 |
Previous Article | Next Article 
The Journal of Neuroscience, April 15, 1998, 18(8):3043-3049
Vagotomy-Induced Enhancement of Mechanical Hyperalgesia in the
Rat Is Sympathoadrenal-Mediated
Sachia G.
Khasar1,
Frederick J.-P.
Miao1,
Wilfrid
Jänig2, and
Jon D.
Levine1
1 Departments of Anatomy, Medicine, and Oral and
Maxillofacial Surgery, Division of Neuroscience and Biomedical Sciences
Program, University of California at San Francisco, San Francisco,
California 94143-0452, and 2 Physiologisches Institut,
Christian-Albrechts-Universität zu Kiel, 24098 Kiel, Germany
We have recently shown that subdiaphragmatic vagotomy enhances
bradykinin-induced hyperalgesic behavior and decreases baseline paw
withdrawal threshold to mechanical stimulation of the hindpaw skin in
rats by a peripheral mechanism. To elucidate the underlying mechanism,
we studied whether lesions of efferent neuroendocrine pathways could
prevent or reverse the potentiating effect of vagotomy. In groups of
sham-vagotomized or vagotomized rats, we surgically removed or
denervated the adrenal medulla. Bradykinin was injected intradermally
into the skin of the dorsal surface of the rat hindpaw. Threshold of
paw withdrawal to mechanical stimulation of the skin was measured.
Vagotomy induced a decrease in mechanical baseline paw withdrawal
threshold and enhancement of bradykinin-induced mechanical hyperalgesic
behavior, both of which were maintained over the 5 week testing period.
Adrenal enucleation or denervation of the adrenal gland by suprarenal
ganglionectomy prevented vagotomy-induced decrease in baseline paw
withdrawal threshold and enhancement of bradykinin-induced
hyperalgesia. In animals that had a demonstrated decrease in baseline
paw withdrawal threshold and enhancement of bradykinin-induced
hyperalgesia 2 weeks after vagotomy, additional denervation of the
adrenal medulla significantly reversed these effects over a 3 week
period.
These results imply that both the decrease in baseline paw withdrawal
threshold and enhancement of bradykinin-induced hyperalgesic behavior
after vagotomy are dependent on a hormonal signal released from the
adrenal medulla and suggest a novel mechanism of sensitization of
cutaneous nociceptors.
Key words:
bradykinin; hyperalgesia; nociception; pain; sympathoadrenal system; vagus
Copyright © 1998 Society for Neuroscience 0270-6474/98/1883043-07$05.00/0
This article has been cited by other articles:

|
 |

|
 |
 
S. G. Khasar, J. Burkham, O. A. Dina, A. S. Brown, O. Bogen, N. Alessandri-Haber, P. G. Green, D. B. Reichling, and J. D. Levine
Stress Induces a Switch of Intracellular Signaling in Sensory Neurons in a Model of Generalized Pain
J. Neurosci.,
May 28, 2008;
28(22):
5721 - 5730.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
C. H. Hubscher and R. D. Johnson
Effects of Chronic Dorsal Column Lesions on Pelvic Viscerosomatic Convergent Medullary Reticular Formation Neurons
J Neurophysiol,
December 1, 2004;
92(6):
3596 - 3600.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
C. Vogel, R. Mossner, M. Gerlach, T. Heinemann, D. L. Murphy, P. Riederer, K.-P. Lesch, and C. Sommer
Absence of Thermal Hyperalgesia in Serotonin Transporter-Deficient Mice
J. Neurosci.,
January 15, 2003;
23(2):
708 - 715.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
K. O. Aley, A. Martin, T. McMahon, J. Mok, J. D. Levine, and R. O. Messing
Nociceptor Sensitization by Extracellular Signal-Regulated Kinases
J. Neurosci.,
September 1, 2001;
21(17):
6933 - 6939.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
E. Lancaster, E. J. Oh, and D. Weinreich
Vagotomy Decreases Excitability in Primary Vagal Afferent Somata
J Neurophysiol,
January 1, 2001;
85(1):
247 - 253.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
S. G. Khasar, G. McCarter, and J. D. Levine
Epinephrine Produces a beta -Adrenergic Receptor-Mediated Mechanical Hyperalgesia and In Vitro Sensitization of Rat Nociceptors
J Neurophysiol,
March 1, 1999;
81(3):
1104 - 1112.
[Abstract]
[Full Text]
[PDF]
|
 |
|
|