Plasma Visfatin Is Increased after High-Intensity Exercise

Background/Aims: Visfatin is a newly characterized protein that is highly expressed in visceral adipose tissue and may play a role in insulin resistance. We investigated the effects of repeated short bouts of high-intensity exercise on plasma visfatin and related metabolic responses. Methods: Six yo...

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Veröffentlicht in:Annals of nutrition and metabolism 2010-01, Vol.57 (1), p.3-8
Hauptverfasser: Ghanbari-Niaki, Abbass, Saghebjoo, Marziyeh, Soltani, Raheleh, Kirwan, John P
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Sprache:eng
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Zusammenfassung:Background/Aims: Visfatin is a newly characterized protein that is highly expressed in visceral adipose tissue and may play a role in insulin resistance. We investigated the effects of repeated short bouts of high-intensity exercise on plasma visfatin and related metabolic responses. Methods: Six young, physically fit men (22.8 ± 2.3 years; 78.5 ± 2.3 kg; and body mass index 22.1 ± 1.2) performed a single session of a running-based anaerobic sprint exercise (7 sets of 6 × 35 m every 10 s, with 1 min rest between sets). Venous blood samples were collected before, immediately after, and 45 and 90 min after exercise to assess plasma visfatin, insulin, glucose, lactate and glutathione responses. Results: After adjustment for postexercise changes in plasma volume, the data indicate a significant increase in plasma visfatin (12.5 ± 2.0 vs. 26.6 ± 3.9 ng/ml, p < 0.02), insulin (p < 0.05), and glucose (p < 0.002) concentrations, and homeostasis model assessment of insulin resistance (p < 0.02), immediately after the exercise session. At 45 min of recovery, all metabolic measures, with the exception of lactate, had returned to baseline levels. Conclusion: The elevation in plasma visfatin, together with increased plasma glucose and insulin concentrations immediately after high-intensity exercise, may sensitize tissues for postexercise glucose uptake and glycogen restoration. Our results also support a temporary and early postexercise anorexigenic metabolic state.
ISSN:0250-6807
1421-9697
DOI:10.1159/000313936