Literature DB >> 20123096

Protection in rats with heatstroke: hyperbaric oxygen vs activated protein C therapy.

Chao-Hung Yeh1, Zhih-Cherng Chen, Chuan-Chih Hsu, Mao-Tsun Lin, Chien-Chang Chen.   

Abstract

The present study was attempted to evaluate the therapeutic effects of activated protein C and/or hyperbaric oxygen in an animal model of heatstroke. Sixty-eight minutes heat stress (43 degrees C) initiated, the anesthetized rats were randomized to several groups and administered: 1) no resuscitation (vehicle solution plus normabaric air, 2) intravenous activated protein C (1mg in 1ml of normal saline per kg of body weight), 3) hyperbaric oxygen (100% oxygen at 202kpa for 17min), and 4) intravenous activated protein C plus hyperbaric oxygen. Another group of rats exposed to room temperature (26 degrees C) was used as normothermic controls. Blood sampling was 0min, 70min, and 85min after heat stress initiated. When the vehicle-treated rats underwent heat exposure, their survival time values found were to be 19-25min. Resuscitation with activated protein C or hyperbaric oxygen significantly and equally improved survival during heatstroke (134-159min). As compared with those of activated protein C or hyperbaric oxygen alone, combined activated protein C and hyperbaric oxygen significantly had higher survival time values (277-347min). All vehicle-treated heatstroke animals displayed systemic response, hypercoagulable state, and hepatic and renal dysfunction. Combined activated protein C and hyperbaric oxygen therapy reduced these heatstroke reactions better than activated protein C or hyperbaric oxygen alone. The results indicate consequently, combined activated protein C and hyperbaric oxygen therapy heightens benefit in combating heatstroke reactions.

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Year:  2010        PMID: 20123096     DOI: 10.1016/j.ejphar.2010.01.013

Source DB:  PubMed          Journal:  Eur J Pharmacol        ISSN: 0014-2999            Impact factor:   4.432


  5 in total

1.  The relationship between N-acetylcysteine, hyperbaric oxygen, and inflammation in a rat model of acetaminophen-induced nephrotoxicity.

Authors:  Hakan Cermik; Mine Yavuz Taslipinar; Ibrahim Aydin; Mehmet Agilli; Fevzi Nuri Aydin; Fatma Ucar; Bilal Firat Alp; Mehmet Toygar; Esin Ozkan; Ertan Altayli; Tuncer Cayci
Journal:  Inflammation       Date:  2013-10       Impact factor: 4.092

2.  Combination treatment with Gua Sha and Blood-letting causes attenuation of systemic inflammation, activated coagulation, tissue ischemia and injury during heatstroke in rats.

Authors:  Wen-zhan Tu; Rui-dong Cheng; Jie Hu; Jie-zhi Wang; Hai-yan Lin; En-miao Zou; Wan-sheng Wang; Xin-fa Lou; Song-he Jiang
Journal:  Chin J Integr Med       Date:  2014-08-07       Impact factor: 1.978

3.  Reduction of ischemic and oxidative damage to the hypothalamus by hyperbaric oxygen in heatstroke mice.

Authors:  Po-An Tai; Chen-Kuei Chang; Ko-Chi Niu; Mao-Tsun Lin; Wen-Ta Chiu; Jia-Wei Lin
Journal:  J Biomed Biotechnol       Date:  2010-06-17

4.  Ischemic and oxidative damage to the hypothalamus may be responsible for heat stroke.

Authors:  Sheng-Hsien Chen; Mao-Tsun Lin; Ching-Ping Chang
Journal:  Curr Neuropharmacol       Date:  2013-03       Impact factor: 7.363

5.  Metabolomic profiling identifies a novel mechanism for heat stroke‑related acute kidney injury.

Authors:  Ling Xue; Wenli Guo; Li Li; Santao Ou; Tingting Zhu; Liang Cai; Wenfei Ding; Weihua Wu
Journal:  Mol Med Rep       Date:  2021-01-28       Impact factor: 2.952

  5 in total

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