Mechanisms of sensitization of the response of single dorsal root ganglion cells from adult rat to noxious heat

被引:47
作者
Galoyan, SM [1 ]
Petruska, JC [1 ]
Mendell, LM [1 ]
机构
[1] SUNY Stony Brook, Dept Neurobiol & Behav, Stony Brook, NY 11794 USA
关键词
capsaicin; dorsal root ganglion; nerve growth factor; nociceptor; pain; sensitization; thermal nociception; TRPV1;
D O I
10.1046/j.1460-9568.2003.02775.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We investigated the regulation by nerve growth factor of the response of sensory neurons to noxious heat (>43 degreesC). In dissociated dorsal root ganglion neurons (<30 mum) from adult rat we demonstrated, using perforated patch clamp recording, that the inward current elicited in response to noxious heating is enhanced by nerve growth factor and reduced by capsazepine. The tachyphylaxis observed in response to the second of two heat pulses was reversed in most cells when nerve growth factor was introduced into the medium during the 5 min between the two heat stimuli, similar to findings using capsaicin [X. Shu & L.M. Mendell (1999) Neurosci. Lett. 274 , 159-162]. The threshold temperature did not change systematically after nerve growth factor. Using antibodies to TRPV1 and trkA in a subset of cells from which we recorded, we found a virtually perfect correlation between expression of TRPV1 and sensitivity to noxious heat. In addition, trkA expression was perfectly correlated with the ability of nerve growth factor to reverse tachyphylaxis. Thus, this physiological test is a reliable measure of trkA expression in cells sensitive to noxious heat. In agreement with studies in heterologous cells expressing trkA and TRPV1, pharmacologically blocking phospholipase C abolished the effect of nerve growth factor on heat-evoked currents in cells verified to express trkA. We conclude that the response of dorsal root ganglion neurons to noxious heat is conditioned by nerve growth factor in the same way as their response to capsaicin and that these responses require the presence of trkA and TRPV1.
引用
收藏
页码:535 / 541
页数:7
相关论文
共 52 条
[1]   STUDIES ON CARRAGEENAN-INDUCED ARTHRITIS IN ADULT-RATS - PRESENCE OF NERVE GROWTH-FACTOR AND ROLE OF SYMPATHETIC INNERVATION [J].
ALOE, L ;
TUVERI, MA ;
LEVIMONTALCINI, R .
RHEUMATOLOGY INTERNATIONAL, 1992, 12 (05) :213-216
[2]   IMMUNOCYTOCHEMICAL LOCALIZATION OF TRKA RECEPTORS IN CHEMICALLY IDENTIFIED SUBGROUPS OF ADULT-RAT SENSORY NEURONS [J].
AVERILL, S ;
MCMAHON, SB ;
CLARY, DO ;
REICHARDT, LF ;
PRIESTLEY, JV .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1995, 7 (07) :1484-1494
[3]   Pain [J].
Basbaum, AI ;
Woolf, CJ .
CURRENT BIOLOGY, 1999, 9 (12) :R429-R431
[4]   The vanilloid receptor: A molecular gateway to the pain pathway [J].
Caterina, MJ ;
Julius, D .
ANNUAL REVIEW OF NEUROSCIENCE, 2001, 24 :487-517
[5]   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
[6]   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
[7]   A novel heat-activated current in nociceptive neurons and its sensitization by bradykinin [J].
Cesare, P ;
McNaughton, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (26) :15435-15439
[8]   Specific involvement of PKC-ε in sensitization of the neuronal response to painful heat [J].
Cesare, P ;
Dekker, LV ;
Sardini, A ;
Parker, PJ ;
McNaughton, PA .
NEURON, 1999, 23 (03) :617-624
[9]   P75 AND TRK - A 2-RECEPTOR SYSTEM [J].
CHAO, MV ;
HEMPSTEAD, BL .
TRENDS IN NEUROSCIENCES, 1995, 18 (07) :321-326
[10]   Bradykinin and nerve growth factor release the capsaicin receptor from PtdIns(4,5)P2-mediated inhibition [J].
Chuang, HH ;
Prescott, ED ;
Kong, HY ;
Shields, S ;
Jordt, SE ;
Basbaum, AI ;
Chao, MV ;
Julius, D .
NATURE, 2001, 411 (6840) :957-962