Vander Heide R S, Angelo J P, Altschuld R A, Ganote C E
Am J Pathol. 1986 Oct;125(1):55-68.
Aggregation of sarcomeres into contraction bands is a prominent feature of the oxygen paradox, the calcium paradox, and caffeine injury to calcium-free perfused hearts. For investigation of the mechanism of contraction banding, it was necessary to devise a method of evaluating the degree of sarcomere contraction and to define objectively a contraction band. Hearts with mechanical detachment of cells caused by hypocalcemic perfusion and isolated myocytes both allow unrestrained contracture of cells and permit direct optical measurements to quantitate the degree of cell contracture. With the use of the calcium paradox as a model of contraction band necrosis, it was found that cells with lengths of less than 37.3 mu could be considered as containing contraction bands. It was found that the mitochondrial inhibitors cyanide and amytal, as well as the uncoupler 2,4-dinitrophenol, allowed cell contracture but inhibited hypercontracture of sarcomeres into contraction bands during both the calcium paradox and caffeine injury to perfused hearts. However, when 2mM adenosine triphosphate (ATP) was included in the perfusion media, contraction band formation occurred despite the continued presence of cyanide or amytal. In isolated myocyte preparations the addition of the glycolytic inhibitor iodoacetate (IAA, 5 mM) and the mitochondrial inhibitor amytal (3 mM) caused relaxed rod-shaped cells (length/width ratio greater than 3:1) to contract into a stable population of square-shaped forms (length/width ratio less than 3:1), indicating an abrupt and severe decline in cellular ATP levels. Removal of amytal from the incubation medium in the presence of IAA produced a significant conversion of square-shaped cells into round-shaped cells containing contraction bands. Either IAA alone or amytal alone resulted in a mixed population of square and round cells. The results indicate that ATP is required for the formation of contraction bands in intact hearts and for the rounding of isolated myocytes. Formation of contraction bands appears to be an energy-dependent process requiring ATP.
肌节聚集成收缩带是氧反常、钙反常以及咖啡因对无钙灌注心脏损伤的一个显著特征。为了研究收缩带形成的机制,有必要设计一种评估肌节收缩程度的方法,并客观地定义收缩带。低钙灌注导致细胞机械性脱离的心脏以及分离的心肌细胞,都允许细胞不受限制地挛缩,并允许进行直接光学测量以定量细胞挛缩程度。以钙反常作为收缩带坏死的模型,发现长度小于37.3微米的细胞可被认为含有收缩带。研究发现,线粒体抑制剂氰化物和戊巴比妥,以及解偶联剂2,4-二硝基苯酚,在钙反常和咖啡因对灌注心脏的损伤过程中,都能使细胞挛缩,但抑制肌节过度收缩形成收缩带。然而,当灌注液中加入2毫摩尔三磷酸腺苷(ATP)时,尽管氰化物或戊巴比妥持续存在,仍会发生收缩带形成。在分离的心肌细胞制剂中,加入糖酵解抑制剂碘乙酸盐(IAA,5毫摩尔)和线粒体抑制剂戊巴比妥(3毫摩尔),会使松弛的杆状细胞(长宽比大于3:1)收缩成稳定的方形细胞群体(长宽比小于3:1),这表明细胞内ATP水平急剧严重下降。在IAA存在的情况下,从孵育培养基中去除戊巴比妥会使方形细胞显著转化为含有收缩带的圆形细胞。单独使用IAA或单独使用戊巴比妥都会导致方形和圆形细胞的混合群体。结果表明,完整心脏中收缩带的形成以及分离心肌细胞的变圆都需要ATP。收缩带的形成似乎是一个依赖能量的过程,需要ATP。