Instituto de Neurociencias de Alicante, Consejo Superior de Investigaciones Científicas - Universidad Miguel Hernández (CSIC-UMH), 03550, Sant Joan d´Alacant, Spain.
Laboratoire de Physiologie de La Reproduction Et Des Comportements, CNRS, IFCE, INRAE, University of Tours, 37380, Nouzilly, France.
Mol Neurobiol. 2023 Aug;60(8):4641-4658. doi: 10.1007/s12035-023-03362-3. Epub 2023 May 2.
Normal aging and many age-related disorders such as Alzheimer's disease cause deficits in olfaction; however, it is currently unknown how natural and pathological aging impacts the detection of social odors which might contribute to the impoverishment of social behavior at old age further worsening overall health. Analysis of the vomeronasal organ, the main gateway to pheromone-encoded information, indicated that natural and pathological aging distinctively affects the neurogenic ability of the vomeronasal sensory epithelium. Whereas cell proliferation remained majorly preserved in 1-year-old APP/PS1 mice, naturally aged animals exhibited significant deficiencies in the number of mature, proliferative, and progenitor cells. These alterations may support age-related deficits in the recognition of social cues and the display of social behavior. Our findings indicate that aging disrupts the processing of social olfactory cues decreasing social odor exploration, discrimination, and habituation in both wild-type senescent (2-year-old) mice and in 1-year-old double mutant model of Alzheimer's disease (APP/PS1). Furthermore, social novelty was diminished in 1-year-old APP/PS1 mice, indicating that alterations in the processing of social cues are accelerated during pathological aging. This study reveals fundamental differences in the cellular processes by which natural and pathological aging disrupts the exploration of social information and social behavior.
正常衰老和许多与年龄相关的疾病(如阿尔茨海默病)会导致嗅觉减退;然而,目前尚不清楚自然衰老和病理衰老如何影响对社交气味的检测,而社交气味的检测可能导致老年社交行为的匮乏,进一步恶化整体健康状况。对犁鼻器(主要的信息素编码的嗅觉感知器官)的分析表明,自然衰老和病理衰老对犁鼻感觉上皮的神经发生能力有明显不同的影响。虽然 1 岁 APP/PS1 小鼠的细胞增殖仍主要保持,但自然衰老的动物在成熟、增殖和祖细胞的数量上存在明显的不足。这些改变可能支持与年龄相关的社交线索识别和社交行为表现的缺陷。我们的研究结果表明,衰老会破坏社交嗅觉线索的处理,减少社交气味的探索、辨别和习惯化,无论是在 2 岁的野生型衰老(衰老)小鼠还是在 1 岁的阿尔茨海默病双突变模型(APP/PS1)中均如此。此外,1 岁 APP/PS1 小鼠对社交新颖性的反应减弱,表明在病理衰老过程中,社交线索处理的改变加速。这项研究揭示了自然衰老和病理衰老破坏社交信息和社交行为探索的细胞过程中的基本差异。