Obesity is often associated with a reduced ventilatory response and a decreased maximal exercise capacity. GABA is a major inhibitory neurotransmitter in the mammalian central nervous system. Altered GABAergic mechanisms have been detected in obese Zucker rats and implicated in their hyperphagic response. Whether altered GABAergic mechanisms also contribute to regulate ventilation and influence exercise capacity in obese Zucker rats is unknown and formed the basis of the present study. Eight lean [317 ± 18 (SD) g] and eight obese (450 ± 27 g) Zucker rats were studied at 12 wk of age. Ventilation at rest and ventilation during hypoxic (10% O2) and hypercapnic (4% CO2) challenges were measured by the barometric method. Peak O2 consumption (V˙o 2 peak) in response to a progressive treadmill test to exhaustion was measured in a metabolic treadmill. Ventilation and V˙o 2 peak were assessed after administration of equal volumes of DMSO (vehicle) and the GABAA receptor antagonist bicuculline (1 mg/kg). In lean animals, bicuculline administration had no effect on ventilation andV˙o 2 peak. In obese rats, bicuculline administration significantly ( P < 0.05) increased resting ventilation (465 ± 53 and 542 ± 72 ml · kg−1 · min−1 for control and bicuculline, respectively), ventilation during exposure to hypoxia (899 ± 148 and 1,038 ± 83 ml · kg−1 · min−1 for control and bicuculline, respectively), andV˙o 2 peak (62 ± 3.7 and 67 ± 3.5 ml · kg−0.75 · min−1 for control and bicuculline, respectively). However, in obese Zucker rats, ventilation in response to hypercapnia did not change after bicuculline administration (608 ± 96 vs. 580 ± 69 ml · kg−1 · min−1). Our findings indicate that endogenous GABA depresses ventilation and limits exercise performance in obese Zucker rats.
