Cyclic AMP stimulates neurite outgrowth of lamprey reticulospinal neurons without substantially altering their biophysical properties.

Reticulospinal (RS) neurons are critical for initiation of locomotor behavior, and following spinal cord injury (SCI) in the lamprey, the axons of these neurons regenerate and restore locomotor behavior within a few weeks. For lamprey RS neurons in culture, experimental induction of calcium influx, either in the growth cone or cell body, is inhibitory for neurite outgrowth. Following SCI, these neurons partially downregulate calcium channel expression, which would be expected to reduce calcium influx and possibly provide supportive conditions for axonal regeneration. In the present study, it was tested whether activation of second messenger signaling pathways stimulates neurite outgrowth of lamprey RS neurons without altering their electrical properties (e.g. spike broadening) so as to possibly increase calcium influx and compromise axonal growth. First, activation of cAMP pathways with forskolin or dbcAMP stimulated neurite outgrowth of RS neurons in culture in a PKA-dependent manner, while activation of cGMP signaling pathways with dbcGMP inhibited outgrowth. Second, neurophysiological recordings from uninjured RS neurons in isolated lamprey brain-spinal cord preparations indicated that dbcAMP or dbcGMP did not significantly affect any of the measured electrical properties. In contrast, for uninjured RS neurons, forskolin increased action potential duration, which might have increased calcium influx, but did not significantly affect most other electrical properties. Importantly, for injured RS neurons during the period of axonal regeneration, forskolin did not significantly alter their electrical properties. Taken together, these results suggest that activation of cAMP signaling by dbcAMP stimulates neurite outgrowth, but does not alter the electrical properties of lamprey RS neurons in such a way that would be expected to induce calcium influx. In conclusion, our results suggest that activation of cAMP pathways alone, without compensation for possible deleterious effects on electrical properties, is an effective approach for stimulating axonal regeneration of RS neuron following SCI.

Localization, pharmacology, and organization of brain locomotor areas in larval lamprey.

In larval lamprey, spinal locomotor activity can be initiated by pharmacological microstimulation from the following higher order brain locomotor areas [Paggett et al. (2004) Neuroscience 125:25-33; Jackson et al. (2007) J Neurophysiol 97:3229-3241]: rostrolateral rhombencephalon (RLR); ventromedial diencephalon (VMD); or dorsolateral mesencephalon (DLM). In the present study, pharmacological microstimulation with excitatory amino acids (EAAs) or their agonists in the brains of in vitro brain/spinal cord preparations was used to determine the sizes, pharmacology, and organization of these locomotor areas. First, the RLR, DLM and VMD locomotor areas were confined to relatively small areas of the brain, and stimulation as little as 50 µm outside these areas was ineffective or elicited tonic or uncoordinated motor activity. Second, pharmacological stimulation with NMDA, kainate, or AMPA in the VMD or DLM reliably initiated well-coordinated spinal locomotor activity. In the RLR, stimulation with all three ionotropic EAA receptor agonists could initiate spinal locomotor activity, but NMDA or AMPA was more reliable than kainate. Third, with synaptic transmission blocked only in the brain, stimulation in the RLR, VMD, or DLM no longer initiated spinal locomotor activity, suggesting that these locomotor areas do not directly activate spinal locomotor networks. Fourth, following a complete transection at the mesencephalon-rhombencephalon border, stimulation in the RLR no longer initiated spinal motor activity. Thus, the RLR locomotor area does not appear able to initiate spinal locomotor activity by neural circuits confined entirely within the rhombencephalon but requires more rostral neural centers, such as those in the VMD and DLM, as previously proposed [Paggett et al. (2004) Neuroscience 125:25-33].

Organization of higher-order brain areas that initiate locomotor activity in larval lamprey.

In the lamprey, spinal locomotor activity can be initiated by pharmacological microstimulation in several brain areas: rostrolateral rhombencephalon (RLR); dorsolateral mesencephalon (DLM); ventromedial diencephalon (VMD); and reticular nuclei. During DLM- or VMD-initiated locomotor activity in in vitro brain/spinal cord preparations, application of a solution that focally depressed neuronal activity in reticular nuclei often attenuated or abolished the locomotor rhythm. Electrical microstimulation in the DLM or VMD elicited synaptic responses in reticulospinal (RS) neurons, and close temporal stimulation in both areas evoked responses that summated and could elicit action potentials when neither input alone was sufficient. During RLR-initiated locomotor activity, focal application of a solution that depressed neuronal activity in the DLM or VMD abolished or attenuated the rhythm. These new results suggest that neurons in the RLR project rostrally to locomotor areas in the DLM and VMD. These latter areas then appear to project caudally to RS neurons, which probably integrate the synaptic inputs from both areas and activate the spinal locomotor networks. These pathways are likely to be important components of the brain neural networks for the initiation of locomotion and have parallels to locomotor command systems in higher vertebrates.

Coordination of locomotor activity in the lamprey: role of descending drive to oscillators along the spinal cord.

In the lamprey and most fish, locomotion is characterized by caudally propagating body undulations that result from a rostrocaudal phase lag for ipsilateral burst activity. One of the mechanisms that might contribute to rostrocaudal phase lags is a gradient of oscillator burst frequencies along the spinal cord that presumably are produced, in part, by descending drive from the brain. The purpose of the present study was to test whether a gradient of oscillator frequencies does exist along the lamprey spinal cord. First, during brain-initiated locomotor activity in in vitro brain/spinal cord preparations, the cycle times (=1/frequency) of locomotor activity generated by the functionally isolated rostral spinal cord (activity blocked in middle and caudal cord) were significantly shorter than control cycle times when the entire spinal cord was generating locomotor activity. Second, the cycle times of locomotor activity generated by the functionally isolated caudal cord (activity blocked in rostral and middle cord) were significantly longer than control cycle times for activity generated by the entire spinal cord. Thus, no one region of the spinal cord appears to dictate the overall cycle times of locomotor activity generated by the entire spinal cord, although overall cycle times tended to be closest to those of the isolated rostral spinal cord. Finally, although short- and long-distance coupling as well as oscillator frequency gradients probably contribute to rostrocaudal phase lags of spinal locomotor activity, the asymmetrical nature of short-distance coupling, in which the descending component dominates, appears to be the main factor.

Axonal regeneration of descending brain neurons in larval lamprey demonstrated by retrograde double labeling.

In larval lamprey, the large, identified descending brain neurons (Müller and Mauthner cells) are capable of axonal regeneration. However, smaller, unidentified descending brain neurons, such as many of the reticulospinal (RS) neurons, probably initiate locomotion, and it is not known whether the majority of these neurons regenerate their axons after spinal cord transection. In the present study, this issue was addressed by using double labeling of descending brain neurons. In double-label control animals, in which Fluoro-Gold (FG) was applied to the spinal cord at 40% body length (BL; measured from anterior to posterior from tip of head) and Texas red dextran amine (TRDA) was applied later to the spinal cord at 20% BL, an average of 98% of descending brain neurons were double labeled. In double-label experimental animals, FG was applied to the spinal cord at 40% BL; two weeks later the spinal cord was transected at 10% BL; and, eight weeks or 16 weeks after spinal cord transection, TRDA was applied to the spinal cord at 20% BL. At eight weeks and 16 weeks after spinal cord transection, an average of 49% and 68%, respectively, of descending brain neurons, including many unidentified RS neurons, were double labeled. These results in larval lamprey are the first to demonstrate that the majority of descending brain neurons, including small, unidentified RS neurons, regenerate their axons after spinal cord transection. Therefore, in spinal cord-transected lamprey, axonal regeneration of descending brain neurons probably contributes significantly to the recovery of locomotor function.

Coordination of spinal locomotor activity in the lamprey: long-distance coupling of spinal oscillators.

The extent and strength of long-distance coupling between locomotor networks in the rostral and caudal spinal cord of larval lamprey were examined with in vitro brain/spinal cord preparations, in which spinal locomotor activity was initiated by chemical microstimulation in the brain, as well as with computer modeling. When locomotor activity and short-distance coupling were blocked in the middle spinal cord for at least 40 segments, burst activity in the rostral and caudal spinal cord was still coupled 1:1, indicating that long-distance coupling is extensive. However, in the absence of short-distance coupling, intersegmental phase lags were not constant but decreased significantly with increasing cycle times, suggesting that long-distance coupling maintains a relatively constant delay rather than a constant phase lag between rostral and caudal bursts. In addition, under these conditions, intersegmental phase lags, measured between rostral and caudal burst activity, were significantly less than normal, and the decrease was greater for longer distances between rostral and caudal locomotor networks. The above result could be mimicked by a computer model consisting of pairs of oscillators in the rostral, middle, and caudal spinal cord that were connected by short- and long-distance coupling. With short-distance coupling blocked in the middle spinal cord, strychnine was applied to either the rostral or caudal spinal cord to convert the pattern locally from right-left alternation to synchronous burst activity. Synchronous burst activity in the rostral spinal cord resulted in a reduction in right-left phase values for burst activity in the caudal cord. These results also could be mimicked by the computer model. Strychnine-induced synchronous burst activity in the caudal spinal cord did not appear to alter the right-left phase values of rostral burst activity. Taken together, the experimental and modeling results suggest that the descending and ascending components of long-distance coupling, although producing qualitatively different effects, are comparatively weak. In particular, the descending component of long-distance coupling appears to become progressively weaker with increasing distance between two given regions of spinal cord. Therefore, short-distance coupling probably contributes substantially to normal rostrocaudal phase lags for locomotor activity along the spinal cord. However, short-distance coupling may be more extensive than "nearest neighbor coupling."

Anatomical regeneration and behavioral recovery following crush injury of the trigeminal root in lamprey.

In normal larval lamprey, bilateral application of horseradish peroxidase (HRP) to the dorsal part of the anterior oral hood labeled subpopulations of trigeminal components on both sides of the brain; peripherally projecting motoneurons, medullary dorsal cells (sensory), and spinal dorsal cells (sensory), as well as centrally projecting afferents in the trigeminal descending tracts. Following unilateral crush injury of the right trigeminal root, HRP labeling of sensory and motor trigeminal components on the right side gradually increased with increasing recovery time, between 2 weeks and 12 weeks postcrush (PC). Axons of trigeminal motoneurons appeared to exhibit robust regeneration, whereas restoration of projections in the descending trigeminal tract ipsilateral to the injury was incomplete. Control experiments indicated that motor and sensory axons from the intact side of the oral hood did not sprout across the midline to the denervated side. Several results suggested that regenerated trigeminal sensory fibers made synapses with brain neurons that have direct or indirect inputs to reticulospinal (RS) neurons. Following a unilateral crush injury of the right trigeminal root, escape behavior in response to stimulation of the right side of the oral hood gradually returned to normal. Muscle recordings at various recovery times confirmed that anatomical regeneration of trigeminal sensory axons was functional. In addition, at 8 or 12 weeks PC, brief stimulation of the oral hood ipsilateral or contralateral to the crush injury elicited synaptic responses in RS neurons on either side of the brain, similar to that in normal animals. In the lamprey, compensatory mechanisms probably allow recovery of behavioral function despite incomplete regeneration of trigeminal sensory axons within the central nervous system.

Adaptive variations of undulatory behaviors in larval lamprey: comparison of swimming and burrowing.

In larval lamprey, movements and muscle activity during swimming and burrowing behaviors were compared. Burrowing consisted of two components: an initial component in which the head was driven into the burrowing medium; and a final component in which the animal pulled the rest of its body into the burrowing medium. The initial component of burrowing was characterized by large undulatory movements and rhythmic muscle burst activity that were similar in form to those during fast swimming, but more intense. During the initial component of burrrowing, burst durations, burst amplitudes, and burst proportions of motor activity were larger than those during swimming, while cycle time was slightly shorter than during swimming. Intersegmental phase lags and right-left phase values were similar for swimming and initial burrowing. The final component of burrowing was characterized by sharp, long-duration flexures on one side of the body, sometimes followed by similar flexures on the other side. Each flexure was produced by long-duration, large-amplitude muscle burst activity on the same side of the body or several shorter sequential bursts with slightly smaller amplitudes. During the final component of burrowing, burst durations and burst amplitudes of motor activity were much larger than those during swimming or during the initial component of burrowing. It is suggested that the motor patterns for swimming and the initial component of burrowing are produced by a common spinal locomotor network. The final component of burrowing may use some of the same neurons in the spinal locomotor networks, but the networks are probably configured differently than the situation during swimming.

Biophysical properties of descending brain neurons in larval lamprey.

In the brains of larval lamprey, biophysical properties of reticulospinal (RS) neurons were determined by applying depolarizing and hyperpolarizing current pulses under current clamp conditions. In response to above threshold depolarizing current pulses, almost all RS neurons produced an initial relatively high spiking frequency (Fi) followed by a variable decay to a steady-state firing frequency (Fss). Spike-frequency adaptation (SFA), defined as [(Fi - Fss)/Fi] x 100%, was minimal at the lowest currents and more pronounced with larger applied current pulses. Some RS neurons, particularly those in the posterior rhombencephalic reticular nucleus (PRRN), either adapted very quickly, and stopped firing, or fired in short bursts during a constant depolarizing current pulse. Several types of RS neurons, including some Muller cells and unidentified neurons in the middle rhombencephalic reticular nucleus (MRRN), displayed delayed excitation (DE) in which spiking in response to a depolarizing current pulse was delayed if preceded by a hyperpolarizing prepulse. Very few neurons fired action potentials following a hyperpolarizing pulse, such as in the case of post-inhibitory rebound (PIR), and no neurons were found that displayed plateau potentials. The possible contributions of these properties to the descending activation of spinal locomotor networks is discussed.

Fluorescent tracers as potential candidates for double labeling of descending brain neurons in larval lamprey.

In larval lamprey, seven fluorescent tracers were tested as potential candidates for retrograde double labeling of descending brain neurons: Fluoro Gold (FG); fluorescein dextran amine (FDA); True Blue (TB); cascade blue dextran amine (CBDA); Fast Blue (FB); Texas red dextran amine (TRDA); and tetramethylrhodamine dextran amine (RDA). The first tracer (FG, TB, FB, or CBDA) was applied to the spinal cord at 40% body length (BL). In separate experiments, the second tracer (TRDA or RDA) was applied to the spinal cord at 20% BL. The tracer combination FG/TRDA was found to have the best optical properties for double labeling. However, application of FG to the spinal cord with the method used for the other tracers resulted in labeling of 'lateral cells' along the sides of the rhombencephalon that were presumed to be non-neuronal and that obscured some of the descending brain neurons. Control experiments suggested that FG was transported in the circulation to the brain, where the tracer was taken up by lateral cells. Therefore, a special technique was developed for applying FG to the spinal cord without allowing the tracer to enter the circulation. In larval lamprey, this important double-labeling technique that was developed for TRDA and FG is being used to examine axonal regeneration and projection patterns of descending brain neurons.

Descending control of turning locomotor activity in larval lamprey: neurophysiology and computer modeling.

The purpose of the present study was to examine the mechanisms that produce natural spontaneous turning maneuvers in larval lamprey. During swimming, spontaneous turning movements began with a larger-than-normal bending of the head to one side. Subsequently, undulations propagated down the body with greater amplitude on the side ipsilateral to the turn. During turning to one side, which usually occurred within one cycle, the amplitude and duration of ipsilateral muscle burst activity as well as overall cycle time increased significantly with increasing turn angle. In in vitro brain/spinal cord preparations, brief electrical stimulation applied to the left side of the oral hood at the onset of locomotor burst activity on the right side of the spinal cord produced turninglike motor activity. During the perturbed cycle, the duration and amplitude of the burst on the right as well as cycle time were significantly larger than during preceding control cycles. In several lower vertebrates, unilateral stimulation in brain stem locomotor regions elicits asymmetric, turninglike locomotor activity. In the lamprey, unilateral chemical microstimulation in brain stem locomotor regions elicited continuous asymmetric locomotor activity, but there was little change in cycle time, as occurs during the single turning cycles in whole animals. The descending mechanisms responsible for producing turning locomotor activity were examined with the use of a computer model consisting of left and right phase oscillators in the spinal cord that were coupled by net reciprocal inhibition. With relatively weak reciprocal coupling, a brief unilateral descending excitatory input to one oscillator produced effects ipsilaterally, but there was little effect on the contralateral oscillator. Turninglike patterns could be produced by each of the following modifications of the model: 1) unilateral descending input and relatively strong reciprocal coupling; 2) unilateral descending input that phase shifted as well as increased the amplitude of the waveform generated by an oscillator on one side; and 3) brief descending modulatory inputs that excited the oscillator on one side and inhibited the contralateral oscillator. In all three cases, there was an increase in "burst" duration ipsilateral to the excitatory input and an increase in cycle time, similar to turning locomotor activity in whole animals. It is likely that turning maneuvers are mediated by descending modulatory inputs primarily to the spinal oscillator networks, which control the timing of burst activity, but perhaps also to motoneurons for axial musculature.

Descending propriospinal neurons in normal and spinal cord-transected lamprey.

The organization and distribution of propriospinal neurons with descending axons were determined via retrograde HRP labeling in normal lamprey and in animals that had behaviorally recovered for various times (4, 8, 16, and 32 weeks) following transection of the rostral spinal cord. In normal animals, descending propriospinal neurons were found in the rostral, middle, and caudal spinal cord. Theoretical analysis indicated that the majority of these neurons had relatively short axons (< 10-15 mm), although a few neurons had relatively long axons (> 30 mm). In spinal cord-transected animals, with increasing recovery times there was a gradual increase in the numbers of labeled propriospinal neurons below the lesion with short-to moderate-length descending axons. The distribution of descending propriospinal neurons and the possible plasticity in this system following spinal cord transection are discussed with regard to activation of spinal motor networks and initiation of locomotor behavior.

Optical imaging of neuronal activity in tissue labeled by retrograde transport of Calcium Green Dextran.

In many neurophysiological studies it is desirable to simultaneously record the activity of a large number of neurons. This is particularly true in the study of vertebrate motor systems that generate rhythmic behaviors, such as the pattern generator for locomotion in vertebrate spinal cord. Optical imaging of neurons labeled with appropriate fluorescent dyes, in which fluorescence is activity-dependent, provides a means to record the activity of many neurons at the same time, while also providing fine spatial resolution of the position and morphology of active neurons. Voltage-sensitive dyes have been explored for this purpose and have the advantage of rapid response to transmembrane voltage changes. However, voltage-sensitive dyes bleach readily, which results in phototoxic damage and limits the time that labeled neurons can be imaged. In addition, the signal-to-noise ratio is typically small, so that averaging of responses is usually required. As an alternative to voltage-sensitive dyes, calcium-sensitive dyes can exhibit large changes in fluorescence. Most neurons contain voltage-sensitive Ca2+ channels, and numerous reports indicate that neuronal activity is accompanied by increased intracellular Ca2+ concentration. In this protocol we describe a method to use retrograde transport of the dextran conjugate of a calcium-sensitive dye (Calcium Green Dextran) to label selectively populations of brain and spinal interneurons in a primitive vertebrate (lamprey), for subsequent video-rate imaging of changes in intracellular fluorescence during neuronal activity. Although described with specific reference to lampreys, the technique has also been applied to embryonic chick spinal cord and larval zebrafish preparations and should be easily adaptable to other systems. The most significant novel feature of the protocol is the use of retrograde axonal transport to selectively fill neurons that have known axonal trajectories. Using lampreys, we have obtained activity-sensitive labeling across longer distances and over a longer transport time (up to 14 mm and 4 days) than has been reported in other species. In addition, retrograde transport allows filling of neurons more deeply within tissue than would be possible with bath application of calcium-sensitive dyes. Furthermore, the dyes are readily taken up by adult tissues, while bath application is usually limited to embryonic and neonatal vertebrate nervous tissues (although the reasons for this limitation are not clear). Attempts to load the AM (acetomethoxy) esters of calcium-sensitive dyes into lamprey spinal cord neurons by bath application have been unsuccessful (McPherson, unpublished observations, and).

Combined retrograde labeling and calcium imaging in spinal cord and brainstem neurons of the lamprey.

Neurons in the brainstem and spinal cord of the lamprey were retrogradely labeled with Calcium Green-dextran, an indicator dye that increases its fluorescence when intracellular calcium levels increase. Optical signals could be recorded from these labeled neurons during spinal cord stimulation, nerve stimulation, or spontaneous activity, up to 4 days after dye application and for distances of 5-14 mm away from the application site. Optical signals were enhanced by 4-AP, a potassium channel blocker, and blocked by cadmium, a calcium channel blocker. Taken together, the results suggest that the optical signals recorded from labeled neurons were due to calcium influx during electrical activity. Thus, retrograde labeling with calcium indicator dyes may provide a general purpose method for simultaneously monitoring the activity-related changes of intracellular calcium in anatomically identified groups of neurons in the lamprey nervous system.

Coupling of spinal locomotor networks in larval lamprey revealed by receptor blockers for inhibitory amino acids: neurophysiology and computer modeling.

1. Receptor blockers for inhibitory amino acids were applied to part or all of the spinal cord of larval lamprey during brain stem-initiated locomotor activity. Blocking glycinergic inhibition with strychnine applied to the entire spinal cord converted the locomotor pattern from left-right alternation to synchronous left-right bursting. The results suggest that left and right oscillators are connected by relatively strong reciprocal inhibitory (glycinergic) connections in parallel with weaker reciprocal excitatory connections. This possible organization was supported by results from a computer model consisting of left and right oscillators connected by reciprocal inhibition and excitation in parallel. In addition, the results suggest that reciprocal inhibition is not required for left-right rhythmicity but rather is involved primarily with phasing of left-right activity. 2. Locally blocking glycinergic inhibition with strychnine in the rostral spinal cord resulted in synchronous left-right burst activity in that region of the cord as well as in more caudal areas of the cord in which reciprocal inhibition should still be functional. 3. Blocking glycinergic inhibition in the caudal spinal cord converted the pattern in that region of the cord to left-right synchronous activity. The effects in the ascending direction on the burst patterns in more rostral areas of the spinal cord were less than those mentioned above in the descending direction with application of strychnine to the rostral spinal cord. 4. With glycinergic inhibition or GABAergic inhibition blocked in the entire spinal cord, stable longitudinal coupling along the spinal cord persisted. This and the neurophysiology results mentioned above suggest that the main mechanism for longitudinal coupling between locomotor networks in adjacent regions of the spinal cord is ipsilateral excitatory connections and not crossed inhibitory connections. This possible organization was supported by results from a computer model, which consisted of a pair of oscillators in the more rostral and more caudal spinal cord that could be connected by various types of coupling schemes. 5. The neurophysiological data above suggest that ipsilateral, excitatory coupling is stronger in the descending direction than in the ascending direction. In the computer model, a dominant descending coupling is a necessary requirement to produce positive longitudinal phase lags.

Time course of locomotor recovery and functional regeneration in spinal cord-transected lamprey: in vitro preparations.

1. Previous studies indicate that after transection of the rostral spinal cord, larval lamprey begin to recover locomotor behavior 2 wk posttransection and recovery is complete at approximately 8 wk. To examine the mechanisms underlying behavioral recovery after spinal cord transection, in the present study the time course and extent of recovery of locomotor function was examined in in vitro brain/spinal cord preparations. With these preparations the contributions of functional regeneration of descending brain stem projections to recovery of spinal locomotor function can be examined in the absence of mechanosensory inputs and descending propriospinal relay systems. 2. In in vitro preparations from normal lamprey, stimulation in brain stem locomotor regions resulted in direct descending activation of locomotor networks in the rostral, middle, and caudal spinal cord. 3. At 4 wk posttransection, in vitro locomotor activity was usually confined to the rostral spinal cord a few millimeters below the transection site. At 8 wk posttransection locomotor activity was present in both the rostral and middle spinal cord, and spinal locomotor networks at these levels could be directly activated by restored descending projections from the brain stem. 4. At 16-32 wk posttransection locomotor activity similar to that seen in normal animals was present along the spinal cord. Additional manipulations suggest that at 32 wk posttransection descending axons from brain stem command/initiation neurons had grown for relatively long distances and could directly activate the locomotor networks in the caudal spinal cord. At each recovery time examined the ranges of locomotor parameters (cycle time, burst proportion, and intersegmental phase lag) overlapped with those in normal animals. 5. In vitro locomotor activity in spinal cord-transected animals could be recorded at progressively more caudal levels below the transection site during the course of recovery. However, locomotor activity in in vitro preparations occurred for shorter distances below the lesion than in whole animals at comparable recovery times. 6. Our recent double-labeling experiments suggest that behavioral recovery in spinal cord-transected lamprey is largely due to true regeneration of preexisting descending axons rather than development of new descending projections. Thus, these results in conjunction with our behavioral, in vitro, and anatomic data suggest that functional regeneration of descending axons from the brain, as well as other mechanisms such as descending propriospinal relay systems and mechanosensory inputs, account for the gradual restoration of locomotor function in spinal cord-transected lamprey.

Extent and time course of restoration of descending brainstem projections in spinal cord-transected lamprey.

The purpose of the present study was to determine the numbers of descending brainstem projections to different levels of the spinal cord in normal larval sea lamprey (Petromyzon marinus) and to examine the restoration of these projections in animals 3-32 weeks after transection of the rostral spinal cord (approximately 10% of body length). In normal animals approximately 1,250, 900, and 825 brainstem neurons projected to 20%, 40%, and 60% of body length, respectively. Spinal projections originated from the diencephalon, mesencephalon, three rhombencephalic reticular nuclei, Müller and Mauthner neurons, and four cell groups in the caudal rhombencephalon. In spinal cord-transected animals the number of brainstem neurons projecting to 20% of body length increased with recovery time, and at 32 weeks post-transection the total number and distribution of brainstem neurons was not significantly different from normal animals. Brainstem projections first appeared at 40% of body length by 8 weeks post-transection, and were present at 60% of body length by 32 weeks post-transection. There was substantial restoration of brainstem projections to 40% of body length but limited restoration to 60% of body length. The approximately 50 brainstem neurons, including some Müller cells, that projected to 60% of body length at 32 weeks post-transection indicate that restoration of descending projections in excess of 50 mm can occur within the central nervous system of this vertebrate. These anatomical results are discussed in relation to the time course of recovery of locomotor function in spinal cord-transected lampreys.

Long distance axonal regeneration of identified lamprey reticulospinal neurons.

Retrograde labeling with horseradish peroxidase was used to examine the time course and extent of axonal regeneration of 12 pairs of individually identifiable reticulospinal Müller cells and 2 pairs of Mauthner cells in larval lamprey that received transections of the rostral spinal cord in the gill region. With increasing recovery times (3-32 weeks post-transection) the descending axons of many of these neurons regenerated to progressively more caudal levels of the spinal cord. These results confirm that some reticulospinal neurons are capable of true regeneration. However, the regenerative capacity of these neurons was not uniform, even for neurons in the same brain stem nucleus in close proximity. For example, at 32 weeks post-transection some identifiable reticulospinal neurons could regenerate their axons to 60% body length or as much as 57 mm below the transection site. In contrast, previous studies indicated regeneration distances of 5-6 mm. Other neurons showed modest axonal regeneration, while one cell type showed very limited regeneration. The factors which may be responsible for the variable extent of regeneration among these neurons are considered.