Abstract

Cardiac arrest is a leading cause of death and disability worldwide. Although many victims are initially resuscitated, they often suffer from serious brain injury, even leading to a “persistent vegetative state”. Therefore, it is need to explore therapies which restore and protect brain function after cardiac arrest. In the present study, using Tg (HuC:GCaMP5) zebrafish as a model, we found the zebrafish brain generated a burst of Ca2+ wave after cardiac arrest by in vivo time-lapse confocal imaging. The Ca2+ wave was firstly initiated at hindbrain and then sequentially propagated to midbrain and telencephalon, the neuron displayed Ca2+ overload after Ca2+ wave propagation. Consistent with this, our study further demonstrated neuronal apoptosis was increased in cardiac arrest zebrafish by TUNEL staining. The cardiac arrest-induced Ca2+ wave propagation can be prevented by general anesthetics such as midazolam or ketamine pretreatment. Moreover, midazolam or ketamine pretreatment dramatically decreased the neuronal apoptosis and improved the survival rate in CA zebrafish. Taken together, these findings provide the first in vivo evidence that general anesthetics pretreatment protects against cardiac arrest-induced brain injury by inhibiting calcium wave propagation in zebrafish.

Highlights

  • Cardiac arrest (CA) remains a primary cause of death and persistent disability throughout the world, despite tremendous improvements in emergency medical care and increased public delivery of bystander cardiopulmonary resuscitation (CPR) [1, 2]

  • Cardiac arrest causes a burst of Ca2+ wave in zebrafish brain

  • We found that the zebrafish brain exhibited a burst of Ca2+ wave after CA

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Summary

Introduction

Cardiac arrest (CA) remains a primary cause of death and persistent disability throughout the world, despite tremendous improvements in emergency medical care and increased public delivery of bystander cardiopulmonary resuscitation (CPR) [1, 2]. Therapeutic hypothermia clearly provides a statistically significant improvement of brain damage in ventricular fibrillation–induced out-of-hospital CA patients, the clinical effect is quite modest, it has been shown at most 20% of victims in whom return of spontaneous circulation benefit from hypothermia treatment [9, 10]. It is essential to decipher the brain injury mechanisms and develop treatments to increase survival and improve quality of life after CA. The CA-induced Ca2+ wave can be inhibited by general anesthetics pretreatment. General anesthetics pretreatment significantly decreased the neuronal death and improved the survival rate and locomotor activity in CA zebrafish. Our study reveals the burst Ca2+ wave propagation after CA contributed to brain injury. General anesthetics pretreatment can inhibit the CA-induced Ca2+ wave and improve neurological outcomes after CA

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