Evidence map›Paper›PMID 40800954›Full record

ArticleImaging neuroscience (Cambridge, Mass.)2025

Delineation of the trigeminal-lateral parabrachial-central amygdala tract in humans.

Batu Kaya, Omar Khalil, Spencer S Abssy, Iacopo Cioffi, Massieh Moayedi

Abstract read
In one paragraph

Article in Imaging neuroscience (Cambridge, Mass.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. Article
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

5 authors.

Batu KayaCentre for Multimodal Sensorimotor and Pain Research, Faculty of Dentistry, University of Toronto, Toronto, ON, Canada.ORCID https://orcid.org/0000-0003-0484-1467
Omar KhalilCentre for Multimodal Sensorimotor and Pain Research, Faculty of Dentistry, University of Toronto, Toronto, ON, Canada.ORCID https://orcid.org/0009-0001-4385-5477
Spencer S AbssyCentre for Multimodal Sensorimotor and Pain Research, Faculty of Dentistry, University of Toronto, Toronto, ON, Canada.ORCID https://orcid.org/0009-0001-7044-3566
Iacopo CioffiCentre for Multimodal Sensorimotor and Pain Research, Faculty of Dentistry, University of Toronto, Toronto, ON, Canada.ORCID https://orcid.org/0000-0002-9708-6765
Massieh MoayediCentre for Multimodal Sensorimotor and Pain Research, Faculty of Dentistry, University of Toronto, Toronto, ON, Canada.ORCID https://orcid.org/0000-0002-7324-2540

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The parabrachial nucleus (PBN) relays interoceptive and exteroceptive information to limbic brain regions. In particular, lateral PBN projections to the central nucleus of the amygdala (CeA) are thought to encode the affective dimension of pain. Pain in the orofacial region is thought to be more unpleasant than pain elsewhere in the body because the face plays an important role in social interactions, feeding, and exploration. The trigeminal nerve (CN V) carries sensory, including nociceptive, information from the orofacial region to the central nervous system. Canonically, the affective dimension of orofacial pain is thought to be encoded by the medial trigeminothalamic tract, which projects to midline thalamic nuclei and further to limbic brain regions. A preclinical study identified an additional circuit that carries orofacial nociceptive information to subcortical limbic brain regions via the lateral PBN. This circuit, from the CN V to the lateral PBN and further to the CeA, is thought to contribute to the heightened negative affect of orofacial pain. However, the CN V-lateral PBN-CeA circuit has yet to be delineated in humans. Here, we aimed to resolve this circuit in humans with diffusion MRI from the Human Connectome Project (HCP) using probabilistic tractography. We first delineated the tract at 7T (n = 150) to determine whether this tract can be resolved. Next, we delineated the tract at the more readily available, but lower resolution 3T field strength (n = 155). Given the growing evidence of sex differences in pain mechanisms, as a secondary aim, we explored whether sex differences in connectivity strengths of the circuit existed in our sample. The basolateral amygdala (BLAT) was used as a negative control, as we did not anticipate CN V-lPBN-BLAT connectivity. The CN V-lPBN-CeA circuit had significantly stronger connectivity strength than the BLAT circuit at both field strengths (both

Indexed as

amygdalabrainconnectivitydiffusion MRIorofacial painpain affectpain unpleasantnessparabrachial nucleusstructural MRItractographyultra-high field imagingwhite matter

Identifiers

PMID40800954
PMCPMC12319760

What Socratic holds

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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 Socratic graph.