Variation in the COMT gene: implications for pain perception and pain treatment

被引:49
作者
Andersen, Sonja [1 ]
Skorpen, Frank [1 ]
机构
[1] Norwegian Univ Sci & Technol NTNU, Dept Lab Med Childrens & Womens Hlth, Lab Ctr, Fac Med, N-7489 Trondheim, Norway
关键词
catechol-O-methyltransferase; descending inhibition; dopamine; haplotype; nociception; noradrenaline; pain; pain sensitivity; polymorphism; SNP; CATECHOL-O-METHYLTRANSFERASE; MESSENGER-RNA; VAL158MET POLYMORPHISM; MECHANICAL HYPERSENSITIVITY; CYTOKINE PRODUCTION; DESCENDING CONTROL; PREFRONTAL CORTEX; DOPAMINE RELEASE; EXPRESSION; ASSOCIATION;
D O I
10.2217/PGS.09.13
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Catechol-O-methyltransferase (COMT) is an enzyme that inactivates biologically-active catechols, including the important neurotransmitters dopamine, noradrenaline and adrenaline. These neurotransmitters are involved in numerous physiological processes, including modulation of pain. Genetic variation in the COMT gene has been implicated in variable response to various experimental painful stimuli, variable susceptibility to develop common pain conditions, as well as the variable need for opioids in the treatment of cancer pain. Increased insight into how genetic variants within the COMT locus affect pain perception will contribute to improved understanding of the mechanisms involved in the development of common human pain disorders and may lead to improved strategies for pain treatment. So far, a remarkable complex relationship between COMT genotypes or haplotypes and pain phenotypes has been revealed.
引用
收藏
页码:669 / 684
页数:16
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