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Exercise training and vascular heterogeneity in db/db mice: evidence for regional- and duration-dependent effects

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Abstract

Exercise training (ET) has several health benefits; however, our understanding of regional adaptations to ET is limited. We examined the functional and molecular adaptations to short- and long-term ET in elastic and muscular conduit arteries of db/db mice in relation to changes in cardiovascular risk factors. Diabetic mice and their controls were exercised at moderate intensity for 4 or 8 weeks. The vasodilatory and contractile responses of thoracic aortae and femoral arteries isolated from the same animals were examined. Blood and aortic samples were used to measure hyperglycemia, oxidative stress, inflammation, dyslipidemia, protein expression of SOD isoforms, COX, eNOS, and Akt. Short-term ET improved nitric oxide (NO) mediated vasorelaxation in the aortae and femoral arteries of db/db mice in parallel with increased SOD2 and SOD3 expression, reduced oxidative stress and triglycerides, and independent of weight loss, glycemia, or inflammation. Long-term ET reduced body weight in parallel with reduced systemic inflammation and improved insulin sensitivity along with increased SOD1, Akt, and eNOS expression and improved NO vasorelaxation. Exercise did not restore NOS- and COX-independent vasodilatation in femoral arteries, nor did it mitigate the hypercontractility in the aortae of db/db mice; rather ET transiently increased contractility in association with upregulated COX-2. Long-term ET differentially affected the aortae and femoral arteries contractile responses. ET improved NO-mediated vasodilation in both arteries likely due to collective systemic effects. ET did not mitigate all diabetes-induced vasculopathies. Optimization of the ET regimen can help develop comprehensive management of type 2 diabetes.

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Data availability

Data of the study are available from the corresponding author upon request.

Abbreviations

COX:

Cyclooxygenase

CRP:

C-reactive protein

EDHF:

Endothelium-dependent hyperpolarizing factor

ET:

Exercise training

eNOS:

Endothelial nitric oxide synthase

GTT:

Glucose tolerance test

PE:

Phenylephrine

mN:

Millinewton

L-NAME:

Nω-Nitro-L-arginine methyl ester

PSS:

Physiologic salt solution

R:

Pearson correlation coefficient

Sed:

Sedentary

SOD:

Superoxide dismutase

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Funding

Nada Sallam received a scholarship from the Ministry of Higher Education, Egypt.

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Authors and Affiliations

Authors

Contributions

Nada Sallam: Conceptualization; Investigation; Methodology; Data curation; Formal analysis; Writing & editing- original draft. Baohua Wang: Methodology. Ismail Laher: Supervision; Funding acquisition; Editing. The authors declare that all data were generated in-house and that no paper mill was used.

Corresponding author

Correspondence to Ismail Laher.

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Ethical approval

This study was carried out following the principles of the Declaration of Helsinki. The experimental animal protocols were approved by University of British Columbia Animal Care Committee (A06-0308).

Competing interests

The authors declare no competing interests.

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Sallam, N.A., Wang, B. & Laher, I. Exercise training and vascular heterogeneity in db/db mice: evidence for regional- and duration-dependent effects. Naunyn-Schmiedeberg's Arch Pharmacol 397, 2421–2436 (2024). https://doi.org/10.1007/s00210-023-02775-0

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  • DOI: https://doi.org/10.1007/s00210-023-02775-0

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