Department of Psychiatry, Hamamatsu University School of Medicine, 1-20-1 Handayama, Higashi-ku, Hamamatsu, Shizuoka 431-3192, Japan.
Peptides. 2024 Jan;171:171133. doi: 10.1016/j.peptides.2023.171133. Epub 2023 Dec 10.
No approved pharmacological intervention currently exists to address the core symptoms of autism spectrum disorder, a prevalent neurodevelopmental condition. However, there is a growing body of empirical evidence highlighting oxytocin's modulatory effects on social and communicative behaviors. Numerous single-dose trials have consistently demonstrated the efficacy of oxytocin in ameliorating behavioral and neural measurements associated with the core symptoms of autism spectrum disorder. Nevertheless, prior investigations involving the repeated administration of oxytocin have yielded disparate findings concerning its effectiveness, particularly in relation to clinical measures of the core symptoms of autism spectrum disorder. Recent studies have also raised the possibility of diminishing efficacy of oxytocin over time, particularly when higher or recurrent dosages of oxytocin are administered. This review article aims to provide an overview of previous studies examining this issue. Furthermore, it aims to discuss the potential mechanisms underlying these effects, including the interaction between oxytocin and vasopressin, as well as potential strategies for addressing the challenges mentioned. This review's overall objective is to provide insights into the potential development of innovative therapeutics to mitigate the core symptoms of autism spectrum disorder, representing potential breakthroughs in the treatment of this complex neurodevelopmental condition.
目前尚无经过批准的药理学干预措施可用于解决自闭症谱系障碍的核心症状,自闭症谱系障碍是一种普遍的神经发育障碍。然而,越来越多的实证证据强调了催产素对社交和沟通行为的调节作用。许多单剂量试验一致表明,催产素可有效改善与自闭症谱系障碍核心症状相关的行为和神经测量。然而,先前涉及催产素重复给药的研究对于其有效性的结果存在差异,特别是在与自闭症谱系障碍核心症状的临床测量相关的方面。最近的研究还提出了催产素随着时间的推移效力可能会降低的可能性,尤其是当给予更高或更频繁的催产素剂量时。本文旨在综述以前研究该问题的研究。此外,还旨在讨论这些影响的潜在机制,包括催产素和加压素之间的相互作用,以及解决所述挑战的潜在策略。本综述的总体目标是深入了解开发创新疗法以减轻自闭症谱系障碍核心症状的潜力,这代表着治疗这种复杂神经发育障碍的潜在突破。