High-Intensity Interval Exercise Regulates Neurotrophic Factors and Astrocyte Activity in the Hippocampus and Cerebral Cortexopen access
- Authors
- Junyoung Hong; Seon-Hee Kim; Jiyeon Kim; Dong-ho Park; Hye Jung Kim; Sang Won Park; Jong-Won Kim; Young Hyun Jung; Seung Pil Yun
- Issue Date
- Nov-2025
- Publisher
- 한국운동생리학회
- Keywords
- High-intensity interval exercises; Astrocyte; Neurotrophic factor; Hippocampus; Cerebral cortex
- Citation
- 운동과학, v.34, no.4, pp 467 - 477
- Pages
- 11
- Indexed
- SCOPUS
KCI
- Journal Title
- 운동과학
- Volume
- 34
- Number
- 4
- Start Page
- 467
- End Page
- 477
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/81941
- ISSN
- 1226-1726
2384-0544
- Abstract
- PURPOSE: Exercise training is widely recognized as a complementary intervention that provides both therapeutic and preventive benefits for neurodegenerative diseases, given its strong association with brain health. Regulating the expression of neurotrophic factors can significantly enhance cognitive function and memory processes, particularly in conditions such as Alzheimer’s disease (AD). However, the effects of high-intensity interval aerobic exercise training (HIE) on brain-derived neurotrophic factors and astrocyte activation in the cortex (CTX) and the hippocampus (HIP) remain unclear. Therefore, this study aimed to investigate whether HIE regulates the expression of neurotrophic factors and neuroinflammatory cytokines in the CTX and HIP.
METHODS: Eighteen-week-old female C57BL/6 mice were assigned to control (Cnt) and HIE groups. After 12 weeks of HIE, the brains were harvested for immunoblotting, immunofluorescence, real-time PCR (qRT-PCR), and terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assays.
RESULTS: HIE increased the expression of glial cell line-derived neurotrophic factor (GDNF) protein in the CTX but not in the HIP.
Additionally, HIE exerted a protective effect against neuroinflammation by significantly upregulating A2-specific astrocytic transcripts.
These findings suggest that HIE promotes neurotrophic and anti-inflammatory responses in both CTX and HIP.
CONCLUSIONS: Our study results suggest that HIE exerts protective regulatory effects on neurotrophic factors, neuroinflammation, and A1/A2 type astrocytic reactivity in CTX and HIP of animal models. These findings suggest that HIE has beneficial effects on brain health. However, as these results were derived from animal studies, further clinical research is required to determine whether similar neuroprotective effects can be observed in humans.
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