Key Laboratory of Brain Functional Genomics of Ministry of Education, Shanghai Key Laboratory of Brain Functional Genomics, School of Life Sciences, East China Normal University, Shanghai, 200062, China.
New York University-East China Normal University Institute of Brain and Cognitive Science, New York University-Shanghai, Shanghai, 200062, China.
J Neurosci. 2023 Apr 19;43(16):2850-2859. doi: 10.1523/JNEUROSCI.2027-22.2023. Epub 2023 Mar 22.
Antidepressants, while effective in treating depression and anxiety disorders, also induce deficits in sensory (particularly auditory) processing, which in turn may exacerbate psychiatric symptoms. How antidepressants cause auditory signature deficits remains largely unknown. Here, we found that fluoxetine-treated adult female rats were significantly less accurate when performing a tone-frequency discrimination task compared with age-matched control rats. Their cortical neurons also responded less selectively to sound frequencies. The degraded behavioral and cortical processing was accompanied by decreased cortical perineuronal nets, particularly those wrapped around parvalbumin-expressing inhibitory interneurons. Furthermore, fluoxetine induced critical period-like plasticity in their already mature auditory cortices; therefore, a brief rearing of these drug-treated rats under an enriched acoustic environment renormalized auditory processing degraded by fluoxetine. The altered cortical expression of perineuronal nets was also reversed as a result of enriched sound exposure. These findings suggest that the adverse effects of antidepressants on auditory processing, possibly because of a reduction in intracortical inhibition, can be substantially alleviated by simply pairing drug treatment with passive, enriched sound exposure. They have important implications for understanding the neurobiological basis of antidepressant effects on hearing and for designing novel pharmacological treatment strategies for psychiatric disorders. Clinical experience suggests that antidepressants adversely affect sensory (particularly auditory) processing, which can exacerbate patients' psychiatric symptoms. Here, we show that the antidepressant fluoxetine reduces cortical inhibition in adult rats, leading to degraded behavioral and cortical spectral processing of sound. Importantly, fluoxetine induces a critical period-like state of plasticity in the mature cortex; therefore, a brief rearing under an enriched acoustic environment is sufficient to reverse the changes in auditory processing caused by the administration of fluoxetine. These results provide a putative neurobiological basis for the effects of antidepressants on hearing and indicate that antidepressant treatment combined with enriched sensory experiences could optimize clinical outcomes.
抗抑郁药在治疗抑郁和焦虑障碍方面非常有效,但也会导致感觉(尤其是听觉)处理能力下降,进而可能加重精神症状。抗抑郁药如何引起听觉特征缺陷在很大程度上仍是未知的。在这里,我们发现与年龄匹配的对照组大鼠相比,氟西汀处理的成年雌性大鼠在执行音调频率辨别任务时准确性明显降低。它们的皮质神经元对声音频率的反应也不那么有选择性。皮质周围神经毡网络(perineuronal nets,PNNs)的退化与皮质内抑制性中间神经元表达的 parvalbumin 减少有关。此外,氟西汀诱导了其已经成熟的听觉皮层类似关键期的可塑性;因此,这些药物处理的大鼠在丰富的听觉环境中短暂饲养,可以使氟西汀引起的听觉处理能力下降恢复正常。皮层 PNNs 的改变表达也因丰富的声音暴露而逆转。这些发现表明,抗抑郁药对听觉处理的不良影响可能是由于皮质内抑制作用减弱所致,通过将药物治疗与被动的、丰富的声音暴露相结合,这种不良影响可以得到显著缓解。这些发现对于理解抗抑郁药对听觉的神经生物学基础以及设计治疗精神障碍的新型药理学治疗策略具有重要意义。临床经验表明,抗抑郁药会对感觉(特别是听觉)处理产生不良影响,这可能会加重患者的精神症状。在这里,我们表明抗抑郁药氟西汀会降低成年大鼠的皮质抑制作用,导致声音的行为和皮质光谱处理能力下降。重要的是,氟西汀在成熟的皮质中诱导了类似关键期的可塑性状态;因此,在丰富的听觉环境中短暂饲养足以逆转氟西汀给药引起的听觉处理变化。这些结果为抗抑郁药对听觉的影响提供了一个潜在的神经生物学基础,并表明抗抑郁治疗与丰富的感官体验相结合可能优化临床结果。