Evidence map›Paper›PMID 35122444›Full record

ArticleThe Journal of physiology2022

A multisynaptic pathway from the ventral midbrain toward spinal motoneurons in monkeys.

Michiaki Suzuki, Ken-Ichi Inoue, Hiroshi Nakagawa, Hiroaki Ishida, Kenta Kobayashi, Tadashi Isa, Masahiko Takada, Yukio Nishimura

Open access · hybridAbstract read
In one paragraph

Article in The Journal of physiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 35% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. Common and Distinct Neural Substrates for Approach- and Avoidance-Motivated Actions.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 1 country.

Michiaki SuzukiNeural Prosthetics Project, Tokyo Metropolitan Institute of Medical Science, Setagaya, Tokyo, Japan.ORCID 0000-0003-0725-0515
Ken-Ichi InoueSystems Neuroscience Section, Primate Research Institute, Kyoto University, Inuyama, Aichi, Japan.
Hiroshi NakagawaSystems Neuroscience Section, Primate Research Institute, Kyoto University, Inuyama, Aichi, Japan.ORCID 0000-0002-0269-8962
Hiroaki IshidaNeural Prosthetics Project, Tokyo Metropolitan Institute of Medical Science, Setagaya, Tokyo, Japan.
Kenta KobayashiSection of Viral Vector Development, National Institute for Physiological Sciences, Okazaki, Aichi, Japan.
Tadashi IsaDepartment of Developmental Physiology, National Institute for Physiological Sciences, Okazaki, Aichi, Japan.ORCID 0000-0001-5652-4688
Masahiko TakadaSystems Neuroscience Section, Primate Research Institute, Kyoto University, Inuyama, Aichi, Japan.
Yukio NishimuraNeural Prosthetics Project, Tokyo Metropolitan Institute of Medical Science, Setagaya, Tokyo, Japan.ORCID 0000-0003-3479-2483
Inuyama Chuo Hospital · JPThe Graduate University for Advanced Studies, SOKENDAI · JPNational Institute for Physiological Sciences · JPTokyo Metropolitan Institute of Medical Science · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Motivation boosts motor performance. Activity of the ventral midbrain (VM), consisting of the ventral tegmental area (VTA), the substantia nigra pars compacta (SNc) and the retrorubral field (RRF), plays an important role in processing motivation. However, little is known about the neural substrate bridging the VM and the spinal motor output. We hypothesized that the VM might exert a modulatory influence over the descending motor pathways. By retrograde transneuronal labelling with rabies virus, we demonstrated the existence of multisynaptic projections from the VM to the cervical enlargement in monkeys. The distribution pattern of spinal projection neurons in the VM exhibited a caudorostral gradient, in that the RRF and the caudal part of the SNc contained more retrogradely labelled neurons than the VTA and the rostral part of the SNc. Electrical stimulation of the VM induced muscle responses in the contralateral forelimb with a delay of a few milliseconds following the responses of the ipsilateral primary motor cortex (M1). The magnitude and number of evoked muscle responses were associated with the stimulus intensity and number of pulses. The muscle responses were diminished during M1 inactivation. Thus, the present study has identified a multisynaptic VM-spinal pathway that is mediated, at least in part, by the M1 and might play a pivotal role in modulatory control of the spinal motor output. KEY POINTS: Motivation to obtain reward is thought to boost motor performance, and activity in the ventral midbrain is important to the motivational process. Little is known about a neural substrate bridging the ventral midbrain and the spinal motor output. Retrograde trans-synaptic experiments revealed that the ventral midbrain projects multisynaptically to the spinal cord in macaque monkeys. Ventral midbrain activation by electrical stimulation generated cortical activity in the motor cortex and forelimb muscle activity. A multisynaptic ventral midbrain-spinal pathway most probably plays a pivotal role in modulatory control of the spinal motor output.

Indexed as

Motor CortexVentral Tegmental AreaAnimalsHaplorhiniMesencephalonMotor Neuronsmotivationnon-human primaterabies virusretrorubral fieldspinal cordtransneuronal labelling

Identifiers

PMID35122444
PMCPMC9306604
OpenAlexW4210283267

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.