Allostatic Mechanisms of Opioid Tolerance Beyond Desensitization and Downregulation

被引:83
作者
Cahill, Catherine M. [1 ]
Walwyn, Wendy [2 ]
Taylor, Anna M. W. [2 ]
Pradhan, Amynah A. A. [3 ]
Evans, Christopher J. [2 ]
机构
[1] Univ Calif Irvine, Dept Anesthesiol & Perioperat Care, 837 Hlth Sci Rd, Irvine, CA 92697 USA
[2] Univ Calif Los Angeles, Hatos Ctr Neuropharmacol, Dept Psychiat & Biobehav Sci, Semel Inst Neurosci & Human Behav, 675 Charles E Young Dr South, Los Angeles, CA 90095 USA
[3] Univ Illinois, Dept Psychiat, 1601 West Taylor St, Chicago, IL 60612 USA
基金
美国国家卫生研究院;
关键词
VENTRAL TEGMENTAL AREA; NUCLEUS-ACCUMBENS SHELL; CONDITIONED PLACE PREFERENCE; PROTEASE-ACTIVATED RECEPTOR-2; MEDIUM SPINY NEURONS; DOPAMINE NEURONS; MORPHINE-WITHDRAWAL; OPIATE REWARD; LATERAL HABENULA; CHRONIC PAIN;
D O I
10.1016/j.tips.2016.08.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Mechanisms of opioid tolerance have focused on adaptive modifications within cells containing opioid receptors, defined here as cellular allostasis, emphasizing regulation of the opioid receptor signalosome. We review additional regulatory and opponent processes involved in behavioral tolerance, and include mechanistic differences both between agonists (agonist bias), and between mu- and delta-opioid receptors. In a process we will refer to as pass-forward allostasis, cells modified directly by opioid drugs impute allostatic changes to downstream circuitry. Because of the broad distribution of opioid systems, every brain cell may be touched by pass-forward allostasis in the opioid-dependent/tolerant state. We will implicate neurons and microglia as interactive contributors to the cumulative allostatic processes creating analgesic and hedonic tolerance to opioid drugs.
引用
收藏
页码:963 / 976
页数:14
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