The neuroanatomical circuitry of jaw muscles has been mostly explored in non‐human animals. A recent rodent study revealed a novel circuit from the central amygdala (CeA) to the trigeminal motor nucleus (5M), which controls biting attacks. This circuit has yet to be delineated in humans. Ultra‐high diffusion‐weighted imaging data from the Human Connectome Project (HCP) allow in vivo delineation of circuits identified in other species—for example, the CeA–5M pathway—in humans. We hypothesized that the CeA–5M circuit could be resolved in humans at both 7 and 3 T. We performed probabilistic tractography between the CeA and 5M in 30 healthy young adults from the HCP database. As a negative control, we performed tractography between the basolateral amygdala (BLAT) and 5M, as CeA is the only amygdalar nucleus with extensive projections to the brainstem. Connectivity strength was operationalized as the number of streamlines between each region of interest. Connectivity strength between CeA–5M and BLAT–5M within each hemisphere was compared, and CeA–5M circuit had significantly stronger connectivity than the BLAT–5M circuit, bilaterally at both 7 T (all p < .001) and 3 T (all p < .001). This study is the first to delineate the CeA–5M circuit in humans.
Orofacial pain is thought to be more unpleasant than pain elsewhere in the body due to the importance of the face in social, feeding, and exploratory behaviors. Nociceptive information from the orofacial region is carried to the brain via the trigeminal nerve (CNV) via the trigeminal brainstem sensory nuclear complex (VBSNC). Pre-clinical evidence revealed a monosynaptic circuit from CNV to the lateral parabrachial nucleus (latPB), which underlies the greater unpleasantness elicited by orofacial pain. The latPB further projects to the central amygdala (CeA), which contributes to the affective component of pain in rodents. However, this circuit has yet to be delineated in humans. Here, we aimed to resolve this circuit using 7T diffusion-weighted imaging from the Human Connectome Project (HCP). We performed probabilistic tractography in 80 participants to resolve the CNV-latPB-CeA circuit. The basolateral amygdala (BLAT) was used as a negative control, given that we did not anticipate CNV-latPB-BLAT connectivity. Connectivity strengths were compared using a repeated- measures ANOVA with factors 'hemisphere' (left; right), and 'target' (CeA; BLAT), with sex included in the model for both pilot and validation samples. Only the 'target' factor was significant in both samples (FPilot= 11.4804, p = 0.005; FValidation= 69.113, p < .001). Post hoc tests showed that the CeA had significantly stronger connectivity strength than the BLAT (pTukey-Pilot = 0.005; pTukey-Validation< 0.001). This study delineates the human CNV-latPB-CeA circuit for the first time in vivo. This circuit may provide a neuroanatomical substrate for the affective dimensions of orofacial pain.
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