资助项目 (674760 0 0 54)
关键词 ST-1 豚鼠 心肌缺血 再灌注损伤 血流动力学 钾通道 guinea-pigs rabbits cardiac ischemia reperfusion hemodynamics ATP-sensitive potassium channel
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  • 1SATO T, SASAKI N, SEHARASEYON J , et al. Selective pharmacological agents implicate mitochondrial hut not sarcolemmal KATP,channels in ischimic cardioprotection [ J ]. Circulation, 2000, 101 :23,18-23,23.
  • 2NAPOLI C, P1N'ID A, C1RIN C. Pharmacological modulation, preclinical studies and new clinical feature of ischemic preconditioning[ J ]. Pharmacology & Theerapeutics, 2000,88 : 311-331.
  • 3KELMER-BRACHT A, ALVAREZ M, BRAClfF A. Effects of stevia rebaudiana natural products on rat liver mitochondria[J]. Biochemical Pharmacology, 1985,34: 1873-1882.
  • 4AINES C P, LIU G S, B1RINC1OGLU M, et al. lschemic preconditiorfing depends on interaction between mitoehondrial KATP channels and actin cytoskeleton[J], Am J Physiol, 1999,276: HI361.
  • 5PARK J W, CHUNG Y S, KIM Y H, et al. lschemic preconditioning reduces O2 generation and prevents respiratory impairment in the mitochondria of post-ischemic reperfused heart of rat[J]. Life Science, 1997, 60:2207-2219.
  • 6JILKINA O, KUZ10 B, GROVER G J, et al. Effects of Kvn, channel opener, P-1075, pinacidil and diazoxide on cnergelitics and contracture function in isolated rat hearts [ J ]. J Mol Cell Cardiol, 2002,34 : 427-440.

同被引文献16

  • 1XU D Y, ZHANG S J, DAVID FOSTER J R, et al. The effects of isosteviol against myocardium injury induced by ischaemia-reperfusion in the isolated guinea pig heart [ J ]. Clin Exp Pharmacolo P,2007,34(5/6) :488-493.
  • 2WONG K L, CHANA P, YANG H Y, et al. Isosteviol acts onpotassium channels to relax isolated aortic strips of Wistar rat [J]. Life Sci,2004,74(19) :2379-2387.
  • 3LIU J C, KAO P F, HSIEH M H, et al. The antihypertensive effect of stevioside derivative isosteviol in spontaneously hypertensive rats [ J ]. Acta Cardiol Sin,2001,17 : 133-140.
  • 4ISHII E L, SCHWAB A J, BRACHT A. Inhibition of monosaccharide transport in the intact rat liver by stevioside [ J ]. Biochem Pharmacol, 1987,36(9) : 1417-1433.
  • 5ISHII E L, BRACHT A. Glucose release by the liver under conditions of reduced activity of glucose 6phosphatase [ J ]. Braz J Med Biol Res, 1987,20(6) :837-843.
  • 6NORDENTOFT I, JEPPESEN P B, HONG J, et al. Isosteviol increases insulin sensitivity and changes gene expression of key insulin regulatory genes and transcription factors in islets of the diabetic KKAy mouse[ J]. Diabetes Obes Metab,2008, 10(10) :939-949.
  • 7MA J, MA Z, WANG J, et al. Isosteviol reduces plasma glucose levels in the intravenous glucose tolerance test in Zucker diabetic fatty rats[ J ]. Diabetes Obes Metab,2007,9 (4) ,597-599.
  • 8AKIHISA T, HAMASAKI Y, TOKUDA H, et al. Microbial transformation of isosteviol and inhibitory effects on epsteinbarr virus activation of the transformation products[ J]. J Nat Prod,2004,67 ( 3 ) :407-410.
  • 9CHANG S F, YANG L M, LO C H, et al. Microbial transformation of isosteviol and bioactivities against the glucocorti-coid/androgen response elements [ J ]. J Nat Prod, 2008,71 ( 1 ) :87-92.
  • 10阿历索保罗CJ,明斯CW,布莱克韦尔.菌物学概论[M].4版.北京:中国农业出版社,2002.

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