Metabolic alterations in dogs with osteosarcoma

Metabolic alterations in dogs with osteosarcoma

Mazzaferro EM; Hackett TB; Stein TP; Ogilvie GK; Wingfield WE; Walton J; Turner AS; Fettman MJ

American Journal Of Veterinary Research

2001

Female; Male; Animals; Non-U.S. Gov't; Research Support; Energy Metabolism/physiology; Nutritional Failure; Densitometry; Dogs; Calorimetry; Bone Neoplasms/metabolism/veterinary; Dog Diseases/metabolism; Glucose/analysis/metabolism; Glycine/blood/metabolism/urine; Indirect/veterinary; Osteosarcoma/metabolism/veterinary; X-Ray/veterinary

OBJECTIVE: To evaluate changes in resting energy expenditure (REE) as well as protein and carbohydrate metabolism in dogs with osteosarcoma (OSA). ANIMALS: 15 weight-stable dogs with OSA that did not have other concurrent metabolic or endocrine illness and twelve 1-year-old sexually intact female Beagles (control dogs). PROCEDURES: Indirect calorimetry was performed on all dogs to determine REE and respiratory quotient (RQ). Stable isotope tracers (15N-glycine, 4.5 mg/kg of body weight, IV; 6,6-deuterium-glucose, 4.5 mg/kg, IV as a bolus, followed by continuous-rate infusion at 1.5 mg/kg/h for 3 hours) were used to determine rate of protein synthesis and glucose flux in all dogs. Dual-energy x-ray absorptiometry (DEXA) scans were performed to determine total body composition. RESULTS: Accounting for metabolic body size, REE in dogs with OSA was significantly higher before and after surgery, compared with REE of healthy control dogs. The RQ values did not differ significantly between groups. Dogs with OSA also had decreased rates of protein synthesis, increased urinary nitrogen loss, and increased glucose flux during the postoperative period. CONCLUSIONS AND CLINICAL RELEVANCE: Alterations in energy expenditure, protein synthesis, urinary nitrogen loss, and carbohydrate flux were evident in dogs with OSA, similar to results documented in humans with neoplasia. Changes were documented in REE as well as protein and carbohydrate metabolism in dogs with OSA. These changes were evident even in dogs that did not have clinical signs of cachexia.

2001

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