Parabrachial complex links pain transmission to descending pain modulation.
Parabrachial complex links pain transmission to descending pain modulation.
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DOI:
10.1097/j.pain.0000000000000688
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发表时间:
2016-12
期刊:
影响因子:
7.4
通讯作者:
Heinricher MM
中科院分区:
文献类型:
--
作者:
Roeder Z;Chen Q;Davis S;Carlson JD;Tupone D;Heinricher MM
The rostral ventromedial medulla (RVM) has a well-documented role in pain modulation, and exerts anti-nociceptive and pro-nociceptive influences mediated by two distinct classes of neurons, OFF-cells and ON-cells. OFF-cells are defined by a sudden pause in firing in response to nociceptive inputs, whereas ON-cells are characterized by a “burst” of activity. Although these reflex-related changes in ON- and OFF-cell firing are critical to their pain-modulating function, the pathways mediating these responses have not been identified. The present experiments were designed to test the hypothesis that nociceptive input to the RVM is relayed through the parabrachial complex (PB). In electrophysiological studies, ON- and OFF-cells were recorded in the RVM of lightly anesthetized male rats before and after an infusion of lidocaine or muscimol into PB. The ON-cell burst and OFF-cell pause evoked by noxious heat or mechanical probing were substantially attenuated by inactivation of the lateral, but not medial, parabrachial area. Retrograde tracing studies showed that neurons projecting to the RVM were scattered throughout PB. Few of these neurons expressed calcitonin gene-related peptide (CGRP), suggesting that the RVM projection from PB is distinct from that to the amygdala. These data show that a substantial component of “bottom-up” nociceptive drive to RVM pain-modulating neurons is relayed through the parabrachial complex. While the parabrachial complex is well-known as an important relay for ascending nociceptive information, its functional connection with the RVM allows the spinoparabrachial pathway to access descending control systems as part of a recurrent circuit.
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影响因子:
5.3
作者:
Bourgeais, L;Monconduit, L;Bernard, JF
通讯作者:
Bernard, JF
影响因子:
5.3
作者:
Carlson, Jonathan D.;Maire, Jennifer J.;Heinricher, Mary M.
通讯作者:
Heinricher, Mary M.
DOI:
10.1098/rstb.1985.0037
发表时间:
1985-01-01
期刊:
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES
影响因子:
--
作者:
FIELDS, HL;HEINRICHER, MM
通讯作者:
HEINRICHER, MM
影响因子:
11.2
作者:
Edelmayer, Rebecca M.;Vanderah, Todd W.;Majuta, Lisa;Zhang, En-Tan;Fioravanti, Beatriz;De Felice, Milena;Chichorro, Juliana G.;Ossipov, Michael H.;King, Tamara;Lai, Josephine;Kori, Shashi H.;Nelsen, Andrew C.;Cannon, Keri E.;Heinricher, Mary M.;Porreca, Frank
通讯作者:
Porreca, Frank
影响因子:
64.5
作者:
Han S;Soleiman MT;Soden ME;Zweifel LS;Palmiter RD
通讯作者:
Palmiter RD