PMID- 10342408 OWN - NLM STAT- MEDLINE DCOM- 19990715 LR - 20220318 IS - 0304-3959 (Print) IS - 0304-3959 (Linking) VI - 80 IP - 3 DP - 1999 Apr TI - Effects of trkB and trkC neurotrophin receptor agonists on thermal nociception: a behavioral and electrophysiological study. PG - 463-470 LID - 10.1016/S0304-3959(99)00042-1 [doi] AB - Nerve-growth factor (NGF), a member of the neurotrophin family, plays an important role in nociceptor function. Prompted by a previous uinexpected finding that NT-4/5, as well as NGF sensitizes single nociceptors to noxious heat, we have explored the relative potency of all neurotrophins in eliciting thermal hyperalgesia. NGF, brain-derived neurotrophic factor (BDNF), NT-4/5 and NT-3 were injected locally into the hind paw of rats, and the behavioral response to noxious heat was compared with that from the other paw that received an identical injection of vehicle. Like NGF, agonists of tyrosine kinaseB (trkB) receptors (NT-4/5 and BDN F) induced thermal hyperalgesia in the first 5 h after treatment (NT-4/5 > BDNF) but the effect had worn off by 24 h. In contrast, the trkC agonist NT-3 had no effect on the response to noxious heat. Electrophysiological recordings from single C-fibres in the in vitro skin-saphenous nerve preparation revealed sensitization to noxious heat stimuli after direct application of BDNF to the receptive field, as previously noted for NT-4/5, and in parallel with the behavioral findings. NT-3 was ineffective as in the behavioral studies. These results suggest that trkB agonists BDNF and NT-4/5 as well as the trkA agonist NGF can regulate nociceptive responses to noxious heat. FAU - Shu, X-Q AU - Shu XQ AD - Department of Neurobiology and Behavior, State University of New York at Stony Brook, Stony Brook, NY 11794, USA. FAU - Llinas, A AU - Llinas A FAU - Mendell, L M AU - Mendell LM LA - eng GR - P01 NS- 14899/NS/NINDS NIH HHS/United States GR - R01 NS 16696/NS/NINDS NIH HHS/United States GR - R01 NS- 32264/NS/NINDS NIH HHS/United States PT - Journal Article PT - Research Support, U.S. Gov't, P.H.S. PL - United States TA - Pain JT - Pain JID - 7508686 RN - 0 (Brain-Derived Neurotrophic Factor) RN - 0 (Nerve Growth Factors) RN - 0 (Neuroprotective Agents) RN - 0 (Neurotrophin 3) RN - 0 (Receptor, Ciliary Neurotrophic Factor) RN - 0 (Receptors, Nerve Growth Factor) RN - 145172-44-7 (neurotrophin 5) RN - EC 2.7.10.1 (Receptor Protein-Tyrosine Kinases) RN - EC 2.7.10.1 (Receptor, trkC) RN - P658DCA9XD (neurotrophin 4) SB - IM MH - Animals MH - Behavior, Animal/*drug effects MH - Brain-Derived Neurotrophic Factor/pharmacology MH - Electrophysiology MH - Female MH - Hot Temperature MH - Hyperalgesia/drug therapy/physiopathology MH - Male MH - Nerve Growth Factors/pharmacology MH - Neuroprotective Agents/*agonists MH - Neurotrophin 3 MH - Nociceptors/*drug effects/physiology MH - Rats MH - Rats, Wistar MH - Reaction Time/drug effects MH - Receptor Protein-Tyrosine Kinases/*chemistry MH - Receptor, Ciliary Neurotrophic Factor MH - Receptor, trkC MH - Receptors, Nerve Growth Factor/*agonists/*chemistry EDAT- 1999/05/26 00:00 MHDA- 1999/05/26 00:01 CRDT- 1999/05/26 00:00 PHST- 1999/05/26 00:00 [pubmed] PHST- 1999/05/26 00:01 [medline] PHST- 1999/05/26 00:00 [entrez] AID - 00006396-199904010-00002 [pii] AID - 10.1016/S0304-3959(99)00042-1 [doi] PST - ppublish SO - Pain. 1999 Apr;80(3):463-470. doi: 10.1016/S0304-3959(99)00042-1.