Volume 17, Number 9,
Issue of May 1, 1997
pp. 3285-3292
Copyright ©1997 Society for Neuroscience
SEROTONERGIC Pontomedullary
Neurons Are Not Activated by Antinociceptive Stimulation in the
Periaqueductal Gray
Received Dec. 9, 1996; revised Jan. 22, 1997; accepted Feb. 11, 1997.
Keming Gao,
Yoo-Hang Hugh Kim, and
Peggy Mason
Department of Pharmacological and Physiological Sciences and the
Committee on Neurobiology, University of Chicago, Chicago, Illinois
60637
The antinociceptive and cardiovascular effects of midbrain
periaqueductal gray (PAG) stimulation are mediated through a relay in
the pontomedullary raphe magnus (RM) and adjacent nucleus reticularis magnocellularis (NRMC). To test whether the neurons important in
mediating PAG-evoked effects are SEROTONERGIC, the
responses of pontomedullary SEROTONERGIC-LIKE cells to PAG
stimulation were tested. SEROTONERGIC-LIKE neurons
(n = 21) were recorded extracellularly in
halothane-anesthetized Sprague Dawley rats. Serotonergic-like neurons
were distinguished by their slow and steady background discharge. Two
neurons that were physiologically characterized as
SEROTONERGIC-LIKE were intracellularly labeled and
processed for serotonin immunoreactivity; both cells tested contained
immunoreactive serotonin. Train stimulation of sites within the
midbrain PAG, at intensities of
50 µA, suppressed the tail
withdrawal from noxious heat and evoked changes in blood pressure and
heart rate. No SEROTONERGIC-LIKE cells were activated by
single-pulse or short-train (two to five pulses) stimulation of the PAG
at antinociceptive intensities. In most cases,
SEROTONERGIC-LIKE cells were unaffected by long-train
stimulation (5-6 sec) of the PAG, which produced antinociception and
cardiovascular changes. In contrast, >50% of the cells in two
nonserotonergic-like cell classes were activated at short latency by
such PAG stimulation. In conclusion, monosynaptic excitation of
SEROTONERGIC cells in RM/NRMC is unlikely to be necessary
for the nociceptive and autonomic modulatory effects of PAG
stimulation.
Key words:
raphe magnus;
serotonin;
monoamine;
pain modulation;
autonomic modulation;
antinociception