%0 Journal Article %J Journal of neurophysiology %D 2010 %T External urethral sphincter motoneuron properties in adult female rats studied in vitro. %A Jonathan S. Carp %A Tennissen, Ann M. %A Liebschutz, Jennifer E. %A Xiang Yang Chen %A Jonathan Wolpaw %K Urethra %X The external urethral sphincter (EUS) muscle plays a crucial role in lower urinary tract function: its activation helps maintain continence, whereas its relaxation contributes to micturition. To determine how the intrinsic properties of its motoneurons contribute to its physiological function, we have obtained intracellular current-clamp recordings from 49 EUS motoneurons in acutely isolated spinal cord slices from adult female rats. In all, 45% of EUS motoneurons fired spontaneously and steadily (average rate = 12-27 pulses/s). EUS motoneurons were highly excitable, having lower rheobase, higher input resistance, and smaller threshold depolarization than those of rat hindlimb motoneurons recorded in vitro. Correlations between these properties and afterhyperpolarization half-decay time are consistent with EUS motoneurons having characteristics of both fast and slow motor unit types. EUS motoneurons with a slow-like spectrum of properties exhibited spontaneous firing more often than those with fast-like characteristics. During triangular current ramp-induced repetitive firing, recruitment typically occurred at lower current levels than those at derecruitment, although the opposite pattern occurred in 10% of EUS motoneurons. This percentage was likely underestimated due to firing rate adaptation. These findings are consistent with the presence of a basal level of persistent inward current (PIC) in at least some EUS motoneurons. The low EUS motoneuron current and voltage thresholds make them readily recruitable, rendering them well suited to their physiological role in continence. The expression of firing behaviors consistent with PIC activation in this highly reduced preparation raises the possibility that in the intact animal, PICs contribute to urinary function not only through neuromodulator-dependent but also through neuromodulator-independent mechanisms. %B Journal of neurophysiology %V 104 %P 1286–1300 %8 09/2010 %G eng %U http://www.ncbi.nlm.nih.gov/pubmed/20573976 %R 10.1152/jn.00224.2010 %0 Journal Article %J Journal of neurophysiology %D 2008 %T An in vitro protocol for recording from spinal motoneurons of adult rats. %A Jonathan S. Carp %A Tennissen, Ann M. %A Mongeluzi, Donna L. %A Dudek, Christopher J. %A Xiang Yang Chen %A Jonathan Wolpaw %K Tissue and Organ Harvesting %X In vitro slice preparations of CNS tissue are invaluable for studying neuronal function. However, up to now, slice protocols for adult mammal spinal motoneurons–the final common pathway for motor behaviors–have been available for only limited portions of the spinal cord. In most cases, these preparations have not been productive due to the poor viability of motoneurons in vitro. This report describes and validates a new slice protocol that for the first time provides reliable intracellular recordings from lumbar motoneurons of adult rats. The key features of this protocol are: preexposure to 100% oxygen; laminectomy prior to perfusion; anesthesia with ketamine/xylazine; embedding the spinal cord in agar prior to slicing; and, most important, brief incubation of spinal cord slices in a 30% solution of polyethylene glycol to promote resealing of the many motoneuron dendrites cut during sectioning. Together, these new features produce successful recordings in 76% of the experiments and an average action potential amplitude of 76 mV. Motoneuron properties measured in this new slice preparation (i.e., voltage and current thresholds for action potential initiation, input resistance, afterhyperpolarization size and duration, and onset and offset firing rates during current ramps) are comparable to those recorded in vivo. Given the mechanical stability and precise control over the extracellular environment afforded by an in vitro preparation, this new protocol can greatly facilitate electrophysiological and pharmacological study of these uniquely important neurons and other delicate neuronal populations in adult mammals. %B Journal of neurophysiology %V 100 %P 474–481 %8 07/2008 %G eng %U http://www.ncbi.nlm.nih.gov/pubmed/18463177 %R 10.1152/jn.90422.2008 %0 Journal Article %J Journal of neurotrauma %D 2006 %T Corticospinal tract transection permanently abolishes H-reflex down-conditioning in rats. %A Xiang Yang Chen %A Yi Chen %A Lu Chen %A Tennissen, Ann M. %A Jonathan Wolpaw %K corticospinal tract %K H-reflex conditioning %K plasticity %K rat %K spinal cord injury %X Previous studies have shown that corticospinal tract (CST) transection, but not transection of other major spinal cord tracts, prevents down-conditioning of the H-reflex, the electrical analog of the spinal stretch reflex. This study set out to determine whether the loss of the capacity for H-reflex down-conditioning caused by CST transection is permanent. Female Sprague-Dawley rats received CST, lateral column (LC), or dorsal column ascending tract (DA) transection at T8-9; 9-10 months later, they were exposed to the H-reflex down-conditioning protocol for 50 days. In the LC and DA rats, H-reflex size fell to 60 (+/- 9 SEM)% and 60 (+/- 19)%, respectively, of its initial size. This down-conditioning was comparable to that of normal rats. In contrast, H-reflex size in the CST rats rose to 170 (+/- 42)% of its initial size. A similar rise does not occur in rats exposed to down-conditioning shortly after CST transection. These results indicate that CST transection permanently eliminates the capacity for H-reflex down-conditioning and has gradual long-term effects on sensorimotor cortex function. They imply that H-reflex down-conditioning can be a reliable measure of CST function for long-term studies of the effects of spinal cord injury and/or for evaluations of the efficacy of experimental therapeutic procedures, such as those intended to promote CST regeneration. The results also suggest that the role of sensorimotor cortex in down-conditioning extends beyond generation of the essential CST activity. %B Journal of neurotrauma %V 23 %P 1705–1712 %8 11/2006 %G eng %U http://www.ncbi.nlm.nih.gov/pubmed/17115915 %R 10.1089/neu.2006.23.1705 %0 Journal Article %J Experimental brain research. Experimentelle Hirnforschung. Expérimentation cérébrale %D 2006 %T Diurnal H-reflex variation in mice. %A Jonathan S. Carp %A Tennissen, Ann M. %A Xiang Yang Chen %A Jonathan Wolpaw %K circadian rhythm %K Electromyography %K implanted electrodes %K Monosynaptic %K Reflex %K Spinal Cord %X Mice exhibit diurnal variation in complex motor behaviors, but little is known about diurnal variation in simple spinally mediated functions. This study describes diurnal variation in the H-reflex (HR), a wholly spinal and largely monosynaptic reflex. Six mice were implanted with tibial nerve cuff electrodes and electrodes in the soleus and gastrocnemius muscles, for recording of ongoing and nerve-evoked electromyographic activity (EMG). Stimulation and recording were under computer control 24 h/day. During a 10-day recording period, HR amplitude varied throughout the day, usually being larger in the dark than in the light. This diurnal HR variation could not be attributed solely to differences in the net ongoing level of descending and segmental excitation to the spinal cord or stimulus intensity. HRs were larger in the dark than in the light even after restricting the evoked responses to subsets of trials having similar ongoing EMG and M-responses. The diurnal variation in the HR was out of phase with that reported previously for rats, but was in phase with that observed in monkeys. These data, supported by those in other species, suggest that the supraspinal control of the excitability of the HR pathway varies throughout the day in a species-specific pattern. This variation should be taken into account in experimental and clinical studies of spinal reflexes recorded at different times of day. %B Experimental brain research. Experimentelle Hirnforschung. Expérimentation cérébrale %V 168 %P 517–528 %8 01/2006 %G eng %U http://www.ncbi.nlm.nih.gov/pubmed/16151781 %R 10.1007/s00221-005-0106-y %0 Journal Article %J Journal of neurophysiology %D 2006 %T H-reflex operant conditioning in mice. %A Jonathan S. Carp %A Tennissen, Ann M. %A Xiang Yang Chen %A Jonathan Wolpaw %K Spinal Cord %X Rats, monkeys, and humans can alter the size of their spinal stretch reflex and its electrically induced analog, the H-reflex (HR), when exposed to an operant conditioning paradigm. Because this conditioning induces plasticity in the spinal cord, it offers a unique opportunity to identify the neuronal sites and mechanisms that underlie a well-defined change in a simple behavior. To facilitate these studies, we developed an HR operant conditioning protocol in mice, which are better suited to genetic manipulation and electrophysiological spinal cord study in vitro than rats or primates. Eleven mice under deep surgical anesthesia were implanted with tibial nerve stimulating electrodes and soleus and gastrocnemius intramuscular electrodes for recording ongoing and stimulus-evoked EMG activity. During the 24-h/day computer-controlled experiment, mice received a liquid reward for either increasing (up-conditioning) or decreasing (down-conditioning) HR amplitude while maintaining target levels of ongoing EMG and directly evoked EMG (M-responses). After 3-7 wk of conditioning, the HR amplitude was 133 +/- 7% (SE) of control for up-conditioning and 71 +/- 8% of control for down-conditioning. HR conditioning was successful (i.e., > or =20% change in HR amplitude in the appropriate direction) in five of six up-conditioned animals (mean final HR amplitude = 139 +/- 5% of control HR for successful mice) and in four of five down-conditioned animals (mean final HR amplitude = 63 +/- 8% of control HR for successful mice). These effects were not attributable to differences in the net level of motoneuron pool excitation, stimulation strength, or distribution of HR trials throughout the day. Thus mice exhibit HR operant conditioning comparable with that observed in rats and monkeys. %B Journal of neurophysiology %V 96 %P 1718–1727 %8 10/2006 %G eng %U http://www.ncbi.nlm.nih.gov/pubmed/16837659 %R 10.1152/jn.00470.2006 %0 Journal Article %J Journal of neuroscience methods %D 2005 %T Long-term spinal reflex studies in awake behaving mice. %A Jonathan S. Carp %A Tennissen, Ann M. %A Xiang Yang Chen %A Gerwin Schalk %A Jonathan Wolpaw %K Electromyography %K implanted electrodes %K Monosynaptic %K Spinal Cord %X The increasing availability of genetic variants of mice has facilitated studies of the roles of specific molecules in specific behaviors. The contributions of such studies could be strengthened and extended by correlation with detailed information on the patterns of motor commands throughout the course of specific behaviors in freely moving animals. Previously reported methodologies for long-term recording of electromyographic activity (EMG) in mice using implanted electrodes were designed for intermittent, but not continuous operation. This report describes the fabrication, implantation, and utilization of fine wire electrodes for continuous long-term recordings of spontaneous and nerve-evoked EMG in mice. Six mice were implanted with a tibial nerve cuff electrode and EMG electrodes in soleus and gastrocnemius muscles. Wires exited through a skin button and traveled through an armored cable to an electrical commutator. In mice implanted for 59-144 days, ongoing EMG was monitored continuously (i.e., 24 h/day, 7 days/week) by computer for 18-92 days (total intermittent recording for 25-130 days). When the ongoing EMG criteria were met, the computer applied the nerve stimulus, recorded the evoked EMG response, and determined the size of the M-response (MR) and the H-reflex (HR). It continually adjusted stimulation intensity to maintain a stable MR size. Stable recordings of ongoing EMG, MR, and HR were obtained typically 3 weeks after implantation. This study demonstrates the feasibility of long-term continuous EMG recordings in mice for addressing a variety of neurophysiological and behavioral issues. %B Journal of neuroscience methods %V 149 %P 134–143 %8 12/2005 %G eng %U http://www.ncbi.nlm.nih.gov/pubmed/16026848 %R 10.1016/j.jneumeth.2005.05.012 %0 Journal Article %J Experimental brain research. Experimentelle Hirnforschung. Expérimentation cérébrale %D 2003 %T Conduction velocity is inversely related to action potential threshold in rat motoneuron axons. %A Jonathan S. Carp %A Tennissen, Ann M. %A Jonathan Wolpaw %K action potential %K conduction velocity %K intra-axonal recording %K myelinated axon %K threshold %X Intra-axonal recordings were performed in ventral roots of rats in vitro to study the conduction velocity and firing threshold properties of motoneuron axons. Mean values +/- SD were 30.5+/-5.6 m/s for conduction velocity and 11.6+/-4.5 mV for the depolarization from the resting potential required to reach firing threshold (threshold depolarization). Conduction velocity varied inversely and significantly with threshold depolarization ( P=0.0002 by linear regression). This relationship was evident even after accounting for variation in conduction velocity associated with action potential amplitude, injected current amplitude, or body weight. Conduction velocity also varied inversely with the time to action potential onset during just-threshold current pulse injection. These data suggest that the time course of depolarization leading to action potential initiation contributes to the speed of conduction in motoneuron axons. %B Experimental brain research. Experimentelle Hirnforschung. Expérimentation cérébrale %V 150 %P 497–505 %8 06/2003 %G eng %U http://www.ncbi.nlm.nih.gov/pubmed/12715118 %R 10.1007/s00221-003-1475-8