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H J Karten

Publications and source records attributed to H J Karten.

At least 73 records · Page 4Linked to original sources
PubMed1985

Topographic representation of visceral target organs within the dorsal motor nucleus of the vagus nerve of the pigeon Columba livia.

Our previous work (Katz and Karten, '83a J. Comp. Neurol. 217:31-46 demonstrated that the dorsal motor nucleus of the vagus nerve (DMN complex) in the pigeon is composed of cytoarchitecturally distinct subnuclei that are distinguished by the size, shape, position, and cytochemical characteristics of their constituent neurons. In view of the diversity of target organs innervated by the vagus nerve, we sought to determine whether the subnuclear heterogeneity of the DMN complex is related to the pattern of target innervation. To test this possibility, retrograde tracing techniques were used to define the subnuclear localization of vagal motoneurons that innervate individual vagal target organs. The distribution of horseradish peroxidase (HRP)-labeled motoneurons within the DMN complex was studied following application of HRP to the cut central end of individual vagal nerve branches and after injection of the tracer into vagal target tissues. In addition, we examined the distribution of acetylcholinesterase depletion within the DMN complex following transection of individual vagal branches. Our data demonstrate that individual vagal target organs have discrete and topographic representations within cytoarchitecturally distinct subnuclei of the DMN complex. Therefore, in the pigeon, the subnuclear distribution of vagal motoneurons plays a critical role in the organization of descending vagal motor pathways. Segregation of visceral representations within the DMN complex may provide a mechanism for organizing functionally diverse afferent inputs to target-specific populations of vagal motoneurons.

Abdomen↗
PubMed1985

Regeneration of peptide-containing retinofugal axons into the optic tectum with reappearance of a substance P-containing lamina.

Twenty-five specimens of Rana pipiens were subjected to a unilateral crush of the optic nerve. Substance P (SP)-, leucine enkephalin (LENK)-, cholecystokinin octapeptide (CCK8)-, and bombesin (BOM)-like immunoreactivities were analyzed in the retinae, optic nerves, and optic tecta, 9 days to 9 months postoperatively, by means of immunohistochemical methods. Peptide-like immunoreactivity was observed in axons within the optic nerve stump retinal to the crush, as in previous studies (Kuljis and Karten, '83b, Kuljis et al., '84). Peptide-containing retinofugal axons began traversing the lesion site between 10 and 20 days postoperatively, in progressively increasing numbers. Ten to 20 days following crush of the optic nerve SP-, LENK-, and CCK8-containing axons could be found in the cerebral stump of the optic nerve and in the optic chiasm, advancing to the side of the brain deafferented by the crush. The number of axons displaying peptide-like immunoreactivity within the optic nerve, retinal or cerebral to the crush, and within the optic chiasm gradually decreased after 2-3 months. The optic nerve contralateral to the procedure displayed only occasional isolated peptide-containing fibers, as in normal optic nerves. The retinae ipsilateral and contralateral to the crush exhibited no change in the normal pattern of peptide-like immunoreactivity, including the absence of demonstrable peptide-like immunoreactivity in the somata of retinal ganglion cells. The optic tectum deafferented by the procedure underwent modifications in the pattern of peptide-like immunoreactivity identical to those reported following unilateral eye enucleation (Kuljis and Karten, '82a, '83a). The patterns of LENK-, CCK8-, and BOM-like immunoreactivities in the tectum were identical to those following irreversible retinal deafferentation as long as 9 months postoperatively. SP-like immunoreactivity, however, was gradually restored in layer 11 of Ramón y Cajal ('46; layer D of Potter, '69) of the superficial (retinorecipient) neuropil 4-6 months postoperatively. The persistence of lamina-specific depletion patterns of LENK-, CCK8-, and BOM-like immunoreactivities in reafferented tecta represents a puzzling observation. The latter findings contrast sharply with the recovery of SP-like immunoreactivity, which occurs long after apparently complete restitution of the retinofugal projection, as shown by anatomical (Stelzner et al., '81), physiological (Maturana et al., '59), and behavioral (Sperry, '44) methods.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗
PubMed1985

Ultrastructure and synaptic contacts of enkephalinergic amacrine cells in the retina of turtle (Pseudemys scripta).

Bistratified amacrine cells of the turtle retina containing enkephalin-like immunoreactivity were examined with the electron microscope with the aid of peroxidase immunocytochemical techniques. Our goal was to determine the nature and the location of the synaptic contacts of these cells and the intracellular localization of the immunoreactivity. There was a diffuse reaction product throughout the cytoplasm which coated the surfaces of all the organelles and a dense reaction product which filled the core of some large cytoplasmic vesicles (130 nm in dia.). These labeled amacrine cells received conventional synaptic contacts from other unlabeled amacrine cells and ribbon synaptic contacts from unlabeled bipolar cells, in both the proximal and distal inner plexiform layer. These enkephalin-positive amacrine cells made conventional synaptic contacts containing unlabeled synaptic vesicles (60 nm in dia.), with ganglion cells in the proximal inner plexiform layer and with bipolar cells in the distal inner plexiform layer. These results suggest that enkephalin-like material coexists with another neurotransmitter within these neurons and that these amacrine cells are able to integrate information from both amacrine cells and bipolar cells and provide synaptic input to bipolar cells, ganglion cells, and possibly other amacrine cells.

Animals↗
PubMed1985

Presence and ontogeny of enkephalin and substance P in the chick ciliary ganglion.

The avian ciliary ganglion has been reported to contain both enkephalin and substance P in preganglionic terminals. However, extensive biochemical characterization of these antigens has not been completed. Using radioimmunoassays specific for Met5- and for Leu5-enkephalin and for substance P we identified immunoreactive substances in ganglionic extracts that comigrate on HPLC columns with standard Met5- and Leu5-enkephalin and with substance P. The ontogeny of Met5-enkephalin and substance P during embryogenesis was determined in ganglionic extracts and we found that the content of Met5-enkephalin in the ganglion reached a peak at embryonic stage 37 whereas the content of substance P in the ganglion reached its maximum in the adult.

Animals↗
PubMed1985

Comparison of olfactory bulb projections in pigeons and turtles.

The projection targets of the olfactory bulb in pigeons and turtles were investigated using autoradiographic techniques. Despite the relatively smaller size of the olfactory bulbs in pigeons, the projection targets of the olfactory bulb are very similar to those in turtles. In both pigeons and turtles, the olfactory bulb projects to the entire rostrocaudal extent of a portion of the dorsolateral telencephalon (which is here recognized as the pyriform cortex in both birds and reptiles) and to portions of the medial telencephalic wall including the medial septal region. In addition, a projection to the olfactory tubercle of the ventral telencephalon is clearly present in turtles and also appears to be present in pigeons. Pigeons and turtles do differ significantly, however, in the extent of the projection to the amygdaloid region. In turtles, olfactory bulb input encompasses the entire mediolateral and rostrocaudal extent of the amygdaloid region, while in pigeons the input is restricted to a small dorsomedial portion of the amygdala termed nucleus taeniae of the archistriatum. The present results suggest that the olfactory bulb projections in birds are generally similar to those in reptiles, with the exception that secondary olfactory bulb projections to the amygdala may be much reduced in birds compared to those in reptiles. The functional significance of the reduction in olfactory input to the amygdala is presently uncertain.

Animals↗
PubMed1984

Catecholamine- and indoleamine-containing neurons in the turtle retina.

We identified a population of presumed dopaminergic amacrine cells and populations of presumed serotonergic bipolar and amacrine cells in the retina of the turtle Pseudemys scripta elegans by a combination of autoradiographic, fluorescence, and immunocytochemical techniques. Antisera directed against the dopamine-synthesizing enzyme, tyrosine hydroxylase (TOH), stained perikarya located at the border of inner nuclear (INL) and inner plexiform (IPL) layers. Processes emitted by these cells arborized in sublaminae 1, 3, and 5 of the IPL. Incubation of retinas in 10(-6) M 3H-dopamine yielded a labeling pattern identical to the staining pattern achieved with TOH antisera, but when the concentration of 3H-dopamine was increased 25-fold, both amacrine and bipolar cells are labeled. Following intraocular injection of dopamine, fluorescence micrography revealed both stained amacrine and bipolar cells. The bipolar cells had Landolt's clubs, pyriform perikarya located in the distal portion of the INL, and axons that coursed horizontally in the INL, then entered the IPL, and ramified in both its superficial and deeper layers. Although no fluorescent neuronal profiles were revealed following injection of serotonin (5HT), bipolar cells identical to those described were visualized with 5HT antisera. The intensity of bipolar cell staining with 5HT antisera was improved by preinjection of the eye with exogenous 5HT. We suggest that the bipolar cell is serotonergic, but that it also can actively accumulate dopamine. The 5HT antisera also stained a population of large amacrine cells whose processes ramified in IPL sublaminae 1, 4, and 5. The same populations of presumed serotonergic bipolar and amacrine cells were labeled following incubation of the eyecup in 10(-6) M 3H-5HT.

Animals↗
PubMed1984

The distribution of enkephalinlike immunoreactivity in the telencephalon of the adult and developing domestic chicken.

Immunohistochemical techniques were used to determine the distribution of enkephalinlike immunoreactivity in the telencephalon of chicken. The densest accumulation of enkephalinergic neurons and fibers was observed within the paleostriatal complex, the avian equivalent of the mammalian basal ganglia. Numerous small enkephalinergic neurons were observed in both lobus parolfactorius (LPO) and the paleostriatum augmentatum (PA), the two components of the small-celled portion of the paleostriatal complex. The enkephalinergic neurons of LPO-PA appeared to give rise to a dense plexus of enkephalinergic fibers within the large-celled zone of the paleostriatal complex, the paleostriatum primitivum (PP). The distribution of enkephalin within the avian paleostriatal complex, when compared to the distribution of enkephalin within the mammalian basal ganglia, supports previous proposals that PP is comparable to the mammalian globus pallidus and that PA-LPO are comparable to the caudate-putamen (Karten and Dubbeldam, '73; Kitt and Brauth, '81; Parent and Olivier, '70; Reiner et al., '83). Observations on the development of enkephalinlike immunoreactivity within the chicken paleostriatal complex also support the suggestion that the major component nuclei of the avian paleostriatal complex have correspondents within the mammalian basal ganglia. Enkephalinlike immunoreactivity was also observed within cell bodies and fibers in other portions of the avian telencephalon. Within the ventrolateral telencephalon, the nucleus accumbens, nucleus of the diagonal band, and tuberculum olfactorium contained enkephalinergic cell bodies and fibers while only enkephalinergic fibers were observed in the portion of the avian telencephalon that has been termed the ventral paleostriatum (Kitt and Brauth, '81; Reiner et al., '83). Within the medial wall of the telencephalon, enkephalinergic fibers were observed in the lateral septal nucleus, while enkephalinergic cell bodies and fibers were observed in the parahippocampal area. Little enkephalinlike immunoreactivity was observed dorsal to the paleostriatal complex except in the hyperstriatum dorsale. Within the hyperstriatum dorsale, a band of enkephalinergic neurons appeared to give rise to an overlying parallel band of dense enkephalinergic fibers. The distribution of enkephalinlike immunoreactivity within the avian telencephalon thus shows remarkable similarity to that seen in the mammalian telencephalon. The largest accumulation of enkephalinlike immunoreactivity within the telencephalon of both vertebrate classes appears to be found within the ventrolateral wall of the telencephalon, including the basal ganglia.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗
PubMed1984

The neural substrate for the pupillary light reflex in the pigeon (Columba livia).

The neural substrate of the pupillary light reflex in the pigeon was investigated using anatomical, stimulation, and lesion techniques. In birds, as in mammals, the sphincter pupillae muscle (which constricts the iris) is innervated by cells in the ciliary ganglion (Pilar and Tuttle, '82). These cells are in turn innervated by cells in the Edinger-Westphal nucleus (EW) (Cowan and Wenger, '68; Narayanan and Narayanan, '76; Lyman and Mugnaini, '80). The efferent link of the pupillary light reflex must therefore involve cells in EW. To study the central course of this reflex pathway, injections of horseradish peroxidase (HRP) were placed in EW. These injections labeled cells in a number of regions including a contralateral pretectal nucleus, area pretectalis (AP). Only a limited number of cells in AP project to EW. Injections of tritiated amino acids into AP labeled a discrete region of the contralateral EW. This projection is confined to a dorsolateral region of caudal EW and overlies the somata of approximately 100 cells. Tritiated proline was injected into the eye, and the results confirmed an earlier report (Reperant, '73) that AP receives retinal input from the contralateral eye. Immunohistochemical studies demonstrated fibers in AP that stained positively for substance-P-like, enkephalin-like and tyrosine-hydroxylase-like immunoreactivity. Injections of HRP were placed in AP to examine the retinal ganglion cells mediating the reflex. Cells with an average diameter of approximately 14 microns (5-25 microns range) were labeled and averaged approximately 6 microns greater in diameter than the retinal ganglion cells (mean = 7.3 microns) labeled by an optic chiasm injection. The cells labeled by AP injections were distributed unevenly throughout the retina with a higher concentration in the central and temporal retina and a paucity in the red field and fovea. Our results demonstrate that AP receives input from a distinct subpopulation of large retinal ganglion cells that comprises a very small percentage of the total population of retinal ganglion cells. Unilateral lesions of AP abolished the pupillary light reflex in the eye contralateral to the lesion; stimulation of AP elicited pupilloconstriction in the eye contralateral to the stimulation site. These results delineate the central course of the pupillary light reflex pathway in the pigeon and identify the retinal ganglion cells that subserve this reflex. They show that, at every point in the pathway, only a few cells mediate this simple reflex.(ABSTRACT TRUNCATED AT 400 WORDS)

Afferent Pathways↗
PubMed1984

Peptide-like immunoreactivity in anuran optic nerve fibers.

Unilateral section, crush, or ligation of the optic nerve was performed in Rana pipiens. Following optic nerve disruption, Substance P (SP)-, leucine-enkephalin (LENK)-, cholecystokinin octapeptide (CCK8)-, and bombesin (BOM)-like immunoreactivities were analyzed in the retinae and optic nerves. Peptide-like immunoreactivity developed in the retinal stump of disrupted optic nerves within 1 hour after surgery and was retained until at least 30 days. Peptide-positive staining in the retinal stump of the optic nerves was abolished by preabsorption of each of the antibodies/antisera with the corresponding synthetic substances. No massive peptide-like immunoreactivity was observed in the cerebral stump of the ligated side, nor in the contralateral, nonoperated, optic nerve. No change in the pattern of peptide-like immunoreactivity was apparent in the retina ipsilateral or contralateral to the experimental procedure. The optic tectum contralateral to the surgical procedure displayed those changes in peptide-like immunoreactivity described previously following retinal deafferentation (Kuljis and Karten, '82a, '83a). Peptide-like immunoreactivity in the stump retinad to the surgical procedure occurred in the form of beaded and fibrillar elements often ending in an irregular expansion near the lesion site. Fluorescent double-label antibody methods demonstrated that SP-like immunoreactivity is present in different processes than those containing LENK, CCK8, or BOM. Electron microscopical immunocytochemistry revealed that peptide-like immunoreactivity is contained within unmyelinated and possibly also within myelinated axons in the stump retinad to the traumatic procedure. Radioimmunoassay studies of SP demonstrated a four- to sixfold increase in SP-like content in the retinal stump of ligated nerves, compared with both the cerebral stump and with the contralateral nonoperated optic nerves. These findings demonstrate the presence of peptide-like immunoreactivity in retinal ganglion cell processes, which is compatible with either a posttraumatic expression of previously repressed peptide-like phenotypes, or, most likely, with the existence of various classes of peptide-containing retinal ganglion cells. The latter prospect strongly suggests that peptide-specific subsets of retinal ganglion cells terminate in highly specific laminae in the optic tectum (Kuljis and Karten, '81, '82a-83a) and presumably differ in their physiological role in vision.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗
PubMed1984

Ontogeny of enkephalin-like immunoreactivity in the rat hippocampus.

The postnatal development of leucine5-enkephalin-like immunoreactivity within the hippocampal formation of the rat has been analyzed using immunocytochemical techniques. From the day of birth to postnatal day three, no intrinsic hippocampal elements exhibit immunoreactivity although labeled axons are found within the fimbria, within the alveus, and in the vicinity of the angular bundle. On postnatal day 4, a few immunoreactive hippocampal neurons can be seen in stratum radiatum of the region CA3 and by postnatal day 8, within the hilus, strata pyramidale and oriens of regio superior, and the subiculum. There is a dramatic increase in the incidence of immunoreactive perikarya between postnatal days 8 and 10 in all fields as well as the appearance of labeled neurons in CA1 stratum pyramidale and stratum granulosum of the dentate gyrus. Two days after the first appearance of immunoreactive perikarya, intensely immunoreactive neurons, labeled much more extensively than is ever seen in the adult, are encountered in each subfield of the hippocampus. The spatio-temporal order in both the emergence of perikaryal immunoreactivity and the transient appearance of intensely immunoreactive neurons follows that of neurogenesis, with immunoreactivity developing 12-14 days after the peak period of last cell division for a given hippocampal region. The incidence of immunoreactive perikarya in the dentate gyrus was quantified in rat pups ranging from postnatal days 8 to 19. The appearance of labeled neurons followed the spatio-temporal gradients that have been described for neurogenesis in this region as well. Immunoreactive perikarya emerged in the suprapyramidal stratum granulosum prior to their emergence in the infrapyramidal zone and in the temporal pole of the dentate earlier than in the mid-dorsoventral dentate. The lateral perforant path and mossy fiber axons, seen to exhibit enkephalin-like immunoreactivity in the adult hippocampal formation, differ in their relative maturity at the age immunoreactivity first appears. Immunoreactivity appears as early as postnatal day 4 in the lateral perforant path, an age at which these axons are just growing into their target field while it is not found within the mossy fibers until after postnatal day 10, an age at which mossy fiber bouton elaboration is well advanced and physiologically competent mossy fiber synapses with the regio inferior pyramidal cells have been established. The latter observation indicates that enkephalin is not necessary for synaptic transmission at the mossy fiber synapse.

Aging↗
PubMed1984

Cluster-and-sheet pattern of enkephalin-like immunoreactivity in the superior colliculus of the cat.

The distribution of enkephalin-like immunoreactivity in the superior colliculus has been studied in the cat with the peroxidase-antiperoxidase method. Two striking patterns of immunoreactivity were observed. In the superficial layers there is a thin, dense horizontal band of immunoreactivity in the neuropil of the most dorsal tier of the superficial gray layer (sublamina 1). Because this sublayer corresponds to the zone of densest contralateral retinotectal projection, an intraocular injection of horseradish peroxidase was made in one cat to allow direct comparison of the distributions of opiate-like immunoreactivity and transported tracer in the contralateral superior colliculus. There was a detailed similarity between the two, including the presence of a gap in both at the presumptive site of the optic disc representation. The presence of enkephalin-like immunoreactivity in neural perikarya in and near sublamina 1 of the superficial gray layer, however, raised the possibility that the immunoreactive band is part of an intrinsic opiate system. Deeper in the superficial gray layer there was appreciable but weaker immunoreactivity in the neuropil and fewer immunoreactive neurons. In the intermediate gray layer and, especially medially, even deeper in the superior colliculus, enkephalin-like immunoreactivity was organized into small (100-300 micron wide) patches. In the intermediate gray layer these tended to be arranged periodically, five-seven patches being spaced at 200-600 micron intervals in caudal transverse sections. In some sections adjoining patches appeared to be fused. The patches were absent or difficult to detect in rostral sections. Caudally, they sometimes were adjacent to blood vessels penetrating the intermediate gray layer, but other times were not. Serial section reconstructions suggested that the patches observed in individual sections are part of larger arrays which have the form of anastomotic bands running in longitudinal directions somewhat oblique to the sagittal plane. It is concluded that an opiate mechanism may play a part in controlling the effects of incoming retinal information in the superficial gray layer, directly or indirectly, and that opiate peptides may also act in modulating one or more afferent or efferent systems of the deep collicular layers. Accordingly, from the functional standpoint, enkephalin-like peptides may influence both visual and sensory motor processing in the superior colliculus.

Animals↗
PubMed1983

Characterization and quantification of peptidergic amacrine cells in the turtle retina: enkephalin, neurotensin, and glucagon.

Immunocytochemical methods were used for selective labeling and characterization of amacrine cells of the turtle (Pseudemys scripta elegans) retina which contained neuropeptide-like immunoreactivity (leu-enkephalin, glucagon, and neurotensin). Processes of amacrine cells arborized in specific strata of the inner plexiform layer (IPL). Different strata were defined in relation to the boundaries of the IPL. Zero represented the strata nearest the inner nuclear layer and 100 represented the strata nearest the ganglion cells. Antisera directed against leu-enkephalin labeled approximately 7,300 amacrine cells in a single turtle retina which were concentrated in the region of the visual streak and decreased in density toward the periphery. In retinal regions outside the visual streak the labeled neurons were similar in size and shape with dendritic arbors which lacked a particular orientation. In contrast, in the visual streak, there were particular neurons which were labeled with enkephalin antiserum which had elongated dendritic arbors that ran parallel to the streak. Both types of amacrine cells with enkephalinergic immunoreactivity sent their dendrites into the 0-20 region and the 65-100 region of the IPL. Antisera directed against glucagon labeled approximately 2,500 amacrine cells in a single turtle retina. These cells were concentrated in areas near the visual streak. Amacrine cells labeled with glucagon antiserum had dendritic arbors which were asymmetrically skewed toward one end of the cell and ramified in the 0-20 strata with sparse projections at the 40 and 80 strata of the IPL. Antisera directed against neurotensin labeled 12,800 amacrine cells in a single turtle retina. These cells were concentrated in the region of the visual streak. Two distinct amacrine cell types were labeled selectively. One type had a large, vertically oriented cell body (10 X 14 micron) which gave rise to a single 2-micron-thick process that branched and ramified within the 45-70 strata. The other amacrine cell type with neurotensin-like immunoreactivity had a smaller cell body (8 micron) that sent numerous thin dendrites into the same 45-70 strata. The present results indicated that various neuropeptides were present in amacrine cells of the turtle retina and that a specific neuropeptide could be found in more than one anatomical type of amacrine cell. Each anatomical type of amacrine cell had a unique dendritic arborization which ramified within particular strata within the IPL.

Animals↗
PubMed1983

The laminar source of efferent projections from the avian Wulst.

Following horseradish peroxidase injections into the pigeon tractus septomesencephalicus, the efferent outflow bundle of the avian Wulst, retrogradely labeled neurons within the Wulst were confined to the superficialmost layer, the hyperstriatum accessorium. These results suggest that the hyperstriatum accessorium is the sole source of Wulst efferent projections. In similarity to the laminar organization of mammalian striate cortex, this efferent layer is juxtaposed to the thalamorecipient layer of Wulst.

Animals↗
PubMed1983

Visceral representation within the nucleus of the tractus solitarius in the pigeon, Columba livia.

This study describes the distribution of organ-specific populations of vagal afferent fibers within the nucleus of the solitary tract (nTS) in the pigeon. The central projections of vagal sensory neurons were visualized by the centripetal and trans-ganglionic transport of horseradish peroxidase from either the central cut ends of peripheral vagal branches or from HRP injection sites in peripheral vagal target tissues. This paper also includes a detailed description of the cytoarchitectural organization of the nTS in the pigeon based on studies of Nissl-stained material. Vagal afferent fibers that innervate different peripheral target organs are partially segregated within cytoarchitecturally distinct subnuclei of the nTS. Gastrointestinal afferents, for example, project primarily to medial subnuclei. On the other hand, pulmonary, and on the basis of earlier studies, cardiovascular afferents, project primarily to lateral subnuclei. Moreover, the rostral to caudal distribution of gastrointestinal afferents corresponds to the rostrocaudal topography of the gastrointestinal tract. In addition, our data demonstrate a projection of gastrointestinal afferents to the lateral descending tract of the trigeminal nerve that appears to terminate in the external cuneate nucleus. The cytoarchitectural organization of visceral representations within the pigeon nTS corresponds closely to recent descriptions of this cell group in mammals. Comparison of our results with studies of the central connections of nTS neurons suggests that the subnuclear distribution of organ-specific vagal afferents within nTS plays a critical role in the organization of ascending and descending visceral afferent pathways.

Animals↗
PubMed1983

Modifications in the laminar organization of peptide-like immunoreactivity in the anuran optic tectum following retinal deafferentation.

Substance P (SP)-, leucine-enkephalin (LENK)-, cholecystokinin octapeptide (CCK8)-, bombesin (BOM)-, and avian pancreatic polypeptide (APP)-like immunoreactivities were analyzed in the optic tectum of Rana pipiens 5-99 days after unilateral eye enucleation, or optic nerve ligation, by means of the peroxidase-antiperoxidase and indirect fluorescence single and double labeling methods. The normal pattern (Kuljis and Karten, '81, '82c) of peptide-like immunoreactivity was observed ipsilaterally to the operation. Contralateral deafferented tectae displayed conspicuous modifications in the normal pattern of peptide-like immunoreactivity unique to each of the substances studied. The modifications of peptide-like immunoreactivity observed varied depending both on the survival time and on the particular peptide analyzed, with either increment or diminution or disappearance--or combinations thereof--in the staining intensity of some of the peptide-positive bands in the superficial one-third (superficial neuropil) of the tectum. The onset of these changes is detectable immunocytochemically between the sixth and tenth day following deafferentation. By 2-4 weeks full expression of the long-term changes is reached with no apparent further modification up to the 99th postoperative day. The rapid onset of these phenomena suggests the existence of a previously unrecognized retinal ganglion cell terminal peptidergic contribution to the tectum and/or rapid transsynaptic effects. The former possibility is suggested by recent observations demonstrating peptide-like immunoreactivity for SP, LENK, CCK8 and BOM in the retinal stump of ligated optic nerves (Kuljis and Karten, '82b). The fact that no vertebrate retinal ganglion cells have been shown to contain any of these peptides (Brecha et al., '79; Famiglietti et al., '80; Eldred and Karten, '81; Karten et al., '82), however, argues against the possibility of a retinal terminal contribution to peptide-like immunoreactivity in the tectum and suggests that transsynaptic phenomena are involved.

Animals↗
PubMed1983

Subnuclear organization of the dorsal motor nucleus of the vagus nerve in the pigeon, Columbia livia.

The present study is the first of two papers describing the cytoarchitectural and functional organization of the dorsal motor nucleus of the vagus nerve (DMN complex) in the pigeon. This paper describes the distribution of vagal motoneurons within the pigeon brainstem, and the cytoarchitectural organization of the DMN complex. Our description is based on studies of Nissl-stained tissue from normal animals and on experimental studies using retrograde tracing techniques. Cells within the DMN complex were classified according to size, morphology, location, and staining characteristics. These studies demonstrate that vagal motoneurons are localized to (1) the DMN complex, (2) the region of the nucleus ambiguus, and (3) the region of the reticular formation extending between the dorsal motor nucleus and the nucleus ambiguus. Our cytoarchitectural indicate that the DMN complex is composed of at least 11 cytoarchitecturally distinct subnuclei. These subnuclei are evident in normal tissue and are especially prominent in cases where HRP backfilling produces a Golgi-like staining of the motoneurons. The subnuclei can be distinguished by their positions within the DMN complex and by the size, shape, and staining characteristics of their constituent neurons. Comparison of these data with studies in other species indicates similar patterns of cytoarchitectural organization in the DMN complex of some mammals. The diversity of nuclear subgroups within the DMN complex may be related to the heterogeneity of target organs innervated by these cells.

Acetylcholinesterase↗
PubMed1983

Localization of neuroactive substances in the vertebrate retina: evidence for lamination in the inner plexiform layer.

The inner plexiform layer (IPL) of the vertebrate retina is a multilaminated region containing bipolar, amacrine, interplexiform and ganglion cell processes. Immunohistochemical methods clearly demonstrate the existence of various neuroactive substances in distinct morphological types of amacrine cells. Sufficient detail in the staining consistently delineates processes containing these neuroactive substances in multiple laminae of the IPL. Thus, the histochemical approach provides a powerful tool for the analysis of the laminar organization of the IPL and can also be used to further clarify the functional role of various transmitter and peptide substances in the retina.

Acetylcholine↗