Post-encoding administration of oxytocin selectively enhances memory consolidation of male faces in females

催产素 编码(内存) 遗产管理(遗嘱认证法) 记忆巩固 心理学 神经科学 政治学 海马体 法学
作者
Jiashen Li,Zhengyue Chen,Wei Liu
标识
DOI:10.1101/2024.06.18.599465
摘要

Abstract Oxytocin plays a critical role in modulating social cognition and enhancing human memory for faces. However, it remains unclear which stage of memory oxytocin affects to enhance face memory. Our study explored oxytocin’s potential to selectively enhance the consolidation of social memories, specifically human faces, and whether this effect varies between genders. In two preregistered, randomized, double-blind, placebo-controlled trials with heterosexual participants (total N=294, comprising 149 males and 145 females), we explored how oxytocin affects memory consolidation. We administered oxytocin immediately after encoding (i.e., Study1) and 30 minutes before retrieval in a parallel study (i.e., Study2). This design allowed us to confirm that oxytocin’s effects were indeed due to consolidation rather than retrieval. We found that administering oxytocin post-encoding, but not before-retrieval, significantly improved female participants’ ability to recognize male faces 24 hours later, with no similar enhancement observed in males recognizing opposite-gender faces. Together with our analyses of social placebo effects and approachability rating during encoding, we concluded that oxytocin enhanced consolidation of long-term social memories in humans. Our results not only advance the understanding of the neurobiological mechanisms underlying social memory consolidation but also highlight oxytocin as a pharmacological tool for selectively enhancing human memory consolidation. Highlights Oxytocin selectively enhances memory consolidation of human faces, with gender-specific effects. In females, oxytocin after encoding improves recognition of male faces after 24 hours. Oxytocin-induced enhancement of social memory is due to enhanced consolidation, not retrieval or encoding. Oxytocin shows potential for selectively modulating memory consolidation in humans.
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