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Emulsified isoflurane postconditioning improves survival and neurological outcomes in a rat model of cardiac arrest

  • Authors:
    • Ya‑Jie Zhang
    • Meng‑Jun Wu
    • Hai Yu
    • Jin Liu
  • View Affiliations / Copyright

    Affiliations: Department of Anesthesiology and Translational Neuroscience Center, West China Hospital, Sichuan University, Chengdu, Sichuan 610041, P.R. China
    Copyright: © Zhang et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 65-72
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    Published online on: May 11, 2017
       https://doi.org/10.3892/etm.2017.4446
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Abstract

Emulsified isoflurane (EIso) has a protective effect against ischemia/reperfusion (I/R) injury in animal models. However, the protective effects of EIso on global cerebral I/R injury remain unclear. The present study aimed to investigate whether EIso postconditioning was able to improve survival and neurological outcomes in a rat model of cardiac arrest (CA). Rats were randomly divided into five groups, namely the control, EIso‑2ml, EIso‑4ml, isoflurane (Iso) and emulsion (E) groups. All rats were resuscitated by a standardized method following 6 min of asphyxia. Furthermore, all interventions were administered immediately following the return of spontaneous circulation (ROSC). The animal survival was recorded daily, and evaluations of behavioral and brain morphology were assessed at 1 and 7 days after ROSC. The results showed that EIso treatment increased the survival rate 7 days after ROSC, with a 41.7% 7‑day survival in the EIso‑2ml group, 66.7% in the EIso‑4ml group and 50% in the Iso group compared with 33.3% survival in the control and E groups. Moreover, the neural deficit score and memory function were improved in the EIso‑4ml group, and this treatment also ameliorated brain hippocampal cell injury and apoptosis. In addition, a better brain protective effect was observed in the EIso‑4ml group compared with the EIso‑2ml, Iso and E groups. In summary, the data of the present study suggest that EIso postconditioning improved the survival and neurological outcomes following CA in a dose-dependent manner.
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Copy and paste a formatted citation
Spandidos Publications style
Zhang YJ, Wu MJ, Yu H and Liu J: Emulsified isoflurane postconditioning improves survival and neurological outcomes in a rat model of cardiac arrest. Exp Ther Med 14: 65-72, 2017.
APA
Zhang, Y., Wu, M., Yu, H., & Liu, J. (2017). Emulsified isoflurane postconditioning improves survival and neurological outcomes in a rat model of cardiac arrest. Experimental and Therapeutic Medicine, 14, 65-72. https://doi.org/10.3892/etm.2017.4446
MLA
Zhang, Y., Wu, M., Yu, H., Liu, J."Emulsified isoflurane postconditioning improves survival and neurological outcomes in a rat model of cardiac arrest". Experimental and Therapeutic Medicine 14.1 (2017): 65-72.
Chicago
Zhang, Y., Wu, M., Yu, H., Liu, J."Emulsified isoflurane postconditioning improves survival and neurological outcomes in a rat model of cardiac arrest". Experimental and Therapeutic Medicine 14, no. 1 (2017): 65-72. https://doi.org/10.3892/etm.2017.4446
Copy and paste a formatted citation
x
Spandidos Publications style
Zhang YJ, Wu MJ, Yu H and Liu J: Emulsified isoflurane postconditioning improves survival and neurological outcomes in a rat model of cardiac arrest. Exp Ther Med 14: 65-72, 2017.
APA
Zhang, Y., Wu, M., Yu, H., & Liu, J. (2017). Emulsified isoflurane postconditioning improves survival and neurological outcomes in a rat model of cardiac arrest. Experimental and Therapeutic Medicine, 14, 65-72. https://doi.org/10.3892/etm.2017.4446
MLA
Zhang, Y., Wu, M., Yu, H., Liu, J."Emulsified isoflurane postconditioning improves survival and neurological outcomes in a rat model of cardiac arrest". Experimental and Therapeutic Medicine 14.1 (2017): 65-72.
Chicago
Zhang, Y., Wu, M., Yu, H., Liu, J."Emulsified isoflurane postconditioning improves survival and neurological outcomes in a rat model of cardiac arrest". Experimental and Therapeutic Medicine 14, no. 1 (2017): 65-72. https://doi.org/10.3892/etm.2017.4446
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