TY - JOUR
T1 - A craniofacial-specific monosynaptic circuit enables heightened affective pain
AU - Rodriguez, Erica
AU - Sakurai, Katsuyasu
AU - Xu, Jennie
AU - Chen, Yong
AU - Toda, Koji
AU - Zhao, Shengli
AU - Han, Bao Xia
AU - Ryu, David
AU - Yin, Henry
AU - Liedtke, Wolfgang
AU - Wang, Fan
PY - 2017/12/1
Y1 - 2017/12/1
N2 - Humans often rank craniofacial pain as more severe than body pain. Evidence suggests that a stimulus of the same intensity induces stronger pain in the face than in the body. However, the underlying neural circuitry for the differential processing of facial versus bodily pain remains unknown. Interestingly, the lateral parabrachial nucleus (PBL), a critical node in the affective pain circuit, is activated more strongly by noxious stimulation of the face than of the hindpaw. Using a novel activity-dependent technology called CANE developed in our laboratory, we identified and selectively labeled noxious-stimulus-activated PBL neurons and performed comprehensive anatomical input-output mapping. Surprisingly, we uncovered a hitherto uncharacterized monosynaptic connection between cranial sensory neurons and the PBL-nociceptive neurons. Optogenetic activation of this monosynaptic craniofacial-to-PBL projection induced robust escape and avoidance behaviors and stress calls, whereas optogenetic silencing specifically reduced facial nociception. The monosynaptic circuit revealed here provides a neural substrate for heightened craniofacial affective pain.
AB - Humans often rank craniofacial pain as more severe than body pain. Evidence suggests that a stimulus of the same intensity induces stronger pain in the face than in the body. However, the underlying neural circuitry for the differential processing of facial versus bodily pain remains unknown. Interestingly, the lateral parabrachial nucleus (PBL), a critical node in the affective pain circuit, is activated more strongly by noxious stimulation of the face than of the hindpaw. Using a novel activity-dependent technology called CANE developed in our laboratory, we identified and selectively labeled noxious-stimulus-activated PBL neurons and performed comprehensive anatomical input-output mapping. Surprisingly, we uncovered a hitherto uncharacterized monosynaptic connection between cranial sensory neurons and the PBL-nociceptive neurons. Optogenetic activation of this monosynaptic craniofacial-to-PBL projection induced robust escape and avoidance behaviors and stress calls, whereas optogenetic silencing specifically reduced facial nociception. The monosynaptic circuit revealed here provides a neural substrate for heightened craniofacial affective pain.
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U2 - 10.1038/s41593-017-0012-1
DO - 10.1038/s41593-017-0012-1
M3 - Article
C2 - 29184209
AN - SCOPUS:85035326089
SN - 1097-6256
VL - 20
SP - 1734
EP - 1743
JO - Nature Neuroscience
JF - Nature Neuroscience
IS - 12
ER -