Gunaydin Serdar, Akbay Esin, Gunertem Orhan Eren, McCusker Kevin, Onur Mehmet Ali, Ozisik Kanat
Department of Cardiovascular Surgery, University of Health Sciences, Ankara, Turkey; Department of Biology, Faculty of Science, Hacettepe University, Ankara, Turkey; and Department of Cardiac Surgery, New York Medical College, New York, New York.
J Extra Corpor Technol. 2020 Dec;52(4):279-288. doi: 10.1182/ject-2000028.
Despite the popularity of single-dose cardioplegic techniques, the time window and targeted population for successful reperfusion remain unclear. We tested currently available techniques based on cell viability and integrity to demonstrate long-term cardioprotection and clarify whether these solutions were performed on neonatal/adult endothelium and myocardium by examining different cell lines. Cell viability with 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) test proliferation assay and membrane integrity with the lactic dehydrogenase (LDH) cytotoxicity test were documented in a cell culture/microscopy setting on adult (human umbilical vein endothelium [HUVEC]), neonatal (H9C2-cardiomyocytes), and myofibroblast (L929) cell lines. Apoptotic cell activity and necrosis were evaluated by acridine orange/propidium iodide (AO/PI) staining. Twenty-four hours after seeding, cells were incubated in control (Dulbecco's modified Eagle), St. Thomas and blood cardioplegia (4:1), histidine-tryptophan-ketoglutarate (HTK), and del Nido solutions at 32°C followed by an additional 6, 24, and 48 hours in standard conditions (37°C, 5% CO2). Experiments were repeated eight times. In MTT cell viability analysis, HTK protection was significantly better than the control medium in L929 cell lines at 48th hours follow-up and acted markedly better on the HUVEC cell line at 24th and 48th hours. del Nido and HTK provided significantly better protection on H9C2 (at 24th and 48th hours). Apoptotic and necrotic cell scoring as a result of AO/PI staining was found consistent with MTT results. The LDH test demonstrated that the level of cell disruption was significantly higher for St. Thomas and blood cardioplegia in H9c2 cells. Experimental studies on cardioplegia aimed at assessing myocardial protection use time-consuming and often expensive approaches that are unrealistic in clinical practice. We have focused on identifying the most effective cell types and the direct consequences of different cardioplegia solutions to document long-term effects that we believe are the most underestimated ones in the cardioplegia literature.
尽管单剂量心脏停搏技术很受欢迎,但成功再灌注的时间窗和目标人群仍不明确。我们基于细胞活力和完整性测试了当前可用的技术,以证明长期心脏保护作用,并通过检查不同细胞系来阐明这些溶液是否作用于新生儿/成人内皮细胞和心肌细胞。在细胞培养/显微镜环境下,使用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)试验增殖分析评估细胞活力,使用乳酸脱氢酶(LDH)细胞毒性试验评估膜完整性,研究对象为成人(人脐静脉内皮细胞[HUVEC])、新生儿(H9C2-心肌细胞)和成纤维细胞(L929)细胞系。通过吖啶橙/碘化丙啶(AO/PI)染色评估凋亡细胞活性和坏死情况。接种24小时后,将细胞在对照(杜氏改良 Eagle培养基)、圣托马斯溶液和血液心脏停搏液(4:1)、组氨酸-色氨酸-酮戊二酸(HTK)溶液以及德尔尼多溶液中于32°C孵育,随后在标准条件(37°C,5%二氧化碳)下再孵育6、24和48小时。实验重复进行8次。在MTT细胞活力分析中,在第48小时的随访中,HTK对L929细胞系的保护作用明显优于对照培养基,在第24小时和第48小时对HUVEC细胞系的作用也明显更好。德尔尼多溶液和HTK对H9C2细胞(在第24小时和第48小时)提供了明显更好的保护。AO/PI染色结果显示的凋亡和坏死细胞评分与MTT结果一致。LDH试验表明,圣托马斯溶液和血液心脏停搏液对H9c2细胞的细胞破坏水平明显更高。旨在评估心肌保护作用的心脏停搏液实验研究采用的方法既耗时又昂贵,在临床实践中不切实际。我们专注于确定最有效的细胞类型以及不同心脏停搏液溶液的直接后果,以记录长期影响,我们认为这些影响在心脏停搏液文献中最被低估。