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Neuronal activity in several brain regions is modulated by dopaminergic inputs. When single neuronal activity/20 trials of single-pulse ventrolateral thalamic (VL) stimulation was extracellularly recorded in the in vivo, anesthetized cat motor cortex, iontophoretic application of dopamine (DA) elicited either suppression or, in a fewer instances, facilitation of evoked unitary responses. The predominant inhibition exerted by DA appeared to be consistent for successive trials, and a D1, D2, and D1/D2 receptor antagonist restored the effect, thereby reflecting a possible coexistence of two DA receptors. By contrast, only a fewer neurons’ response to DA displayed facilitation, which was not attenuated by DA antagonists. Moreover, subsequent trials with receptor agonist and antagonists induced inconsistent effects. Except for the jitters, single unit spikes showed invariant latency, which was constant during all recording parameters, and the mean latency remained unchanged. The modulatory effects mediated by DA did not reveal any substantial difference between short- and long-latency responses. Both pyramidal tract neurons and non-pyramidal tract neurons, determined on the basis of antidromic potentials from the pyramidal tract, responded to DA essentially in a similar manner. It appears that DA overall inhibits cat motor cortical neuronal activity in response to VL inputs. We propose that such DAergic inhibition of thalamocortical excitation in the motor cortex could be critical for ongoing sensorimotor transformation.

Mental-sweating response (MSR) was observed in the palm when the subject was asked to perform a mentally stressful task such as memory recall or mental calculation. About 4 s before the development of MSR, small MSR-related wavelets (MSR wavelets) and large waves were randomly generated on electroencephalograph. After differentiating the two types of waves, we calculated locations of the current dipole of MSR wavelets using the two-dipole model of the SSB/dipole tracing method. The result showed that one current dipole of MSR wavelets was consistently located in the hippocampus while the other dipole was widely dispersed in the cortex during memory recall and mental calculation.

Preceding mental sweating response (MSR) during mental stress, small wavelets and large waves are observed on EEG. In the present study, locations of current sources of the large waves were estimated. The results revealed that the current dipole was estimated around the orbits, reflecting activity of the eyelid or eye muscles.

A theoretical framework is presented that describes a way in which the inverse dynamics equations of motion of planar two-joint arm movements (EX-model) are reformulated in a simple form. A single point was assumed to define both the wrist and elbow joint centers, and thus the motion of two points in extrinsic space was represented by second-order differential equations to provide the variables in the reformulation (RE-) model. Through an analytical processes, it was shown that the RE-model for reproducing the shoulder joint torque consists of the linearly scaled moment per unit mass responsible for accelerating the wrist and elbow points about the shoulder joint, while that for reproducing the elbow joint torque consists of the linearly scaled moment per unit mass responsible for accelerating the wrist point about the elbow. The scaling factors for variables in the RE-model were based solely on the values for segment lengths, while in the EX-model the inertial parameter data for the segments are involved in its representation. The inertial parameter data of six-arm specimens from the cadaver experiment of Chandler et al. (1975, AMRL Technical Report, Wright-Patterson Air Force Base, OH) were used to develop and verify the numeric solutions of the RE-model. The adequacy of the model varied somewhat among subjects, but minor changes of the physical parameters of the arm segments enabled perfect reformulation, regardless of the specimens. The potential abilities of the RE-model to deal with the complexities in motor control with more simple control schemes are discussed.

The effects of dopamine (DA) and its antagonists on the transcallosal activity of pyramidal tract neurons (PTNs) and non-PTNs in the anesthetized cat motor cortex were studied with iontophoretic applications; dopamine, SCH 23390 (D1 antagonist), sulpiride (D2 antagonist) and haloperidol. Neuronal activity was recorded with a multi-barreled glass microelectrode. Transcallosal neuronal activity was evoked by stimulation of the contralateral motor cortex. The number of spikes thus activated was counted for the control and test conditions after application of each drug: (1) dopamine application decreased the number of spikes evoked by transcallosal stimulation; (2) application of SCH 23390, sulpiride and haloperidol restored these decreased spike numbers to the control level; (3) latency of neuronal response to transcallosal stimulation was not affected by the application of either DA, SCH 23390, sulpiride or haloperidol; and (4) there was no significant difference between PTNs and non-PTNs in the manner of response to DA and its antagonist applications. Our conclusion is that dopamine modulated the transcallosal neuronal response in the cat motor cortex in a suppressive manner. This fact suggested that interhemispheric neuronal communications could be subjected to suppressive modification by the dopaminergic system.

The purpose of this study was to investigate the cortical motor areas activated in relation to unilateral complex hand movements of either hand, and the motor area related to motor skill learning. Regional cerebral blood flow (rCBF) was measured in eight right-handed healthy male volunteers using positron emission tomography during a two-ball-rotation task using the right hand, the same task using the left hand and two control tasks. In the two-ball-rotation tasks, subjects were required to rotate the same two iron balls either with the right or left hand. In the control task, they were required to hold two balls in each hand without movement. The primary motor area, premotor area and cerebellum were activated bilaterally with each unilateral hand movement. In contrast, the supplementary motor area proper was activated only by contralateral hand movements. In addition, we found a positive correlation between the rCBF to the premotor area and the degree of improvement in skill during motor task training. The results indicate that complex hand movements are organized bilaterally in the primary motor areas, premotor areas and cerebellum, that functional asymmetry in the motor cortices is not evident during complex finger movements, and that the premotor area may play an important role in motor skill learning.

Investigation of the vestibulo-ocular system of the squirrel monkey was reviewed in consideration of space motion sickness (SMS), or which is recently more often termed as space adaptation syndrome (SAS). Since the first launching of the space satellite, Sputnik [correction of Sputonik] in October 1957, many experiments were carried out in biological and medical fields. A various kind of creatures were used as experimental models from protozoa to human beings. Rats and monkeys are most favorite animals, particularly the non-human primate seems to be the one, because of its phylogenetic relatives akin to the human beings. Chimpanzees, rhesus monkeys, pig tailed-monkeys, red-faced monkeys and squirrel monkeys have been used mostly in American space experiments. Russian used rhesus monkeys. Among these, however, the squirrel monkey has an advantage of the small size of the body, ranging from 600- l000g in adult. This small size as a primate is very advantageous in experiments conducted in a narrow room of the space satellite or shuttle because of its space-saving. The squirrel monkey has another advantage to rear easily as is demonstrated to keep it as a pet. Accordingly, this petit animal provides us a good animal model in biological and medical experiments in space craft. The size of the brain of the squirrel monkey is extraordinary large relative to the body size, which is even superior to that of the human beings. This is partly owed to enlargement of the occipito-temporal cortices, which are forced to well develop for processing a huge amount of audio-visual information indispensable to the arboreal habitant to survive in tropical forest. The vestibular system of the squirrel monkey seems to be the most superior as well, when judged from it relative size of the vestibular nuclear complex. Balancing on swinging twigs or jumping from tree to tree developed the capability of this equilibrium system. Fernandez, Goldberg and his collaborators used the squirrel monkey to elucidate functions of the peripheral vestibular system. A transfer function was proposed to explain the behaviors of regular and irregular unit activity of vestibular nerve fibers. The physiologic characteristics of the second order vestibular neuron was investigated in combination of electrophysiological and micro-morphological way, with using WGA-HRP methods, in relation to somato-motor and eye movements. Interconnections between vestibular neurons and cerebellum, interstitial nucleus of Cajal, oculomotor nuclear complex, superior colliculus and cervical spinal cord were elucidated. In physiological field of the vestibular system, the vestibulo-ocular reflex is well studied and results obtained from the squirrel monkey experiments were reviewed. The squirrel monkey, particularly the Bolivian, is a unique animal in that it is vulnerable to motion sickness induced by visual-motion stimulation with phase mismatch of the two stimuli. Experimental results of labyrinthectomy or bilateral ablation of the maculae staticae led to the conclusion that both semicircular and otolith organs are involved in the genesis of space motion sickness. On the other hand, destruction of the area postrema, acknowledged as the vomiting center to chemical stimulants, produced controversial results. However, it must be pointed out that the a human subject underwent to resection of the area postrema, became insensitive to administration of apomorphine, a well known chemical stimulant of vomiting. Finally the experiments in space revealed the presence of at least two origins of caloric nystagmus, that is, attributable to convection and non-convection current of the endolymphatic fluid.

The effects of a specific GABA B receptor antagonist, p -(3-aminopropyl)- p -diethoxymethyl-phosphonic acid (CGP 35348), on pyramidal tract neuron responses to transcallosal stimulation were investigated in the cat motor cortex in vivo. The paired-pulse method was used to obtain more insight into the role of GABA B receptors. At a 200-ms inter-stimulus interval the spike response was inhibited in 75% of the neurons. There was an approximately 40% depression of the mean spike value in the control. CGP 35348 reduced paired-pulse inhibition, while (−)-baclofen increased it. Stronger drug effects on the second stimulation-induced response possibly indicate their presynaptic action on GABA B receptors.

Effects of constant magnetic field (CMF, 0.65T) on muscle tension were studied in the bullfrog sartorius muscle. Muscles were stimulated every 30mins during exposure to a CMF for up to ten hrs. Tension developed at each time point decreased with time. However, the rate of decrease was smaller for test than for control muscles, and tension was larger in test than in control muscles.

The effects of a specific GABAB receptor antagonist, p-(3-aminopropyl)-p-diethoxymethyl-phosphonic acid (CGP 35348), on pyramidal tract neuron responses to transcallosal stimulation were investigated in the cat motor cortex in vivo. Iontophoretic application of CGP 35348 significantly increased the number of spikes from 10.3 +/- 4.4 (control; n = 27; mean +/- S.D.) to 16.7 +/- 7.2 (CGP 35348) for 20 transcallosal stimulation trials, while the latency of neuronal activity was significantly shortened from 4.4 +/- 2.1 ms (control; n = 27; mean +/- S.D.) to 3.8 +/- 1.7 ms (CGP 35348). In conclusion, CGP 35348 facilitated transcallosal synaptic transmission between pyramidal tract neurons by removal of GABAB inhibition.

The topography of the commissural fibers in the corpus callosum (CC) of the cat was systematically investigated using the WGA-HRP method. WGA-HRP was injected into various parts of the cerebral cortex and locations of WGA-HRP-stained commissural fibers in the CC were examined. Commissural fibers were arranged in a topological fashion in the CC. Cortical areas rostral to the cruciate sulcus (CrS), corresponding to motor or premotor cortices, projected fibers into the genu of the CC, while fibers from the cortex caudal to the CrS passed through the CC slightly caudal to the genu. When WGA-HRP was injected into the lateral gyrus (LG), it was observed that fibers from the anterior LG passed through the anterior one-third of the CC, whereas those from the posterior LG passed through or near the splenium, and fibers from the middle LG passed between those from the anterior and posterior LG. Similarly, the suprasylvian gyrus (SSG) projected commissural fibers in the CC in a rostrocaudal topological manner. Fibers from the anterior SSG passed through the anterior one-third of the CC, and those from the middle SSG through the middle one-third of the CC and upper part of the splenium. Injection into the most posterior part of the middle SSG revealed fibers passing through the caudal end of the splenium. Callosal fibers from the anterior SSG were focused on in this study, because this area (area 2v) is considered one of the vestibular projection cortices and is an area of special interest to the authors. Callosal fibers from the anterior SSG were observed to pass through the anterior one-third of the body of the CC. When WGA-HRP was injected into auditory areas, fibers from the anterior and middle ectosylvian gyri (ESG) were observed to pass through the posterior one-third of the body of the CC or through the splenium, while fibers from the posterior ESG passed through the splenium. WGA-HRP was also injected into the cingulate gyrus (CiG). Fibers from the anterior CiG (area 24) passed through the anterior portion of the CC while those from the posterior CiG (area 23) passed through the posterior portion of the CC.

Force response and surface electromyographic (EMG) activity of extrinsic extensors and flexors of the hand were measured under 6 target force conditions during rapid pulse isometric contractions (power grip) targeted using an oscilloscope display of exerted and target forces. For target forces ranging from 16.7% to 50% of maximum voluntary contraction (MVC), the rate of force rise increased with the peak force, while the time to peak force remained almost constant. However, at target forces between 66.7% and 100.0% MVC, the rate of force rise leveled off and the time to peak force was prolonged. In association with these changes in force trajectories, modulation of the EMG activity of the flexor digitorum superficials muscle was observed. At the lowest target force (16.7 MVC), the EMG of this muscle showed a single initial activity; the activity increased linearly up to the 50% MVC target force, while the duration was relatively constant. However, at target forces above 50% MVC, no further increase of the initial activity was observed, while the amplitude and duration of an additional activity progressively increased. These results indicate that the neural control of rapid isometric contraction at target forces at and below 50% MVC differs from that operating at larger target force levels.

The effects of long exposure of the frog sciatic nerve to a large static magnetic field (0.7T) was investigated. The amplitude or conduction velocity of nerve activity was hardly affected by long exposure to large static magnetic field. However, the recovery curve of nerve activity was larger for the nerve exposed to the large magnetic field.

Studies of the vestibular system in squirrel monkeys in consideration of space motion sickness (SMS) or space adaptation syndrome (SAS) were reviewed. First, the phylogenetic position of the squirrel monkey was considered. Then the anatomico-physiological studies of both the peripheral and the central vestibular systems were described, because the vestibular system is crucially important in the genesis of SMS (SAS). In this connection, the ablation studies of labyrinth, semicircular canals, and other SAS-related areas were referred to, and consideration was made for experiments about caloric irrigation of the ear. A hypothetic model was then proposed for the genesis of SAS.

The role of dopamine (DA) on motor cortical pyramidal tract neurons (PTNs) was studied in anesthetized cats with in vivo extracellular recordings in response to transcallosal (TC) and ventrolateral (VL) thalamic stimulations. An antidromic PT potential was evoked to recognize PTNs. In most PTNs, iontophoretic application of DA significantly reduced the spike activity exerted by 20 single-pulse stimulations. Both D 1 -like and D 2 -like receptor antagonists blocked (disinhibited) the effect in a similar way regardless of TC and VL stimulations, suggesting colocalization of two receptors. Except for the presence of jittering, the mean latency was usually fixed and short. These findings indicate that ventral midbrain DA imposes an intense suppression in modulating PTNs response to both callosal and thalamocortical excitatory inputs in motor cortex. Such DAergic suppression could play pivotal role to improve motor and sensorimotor signal integration.

In order to determine whether Ala-Pro-Gly-Try-NH2 (APGW-amide) could affect mammalian excitable cells, we investigated the effect of APGW-amide in PC12 cells. APGW-amide caused a rapid [Ca2+]i elevation, which was completely prevented by elimination of extracellular Ca2+ with EGTA and inhibited by two L-type Ca2+ channel blockers. [Ca2+]i elevation was also blocked by a specific PKC inhibitor and prolonged pretreatment of cells with PMA. These results indicate that APGW-amide elevates [Ca2+]i in PC12 cells, possibly by Ca2+ influx via L-type Ca2+ channel activated by PKC.

Effects of a constant magnetic field (CMF) of 0.65 T on muscle tension over 9 h were studied in the neuromuscular preparation of the bullfrog sartorius muscle. Tension was developed every 30 min by stimulation of the sciatic nerve (nerve stimulation) or of the sartorius muscle itself (muscle stimulation). In sciatic nerve stimulation, tension decreased rapidly for the first 3–4 h at a similar rate in both test (exposed to CMF) and control muscles. However, the rate of decrease became smaller and almost leveled off after 3–4 h in the test muscles, whereas tension continued to decrease monotonically in control muscles. The slope of the decrease for these later periods was significantly different between the test and the control conditions. Accordingly, tension was larger in test than in control muscles. In muscle stimulation, tension decreased monotonically from the start of experiments in control muscles, while tension in test muscles maintained their initial values for almost 3 h. Thereafter they started to decrease with a similar rate to the control. Hence, tension was always larger in test than in control muscles. A similar pattern of temporal change was observed for the rate of rise of the maximum tension for nerve or muscle stimulation. However, a significant difference was detected only in the case of muscle stimulation. The present results showed that a strong CMF of 0.65 T had biological effects on tension development of the bullfrog sartorius muscle by stimulation of the sciatic nerve as well as by stimulation of muscle itself. The presence of a small AC magnetic field component leaves open the possibility of an AC, rather than a CMF effect. Bioelectromagnetics 22:53–59, 2001. © 2001 Wiley-Liss, Inc.

GABAergic and dopaminergic influences in the cortex have been found to be inhibitory and predominantly inhibitory, respectively. Activation of GABAB receptors produces slow IPSPs with long duration while postsynaptic activation of GABAA receptors evokes fast IPSPs with an increase in Cl- conductance. GABAB-mediated slow (late) IPSPs accompanied by an increase in K+ conductance build up very slowly and continue to develop for more than 500 ms in cat cerebral cortical neurons. Suppression of cortical IPSPs by GABAB antagonists is suggested to be involved in postsynaptic events. Our study, however, elucidated that GABAB receptor antagonists CGP35348 and phaclofen shortened the transcallosal response latency of cat motor cortical neurons predominantly presynaptically. Shortening of the latency by postsynaptic mechanism was also observed in some neurons. On the other hand, iontophoretic dopamine (DA) application reduced the action potentials. The complex DAergic modulation is known to be mediated by D1 and D2 receptors positively and negatively coupled to adenylate cyclase, respectively. The inhibitory effect of DA on EPSCs via both D1 and D2 receptors has already been reported. Recently, the presence of DA receptor in presynaptic terminals has been suggested. However, our experiments elucidated that D1 antagonists SCH23390 (SCH) and D2 antagonists sulpiride (SUL) and haloperidol (HAL) facilitated the transcallosal activity on cat motor neurons by blocking the suppressive effect of DA but did not change the response latency.

Achatin-I, a neuropeptide isolated from the ganglia of Achatina fulica Ferussac, was proposed as an excitatory neurotransmitter and neuromodulator for A. fulica neurons (Kamatani et al. 1989; Kim et al. 1991; Liu and Takeuchi 1993). This peptide induced an inward current (Iin) on the giant neuron type, periodically oscillating neuron (PON). This Iin was found to be Na2+-dependent and is mediated by the cyclic AMP-PKA and calmodulin systems (Kim et al. 1991; Emaduddin et al. 1996). It was also found that some histamine H1 receptor antagonists inhibited this Iin (Santos et al. 1995). This paper, which is a part of studies on the characterization of Iin induced by achatin-I on PON, describes the suppressing effects of some H1 receptor antagonists and their analogues on this current. Their structure-activity relationship was also elucidated.

1. Modulatory effects of APGW-amide (Ala-Pro-Gly-Trp-NH 2 ), proposed as an inhibitory neurotransmitter of Achatina neurons, perfused at 3×10 −6 M on the currents induced by small-molecule putative neurotransmitters were examined by using Achatina giant neuron types, v-RCDN (ventral-right cerebral distinct neuron), TAN (tonically autoactive neuron) and RAPN (right anterior pallial nerve neuron), under voltage clamp.These putative neurotransmitters were ejected locally to the neuron by brief pneumatic pressure. 2. Outward current ( I out ) induced by erythro-β-hydroxy- L -glutamic acid (erythro- L -BHGA) on v-RCDN, which was probably K + dependent, was enhanced with membrane conductance ( g ) increase under APGW-amide. From dose (pressure duration)-response curves of erythro- L -BHGA measured in physiological solution (control curve) and with APGW-amide (drug curve), ED 50 values of the two curves were nearly comparable, whereas E max of the drug curve was significantly larger than that of the other. From a Lineweaver-Burk plot of these data, the cross point of the control line and the drug line was on the abscissa. 3. K + -dependent I out caused by dopamine (DA) on v-RCDN was inhibited with a g increase by APGW-amide. The inhibition of this current caused by APGW-amide was mainly in a noncompetitive and partly uncompetitive manner. 4. 5-Hydroxytryptamine (5-HT) produced an inward current ( I in ) with two (fast and slow) components on TAN, which was probably Na + dependent. The fast component of the I in was inhibited by APGW-amide. The inhibition was mainly in a noncompetitive manner. 5. The currents induced by acetylcholine, γ-aminobutyric acid and L -glutamic acid on Achatina neuron types were not affected by APGW-amide. 6. The inhibitory effects of APGW-amide on the I in (fast component) induced by 5-HT were nearly equipotent or a bit stronger than those on the I out caused by DA. 7. The g increase produced by APGW-amide would be a cause for inhibiting the I out induced by DA. In addition, we consider that APGW-amide affects intracellular signal transduction systems or ionic channels, thus modulating these currents.

1. Modulatory effects of APGW-amide (Ala-Pro-Gly-Trp-NH2), proposed as an inhibitory neurotransmitter of Achatina neurons, perfused at 3 x 10(-6) M on the currents induced by neuroactive peptides, ejected by brief pressure, were examined by using Achatina giant neuron types, v-RCDN (ventral-right cerebral distinct neuron) and PON (periodically oscillating neuron), under voltage clamp. 2. Outward current (Iout) caused by FMRFamide (Phe-Met-Arg-Phe-NH2) on v-RCDN, which was probably K+ dependent, was inhibited with membrane conductance (g) increase by APGW-amide. From the dose (pressure duration)-response curves of FMRFamide and a Lineweaver-Burk plot of these data, the inhibition caused by APGW-amide was mainly in an uncompetitive manner. 3. Iout caused by APGW-amide on v-RCDN, which was probably K+ dependent, was inhibited with g increase by APGW-amide. The inhibition caused by APGW-amide was partly in a competitive manner and partly in a noncompetitive manner. 4. Iout caused by [Ser2]-Mytilus inhibitory peptide, [Ser2]-MIP (Gly-Ser-Pro-Met-Phe-Val-NH2) on v-RCDN, which was probably K+ dependent, was inhibited with g increase by APGW-amide. Because the modulation of this current was not so marked, a dose-response study of this compound was not carried out. Iin induced by oxytocin on PON was not affected by APGW-amide. 5. From the dose-response curves of APGW-amide, perfused consecutively, the inhibitory effects of APGW-amide on the Iout caused by APGW-amide were stronger than those on the Iout caused by FMRFamide. 6. The inhibition of the APGW-amide-induced Iout on v-RCDN by APGW-amide was partly due to the competition in the receptor sites and partly to the g increase. The inhibition by APGW-amide on the Iout induced by FMRFamide and [Ser2]-MIP would be partly due to the g increase. In addition, we consider that APGW-amide affects intracellular signal transduction systems or ionic channels, thus modulating these currents. 7. The currents modulated by APGW-amide were different from those modulated by achatin-1, another Achatina endogenous neuroexcitatory peptide. We consider that the mechanisms underlying the modulatory effects of APGW-amide are different from those of achatin-I.

GABAergic characteristics of transcallosal activity of cat pyramidal tract neurons (PTNs) and non-PTNs (nPTNs) were studied with stressing on GABAB receptors. PTNs and nPTNs were further classified into group 1 (10 ms) and group 2 (10 ms) based on the latency upon transcallosal stimulation. However, mainly the results of group 1 neurons were presented here, due to the small number of group 2 neurons. GABA, bicuculline, CGP 35348 and phaclofen were iontophoretically applied. The spike number to 20 trials of transcallosal stimulation was 8.9 +/- 4.3 (mean +/- S.D.) for group 1 PTNs (n = 14) and 10.4 +/- 4.5 for group 1 nPTNs (n = 38) under the control conditions. CGP 35348, phaclofen and bicuculline significantly increased the spike numbers in both cases. The increase was greater for nPTNs than for PTNs. GABA decreased them. The transcallosal latency was 3.9 +/- 1.1 ms for PTNs under the control conditions. CGP 35348, phaclofen and bicuculline significantly shortened the latency, and GABA elongated it. The transcallosal latency for nPTNs under the control conditions was 2.7 +/- 1.2 ms. This was significantly shortened by application of CGP 35348, phaclofen or bicuculline. GABA restored it. In conclusion, CGP 35348, phaclofen and bicuculline increased spike discharge and shortened the latency upon transcallosal stimulation for both group 1 PTNs and nPTNs.

The pattern of radioactive 2-deoxy-D-glucose (2-DG) uptake in the rostral mesial cortex was investigated in seven hemispheres of four task-performing monkeys (a delayed-response task performed with a forelimb). A two-dimensional 2-DG map was constructed from frontal sections. Blob-like 2-DG incorporation sites (2-DG active sites) were observed in single frontal sections, e.g., in the anterior cingulate gyrus (CiG) and supplementary and primary motor cortices in the mesial surface, and around the superior precentral sulcus in the premotor area. Blob-like 2-DG incorporation sites were also observed in the medial part of the dorsal frontal cortex near the midline. However, most of these blob-like 2-DG active sites were revealed in fact not to be blobs. They formed rostrocaudally continuous streaks when they were constructed in a two-dimensional map. Streaks fused with one another in some areas, and gave off branches in other areas. These 2-DG uptake patterns were similar between the paired left and right hemispheres of three brains. It is highly probable that these 2-DG active streaks (or blobs) reflected neuronal activity related to somatomotor and/or eye movements, because the 2-DG-labeled areas included motor, premotor, supplementary motor, and possibly part of the supplementary eye fields. It is also probable that this 2-DG incorporation was related to cognitive or memory functions, because neuronal activity related to performance of a delayed-response was reported in the rostral mesial cortex and in the CiG.

The present study was designed with two intentions; Are the effects of angular velocity detectable in the cardiovascular responses during the hyper-G? Another is object to examine how the otolith signal could modify the cardiovascular responses provoked by the exposure to the hyper-G. NASA/KC-135 hyper-gravity flight was used to generate high gravito-inertial forces to exclude a possible effect of angular velocity. Six healthy subjects was indicated to make dorsal flexion of the neck to reduce the otolith input. An exposure to +l.8Gz stress resulted in a remarkable increase of systolic and diastolic blood pressure, thereby pulse pressure became a little bit narrower. R-R interval revealed a tachycardia during the hyper-G except one subject. The present experiment bore the similar cardiovascular responses as those observed in the previous studies with a short rotating radius, suggesting that almost no effect of angular velocity acts on their responses. A weaker otolith input could possibly work on them. However a systematical observation can not recognize among the subjects for the vestibular effect on the cardiovascular responses. This fact of vestibular qualification leads us to speculate that it would depend on the subjects or other factors.

Neuronal responses to electrical stimulation at the horizontal ampulla (HA), vestibular nerve (at the windows) and corpus callosum (CC) were investigated in neurons in the anterior suprasylvian gyrus of the cat. The field potentials to HA stimulation had short latency: 2.9 +/- 0.3 (mean +/- SD) ms from the stimulus to the onset and 5.6 +/- 1.9 ms to the peak. The focus of the evoked potentials was located in the anterior suprasylvian (ASS) gyrus or near the ASS sulcus. HA stimulation activated 6 neurons out of 674 examined, with the mean latency of 4.3 +/- 1.1 ms. Of these 6, four neurons also responded to window stimulation. Fifty-six neurons responded to window stimulation with the mean latency of 6.1 +/- 2.4 ms. The mean latency for CC stimulation was 1.9 +/- 0.9 ms (n = 76). Four neurons responded to CC stimulation antidromically (mean = 0.9 +/- 0.3 ms) and one of them also responded orthodromically. The convergence of CC inputs in relation to HA or window stimulation was examined. One (17%) of the 6 HA-activated cells responded to CC stimulation, compared with 8 (14%) of the 56 neurons activated by window stimulation. The other 612 neurons did not respond to either HA or window stimulation, and 80 (13%) of the 612 responded to CC stimulation. Therefore, it is concluded that neurons in the ASS gyrus received callosal input equally irrespective of the presence or absence of responses to ampulla or window stimulation. WGA-HRP was injected in the ASS gyrus to identify the passing callosal fibers in the CC. Fibers from the ASS area passed at the rostral third of the CC. The present results indicate that the ASS area received vestibular projection with short latency, but responses of this projection did not seem to be very strong, at least from the present unit study, to HA stimulation. Discussion was made on the poor neuronal responses to electrical HA stimulation in comparison with previous studies. Also consideration was made on neuronal activity to CC stimulation.

Vestibulo-autonomic function was examined as the change of cardiac parameters (HR and SV) to +Gz and -Gx accelerations for 1,000 s in intact and bilaterally labyrinthectomized monkeys. Under anesthetized conditions, HR and SV slightly changed to +2Gz acceleration in both monkeys. In +3Gz acceleration, changes were remarkable and significant. HR increased in intact monkeys by as much as 30% while it decreased in labyrinthectomized monkeys, although a moderate initial increase was observed. SV decreased in intact as well as labyrinthectomized monkeys, but the reduction was significant and larger for the latter. This implies that vestibular input could modulate autonomic function. For larger +Gz, both intact and labyrinthectomized monkeys could tolerate no more due to severe cardiac dysfunction (rapid HR and SV decrease) which appeared soon after +4Gz application. In case of -Gx application, HR increased, although slightly, in proportion to the amplitude of applied -Gx in both monkeys, with less changes in labyrinthectomized ones. SV hardly changed in smaller -Gx, while it increased in larger -Gx. Difference between intact and labyrinthectomized monkeys was observed in -6Gx and -8Gx conditions.

Changes of ECG due to long and intense -Gz acceleration was investigated in anesthetized Syrian golden hamsters. The R-R interval decreased (heart rate increased) slightly at the very initial phase of steady -Gz load. However, the R-R interval increased during the rest of the whole steady -Gz period. The P-R interval increased with a smaller -Gz load (-4 and -6 Gz), but it decreased with a larger -Gz (-8 and -10 Gz). The size of the QRS complex was measured as R amplitude. It decreased in all -Gz conditions. Effects were a little different for smaller and larger -Gz, as was observed in the case of P-R changes. Pathological ECGs were frequently observed. They were: (1) Arrhythmia of heart rate with or without atrio-ventricular blocks. (2) Abnormal P wave; e.g., splitting, flattening, or abolition of P wave. (3) Alteration of the QRS complex in amplitude or contour. (4) Changes in ST-T components. In spite of all these changes, however, it should be noted that several Syrian golden hamsters could tolerate up to -10 Gz for as long as 1,000 s.

Alzheimer or Parkinson patients suffer from some memory deficits in the later course of their illness. It is also reported that MPTP-treated monkeys showed cognitive disturbances without Parkinsonian motor deficits.1 Therefore, it would be very helpful to determine the activity of memory-related structures in the normal brain for the development of more appropriate therapeutic or clinical treatments. In the present study, the 2-deoxy-d-glucose (2-DG) method2 was employed to reveal active sites in the brain while the monkey was performing a delayed response. This paradigm is known to test for short-term memory. The results have been already published in final form.3,4

During three different motor tasks of finger, wrist and arm movements on either side, 80 pyramidal tract neuron (PTN) activities were recorded in the monkey motor cortex. They were divided into three groups; PTNs related to controlateral movement (contra-PTNs), those related to ipsilateral movementt lateral movement (bilaterai-PTNs) and those related to ipsilateral movement (ipsi-PTNs). The latency histogram of the antidromic activation was similar for contra-PTNs as well as ipsi- and bilateral-PTNs in the fast PTN group, but most of slow PTNs appeared among contra-PTNs. Intracortical microstimulation (ICMS) was delivered to correlate muscular contraction with PTN acticity. Most of slow PTNs were related to proximal muscular contraction and PTNs related to proximal muscles appeared more in ipsi- and bilateral-PTNs than in contra-PTNs.

The neuronal activity in the motor cortex of the rhesus monkey was investigated in three different tasks performed with finger, wrist, and arm movements. A total of 125 neuronal activities were analysed. They were classified into five groups in terms of muscular contractions provoked by intracortical stimulation; neurons related to contractions of finger, wrist, elbow, shoulder, or trunk muscles. The neuronal activities in three tasks performed with finger, wrist, or arm movements were investigated for each group. Most of the neurons related to the contractions of elbow, shoulder, or trunk muscles were associated solely with arm movement. Smaller numbers of neuronal activities changed their firing frequencies in association with two or three tasks. Neurons related to the contractions of finger and wrist muscles showed various firing patterns in the three tasks; some responded to a single task with wrist or arm movement, while others changed their activities in association with more than one task. The presence of multi-task related neurons is discussed with respect to the multisegmental termination of corticospinal axons in the spinal cord.