Producción CientíficaAcetylcholine and nicotinic agents excite cat carotid body chemoreceptors and modify their response to natural stimuli. The present
experiments utilized [125I]a-bungarotoxin ([125I]a-BGT) to localize within the chemosensory tissue the possible sites of action of exogenous
and endogenous nicotinic cholinergic substances. In vitro equilibrium binding studies of intact carotid bodies determined a K d of
5.57 nM and a Bma x of 9.21 pmol/g of tissue. Chronic section (12-15 days) of the carotid sinus nerve (CSN) did not change the amount
of displaceable toxin binding. In contrast, the specific binding was reduced by 46% following removal of the superior cervical ganglion.
Light microscope autoradiography of normal, CSN-denervated and sympathectomized carotid bodies revealed displaceable binding
sites concentrated in lobules of type I and type II cells. Treatment of carotid bodies with 50 nM a-BGT in vitro reduced by 50% the
release of [3H]dopamine (synthesized from [3H]tyrosine) caused by hypoxia or nicotine, and also significantly reduced the stimulus-.
evoked discharges recorded from the CSN. The data suggest (1) an absence of ct-BGT binding sites on the afferent terminals of the
CSN and (2) that nicotinic receptors located within parenchymal cell lobules may modulate the release of catecholamines from these cells
