PMID- 10783401 OWN - NLM STAT- MEDLINE DCOM- 20000602 LR - 20191023 IS - 1529-2401 (Electronic) IS - 0270-6474 (Print) IS - 0270-6474 (Linking) VI - 20 IP - 10 DP - 2000 May 15 TI - Cervical dorsal rhizotomy increases brain-derived neurotrophic factor and neurotrophin-3 expression in the ventral spinal cord. PG - RC77 AB - Although neurotrophic factors have been implicated in several forms of neuroplasticity, little is known concerning their potential role in spinal plasticity. Cervical dorsal rhizotomy (CDR) enhances serotonin terminal density near (spinal) phrenic motoneurons and serotonin-dependent long-term facilitation of phrenic motor output (Kinkead et al., 1998). We tested the hypothesis that selected neurotrophic factors change in a manner consistent with an involvement in this model of spinal plasticity. Brain-derived neurotrophic factor (BDNF), neurotrophin-3 (NT-3), glial cell line-derived neurotrophic factor (GDNF), and transforming growth factor-beta(1) (TGF-beta(1)) concentrations were measured (ELISA) in three regions of interest to respiratory control: (1) ventral cervical spinal segments associated with the phrenic motor nucleus (C3-C6), (2) ventral thoracic spinal segments associated with inspiratory intercostal motor output (T3-T6) and (3) the diaphragm. Tissues were harvested from rats 7 d after bilateral CDR and compared with sham-operated and unoperated control rats. CDR increased BDNF (110%; p = 0.002) and NT-3 (100%; p = 0.002) in the cervical and NT-3 in the thoracic spinal cord (98%; p = 0.009). GDNF and TGF-beta(1) were not altered by CDR in any tissue. Immunohistochemistry localized BDNF and NT-3 to motoneurons and interneurons of the ventral spinal cord. These studies provide novel, suggestive evidence that BDNF and NT-3, possibly through their trophic effects on serotonergic neurons and/or motoneurons, may underlie serotonin-dependent plasticity in (spinal) respiratory motor control after CDR. FAU - Johnson, R A AU - Johnson RA AD - Department of Comparative Biosciences, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA. FAU - Okragly, A J AU - Okragly AJ FAU - Haak-Frendscho, M AU - Haak-Frendscho M FAU - Mitchell, G S AU - Mitchell GS LA - eng GR - HL03874/HL/NHLBI NIH HHS/United States GR - HL36780/HL/NHLBI NIH HHS/United States GR - HL53319/HL/NHLBI NIH HHS/United States PT - Journal Article PT - Research Support, U.S. Gov't, P.H.S. PL - United States TA - J Neurosci JT - The Journal of neuroscience : the official journal of the Society for Neuroscience JID - 8102140 RN - 0 (Brain-Derived Neurotrophic Factor) RN - 0 (Gdnf protein, rat) RN - 0 (Glial Cell Line-Derived Neurotrophic Factor) RN - 0 (Nerve Growth Factors) RN - 0 (Nerve Tissue Proteins) RN - 0 (Neurotrophin 3) RN - 0 (Transforming Growth Factor beta) SB - IM MH - Animals MH - Brain-Derived Neurotrophic Factor/*metabolism MH - Diaphragm/metabolism MH - Enzyme-Linked Immunosorbent Assay MH - Glial Cell Line-Derived Neurotrophic Factor MH - Interneurons/metabolism MH - Male MH - Motor Neurons/metabolism MH - *Nerve Growth Factors MH - Nerve Tissue Proteins/metabolism MH - Neurotrophin 3/*metabolism MH - Rats MH - Rats, Sprague-Dawley MH - Rhizotomy MH - Spinal Cord/*metabolism/physiology MH - Transforming Growth Factor beta/metabolism PMC - PMC6772689 EDAT- 2000/04/28 00:00 MHDA- 2000/06/10 00:00 PMCR- 2000/11/15 CRDT- 2000/04/28 00:00 PHST- 2000/04/28 00:00 [pubmed] PHST- 2000/06/10 00:00 [medline] PHST- 2000/04/28 00:00 [entrez] PHST- 2000/11/15 00:00 [pmc-release] AID - 20004209 [pii] AID - 4209 [pii] AID - 10.1523/JNEUROSCI.20-10-j0005.2000 [doi] PST - ppublish SO - J Neurosci. 2000 May 15;20(10):RC77. doi: 10.1523/JNEUROSCI.20-10-j0005.2000.