Effect of cerebral mild hypothermia on cerebral mitochondrial ATPase activity in neonatal rats with hypoxic-ischemic brain damage
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    Abstract:

    OBJECTIVE: To study the effect of cerebral mild hypothermia on cerebral mitochondrial ATPase activities in neonatal rats with hypoxic-ischemic brain damage(HIBD), METHODS: Eighty-four seven-day-old Wistar rats were randomly assigned into four groups: sham-operated normothermic, sham-operated mild hypothermic, HIBD normothermic and HIBD mild hypothemic, HIBD was induced by left common carotid artery ligation, followed by 8% hypoxia exposure. At each time interval of 2, 6, and 12 hrs post-hypoxia-ischemia (HI), 7 rats were sacrificed and the brain tissues were sampled for detecting the activities of mitochondrial Na+K+ATPase and Ca2+ATPase. RESULTS: The activities of mitochondrial Ca2+ATPase decreased significantly in the two HIBD groups compared with those of the two sham-operated groups at 2, 6, and 12 hrs post-HI. The HIBD mild hypothemic group had higher mitochondrial Ca2+ATPase activities compared with the HIBD normothermic group at 2, 6, and 12 hrs post-HI (5.25±0.61 μmol/mgPr. h vs 3.17±0.81 μmol/mgPr, h, 4.59±0.81 μmol/mgPr. h vs 2.26±0.53 μmol/mgPr. h, 4.61±0.62 μmol/mgPr. h vs 1.31±0.78 μmol/mgPr. H, respectively) (P<0.01). The activities of mitochondrial Na+K+ATPase decreased significantly in the two HIBD groups compared with those of the two sham-operated groups at 6 and 12 hrs post-HI. A significant difference was observed in the mitochondrial Na+K+ATPase activities between the HIBD mild hypothemic and HIBD normothermic groups at 6 and 12 hrs post-HI(5.25±0.66 μmol/mg Pr. h vs 3.76±0.78 μmol/mgPr. h, 4.74±0.80 μmol/mgPr. h vs 3.12±0.53 μmol/mgPr, h; P<0.01). CONCLUSIONS: Mild hypothermia following HIBD inhibits the decline in cerebral mitochondrial Ca2+ and Na+K+ ATPase activities in neonatal rats, thus providing protective effects against HIBD.[Chin J Contemp Pediatr, 2007, 9 (4):305-307]

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姚笠, 程琳, 于立君.头部贴敷式亚低温对HIBD新生大鼠脑组织线粒体ATP酶活性的影响[J].中国当代儿科杂志英文版,2007,9(4):305-307

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  • Online: September 08,2009
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