(Hypertension. 2001;37:1292.)
© 2001 American Heart Association, Inc.
Scientific Contributions |
From the Hypertension and Vascular Disease Center, Wake Forest University School of Medicine, Winston-Salem, NC.
Correspondence to Debra I. Diz, PhD, The Hypertension and Vascular Disease Center, Wake Forest University School of Medicine, Medical Center Blvd, Winston-Salem, NC 27157-1032. E-mail ddiz{at}wfubmc.edu
AbstractAngiotensin
(Ang) II receptors in the solitary tract nucleus (nTS) are located on
vagal sensory-afferent fiber terminals as well as on neuronal cell
bodies. Results from in vitro slice preparations indicate that
50%
of the neuronal excitatory actions of Ang II result from actions at
presynaptic receptors. The differential contribution of actions on
fiber terminals versus neuronal cell soma to the
cardiovascular effects of Ang II in the nTS is not
known. We used antisense oligonucleotides to the
angiotensin type 1 (AT1) receptor,
which should reduce receptors on neurons within the injection site but
not those on fiber terminals projecting to the nTS. Ang II
injections (250 fmol/30 nL) into the nTS reduced blood pressure by
14±1 mm Hg and heart rate by 13±1 bpm (n=8) in male
Sprague-Dawley rats anesthetized with chloralose/urethane.
Although there was still a significant fall in pressure that was
induced by Ang II at 90 and 150 minutes after
AT1 antisense (164 pmol/120 nL) was injected
into the nTS, the response was blunted 50%
(P<0.01). Heart rate responses
were completely blocked at the 150-minute time point. Scrambled
sequence oligonucleotides did not alter Ang II
responses at any time. There was a 40% reduction in
125I[Sar1Thr8]-Ang
II binding when antisense-injected and noninjected sides of the nTS
were compared with receptor autoradiography. This
finding is consistent with the continued presence of
AT1 receptors on afferent fibers. This unique
strategy illustrates that both presynaptic fiber terminals and nTS
neurons are involved in the blood pressure lowering actions of Ang II,
whereas heart rate responses are largely due to actions directly on nTS
neurons and activation of vagal efferent pathways.
Key Words: solitary tract nucleus medulla oblongata circulation angiotensin II microinjections oligodeoxynucleotides, antisense receptors, angiotensin
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