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J Physiol Volume 566, Number 2, 559-573, July 15, 2005 DOI: 10.1113/jphysiol.2005.086322
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Hypoxic activation of arterial chemoreceptors inhibits sympathetic outflow to brown adipose tissue in rats

C. J Madden1 and S. F Morrison1

1 Neurological Sciences Institute, Oregon Health & Science University, Beaverton, OR 97006, USA

In urethane–chloralose anaesthetized, neuromuscularly blocked, artificially ventilated rats, we demonstrated that activation of carotid chemoreceptors inhibits the elevated levels of brown adipose tissue (BAT) sympathetic nerve activity (SNA) evoked by hypothermia, by microinjection of prostaglandin E2 into the medial preoptic area or by disinhibition of neurones in the raphe pallidus area (RPa). Peripheral chemoreceptor stimulation with systemic administration of NaCN (50 µg in 0.1 ml) or with hypoxic ventilation (8% O2–92% N2, 30 s) completely inhibited BAT SNA. Arterial chemoreceptor-evoked inhibition of BAT SNA was eliminated by prior bilateral transections of the carotid sinus nerves or by prior inhibition of neurones within the commissural nucleus tractus solitarii (commNTS) with glycine (40 nmol/80 nl) or with the GABAA receptor agonist muscimol (160 pmol/80 nl; 77 ± 10% attenuation), or by prior blockade of ionotropic excitatory amino acid receptors in the commNTS with kynurenate (8 nmol/80 nl; 82 ± 10% attenuation). Furthermore, activation of commNTS neurones following local microinjection of bicuculline (30 pmol/60 nl) completely inhibited the elevated level of BAT SNA resulting from disinhibition of neurones in the RPa. These results demonstrate that hypoxic stimulation of arterial chemoreceptor afferents leads to an inhibition of BAT SNA and BAT thermogenesis through an EAA-mediated activation of second-order, arterial chemoreceptor neurones in the commNTS. Peripheral chemoreceptor-evoked inhibition of BAT SNA could directly contribute to (or be permissive for) the hypoxia-evoked reductions in body temperature and oxygen consumption that serve as an adaptive response to decreased oxygen availability.

(Received 8 March 2005; accepted after revision 29 April 2005; first published online 5 May 2005)
Corresponding author C. J. Madden: Neurological Sciences Institute/OHSU, 505 NW 185th Avenue, Beaverton, OR 97006, USA. Email: maddench{at}ohsu.edu




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