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  • 1
    Online Resource
    Online Resource
    The Company of Biologists ; 1986
    In:  Journal of Experimental Biology Vol. 124, No. 1 ( 1986-09-01), p. 53-72
    In: Journal of Experimental Biology, The Company of Biologists, Vol. 124, No. 1 ( 1986-09-01), p. 53-72
    Abstract: Although there is considerable evidence that depolarization of nerve cell terminals leads to the entry of Ca2+ and to the secretion of neurohormones and neurotransmitters, the details of how ionic currents control the release of neuroactive substances from nerve terminals are unknown. The small size of most nerve terminals has precluded direct analysis of membrane ionic currents and their influence on secretion. We now report that it is possible, using patch-clamp techniques, to study stimulus-secretion coupling in isolated peptidergic nerve terminals. Sinus gland terminals from Cardisoma are easily isolated following collagenase treatment and appear morphologically and electrically very similar to nondissociated nerve endings. We have observed two types of single-channel currents not previously described. The first (‘f’) channel is activated by intracellular Na+ and the second (‘s’) by intracellular Ca2+. Both show little selectivity between Na+ and K+. In symmetrical K+, these cation channels have mean conductances of 69 and 213 pS, respectively. Furthermore, at least three types of Ca2+ channels can be reconstituted from nerve terminal membranes prepared from sinus glands. Nerve terminals can also be isolated from the rat neural lobe. These neuro-secretosomes release oxytocin and vasopressin, in response to membrane depolarization, only in the presence of external Ca2+. The depolarization of the nerve endings is associated with an increase in intracellular free Ca2+ concentration and this increase, measured using a fluorescent indicator, is abolished by Ca2+ channel blockers. Channels similar in their properties to the f and s channels also exist in rat neural lobe endings. Since these channels have not been found in other neurones or neuronal structures they may be unique to peptidergic nerve terminals.
    Type of Medium: Online Resource
    ISSN: 0022-0949 , 1477-9145
    Language: English
    Publisher: The Company of Biologists
    Publication Date: 1986
    detail.hit.zdb_id: 1482461-9
    SSG: 12
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  • 2
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 1986
    In:  Nature Vol. 319, No. 6052 ( 1986-1), p. 410-412
    In: Nature, Springer Science and Business Media LLC, Vol. 319, No. 6052 ( 1986-1), p. 410-412
    Type of Medium: Online Resource
    ISSN: 0028-0836 , 1476-4687
    RVK:
    RVK:
    RVK:
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 1986
    detail.hit.zdb_id: 120714-3
    detail.hit.zdb_id: 1413423-8
    SSG: 11
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  • 3
    Online Resource
    Online Resource
    Portland Press Ltd. ; 1987
    In:  Bioscience Reports Vol. 7, No. 5 ( 1987-05-01), p. 411-426
    In: Bioscience Reports, Portland Press Ltd., Vol. 7, No. 5 ( 1987-05-01), p. 411-426
    Abstract: In the present paper we discuss the properties of a recently developed preparation of isolated neurosecretory nerve endings obtained from the rate neurohypophysis. These nerve terminals release two neurohormones, oxytocin and vasopressin, which are easily assayed by radioimmunoassay. Depolarization-induced secretion is dependent on the same parameters as those regulating release from the whole neural lobe. The isolated nerve endings can be permeabilized by means of digitonin; a treatment which gives direct access to the cytoplasm allowing the study of the minimal requirements for inducing neuropeptide release. Furthermore, some nerve endings are large enough to allow the use of the patch-clamp technique. In the present paper we present evidences which show that the isolated neurohypophysial nerve terminals represent a protent tool for studying the mechanism of stimulus-secretion.
    Type of Medium: Online Resource
    ISSN: 0144-8463 , 1573-4935
    Language: English
    Publisher: Portland Press Ltd.
    Publication Date: 1987
    detail.hit.zdb_id: 2014993-1
    SSG: 12
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  • 4
    Online Resource
    Online Resource
    Elsevier BV ; 1989
    In:  Neuron Vol. 2, No. 5 ( 1989-5), p. 1419-1426
    In: Neuron, Elsevier BV, Vol. 2, No. 5 ( 1989-5), p. 1419-1426
    Type of Medium: Online Resource
    ISSN: 0896-6273
    Language: English
    Publisher: Elsevier BV
    Publication Date: 1989
    detail.hit.zdb_id: 2001944-0
    SSG: 12
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