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J B Kelly

Publications and source records attributed to J B Kelly.

At least 37 records · Page 2Linked to original sources
PubMed1996

Contribution of the dorsal nucleus of the lateral lemniscus to binaural responses in the inferior colliculus of the rat: interaural time delays.

The contribution of the dorsal nucleus of the lateral lemniscus (DNLL) to binaural responses in the inferior colliculus of the rat was determined for a wide range of interaural time differences (ITDs). Single-unit action potentials were recorded from the inferior colliculus before and after local injection of the excitatory amino acid antagonist kynurenic acid into the DNLL. Binaural properties were determined by manipulating the time difference between paired clicks delivered to the ears ipsilateral and contralateral to the recording site. The probability of an action potential decreased as contralateral stimulation was delayed, relative to ipsilateral stimulation. These data generated a sigmoidal ITD curve for delays between -1.0 and + 1.0 msec. By extending the time intervals beyond 1 msec, it was possible to determine the trailing edge of the inhibition produced by ipsilateral stimulation. The duration of the inhibitory effect varied from cell to cell but lasted as long as 20 msec in some cases. Injection of kynurenic acid into the DNLL contralateral to the recording site reduced the extent of both short (0-1 msec) and long-lasting (1-20 msec) inhibition in the inferior colliculus. No effect was seen after injections ipsilateral to the recording site. The data demonstrate that the DNLL plays an important role in shaping ITD responses in the inferior colliculus and contributes to both the short and long-lasting inhibition produced by stimulation of the ipsilateral ear.

Acoustic Stimulation↗
PubMed1996

Effects of bilateral auditory cortical lesions on gap-detection thresholds in the ferret (Mustela putorius).

Ferrets were tested for their ability to detect temporal gaps in noise before and after bilateral lesions of the primary auditory cortex. Thresholds for gap detection were determined first for normal animals with band-pass noises at various center frequencies (0.5 to 32 kHz) and at 8 kHz with various sound pressure levels (-10-70 dB). Gap-detection ability improved steadily as sound pressure increased up to 70 dB. No systematic relation was found between threshold and center frequency. To determine the effects of brain damage, ferrets were tested with 8-kHz band-pass noise at 70 dBSPL. After bilateral lesions of auditory cortex, ferrets were still capable of detecting gaps, but the mean threshold was elevated from 10.1 to 20.1 ms. The data demonstrate that auditory cortex is important for perceptual tasks requiring fine temporal resolution.

Animals↗
PubMed1996

Sound localization after kainic acid lesions of the dorsal nucleus of the lateral lemniscus in the albino rat.

The ability of rats to localize sounds in space was determined before and after kainic acid lesions of the dorsal nucleus of the lateral lemniscus (DNLL). The rats were trained to approach a 45-ms noise burst delivered from loudspeakers on the right or left of midline. Lesions were made by local injection of kainic acid into the DNLL. Rats with unilateral lesions of DNLL were impaired in their postoperative ability to localize a single noise burst. Rats with bilateral lesions also had deficits in postoperative performance, but the severity of the impairment was not substantially greater than that expected from a unilateral lesion. The mean pre- and postoperative minimum audible angles were 14.8 degrees and 40.4 degrees for rats with complete unilateral lesions and 13.5 degrees and 36.0 degrees for rats with bilateral lesions.

Acoustic Stimulation↗
PubMed1996

In vitro brain slice studies of the rat's dorsal nucleus of the lateral lemniscus. III. synaptic pharmacology.

1. The synaptic pharmacology of the dorsal nucleus of the lateral lemniscus (DNLL) of the rat was investigated in a brain slice preparation of the auditory midbrain. The brain slice was cut in the coronal plane and placed in a small recording chamber where warm, oxygenated saline was continuously perfused over and underneath the tissue. Intracellular recordings were made with glass microelectrodes filled with 4 M potassium acetate. Synaptic potentials were elicited by electrical stimulation of the lateral lemniscus or commissure of Probst and pharmacological effects were tested by bath application of amino acid agonists and antagonists. 2. The cells in DNLL were challenged with the excitatory amino acid (EAA) agonists, alpha-amino-3-hydroxy-5-methyl-4-isoxazole-propionic acid (AMPA), N-methyl-D-aspartic acid (NMDA) in 0 Mg2+, and L-glutamate. Each of these caused a depolarization of the cell membrane, a reduction in cell membrane resistance, and the onset of spontaneous firing. 3. Short-latency excitatory postsynaptic potentials (EPSPs) were evoked by stimulation of the lateral lemniscus in 77% of the neurons tested. The mean latency to initial depolarization was 0.9 ms. A single spike with relatively constant latency (mean 1.5 ms) was typically elicited when the strength of lemniscal stimulation was increased. A longer-latency EPSP (mean 2.9 ms) was seen in 34% of the neurons tested either with the slice in normal saline or after pharmacological block of the earlier, short-latency EPSP. The long-latency EPSP was followed by a single spike of multiple spikes with highly variable latencies (range 3.2-24 ms). In 28% of the neurons tested, both early and late EPSPs were observed in response to stimulation of a single location on the lateral lemniscus. 4. Stimulation of the commissure of Probst elicited short-latency EPSPs (mean 0.9 ms) in 37% of the neurons tested. Longer-latency EPSPs (mean 3.0 ms) were found in only 3% of the neurons in response to commissural stimulation. 5. The nonspecific EAA antagonist kynurenic acid blocked both short-and long-latency EPSPs evoked by either lemniscal or commissural stimulation. The non-NMDA antagonist 6-cyano-7-nitro-quinoxaline-2,3-dione (CNQX), at very low concentrations, blocked the short-latency EPSPs but had no effect on the longer-latency EPSPs. The short-latency EPSPs were unaffected by the NMDA antagonist D,L-2-amino-5-phosphonovaleric acid (APV). In contrast, the longer-latency EPSPs were blocked by APV, but never by CNQX. 6. DNLL neurons were affected by the inhibitory amino acid agonists gamma-aminobutyric acid (GABA) and glycine. The membrane resistance of the neurons was decreased by GABA and glycine in a solution of either normal or calcium-free saline in a concentration-dependent manner. 7. Inhibitory postsynaptic potentials (IPSPs) were elicited by stimulation of the lateral lemniscus in 53% of the neurons and the commissure of the Probst in 18% of the neurons tested. The mean latencies were 1.0 and 0.9 ms, respectively. The reversal potentials of the IPSPs were around -70 mV. 8. The IPSPs evoked by stimulation of the lateral lemniscus were blocked by the glycine receptor antagonist strychnine, but not by the GABA receptor antagonist bicuculline, whereas the IPSPs elicited by stimulation of the commissure of Probst were blocked by bicuculline but not strychnine.

6-Cyano-7-nitroquinoxaline-2,3-dione↗
PubMed1996

Potassium currents and membrane excitability of neurons in the rat's dorsal nucleus of the lateral lemniscus.

1. The contribution of voltage-activated outward potassium currents to membrane excitability of neurons in the rat's dorsal nucleus of the lateral lemniscus (DNLL) was studied in a brain slice preparation using whole cell patch-clamp and intracellular recordings. Voltage-clamp methods and pharmacological manipulations were used to examine the currents regulating membrane dynamics in DNLL. 2. A delayed sustained outward current was evoked by applying depolarizing voltage steps across the cell membrane from a holding potential of -50 mV. An additional transient outward current was evoked when the depolarizing steps were preceded by a hyperpolarizing prepulse of -110 or -120 mV. 3. The transient outward current peaked within 6.8 ms of the onset of a depolarizing pulse. It decayed with a time constant of 12.3 ms for a 60-mV depolarizing voltage shift. Half-inactivation of this current occurred at -81.3 mV. The time constant for removal of the inactivation was 17.4 ms. The transient current had a high sensitivity to 4-aminopyridine (4-AP). 4. The sustained current was activated more slowly and was more sensitive to tetraethylammonium (TEA) than the transient current. The sustained current had both Ca2+-dependent and Ca2+-independent components. The Ca2+-dependent portion emerged at potentials of about -35 mV and was activated fully at +10 mV. The Ca2+-independent component was activated at potentials more positive than -40 mV and increased in magnitude with further depolarization. Inactivation of the Ca2+-independent component was voltage dependent. Also, TEA suppressed the Ca2+-independent compound. 5. The transient current in DNLL neurons closely resembled the A current (IA) described for hippocampal and other neurons in both kinetics and pharmacology. The Ca2+-independent component of the sustained current resembled the K current (IK) described for other neurons in both its properties of activation and inactivation and its pharmacology. 6. The outward current of some DNLL neurons was found to contain a dendrotoxin-sensitive component. This component reached its peak at 6.8 ms and had voltage-sensitive time constants of decay of 25.5 and 8.5 ms with voltage steps of 40 and 60 mV, respectively. 7. Application of 4-AP and TEA markedly prolonged the spike width, abolished the fast component of the after hyperpolarization and depolarized the cell membrane. Also, the number of action potentials produced by positive current injection increased under the influence of 4-AP and TEA. Membrane excitability and spike repolarization were dependent on both 4-AP-sensitive transient and TEA-sensitive sustained currents. 8. Neurons in DNLL typically exhibit a steady discharge of action potentials in response to sustained membrane depolarization. The rate and temporal pattern of production of action potentials in these cells are determined by the combination of transient and sustained potassium channels.

Action Potentials↗
PubMed1996

Sound localization after transection of the commissure of Probst in the albino rat.

1. The ability of rats to localize sounds in space was determined before and after cutting of the commissure of Probst. The commissure of Probst was transected at its midline decussation with a microknife inserted into the brain according to stereotaxic coordinates. Six animals were tested after extensive lesions that destroyed all of the commissure of Probst fibers. An additional animal was tested after a smaller lesion that destroyed most of the commissure of Probst but left some fibers intact. Three control animals were tested before and after surgical intervention that did not involve the commissure of Probst. 2. The animals were tested in a semicircular apparatus with loudspeakers located on the right or left of midline. They were trained to make a response toward the left or right in the direction of the active loudspeaker. Correct reponses were rewarded by delivery of a small quantity of water from spouts located at +30 and -30 degrees azimuth. Tests of sound localization were conducted with a single broadband noise burst, 45 ms in duration, presented at the beginning of each trial. The position of the active loudspeakers was varied from trial to trial and performance at different speaker angles was calculated to determine psychometric curves. Minimum audible angles were estimated by interpolation from a performance level of 75% correct. 3. After postoperative testing was completed, the effectiveness of the lesions was confirmed by cell counts to determine the extent of retrograde degeneration in the dorsal nucleus of the lateral lemniscus (DNLL). These data showed that most of the contralaterally projecting neurons in DNLL underwent retrograde degeneration and the number of neurons was reduced by 60-65%. Ninety to 95% of the contralaterally projecting neurons in the DNLL disappeared within 7 wk after transection of the commissure of Probst. 4. The condition of damaged commissural fibers was further confirmed by tract tracing methods. A unilateral Fluoro-Gold injection was made into the inferior colliculus and the auditory brain stem was examined for retrograde label. No labeled neurons were seen in the contralateral DNLL in cases with complete transection of the commissure of Probst. In addition, the distribution of Fluoro-Gold labeling in other brain stem auditory structures was similar to that seen in normal animals. This result confirmed that the transection of the commissure of Probst was successful and that projections to other auditory structures remained intact. 5. Transection of the commissure of Probst produced marked deficits in midline sound localization. Although sound localization was still possible, there was a degradation in the ability of rats to localize sounds in the horizontal plane. The mean minimum audible angle was elevated 22.1 degrees after destruction of the commissure of Probst compared with a shift of only 2.0 degrees in control animals.

Animals↗
PubMed1995

Inhibition in the superior olivary complex: pharmacological evidence from mouse brain slice.

1. The effects of gamma-aminobutyric acid (GABA) and glycine and their respective antagonists were determined for neurons in the mouse superior olivary complex. Brain slices (400 microns) were cut in the frontal plane and maintained in an oxygenated saline solution for physiological recording. Recordings were made from neurons in the lateral superior olive (LSO) or medial nucleus of the trapezoid body (MNTB) with glass micropipettes filled with 4 M potassium acetate. 2. Ipsilateral and contralateral synaptic responses were elicited by applying current pulses to the trapezoid body through bipolar stimulating electrodes located at positions lateral and medial to the olivary complex. Both intracellular and extracellular recordings were studied before, during, and after application of drugs to the saline bath containing the tissue slice. 3. Intracellular recordings from 10 neurons in LSO showed that GABA (1-10 mM) caused a concentration-dependent drop in membrane resistance and either reduced or blocked postsynaptic excitatory responses. Similar effects were found in five cells tested with glycine (1-10 mM). Three neurons tested with both GABA and glycine were affected by both drugs. Extracellular spikes were blocked in 53 out of 67 LSO neurons tested with GABA and 29 out of 35 neurons tested with glycine. Seventeen out of 23 neurons tested with both GABA and glycine were affected by both. 4. GABA had a powerful blocking effect on extracellularly recorded action potentials evoked by current-pulse stimulation of the trapezoid body in seven LSO neurons tested after adding the glycine receptor antagonist, strychnine (1 microM), to the bath. GABA also lowered the membrane resistance of one LSO neuron in which intracellular recordings were made in the presence of strychnine. 5. Neurons in MNTB also were affected by GABA and glycine but the proportion of sensitive cells was less than in LSO. GABA reduced membrane resistance in 6 out of 16 neurons and glycine produced a similar effect in 14 out of 26 neurons from which intracellular recordings were made. Six out of 14 neurons tested with GABA and glycine responded to both. Extracellular spikes were eliminated or reduced in amplitude by GABA in 15 out of 44 cells and by glycine in 40 out of 68 cells tested. Eleven out of 29 cells from which extracellular recordings were made were affected by both. 6. The glycine antagonist, strychnine (0.25 - 1.0 muM), blocked both ipsilateral and contralateral inhibitory postsynaptic potentials (IPSPs) in LSO.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗
PubMed1995

In vitro brain slice studies of the rat's dorsal nucleus of the lateral lemniscus. I. Membrane and synaptic response properties.

1. We examined the physiological properties of neurons in the dorsal nucleus of the lateral lemniscus (DNLL) of the rat in a 400-microns tissue slice taken in the frontal plane through the auditory midbrain. The brain slice was placed in a small chamber and was perfused fully submerged in a warm, continuously circulating oxygenated saline solution. We made intracellular recordings with glass pipettes filled with 4 M potassium acetate. Synaptic potentials were evoked by electrical stimulation of either the lateral lemniscus or the commissure of Probst. 2. We tested the membrane characteristics of DNLL neurons by recording the electrical potentials produced by intracellular injection of positive or negative current. Typically, DNLL neurons had nearly linear current-voltage curves and responded to depolarizing currents with a sustained train of action potentials. Injection of intense or prolonged depolarizing currents frequently resulted in a pronounced afterhyperpolarization of the cell membrane. Intense hyperpolarizing currents were often followed by a large rebound depolarization. 3. The action potentials of most DNLL neurons were characterized by a double undershoot, i.e., the initial hyperpolarization after a spike was followed by a second, longer-latency hyperpolarization. Seventy-nine percent of the cells recorded had this type of double undershoot. The remaining cells had a single undershoot in which the postspike hyperpolarization was followed by a steady return to resting potential without any indication of a second phase of hyperpolarization. 4. Electrical stimulation of the lateral lemniscus evoked both excitatory postsynaptic potentials (EPSPs) and inhibitory postsynaptic potentials (IPSPs) in DNLL. The EPSPs were evoked alone without any evidence of an IPSP in 67% of neurons and IPSPs were evoked alone in 6% of the neurons from which recordings were made. In 27% of the recordings both EPSPs and IPSPs were elicited in the same neuron by stimulation of a single location on the lateral lemniscus. 5. The combined EPSPs and IPSPs produced by lemniscal stimulation could often be dissociated by their different thresholds and/or different response latencies. For 35% of the neurons in which both an EPSP and IPSP were present, the IPSP had a lower threshold; for 23% of the cells, the EPSP had a lower threshold. For the remaining cells the thresholds for producing an EPSP and IPSP were the same. 6. DNLL neurons were capable of responding with great fidelity to a single pulse of stimulation delivered to the lateral lemniscus, i.e., an action potential was evoked after every stimulus.(ABSTRACT TRUNCATED AT 400 WORDS)

Action Potentials↗
PubMed1995

In vitro brain slice studies of the rat's dorsal nucleus of the lateral lemniscus. II. Physiological properties of biocytin-labeled neurons.

1. We made intracellular recordings from neurons in rat dorsal nucleus of the lateral lemniscus (DNLL), determined intrinsic and synaptic physiological properties, and labeled the cells by intracellular injection of biocytin. Biocytin-labeled neurons were reconstructed and classified according to their somatic and dendritic morphology. 2. We identified a diversity of morphological cell types in DNLL. Five main groups of neurons were recognized: multipolar; elongate I, II, and III; and round. The multipolar cells were characterized by several large dendrites with multiple branches that spread over large areas within the DNLL. The dendrites radiated equally in all directions. 3. Elongate cells were characterized by extended cell bodies with polar dendrites. In the case of elongate I and II cells, the dendrites were preferentially oriented in the horizontal plane and the dendritic branches extended across most of the cytoarchitectonic breadth of DNLL from the medial to lateral borders. The classification of elongate II was reserved for a single neuron with profuse dendritic branching that fanned out dorsoventrally along the margins of DNLL. This neuron was unique in our sample and was distinguished from the more common elongate I cells, which had less profuse dorsoventral dendritic branching. Elongate III cells had extended cell bodies, but their dendrites did not extend across the DNLL and showed no preferential orientation. 4. Round neurons had relatively small, round cell bodies and radial dendrites that extended over large areas within DNLL. These cells were quite common in our sample and are almost certainly not the same as the infrequently encountered small round cells found in Nissl-stained sections. Some biocytin-labeled neurons were difficult to classify as either multipolar, elongate I, II, or III, or round. These neurons had properties that most closely resembled elongate III cells, but they were treated separately here to minimize heterogeneity within morphological categories. 5. The intrinsic physiological properties measured in this study were uncorrelated with the morphological class of DNLL neurons. All DNLL neurons had similar current-voltage curves regardless of their anatomic category. Intracellular injection of positive current produced a sustained series of action potentials, the number of which was related to the magnitude of current injection. The interspike intervals were regular, although some cells had a tendency toward an increase or decrease in the length of the interval with prolonged current injection. The interspike intervals were regular, although some cells had a tendency toward an increase or decrease in the length of the interval with prolonged current injection. Injection of negative current produced a hyperpolarization that was proportional to the current strength.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗
PubMed1994

Three-dimensional reconstructions of autonomic projections to the gastrointestinal tract.

Three-dimensional reconstruction protocols in confocal microscopy are typically considered in terms of rendering separate stacks of optical sections. Single stacks, however, include volumes that are often too small to permit descriptions of entire neurons, complete axonal arbors, or complex neural networks. Furthermore, traditional tissue preparation protocols generally yield specimens too limited to permit reconstructions of complex neural systems. For 3-D analyses of extensive networks such as the autonomic nervous system projections within the viscera, it is critical to incorporate appropriate tissue techniques, including suitable tracer protocols, into the reconstruction strategy. This report summarizes complementary technologies, including whole mount procedures, tracer techniques for identifying single fibers in situ, and methods of examining stacks of optical images, which make it practical to describe the complete terminal field of an individual axon in the gastrointestinal tract. Such methods establish that vagal motor axons travel long distances within their target organs, collateralize frequently, and ramify extensively. Vagal afferents have extensive, complex, and, in some cases, polytopic arbors within target tissues.

Animals↗
PubMed1994

Physiological evidence for ipsilateral inhibition in the lateral superior olive: synaptic responses in mouse brain slice.

The incidence of ipsilateral inhibition in the lateral superior olive (LSO) was examined in a brain slice preparation of the mouse superior olivary complex. A 400 microns brain slice was taken in the frontal plane and maintained in a warm, oxygenated saline solution. Intracellular recordings were made from the LSO with micropipettes filled with 4 M potassium acetate. Synaptic responses were elicited by electrical stimulation of the trapezoid body in different slices at various locations between the cochlear nucleus and the ipsilateral superior olivary complex (SOC). The results show that ipsilateral stimulation can evoke inhibitory as well as excitatory postsynaptic potentials. The ipsilateral IPSPs have short latencies and are elicited by stimulation of the trapezoid body at any point along its course between cochlear nucleus and LSO. Short-latency IPSPs can also be produced by direct stimulation of the ventral cochlear nucleus itself. Ipsilateral IPSPs are blocked by low concentrations of the glycine antagonist, strychnine. In addition, bath application of sodium pentobarbital in one case eliminated ipsilateral IPSPs without eliminating EPSPs. The results suggest that there is a rapidly conducting, glycinergic pathway from cochlear nucleus through the trapezoid body to the LSO on the same side of the brain. This pathway is probably served by either a direct projection from the ventral cochlear nucleus to the LSO or an indirect one from cochlear nucleus to LSO through the lateral nucleus of the trapezoid body (LNTB).

Action Potentials↗
PubMed1994

Sound localization after unilateral lesions of inferior colliculus in the ferret (Mustela putorius).

1. The ability of ferrets to localize sounds in space was determined before and after large unilateral lesions of the inferior colliculus. Three animals sustained restricted lesions that destroyed the inferior colliculus caudally but spared some tissue rostrally. These restricted lesions did not extend substantially beyond the cytoarchitectonic boundaries of the inferior colliculus. Four animals received more extensive lesions that destroyed all of the inferior colliculus, including the rostral pole. These lesions also involved to various degrees other midbrain structures, including the dorsal nucleus of the lateral lemniscus and the lateral tegmentum. Psychophysical curves and minimum audible angles were obtained for midline and left and right lateral fields. Comparisons were made of deficits ipsilateral and contralateral to the lesion. 2. The animals were tested in a semicircular apparatus with loudspeakers located at various positions around the periphery. Separate sound localization tests were conducted for midline, left, and right field positions. In each test the animals were trained first to discriminate between speakers separated by 60 degrees. They were then tested with progressively smaller angles of speaker separation to obtain their psychophysical threshold (minimum audible angle). All critical tests of sound localization were based on the ability of animals to identify the location of a 45-ms noise burst presented at the beginning of each trial. Correct responses were rewarded by delivery of a small quantity of water from spouts located around the perimeter of the apparatus. 3. Unilateral lesions restricted to the inferior colliculus had relatively little effect on sound localization. All three animals with restricted lesions were still capable of localizing a single noise burst and minimum audible angles were similar before and after surgery for midline, left, and right field tests. There was no difference in postoperative performance ipsilateral and contralateral to the lesion site. 4. More extensive unilateral lesions that included the dorsal nucleus of the lateral lemniscus and the lateral tegmentum as well as the inferior colliculus resulted in severe deficits in sound localization. Each of the four animals with large unilateral lesions had a substantial impairment in sound localization in the field contralateral to the lesion site. Postoperative performance in the contralateral field was too low to obtain a minimum audible angle for these animals. Midline sound localization was also affected in some cases but ipsilateral sound localization was only slightly affected.

Animals↗
PubMed1994

Binaural organization of primary auditory cortex in the ferret (Mustela putorius).

1. The distribution of binaural responses within the ferret's primary auditory cortex was determined by standard microelectrode mapping techniques. Single and multiple unit responses were recorded from the middle ectosylvian gyrus of barbiturate-anesthetized animals with tungsten microelectrodes (1.2-1.8 M omega) inserted into the brain perpendicular to the cortical surface. The characteristic frequency (CF) and binaural response characteristics were determined for each point sampled. 2. Gated pure tones were delivered independently to the two ears through a sealed sound system, and binaural response types were determined by comparison of evoked activity for monaural and binaural stimulation. Most binaural responses fell into one of three major groups: binaural summation (EE/F), binaural suppression (EO/I), or mixed binaural summation and suppression. 3. The neurons tended to be grouped together on the basis of their binaural response properties. Zones of binaural summation and suppression extended across the surface of the middle ectosylvian gyrus and intersected with regions of sound frequency representation. 4. Particular attention was paid to the distribution of binaural responses within isofrequency contours in the ferret's primary auditory cortex (AI). Along the length of each isofrequency contour, areas of EE/F alternated with areas of EO/I. The summation areas were typically between 0.5 and 0.7 mm wide. Single neurons with mixed binaural response properties were frequently found between groups of EE/F and EO/I cells. The mixed responses appeared to mark a transition in location between zones of summation and suppression responses. 5. The distribution of interaural intensity difference (IID) thresholds was also examined along the length of isofrequency contours. No systematic relation was found between IID threshold and the distance along an isofrequency contour.

Animals↗
PubMed1994

The determination of child custody.

This article reviews briefly the history of child custody decision making and describes current custodial arrangements in the United States. It examines both the manner in which parents and courts make decisions regarding custody and access, and the changes in visiting patterns in recent decades. The author discusses the impact of reforms in the law and the implementation of newer dispute resolution and educational interventions, and then makes recommendations for policy and practice.

Child↗
PubMed1993

Effects of superior olivary complex lesions on binaural responses in rat auditory cortex.

Unilateral or bilateral lesions of the superior olivary complex (SOC) were made by local injection of kainic acid through a micropipette lowered stereotaxically into the rat's auditory brain stem. The lesions had the effect of destroying cell bodies in the superior olive without disrupting fibers of passage. After a recovery period of approximately one month physiological recordings were made with tungsten microelectrodes from the auditory cortex of normal animals and animals with SOC lesions. For animals with unilateral SOC lesions recordings were made either ipsilateral or contralateral to the site of damage. Monaural and binaural tone bursts (110 ms duration) were presented dichotically through a sealed sound delivery system and binaural interaction patterns were determined by comparison of monaural and binaural responses. Some cells were excited by stimulation of either ear and facilitated by binaural stimulation (binaural summation or EE cells), whereas others were excited by contralateral stimulation and inhibited by simultaneous ipsilateral stimulation (binaural suppression or EI cells). Both binaural summation and suppression responses were still present following unilateral SOC lesions. Interaural intensity difference thresholds were within the normal range and no differences were found between animals with lesions placed ipsilateral or contralateral to the recording site. Following a bilateral lesion in one case, both binaural summation and suppression responses were still present. The bilateral lesion had the effect of shifting the average interaural intensity difference thresholds in favor of the contralateral ear. These data suggest that binaural interactions above the level of the superior olive contribute to physiological responses in auditory cortex and that binaural responses in the rat's auditory cortex are shaped by both olivary and supraolivary interactions.

Animals↗
PubMed1993

Response of neurons in the lateral superior olive and medial nucleus of the trapezoid body to repetitive stimulation: intracellular and extracellular recordings from mouse brain slice.

The responses of neurons in the lateral superior olive (LSO) and medial nucleus of the trapezoid body (MNTB) to repeated electrical stimulation of the trapezoid body were investigated in a brain slice preparation of the mouse superior olivary complex. Brain slices, 400-500 microns thick, were cut in the frontal plane and were maintained for physiological recording in a bath of warm, oxygenated saline. Both intracellular and extracellular recordings were made with glass micropipettes filled with 4 M potassium acetate. Bipolar stimulating electrodes were placed on the trapezoid body ipsilateral and contralateral to the superior olive. Current levels were set so that an ipsilateral pulse elicited a single action potential in LSO and a contralateral pulse elicited a single action potential in MNTB. Trapezoid body fibers were then stimulated with trains consisting of 10 current pulses. Repeated stimulation at low rates resulted in a number of spikes equal to the number of current pulses. Pulse rate was then increased to determine the limits of response to repeated stimulation. In the MNTB, neurons were capable of following very high rates of stimulation without reduction in response probability. On the average, MNTB neurons responded with a probability of 0.9 at 667 Hz. In contrast, most LSO neurons were incapable of following high rates of stimulation. LSO neurons responded with a probability of 0.9 at 125 Hz. For some LSO neurons, application of strychnine (0.5 microM) to the bath increased the probability of firing at high rates. MNTB neurons were unaffected by strychnine.

Acoustic Stimulation↗
PubMed1992

Effects of superior olivary complex lesions on binaural responses in rat inferior colliculus.

Unilateral or bilateral lesions of the superior olivary complex (SOC) were made by local injection of kainic acid through a micropipette lowered stereotaxically into the rat's auditory brainstem. The lesions had the effect of destroying cell bodies in the superior olive without disrupting fibers of passage. After a recovery period of approximately one month, physiological recordings were made with tungsten micro-electrodes from the central nucleus of the inferior colliculus of animals with SOC lesions. For animals with unilateral lesions recordings were made either ipsilateral or contralateral to the site of damage. Results were compared with data from normal control cases. Monaural and binaural tone bursts were presented through a sealed sound delivery system and binaural interaction patterns were determined. Both binaural summation and suppression responses were still present following unilateral SOC lesions. Interaural intensity difference thresholds were within the normal range and no differences were found between animals with lesions placed ipsilateral or contralateral to the recording site. Binaural summation and suppression responses were also present following bilateral lesions. Bilateral lesions had the effect of shifting the average interaural intensity difference thresholds in favor of the contralateral ear. But, in general, binaural interactions were remarkably little affected by bilateral destruction of the SOC.

Acoustic Stimulation↗