Abstract

Human and animal studies have elucidated the apparent neurodevelopmental effects resulting from neonatal anesthesia. Observations of learning and behavioral deficits in children, who were exposed to anesthesia early in development, have instigated a flurry of studies that have predominantly utilized animal models to further interrogate the mechanisms of neonatal anesthesia-induced neurotoxicity. Specifically, while neonatal anesthesia has demonstrated its propensity to affect multiple cell types in the brain, it has shown to have a particularly detrimental effect on the gamma aminobutyric acid (GABA)ergic system, which contributes to the observed learning and behavioral deficits. The damage to GABAergic neurons, resulting from neonatal anesthesia, seems to involve structure-specific changes in excitatory-inhibitory balance and neurovascular coupling, which manifest following a significant interval after neonatal anesthesia exposure. Thus, to better understand how neonatal anesthesia affects the GABAergic system, we first review the early development of the GABAergic system in various structures that have been the focus of neonatal anesthesia research. This is followed by an explanation that, due to the prolonged developmental curve of the GABAergic system, the entirety of the negative effects of neonatal anesthesia on learning and behavior in children are not immediately evident, but instead take a substantial amount of time (years) to fully develop. In order to address these concerns going forward, we subsequently offer a variety of in vivo methods which can be used to record these delayed effects.

Highlights

  • The disproportionate neurotoxic and neuroapoptotic effects of neonatal anesthesia can negatively affect the GABAergic system in structures associated with learning and behavior, during their critical periods of development

  • We conclude, neonatal anesthesia’s effect on GABAergic development can account for some of the delayed learning and behavioral abnormalities seen in older children

  • Animal models have definitively concluded that neuroapoptosis is evident throughout the brain following neonatal anesthesia exposure in animals

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Summary

Introduction

Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations. Wilder et al [2] identified a significant relationship between anesthesia exposure before the age of four and math learning disabilities, and Chemaly and colleagues [3] found a significant relationship between anesthesia exposure and long-term abnormal behavior, where the likelihood of abnormal behavior increased with anesthesia duration but decreased as the child grew older These notable studies highlight the potential consequences of neonatal anesthesia exposure, for which, several further studies and reviews have provided converging evidence [2,4,5,6,7,8]. Taking into account the importance of the GABAergic system in neuronal networks, we will briefly review the functions of this system and the critical period of its development, around the time of neonatal anesthesia exposure This will provide context to the subsequent analysis of the neurotoxic and neuroapoptotic consequences of neonatal anesthesia during GABAergic development, and how this may be related to the learning and behavioral deficits observed following neonatal anesthesia exposure. Sci. 2021, 22, 12951 will discuss current and prospective methodologies that can be applied in vivo to detect changes in the natural GABAergic functioning and development in children following neonatal anesthesia

GABAergic Inhibition and Neurovascular Coupling
Structure-Specific GABAergic System Function
Physiology of the E-I Balance
GABA Signaling Development
Neuroapoptosis in GABAergic Structures
Short-Term Neurotoxicity
Long-Term Neurovascular Coupling Deficiency
E-I Imbalance after Neonatal Anesthesia
Methodological Outlook
Neuroimaging Techniques
Neuroimaging Alternatives
Findings
Concluding Remarks
Full Text
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