单次长时间应激模型引起的视觉特性的性别差异

IF 4.6 2区 医学 Q1 NEUROSCIENCES
Qianhui Xia, Xi Kuang, Wei Meng, Fei Yin, Chenchen Ma, Yupeng Yang
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引用次数: 0

摘要

创伤后应激障碍(PTSD)患者的症状表现存在性别差异,女性比男性更容易出现侵入性症状和回避症状,这突出表明在研究和治疗过程中需要考虑性别因素。我们的研究利用单次长期应激(SPS)模型(创伤后应激障碍的部分有效啮齿类动物模型)深入研究了应激诱导的视觉损伤的性别特异性。雄性 SPS 小鼠表现出初级视觉皮层(V1)神经元的最佳空间频率(SF)增高,而雌性 SPS 小鼠则表现出 V1 神经元的最佳时间频率(TF)降低。这一现象一直持续到SPS建模后的第29天,这可能是观察到雄性SPS小鼠在视觉水任务中视觉敏锐度提高的生理基础。此外,我们的研究还发现,促肾上腺皮质激素释放因子受体1能调节小鼠V1的最佳TF和最佳SF,但不表现出性别差异。这些发现表明,严重应激会对视觉功能产生性别特异性影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sex-specific alterations in visual properties induced by single prolonged stress model

Patients with post-traumatic stress disorder (PTSD) exhibit sex differences in symptomology, with women more likely to report higher rates of intrusive and avoidance symptoms than men, underscoring the need for sex-informed approaches to research and treatment. Our study delved into the sex-specific aspects of stress-induced visual impairments using the single prolonged stress (SPS) model, a partially validated rodent model for PTSD. Male SPS mice exhibit heightened optimal spatial frequency (SF) of primary visual cortex (V1) neurons, while female counterparts exhibit decreased optimal temporal frequency (TF) of V1 neurons. This phenomenon persisted until the 29th day after SPS modeling, and it may be the physiological basis for the observed increase in visual acuity in male SPS mice in visual water task. Furthermore, our study found that corticotropin-releasing factor receptor 1 regulated optimal TF and optimal SF of V1 in mice, but did not exhibit sex differences. These findings indicated that severe stress induces sex-specific effects on visual function.

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来源期刊
Neuropharmacology
Neuropharmacology 医学-神经科学
CiteScore
10.00
自引率
4.30%
发文量
288
审稿时长
45 days
期刊介绍: Neuropharmacology publishes high quality, original research and review articles within the discipline of neuroscience, especially articles with a neuropharmacological component. However, papers within any area of neuroscience will be considered. The journal does not usually accept clinical research, although preclinical neuropharmacological studies in humans may be considered. The journal only considers submissions in which the chemical structures and compositions of experimental agents are readily available in the literature or disclosed by the authors in the submitted manuscript. Only in exceptional circumstances will natural products be considered, and then only if the preparation is well defined by scientific means. Neuropharmacology publishes articles of any length (original research and reviews).
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