Anatomical Projections Research Articles

Influence of nucleus tractus solitarius stimulation and baroreceptor activation on rat parabrachial neurons

The parabrachial nucleus (PBN) within the dorsolateral pons is a major recipient of autonomic-related inputs from more caudal levels of the brainstem and in particular, the nucleus of the solitary tract (NTS). Although the anatomical projections from the NTS to the PBN are well characterized, less is known concerning the influence of activating NTS efferents on PBN neurons and the response of the latter to cardiovascular-related inputs. The present study examined the response of PBN neurons to electrical stimulation of the depressor area within the NTS in urethane anesthetized rats, and subsequently, the influence of arterial baroreceptor activation and systemic angiotensin II (ANC II) on these cells. Extracellular single-unit PBN recordings indicated that 92 of 227 (40.5%) cells were orthodromically excited and 35 of 227 (15.4%) inhibited consequent to NTS stimulation. Ten (4.5%) PBN cells displayed antidromic activation from the NTS. Of 41 of 119 neurons responding to both NTS stimulation and baroreceptor activation, 29.3% revealed a excitatory and 31.7% an inhibitory response to the two stimuli. Fifteen PBN cells responded to NTS stimulation, baroreceptor activation, and the administration of systemic ANG II, with six cells displaying either an excitatory or inhibitory response to all three stimuli. These observations provide electrophysiological support for reciprocal connections between the NTS and PBN and indicate the presence of both excitatory and inhibitory projections to the pontine nucleus. A population of neurons influenced by activation of NTS efferents also reveal a similarity of responses to inputs originating from peripheral arterial baroreceptors and systemic ANG II.

Anatomic and machine projection angles of various radiographic imaging systems used for cardiac angiography

Quantitation of coronary artery dimensions in serial angiographic studies requires an awareness of the variety, complexity, and implications of radiographic imaging equipment used for coronary arteriography. Recognition of the geometric complexities inherent in angiographic imaging systems is important in understanding complex image rotations and ensuring identity of projections when serial comparison is desired. Tables, figures, and formulae are provided to permit translation of machine angles into patient reference angles and vice versa.

Efferent pathway of the amygdala involved in conditioned fear as measured with the fear-potentiated startle paradigm.

Fear-potentiated startle in the rat is a measure of conditioned fear that is blocked by lesions of the central nucleus of the amygdala. In a companion study, Rosen, Hitchcock, Sananes, Miserendino, and Davis (1991) demonstrated a direct anatomical projection from the central nucleus to the brainstem startle reflex circuit. In the present study, fear-potentiated startle was blocked by lesions that interrupted this pathway at 3 different levels or by a crossed lesion that interrupted the pathway at its source on one side and at a more caudal level on the other side. Although synaptic relays have not been ruled out entirely, the data suggest that the direct projection from the central nucleus of the amygdala to the startle circuit mediates the expression of fear-potentiated startle. These findings are consistent with the literature indicating that efferent projections from the central nucleus to various brainstem structures are involved in the expression of several conditioned fear responses.

A circuit for detection of interaural time differences in the brain stem of the barn owl

Detection of interaural time differences underlies azimuthal sound localization in the barn owl Tyto alba. Axons of the cochlear nucleus magnocellularis, and their targets in the binaural nucleus laminaris, form the circuit responsible for encoding these interaural time differences. The nucleus laminaris receives bilateral inputs from the cochlear nucleus magnocellularis such that axons from the ipsilateral cochlear nucleus enter the nucleus laminaris dorsally, while contralateral axons enter from the ventral side. This interdigitating projection to the nucleus laminaris is tonotopic, and the afferents are both sharply tuned and matched in frequency to the neighboring afferents. Recordings of phase-locked spikes in the afferents show an orderly change in the arrival time of the spikes as a function of distance from the point of their entry into the nucleus laminaris. The same range of conduction time (160 mu sec) was found over the 700-mu m depth of the nucleus laminaris for all frequencies examined (4-7.5 kHz) and corresponds to the range of interaural time differences available to the barn owl. The estimated conduction velocity in the axons is low (3-5 m/sec) and may be regulated by short internodal distances (60 mu m) within the nucleus laminaris. Neurons of the nucleus laminaris have large somata and very short dendrites. These cells are frequency selective and phase-lock to both monaural and binaural stimuli. The arrival time of phase-locked spikes in many of these neurons differs between the ipsilateral and contralateral inputs. When this disparity is nullified by imposition of an appropriate interaural time difference, the neurons respond maximally. The number of spikes elicited in response to a favorable interaural time difference is roughly double that elicited by a monaural stimulus. Spike counts for unfavorable interaural time differences fall well below monaural response levels. These findings indicate that the magnocellular afferents work as delay lines, and the laminaris neurons work as co-incidence detectors. The orderly distribution of conduction times, the predictability of favorable interaural time differences from monaural phase responses, and the pattern of the anatomical projection from the nucleus laminaris to the central nucleus of the inferior colliculus suggest that interaural time differences and their phase equivalents are mapped in each frequency band along the dorsoventral axis of the nucleus laminaris.

Delayed, frequency-specific inhibition in the cochlear nuclei of mice: a mechanism for monaural echo suppression

To understand how auditory information is processed in the cochlear nuclei, it is crucial to know what circuitry exists and how it functions. Previous anatomical experiments have shown that neurons in the deep layer of the dorsal cochlear nucleus (DCN) project topographically to the anteroventral cochlear nucleus (AVCN) (Wickesberg and Oertel, 1988). Because interneurons in the DCN and their targets in AVCN are excited by the same group of auditory nerve fibers, the projection is frequency-specific. Here we report that microinjections of glutamate in the DCN evoke trains of IPSPs in individual, impaled AVCN neurons in brain slices of the cochlear nuclear complex. Only injections along a rostrocaudal band in the DCN, matching the anatomical projection of tuberculoventral neurons, evoke IPSPs; elsewhere, there were no responses to the glutamate. The inhibition is blocked by 0.5 microM strychnine. Both bushy and stellate cells are targets of the inhibitory projection. Inhibition in the AVCN is delayed by an additional synaptic delay with respect to the excitation. Delayed, frequency-specific inhibition allows the first wavefront to be transmitted to higher auditory centers by bushy and stellate cells, while following inputs encoding signals of similar frequencies are attenuated at least for the duration of an IPSP. These findings are consistent with results from psychoacoustic experiments and suggest that this circuit provides a source of monaural echo suppression.

Respiratory activity in retrotrapezoid nucleus in cat

An anatomic projection from the retrotrapezoid nucleus to the ventral respiratory group in cat was previously reported by our laboratory (J. C. Smith, D. E. Morrison, H. H. Ellenberger, M. R. Otto, and J. L. Feldman. J. Comp. Neurol. 281: 69-96, 1989). We now report on the properties of neurons in the retrotrapezoid nucleus, investigated with extracellular recording techniques in 10 chloralose-urethane anesthetized, paralyzed, mechanically ventilated cats. A ventral exposure of the medulla facilitated recording from neurons in the retrotrapezoid nucleus, located ventral to the facial nucleus near the medullary surface. Respiratory-modulated, as well as irregularly discharging, spontaneous unit activity was recorded within the retrotrapezoid nucleus. Twelve respiratory-modulated units in the retrotrapezoid nucleus exhibited inspiratory (8 units), expiratory (3 units), or multimodal (1 unit) discharge patterns. Chemical activation of an inspiratory unit in the retrotrapezoid nucleus by pressure ejection of DL-homocysteic acid (less than 0.5 nl of 10 mM solution) demonstrated that the respiratory-modulated activity originated from the cell soma and not fibers of passage coursing through the retrotrapezoid nucleus region. Electrical microstimulation (20-40 microA, approximately 70-microseconds duration, biphasic pulse) within the ipsilateral ventral respiratory group elicited antidromic activation of 7 units in the retrotrapezoid nucleus, three of which were not spontaneously active. Electrical stimulation (5-80 microA, 70-microseconds pulse width, 100 Hz, 400- to 500-ms trains) at sites within retrotrapezoid nucleus affected the respiratory motor output when delivered during late expiration, eliciting premature onset of inspiration. These results suggest that retrotrapezoid nucleus projections to the ventral respiratory group (and dorsal respiratory group) may influence respiratory timing and pattern, perhaps by conveying signals originating in the rostral ventrolateral medulla that result from ventral surface perturbations.

The projection from medial geniculate to field AI in cat: organization in the isofrequency dimension

The topography of the anatomical projection from isofrequency contours (IFCs) in auditory thalamus to IFCs in primary auditory cortex (field AI) was investigated in the cat. In each experiment, a best-frequency map of AI was obtained with electrophysiological recording techniques. Then, different retrogradely transported tracers (HRP, fluorescent dyes) were introduced into AI. In some experiments, different parts (e.g., dorsal, central, and ventral) of a previously mapped IFC were injected, each part with a different tracer. In other experiments, 2 or 3 rows of tracer injections were made at different dorsoventral levels of AI, over a large frequency range (5-38 kHz); each injection row was oriented orthogonal to the IFCs and contained a different tracer. The main mass of the labeled thalamic cells was found in the ventral nucleus of the medial geniculate body (MGv). The MGv cells projecting to a limited sector (1-2 mm in length in most experiments) of an IFC in AI form one or several densely packed neuron clusters of variable shape. The cells labeled by a given tracer are largely separated in space from cells labeled by a different tracer. Thus, different sectors of a cortical IFC receive input from different portions of the corresponding thalamic IFC. As a general rule, cells labeled from dorsal (ventral) injections are centered rostrally (caudally) in the part of MGv innervating AI. However, the topographic details are variable between individuals, and the rostrocaudal gradient is complicated by numerous irregularities and gradients. Previous studies of the auditory thalamocortical projection in the cat have not recognized the topographic order in the isofrequency dimension. Instead, it was believed that different sectors of a cortical IFC were innervated by coincident thalamic populations.

Response Characteristics of Four Wide-Field Motion-Sensitive Descending Interneurones IN Apis Melufera

ABSTRACT The anatomical projections and directional tuning of four descending interneurones sensitive to wide-field motion over the compound eyes are described. The cells are slow to adapt, resistant to habituation and their responses are dependent on the contrast frequency of the periodic patterns used as stimuli. Two of the cells (DNIV2 and DNIV4) are maximally stimulated by movement around the longitudinal axis of the bee (simulated roll), one (DNII2) by movement around the horizontal axis (simulated pitch) and one (DNVI1) by movement around the vertical axis (simulated yaw). The cells are binocular, their directional response being shaped by the interaction of the inputs from each eye. The cells which respond predominantly to roll (DNIV2 and DNIV4) have their arborizations restricted to the ipsilateral side of the brain and thoracic ganglia, i.e. the side which contains the cell soma. The cell responding to pitch (DNII2) has its arborizations distributed bilaterally, invading similar regions of the neuropile in both sides of the brain and thoracic ganglia. The cell which responds to yaw (DNVI1) has its major dendritic field in the ipsilateral side of the brain and descends into the thoracic ganglia in the contralateral side. The majority of its arborizations in the thoracic ganglia are confined to the contralateral neuropile.

Auditory cortical projection from the anterior ectosylvian sulcus (Field AES) to the superior colliculus in the cat: an anatomical and electrophysiological study.

Sensory activity in the deep layers of the superior colliculus (SC) is strongly influenced by descending cortical inputs. Elimination (permanent or reversible) of specific regions of visual or somatosensory cortex, known to have direct access to the SC, abolishes or dramatically reduces SC responses to stimuli from those modalities. While many SC neurons are also responsive to auditory cues, the origin of auditory corticotectal connections is not clear at present and their affect on activity in the SC is unknown. Therefore, the present study was undertaken to determine the origin, organization, and functional characteristics of auditory corticotectal projections. Of the auditory cortices (AI; AII; Fields A, P, and VP), only the auditory subregion of the banks of the anterior ectosylvian sulcus (Field AES) showed a robust anatomical projection to the SC. These data were confirmed physiologically: auditory neurons in Field AES projected to the SC and auditory SC neurons responded to stimulation of the Field AES. However, neither anatomical nor physiological techniques revealed a clear topographic relationship between the Field AES and the SC but suggested instead a diffuse and extremely divergent/convergent projection. Stimulation and cryoblockade of Field AES demonstrated the excitatory nature of this corticotectal pathway, whose influence was most evident on SC responses to stimuli of reduced intensity. Given the short latency of this ear-cortex-SC circuit and its excitatory influence on unimodal as well as on multisensory auditory neurons, it seems likely that Field AES plays a significant role in facilitating SC responses to auditory stimuli.

Nucleus cuneiformis and pain modulation: anatomy and behavioral pharmacology

The anatomical substrate and behavioral pharmacology of stimulation-produced analgesia resulting from electrical stimulation of the pontomesencephalic nucleus cuneiformis (NCF) was determined in the present study. Maximum increase in nociceptive tail-flick latencies following NCF stimulation occurred during the first 5 min post stimulation and decreased afterwards. The increased reflex latency could be attenuated by prior treatment with the narcotic antagonist, naloxone or the cholinergic antagonist, scopolamine. The anatomical projections of NCF were identified in autoradiographic and histochemical studies. Ipsilateral fibers coursed caudal from the NCF injection site through the ventral pontine reticular formation to innervate nucleus raphe magnus and the ipsilateral nucleus magnocellularis. At rostral medullary levels fibers coursed dorsolateral to innervate the ipsilateral nucleus reticularis parvocellularis. Descending contralateral fibers crossed through the decussation of the superior cerebellar peduncle, then coursed ventrolaterally projecting to the contralateral nucleus magnocellularis. Two primary groups of ascending fibers were observed. The dorsally located group ascended through the central tegmental tract projecting to the dorsal raphe, ipsilateral periaqueductal gray, nucleus parafascicularis and centromedianus, the intermediolateral and lateral thalamic nuclei. The ventrolateral from the injection site projecting to the substantia nigra, zona compacta, ventral tegmental area of Tsai, zona incerta, Fields of Forel, lateral hypothalamic nucleus and nucleus reuniens. These anatomic and behavioral data suggest that NCF plays an important role in sensory/motor integration relevant to pain transmission.

Functional metabolic mapping during forelimb movement in rat. I. Stimulation of motor cortex

The quantitative 14C-deoxyglucose (DG) autoradiographic technique has been used to study changes in cerebral metabolism during forelimb movements induced by graded stimulation of motor cortex. Experiments were directed at studying basic physiologic and anatomic aspects of the metabolic changes. Single shocks caused movement without metabolic change, whereas low-frequency trains caused seizures. Repetitive high-frequency train stimuli of short duration (500 Hz for 20 msec) caused jerk movements coupled with DG uptake in pathways. With stimulation of the forelimb motor zone at frequencies of 15-30/min there was prominent activation of cortical columns and strips in ipsilateral SI, SII, and MII, and contralateral MI and SI. Higher frequencies (120/min) were required to cause significant changes in DG in subcortical circuits. The most prominent changes occurred within a longitudinal corridor in dorsal thalamus and a ventral corridor in second-order sites in basal ganglia. Metabolic activation also occurred in contralateral cerebellum, the cuneate nucleus, and dorsal horn of the cervical spinal cord. Changes in these latter two sites were largely eliminated by removing feedback sensory activity. Stimulation of the forelimb sensory zone activated different sites in caudatoputamen and thalamus but similar zones in midbrain and cerebellum. The magnitude of the metabolic response in distant sites depended on the frequency of cortical stimulation. Different frequency-response relationships in different sites seemed to reflect the nature of the cortical input as well as differential effects of anesthesia. The pattern of the metabolic response was studied by comparing sites of activation with sites of the anatomic projections from motor and sensory cortical zones. 3H- and 14C-labeled amino acids were used to map the site and relative strength of pathways. Results revealed good correlation between the site of anatomic projection and the site of DG uptake but no consistent relationship between the relative strength of a projection and the magnitude of metabolic change within its field. Changes in glucose utilization with metabolic mapping experiments depend on the nature, strength, and frequency of stimulation; the site and nature of anatomic projection; the effects of anesthesia; and the strength of sensory feedback associated with the induced behavior.

Modulatory influences of red nucleus stimulation on the somatosensory responses of cat trigeminal subnucleus oralis neurons

Little is known of the effect of red nucleus (RN) stimulation on somatosensory neurons despite its known anatomic projections to somatosensory relay nuclei. The effect of RN stimulation on the somatosensory responses of trigeminal subnucleus oralis (Vo) neurons was investigated in chloralose- or barbiturate-anesthetized cats. Arrays of bipolar stimulating electrodes were inserted into the contralateral and ipsilateral RN and the contralateral thalamus. Extracellular single-unit recordings were obtained in Vo with tungsten microelectrodes. Neurons in Vo were excited to just suprathreshold by electrical stimulation within their receptive fields. Red nucleus influences were studied by applying 100-ms, 500-Hz conditioning trains to the contralateral or ipsilateral RN 130 ms prior to the peripheral test stimulus. The effect of RN stimulation was also tested on mechanically evoked responses of Vo cells. The somatosensory responses of most cells ( 70 73 ) were inhibited after RN stimulation. Some of these cells ( 15 70 ) could be antidromically activated from the contralateral thalamus. Stimulation of the RN resulted in excitation followed by inhibition in nine Vo cells. The results suggest that the RN may modulate transmission of somatosensory information through Vo.

The development of the nucleus isthmi in Xenopus laevis. I. Cell genesis and the formation of connections with the tectum.

The nucleus isthmi (NI) of the amphibian relays visual input from one tectum to the other tectum and thus brings a visual map from the eye to the ipsilateral tectum. This isthmotectal visual map develops slowly; it is first detected electrophysiologically at stages 60-62, the age at which the eyes begin their dorsalward migration and the region of binocular overlap beings to increase in extent. During this critical period of life, normal binocular visual input is required for establishment of normal topographic isthmotectal projections. In this study, we have used anatomical methods to trace cell birth, cell death, and formation of connections by the nucleus isthmi during the critical period. Tritiated thymidine labelling demonstrates that cells in the nucleus isthmi are generated throughout most of tadpole life (stages 29-62). Most cells conform to an orderly ventrodorsal gradient starting from stage 29 and extending to stages 56; later cells are inserted at apparently random locations in the nucleus. We have re-examined the hypothesis of Tay and Straznicky ('80) that the order of cell genesis in the NI and tectum could help establish proper isthmotectal connections, and we find that a timing mechanisms does not explain the two-dimensional topography of the isthmotectal map but that timing may aid in proper mediolateral positioning of isthmotectal axons at the points where they first enter the tectum. Horseradish peroxidase labelling was used to investigate whether anatomical projections from tectum to NI and from NI to tectum are present prior to the onset of eye migration. The results show that there are tectoisthmotectal projections by stage 52. Moreover, isthmotectal axons grow into as yet monocular tectal regions prior to the onset of eye migration. At stage 60, when binocular overlap begins, isthmotectal axons are visible throughout the tectum but are densely branched only at the rostral tectal margin, the location where they are predicted to occur on the basis of electrophysiological maps.

Neurogenesis in the olfactory tubercle and islands of Calleja in the rat

Neurogenesis in the rat olfactory tubercle and islands of Calleja was examined with [3H]thymidine autoradiography. Animals in the prenatal groups were the offspring of pregnant females given an injection of [3H]thymidine on two consecutive gestational days. Ten groups of embryos (E) were exposed to [3H]thymidine on E12–E13, E13–E14 4 E21–E22, respectively. Three groups of postnatal animals (P) were given four consecutive injections of [3H]thymidine on P0–P3, P2–P5, and P4–P7, respectively. On P60, the percentage of labeled cells and the proportion of cells originating during either 24 or 48 h periods were quantified at several anatomical levels. Three populations of neurons were studied: 1.(1) large cells in layer III2.(2) small to medium-sized cells in layers II and III, and in the striatal bridges3.(3) granule cells in the islands of Calleja. Neurogenesis is sequential between these three populations with No. 1 oldest and No. 3 youngest. The large neurons in layer III originate mainly between E13 and E16 in a strong lateral-to-medial gradient. Neurons in population No. 2 are generated between E15 and E20, also in a lateral-to-medial gradient; neurogenesis is simultaneous along the superficialdeep plane. Granule cells in the smaller islands of Calleja are generated between E17 and E22 in combined lateral-to-medial and superficial-to-deep gradients. Neurons in the large island of Calleja are generated mainly between E19 and E22 in a strong rostral-to-caudal gradient. Neurogenesis is reduced to < 10% in both populations No. 2 and No. 3, occurring mainly between P0 and P4. The neurogenetic patterns in populations No. 2 and No. 3 are similar to those in the striatum, while neurogenesis in population No. 1 fits into the pattern of the globus pallidus and substantia innominata. These developmental patterns indicate that the olfactory tubercle is a mixed striato-pallidal system rather than an olfactory cortical area. The lateral-to-medial neurogenetic gradient shown in each neuronal population in the olfactory tubercle correlates with both differential anatomical projections and differential neurochemical characteristics along the lateral-medial plane.

Neurogenesis of the magnocellular basal telencephalic nuclei in the rat

Neurogenesis in the magnocellular basal telencephalic nuclei of the rat was examined with [3H]thymidine autoradiography. The experimental animals were the offspring of pregnant females given two injections of [3H]thymidine on consecutive embryonic (E) days (E12–E13, E13–E14, … E21–E22). On postnatal day (P) 60, the percentage of labeled cells and the proportion of cells originating during 24 h periods were quantified at several anatomical levels throughout the magnocellular basal telencephalic nuclei. The neurons of the horizontal limb of the diagonal band originate mainly between E13 and E16 in a combined rostral-to-caudal and lateral-to-medial gradient. The neurogenetic gradients in the horizontal limb are continued by generation patterns of cells in the vertical limb of the diagonal band-medial septal complex, the large cells in the polymorph layer of the olfactory tubercle, and the large cells of the anterior amygdaloid area. The substantia innominata originates between E13 and E17 in combined caudal-to-rostral and lateral-to-medial gradients. The globus pallidus originates between E13 and E17 in combined caudal-to-rostral, ventral-to-dorsal and medial-to-lateral gradients. The entopeduncular nucleus originates between E12 and E14 in a ‘sandwich’ gradient where neurons in the core of the nucleus are older than those in either the anterior or posterior ends. There is an overall superficial (ventral) to deep (dorsal) neurogenetic gradient between the magnocellular basal nuclei present at any given rostrocaudal level. An important finding is that neurogenetic gradients in the individual components of the magnocellular basal nuclei are alike (with the possible exception of the entopeduncular nucleus) indicating they are part of a single system. Finally, evidence is presented that neurogenetic gradients in the magnocellular basal telencephalic neurons can be correlated with their anatomical projections to the cerebral cortex.

Effects of neonatal whisker lesions on mouse central trigeminal pathways.

The mystacial vibrissae or whiskers on the face have a large representation in the rodent central nervous system. In rats and mice the projections arising from each vibrissa can be demonstrated histologically in five separate parts of the central trigeminal pathway. At every location, the pattern of the projections is isomorphic to the pattern of the facial vibrissae. For example, in the somatosensory cortex (SmI), multicellular cytoarchitectonic units in layer IV--termed barrels--correspond anatomically and functionally to the contralateral whiskers. The cortical barrels are absent at birth and their cytoarchitectonic pattern can be altered by neonatal whisker lesions. The effect is graded such that whisker damage on or after postnatal day (PND) 6 does not produce changes in the anatomical somatotopy. We undertook the present study to determine whether similar "critical periods" for susceptibility to vibrissa damage exist in the subcortical trigeminal stations of mice. In particular, we wished to find out whether subcortical projections are susceptible to whisker damage in a sequence which parallels other described developmental sequences, as has been concluded from previous work on the mouse (Woolsey et al., '79), or whether the "critical periods" are related to other aspects of development as has been concluded from work on the rat (Belford and Killackey, '80). Neonatal Swiss Webster mice sustained lesions of a single row of whiskers on PND 1, 2, 3, 4, or 5. The animals survived to adulthood. Their brains were sectioned and stained for the mitochondrial enzyme, succinic dehydrogenase (SDH), which demonstrates whisker somatotopy in all central nervous system (CNS)stations. The whisker representations at each level of the pathway, often in the same individual, were reconstructed from serial sections to assess qualitative and quantitative changes in somatotopy. Histological sections through the faces of the experimental animals were used to determine the extent of whisker damage and to show that few nerve fibers innervate the damaged zone on the face. In the brainstem representations, the zones corresponding to the damaged whiskers are shrunken and pale, regardless of the animal's age at vibrissa damage; this probably reflects the degeneration of the primary afferents. In the thalamus and the cortex, whisker damage at later postnatal times has progressively less effect on the anatomical projections patterns. Based on the changes in the projection patterns related to the damaged vibrissae and the changes in the projection patterns related to the remaining, intact vibrissae,(ABSTRACT TRUNCATED AT 400 WORDS)

The termination pattern of sciatic nerve afferents in the substantia gelatinosa of neonatal rats

A study was carried out to determine at what stage of development the adult pattern of primary afferent projections to the substantia gelatinosa (SG) is first established. Horseradish peroxidase conjugated wheat-germ agglutinin (WGA-HRP) was applied to cut ends of sciatic nerves at mid-thigh level in adult and neonatal rats aged 1–16 days. The distribution of transganglionically transported label in primary afferent terminals in SG was reconstructed from transverse sections of spinal cord segments L1 to S1. The distinctive U-shaped projection field of the sciatic nerve in SG of the adult was found to exist in miniature form already in the second postnatal day 24 h after WGA-HRP had been applied. The highly specific somatotopic projections of primary afferents to SG are probably established before birth. Any delay in the maturation of functional specificity in the dorsal horn of the neonate cannot be attributed to the absence or disorganization of anatomical projections to SG of primary afferent inputs.

Lateral visual pathway of giant barnacle.

1. We have studied the responses to light, conduction down the axons, and anatomical projections of the photoreceptors of the lateral eye in the giant barnacle, Balanus nubilus. By recording intracellularly from ganglion cells that respond to visual input, we have described convergence of the lateral and median visual pathways. 2. Each lateral eye contains three photoreceptor cells, two large and one small. Cobalt filling of single large lateral receptor axons demonstrated that they end in a restricted ovoid bush on the ipsilateral side of the ganglion in approximately the same region in which the median receptors arborize. 3. The lateral receptors have dark resting potentials and responses to light similar to those previously described for the receptors of the median eye. Like the median receptors, the lateral receptors conduct visual signals decrementally, although their axons may be twice as long (14-25 mm). 4. Passing current of either polarity into either of the large receptors produced no detectable voltage change in the other cell. Action potentials elicited in either cell by stimulating it in the presence of tetraethylammonium ion were not detected in the other cell. Light-induced membrane noise in one cell did not correlate with noise in the other. Thus, like the receptors of the median eye, the large receptors of the lateral eye are not electrically coupled. 5. By shadowing each ocellus individually, we have shown that the signals from the median and lateral photoreceptors converge at the level of the second-order cells described for the median pathway. Shadowing the median or a lateral eye gave rise to synergistic responses in second-, third-, and all higher order ganglion cells studied. No cells were found that were driven solely by the lateral eyes. Thus, the lateral and median visual pathways are highly convergent.

Parabrachial area as mediator of bradycardia in rabbits

This study examined the role of the parabrachial nucleus (PBN) in the mediation of bradycardia and in the reception of barosensory information. The 82 rabbits in the investigation were anesthetized with ethyl carbamate. Train stimulation of medial or lateral PBN produced primary bradycardia (mean peak change: −74 beats/min) associated with a pressor response (average peak mean change: +10 mm Hg) of longer latency. Section of the cervical vagus nerves indicated that the bradycardia was mediated primarily by the parasympathetic nervous system. Heart rate and blood pressure responses to train stimulation did not vary systematically as a function of respiratory pattern; paralyzing animals with decamethonium hydrochloride and artificially ventilating them also did not influence the cardiovascular responses to stimulation. Single-pulse stimulation of PBN in conjunction with extracellular single neuron recording established that neurons originating in or projecting through PBN project to the commissural region of nucleus tractus solitarius (NTS) where synapse is made with neurons receiving barosensory input. In addition to establishing the existence of descending functional projections passing from PBN to NTS, injections of HRP into PBN revealed direct descending anatomical projections to PBN from regions of the forebrain previously implicated in the mediation of bradycardia. These included central nucleus of amygdala, lateral preoptic region, medial forebrain bundle, bed nucleus of stria terminals, anterior and lateral hypothalamus. and zona incerta. The present investigation also indicated that PBN receives barosensory information. Single-pulse electrical stimulation of the aortic nerve (AN) activated neurons in NTS at an average latency of 7.5 ms and in PBN at a mean latency of 12.1 ms. Mean latency of 9 neurons in NTS activated antidromically by PBN stimulation was 3.4 ms. Conduction velocity of the monosynaptic fibers projecting from NTS to PBN was approximately 3.5. m/s, which would be characteristic of finely myelinated fibers. Injection of HRP into PBN confirmed the existence of direct ascending projections to PBN from regions of NTS (e.g. lateral commissural area) previously shown to receive primary barosensory input. However, the finding that only 1 of 9 NTS neurons antidromically activated by PBN stimulation also received barosensory stimulation, indicates that additional study is needed of the mono- and oligosynaptic functional projections from NTS to PBN. The present study did provide evidence that PBN both receives barosensory information at short latency over a direct route, and serves as a relay for descending projections mediating bradycardia.

1611 ULTRASOUND-AUTOPSY CORRELATION OF THE INFANT BRAIN

Cranial ultrasound examinations were performed in five newborns and five infants under a year of age in the period immediately after death. Scans were made in multiple coronal planes angled from the anterior fontanelle. After autopsy, the brains were fixed in formalin and then sectioned in planes corresponding to the ultrasound scans. These anatomic projections are not standard and are unfamiliar even in computed tomography. Comparison of brain sections with scans revealed the anatomic basis for the echoes. Diagnostic ultrasound of the central nervous system is a noninvasive and relatively inexpensive new technique which is especially valuable during infancy while the anterior fontanelle is unossified and can act as a sonolucent window. It can be used to diagnose a variety of solid and cystic lesions and is ideally suited to follow-up examinations. Illustrative examples include a choroid plexus papilloma, a vein of Galen malformation and intracranial hemorrhage Anatomy, pathology, and the ultrasound scans are correlated.