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体外低温保存后心肌细胞的功能和生化变化。保存液的保护作用。

Cardiac myocyte functional and biochemical changes after hypothermic preservation in vitro. Protective effects of storage solutions.

作者信息

Orita H, Fukasawa M, Hirooka S, Uchino H, Fukui K, Kohi M, Washio M

机构信息

Second Department of Surgery, Yamagata University School of Medicine, Japan.

出版信息

J Thorac Cardiovasc Surg. 1994 Jan;107(1):226-32.

PMID:8283890
Abstract

In this study, we evaluated cardiac myocyte viability and function under hypothermic conditions with four types of storage solutions, saline solution, Euro-Collins solution, University of Wisconsin solution, and MCDB 107 medium. Cardiac myocytes were isolated from neonatal rat ventricles by collagenase dispersion and cultured for 4 days with MCDB 107 medium. A total of 12.5 x 10(5) myocytes per culture dish was used and the myocytes were incubated at 4 degrees C for 6, 12, 18, and 24 hours in the various storage solutions. After each incubation time, creatine kinase and lactate dehydrogenase were measured in the storage solutions. The myocytes were then incubated for 24 hours at 37 degrees C to evaluate the recovery of the myocyte beating rate. In the MCDB 107 group (n = 7), the recovery ratio of myocyte beating rate was complete by 12 hours, then decreased to 44.8% of control (beating rate before hypothermic incubation) at 24 hours. The saline, Euro-Collins, and University of Wisconsin groups (n = 7 each) had significantly lower recovery ratios than the MCDB 107 group (at 12 hours: 61.0%, 32.2%, and 48.9%; at 18 hours: 0.0%, 5.5%, and 15.1% of control, respectively). Release of creatine kinase and lactate dehydrogenase in the MCDB 107 group gradually increased and at 24 hours was 143.2 mIU/flask and 486.2 mIU/flask, respectively. However, the saline and University of Wisconsin groups had significantly increased creatine kinase and lactate dehydrogenase values at 24 hours (creatine kinase: 334.6 and 319.6 mIU/flask; lactate dehydrogenase: 821.6 and 654.4 mIU/flask, respectively). The Euro-Collins group showed the greatest increase in both markers (creatine kinase: 1587.5, lactate dehydrogenase: 2106.9 mIU/flask). In summary, saline and University of Wisconsin solutions showed a beneficial effect on recovery of myocyte viability at 12 hours compared with Euro-Collins solution, however MCDB 107 medium had the best overall protective effect on cultured myocytes. Accordingly, alternate hypothermic storage solutions, such as cell-culture medium, may have protective characteristics that are suitable for cardiac preservation.

摘要

在本研究中,我们使用四种保存溶液(生理盐水、欧洲柯林斯溶液、威斯康星大学溶液和MCDB 107培养基)评估低温条件下心肌细胞的活力和功能。通过胶原酶分散法从新生大鼠心室分离心肌细胞,并用MCDB 107培养基培养4天。每个培养皿使用总共12.5×10⁵个心肌细胞,并将心肌细胞在4℃下于各种保存溶液中孵育6、12、18和24小时。每次孵育时间后,测量保存溶液中的肌酸激酶和乳酸脱氢酶。然后将心肌细胞在37℃下孵育24小时,以评估心肌细胞搏动率的恢复情况。在MCDB 107组(n = 7)中,心肌细胞搏动率的恢复率在12小时时完全恢复,然后在24小时时降至对照(低温孵育前的搏动率)的44.8%。生理盐水、欧洲柯林斯和威斯康星大学组(每组n = 7)的恢复率明显低于MCDB 107组(12小时时:分别为对照的61.0%、32.2%和48.9%;18小时时:分别为对照的0.0%、5.5%和15.1%)。MCDB 107组中肌酸激酶和乳酸脱氢酶的释放逐渐增加,在24小时时分别为143.2 mIU/瓶和486.2 mIU/瓶。然而,生理盐水和威斯康星大学组在24小时时肌酸激酶和乳酸脱氢酶值显著升高(肌酸激酶:分别为334.6和319.6 mIU/瓶;乳酸脱氢酶:分别为821.6和654.4 mIU/瓶)。欧洲柯林斯组的两种标志物升高幅度最大(肌酸激酶:1587.5,乳酸脱氢酶:2106.9 mIU/瓶)。总之,与欧洲柯林斯溶液相比,生理盐水和威斯康星大学溶液在12小时时对心肌细胞活力的恢复显示出有益作用,然而MCDB 107培养基对培养的心肌细胞具有最佳的总体保护作用。因此,替代的低温保存溶液,如细胞培养基,可能具有适合心脏保存的保护特性。

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