Title | Motor unit properties after operant conditioning of rat H-reflex. |
Publication Type | Journal Article |
Year of Publication | 2001 |
Authors | Carp, JS, Chen, XY, Sheikh, H, Wolpaw, J |
Journal | Experimental brain research. Experimentelle Hirnforschung. Expérimentation cérébrale |
Volume | 140 |
Pagination | 382–386 |
Date Published | 10/2001 |
ISSN | 0014-4819 |
Keywords | H-Reflex, motor unit type, operant conditioning, plasticity, triceps surae |
Abstract | Operant conditioning of the H-reflex produces plasticity at several sites in the spinal cord, including the motoneuron. This study assessed whether this spinal cord plasticity is accompanied by changes in motor unit contractile properties. Thirty-one adult male Sprague-Dawley rats implanted for chronic recording of triceps surae electromyographic activity and H-reflex elicitation were exposed for at least 40 days to HRup or HRdown training, in which reward occurred when the H-reflex was greater than (12 HRup rats) or less than (12 HRdown rats) a criterion value, or continued under the control mode in which the H-reflex was simply measured (7 HRcon rats). At the end of H-reflex data collection, rats were anesthetized and the contractile properties of 797 single triceps surae motor units activated by intraaxonal (or intramyelin) current injection were determined. Motor units were classified as S, FR, Fint, or FF on the basis of sag and fatigue properties. Maximum tetanic force and twitch contraction time were also measured. HRdown rats exhibited a significant increase in the fatigue index of fast-twitch motor units. This resulted in a significant decrease in the percentage of Fint motor units and a significant increase in that of FR motor units. HRup conditioning had no effect on fatigue index. Neither HRup nor HRdown conditioning affected maximum tetanic force or twitch contraction time. These data are consistent with the hypothesis that conditioning mode-specific change in motoneuron firing patterns causes activity-dependent change in muscle properties. |
URL | http://www.ncbi.nlm.nih.gov/pubmed/11681314 |
DOI | 10.1007/s002210100830 |