An extended amygdala-midbrain circuit controlling cocaine withdrawal-induced anxiety and reinstatement.
An extended amygdala-midbrain circuit controlling cocaine withdrawal-induced anxiety and reinstatement.
复制标题
一个扩展的杏仁核-中脑回路控制可卡因戒断引起的焦虑和恢复。
DOI:
10.1016/j.celrep.2022.110775
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发表时间:
2022-05-03
期刊:
影响因子:
8.8
通讯作者:
Beier, Kevin T.
中科院分区:
文献类型:
--
作者:
Tian, Guilian;Hui, May;Macchia, Desiree;Derdeyn, Pieter;Rogers, Alexandra;Hubbard, Elizabeth;Liu, Chengfeng;Vasquez, Jose J.;Taniguchi, Lara;Bartas, Katrina;Carroll, Sean;Beier, Kevin T.
Although midbrain dopamine (DA) circuits are central to motivated behaviors, our knowledge of how experience modifies these circuits to facilitate subsequent behavioral adaptations is limited. Here we demonstrate the selective role of a ventral tegmental area DA projection to the amygdala (VTADA→amygdala) for cocaine-induced anxiety but not cocaine reward or sensitization. Our rabies virus-mediated circuit mapping approach reveals a persistent elevation in spontaneous and task-related activity of inhibitory GABAergic cells from the bed nucleus of the stria terminalis (BNST) and downstream VTADA→amygdala cells that can be detected even after a single cocaine exposure. Activity in BNSTGABA→midbrain cells is related to cocaine-induced anxiety but not reward or sensitization, and silencing this projection prevents development of anxiety during protracted withdrawal after cocaine administration. Finally, we observe that VTADA→amygdala cells are strongly activated after a challenge exposure to cocaine and that activity in these cells is necessary and sufficient for reinstatement of cocaine place preference. Tian et al. show that an elevation of BNSTGABA→midbrain cell activity is related to withdrawal anxiety that manifests after a single cocaine exposure. Inhibition or activation of the BNSTGABA→ VTADA→amygdala pathway bidirectionally controls cocaine-induced withdrawal anxiety. Activation of VTADA→amygdala cells is also sufficient to drive robust reinstatement of cocaine-induced place preference.
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DOI:
10.1073/pnas.0700293104
发表时间:
2007-03-20
影响因子:
11.1
作者:
Armbruster, Blaine N.;Li, Xiang;Roth, Bryan L.
通讯作者:
Roth, Bryan L.
影响因子:
2.5
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通讯作者:
Swanson, LW
DOI:
10.1016/j.pnpbp.2009.07.010
发表时间:
2009-11-13
影响因子:
5.6
作者:
Jalabert, Marion;Aston-Jones, Gary;Herzog, Etienne;Manzoni, Olivier;Georges, Francois
通讯作者:
Georges, Francois
影响因子:
3.4
作者:
Francesconi W;Szücs A;Berton F;Koob GF;Vendruscolo LF;Sanna PP
通讯作者:
Sanna PP
影响因子:
16.2
作者:
Bromberg-Martin, Ethan S.;Matsumoto, Masayuki;Hikosaka, Okihide
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