Selected Contribution: Hypersensitivity of pulmonary C fibers induced by adenosine in anesthetized rats

Departments of 1 Physiology and 2 Medicine, University of Kentucky Medical Center, Lexington, Kentucky 40536 Submitted 31 January 2003 ; accepted in final form 12 May 2003 Compelling clinical evidence implicates the potential role of adenosine in development of airway hyperresponsiveness and suggests involvement of pulmonary sensory receptors. This study was carried out to determine the effect of a low dose of adenosine infusion on sensitivity of pulmonary C-fiber afferents in anesthetized open-chest rats. Infusion of adenosine (40 µg · kg - 1 · min - 1 iv for 90 s) mildly elevated baseline activity of pulmonary C fibers. However, during adenosine infusion, pulmonary C-fiber responses to chemical stimulants and lung inflation (30 cmH 2 O tracheal pressure) were markedly potentiated; e.g., the response to right atrial injection of capsaicin (0.25 or 0.5 µg/kg) was increased by more than fivefold (change in fiber activity = 2.64 ± 0.67 and 16.27 ± 3.11 impulses/s at control and during adenosine infusion, n = 13, P < 0.05), and this enhanced response returned to control in 10 min. The potentiating effect of adenosine infusion was completely blocked by pretreatment with 8-cyclopentyl-1,3-dipropylxanthine (100 µg/kg), a selective antagonist of the adenosine A 1 receptor, but was not affected by 3,7-dimethyl-1-propargylxanthine (1 mg/kg), an A 2 -receptor antagonist, or 3-ethyl-5-benzyl-2-methyl-4-phenylethynyl-6-phenyl-1,4-(±)-dihydropyridine-3,5-dicarboxylate (2 mg/kg), an A 3 -receptor antagonist. This potentiating effect was also mimicked by N 6 -cyclopentyladenosine (0.25 µg·kg - 1 ·min - 1 for 90 s), a selective agonist of the adenosine A 1 receptor. In conclusion, our results showed that infusion of adenosine significantly elevated the sensitivity of pulmonary C-fiber afferents in rat lungs and that this potentiating effect is likely mediated through activation of the adenosine A 1 receptor. airway hyperresponsiveness; dyspnea; lung afferents; adenosine receptor; chemical irritants Address for reprint requests and other correspondence: L.-Y. Lee, Dept. of Physiology, University of Kentucky Medical Center, 800 Rose St., Lexington, KY 40536-0298 (E-mail: lylee{at}uky.edu ).