Sigma 1 receptor: A new therapeutic target for pain

被引:106
作者
Zamanillo, Daniel [1 ]
Romero, Luz [1 ]
Merlos, Manuel [1 ]
Miguel Vela, Jose [1 ]
机构
[1] Esteve, Drug Discovery & Preclin Dev, Barcelona 08028, Spain
关键词
Sigma; 1; receptor; Pain; Analgesia; Opioid; Neuropathic; Sensitization; METHYL-D-ASPARTATE; GUINEA-PIG BRAIN; RAT HIPPOCAMPAL SLICES; NEUROSTEROID PREGNENOLONE SULFATE; INDUCED SPINAL SENSITIZATION; STEROL C-8-C-7 ISOMERASE; KAPPA-OPIOID RECEPTORS; CENTRAL-NERVOUS-SYSTEM; NMDA-INDUCED PAIN; NEUROPATHIC PAIN;
D O I
10.1016/j.ejphar.2013.01.068
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Sigma 1 receptor (sigma(1) receptor) is a unique ligand-regulated molecular chaperone located mainly in the endoplasmic reticulum and the plasma membrane. sigma(1) receptor is activated under stress or pathological conditions and interacts with several neurotransmitter receptors and ion channels to modulate their function. The effects reported preclinically with sigma(1) receptor ligands are consistent with a role for sigma(1) receptor in central sensitization and pain hypersensitivity and suggest a potential therapeutic use of sigma(1) receptor antagonists for the management of neuropathic pain as monotherapy. Moreover, data support their use in opioid adjuvant therapy: combination of sigma(1) receptor antagonists and opioids results in potentiation of opioid analgesia, without significant increases in opioid-related unwanted effects. Results from clinical trials using selective sigma(1) receptor antagonists in several pain conditions are eagerly awaited to ascertain the potential of sigma(1) receptor modulation in pain therapy. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:78 / 93
页数:16
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