Evidence mapPaperPMID 40217474Full record

ArticleBMC sports science, medicine & rehabilitation2025

Aerobic training and vitamin D supplementation effects on diabetes-related parameters in a rat model of type 2 diabetes.

Zahra Hoseini, Nasser Behpour, Rastegar Hoseini

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Article in BMC sports science, medicine & rehabilitation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

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4citing papers in PubMed, 1 pooled it
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Emerging roles of spexin in cardiovascular homeostasis.Frontiers in cardiovascular medicine · 2026
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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Zahra HoseiniDepartment of Exercise Physiology, Faculty of Sport Sciences, Razi University, Kermanshah, Iran.
Nasser BehpourDepartment of Exercise Physiology, Faculty of Sport Sciences, Razi University, Kermanshah, Iran. n_behpoor@yahoo.com.
Rastegar HoseiniDepartment of Exercise Physiology, Faculty of Sport Sciences, Razi University, Kermanshah, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDiabetes mellitus (DM) is characterized by disturbances in glucose, lipid, and energy metabolism, including dyslipidemia and dysregulation of metabolic peptides like spexin; however, the effects of combined interventions, such as aerobic training and nutritional intervention, on these parameters are not fully elucidated. The objective of this study was to investigate the influences of aerobic training (AT) and vitamin D (Vit D) supplementation on the lipid profile and spexin levels in a model of rats with type 2 diabetes (T2D).

methodsA total of 56 male Wistar rats were divided into two groups: SHAM (non-diabetic control; n = 8) and diabetic (n = 48). The diabetic rats were further divided into six groups: AT with high doses of vitamin D (D + AT + HD; 10,000 IU/kg/week), AT with moderate doses of vitamin D (D + AT + MD; 5,000 IU/kg/week), high doses of vitamin D (D + HD; 10,000 IU/kg/week), moderate doses of vitamin D (D + MD; 5,000 IU/kg/week), AT receiving vehicle (sesame oil; D + AT + oil), and control (oil-receiving; D + C). To induce type 2 diabetes, rats were first fed a high-fat diet (HFD) for 2 weeks to induce obesity, followed by an intraperitoneal injection of 110 mg/kg nicotinamide and 55 mg/kg streptozotocin (STZ) dissolved in 0.1 M citrate buffer (pH 4.5). Blood samples were collected 48 h after the last training session under anesthesia for measuring spexin levels, and lipid profile parameters. Statistical analyses were performed using the paired t-test, one-way analysis of variance (ANOVA), and Tukey post hoc test.

resultsCompared to the SHAM rats, there were significant increases in body weight, BMI, FI, and WC in the diabetic rats (p < 0.001). Also, there was a significant decrease in body weight, BMI, FI, and WC of the diabetic groups who received interventions, especially in D + AT + HD (body weight: -11.07%, BMI: -10.25%, FI: -19.16%, WC: -16.54%). The lipid profiles were significantly improved, with the lowest total cholesterol (TC), triglycerides (TG), and low-density lipoprotein (LDL) levels and the highest high-density lipoprotein (HDL) levels being found in the D + AT + HD group compared with the D + C group (p < 0.05). Moreover, the D + AT + HD group had elevated spexin levels compared with the other diabetic groups, which may play a metabolic role.

conclusionAT and Vit D supplementation effectively normalized serum lipids and increased spexin levels in T2D rats. These findings suggest that AT and Vit D supplementation may serve as potential therapeutic strategies for managing T2D and its associated complications. Further studies are needed to elucidate the underlying mechanisms and to evaluate the long-term effects of these interventions in humans.

Indexed as

ExerciseHOMA-IRMetabolic disorderVitamin D

Identifiers

PMID40217474
PMCPMC11987209

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.