Usefulness of knockout mice to clarify the role of the opioid system in chronic pain

被引:28
|
作者
Maldonado, Rafael [1 ,2 ]
Eladi Banos, Josep [1 ,2 ]
Cabanero, David [1 ]
机构
[1] Univ Pompeu Fabra, Dept Expt & Hlth Sci, Lab Neuropharmacol, Barcelona, Spain
[2] Hosp del Mar Med Res Inst IMIM, Barcelona, Spain
关键词
NOCICEPTIN/ORPHANIN FQ RECEPTOR; ENDOGENOUS BETA-ENDORPHIN; STRESS-INDUCED ANALGESIA; MORPHINE-TOLERANCE; NEUROPATHIC PAIN; ORPHANIN FQ/NOCICEPTIN; MOUSE MODELS; SPINAL-CORD; ANTINOCICEPTIVE RESPONSES; GENETIC DISSOCIATION;
D O I
10.1111/bph.14088
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Several lines of knockout mice deficient in the genes encoding each component of the endogenous opioid system have been used for decades to clarify the specific role of the different opioid receptors and peptide precursors in many physiopathological conditions. The use of these genetically modified mice has improved our knowledge of the specific involvement of each endogenous opioid component in nociceptive transmission during acute and chronic pain conditions. The present review summarizes the recent advances obtained using these genetic tools in understanding the role of the opioid system in the pathophysiological mechanisms underlying chronic pain. Behavioural data obtained in these chronic pain models are discussed considering the peculiarities of the behavioural phenotype of each line of knockout mice. These studies have identified the crucial role of specific components of the opioid system in different manifestations of chronic pain and have also opened new possible therapeutic approaches, such as the development of opioid compounds simultaneously targeting several opioid receptors. However, several questions still remain open and require further experimental effort to be clarified. The novel genetic tools now available to manipulate specific neuronal populations and precise genome editing in mice will facilitate in a near future the elucidation of the role of each component of the endogenous opioid system in chronic pain.
引用
收藏
页码:2791 / 2808
页数:18
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