2004Chinese Journal of Critical Care MedicineRequires access

Caspase inhibitor reduces myocyte cell apoptosis induced by hypoxia in vitro

Zheng Shi

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Abstract

Objective To investigate the significance of caspase inhibitor in neonatal cardiomyocyte apoptosis induced by hypoxia. Methods The cultured cardiomyocytes from 2 - 3 d newborn SD rats were randomly divided into 3 groups: control group, ischemic 72 h group and caspase inhibitor group. Cardiomyocyte apoptosis was detected by TUNEL and flow cytometry. The caspase - 3 activity was detected by caspase - 3 fluorescent assay kit . Results TUNEL method and flow cytometry analysis showed that apoptosis indexes and the percentage of apoptosis cells in caspase inhibitor group was (14.10±2.56)% and (14.93 ± 2.47)% respectively, and compared with the ischemic 72 h group(46.49 ± 4.93) % and (48.43±4.18) % , were significantly lower( P 0.01) .caspase - 3 activity analysis showed that caspase - 3 activity in caspase inhibitor group was reduced 52.85% relative to ischemic 72 h group. Conclusion caspase inhibitor can efficiently inhibit apoplosis of neonatal cardiomyocytes after hypoxia insult, caspase inhibitor can efficiently inhibit activity of caspase - 3 in cultured neonatal cardiomyocytes after hypoxia insult.

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Objective To investigate the significance of caspase inhibitor in neonatal cardiomyocyte apoptosis induced by hypoxia. Methods The cultured cardiomyocytes from 2 - 3 d newborn SD rats were randomly divided into 3 groups: control group, ischemic 72 h group and caspase inhibitor group. Cardiomyocyte apoptosis was detected by TUNEL and flow cytometry. The caspase - 3 activity was detected by caspase - 3 fluorescent assay kit . Results TUNEL method and flow cytometry analysis showed that apoptosis indexes and the percentage of apoptosis cells in caspase inhibitor group was (14.10±2.56)% and (14.93 ± 2.47)% respectively, and compared with the ischemic 72 h group(46.49 ± 4.93) % and (48.43±4.18) % , were significantly lower( P 0.01) .caspase - 3 activity analysis showed that caspase - 3 activity in caspase inhibitor group was reduced 52.85% relative to ischemic 72 h group. Conclusion caspase inhibitor can efficiently inhibit apoplosis of neonatal cardiomyocytes after hypoxia insult, caspase inhibitor can efficiently inhibit activity of caspase - 3 in cultured neonatal cardiomyocytes after hypoxia insult.

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Available abstract

Objective To investigate the significance of caspase inhibitor in neonatal cardiomyocyte apoptosis induced by hypoxia. Methods The cultured cardiomyocytes from 2 - 3 d newborn SD rats were randomly divided into 3 groups: control group, ischemic 72 h group and caspase inhibitor group. Cardiomyocyte apoptosis was detected by TUNEL and flow cytometry. The caspase - 3 activity was detected by caspase - 3 fluorescent assay kit . Results TUNEL method and flow cytometry analysis showed that apoptosis indexes and the percentage of apoptosis cells in caspase inhibitor group was (14.10±2.56)% and (14.93 ± 2.47)% respectively, and compared with the ischemic 72 h group(46.49 ± 4.93) % and (48.43±4.18) % , were significantly lower( P 0.01) .caspase - 3 activity analysis showed that caspase - 3 activity in caspase inhibitor group was reduced 52.85% relative to ischemic 72 h group. Conclusion caspase inhibitor can efficiently inhibit apoplosis of neonatal cardiomyocytes after hypoxia insult, caspase inhibitor can efficiently inhibit activity of caspase - 3 in cultured neonatal cardiomyocytes after hypoxia insult.

Key concepts: Apoptosis, TUNEL assay, Hypoxia (environmental), Medicine, Flow cytometry, Caspase 3, Caspase-9, Caspase

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