Altered thermal selection behavior in mice lacking transient receptor potential vanilloid 4

被引:196
作者
Lee, HS
Iida, T
Mizuno, A
Suzuki, M
Caterina, MJ
机构
[1] Johns Hopkins Univ, Sch Med, Dept Biol Chem, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Neurosci, Baltimore, MD 21205 USA
[3] Jichi Med Sch, Dept Pharmacol, Minami Kawachi, Tochigi 3290498, Japan
关键词
TRPV4; thermosensation; warm; heat; temperature; pain;
D O I
10.1523/JNEUROSCI.4745.04.2005
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Transient receptor potential vanilloid 4 (TRPV4), a cation channel responsive to hypotonicity, can also be activated by warm temperatures. Moreover, TRPV4(-/-) mice reportedly exhibit deficits in inflammation-induced thermal hyperalgesia. However, it is unknown whether TRPV4 or related transient receptor potential channels account for warmth perception under injury-free conditions. We therefore investigated the contribution of TRPV4 to thermosensation and thermoregulation in vivo. On a thermal gradient, TRPV4(-/-) mice selected warmer floor temperatures than wild-type littermates. In addition, whereas wild-type mice failed to discriminate between floor temperatures of 30 and 34 degreesC, TRPV4(-/-) mice exhibited a strong preference for 34 degreesC. TRPV4(-/-) mice also exhibited prolonged withdrawal latencies during acute tail heating. TRPV4(-/-) and wild-type mice exhibited similar changes in behavior on a thermal gradient after paw inflammation. Circadian body temperature fluctuations and thermoregulation in a warm environment were also indistinguishable between genotypes. These results demonstrate that TRPV4 is required for normal thermal responsiveness in vivo.
引用
收藏
页码:1304 / 1310
页数:7
相关论文
共 31 条
[1]   Transient receptor potential vanilloid 4 is essential in chemotherapy-induced neuropathic pain in the rat [J].
Alessandri-Haber, N ;
Dina, OA ;
Yeh, JJ ;
Parada, CA ;
Reichling, DB ;
Levine, JD .
JOURNAL OF NEUROSCIENCE, 2004, 24 (18) :4444-4452
[2]   Hypotonicity induces TRPV4-mediated nociception in rat [J].
Alessandri-Haber, N ;
Yeh, JJ ;
Boyd, AE ;
Parada, CA ;
Chen, XJ ;
Reichling, DB ;
Levine, JD .
NEURON, 2003, 39 (03) :497-511
[3]   The vanilloid receptor: A molecular gateway to the pain pathway [J].
Caterina, MJ ;
Julius, D .
ANNUAL REVIEW OF NEUROSCIENCE, 2001, 24 :487-517
[4]   Impaired nociception and pain sensation in mice lacking the capsaicin receptor [J].
Caterina, MJ ;
Leffler, A ;
Malmberg, AB ;
Martin, WJ ;
Trafton, J ;
Petersen-Zeitz, KR ;
Koltzenburg, M ;
Basbaum, AI ;
Julius, D .
SCIENCE, 2000, 288 (5464) :306-313
[5]   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
[6]   A capsaicin-receptor homologue with a high threshold for noxious heat [J].
Caterina, MJ ;
Rosen, TA ;
Tominaga, M ;
Brake, AJ ;
Julius, D .
NATURE, 1999, 398 (6726) :436-441
[7]  
CHOI Y, 1994, PAIN, V59, P369, DOI 10.1016/0304-3959(94)90023-X
[8]   TRPV3 and TRPV4 mediate warmth-evoked currents in primary mouse keratinocytes [J].
Chung, MK ;
Lee, H ;
Mizuno, A ;
Suzuki, M ;
Caterina, MJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (20) :21569-21575
[9]   Warm temperatures activate TRPV4 in mouse 308 keratinocytes [J].
Chung, MK ;
Lee, H ;
Caterina, MJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (34) :32037-32046
[10]   Vanilloid receptor-1 is essential for inflammatory thermal hyperalgesia [J].
Davis, JB ;
Gray, J ;
Gunthorpe, MJ ;
Hatcher, JP ;
Davey, PT ;
Overend, P ;
Harries, MH ;
Latcham, J ;
Clapham, C ;
Atkinson, K ;
Hughes, SA ;
Rance, K ;
Grau, E ;
Harper, AJ ;
Pugh, PL ;
Rogers, DC ;
Bingham, S ;
Randall, A ;
Sheardown, SA .
NATURE, 2000, 405 (6783) :183-187