Organization of Multisynaptic Inputs from Prefrontal Cortex to Primary Motor Cortex as Revealed by Retrograde Transneuronal Transport of Rabies Virus

The organization of multisynaptic projections from the prefrontal cortex to the primary motor cortex (MI) was examined in macaque monkeys by retrograde transneuronal transport of rabies virus. In the first series of experiments, the virus was injected into the MI forelimb region, and the time-dependent distribution patterns of transsynaptic labeling were analyzed in the frontal lobe with various survivals (2-4 d). Two days after the viral injection, neuronal labeling emerged in the caudal aspects of the nonprimary motor-related areas that are known to project to the MI directly. At the same time, the motor thalamus contained labeled neurons. On the third day, cortical labeling extended into the rostral motor-related areas and, also, prearcuate area 8. Moreover, a number of labeled neurons were located in the internal pallidum and the cerebellar nuclei. At the 4 d postinjection period, neuronal labeling occurred widely in prefrontal areas as well as in the putamen and the cerebellar cortex. In the second series of experiments, the viral injection was made into the MI hindlimb region, and the distribution pattern of prefrontal labeling on the fourth day was compared with that in the forelimb-injection case. The labeled neurons in each prefrontal area were much fewer in the hindlimb-injection case than in the forelimb-injection case. Whereas ventral area 46 was most densely labeled from the forelimb region, only sparse labeling from the hindlimb region was observed in this prefrontal area. The present results suggest the importance of ventral area 46 in the cognitive control of forelimb movements.

[1]  M. Inase,et al.  Organization of prefrontal outflow toward frontal motor‐related areas in macaque monkeys , 2004, The European journal of neuroscience.

[2]  P. Strick,et al.  Macro-architecture of basal ganglia loops with the cerebral cortex: use of rabies virus to reveal multisynaptic circuits. , 2004, Progress in brain research.

[3]  P. Strick,et al.  Cerebellar Loops with Motor Cortex and Prefrontal Cortex of a Nonhuman Primate , 2003, The Journal of Neuroscience.

[4]  Yoshikazu Isomura,et al.  Neural Coding of “Attention for Action” and “Response Selection” in Primate Anterior Cingulate Cortex , 2003, The Journal of Neuroscience.

[5]  Akira Noguchi,et al.  Cross‐reactive antigenicity of nucleoproteins of lyssaviruses recognized by a monospecific antirabies virus nucleoprotein antiserum on paraffin sections of formalin‐fixed tissues , 2003, Pathology international.

[6]  Keiji Tanaka,et al.  Neuronal Correlates of Goal-Based Motor Selection in the Prefrontal Cortex , 2003, Science.

[7]  J. Grafman,et al.  Dissociating the roles of the rostral anterior cingulate and the lateral prefrontal cortices in performing two tasks simultaneously or successively. , 2003, Cerebral cortex.

[8]  G. Luppino,et al.  ß Federation of European Neuroscience Societies Prefrontal and agranular cingulate projections to the dorsal premotor areas F2 and F7 in the macaque monkey , 2022 .

[9]  P. Strick,et al.  An unfolded map of the cerebellar dentate nucleus and its projections to the cerebral cortex. , 2003, Journal of neurophysiology.

[10]  A. Turken,et al.  Dissociation between conflict detection and error monitoring in the human anterior cingulate cortex , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[11]  Anthony R. Dickinson,et al.  Non-spatial, motor-specific activation in posterior parietal cortex , 2002, Nature Neuroscience.

[12]  T. Paus Primate anterior cingulate cortex: Where motor control, drive and cognition interface , 2001, Nature Reviews Neuroscience.

[13]  Atsushi Nambu,et al.  Somatotopic arrangement and corticocortical inputs of the hindlimb region of the primary motor cortex in the macaque monkey , 2001, Neuroscience Research.

[14]  P. Strick,et al.  Rabies as a transneuronal tracer of circuits in the central nervous system , 2000, Journal of Neuroscience Methods.

[15]  J. Price,et al.  Prefrontal cortical projections to the striatum in macaque monkeys: Evidence for an organization related to prefrontal networks , 2000, The Journal of comparative neurology.

[16]  K. Hikosaka,et al.  Delay activity of orbital and lateral prefrontal neurons of the monkey varying with different rewards. , 2000, Cerebral cortex.

[17]  D. Hoffman,et al.  Muscle and movement representations in the primary motor cortex. , 1999, Science.

[18]  H. Barbas,et al.  Medial Prefrontal Cortices Are Unified by Common Connections With Superior Temporal Cortices and Distinguished by Input From Memory‐Related Areas in the Rhesus Monkey , 1999, The Journal of comparative neurology.

[19]  Masamichi Sakagami,et al.  The hierarchical organization of decision making in the primate prefrontal cortex , 1999, Neuroscience Research.

[20]  W. Schultz,et al.  Relative reward preference in primate orbitofrontal cortex , 1999, Nature.

[21]  P. Strick,et al.  The Organization of Cerebellar and Basal Ganglia Outputs to Primary Motor Cortex as Revealed by Retrograde Transneuronal Transport of Herpes Simplex Virus Type 1 , 1999, The Journal of Neuroscience.

[22]  E. Miller,et al.  Memory fields of neurons in the primate prefrontal cortex. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[23]  J. Tanji,et al.  Task-dependent selectivity of movement-related neuronal activity in the primate prefrontal cortex. , 1998, Journal of neurophysiology.

[24]  M. Inase,et al.  Corticostriatal projections from the somatic motor areas of the frontal cortex in the macaque monkey: segregation versus overlap of input zones from the primary motor cortex, the supplementary motor area, and the premotor cortex , 1998, Experimental Brain Research.

[25]  P. Strick,et al.  Spinal Cord Terminations of the Medial Wall Motor Areas in Macaque Monkeys , 1996, The Journal of Neuroscience.

[26]  H. Koprowski,et al.  Laboratory Techniques in Rabies , 2022 .

[27]  J. Price,et al.  Limbic connections of the orbital and medial prefrontal cortex in macaque monkeys , 1995, The Journal of comparative neurology.

[28]  J. Price,et al.  Sensory and premotor connections of the orbital and medial prefrontal cortex of macaque monkeys , 1995, The Journal of comparative neurology.

[29]  J. Tanji,et al.  Spatial distribution of thalamic projections to the supplementary motor area and the primary motor cortex: A retrograde multiple labeling study in the macaque monkey , 1995, The Journal of comparative neurology.

[30]  G. Ugolini Specificity of rabies virus as a transneuronal tracer of motor networks: Transfer from hypoglossal motoneurons to connected second‐order and higher order central nervous system cell groups , 1995, The Journal of comparative neurology.

[31]  C. Bruce,et al.  Topography of projections to posterior cortical areas from the macaque frontal eye fields , 1995, The Journal of comparative neurology.

[32]  E. Chudler,et al.  Somatosensory, multisensory, and task-related neurons in cortical area 7b (PF) of unanesthetized monkeys. , 1994, Journal of neurophysiology.

[33]  J. B. Preston,et al.  Interconnections between the prefrontal cortex and the premotor areas in the frontal lobe , 1994, The Journal of comparative neurology.

[34]  I. Darian‐Smith,et al.  Multiple corticospinal neuron populations in the macaque monkey are specified by their unique cortical origins, spinal terminations, and connections. , 1994, Cerebral cortex.

[35]  G. Rizzolatti,et al.  Corticocortical connections of area F3 (SMA‐proper) and area F6 (pre‐SMA) in the macaque monkey , 1993, The Journal of comparative neurology.

[36]  P. Goldman-Rakic,et al.  Prefrontal connections of medial motor areas in the rhesus monkey , 1993, The Journal of comparative neurology.

[37]  J Tanji,et al.  Input organization of distal and proximal forelimb areas in the monkey primary motor cortex: A retrograde double labeling study , 1993, The Journal of comparative neurology.

[38]  P. Goldman-Rakic,et al.  Dissociation of object and spatial processing domains in primate prefrontal cortex. , 1993, Science.

[39]  RP Dum,et al.  Topographic organization of corticospinal projections from the frontal lobe: motor areas on the lateral surface of the hemisphere , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[40]  A. Graybiel,et al.  Two input systems for body representations in the primate striatal matrix: experimental evidence in the squirrel monkey , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[41]  PL Strick,et al.  The origin of thalamic inputs to the "hand" representation in the primary motor cortex , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[42]  P. Goldman-Rakic,et al.  Neuronal activity related to saccadic eye movements in the monkey's dorsolateral prefrontal cortex. , 1991, Journal of neurophysiology.

[43]  S P Wise,et al.  A neurophysiological comparison of three distinct regions of the primate frontal lobe. , 1991, Brain : a journal of neurology.

[44]  RP Dum,et al.  The origin of corticospinal projections from the premotor areas in the frontal lobe , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[45]  K. Kubota,et al.  Disinhibition in the monkey prefrontal cortex, by injecting bicuculline, induces forelimb movements learned in a GO/NO-GO task , 1990, Neuroscience Research.

[46]  P. Goldman-Rakic,et al.  Visuospatial coding in primate prefrontal neurons revealed by oculomotor paradigms. , 1990, Journal of neurophysiology.

[47]  S. Haber,et al.  Topographic organization of the ventral striatal efferent projections in the rhesus monkey: An anterograde tracing study , 1990, The Journal of comparative neurology.

[48]  D. Pandya,et al.  Prefrontal cortex in relation to other cortical areas in rhesus monkey: architecture and connections. , 1990, Progress in brain research.

[49]  P. Goldman-Rakic,et al.  Posterior parietal cortex in rhesus monkey: II. Evidence for segregated corticocortical networks linking sensory and limbic areas with the frontal lobe , 1989, The Journal of comparative neurology.

[50]  D. Pandya,et al.  Architecture and intrinsic connections of the prefrontal cortex in the rhesus monkey , 1989, The Journal of comparative neurology.

[51]  D. Pandya,et al.  Frontal lobe connections of the superior temporal sulcus in the rhesus monkey , 1989, The Journal of comparative neurology.

[52]  K Watanabe,et al.  Connections of area 8 with area 6 in the brain of the macaque monkey , 1988, The Journal of comparative neurology.

[53]  H. Barbas Anatomic organization of basoventral and mediodorsal visual recipient prefrontal regions in the rhesus monkey , 1988, The Journal of comparative neurology.

[54]  D. Pandya,et al.  Architecture and frontal cortical connections of the premotor cortex (area 6) in the rhesus monkey , 1987, The Journal of comparative neurology.

[55]  L A Krubitzer,et al.  Frontal eye field as defined by intracortical microstimulation in squirrel monkeys, owl monkeys, and macaque monkeys II. cortical connections , 1986, The Journal of comparative neurology.

[56]  L A Krubitzer,et al.  Frontal eye field as defined by intracortical microstimulation in squirrel monkeys, owl monkeys, and macaque monkeys II. cortical connections , 1986, The Journal of comparative neurology.

[57]  M. Mesulam,et al.  Cortical afferent input to the principals region of the rhesus monkey , 1985, Neuroscience.

[58]  T. Kaneko,et al.  An anterograde-retrograde transneuronal transport of conjugates of wheat germ agglutinin with horseradish peroxidase (WGA-HRP): labeling of neurons in the reticular nucleus of the thalamus with WGA-HRP injected into the posterior column nuclei in the cat , 1984, Brain Research.

[59]  A P Georgopoulos,et al.  On the relations between the direction of two-dimensional arm movements and cell discharge in primate motor cortex , 1982, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[60]  I. Hamada,et al.  Topographical projections from the prefrontal cortex to the post-arcuate area in the rhesus monkey, studied by retrograde axonal transport of horseradish peroxidase , 1980, Neuroscience Letters.

[61]  P. Strick,et al.  Frontal lobe inputs to primate motor cortex: evidence for four somatotopically organized ‘premotor’ areas , 1979, Brain Research.

[62]  P. Yager,et al.  A rapid tissue culture test for determining rabies neutralizing antibody. , 1973, Monograph series. World Health Organization.