期刊文献+

体外循环中磷酸肌酸对未成熟心肌的保护作用 被引量:2

Protective effects of phosphocreatine crystalloid cardioplegia on immature heart during cardiopulmonary bypass
下载PDF
导出
摘要 目的 研究人未成熟心肌在心肌停跳条件下高能化合物耗竭情况及磷酸肌酸 ( CP)对于未成熟心肌能量代谢的影响 .方法 先心病患儿 18例按体质量、性别、年龄相近似配成 9对 ,对每组中两个个体随机分配给两种处理 , 组为本院使用的改良停搏液 , 组改良停搏液加磷酸肌酸 10 m L .L- 1 ,分别于心肌缺血前后取右心耳心肌组织 HPL C测定心肌能量物质 CP,ATP,ADP及 AMP.结果 两组术前 L A,CK- MB水平无显著差异 ,而比较缺血未复灌 10 ,30 ,5 0 min发现 组L A,CK- MB漏出量均较少 ( P<0 .0 5 ) .两组术前心肌各能量物质 ( ATP,ADP,AMP,CP)水平相似 ;在缺血再灌注后心肌各能量物质 ( ATP,ADP,AMP,CP) 组 ATP,AMP,CP含量均明显高于 组 ,ATP ( 0 .1983 m mol.g- 1 ,0 .10 36 mmol.g- 1 ,P=0 .0 0 8) ,AMP( 0 .10 82 mmol.g- 1 ,0 .0 5 72 mmol.g- 1 ,P=0 .0 11) ,CP( 0 .4974mmol.g- 1 ,0 .3743mmol.g- 1 ,P=0 .0 0 5 )总非扩散核苷酸 TNN* (除 IMP) ( 0 .46 0 9mmol.g- 1 ,0 .2 90 4mmol.g- 1 )的恢复均优于 组 ,但是两组 ADP( 0 .15 98mmol.g- 1 ,0 .12 96 mmol.g- 1 ,P=0 .345 )无差异 . 组超微结构明显优于 组 .结论 目前心肌保护条件下加入 CP对于未成熟心肌能量物质保存有一定意义 ,即通过减少高能磷? AIM To study protective effects of phosphocreatine (cp) crystalloid cardioplegia on immature heart during cardiopulmonary bypass. METHODS Infants (less than 24 months old) with congenital heart disease were randomly divided into two groups (n=9 each group). There were 12 boys and 6 girls with a mean age of 11.8 months. The mean body mass was 9.7 kg with a range of 3.0 to 12 kg. Group I received modified St. Thomas II solution. Group II with addition of creatine phosphoate (CP: 10 mmol·L -1 ). The level of ATP, ADP, AMP, CP (preoperation, postoperation) in right cardiac atrium and the MB isoenzyme of creatine kinase (CKMB), lactic acid (LA) at each time point (preoperation, the end of arrest, 10 min, 30 min, 50 min of reperfuse) were measured. Postischemic ultrastrature in heart was observed in two groups. RESULTS ①CKMB (at the end of arrest, 10 min, 30 min, 50 min of reperfuse) released in group II were lower than those in group I (P=0.011). ②Although the baseline concentrations of ATP, ADP, AMP, CP were similar during the preischemic in two groups, the rate of highenergy phosphate depletion was attenuated during operation in group II. On reperfusion, the recovery of ATP ( 0.1983 mmol·g -1 , 0.1036 mmol·g -1 , P=0.008) , AMP ( 0.1082 mmol·g -1 , 0.0572 mmol·g -1 , P=0.011), and CP ( 0.4974 mmol·g -1 , 0.3743 mmol·g -1 , P=0.005) was greater in group II than in group I. While no difference was observed in ADP (0.1598 mmol·g -1 , 0.1296 mmol·g -1 , P= 0.345 ), the total non diffusible nucleotides (TNN* except IMP) in group II reach a much greater degree than that of group I ( 0.4609 mmol·g -1 , 0.2904 mmol·g -1 ). ③LA (at the end of arrest, 10 min, 30 min, 50 min of reperfuse) released at lower degree in group II than group I. ④Postischemic myocardial ultrastrature of group II was more excellent than in group I. CONCLUSION CP causes beneficial changes in highenergy phosphate metabolism subjected to cardioplegic arrest and ischemia. It is associated with a decreased rate of highenergy phosphate depletion and the increased recovery of ATP and phosphocreatine levels during reperfusion. Changes in energy metabolism may play a role in the cardioprotection by phosphocreatine during the prolonged hypothermic cardiac arrest.
出处 《第四军医大学学报》 2000年第5期564-567,共4页 Journal of the Fourth Military Medical University
基金 国家自然科学基金资助项目!(39500144)
关键词 磷酸肌酶 体外循环 未成熟心肌 保护作用 phosphocreatine high-performance liquid chromatography immature heart adenosine triphosphate adenosine diphosphate adenosine monophosphate lactic acid
  • 相关文献

参考文献5

  • 1[1] Anderson P, Glick K, Manring A et al. Developmental change s in cardiac contractibility in fetal and pestnatal sheep; in vitro and vivo [J].Am J Physiol,1 984;247(3pt2):H371-379.
  • 2[2] Unitt Jf, Schrader J, Brumotte F. Determination of free creatine and phosphocreatine concentration in the isolated rat heart by 1H and 31 P-NMR [J]. Biochim Bi ophys Acta, 1992;1133(2):115-120.
  • 3[3] Hearse DJ. Creatine phosphoate and protection against reperfution in duced arrhythmias in the rat [J]. Europ J Pharm, 1986;131(1):21-30.
  • 4[4] Marshall RJ, Parratt JR. Reduction in vertricular arrhythmias follow ing acute coronary artery ligation in the dog after the administration of creatine phosphate [J]. Naunyn Schmiedeberg's Arch Pharmacol, 1974;281(4):437-441.
  • 5[5] Klungsoyr L. Interaction between energy charge and product feedback in the regulation of biosynthetic enzymes. Asparokinase: Phosphribosyl adenosine triphosphate syntetase and phophoribosyl pyrophosphate synthetase [J].Biochemistry,1968;7(11):4035-4039.

同被引文献31

  • 1Morita K, Ihnken K, Buckberg GD, et al. Studies of hypoxemic/reoxygenation injury: with aortic clamping. Ⅻ. Delay of cardiac reoxygenation damage in the presence of cyanosis: A new concept of controlled cardiac reoxygenation. J Thorac Cardiovasc Surg, 1995, 110:1265~1273
  • 2Bolling KS, Halldorsson A, Allen BS,et al. Prevention of the hypoxic reoxygenation injury with the use of a leukocyte- depleting filter. J Thorac Cardiovasc Surg, 1997 Jun, 113(6): 1081 ~1089, Disscussion 1089~1090
  • 3Hayashi Y, Sawa Y, Nishimura M, et al. Clinical evaluation of leukocyte -depleted blood cardioplegia for pediatric open heart operation. Ann Thorac Surg,2000, 69: 1914~1919
  • 4Plessis A J, Jonas RA, Wypij D, et al.Perioperative effects of alpha stat versus pH stat strategies for deep hypothermic cardiopulmonary bypass in infants. J Thorac Cardiovasc Surg, 1997, 114:991 ~ 1001
  • 5Castaneda AR, Jonas RA, Mayer JE, et al. Cardiac surgery of the neonate and infant. New York: WB saunders, 1994
  • 6Baker EJ, Baker JE. Calcium and cardioplegic protection of the ischemic immature heart: Impact of hypoxemia from birth. Ann Thorac Surg, 1994, 58(4):1123~1130
  • 7Baker JE, Boerboom IE, Olinger GN, et al. Age and protection of the ischemic myocardium: is alkaline cardioplegia appropriate? Ann Thorac Surg, 1993, 55(3) :747~749
  • 8Katayama O, Amrani M, Ledingham S,et al. Effect of cardioplegia infusion Pressure on coronary artery endothelium and cardiac mechanical function. Eur J Cardiovasc Surg, 1997 Apr, 11 (4): 751 ~762
  • 9Orita H, Fukasawa M, Hirooka S, et al. In vitro evaluation of nicorandil,diltiazen and prostaglandin E on hypothermic injury to immature myocytes.J Surg Res, 1995 Mar, 58(3):313~320
  • 10Awad WI, Shattock MJ, ClAmber DJ.Ischemic preconditioning in immature myocardium. Circulation, 1998 Nov,98(19 suppl) Ⅱ :206 ~ 213

引证文献2

二级引证文献5

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部