» Articles » PMID: 38380151

Influence of Short-term Hypoxic Exposure on Spatial Learning and Memory Function and Brain-derived Neurotrophic Factor in Rats-A Practical Implication to Human's Lost Way

Overview
Specialty Psychology
Date 2024 Feb 21
PMID 38380151
Authors
Affiliations
Soon will be listed here.
Abstract

The present study aimed to investigate the effects of a short period of normobaric hypoxic exposure on spatial learning and memory, and brain-derived neurotrophic factor (BDNF) levels in the rat hippocampus. Hypoxic conditions were set at 12.5% O. We compared all variables between normoxic trials (Norm), after 24 h (Hypo-24 h), and after 72 h of hypoxic exposure (Hypo-72 h). Spatial learning and memory were evaluated by using a water-finding task in an open field. Time to find water drinking fountains was significantly extended in Hypo 24 h (36.2 ± 21.9 s) compared to those in Norm (17.9 ± 12.8 s; < 0.05), whereas no statistical differences between Norm and Hypo-72 h (22.7 ± 12.3 s). Moreover, hippocampal BDNF level in Hypo-24 h was significantly lower compared to Norm (189.4 ± 28.4 vs. 224.9 ± 47.7 ng/g wet tissue, < 0.05), whereas no statistically differences in those between Norm and Hypo-72 h (228.1 ± 39.8 ng/g wet tissue). No significant differences in the changes in corticosterone and adrenocorticotropic hormone levels were observed across the three conditions. When data from Hypo-24 h and Hypo-72 h of hypoxia were pooled, there was a marginal negative relationship between the time to find drinking fountains and BDNF ( < 0.1), and was a significant negative relationship between the locomotor activities and BDNF ( < 0.05). These results suggest that acute hypoxic exposure (24 h) may impair spatial learning and memory; however, it recovered after 72 h of hypoxic exposure. These changes in spatial learning and memory may be associated with changes in the hippocampal BDNF levels in rats.

Citing Articles

Aerobic exercise training improves learning and memory performance in hypoxic-exposed rats by activating the hippocampal PKA-CREB-BDNF signaling pathway.

Luo S, Shi L, Liu T, Jin Q BMC Neurosci. 2025; 26(1):13.

PMID: 39984845 PMC: 11846353. DOI: 10.1186/s12868-025-00935-x.

References
1.
Yogev-Seligmann G, Hausdorff J, Giladi N . The role of executive function and attention in gait. Mov Disord. 2007; 23(3):329-42. PMC: 2535903. DOI: 10.1002/mds.21720. View

2.
Buchman A, Yu L, Boyle P, Schneider J, De Jager P, Bennett D . Higher brain BDNF gene expression is associated with slower cognitive decline in older adults. Neurology. 2016; 86(8):735-41. PMC: 4763800. DOI: 10.1212/WNL.0000000000002387. View

3.
Miyamoto Y, Yamada K, Noda Y, Mori H, Mishina M, Nabeshima T . Hyperfunction of dopaminergic and serotonergic neuronal systems in mice lacking the NMDA receptor epsilon1 subunit. J Neurosci. 2001; 21(2):750-7. PMC: 6763826. View

4.
Zhang W, Shi Y, Peng Y, Zhong L, Zhu S, Zhang W . Neuron activity-induced Wnt signaling up-regulates expression of brain-derived neurotrophic factor in the pain neural circuit. J Biol Chem. 2018; 293(40):15641-15651. PMC: 6177598. DOI: 10.1074/jbc.RA118.002840. View

5.
Johnson A . Hippocampal Vascular Supply and Its Role in Vascular Cognitive Impairment. Stroke. 2023; 54(3):673-685. PMC: 9991081. DOI: 10.1161/STROKEAHA.122.038263. View