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Apoptosis in pressure overload-induced heart hypertrophy in the rat.

机译:大鼠压力超负荷引起的心脏肥大中的细胞凋亡。

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摘要

Pressure overload induces cardiac growth in the rat, which implies the hypertrophy of cardiac muscle cells and proliferation of nonmuscle cells. The cardiac cell loss observed in parallel has generally been attributed to necrosis. Using an in situ assay, we demonstrated a phase of apoptosis or programmed cell death during the first 7 d after pressure overload with a peak at day 4 while cardiac growth continued for over 30 d. The increase in apoptosis was confirmed by quantification of 180-1500-bp DNA oligonucleosomes with agarose gel electrophoresis and in situ labeling via 3'-terminal deoxynucleotidyl transferase assay. While some apoptosis was observed in the basal state in nonmuscle cells, pressure overload induced apoptosis mainly in cardiomyocytes. These data suggest that cardiac hypertrophy is initiated by a wave of apoptosis of cardiomyocytes. Thus, apoptosis may be involved in the pathogenesis of heart remodeling.
机译:压力超负荷诱导大鼠心脏生长,这意味着心肌细胞肥大和非肌肉细胞增殖。并行观察到的心脏细胞丢失通常归因于坏死。使用原位分析,我们证明了压力超负荷后的前7 d凋亡或程序性细胞死亡的阶段,第4天达到峰值,而心脏持续生长超过30 d。通过琼脂糖凝胶电泳定量180-1500-bp DNA寡核小体并通过3'-末端脱氧核苷酸转移酶测定原位标记,证实了细胞凋亡的增加。虽然在非肌肉细胞中观察到一些处于基础状态的凋亡,但是压力超负荷主要在心肌细胞中诱导凋亡。这些数据表明,心肌肥大是由心肌细胞的凋亡波引发的。因此,凋亡可能与心脏重塑的发病机制有关。

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