Why the study?
Long-term operations at high altitude may trigger health complications, and chronic exposure to high altitude has specifically been associated with deficits in cognitive function.
Does chronic exposure to high altitude impair cognitive function and alter synaptic protein expression in C57BL/6 male mice?
Does chronic exposure to high altitude impair cognitive function and alter synaptic protein expression in C57BL/6 male mice?
Chronic exposure to high altitude induces hippocampal memory impairment and region-specific downregulation of synaptic and astroglial proteins in mice.
Raises caution for cognitive risks at altitude; hypothesis-generating for human translation and synaptic targets.
Long-term operations carried out at high altitude (HA) by military personnel, pilots, and astronauts may trigger health complications. In particular, chronic exposure to high altitude (CEHA) has been associated with deficits in cognitive function. In this study, we found that mice exposed to chronic HA (5000 m for 12 weeks) exhibited deficits in learning and memory associated with hippocampal function and were linked with changes in the expression of synaptic proteins across various regions of the brain. Specifically, we found decreased levels of synaptophysin (SYP) (p < 0.05) and spinophilin (SPH) (p < 0.05) in the olfactory cortex, post synaptic density-95 (PSD-95) (p < 0.05), growth associated protein 43 (GAP43) (p < 0.05), glial fibrillary acidic protein (GFAP) (p < 0.05) in the cerebellum, and SYP (p < 0.05) and PSD-95 (p < 0.05) in the brainstem. Ultrastructural analyses of synaptic density and morphology in the hippocampus did not reveal any differences in CEHA mice compared to SL mice. Our data are novel and suggest that CEHA exposure leads to cognitive impairment in conjunction with neuroanatomically-based molecular changes in synaptic protein levels and astroglial cell marker in a region specific manner. We hypothesize that these new findings are part of highly complex molecular and neuroplasticity mechanisms underlying neuroadaptation response that occurs in brains when chronically exposed to HA.
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Sharma et al. (2019) studied this question.
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