An epigenetic rheostat of experience: DNA methylation of OXTR as a mechanism of early life allostasis.
An epigenetic rheostat of experience: DNA methylation of OXTR as a mechanism of early life allostasis.
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DOI:
10.1016/j.cpnec.2021.100098
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发表时间:
2021-11
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Oxytocin is a neuropeptide hormone which is involved in regulation of social behavior, stress response, muscle contraction, and metabolism. Oxytocin signaling is dependent on its binding to the oxytocin receptor, coded for by the OXTR gene. Many studies have examined the role of epigenetic regulation of OXTR in neurological and behavioral outcomes in both humans and animal models. Here, we review these studies, critically analyze their findings in the context of oxytocin's role as an allostatic hormone, and provide suggestions for future research. We use OXTR as a model for how those in the field of psychoneuroendocrinology should perform epigenetic studies in order to maximize both biological relevance and potential for biomarker development. Oxytocin is now recognized as an allostatic hormone preparing individuals for future social and nonsocial environments. Early life experiences alter DNA methylation of the oxytocin receptor gene (OXTR) in both humans and model organisms. DNA methylation of OXTR may be a key mediator of oxytocin's effects as an allostatic hormone. Further mechanistic work is needed to understand OXTR methylation’s role in adaptive processes and its use as a biomarker.