Animal model systems represent an important adjunct and surrogate for studies of osteoarthritis (OA) in humans. They provide a means to study OA pathophysiology as well as aid in the development of therapeutic agents and biological markers for diagnosing and prognosing the disease. Thus, it is of great importance for the OA scientific community, both in academic as well as industrial research, to standardize scoring systems for evaluating the OA disease process and to make results between different studies comparable. The task of the histopathology initiative of OARSI was to achieve a consensus of scoring systems for the most important species used in OA animal model research (dog, guinea pig, horse, mouse, rabbit, rat, and sheep/goat), which are presented in the various chapters in this special volume of Osteoarthritis & Cartilage together with extra chapters on basic methodology (histochemistry, statistics, morphometry), the specific terminology and a general discussion of animal models in OA research. Standardized definitions are suggested for basic but essential terms such as "grading" and "staging" in order to promote their consistent use and thereby promote improved understanding and data interpretation across all model systems. Thus, this introductory chapter presents an overview of the guiding principles for assessment of important OA animal model systems. Use of such systems, independently or in conjunction with other systems in parallel, should facilitate comparability of results across animal model studies.

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Simple SummaryThere is currently limited information on the types, or risk, of injuries occurring for horses racing in flat races in New Zealand. Race reports and records from six racing seasons were used to determine the reasons why horses failed to finish a race. In total, 544 horses failed to complete a race, of which 177 were due to veterinary events. Most of the veterinary events that occurred during a race were classed as musculoskeletal injuries (136/177; 77%). The rate of musculoskeletal injuries during a race, 0.72 per 1000 starts, was lower than the rates reported for other racing jurisdictions. The condition of the track and the distance of the race were associated with the rate of musculoskeletal injury during a race. There may be differences in the training programmes and racing schedules for horses in the southern hemisphere, which may have contributed to the low rates reported in this study.AbstractThe objective of the study was to determine the incidence of veterinary events that resulted in a horse failing to finish a race and identify risk factors for musculoskeletal injury (MSI) during a race. Data were obtained on Thoroughbred flat race starts in New Zealand between 1 August 2005 and 31 July 2011 (six racing seasons). Stipendiary Steward’s reports were key-word searched to identify veterinary events that prevented a horse from finishing a race. Race data were used calculate the incidence of veterinary events per 1000 horse starts and Poisson regression was used to investigate risk factors for MSI. There were 188,616 race starts and 177 reported veterinary events. The incidence of MSI on race day was 0.72 per 1000 starts, whilst the incidence of respiratory events was 0.21 per 1000 starts. The rate of MSI was significantly lower on ‘dead’ and ‘slow’ tracks compared with ‘good’ tracks and significantly greater in longer races (≥1671 m) compared with races of ≤1200 m. The rate of MSI during flat races in New Zealand appears lower than that reported worldwide, which may be due to the management and training of horses in New Zealand or differences in case definitions used in comparable studies.

This study investigated the influence of changing recumbency and mode of ventilation over repeated anesthesias on the alveolar to arterial oxygen tension gradient (PA–aO2) and laboratory analytes in eight horses during a year-long imaging study. Anesthesia was induced with xylazine, diazepam or guaifenesin, and ketamine and maintained with isoflurane. Horses were positioned in right or left lateral recumbency for computed tomography. Ventilation was controlled during 47% of the anesthetics. Blood was sampled from an arterial catheter prior to (30 ± 5 min from connection to anesthetic circuit), within 5 min of changing lateral recumbency, and prior to circuit disconnection (24 ± 6 min after second sample) for measurement of pH, partial pressure of arterial oxygen (PaO2) and partial pressure of arterial carbon dioxide, blood glucose and electrolytes. PA–aO2 was calculated. Data from five anesthetic episodes for each horse were summarized as mean ± standard error and analyzed using a mixed-model ANOVA. t tests were used for pairwise comparisons (P<0.05). PaO2 decreased after turning (198 vs. 347 mmHg), then increased to 291 mmHg prior to disconnection. Correspondingly, PA–aO2 was wider (252 vs.120 mmHg), and improved before disconnection (190 mmHg). Body temperature, ionized-Ca2+ and blood glucose were lower, and Na+ was higher at the last time point. In conclusion, turning anesthetized horses decreases PaO2 and results in a widening PA–aO2 suggesting a cautious approach in animals with pre-existing hypoxemia.