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  • Pain/*physiopathology  (5)
  • American Association for the Advancement of Science (AAAS)  (5)
  • Springer Nature
  • American Geophysical Union (AGU)
  • 1980-1984  (5)
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Schlagwörter
Verlag/Herausgeber
  • American Association for the Advancement of Science (AAAS)  (5)
  • Springer Nature
  • American Geophysical Union (AGU)
Erscheinungszeitraum
  • 1980-1984  (5)
Jahr
  • 1
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    Ventral posterior thalamic neurons differentially responsive to noxious stimulation of the awake monkey (1983)
    American Association for the Advancement of Science (AAAS)
    Details
    Publikationsdatum: 1983-08-12
    Beschreibung: Of 76 cutaneously activated neurons recorded from the ventral posterior thalamus of awake, behaving monkeys, nine were weakly excited by innocuous skin stimulation and responded maximally only when noxious mechanical cutaneous stimuli were delivered within small, contralateral receptive fields. These results show that neurons capable of encoding the spatial and temporal features of noxious stimuli are located in the ventral posterior thalamus of the awake primate.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Casey, K L -- Morrow, T J -- NS 12581/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 1983 Aug 12;221(4611):675-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6867738" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; Cats ; Consciousness/physiology ; Electric Stimulation ; Neurons, Afferent/physiology ; Pain/*physiopathology ; Physical Stimulation ; Rats ; Saimiri ; Thalamic Nuclei/physiology ; Thalamus/cytology/*physiology
    Print ISSN: 0036-8075
    Digitale ISSN: 1095-9203
    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Publiziert von American Association for the Advancement of Science (AAAS)
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
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    Long-term stress-induced analgesia and activation of the opiate system (1981)
    American Association for the Advancement of Science (AAAS)
    Details
    Publikationsdatum: 1981-09-18
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Grau, J W -- Hyson, R L -- Maier, S F -- Madden, J 4th -- Barchas, J D -- New York, N.Y. -- Science. 1981 Sep 18;213(4514):1409-11.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7268445" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Analgesia ; Animals ; Electroshock ; Endorphins/antagonists & inhibitors/*physiology ; Naltrexone/pharmacology ; Pain/*physiopathology ; Rats ; Stress, Physiological/*physiopathology ; Tail ; Time Factors
    Print ISSN: 0036-8075
    Digitale ISSN: 1095-9203
    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Publiziert von American Association for the Advancement of Science (AAAS)
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
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    Corticosterone: a critical factor in an opioid form of stress-induced analgesia (1982)
    American Association for the Advancement of Science (AAAS)
    Details
    Publikationsdatum: 1982-03-19
    Beschreibung: The finding that some opioid-mediated forms of stress-induced analgesia are antagonized by hypophysectomy and dexamethasone has led to the suggestion that beta-endorphin, released from the pituitary, may mediate these analgesic reactions. "Long-term analgesia" (an opioid-mediated form of stress-induced analgesia), which is blocked by dexamethasone and hypophysectomy, was also blocked by adrenalectomy and reinstated with corticosterone therapy. Corticosterone is proposed to play a permissive role in long-term analgesia and to be a critical hormone mediating this phenomenon.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉MacLennan, A J -- Drugan, R C -- Hyson, R L -- Maier, S F -- Madden, J 4th -- Barchas, J D -- MH 23861/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 1982 Mar 19;215(4539):1530-2.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7063862" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Adrenalectomy ; Analgesia ; Animals ; Corticosterone/*physiology ; Dexamethasone/pharmacology ; Endorphins/*physiology ; Hypophysectomy ; Pain/*physiopathology ; Rats ; Stress, Physiological/*physiopathology
    Print ISSN: 0036-8075
    Digitale ISSN: 1095-9203
    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Publiziert von American Association for the Advancement of Science (AAAS)
    Standort Signatur Erwartet Verfügbarkeit
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  • 4
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    Opioid and nonopioid mechanisms of stress analgesia (1980)
    American Association for the Advancement of Science (AAAS)
    Details
    Publikationsdatum: 1980-05-09
    Beschreibung: Inescapable foot shock in rats caused profound analgesia that was antagonized by naloxone or dexamethasone when shock was delivered intermittently for 30 minutes, but not when it was delivered continuously for 3 minutes. Thus, depending only on its temporal characteristics, foot-shock stress appears to activate opioid or nonopioid analgesia mechanisms. Certain forms of stress may act as natural inputs to an endogenous opiate analgesia system.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lewis, J W -- Cannon, J T -- Liebeskind, J C -- New York, N.Y. -- Science. 1980 May 9;208(4444):623-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7367889" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): *Analgesia ; Animals ; Dexamethasone/*pharmacology ; Electroshock ; Endorphins/*physiology ; Male ; Naloxone/pharmacology ; Pain/*physiopathology ; Pituitary Gland/physiology ; Rats ; Stress, Physiological/*physiopathology ; Time Factors
    Print ISSN: 0036-8075
    Digitale ISSN: 1095-9203
    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Publiziert von American Association for the Advancement of Science (AAAS)
    Standort Signatur Erwartet Verfügbarkeit
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  • 5
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    Intrinsic mechanisms of pain inhibition: activation by stress (1984)
    American Association for the Advancement of Science (AAAS)
    Details
    Publikationsdatum: 1984-12-14
    Beschreibung: Portions of the brain stem seem normally to inhibit pain. In man and laboratory animals these brain areas and pathways from them to spinal sensory circuits can be activated by focal stimulation. Endogenous opioids appear to be implicated although separate nonopioid mechanisms are also evident. Stress seems to be a natural stimulus triggering pain suppression. Properties of electric footshock have been shown to determine the opioid or nonopioid basis of stress-induced analgesia. Two different opioid systems can be activated by different footshock paradigms. This dissection of stress analgesia has begun to integrate divergent findings concerning pain inhibition and also to account for some of the variance that has obscured the reliable measurement of the effects of stress on tumor growth and immune function.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Terman, G W -- Shavit, Y -- Lewis, J W -- Cannon, J T -- Liebeskind, J C -- MH 15795/MH/NIMH NIH HHS/ -- NS-07628/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 1984 Dec 14;226(4680):1270-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6505691" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Adaptation, Physiological ; Adrenalectomy ; Anesthesia ; Animals ; Brain Stem/physiology ; Conditioning (Psychology) ; Electroshock ; Endorphins/physiology ; Histamine/physiology ; Humans ; Hypophysectomy ; Immunosuppression ; Naltrexone/pharmacology ; Neoplasms/physiopathology ; Nociceptors/physiology ; Pain/*physiopathology ; Pentobarbital/pharmacology ; Rats ; Stress, Physiological/*physiopathology
    Print ISSN: 0036-8075
    Digitale ISSN: 1095-9203
    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Publiziert von American Association for the Advancement of Science (AAAS)
    Standort Signatur Erwartet Verfügbarkeit
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