Maximal exercise test is a useful method for physical capacity and oxygen consumption determination in streptozotocin-diabetic rats

BACKGROUND: The aim of the present study was to investigate the relationship between speed during maximum exercise test (ET) and oxygen consumption (VO(2)) in control and STZ-diabetic rats, in order to provide a useful method to determine exercise capacity and prescription in researches involving STZ-diabetic rats. METHODS: Male Wistar rats were divided into two groups: control (CG, n = 10) and diabetic (DG, n = 8). The animals were submitted to ET on treadmill with simultaneous gas analysis through open respirometry system. ET and VO(2 )were assessed 60 days after diabetes induction (STZ, 50 mg/Kg). RESULTS: VO(2 )maximum was reduced in STZ-diabetic rats (72.5 ± 1 mL/Kg/min(-1)) compared to CG rats (81.1 ± 1 mL/Kg/min(-1)). There were positive correlations between ET speed and VO(2 )(r = 0.87 for CG and r = 0.8 for DG), as well as between ET speed and VO(2 )reserve (r = 0.77 for CG and r = 0.7 for DG). Positive correlations were also obtained between measured VO(2 )and VO(2 )predicted values (r = 0.81 for CG and r = 0.75 for DG) by linear regression equations to CG (VO(2 )= 1.54 * ET speed + 52.34) and DG (VO(2 )= 1.16 * ET speed + 51.99). Moreover, we observed that 60% of ET speed corresponded to 72 and 75% of VO(2 )reserve for CG and DG, respectively. The maximum ET speed was also correlated with VO(2 )maximum for both groups (CG: r = 0.7 and DG: r = 0.7). CONCLUSION: These results suggest that: a) VO(2 )and VO(2 )reserve can be estimated using linear regression equations obtained from correlations with ET speed for each studied group; b) exercise training can be prescribed based on ET in control and diabetic-STZ rats; c) physical capacity can be determined by ET. Therefore, ET, which involves a relatively simple methodology and low cost, can be used as an indicator of cardio-respiratory capacity in future studies that investigate the physiological effect of acute or chronic exercise in control and STZ-diabetic male rats.