SEROTONERGIC Pontomedullary Neurons Are Not Activated by Antinociceptive Stimulation in the Periaqueductal Gray

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 asserotonergic-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 ofserotonergic cells in RM/NRMC is unlikely to be necessary for the nociceptive and autonomic modulatory effects of PAG stimulation.

[1]  K. Fuxe,et al.  EVIDENCE FOR THE EXISTENCE OF MONOAMINE-CONTAINING NEURONS IN THE CENTRAL NERVOUS SYSTEM. I. DEMONSTRATION OF MONOAMINES IN THE CELL BODIES OF BRAIN STEM NEURONS. , 1964, Acta physiologica Scandinavica. Supplementum.

[2]  J. B. Ranck,et al.  Which elements are excited in electrical stimulation of mammalian central nervous system: A review , 1975, Brain Research.

[3]  T. Yaksh,et al.  Antagonism by methysergide and cinanserin of the antinociceptive action of morphine administered into the periaqueductal gray , 1976, Brain Research.

[4]  J. Besson,et al.  The topographical distribution of serotoninergic terminals in the spinal cord of the cat: biochemical mapping by the combined use of microdissection and microassay procedures , 1977, Brain Research.

[5]  H. Fields,et al.  Evidence that an excitatory connection between the periaqueductal gray and nucleus raphe magnus mediates stimulation produced analgesia , 1979, Brain Research.

[6]  J. Dostrovsky,et al.  Electrophysiological evidence for a projection of the periaqueductal gray matter to nucleus raphe magnus in cat and rat , 1980, Brain Research.

[7]  M. Gilbey,et al.  The response of individual sympathetic preganglionic neurones to microelectrophoretically applied endogenous monoamines , 1981, Brain Research.

[8]  M. Zimmermann,et al.  Serotonergic mediation of descending inhibition from midbrain periaqueductal gray, but not reticular formation, of spinal nociceptive transmission in the cat , 1981, Pain.

[9]  M. Yoshimura,et al.  Intracellular recordings from lateral horn cells fo the spinal cord in vitro. , 1982, Journal of the autonomic nervous system.

[10]  W. Willis,et al.  The effects of serotonin antagonists on the inhibition of primate spinothalamic tract cells produced by stimulation in nucleus raphe magnus or periaqueductal gray. , 1982, The Journal of pharmacology and experimental therapeutics.

[11]  R. M. Bowker,et al.  Transmitters of the raphe-spinal complex: Immunocytochemical studies , 1982, Peptides.

[12]  K. Kadzielawa Antagonism of the excitatory effects of 5-hydroxytryptamine on sympathetic preganglionic neurones and neurones activated by visceral afferents , 1983, Neuropharmacology.

[13]  A. Beitz,et al.  The periaqueductal gray-raphe magnus projection contains somatostatin, neurotensin and serotonin but not cholecystokinin , 1983, Brain Research.

[14]  A I Basbaum,et al.  Endogenous pain control systems: brainstem spinal pathways and endorphin circuitry. , 1984, Annual review of neuroscience.

[15]  R. Mccall Evidence for a serotonergically mediated sympathoexcitatory response to stimulation of medullary raphe nuclei , 1984, Brain Research.

[16]  S. Hilton,et al.  Ventral medullary neurones excited from the hypothalamic and mid-brain defence areas. , 1984, Journal of the autonomic nervous system.

[17]  J. Sandkühler,et al.  Relative contributions of the nucleus raphe magnus and adjacent medullary reticular formation to the inhibition by stimulation in the periaqueductal gray of a spinal nociceptive reflex in the pentobarbital-anesthetized rat , 1984, Brain Research.

[18]  N. Barbaro,et al.  Midbrain stimulation inhibits tail-flick only at currents sufficient to excite rostral medullary neurons , 1984, Brain Research.

[19]  M. Alexander,et al.  Principles of Neural Science , 1981 .

[20]  G. Gebhart,et al.  Stimulation-produced spinal inhibition from the midbrain in the rat is mediated by an excitatory amino acid neurotransmitter in the medial medulla , 1986, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[21]  J. Besson,et al.  Is there a serotonergic tonic descending inhibition on the responses of dorsal horn convergent neurons to C-fibre inputs? , 1987, Brain Research.

[22]  D. C. West,et al.  Autoradiographic and electrophysiological evidence for excitatory amino acid transmission in the periaqueductal gray projection to nucleus raphe magnus in the rat , 1988, Neuroscience Letters.

[23]  A. Basbaum,et al.  An ultrastructural study of the projections from the midbrain periaqueductal gray to spinally projecting, serotonin-immunoreactive neurons of the medullary nucleus raphe magnus in the rat , 1988, Brain Research.

[24]  N. El-Yassir,et al.  Heterogenous effects of serotonin in the dorsal horn of rat: the involvement of 5-HT1 receptor subtypes , 1988, Brain Research.

[25]  P. Mason,et al.  Axonal trajectories and terminations of on‐ and off‐cells in the cat lower brainstem , 1989, The Journal of comparative neurology.

[26]  H. Praag,et al.  The role of glutamate in opiate descending inhibition of nociceptive spinal reflexes , 1990, Brain Research.

[27]  C. Polosa,et al.  The effects of 5-hydroxytryptamine on cat sympathetic preganglionic neurons in vitro. , 1990, The Kurume medical journal.

[28]  N. Akaike,et al.  Serotonin suppressesN-methyl-d-aspartate responses in acutely isolated spinal dorsal horn neurons of the rat , 1990, Brain Research.

[29]  T. Lovick Interactions Between Descending Pathways from the Dorsal and Ventrolateral Periaqueductal Gray Matter in the Rat , 1991 .

[30]  R. Bandler,et al.  The Midbrain Periaqueductal Gray Matter , 1991, NATO ASI Series.

[31]  Duggan Aw Neuropharmacology of pain. , 1992 .

[32]  A. Duggan Neuropharmacology of pain. , 1992, Current opinion in neurology and neurosurgery.

[33]  N. Rajaofetra,et al.  5-Hydroxytryptamine, substance P and thyrotropin-releasing hormone synapses in the intermediolateral cell column of the rat thoracic spinal cord , 1992, Neuroscience Letters.

[34]  A. D. Smith,et al.  Monosynaptic projections from the rostral ventrolateral medulla oblongata to identified sympathetic preganglionic neurons , 1993, Neuroscience.

[35]  Peng Li,et al.  Post-synaptic activity evoked in the rostral ventrolateral medullary neurones by stimulation of the defence areas of hypothalamus and midbrain in the rat , 1993, Neuroscience Letters.

[36]  J. Deuchars,et al.  Localization of cardiac vagal preganglionic motoneurones in the rat: Immunocytochemical evidence of synaptic inputs containing 5‐hydroxytryptamine , 1993, The Journal of comparative neurology.

[37]  N. Mizuno,et al.  Demonstration of axon terminals of projection fibers from the periaqueductal gray onto neurons in the nucleus raphe magnus which send their axons to the trigeminal sensory nuclei , 1993, Brain Research.

[38]  P. Guyenet,et al.  Role of serotonin and catecholamines in sympathetic responses evoked by stimulation of rostral medulla. , 1994, The American journal of physiology.

[39]  M. Urban,et al.  Nuclei within the rostral ventromedial medulla mediating morphine antinociception from the periaqueductal gray , 1994, Brain Research.

[40]  K. Inui,et al.  Facilitation of the arterial baroreflex by the ventrolateral part of the midbrain periaqueductal grey matter in rats. , 1994, The Journal of physiology.

[41]  H. Fields,et al.  Serotonin immunoreactivity is contained in one physiological cell class in the rat rostral ventromedial medulla , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[42]  J. Chalmers,et al.  Serotonin inputs to rabbit sympathetic preganglionic neurons projecting to the superior cervical ganglion or adrenal medulla , 1995, The Journal of comparative neurology.

[43]  K. Inui,et al.  Facilitation of the arterial baroreflex by the preoptic area in anaesthetized rats. , 1995, The Journal of physiology.

[44]  W. Willis,et al.  The efferent projections of the periaqueductal gray in the rat: A Phaseolus vulgaris‐leucoagglutinin study. II. Descending projections , 1995, The Journal of comparative neurology.

[45]  L. Schenberg,et al.  Attenuation of the midbrain-evoked defense reaction by selective stimulation of medullary raphe neurons in rats. , 1995, The American journal of physiology.

[46]  P. Mason,et al.  Effects of isoflurane concentration on the activity of pontomedullary raphe and medial reticular neurons in the rat , 1995, Brain Research.

[47]  W D Willis,et al.  The role of 5-HT3 receptors in periaqueductal gray-induced inhibition of nociceptive dorsal horn neurons in rats. , 1996, The Journal of pharmacology and experimental therapeutics.

[48]  P. Mason,et al.  Physiological identification of pontomedullary serotonergic neurons in the rat. , 1997, Journal of neurophysiology.