| Literature DB >> 33141436 |
Andriy Yabluchanskiy1, Adam Nyul-Toth1,2, Anna Csiszar1, Rafal Gulej3, Debra Saunders3, Rheal Towner3, Monroe Turner4, Yuguang Zhao4, Dema Abdelkari4, Bart Rypma4,5, Stefano Tarantini1,6,7.
Abstract
The present and future research efforts in cognitive neuroscience and psychophysiology rely on the measurement, understanding, and interpretation of blood oxygenation level-dependent (BOLD) functional magnetic resonance imaging (fMRI) to effectively investigate brain function. Aging and age-associated pathophysiological processes change the structural and functional integrity of the cerebrovasculature which can significantly alter how the BOLD signal is recorded and interpreted. In order to gain an improved understanding of the benefits, drawbacks, and methodological implications for BOLD fMRI in the context of cognitive neuroscience, it is crucial to understand the cellular and molecular mechanism of age-related vascular pathologies. This review discusses the multifaceted effects of aging and the contributions of age-related pathologies on structural and functional integrity of the cerebral microcirculation as they has been investigated in animal models of aging, including age-related alterations in neurovascular coupling responses, cellular and molecular mechanisms involved in microvascular damage, vascular rarefaction, blood-brain barrier disruption, senescence, humoral deficiencies as they relate to, and potentially introduce confounding factors in the interpretation of BOLD fMRI.Entities:
Keywords: aging; microcirculation; neurovascular coupling; senescence
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Year: 2020 PMID: 33141436 PMCID: PMC9166153 DOI: 10.1111/psyp.13718
Source DB: PubMed Journal: Psychophysiology ISSN: 0048-5772 Impact factor: 4.348