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Acute and chronic effects of high-intensity interval training on selected exerkine secretion in health, disease, and aging: a systematic review.

PMID: 41659923 · DOI: 10.3389/fphys.2025.1733269 · Frontiers in physiology, 2025 · Zbigniew Jost, Agata Rozynkowska, Michalina Głąb, Alicja Sitkiewicz, Mia Goiko, Radosław Laskowski, Fabian Herold, Zsolt
📄 Abstract

In contemporary research practice, high-intensity interval training (HIIT) has received growing attention compared to other types of endurance training [e.g., moderate-intensity continuous training (MICT)]. This is primarily related to HIIT's ability to induce higher metabolic stress, driving an increased exerkine secretory response (i.e., of specific proteins) compared to MICT. To date, previous reviews on HIIT have primarily focused on single exerkines, while a more comprehensive analysis, as required to gain a more comprehensive understanding of the complex exercise-related physiological processes, is absent. To reduce non-exercise protocol-related outcome heterogeneity, the rigorous inclusion criteria (i.e., exercise intensity in the HIIT adjusted for the target population of healthy, diseased, or older individuals, and not taking any medications) were applied. A total of 39 studies were selected for the systematic review, with fourteen, twenty-two, and three for the acute, chronic, and both acute and chronic effects of HIIT on exerkine concentrations, respectively. Acute HIIT appears to result in greater changes in BDNF and VEGF concentration than the control group performing lower-intensity exercise or no exercise. Metabolically active exerkine, such as adiponectin, mainly fluctuates among overweight and obese participants. This systematic review did not yield any definitive results regarding alterations in IGF-1, irisin, cortisol, and interleukin levels. Tendentially, HIIT is more effective than MICT and non-exercise interventions to induce a greater secretory response of certain exerkines, such as BDNF, VEGF and adiponectin. Evidence regarding exerkine secretion in response to HIIT among older adults remains limited, highlighting the need for further investigation. Identifier CRD420251003743.

Confidence: 0.1 · 4 полей извлечено
Идентификация (6 полей)
Target
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Protein family
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Subcellular loc.
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Isoforms (metab/obesity)
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Механизм действия (21 полей)
Mechanism
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Mutations (obesity/lean)
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Activity (obesity)
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Activity temporal
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Energy balance
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Appetite
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Fat metabolism
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Lipolysis
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Thermogenesis
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Muscle metabolism
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Inflammation
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Glucose metabolism
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AA metabolism
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Hormonal pathways
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Cell death
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Adipocyte fibrosis
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Upstream (biochem)
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Upstream (physiol)
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Downstream (biochem)
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Downstream (physiol)
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PTMs
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Экспрессия (8 полей)
Tissue expression
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In vitro
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In vivo
High-intensity interval training (HIIT) effects on exerkine secretion in humans (systematic review of 39 studies); HIIT effects on neuroplasticity-related proteins in cerebrum of postnatally growth-restricted mice; HIIT promotes adipose tissue browning via IL-27/p38 MAPK-PGC-1α pathway in diet-induced obese rats; Association between adenylate cyclase 3 gene polymorphism and HIIT effect on blood lipids in humans.
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In silico
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Genetic association
Association between polymorphisms of the adenylate cyclase 3 gene rs2241759 and the effect of high-intensity interval training on blood lipid profiles.
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Ex vivo
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Animal model
Postnatally growth-restricted mice; diet-induced obese Sprague-Dawley rats.
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Diet/model
Diet-induced obesity in rats.
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Клиника (11 полей)