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Ascending multisynaptic pathways from the trigeminal ganglion to the anterior cingulate cortex
Authors:Koichi Iwata  Shigehiro Miyachi  Michiko Imanishi  Yoshiyuki Tsuboi  Junichi Kitagawa  Kohei Teramoto  Suzuro Hitomi  Masamichi Shinoda  Masahiro Kondo  Masahiko Takada
Affiliation:aDepartment of Physiology, Nihon University School of Dentistry, 1-8-13 Kandasurugadai, Chiyoda-ku, Tokyo, 101-8310, Japan;bDivision of Applied System Neuroscience, Advanced Medical Research Center, Nihon University, Graduate School of Medical Science, 30-1 Ohyaguchi-Kamimachi, Itabashi-ku, Tokyo 173-8610, Japan;cDivision of Functional Morphology, Dental Research Center, Nihon University School of Dentistry, Tokyo 101-8310, Japan;dTokyo Metropolitan Institute for Neuroscience, Tokyo Metropolitan Organization for Medical Research, Fuchu, Tokyo 183-8526, Japan;ePrimate Research Institute, Kyoto University, Inuyama, Aichi 484-8506, Japan;fDepartment of Dysphasia Rehabilitation, Nihon University School of Dentistry, 1-8-13 Kandasurugadai, Chiyoda-ku, Tokyo 101-8310, Japan
Abstract:By means of retrograde transneuronal transport of rabies virus, ascending multisynaptic pathways from the trigeminal ganglion (TG) to the anterior cingulate cortex (ACC) were identified in the rat. After rabies injection into an electrophysiologically defined trigeminal projection region of the ACC, transsynaptic labeling of second-order neurons via the medial thalamus (including the parafascicular nucleus) was located in the spinal trigeminal nucleus pars caudalis. Third-order neuron labeling occurred in the TG. Most of these TG neurons were medium- or large-sized cells giving rise to myelinated Aδ or Aβ afferent fibers, respectively. By contrast, TG neurons labeled transsynaptically from the orofacial region of the primary somatosensory cortex contained many small cells associated with unmyelinated C afferent fibers. Furthermore, the TG neurons retrogradely labeled with fluorogold injected into the mental nerve were smaller in their sizes compared to those labeled with rabies. Our extracellular unit recordings revealed that a majority of ACC neurons responded to trigeminal nerve stimulation with latencies of shorter than 20 ms. Thus, somatosensory information conveyed to the ACC by multisynaptic ascending pathways derived predominantly from myelinated primary afferents (i.e., the medial nociceptive system) and may be used to subserve affective-motivational aspects of pain. Lack of overlap with the lateral nociceptive system is notable and suggests that the medial and lateral nociceptive systems perform separate and non-overlapping functions.
Keywords:Abbreviations: ac, anterior commissure   ACC, anterior cingulate cortex   BLA, basolateral amygdaloid nucleus   cb, cingulum bundle   CeA, central amygdaloid nucleus   CL, centrolateral thalamic nucleus   CM, centromedial thalamic nucleus   cp, cerebral peduncle   CPu, caudate&ndash  putamen   fr, fasciculus retroflexus   HP, hypothalamic nuclei   LHb, lateral habenular nucleus   LO, lateral orbital cortex   LPb, lateral parabrachial nucleus   LV, lateral ventricle   MD, mediodorsal thalamic nucleus   MPb, medial parabrachial nucleus   mt, mammillothalamic tract   NA, nucleus accumbens   PIR, piriform cortex   PC, paracentral thalamic nucleus   PF, parafascicular thalamic nucleus   RAIC, rostral agranular insular cortex   rf, rhinal fissure   scp, superior cerebellar peduncle   Sm, submedius thalamic nucleus   SRD, subnucleus reticularis dorsalis   TG, trigeminal ganglion   VBc, ventrobasal thalamic complex   VO, ventral orbital cortex   ZI, zona incerta   3v, third ventricle   I, lamina I of Vc   II, lamina II of Vc   III, lamina III of Vc   Vc, spinal trigeminal nucleus pars caudalis   Vo, spinal trigeminal nucleus pars oralis
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