PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 29232839-6 2017 However, the sedative-hypnotic effects were blocked by the type A GABA (GABAA) receptor antagonists bicuculline and flumazenil. Flumazenil 116-126 gamma-aminobutyric acid (GABA) A receptor, subunit gamma 1 Mus musculus 72-77 2554616-5 1989 Systemic flumazepil administration contributed to the memory trace reproduction against the background of GABA-A receptors activation by muscimol in the dose of 0.5 mg/kg. Flumazenil 9-19 gamma-aminobutyric acid (GABA) A receptor, subunit gamma 1 Mus musculus 106-112 33143464-4 2021 The effect of selective receptor antagonist GABAA on anticonvulsant activity was investigated with flumazenil. Flumazenil 99-109 gamma-aminobutyric acid (GABA) A receptor, subunit gamma 1 Mus musculus 44-49 28551554-7 2017 Ketanserin (6mug), a 5-HT2A/C receptor antagonist, and flumazenil (6mug), a GABAA receptor antagonist, abolished the antihyperalgesic effect of mexicanolide 1 (3mug). Flumazenil 55-65 gamma-aminobutyric acid (GABA) A receptor, subunit gamma 1 Mus musculus 76-81 23806621-10 2013 The GABAA inverse agonist, FG-7142, reduced sociability and this was reversed by the GABAA antagonist, flumazenil and dcycloserine, but not by clozapine, or the GABAA benzodiazepine anxiolytic, alprazolam. Flumazenil 103-113 gamma-aminobutyric acid (GABA) A receptor, subunit gamma 1 Mus musculus 4-9 28111292-4 2017 Midazolam-induced p-MEK1/2 upregulation was prevented by pretreatment (30min) with flumazenil (10mg/kg), indicating the involvement of GABAA receptors. Flumazenil 83-93 gamma-aminobutyric acid (GABA) A receptor, subunit gamma 1 Mus musculus 135-140 27573669-9 2016 These effects of (-)-alpha-pinene on sleep and inhibitory synaptic response were mimicked by zolpidem, acting as a modulator for GABAA-BZD receptors, and fully antagonized by flumazenil, an antagonist for GABAA-BZD receptor. Flumazenil 175-185 gamma-aminobutyric acid (GABA) A receptor, subunit gamma 1 Mus musculus 205-210 21518336-6 2011 The anti-epileptic effect of magnolol was reversed by the GABA(A)/benzodiazepine receptor antagonist flumazenil. Flumazenil 101-111 gamma-aminobutyric acid (GABA) A receptor, subunit gamma 1 Mus musculus 58-89 11669460-6 2001 TJ-24-induced SI behavior was significantly blocked by the GABA(A)/BZP receptor inverse agonist Ro 15-4513 and the GABA(A)/BZP receptor antagonist flumazenil. Flumazenil 147-157 gamma-aminobutyric acid (GABA) A receptor, subunit gamma 1 Mus musculus 115-135 17570441-8 2007 In addition, the anxiolytic-like properties of sinapic acid examined in the EPM test were blocked by flumazenil or bicuculline, which are GABA(A) antagonists. Flumazenil 101-111 gamma-aminobutyric acid (GABA) A receptor, subunit gamma 1 Mus musculus 138-145 21945440-5 2011 The hypnotic activity of ILTG was fully inhibited by flumazenil (FLU), a specific gamma-aminobutyric acid type A (GABA(A))-benzodiazepine (BZD) receptor antagonist. Flumazenil 53-63 gamma-aminobutyric acid (GABA) A receptor, subunit gamma 1 Mus musculus 114-152 21945440-5 2011 The hypnotic activity of ILTG was fully inhibited by flumazenil (FLU), a specific gamma-aminobutyric acid type A (GABA(A))-benzodiazepine (BZD) receptor antagonist. Flumazenil 65-68 gamma-aminobutyric acid (GABA) A receptor, subunit gamma 1 Mus musculus 114-152 15582681-13 2004 The inhibition of U50 tolerance by melatonin was reversed by the chronic treatment with flumazenil (0.1 mg/kg), a benzodiazepine receptor antagonist and picrotoxin (1 mg/kg), a GABAA-gated chloride channel blocker. Flumazenil 88-98 gamma-aminobutyric acid (GABA) A receptor, subunit gamma 1 Mus musculus 177-182 8972548-4 1996 In contrast, progesterone (1 mg/kg, for 9 days) produced a significant antistress effect, which was blocked by GABA-A antagonists picrotoxin (1 mg/kg) and bicuculline (1 mg/kg), but not by flumazenil (2 mg/kg), a specific benzodiazepine (BZD) antagonist. Flumazenil 189-199 gamma-aminobutyric acid (GABA) A receptor, subunit gamma 1 Mus musculus 111-117