Pregled bibliografske jedinice broj: 41343
[3H]Flunitrazepam binding to recombinant alpha1 beta2 gamma 2s GABA-A receptors stably expressed in HEK 293 cells
[3H]Flunitrazepam binding to recombinant alpha1 beta2 gamma 2s GABA-A receptors stably expressed in HEK 293 cells // Biomedicine and pharmacotherapy, 55 (2001), 4; 221-228 (međunarodna recenzija, članak, znanstveni)
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Naslov
[3H]Flunitrazepam binding to recombinant alpha1 beta2 gamma 2s GABA-A receptors stably expressed in HEK 293 cells
Autori
Peričić, Danka ; Jazvinšćak, Maja ; Mirković, Kety
Izvornik
Biomedicine and pharmacotherapy (0753-3322) 55
(2001), 4;
221-228
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
[3H]flunitrazepam; GABA-A receptor recombinant; allosteric interactions
Sažetak
The interaction of selected compounds with the binding of the benzodiazepine [H-3]flunitrazepam to membranes isolated from human embryonic kidney (HEK) 293 cells,stably transfected with the alpha (1)beta (2)gamma(2S) subtype of GABA(A) receptors, was studied. This subtype of GABA(A) receptors is the most common type of GABA(A)receptor found in the brain, and benzodiazepines are drugs known to enhance the effects of the nhibitory neurotransmitter gamma-amino butyric acid (GABA) by binding to the benzodiazepine binding sites which are part of the GABA(A) receptor complex. Scatchard analysis of binding data revealed the existence of a single type of binding site for [H-3]flunitrazepam. GABA and thiopental enhanced, while the antagonist of central benzodiazepine binding sites - flumazenil, benzodiazepines such as clonazepam,flunitrazepam and diazepam, and the triazolopyridazine CI 218,872 - displaced with nanomolar potency the binding of [H-3]flunitrazepam. A partial displacement was obtained with the antagonist of the peripheral benzodiazepine binding sites - PK 11195 - and with the neurosteroid dehydroepiandrosterone sulfate. The potency of drugs to enhance or inhibit [H-3]flunitrazepam binding mainly corresponded to that observed for the modulation of the binding of [H-3]flunitrazepam to the native type 1 benzodiazepine binding sites. This, as well as a high density of expressed binding sites, makes the cell line under study a very reliable and economical model for the testing of effects of different compounds at the GABA(A) receptor.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE
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