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a role for sigma receptors in stimulant self administration and addictionσ的作用受体兴奋剂自我管理和上瘾
Pharmaceuticals 2011, 4, 880-914; doi:10.3390/ph4060880
OPEN ACCESS
pharmaceuticals
ISSN 1424-8247
/journal/pharmaceuticals
Review
A Role for Sigma Receptors in Stimulant Self Administration
and Addiction
Jonathan L. Katz *, Tsung-Ping Su, Takato Hiranita, Teruo Hayashi, Gianluigi Tanda, Theresa
Kopajtic and Shang-Yi Tsai
Psychobiology and Cellular Pathobiology Sections, Intramural Research Program, National Institute
on Drug Abuse, National Institutes of Health, Department of Health and Human Services, Baltimore,
MD, 21224, USA
* Author to whom correspondence should be addressed; E-Mail: Jkatz@.
Received: 16 May 2011; in revised form: 11 June 2011 / Accepted: 13 June 2011 /
Published: 17 June 2011
Abstract: Sigma receptors (σRs) represent a structurally unique class of intracellular
1 1
proteins that function as chaperones. σRs translocate from the mitochondria-associated
1
membrane to the cell nucleus or cell membrane, and through protein-protein interactions
influence several targets, including ion channels, G-protein-coupled receptors, lipids, and
other signaling proteins. Several studies have demonstrated that σR antagonists block
stimulant-induced behavioral effects, including ambulatory activity, sensitization, and
acute toxicities. Curiously, the effects of stimulants have been blocked by σR antagonists
tested under place-conditioning but not self-administ
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