Heritability of nociception. III. Genetic relationships among commonly used assays of nociception and hypersensitivity

被引:157
作者
Lariviere, WR
Wilson, SG
Laughlin, TM
Kokayeff, A
West, EE
Adhikari, SM
Wan, Y
Mogil, JS
机构
[1] Univ Illinois, Dept Psychol, Champaign, IL 61820 USA
[2] Univ Illinois, Neurosci Program, Champaign, IL 61820 USA
关键词
genetic correlation; strain difference; stimulus modality; hyperalgesia; allodynia;
D O I
10.1016/S0304-3959(01)00492-4
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
We and others have previously demonstrated that nociception in the mouse is heritable. A genetic correlation analysis of 12 common measures of nociception among a common set of inbred strains revealed three major clusters (or 'types') of nociception in this species. In the present study, we re-evaluated the major types of nociception and their interrelatedness using ten additional assays of nociception and hypersensitivity, including: three thermal assays (tail withdrawal from 47.5degreesC water or -15degreesC ethanol; tail flick from radiant heat), two chemical assays of spontaneous nociception (bee venom test; capsaicin test) and their subsequent thermal hypersensitivity states (including contralateral hypersensitivity in the bee venom test), a mechanical nociceptive assay (tail-clip test), and a mechanical hypersensitivity assay (intrathecal dynorphin). Confirming our earlier findings, the results demonstrate distinct thermal and chemical nociceptive types. It is now clear that mechanical hypersensitivity and thermal hypersensitivity are genetically dissociable phenomena. Furthermore, we now see at least two distinct types of thermal hypersensitivity: afferent-dependent, featuring a preceding significant period of spontaneous nociceptive behavior associated with afferent neural activity, and non-afferent-dependent. In conclusion, our latest analysis suggests that there are at least five fundamental types of nociception and hypersensitivity: (1) baseline thermal nociception; (2) spontaneous responses to noxious chemical stimuli; (3) thermal hypersensitivity; (4) mechanical hypersensitivity; and (5) afferent input-dependent hypersensitivity. (C) 2002 International Association for the Study of Pain. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:75 / 86
页数:12
相关论文
共 60 条
[11]   The capsaicin receptor: a heat-activated ion channel in the pain pathway [J].
Caterina, MJ ;
Schumacher, MA ;
Tominaga, M ;
Rosen, TA ;
Levine, JD ;
Julius, D .
NATURE, 1997, 389 (6653) :816-824
[12]   QUANTITATIVE ASSESSMENT OF TACTILE ALLODYNIA IN THE RAT PAW [J].
CHAPLAN, SR ;
BACH, FW ;
POGREL, JW ;
CHUNG, JM ;
YAKSH, TL .
JOURNAL OF NEUROSCIENCE METHODS, 1994, 53 (01) :55-63
[13]   Establishment of bee venom-induced contralateral heat hyperalgesia in the rat is dependent upon central temporal summation of afferent input from the site of injury [J].
Chen, HS ;
Chen, J ;
Chen, J ;
Guo, WG ;
Zheng, MH .
NEUROSCIENCE LETTERS, 2001, 298 (01) :57-60
[14]   Pivotal role of capsaicin-sensitive primary afferents in development of both heat and mechanical hyperalgesia induced by intraplantar bee venom injection [J].
Chen, J ;
Chen, HS .
PAIN, 2001, 91 (03) :367-376
[15]   Primary hyperalgesia to mechanical and heat stimuli following subcutaneous bee venom injection into the plantar surface of hindpaw in the conscious rat: a comparative study with the formalin test [J].
Chen, J ;
Luo, C ;
Li, HL ;
Chen, HS .
PAIN, 1999, 83 (01) :67-76
[16]   ROLE OF PERI-AXONAL INFLAMMATION IN THE DEVELOPMENT OF THERMAL HYPERALGESIA AND GUARDING BEHAVIOR IN A RAT MODEL OF NEUROPATHIC PAIN [J].
CLATWORTHY, AL ;
ILLICH, PA ;
CASTRO, GA ;
WALTERS, ET .
NEUROSCIENCE LETTERS, 1995, 184 (01) :5-8
[17]   ESTIMATION OF GENETIC CORRELATION - INTERPRETATION OF EXPERIMENTS USING SELECTIVELY BRED AND INBRED ANIMALS [J].
CRABBE, JC ;
PHILLIPS, TJ ;
KOSOBUD, A ;
BELKNAP, JK .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1990, 14 (02) :141-151
[18]   Genetics of mouse behavior: Interactions with laboratory environment [J].
Crabbe, JC ;
Wahlsten, D ;
Dudek, BC .
SCIENCE, 1999, 284 (5420) :1670-1672
[19]   Possible role of inflammatory mediators in tactile hypersensitivity in rat models of mononeuropathy [J].
Cui, JG ;
Holmin, S ;
Mathiesen, T ;
Meyerson, BA ;
Linderoth, B .
PAIN, 2000, 88 (03) :239-248
[20]  
D'amour FE, 1941, J PHARMACOL EXP THER, V72, P74