SEROTONIN IMMUNOREACTIVITY IS CONTAINED IN ONE PHYSIOLOGICAL CELL CLASS IN THE RAT ROSTRAL VENTROMEDIAL MEDULLA

被引:113
作者
POTREBIC, SB
FIELDS, HL
MASON, P
机构
[1] HARVARD UNIV, SCH MED, NEUROSCI PROGRAM, BOSTON, MA 02143 USA
[2] UNIV CALIF SAN FRANCISCO, KECK CTR INTEGRAT NEUROSCI, SAN FRANCISCO, CA 94143 USA
[3] UNIV CALIF SAN FRANCISCO, DEPT PHYSIOL, SAN FRANCISCO, CA 94143 USA
关键词
RAPHE MAGNUS; ANTINOCICEPTION; OPIOID ANALGESIA; 5-HT; INDOLEAMINE; STATE DEPENDENCE;
D O I
10.1523/JNEUROSCI.14-03-01655.1994
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Neurons in the rostral ventromedial medulla (RVM) are the major source of serotonergic projections to the dorsal horn. A large body of evidence implicates RVM serotonergic neurons in the modulation of spinal nociceptive transmission. Three physiological classes of RVM neurons, on, off, and neutral cells, are postulated to have different nociceptive modulatory effects on spinal nocifensor reflexes. This study was undertaken to determine which RVM cell class(es) contains 5-HT. In anesthetized rats, RVM neurons were identified by their responses to noxious cutaneous stimuli, intracellularly labeled, and processed for 5-HT immunocytochemistry. Labeled neurons were examined with epifluorescence and imaged using a confocal laser microscope. A total of 25 RVM neurons were intracellularly labeled. No off (n = 9) or on (n = 8) cells were serotonergic. Half of the neutral cells (4 of 8) demonstrated 5-HT immunoreactivity. These results call for a reevaluation of the mechanisms of RVM modulatory influence on spinal cord nociceptive transmission. The finding that some neutral cells are serotonergic strongly suggests that serotonergic neutral cells are involved in the modulation of spinal nociceptive transmission. Additionally, inhibition of spinal nociceptive transmission by off cells is unlikely to involve 5-HT release. Finally, since opioid administration does not alter the firing of RVM neutral cells, the results of the present study indicate that serotonergic RVM neurons do not directly mediate the effects of supraspinal opioids in the rat.
引用
收藏
页码:1655 / 1665
页数:11
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