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Introduction: Food-specific inhibitory control plays a critical role in maintaining a healthy body weight. However, limited research has explored how different exercise modalities influence this form of control in adults with obesity, particularly regarding the underlying neural mechanisms. This study aimed to examine the acute effects of short-term high-intensity interval exercise (HIIE) and moderate-intensity aerobic exercise (MIAE) on food-related inhibitory function in obese adults, and to assess whether sex differences modulate the response to exercise interventions. The findings aim to provide evidence-based guidance for the personalized design of exercise prescriptions targeting dietary behavior regulation in this population.
Methods: A total of 32 obese adults participated in a within-subjects randomized crossover design. Each individual completed three separate sessions: (1) 15 min of HIIE on a power-adjusted cycle ergometer, (2) 30 min of MIAE, and (3) a 30-min resting control condition. After each session, participants performed a food-related Go/NoGo task during which behavioral responses (reaction time and accuracy) and event-related potential (ERP) components (N2 and P3 amplitudes) were recorded.
Results: Across all image types, both male and female participants demonstrated shorter reaction times following HIIE and MIAE compared to the control condition. In males, reaction times were tended to be shorter under HIIE than under MIAE, although no significant differences in accuracy were observed across conditions. Additionally, female participants showed enhanced N2 amplitudes in NoGo trials involving low-calorie food images under the HIIE condition, and no significant difference between NoGo and Go P3 amplitudes when responding to high-calorie food stimuli.
Conclusion: (1) HIIE may enhance behavioral response speed in obese males through non-inhibitory optimization of the prefrontal-striatal pathway, reflecting the neural efficiency hypothesis associated with short-term exercise; (2) MIAE may improve conflict monitoring in obese females, facilitating a shift in inhibitory control over high-calorie foods from active suppression to automated processing. These findings highlight the importance of tailoring food inhibition interventions to account for exercise intensity adaptability and sex-specific neuro-metabolic targets, providing a scientific rationale for personalized exercise prescription. Future studies should further investigate the causal mechanisms through which HIIE modulates food-related inhibition and explore neuroregulatory targets for optimizing exercise-based interventions.
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http://dx.doi.org/10.3389/fpsyg.2025.1634569 | DOI Listing |
Arch Pharm (Weinheim)
September 2025
Chemistry Department, Faculty of Science, Ain Shams University, Cairo, Egypt.
Through applying the hybridization technique, new coumarin derivatives (2-17) were prepared with substitution at coumarin C-3 utilizing various heterocyclic derivatives, aiming to afford multi-target carbonic anhydrases (CAs) IX/XII and topoisomerase II (Topo II) inhibitors with potent antiproliferative activity. Eight different cell lines were used to evaluate the growth inhibition percentages (GI%) of cancer cells determined by coumarin analogues 1-17. Analogues 16 and 17 had the most substantial cytotoxic effects, achieving mean GI% of 86.
View Article and Find Full Text PDFNeotrop Entomol
September 2025
Dept of Zoology, Government College Univ Lahore, Lahore, Pakistan.
The control of dengue vector mosquitoes by utilizing plant-based eco-friendly larvicides is pivotal in suppressing the spread of dengue with minimum environmental toxicity. This study aimed to evaluate the larvicidal activity of nanoliposomes containing p-cresol and Myristica fragrans Houtt. essential oil (EO) against Aedes aegypti L.
View Article and Find Full Text PDFBioorg Med Chem Lett
September 2025
Department of Chemical Engineering, Analysis and Test Center, Shenyang University of Chemical Technology, Shenyang 110142, China. Electronic address:
Asiatic acid (AA) was used as the lead compound and 22 inhibitors of specificity protein 1 (Sp1) were designed and synthesized with modification at A ring and C-28 position of AA, whose structures were confirmed by HRMS, H NMR and C NMR. The growth inhibitory effects of Asiatic acid derivatives on human breast cancer cells (MCF-7) and cervical cancer cells (Hela) were determined by tetramethyl azole salt (3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide, MTT) colorimetric assay. The results showed that all of these compounds inhibited the proliferation of HeLa and MCF-7 cells, and all the derivatives showed stronger tumor cytotoxicity than AA, among which compounds I, II, and III were comparable to the positive control drug cisplatin.
View Article and Find Full Text PDFOsteoarthritis Cartilage
September 2025
Department of Clinical & Experimental Medicine, Brighton & Sussex Medical School, Brighton BN1 9PX, UK. Electronic address:
Objective: Therapeutic potential of selective aggrecanase inhibition in osteoarthritis (OA) was previously demonstrated using a variant of endogenous tissue inhibitor of metalloproteinase-3 (TIMP-3); however, this relied on transgenic mice overexpressing TIMP-3. Here, we develop a translational approach for harnessing the aggrecanase-selective inhibitory activity of TIMP-3 using the latency associated peptide (LAP) technology.
Methods: We successfully produced and purified recombinant LAP-TIMP-3 fusion proteins and determined the pharmacokinetics of these proteins in vivo following systemic injection.
PLoS One
September 2025
Shenzhen University Institute for Advanced Study, Shenzhen, Guangdong, China.
Trichophyton rubrum, a dermatophyte, demonstrates a notable ability to form mature biofilms on skin and associated surfaces, strengthening its resistance to antifungal agents. This characteristic poses intricate challenges in dermatological research and therapeutic strategies, underscoring the need for innovative approaches to effectively manage fungal infections. This work assessed the impact of the anti-biofilm enzymes, i.
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