Why the study?
To investigate the function of perivascular adipose tissue on vascular contractility within resistant arteries in high-fat diet induced obese rats after long-term aerobic exercise.
Long-term aerobic exercise restores the anti-contractile function of perivascular adipose tissue in resistance arteries impaired by obesity, potentially via H2S.
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Aerobic exercise may restore impaired PVAT anti-contractile effects in obese resistance arteries; leaves open translation to human vascular outcomes.
This study investigated the function of perivascular adipose tissue (PVAT) on vascular contractility within resistant arteries in high‐fat diet induced obese rats after long‐term aerobic exercise. Male Sprague‐Dawley rats were subjected to normal diet control group (N‐CTRL), normal diet exercise group (N‐EX), high‐fat diet control group (H‐CTRL), and high‐fat diet exercise group (H‐EX) (n = 8 in each group). After intervention, adipose tissues morphology was observed. Vasomotor function of mesenteric arteries with or without PVAT were assessed; mesenteric PVAT isolated from each group were transferred to chambers bath with untreated vessels (without PVAT) to evaluate the independent effect. Isolated PVAT was further pre‐treated with inhibitor of cystathionine‐γ‐lyase (CSE), a key hydrogen sulphide (H2S) enzyme. Results showed that the size of lipid droplet around mesenteric arteries from H‐EX was significantly reduced (P < .05); uncoupling protein1 (UCP1) in PVAT from H‐EX was enhanced. In N‐CTRL, N‐EX, and H‐EX, vessels without PVAT showed higher sensitivity to serotonin (5‐HT) than that with intact PVAT. Vascular tension by 5‐HT was significantly reduced in H‐EX than H‐CTRL (P < .05) in vessels with PVAT. Transferred PVAT from H‐EX compared with H‐CTRL significantly reduced vascular sensitivity to 5‐HT (P < .05), and this effect was eliminated through inhibiting CSE. In summary, the anti‐contractile effect of PVAT on resistance artery was impaired in obesity but restored by long‐term aerobic exercise. The function of PVAT modified by obesity or by exercise has an independent influence on vascular reactivity, and PVAT derived H2S may participate in this process.
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Liao et al. (2020) studied this question.
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