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The aging mouse brain: cognition, connectivity and calcium.
Radulescu, Carola I; Cerar, Veronika; Haslehurst, Peter; Kopanitsa, Maksym; Barnes, Samuel J.
Afiliação
  • Radulescu CI; UK Dementia Research Institute, Department of Brain Sciences, Imperial College London, Hammersmith Hospital Campus, Du Cane Road, London, W12 0NN, UK.
  • Cerar V; UK Dementia Research Institute, Department of Brain Sciences, Imperial College London, Hammersmith Hospital Campus, Du Cane Road, London, W12 0NN, UK.
  • Haslehurst P; Department of Pharmacology, University of Oxford, Oxford, OX1 3QT, UK.
  • Kopanitsa M; UK Dementia Research Institute, Department of Brain Sciences, Imperial College London, Hammersmith Hospital Campus, Du Cane Road, London, W12 0NN, UK.
  • Barnes SJ; UK Dementia Research Institute, Department of Brain Sciences, Imperial College London, Hammersmith Hospital Campus, Du Cane Road, London, W12 0NN, UK. Electronic address: samuel.barnes@imperial.ac.uk.
Cell Calcium ; 94: 102358, 2021 03.
Article em En | MEDLINE | ID: mdl-33517250
ABSTRACT
Aging is a complex process that differentially impacts multiple cognitive, sensory, neuronal and molecular processes. Technological innovations now allow for parallel investigation of neuronal circuit function, structure and molecular composition in the brain of awake behaving adult mice. Thus, mice have become a critical tool to better understand how aging impacts the brain. However, a more granular systems-based approach, which considers the impact of age on key features relating to neural processing, is required. Here, we review evidence probing the impact of age on the mouse brain. We focus on a range of processes relating to neuronal function, including cognitive abilities, sensory systems, synaptic plasticity and calcium regulation. Across many systems, we find evidence for prominent age-related dysregulation even before 12 months of age, suggesting that emerging age-related alterations can manifest by late adulthood. However, we also find reports suggesting that some processes are remarkably resilient to aging. The evidence suggests that aging does not drive a parallel, linear dysregulation of all systems, but instead impacts some processes earlier, and more severely, than others. We propose that capturing the more fine-scale emerging features of age-related vulnerability and resilience may provide better opportunities for the rejuvenation of the aged brain.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Encéfalo / Envelhecimento / Cálcio / Cognição / Rede Nervosa Limite: Animals Idioma: En Revista: Cell Calcium Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Encéfalo / Envelhecimento / Cálcio / Cognição / Rede Nervosa Limite: Animals Idioma: En Revista: Cell Calcium Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Reino Unido