Proceedings of The Physiological Society

Europhysiology 2018 (London, UK) (2018) Proc Physiol Soc 41, PCA180

Poster Communications

Elevated systemic oxidative-nitrosative stress and cerebrovascular function in professional rugby union players: the link to impaired cognition

T. S. Owens2, T. A. Calverley1, B. S. Stacey2, C. J. Marley2, G. Rose2, L. Fall2, G. L. Jones2, P. Williams1, M. J. Steggall2, D. M. Bailey2

1. Faculty of Life Sceinces and Education, Univeristy of South Wales, Pontypridd, United Kingdom. 2. Neurovascular Research Laboratory, Univeristy of South Wales, Pontypridd, United Kingdom.


Sports-related concussion (SRC) represents a growing public health concern in rugby union, yet remains one of the least understood injuries facing the community today. There is concern that prior SRC may contribute to long-term neurologic sequelae in later-life(1). This may be due to an accelerated decline in cerebral perfusion, a major risk factor for neurocognitive decline (2), though the underlying mechanisms remain inconclusive. It was hypothesised that recurrent SRC in current professional rugby union players would result in elevated systemic oxidative-nitrosative stress(3), reflected by a free radical-mediated reduction in bioactive nitric oxide (NO) metabolite bioavailability and impaired cerebrovascular and cognitive function. A longitudinal study design was adopted across the 2017-2018 rugby season. Ethical approval was obtained from the University of South Wales Ethics Committee. Data collection is ongoing and the current report documents result from the pre-season data collection. Participants were divided into two separate groups; 23 professional rugby union players (aged 26 ± 5 years) and 22, age- and physical activity-matched non-concussed controls (27 ± 8 years). Pre-season measurements were performed for cerebrovascular function (Doppler ultrasound of middle cerebral artery velocity (MCAv) at rest and in response to hypocapnia/hypercapnia), venous concentrations of the ascorbate radical (electron paramagnetic resonance spectroscopy), and bioactive NO metabolites (nitrite and S-nitrosothiols, ozone-based chemiluminescence) including cognition (neuropsychometric tests). The rugby players expressed greater oxidative-nitrosative stress confirmed by a systemic elevation in ascorbate radical (P < 0.05 vs. control) and reduction in cumulative bioactive NO (P < 0.05 vs. control). The players performed worse in the Rey Auditory Verbal Learning Test B (learning and memory) and the Grooved Pegboard test using both the dominant and non-dominant hands (visuomotor coordination, P < 0.05 vs. control). No between-group differences in cerebral perfusion at rest (MCAv:54 ± 13 cm.s-1 vs. 59 ± 12 cm.s-1, P > 0.05) or in response to the CO2 challenges were observed (CVRCO2Hypo: 2.58 ± 1.01 cm.s-1 vs. 2.58 ± 0.75 cm.s-1, P > 0.05 and CVRCO2Hyper: 2.69 ± 1.07 cm.s-1 vs. 3.35 ± 1.28 cm.s-1, P > 0.05) The present study identified that the rugby players are characterised by impaired cognitive function subsequent to elevated systemic-oxidative-nitrosative stress. This appears to be independent of any functional impairment in cerebrovascular function. Given the potential long term trajectory towards accelerated cognitive decline following SRC, prophylaxis to increase NO bioavailability warrants consideration (4).

Where applicable, experiments conform with Society ethical requirements