Degenerative joint diseases, such as osteoarthritis, adversely impact the health of the equine athlete as well as the economics of the equine industry. Our understanding of the aetiology of osteoarthritis, although not nearly exhaustive, has increased substantially in recent years. Molecules, including cytokines, inflammatory mediators, and metalloproteinases, have been identified and associated with the progression of joint disease. Several factors, including trauma to the joint, immobilization, conformation, shoeing, and ageing, have been linked with osteoarthritis. Our continued efforts into elucidating critical biological mediators and risk factors, coupled with better chondroprotective therapies and diagnostic tools, should facilitate our ability to maintain the skeletal health of the equine athlete

The purpose of this work is to investigate the effects of body mass (BM), velocity (V), and hoof shape on compressive surface strains in the wall of the front hoof at the trot. Toe angle (TA), heel angle (HA), toe length (TL), medial and lateral wall length (MWL, LWL) and BM were measured for nine adult, unshod Standardbreds. Five rosette gauges were glued around the circumference of the left forehoof of each animal which was then trotted on a treadmill at a set range of velocities from 3.5 to 7.5 m s−1. Analysis of variance (ANOVA) of principal compressive strains ɛ2 at midstance identified that all primary variables (BM, V, TA, HA, etc.) had a significant effect as did the interactions of TA×HA and BM×TA. These significant variables explained over 96% of the variation in ɛ2. Multiple regression of ɛ2 on these variables gave equations which accurately predicted ɛ2 within 3%, but the individual coefficients did not accurately describe how each variable affected ɛ2. Further tests using bivariate regression gave equations that enabled ɛ2 data to be standardized for BM and V at the gauge locations used here. Strain ɛ2 increased linearly with mass and curvilinearly with velocity (ɛ2∝V+V2), and both caused redistribution of strain to the dorsum and lateral quarter. Variation in each shape variable caused redistribution rather than simple increase or decrease in strains. The primary conclusion with regard to hoof shape is that the effects of change in any one measurement on strain magnitudes are affected by the values of all other measurements. Resolving the interplay among measurements in their effects on ɛ2 will need a considerably larger sample size than that used here.

The objective of this experiment was to compare the physiological changes that occurred in horses competing in the cross-country portion of Training, Preliminary and Intermediate horse trials. The hypothesis was that temperature (T), heart rate (HR), respiratory rate (RR), and on-site acid–base and electrolyte monitoring would allow differentiation between difficulty levels in horse trials. Sixteen client-owned horses competing at the Trojan-Horse Spring Horse Trials in Cave Creek, Arizona, USA, were studied. T, HR, RR and anaerobic lithium-heparinized jugular venous samples were obtained before, and 1–2 min after, cross-country exercise. Samples were analysed for blood gases (body temperature-corrected) and concentrations of sodium ([Na+]), potassium ([K+]), chloride ([Cl−]), ionized calcium ([Ca2+]i), blood urea nitrogen ([BUN]) and glucose ([GLC]) using a point-of-care analyser. Results were compared using analysis of variance with the level of significance set at P<0.05. In all groups, exercise increased T, HR, RR, packed cell volume and haemoglobin concentration, and decreased partial pressure of CO2 (PCO2), [total CO2 concentration], bicarbonate concentration ([HCO3−]) and [Ca2+]i (P<0.05). Post-exercise RR was higher, and pH, PCO2, [tCO2], [HCO3−] and base excess were lower, in Intermediate and sometimes Preliminary horses compared with Training horses (P<0.05). It was concluded that horse trials caused milder, but otherwise similar, physical, blood gas and electrolyte changes to those observed in complete three-day events. Physical and point-of-care plasma acid–base and electrolyte monitoring allowed differentiation between horses competing at various levels of difficulty in a horse trial.

The impact of stress fractures on competitive event horses in the UK is completely unknown. Ninety-one replies to 450 questionnaires sent to competitive event riders across the UK indicated that 11 horses, representing 12% of the responders, had a confirmed stress fracture. As data on the total number of horses owned or ridden by the riders were not available, the true prevalence of stress fractures in this sample of horses could not be directly assessed. Within the bounds of this study, competitive level of the rider had a significant effect on stress fracture prevalence (X2(0.05, df. 2) = 24.74, P<0.05), as did years of eventing experience (X2(0.05, df. 1) = 27.80, P<0.01). Training regime was also influential (X2(0.05,df. 1) = 26.30, PX20.01). There was a predominance of fractures in geldings (X2(0.05, df. 1) = 24.45, P<0.03); however, geldings constituted 82% of reported cases. Thoroughbred cross horses had a significantly lower incidence of stress fractures than Thoroughbreds (X2(0.05, df. 1) = 20.82, P<0.01) but constituted only 18% of the sample. Horses in the oldest age category (9–12 years) had 6% of all stress fractures (X2(0.05, df. 2) = 24.54, P<0.1). All fractures occurred on the foreleg at the knee or below, with no significant effect of anatomical location. Seventy-three per cent of horses were not competing when diagnosed (X2(0.05, df. 1) = 22.27, P<0.1). These data indicate that useful preliminary data were yielded by the questionnaire and that further research with a larger sample size is justified.

This brief review examines the athletic potential of mammals in general and the horse in particular as it relates to oxygen (O2) transport and utilization. The horse has been bred selectively for over six millennia based upon its ability to run fast. Whereas this has optimized cardiovascular and muscle function and the capacity to deliver and utilize O2, it has resulted in lung failure during intense exercise. Horses in their athletic prime are considered and attention is focused on their maximal capacities as related to O2 transport, irrespective of age per se. Following a few comments on the history of O2, this review moves from established principles of O2 transport at the integrative organ level to the microcirculation and the processes and principles that govern O2 offloading, where much remains to be discovered. Four principal questions are addressed: (1) as an athlete, what are the most outstanding physiological characteristics of the horse? (2) what anatomical and physiological capacities facilitate this superlative performance and such prodigious O2 fluxes (i.e. maximal VO2)? (3) do cardiovascular dynamics or intramuscular energetic processes limit VO2 kinetics (i.e. the speed at which VO2 increases at the onset of exercise)? VO2 kinetics determine the size of the O2 deficit and as such represent an important determinant of muscle metabolism and fatigue; and (4) what determines the efficacy of muscle microcirculatory O2 exchange?

This paper reviews the acute and chronic effects of feeding, diet composition and daily variation on equine acid–base status. The dietary cation–anion difference (DCAD) has a marked effect on blood acid–base balance in both the short term and long term. In general, diets with a low DCAD generate an acute acidosis that develops into a persistent though mild systemic, strong ion acidosis with long-term feeding. In contrast, high-DCAD diets result in a mild, persistent strong ion alkalosis characterized by elevated plasma pH, [HCO3] and total CO2 (TCO2). The acute blood acid–base responses to feeding include alterations in plasma pH and plasma concentrations of HCO3, TCO2, Cl−, Na+, K+ and protein. The forage component of the diet appears to be primarily responsible for the acute responses. There is limited research examining abrupt alterations in DCAD and the influence of daily variation on equine plasma acid–base balance. It is concluded that the composition of the diet, duration of adaptation to the diet, timing of feeding and time of day need to be considered when examining acid–base balance in horses.

High altitude acclimatization produces a suite of physiological changes that might support an improved athletic performance at low altitude and thus lead to the strategy of athletic training at high altitude. Although there is substantial literature on high altitude physiology in humans, there are few studies on horses. Our interest in the physiological responses to high altitude in equids has been driven by the concerns of how athletic performance is altered at altitude and how conditioning at altitude may improve performance subsequently at low altitude. This review serves to illustrate what is currently know about the physiological changes of horses to altitude, at rest and during exercise, and to highlight how performance is impacted both at high altitude and subsequent return to low altitude.

In Standardbreds, the main aim of early training (begun during the growth period) is the mechanization of athletes leading to a particular gait called the ‘flying trot’. The present cross-sectional study was undertaken to investigate the biomechanical and physiological factors involved in this gait change, and aimed to analyse the effect of age on gait and energetic variables in a population of Standardbred horses under training. One hundred and forty-three horses aged from two to seven years were tested on a track at three speeds (8.5, 10 and 11.6 m s−1) with a gait-analysis system. Gait variables (temporal and linear variables, symmetry, regularity, two-beat rhythm, dorso-ventral, longitudinal and lateral activities) were compared between four age groups (two-, three-, four-, and five-year-olds and above). After a standardized exercise test, two energetic variables (V4 and V200) were also compared between these groups. Most variables were influenced by age/training status. The results indicated that, from young to mature racehorses, stride length and duration increase; and gait becomes more symmetric and more regular. We also observed a decrease in dorso-ventral, longitudinal and lateral activities, i.e. a decrease of thoracic displacements. These differences could be elucidated at slow speed and were still obvious at high speed. V4 and V200 also increased significantly with age/training status. All of these results indicate an improvement in co-ordination and a decrease in metabolic cost with increasing age/training status. Thus gait acquisition could be related to an improvement in trotting efficiency.

The purpose of this study was to demonstrate whether acute vascular occlusion was safe and if it would result in changes to limb muscle size in horses. Six healthy, unfit Standardbred mares were used. Horses (standing at rest) wore an occlusion cuff at the most proximal position of the left forelimb. The right forelimb was used as control. An occlusion pressure of 200 mmHg was set for 5 min followed by a 2 min recovery. Three sets of occlusions were given to each horse. Muscle thickness was measured using B-mode ultrasound. The circumference of the forelimb and first phalanx was measured using a flexible tape measure. Pulsed-wave Doppler was performed on the radialis artery with a 5–10 MHz mechanical transducer at baseline and at each occlusion. Peak flow velocity (PFV) and the flow velocity integral (FVI) were measured each time. Mid-forelimb, but not first phalanx, girth was increased (P<0.05) in the occluded but not in the control leg following occlusion. Extensor and flexor muscle thickness was increased (P<0.05) in the occluded but not in the control leg. There were no changes (P>0.05) in PFV or FVI at any measurement time point. Acute vascular occlusion may be a suitable and safe model for studying muscle hypertrophy in horses.

Carbohydrate and fat are the predominant sources of energy during exercise in mammals. Carbohydrates, such as muscle glycogen and plasma glucose, and fats from adipose tissue and intramuscular triglycerides are oxidized during exercise in amounts and proportions that vary depending on the exercise intensity, level of fitness and nutritional status. In horses, muscle glycogen, and to a lesser extent plasma glucose, are oxidized in substantial amounts during low-, moderate- and high-intensity exercise. Carbohydrate availability to skeletal muscle affects exercise performance in humans, however this relationship is not well outlined in horses. Glucose supplementation by intravenous administration during exercise in horses increases duration of moderate-intensity exercise. However, the effect of glucose supplementation by ingestion of a soluble carbohydrate-rich meal prior to exercise on athletic performance has not been established in horses. Low muscle glycogen concentrations prior to exercise in horses are associated with decreased time to exhaustion at moderate- and high-intensity exercise. Nutritional interventions intended to enhance muscle glycogen resynthesis have proved less successful in horses than in other species. Replenishment of muscle glycogen after strenuous exercise in horses is not complete until 48–72 h after exercise, whereas in humans and laboratory animals it is complete by 24 h. The slower rate of muscle glycogen replenishment after exercise in horses may be related to an inherent lower ability to digest starch and other sources of glucose, a lower ability to synthesize muscle glycogen, or both. The aim of this review is to describe the present understanding of carbohydrate metabolism in the exercising horse, its implications on nutrition and athletic performance, and to contrast it with that in other species.

Chemical pollutants, for example ozone, have been demonstrated to have detrimental effects on the cardiorespiratory system in human beings. Inhalation of pollutants may therefore impact on the performance of athletes at the 2004 Athens Olympic Games. Horses will also be exposed to these pollutants contained within the large volume of air they inhale during exercise. Opportunely, the equine events will be staged outside of Athens and as a result the concentration of atmospheric chemical pollutants is likely to be lower than that experienced by many of the human athletes. The horses' housing environment should also be carefully considered as a source of pollutants, as certain bedding materials can release dust, mould spores and irritants that may induce airway inflammation. In order to achieve the highest level of performance it is essential that both horse and rider be in good health and therefore the influence of environmental pollutants on lung function should to be minimized.

We studied the extent to which intra-articular hyaluronic acid (HA) administered to horses with experimentally induced synovitis in the third middle carpal joint altered cartilage proteoglycans (PGs) and the biomechanical properties of the third carpal bone. Intra-articular HA (Hylartin-V®) was administered to the middle carpal joints of healthy horses before and after the induction of synovitis by Escherichia coli lipopolysaccharide (LPS). Two groups of horses received intra-articular HA only, with evaluation 2 and 6 weeks later (group 2 and group 4). Two other groups (group 1 and group 3) received LPS followed by intra-articular HA and evaluation 2 and 6 weeks later. Ex vivo third carpal bone cartilage PG synthesis was measured by 35SO4 incorporation and third carpal bone cartilage PG content was determined by an assay for glucuronic acid. Biomechanical properties were measured by indentation testing. At the 2-week evaluation, HA did not ablate the quantitative reduction in PG synthesis and PG content in animals with experimental synovitis. However, by 6 weeks, there was a significant rebound effect in that PG synthesis and PG content were elevated in horses with experimental synovitis that had received intra-articular HA, compared with horses that had received HA only for that period of time. There were also alterations in the gel filtration profiles of newly synthesized PGs on Sepharose CL-2B among the groups. However, there were no de novo PG species associated with any of the treatments. Furthermore, we found that the biomechanical properties of third carpal bone cartilage were not altered in any of the groups. These studies showed that intra-articular HA administered to horses with experimentally induced synovitis did not provide short-term (i.e. 2-week) benefit to third carpal bone cartilage PG synthesis. However, a long-term benefit of intra-articular HA may occur after the acute effects of synovitis on PG synthesis and PG content subside.

This study examined the effects of a rider on the angular momentum and angular velocity of the jumping horse, particularly during the flight phase. Sagittal plane video recordings were digitized of eight horses jumping a vertical fence (1 m high) under two conditions: Loose and Ridden. An experienced rider rode the horses during the Ridden condition. Using appropriate segmental inertial data for the horse and rider, angular momentum and angular velocity were calculated for the Loose and Ridden conditions. Estimates of the various rider effects on angular momentum and angular velocity were obtained by comparison of Loose and Ridden conditions and examination of the contributions of the horse and rider segments to the total angular momentum. The results showed that the rider's effect on angular momentum was significant but that the rider's segmental contribution to the angular momentum of the horse–rider system was minimal. Repeated-measures ANOVA revealed that the rider had a significant effect on the angular momentum and angular velocity of the horse during the flight phase (P<0.01). However, the rider did not have a significant effect on the transfer of angular momentum during the flight. We concluded that the rider's instruction has a greater influence on the horse's motion than the mechanical transfer between rider and horse.

Furosemide (FUR) and the equine nasal strip (NS) decrease exercise-induced pulmonary haemorrhage (EIPH) compared with control (CON) conditions in the Thoroughbred horse during near-maximal running trials. As FUR and NS have potential performance-enhancing properties, we studied Thoroughbreds running to fatigue to test the hypothesis that time-to-fatigue (TTF) would be increased, yet EIPH reduced, in FUR and NS compared with CON. Thoroughbred geldings (n=6) were run to volitional fatigue on a level treadmill (1 m s−1 increment per minute from an initial trot) every two weeks (order randomized) under CON, NS, FUR (1 mg kg−1; 4 h prior) and FUR+NS conditions. Pulmonary arterial pressure (Ppa) and pulmonary gas exchange were measured throughout exercise, while arterial blood gases were sampled at the end of each 1-min stage. EIPH severity was quantified via bronchoalveolar lavage (BAL) at 30 min post-exercise. TTF was increased for all experimental conditions (i.e. an additional 20±13, 28±8 and 40±6 s for NS, FUR and FUR+NS, respectively; P<0.05) compared with CON. Peak mean Ppa was significantly reduced (P<0.05) for FUR (93.6±6.3 mmHg) and FUR+ NS (95.4±5.1 mmHg), yet unchanged with NS (98.0±5.8 mmHg; P>0.05) compared with CON (100.5±4.9 mmHg). All three experimental conditions exhibited a significant reduction in EIPH compared with CON (64.1±36.8× 6 red blood cells (RBCs) ml−1); however, no significant difference was noted between these conditions (×106 RBCs ml−1: 29.1±16.8, 20.9±13.1 and 26.7±19.8 for NS, FUR and FUR+NS, respectively). Furthermore, no differences for either end-exercise cardiorespiratory (i.e. V˙O2 or V˙CO2) or blood-borne metabolic (i.e. blood gases, lactate or pH) variables were observed. These findings demonstrate that both FUR and NS enhance TTF and reduce EIPH to a similar degree during high-speed treadmill running to fatigue.

The purpose of the present study was to determine the time course and magnitude of changes in extracellular and intracellular fluid volumes in relation to changes in total body water during prolonged submaximal exercise and recovery in horses. Seven horses were physically conditioned over a 2-month period and trained to trot on a treadmill. Total body water (TBW), extracellular fluid volume (ECFV) and plasma volume (PV) were measured at rest using indicator dilution techniques (D2O, thiocyanate and Evans Blue, respectively). Changes in TBW were assessed from measures of body mass, and changes in PV and ECFV were calculated from changes in plasma protein concentration. Horses exercised by trotting on a treadmill for 75–120 min incurred a 4.2% decrease in TBW. During exercise, the entire decrease in TBW (mean±standard error: 12.8±2.0 l at end of exercise) could be attributed to the decrease in ECFV (12.0±2.4 l at end of exercise), such that there was no change in intracellular fluid volume (ICFV; 0.9±2.4 l at end of exercise). PV decreased from 22.0±0.5 l at rest to 19.8±0.3 l at end of exercise and remained depressed (18–19 l) during the first 2 h of recovery. Recovery of fluid volumes after exercise was slow, and characterized by a further transient loss of ECFV (first 30 min of recovery) and a sustained increase in ICFV (between 0.5 and 3.5 h of recovery). Recovery of fluid volumes was complete by 13 h post exercise. It is concluded that prolonged submaximal exercise in horses favours net loss of fluid from the extracellular fluid compartment.

Training and competing at elite as well as sub-elite level requires an optimal functioning of the body. This review looks at the case of the Kenyan runners, who consume a relatively high-quality diet based on vegetable sources with maize and kidney beans as the staple foods. The diet is high in carbohydrate and total protein, but low to borderline in a few essential amino acids. The timing of diet intake – immediately after training sessions – is optimal for skeletal muscle glycogen resynthesis that is enhanced without the help of insulin up to 60 min after cessation of exercise. Whether the total energy intake of the Kenyan runners is adequate is debatable. However, chronic undernutrition is not possible for athletes who engage in daily high-quality and -quantity physical exercise throughout most of the year. It is suggested that Kenyan runners participate in well-controlled, laboratory studies to investigate the quality of local foods and performance, as well as possible physiological adaptation mechanisms among athletes with a high habitual energy turnover.

Temporal stride characteristics of the canter were compared between performance-shod (PS) and light-shod (LS) Tennessee Walking Horses, which generally differ in training and shoeing methods. Four consecutive strides for ten PS and ten LS horses were filmed (30 Hz), and frame-by-frame analysis performed to determine stride duration and individual limb stance duration. Also analysed was the percentage of stride duration devoted to single, bipedal or tripedal limb support. Footfall sequence for PS was trailing hind (TrH), leading hind (LdH), trailing fore (TrF) and leading fore (LdF), whereas footfall sequence for LS horses varied, with the majority of LS performing a sequence of TrH–TrF–LdH–LdF. Stride duration was greater for PS. As a percentage of stride duration, PS demonstrated greater duration of TrF and LdF, while LS demonstrated greater LdH duration. Hind and fore single limb support, and tripedal support, were greater for LS; however, PS utilized bipedal support to a larger extent than LS. Hind or forelimb bipedal support was demonstrated only in PS, while only LS demonstrated lateral bipedal support. Thus, while both performance- and light-shod Tennessee Walking Horses perform the canter, temporal variables for this gait differ dramatically between the two groups.