Ascending multisynaptic pathways from the trigeminal ganglion to the anterior cingulate cortex |
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Authors: | Koichi Iwata Shigehiro Miyachi Michiko Imanishi Yoshiyuki Tsuboi Junichi Kitagawa Kohei Teramoto Suzuro Hitomi Masamichi Shinoda Masahiro Kondo Masahiko Takada |
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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 |
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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. |
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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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