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Department of Physiology, Wayne State University, School of Medicine, Detroit, Michigan 48201
Selective activation of adenosine
A1 and A2a receptors in the subpostremal
nucleus tractus solitarius (NTS) increases and decreases mean arterial
pressure (MAP), respectively, and decreases heart rate (HR). We have
previously shown that the decreases in MAP evoked by NTS
A2a receptor stimulation were accompanied with differential
sympathetic responses in renal (RSNA), lumbar (LSNA), and preganglionic
adrenal sympathetic nerve activity (pre-ASNA). Therefore, now we
investigated whether stimulation of NTS A1 receptors via
unilateral microinjection of
N6-cyclopentyladenosine (CPA) elicits
differential activation of the same sympathetic outputs in
-chloralose-urethane-anesthetized male Sprague-Dawley
rats. CPA (0.33-330.0 pmol in 50 nl) evoked dose-dependent
increases in MAP, variable decreases in HR, and differential increases
in all recorded sympathetic outputs:
pre-ASNA 
RSNA
LSNA. Sinoaortic denervation + vagotomy abolished the MAP and
LSNA responses, reversed the normal increases in RSNA into decreases,
and significantly attenuated increases in pre-ASNA. NTS ionotropic
glutamatergic receptor blockade with kynurenate sodium (4.4 nmol/100
nl) reversed the responses in MAP, LSNA, and RSNA and attenuated the
responses in pre-ASNA. We conclude that afferent inputs and intact
glutamatergic transmission in the NTS are necessary to mediate the
pressor and differential sympathoactivatory responses to stimulation of
NTS A1 receptors.
nucleus of the solitary tract; purinergic receptors; adrenal sympathetic nerve; renal sympathetic nerve; lumbar sympathetic nerve
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