Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Bulletin of experimental biology and medicine 83 (1977), S. 332-334 
    ISSN: 1573-8221
    Keywords: diazepam ; bicuculline ; γ-aminobutyric acid ; thiosemicarbazide
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Bicuculline, a specific blocking agent of GABA-ergic receptors, in doses of 0.5 and 1 mg/kg (subcutaneously); and thiosemicarbazide, which inhibits GABA (γ-aminobutyric acid) synthesis in the brain, in doses of 5 and 8 mg/kg (subcutaneously); are antagonists of diazepam and weaken its tranquilizing action during conflict behavior in experimental rats. Bicuculline exhibits stronger antagonism toward diazepam than thiosemicarbazide. The results are evidence that GABA-ergic mechanisms may participate in the tranquilizing action of the benzodiazepines.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Bulletin of experimental biology and medicine 79 (1975), S. 270-273 
    ISSN: 1573-8221
    Keywords: paroxysmal states ; thiosemicarbazide ; γ-aminobutyric acid (GABA) ; anticonvulsants (diazepam) ; brain mitochondria
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Diazepam is highly effective in the prevention of convulsions induced by thiosemicarbazide (TSC), i.e., due to γ-aminobutyric acid (GABA) deficiency. Electrophysiological experiments to record the recovery cycle of the interzonal response of the cat motor cortex showed that diazepam reduces the amplitude of the test response, indicating the strengthening of inhibition. This test revealed antagonism of diazepam to bicuculline, specifically blocking GABA-ergic receptors, and to TSC. Diazepam was shown to be capable of increasing the GABA concentration in the brain by inhibiting the activity of GABA transaminase in the mitochondrial fraction of brain tissue.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Bulletin of experimental biology and medicine 88 (1979), S. 711-714 
    ISSN: 1573-8221
    Keywords: GABA ; morphine ; cyclic nucleotides ; opiate receptors ; bicuculline ; thiosemicarbazide ; analgesia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract In order to detect possible interaction between GABA and opiates, the effects of GABA-ergic drugs on analgesia induced by morphine were studied. The vocalization response to electrical stimulation of the tail in rats was used as an index of the action of morphine. Thiosemicarbazide, an inhibitor of glutamate decarboxylase, and bicuculline, which blocks GABA-ergic receptors, drugs which, it is suggested, can be considered as a group of GABA-negative compounds, weaken and shorten the effect of morphine. Depakine, an inhibitor of α-ketoglutarate-GABA-transaminase, like GABA itself, given in large doses (GABA-positive effects) strengthens morphine analgesia and prolongs its effect. The possible causes of these relations between GABA and opiates are discussed.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...