(Hypertension. 1998;32:939-944.)
© 1998 American Heart Association, Inc.
Scientific Contributions |
From the Department of Education and Medical Research, Veterans General HospitalTaipei (J.Y.H.C., W-C.C., H-Y.L.), and Center for Neuroscience, National Yang-Ming University (S.H.H.C.), Taipei, Taiwan, Republic of China.
Correspondence to Julie Y.H. Chan, PhD, Department of Education and Medical Research, Veterans General HospitalTaipei, Taipei 11217, Taiwan, Republic of China. E-mail yhwa{at}vghtpe.gov.tw
AbstractWe delineated the functional role of Fos protein at the nucleus tractus solitarii in the manifestation of reduced baroreceptor reflex control of heart rate during hypertension, using spontaneously hypertensive rats (SHR), stroke-prone SHR, Wistar-Kyoto rats, or Sprague-Dawley rats. Microinjection into the bilateral nucleus tractus solitarii of an antisense oligonucleotide that targets against the initiation codon of c-fos mRNA significantly potentiated the baroreceptor reflex in response to 30 minutes of sustained increase in blood pressure. Of particular note was the restoration of both the impaired sensitivity and capacity of baroreceptor reflex in SHR and stroke-prone SHR to levels comparable to those in normotensive rats. Likewise, the number of Fos-immunoreactive nuclei evoked by the sustained increase in blood pressure in the caudal nucleus tractus solitarii of SHR and stroke-prone SHR was reduced, after this antisense c-fos treatment, to the basal level exhibited by the normotensive animals. Control treatment with the corresponding sense oligonucleotide, an antisense oligonucleotide that targets against a different portion of the coding sequence of the c-fos mRNA or artificial cerebrospinal fluid, on the other hand, elicited no discernible effect on either the baroreceptor reflex response or the induced expression of Fos protein in the nucleus tractus solitarii by baroreceptor activation. We also found that the basal level of Fos expression in the caudal nucleus tractus solitarii was significantly elevated in the SHR and stroke-prone SHR. Together, these novel findings suggest that an elevated expression of basal Fos protein in the NTS during hypertension may be associated with the dysfunction in baroreceptor reflex control of heart rate.
Key Words: antisense elements baroreflex hypertension, genetic rats
This article has been cited by other articles:
![]() |
R. Ambalavanar, Y. Tanaka, W. S. Selbie, and C. L. Ludlow Neuronal Activation in the Medulla Oblongata During Selective Elicitation of the Laryngeal Adductor Response J Neurophysiol, November 1, 2004; 92(5): 2920 - 2932. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. H. H. Chan, K.-F. Chang, C.-C. Ou, and J. Y. H. Chan Nitric Oxide Regulates c-fos Expression in Nucleus Tractus Solitarii Induced by Baroreceptor Activation via cGMP-Dependent Protein Kinase and cAMP Response Element-Binding Protein Phosphorylation Mol. Pharmacol., February 1, 2004; 65(2): 319 - 325. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. H.H. Chan, L.-L. Wang, K.-F. Chang, C.-C. Ou, and J. Y.H. Chan Altered Temporal Profile of Heat Shock Factor 1 Phosphorylation and Heat Shock Protein 70 Expression Induced by Heat Shock in Nucleus Tractus Solitarii of Spontaneously Hypertensive Rats Circulation, January 21, 2003; 107(2): 339 - 345. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Y.H. Chan, L.-L. Wang, H.-Y. Lee, and S. H.H. Chan Augmented Upregulation by c-fos of Angiotensin Subtype 1 Receptor in Nucleus Tractus Solitarii of Spontaneously Hypertensive Rats Hypertension, September 1, 2002; 40(3): 335 - 341. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. H.F. Luoh and S. H.H. Chan Inhibition of Baroreflex by Angiotensin II via Fos Expression in Nucleus Tractus Solitarii of the Rat Hypertension, July 1, 2001; 38(1): 130 - 135. [Abstract] [Full Text] [PDF] |
||||
![]() |
P.-L. Li, Y.-M. Chao, S. H. H. Chan, and J. Y. H. Chan Potentiation of Baroreceptor Reflex Response by Heat Shock Protein 70 in Nucleus Tractus Solitarii Confers Cardiovascular Protection During Heatstroke Circulation, April 24, 2001; 103(16): 2114 - 2119. [Abstract] [Full Text] [PDF] |
||||
|
Hypertension Home | Subscriptions | Archives | Feedback | Authors | Help | AHA Journals Home | Search Copyright © 1998 American Heart Association, Inc. All rights reserved. Unauthorized use prohibited. |