Thromb Haemost 2013; 110(06): 1232-1240
DOI: 10.1160/TH13-04-0295
Platelets and Blood Cells
Schattauer GmbH

Effects of high-amount–high-intensity exercise on in vivo platelet activation: Modulation by lipid peroxidation and AGE/RAGE axis

Francesca Santilli
1   Internal Medicine and Center of Excellence on Aging, “G. d’Annunzio” University of Chieti, Chieti, Italy
,
Natale Vazzana
1   Internal Medicine and Center of Excellence on Aging, “G. d’Annunzio” University of Chieti, Chieti, Italy
,
Pierpaolo Iodice
2   Department of Neuroscience and Imaging, “G. d’Annunzio” University of Chieti, Chieti, Italy
,
Stefano Lattanzio
1   Internal Medicine and Center of Excellence on Aging, “G. d’Annunzio” University of Chieti, Chieti, Italy
,
Rossella Liani
1   Internal Medicine and Center of Excellence on Aging, “G. d’Annunzio” University of Chieti, Chieti, Italy
,
Rosa Grazia Bellomo
3   Department of Human Movement, “G. d’Annunzio” University of Chieti
,
Gianfranco Lessiani
1   Internal Medicine and Center of Excellence on Aging, “G. d’Annunzio” University of Chieti, Chieti, Italy
,
Francesca Perego
4   Internal Medicine III, Luigi Sacco Hospital, University of Milan, Milan, Italy
,
Raoul Saggini
2   Department of Neuroscience and Imaging, “G. d’Annunzio” University of Chieti, Chieti, Italy
,
Giovanni Davì
1   Internal Medicine and Center of Excellence on Aging, “G. d’Annunzio” University of Chieti, Chieti, Italy
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Publikationsverlauf

Received: 11. April 2013

Accepted after major revision: 09. August 2013

Publikationsdatum:
30. November 2017 (online)

Summary

Physical activity is associated with cardiovascular risk reduction, but the effects of exercise on platelet activation remain controversial. We investigated the effects of regular high-amount, high intensity aerobic exercise on in vivo thromboxane (TX)-dependent platelet activation and plasma levels of platelet-derived proteins, CD40L and P-selectin, and whether platelet variables changes may be related to changes in high-density lipoprotein (HDL) and in the extent of oxidative stress and oxidative stress-related inflammation, as reflected by urinary isoprostane excretion and endogenous soluble receptor for advanced glycation end-products (esRAGE), respectively. Urinary excretion of 11-dehydro-TXB2 and 8-iso-prostaglandin (PG)F and plasma levels of P-selectin, CD40L and esRAGE were measured before and after a eight-week standardised aerobic high-amount–high-intensity training program in 22 sedentary subjects with low-to-intermediate risk. Exercise training had a clear beneficial effect on HDL cholesterol (+10%, p=0.027) and triglyceride (-27%, p=0.008) concentration. In addition, a significant (p<0.0001) decrease in urinary 11-dehydro-TXB2 (26%), 8-iso-PGF (21 %), plasma P-selectin (27%), CD40L (35%) and a 61% increase in esRAGE were observed. Multiple regression analysis revealed that urinary 8-iso-PGF [beta=0.33, SEM=0.116, p=0.027] and esRAGE (beta=-0.30, SEM=31.3, p=0.046) were the only significant predictors of urinary 11-dehydro-TXB2 excretion rate over the training period. In conclusion, regular high-amount–high-intensity exercise training has broad beneficial effects on platelet activation markers, paralleled and possibly associated with changes in the lipoprotein profile and in markers of lipid peroxidation and AGE/RAGE axis. Our findings may help explaining why a similar amount of exercise exerts significant benefits in preventing cardiovascular events.

 
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