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J S Altman

Publications and source records attributed to J S Altman.

31 records · Page 2Linked to original sources
PubMed1984

Identifiable neurons in the locust central nervous system that react with antibodies to serotonin.

A detailed account is given of a number of neurons in the locust central nervous system that react with antibody raised to serotonin-albumin complex. The antibody was applied to a series of frozen sections of locust ganglia and visualized by using the peroxidase immunohistochemical procedure. The neurons described include certain afferents and their related neuropiles, a small number of efferents and several systems of interneurons, some of which are segmentally repeated, some run from the brain through the whole nerve cord, while others are confined to the brain. It has been possible to identify many of the neurons from previous descriptions obtained from cobalt, Golgi, and osmium ethyl gallate methods.

Animals↗
PubMed1983

A cobalt study of medullary sensory projections from lateral line nerves, associated cutaneous nerves, and the VIIIth nerve in adult Xenopus.

The medullary projections of the anterior lateral line nerve, dorsal branch (Alln.d), the posterior lateral line nerve, dorsal branch (PLLn.d), associated cutaneous nerves, and the VIIIth nerve in Xenopus laevis have been delineated by axonal infusion of cobalt chloride and silver intensification. The peripheral innervation of the posterior lateral line sense organs has also been traced. From wholemount and sectioned preparations, we describe three central projections, extending the length of the ipsilateral medulla but occupying distinct zones: lateral line afferents dorsomedially, stato-acoustic dorsolaterally, and cutaneous ventrolaterally. Arborizations of ALLn.d and PLLn.d afferents are morphologically similar, intermingling throughout the lateral line lobe. Each divides into ascending and descending limbs bearing collaterals, which terminate in the lateral line neuropile and nucleus. Evidence is presented for directional and positional mapping in the branching of individual PLLn.d afferents and for topography in the ALLn.d projection. Second-order neurones have been identified by transneuronal staining and their axons traced into the contralateral torus semicircularis. The morphology of efferent neurones is also described. Rostral branches of PLLn.d also contain cutaneous afferents which run through the medulla into the spinal cord, similar to the nerve V (cutaneous) projection. In nerve VIII preparations, the projection to the compact cochlear nucleus and the massive vestibular projection are identified. Cutaneous and vestibular but not lateral line afferents extend into the cerebellum. The separation of VIIIth nerve and lateral line afferents in Xenopus medulla is considered as evidence against the validity of the acousticolateralis concept. Information processing in the lateral line lobe is discussed in relation to connectivity patterns between first- and second-order neurones.

Afferent Pathways↗
PubMed1982

Cobalt mapping of the nervous system: how to avoid artifacts.

Infusion of cobalt ions into cut axons is an established method for tracing neuron projections in the central nervous system. Artifacts, where unintended neurons are stained, however, have been reported, leading to difficulties in interpretation. Experiments in the locust Schistocerca gregaria Forskål show that such artifacts can be induced through damage to axons caused by cutting peripheral nerves and by using high cobalt chloride concentrations (0.4M and above). Mixtures of cobalt and nickel chlorides and nickel chloride alone were introduced into different branches of the same nerve and developed with rubeanic acid to give precipitates of different colors in the two sets of axons. Preparations were examined with the light microscope, where mixing of ions would appear as intermediate colors, and by x-ray probe microanalysis. No evidence for leakage of metal ions from the filled axons or for ion uptake by other axons could be detected, provided that low concentrations of cobalt and nickel chlorides were used and nerve cutting was reduced to a minimum by making preparations in vivo. If extreme conditions are avoided when making the preparation, the risk of producing artifacts is minimized, thus enabling the cobalt method to be used with greater confidence for describing neuronal projections.

Animals↗
PubMed1979

Suboesophageal neurons involved in head movements and feeding in locusts.

The projections of nerves 6 and 7 of the locust suboesophageal ganglion (SOG) were stained by axonal filling with cobalt chloride. Nerve 6 contains two motoneurons which innervate neck muscles 50 and 51. Sensory neurons innervating hairs on the dorso-occipital region of the head also enter the ganglion through nerve 6 and terminate in a small bilateral plexus. The projections of the head hairs in nerve 6 do not overlap the arborizations of the motoneurons or the neurons of nerve 7, but lie in the same area as descending sensory neurons from wind-sensitive hairs of the front of the head. One branch of nerve 7 (7B) contains two fibres which innervate the salivary gland. These 'salivary' neurons (labelled SN1 and SN2) have their cell bodies in the ganglion. The second branch, 7A, contains sensory neurons from the submentum of the labium, which form four sensory plexuses, two dorsal and two ventral. The sensory plexuses from the submentum have specific regions of overlap with the salivary neurons and with the neck muscle motoneurons. We interpret these as indicating a flow of information from labial receptors signalling head and mouthpart movement to neurons involved in salivation and head movement. We further postulate that the anatomical separation of the various sensory plexuses is indicative of functional localization within the ganglion.

Animals↗
PubMed1977

The locust wing hinge stretch receptors. I. Primary sensory neurones with enormous central arborizations.

In locusts a single-celled stretch receptor (SR) neurone at the base of each wing monitors wing elevation and contributes to the control of the flight motor output. The central projections of these neurones are very complex but consistent in detail in the three species studied (Chortoicetes, Locusta and Schistocerca). The hindwing SR projects to the second and third thoracic ganglia, the forewing SR to the first, second and third thoracic ganglia. Both send fine axons into the abdominal connective. Within the ganglia each SR forms an extensive arborization, entirely ipsilateral and mainly in the dorsal neuropile, divided into medial, mediolateral, and lateral branches. The projections of the two ipsilateral SR neurones overlap almost completely in the second and third ganglia. There are recurrent loops between branches of a single neurone both within and between ganglia. Light microscope analysis shows apparent contacts between the SR aneurones and flight motor neurones and other wing sensory afferents, as well as long interneurones, other motor neurones and two types of multiaxonal neurones of unknown function. There are three groups of contacts between each SR and a flight motor neurone: laterally on the main branches, medially with the terminal twigs; and in the anterior dorso-medial glomerulus, where the inter ganglionic recurrent branch also terminates. All contacts are ipsilateral except for those with the contralateral branches of the dorsal longitudinal muscle motor neurones. We suggest that the SR neurones are multifunctional. Differential information transfer could result both from the spatial distribution of synaptic connections with the motor neurones and from filtering caused by low safety factors at branch junctions. Information in the lateral branching could be used for general excitation and control of firing frequency of the motor neurones; that in the medial branch for wing control and co-ordination.

Animals↗
PubMed1977

The locust wing hinge stretch receptors. II. Variation, alternative pathways and "mistakes" in the central arborizations.

The central arborizations of the stretch receptor (SR) neurones are very consistent from one individual to another. Superimposition of normalized neurones from eight individuals of Locusta show very little variation even in the detailed branching pattern. There is, however, a commonly found alternative course for the main medial branch in the metathoracic ganglion. Rare, radical departures from the normal branching pattern are termed "mistakes." Only three have been found, all in the forewing SR projection, one with an extra branch and two with missing branches. Terminals of twigs in the alternative region of the medial branch occupy consistent positions in the neuropile, although these are reached by different routes. Mistakes have terminals in areas normally containing SR endings. Both these findings suggest that there may be labelled sites in the neuropile which the growing tips of the SR neurones seek out.

Animals↗
PubMed1976

Spatial distribution of synapses onto thoracic motor neurones in locusts.

Aggregates of synaptic vesicles, stained black by the zinc iodideosmium procedure, can be visualised with the light microscope in 1 mum plastic sections. This allows the main branches of a neurone to be reconstructed relatively rapidly and the associated vesicle aggregates to be plotted. By resectioning, the identity of the vesicle aggregates has been confirmed with the electron microscope. Two flight motor neurones in the mesothoracic ganglion of the locust have been examined. One is identified as a dorsal longitudinal muscle motor neurone (muscle 112) and the other is probably a subalar neurone (muscle 99). Both have a large density of vesicle aggregates on the neuropilar segment, the widest part of the main neuronal axis, but few on the neurite within 250 mum of the cell body. The larger branches arising from the neuropilar segment tend to have a lower density of aggregates than fine branches, which suggests that synapses to the branches may occur mainly on the distal twigs. These results are an important preliminary step in determining the integrative functions of such neurons and have immediate implications in the interpretation of microelectrode recordings.

Animals↗