Literature DB >> 17940707

Effects of different modes of intermittent hypobaric hypoxia on ischemia/reperfusion injury in developing rat hearts.

Hao Zhang1, Chang-Ying Yang, Ying-Ping Wang, Xin Wang, Fang Cui, Zhao-Nian Zhou, Yi Zhang.   

Abstract

The aim of the present study was to explore the effects of two different modes of intermittent hypobaric hypoxia (IHH) on myocardial ischemia/reperfusion injury in developing rat hearts. Postnatal male sprague-Dawley rats (n=72) were divided randomly into 3 groups: intermittent hypoxia at 3 000 m (IHH3000) group, intermittent hypoxia at 5 000 m (IHH5000) group and control group. The isolated hearts were perfused in the Langendorff apparatus, undergoing 30 min of global ischemia and 60 min of reperfusion. Cardiac function, coronary flow and lactate dehydrogenase (LDH) activity were recorded at 5 min before ischemia and 1, 5, 10, 20, 30, 60 min during reperfusion, respectively. The heart weight was measured at the end of the experiment. The results showed that: (1) There was no difference in body weight gaining between IHH3000 and control groups. The gain of body weight in IHH5000 group was much lower than that in IHH3000 and control groups (P<0.01). (2) Compared with that in the control group, the recovery of cardiac function in IHH3000 group was enhanced at 60 min after ischemia/reperfusion, coronary flow was increased, and LDH activity was decreased (P<0.05), meaning a cardioprotective effect occurred. There was no significant difference in heart weight between IHH3000 and control groups. In addition, cardiac function restored better in IHH3000 group after 42 d of hypoxic exposure than that after 28 d of hypoxic exposure (P<0.05). (3) Compared with that in the control group, the recovery of cardiac function in IHH5000 group was lower, coronary flow was decreased, and LDH activity was increased (P<0.05). There was a hypertrophy in the right ventricle in IHH5000 group. All changes indicated definitely that a detrimental effect developed in IHH5000 group. The results suggest that proper IHH can protect developing rat hearts against ischemia/reperfusion injury while this effect could be affected by the modes of intermittent hypoxic exposure.

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Year:  2007        PMID: 17940707

Source DB:  PubMed          Journal:  Sheng Li Xue Bao        ISSN: 0371-0874


  5 in total

1.  Intermittent hypobaric hypoxia preconditioning induced brain ischemic tolerance by up-regulating glial glutamate transporter-1 in rats.

Authors:  Shu-Juan Gong; Ling-Yu Chen; Min Zhang; Jian-Xue Gong; Ya-Xian Ma; Jian-Mei Zhang; Yu-Jing Wang; Yu-Yan Hu; Xiao-Cai Sun; Wen-Bin Li; Yi Zhang
Journal:  Neurochem Res       Date:  2011-11-12       Impact factor: 3.996

Review 2.  Cardioprotection by intermittent hypoxia conditioning: evidence, mechanisms, and therapeutic potential.

Authors:  Robert T Mallet; Eugenia B Manukhina; Steven Shea Ruelas; James L Caffrey; H Fred Downey
Journal:  Am J Physiol Heart Circ Physiol       Date:  2018-04-13       Impact factor: 4.733

3.  K(ATP) channels and MPTP are involved in the cardioprotection bestowed by chronic intermittent hypobaric hypoxia in the developing rat.

Authors:  Hui-min Bu; Chang-ying Yang; Mei-ling Wang; Hui-jie Ma; Hong Sun; Yi Zhang
Journal:  J Physiol Sci       Date:  2015-04-11       Impact factor: 2.781

Review 4.  Cardiac response to chronic intermittent hypoxia with a transition from adaptation to maladaptation: the role of hydrogen peroxide.

Authors:  Xia Yin; Yang Zheng; Quan Liu; Jun Cai; Lu Cai
Journal:  Oxid Med Cell Longev       Date:  2012-05-20       Impact factor: 6.543

5.  Enhancement of Glucose Metabolism via PGC-1α Participates in the Cardioprotection of Chronic Intermittent Hypobaric Hypoxia.

Authors:  Xuyi Li; Yan Liu; Huijie Ma; Yue Guan; Yue Cao; Yanming Tian; Yi Zhang
Journal:  Front Physiol       Date:  2016-06-08       Impact factor: 4.566

  5 in total

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