Be. Richardson et al., EFFECT OF ANTAGONISM AT CENTRAL-NERVOUS-SYSTEM M3-MUSCARINIC-RECEPTORS ON LARYNGEAL CHEMORESPONSE, The Annals of otology, rhinology & laryngology, 106(11), 1997, pp. 920-926
The laryngeal chemoresponse (LCR), comprising laryngeal adductor spasm
, central apnea, and subsequent cardiovascular instability, is thought
to be a factor in sudden infant death syndrome. A muscarinic subtype
receptor, M3, appears to be involved in central respiratory drive and
control. Both the duration of the LCR apnea and levels of M3 receptor
messenger RNA in the brain stem change according to postnatal age. Thi
s study examined the effect of central nervous system antagonism at M3
receptors on the LCR with respect to animal age and dose of antagonis
t. Ten piglets in each of three age groups (group 1, 5 to 8 days; grou
p 2, 18 to 21 days; and group 3, 40 to 43 days) received a series of f
our increasing doses of an M3 antagonist p-fluoro-hexahydro-siladiphen
idol) by intracerebral ventricle injection. The LCR was evoked at base
line and after each dose of antagonist. An effect on susceptible anima
ls (groups 1 and 2) was evident by the second antagonist dose, and per
sisted for the remainder of the experiment (2 hours). At completion of
the experiment, mean apnea duration had decreased in group 1 (61%, p
<.05), and group 2 (57%, p <.05), but was unchanged in group 3 (<10%,
p not significant). Length of mean baseline apneas correlated directly
with degree of apnea shortening. The reduction is not attributable to
changes in arterial PO2 or PCO2 or baseline respiratory rate. These r
esults support an age-related influence on the LCR by M3 receptors in
younger animals that decreases with maturation.