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Träfflista för sökning "LAR1:gu ;mspu:(article);srt2:(1970-1974)"

Sökning: LAR1:gu > Tidskriftsartikel > (1970-1974)

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21.
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22.
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23.
  • Frisén, Lars, 1939 (författare)
  • The cartographic deformations of the visual field.
  • 1970
  • Ingår i: Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde. - 0030-3755. ; 161:1, s. 38-54
  • Tidskriftsartikel (refereegranskat)
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24.
  • Frisén, Lars, 1939, et al. (författare)
  • Unsharp masking in fundus photography.
  • 1973
  • Ingår i: Investigative ophthalmology. - 0020-9988. ; 12:6, s. 461-4
  • Tidskriftsartikel (refereegranskat)
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25.
  • Hongo, T., et al. (författare)
  • The rubrospinal tract. III. Effects on primary afferent terminals
  • 1972
  • Ingår i: Experimental Brain Research. - 0014-4819 .- 1432-1106. ; 15, s. 39-53
  • Tidskriftsartikel (refereegranskat)abstract
    • 1. Effects evoked by stimulation of the red nucleus on primary afferent terminals in the lower lumbar segments of cats have been investigated by recording dorsal root potentials (DRPs) and by recording (intracellularly and by excitability measurements) the primary afferent depolarization (PAD) evoked in terminals of different afferent systems. Control experiments suggest that the effects are mediated by the rubrospinal tract. 2. Stimulation of the red nucleus evoked a large DRP and correspondingly there was a pronounced PAD in Ib and low threshold cutaneous afferents. A dual effect was found in Ia afferent terminals; sometimes a weak PAD was detected while in other cases there was dominating primary afferent hyperpolarization (PAH). 3. Rubrospinal volleys are found to facilitate transmission of DRPs evoked from Ia, Ib, cutaneous and high threshold muscle afferents, presumably by exerting an excitatory action on the interneurones mediating the effect from these afferents. Stimulation of the red nucleus may also inhibit transmission in the pathway mediating depolarization of Ia afferent terminals from Ia afferents, probably by activating a segmental pathway from the flexor reflex afferents from which the same effect is evoked. It is postulated that the PAH evoked in Ia afferents from the red nucleus is due to this inhibitory effect and caused by a removal of a tonic PAD in them. 4. The possible role in motor regulation of the rubral effects on primary afferent terminals is discussed in relation to the rubrospinal effects on reflex pathways to motoneurones. This work was supported by the Swedish Medical Research Council (Project No. 14X-94-07C). © 1972 Springer-Verlag.
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26.
  • Hongo, T., et al. (författare)
  • The rubrospinal tract. IV. Effects on interneurones
  • 1972
  • Ingår i: Experimental Brain Research. - 0014-4819 .- 1432-1106. ; 15, s. 54-78
  • Tidskriftsartikel (refereegranskat)abstract
    • 1. The effect of stimulation of the red nucleus on interneurones in the dorsal horn and intermediate region in the lower lumbar spinal cord has been investigated in cats. It has been ascertained that the effects are mediated by the rubrospinal tract. 2. Extracellular monosynaptic focal potentials evoked by single volleys in the rubrospinal tract were recorded in Rexed's layer VI and VII from a region partly overlapping with that in which focal potentials from group I muscle afferents are evoked, but extending more ventrally. 3. Monosynaptic excitatory action from the rubrospinal tract (recorded in 60 of 340 interneurones) was found in two main categories of interneurones: a) cells monosynaptically activated or disynaptically inhibited from group I muscle afferents and b) cells di- or polysynaptically activated from the flexor reflex afferents or exclusively from cutaneous afferents. The cells under a) are located more dorsally than those under b) but both within the region in which rubral focal monosynaptic potentials are recorded. There was no evidence suggesting that rubrospinal fibres have monosynaptic connexions with interneurones not influenced from primary afferents. 4. Many of the group I interneurones in the intermediate region are without monosynaptic connexions from the rubrospinal tract as are the dorsal horn cells monosynaptically activated from cutaneous afferents and dorsally located cells which do not receive monosynaptic connexions from primary afferents but are polysynaptically activated from the FRA. 5. Late (di- or polysynaptic) excitatory, inhibitory or mixed postsynaptic rubral effects are common and were found in interneurones with or without monosynaptic connexions from primary afferents but receiving similar effects from the FRA. The occurrence of spatial facilitation between peripheral nerves and the rubrospinal tract in evoking late PSPs suggests that the late rubral PSPs are evoked by activation of interneurones transmitting actions from primary afferents. 6. Some consequences of the conjoint control of interneurones from primary afferents and the rubrospinal tract are discussed. The monosynaptic effects from the rubrospinal tract are considered in relation to the rubral control of Ib reflex pathways and to the disynaptic rubromotoneuronal PSPs evoked by monosynaptic activation of last order interneurones of polysynaptic reflex pathways from primary afferents. The late rubral effects on interneurones are discussed in relation to interactive mechanisms between segmental interneuronal pathways. Rubrospinal and corticospinal effects are compared. This work was supported by the Swedish Medical Research Council (Project No. 14X-9407C). © 1972 Springer-Verlag.
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27.
  • Hultborn, Hans, et al. (författare)
  • Neuronal pathway of the recurrent facilitation of motoneurones
  • 1971
  • Ingår i: The Journal of Physiology. - : Wiley. - 0022-3751 .- 1469-7793. ; 218, s. 495-514
  • Tidskriftsartikel (refereegranskat)abstract
    • 1. The recurrent facilitation of motoneurones is a disinhibition, i.e. a release of the motoneurones from a sustained hyperpolarization evoked by tonically active inhibitory interneurones. Only two groups of interneurones are known to receive recurrent inhibition from motor axon collaterals via Renshaw cells; the interneurones mediating the reciprocal Ia inhibition and the Renshaw cells themselves. The properties of these two groups of neurones were studied to determine if they could produce the tonic inhibition of motoneurones removed during recurrent facilitation. 2. It was found that the tonic firing of Ia inhibitory interneurones is sensitive to anaesthetics to the same degree as is recurrent facilitation. The range of frequencies of tonic discharges of Renshaw cells appeared to be similarly low in unanaesthetized and anaesthetized preparations although in individual cells the discharge rates were decreased by anaesthesia. 3. The recurrent inhibition of Ia interneurones inhibiting a given group of motoneurones and the recurrent facilitation of the same group of motoneurones were, as a rule, evoked from the same nerves, although in some cats the origin of the recurrent facilitation was somewhat wider. In contrast no evidence could be found that the Renshaw cells which inhibit a functional group of motoneurones are inhibited by volleys in the nerves from which recurrent facilitation is regularly evoked. 4. It was concluded that the recurrent facilitation is caused mainly by inhibition of the tonic activity of Ia inhibitory interneurones and that it is thus a manifestation of the recurrent control of Ia reciprocal inhibition of motoneurones. © 1971 The Physiological Society
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28.
  • Hultborn, Hans, et al. (författare)
  • Recurrent inhibition from motor axon collaterals of transmission in the Ia inhibitory pathway to motoneurones
  • 1971
  • Ingår i: The Journal of Physiology. - : Wiley. - 0022-3751 .- 1469-7793. ; 215, s. 591-612
  • Tidskriftsartikel (refereegranskat)abstract
    • 1. The effects of impulses in recurrent motor axon collaterals on reflex transmission from different types of primary afferents to motoneurones were investigated in the cat by conditioning of PSPs evoked in motoneurones. 2. IPSPs evoked by volleys in large muscle spindle (Ia) afferents were effectively decreased when preceded by an antidromic stimulation of ventral roots. Some IPSPs from group II muscle afferents and low threshold cutaneous afferents were also slightly depressed, while other PSPs were unaffected. 3. The depression of the IPSPs could be evoked by antidromic volleys, which produced neither conductance changes in the motoneurones nor depolarization of Ia afferent terminals. 4. The effect on the Ia IPSPs is most likely due to post‐synaptic inhibition of the Ia inhibitory interneurones, evoked through α‐motor axon collaterals and Renshaw cells. The depression of some IPSPs from flexor reflex afferents is explained by a convergence of excitatory effects from these afferents on the Ia inhibitory interneurones. 5. The results indicate a selective recurrent control from motor axon collaterals of the interneurones in the reciprocal Ia inhibitory pathway to motoneurones. © 1971 The Physiological Society
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29.
  • Hultborn, Hans, et al. (författare)
  • Recurrent inhibition of interneurones monosynaptically activated from group Ia afferents
  • 1971
  • Ingår i: The Journal of Physiology. - : Wiley. - 0022-3751 .- 1469-7793. ; 215, s. 613-636
  • Tidskriftsartikel (refereegranskat)abstract
    • 1. Interneurones monosynaptically excited from large muscle spindle (Ia) afferents and inhibited from motor axon collaterals were searched for in the lumbar spinal cord of the cat. 2. Monosynaptic Ia excitation was found in sixty‐seven of sixty‐nine interneurones inhibited by antidromic volleys. These interneurones were excited from Ia afferents from one or a few muscles (mainly close synergists). Volleys in high threshold muscle and skin afferents (FRA) evoked polysynaptic excitation or inhibition. Weak inhibition from Ia afferents (from antagonists to those giving Ia excitation) was seen in a few cells. Monosynaptic excitation was evoked from the ventral quadrant of the spinal cord and polysynaptic excitation from the dorsal quadrant. 3. Inhibition from motor axon collaterals was evoked with a latency (1·2–2·0 msec) suggesting a disynaptic linkage and had the same time course as in motoneurones. It prevented synaptic activation of 60% of interneurones and decreased the firing index and delayed generation of spikes in the remaining. 4. The interneurones with convergence of monosynaptic Ia excitation and inhibition from motor axon collaterals were found in the ventral horn dorsomedial to motor nuclei. No inhibition by antidromic volleys could be detected in interneurones located in intermediate nucleus and activated monosynaptically from Ia, Ib, group I or cutaneous afferents. 5. It was concluded that the ventral Ia interneurones inhibited by volleys in recurrent motor axon collaterals mediate the reciprocal Ia inhibition to motoneurones. © 1971 The Physiological Society
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30.
  • Hultborn, Hans, et al. (författare)
  • Relative contribution from different nerves to recurrent depression of Ia IPSPs in motoneurones
  • 1971
  • Ingår i: The Journal of Physiology. - : Wiley. - 0022-3751 .- 1469-7793. ; 215, s. 637-664
  • Tidskriftsartikel (refereegranskat)abstract
    • 1. The pattern of depression of Ia IPSPs by volleys in recurrent motor axon collaterals was investigated in motoneurones supplying hind‐limb muscles in the cat. The test IPSPs were evoked by stimulation of dorsal roots and the conditioning antidromic volleys by stimulation of motor fibres in different peripheral muscle nerves. 2. In all motor nuclei investigated the strongest depression of Ia IPSPs is evoked from motor fibres to muscles whose Ia afferents produce the IPSPs. For example, the Ia IPSP from the knee extensor recorded in motoneurones to a knee flexor is most effectively depressed by antidromic stimulation of motor fibres to the knee extensor. 3. The origin of recurrent inhibition of α‐motoneurones and of Ia inhibitory interneurones with the same Ia input display a striking similarity. This suggests that the same population of Renshaw cells mediates effects to motoneurones and to Ia inhibitory interneurones. 4. The functional significance of impulses in motor axon collaterals was discussed and it was suggested that they have an important role in the control of the excitatory as well as inhibitory Ia actions to motoneurones. The recurrent inhibition may limit the Ia effects to excitation of homonymous motoneurones, which would provide optimal conditions for control of individual muscles via the γ‐loop. © 1971 The Physiological Society
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