Kb. Bach et al., Post-hypoxia frequency decline in rats: sensitivity to repeated hypoxia and alpha(2)-adrenoreceptor antagonism, BRAIN RES, 817(1-2), 1999, pp. 25-33
We tested the hypothesis that the post-hypoxia frequency decline of phrenic
nerve activity following brief, isocapnic hypoxic episodes in rats is dimi
nished by prior hypoxic episodes and alpha(2)-adrenoreceptor antagonism. An
esthetized (urethane), artificially ventilated (F-IO2 = 0.50) and vagotomiz
ed rats were presented with two or three, 5 min episodes of isocapnic hypox
ia (F-IO2 =o.11) separated by 30 min of control, hyperoxic conditions. Phre
nic nerve discharge, end-tidal CO, and arterial blood gases were measured b
efore during and after hypoxia. The average maximum frequency decline, meas
ured 5 min after the first hypoxic episode, was 26 +/- 7 bursts/min below p
re-hypoxic baseline values (a 70 +/- 16% decrease). By 30 min post-hypoxia,
frequency had returned to baseline. Two groups of rats were then administe
red either: (1) saline (sham) or (2) the alpha(2)-receptor antagonist, RX82
1002 HCl (2-[2-(2-Methoxy-1,4-benzodioxanyl)l imidazoline hydrochloride; 0.
25 mg/kg, i.v.). Isocapnic hypoxia was repeated 10 min later. In sham rats,
the post-hypoxia frequency decline (PHFD) was significantly attenuated rel
ative to the initial (control) response. However, PHFD was attenuated signi
ficantly more in RX821002-treated vs. sham rats (-3 +/- 3 bursts/min vs. -1
2 +/- 4 bursts/min @ 5 min post hypoxia for RX821002 and sham-treated, resp
ectively; p < 0.05). We conclude that the magnitude of PHFD is dependent on
the prior history of hypoxia and that alpha(2) adrenoreceptor activation p
lays a role in its underlying mechanism. (C) 1999 Elsevier Science B.V. All
rights reserved.