Fremes S E, Li R K, Weisel R D, Mickle D A, Furukawa R D, Tumiati L C
Division of Cardiovascular Surgery, University of Toronto, Ontario, Canada.
Ann Thorac Surg. 1991 Oct;52(4):1021-5. doi: 10.1016/0003-4975(91)91271-v.
Previous studies from this institution have suggested that University of Wisconsin solution is preferred for prolonged cardiac storage and preserves high-energy phosphates better than other storage fluids. University of Wisconsin solution contains adenosine (5 mmol/L), which may maintain the concentration of myocardial adenine nucleotides. Cultures of human adult myocytes were grown from left ventricular biopsy specimens obtained from patients undergoing coronary bypass procedures. Cells (seven to nine dishes per group) were rinsed of culture medium and stored at 0 degrees C in University of Wisconsin solution. Cells were analyzed for adenine nucleotide content after 1, 6, 12, and 24 hours of storage by high-performance liquid chromatography (units = nmol/microgram DNA) and compared with control samples (0 hour). Adenosine concentration increased from 0.03 +/- 0.02 (mean +/- standard deviation) to 1.77 +/- 1.03 by 1 hour (p less than 0.0001, analysis of variance) and remained increased thereafter. Adenosine was largely degraded to inosine (0 hours, 0.03 +/- 0.03; 6 hours, 0.88 +/- 0.56; p less than 0.001) and hypoxanthine (0 hours, 0.01 +/- 0.01; 6 hours, 0.15 +/- 0.09; p = 0.004). Measured levels of xanthine and uric acid were extremely low at all time intervals. Adenosine triphosphate levels were maintained at 1 hour (0 hours, 0.64 +/- 0.38; 1 hour, 0.67 +/- 0.45) but declined thereafter (6 hours, 0.21 +/- 0.21; 12 hours, 0.11 +/- 0.09; 24 hours, 0.04 +/- 0.03; p less than 0.0001). Levels of adenosine diphosphate (p = 0.007) and adenosine monophosphate (p less than 0.05) decreased to approximately 25% of original values by 24 hours.(ABSTRACT TRUNCATED AT 250 WORDS)
该机构之前的研究表明,威斯康星大学溶液更适合用于长时间的心脏保存,并且与其他保存液相比,能更好地保存高能磷酸盐。威斯康星大学溶液含有腺苷(5毫摩尔/升),这可能维持心肌腺嘌呤核苷酸的浓度。人类成年心肌细胞培养物来自接受冠状动脉搭桥手术患者的左心室活检标本。细胞(每组七到九个培养皿)用培养基冲洗后,在0摄氏度下保存在威斯康星大学溶液中。通过高效液相色谱法(单位 = 纳摩尔/微克DNA)在储存1、6、12和24小时后分析细胞的腺嘌呤核苷酸含量,并与对照样品(0小时)进行比较。腺苷浓度在1小时内从0.03±0.02(平均值±标准差)增加到1.77±1.03(方差分析,p<0.0001),此后一直保持升高。腺苷大部分降解为肌苷(0小时,0.03±0.03;6小时,0.88±0.56;p<0.001)和次黄嘌呤(0小时,0.01±0.01;6小时,0.15±0.09;p = 0.004)。在所有时间间隔测量的黄嘌呤和尿酸水平都极低。三磷酸腺苷水平在1小时时维持在(0小时,0.64±0.38;1小时,0.67±0.45),但此后下降(6小时,0.21±0.21;12小时,0.11±0.09;24小时,0.04±0.03;p<0.0001)。到24小时时,二磷酸腺苷(p = 0.007)和一磷酸腺苷(p<0.05)水平降至原始值的约25%。(摘要截断于250字)