PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 21978215-6 2011 Intraperitoneal injection of diazepam, an anxiolytic agent, but not indomethacin, an antipyretic, significantly reduced both the stress-induced hyperthermia and Fos expression in these medullary raphe neuronal populations. Diazepam 29-37 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 161-164 25553641-7 2015 VEO and diazepam significantly increased c-fos expression in the lateral division of the central amygdaloid nucleus (CeL). Diazepam 8-16 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 41-46 24797330-0 2014 Distribution of Fos-immunoreactive cells in rat forebrain and midbrain following social defeat stress and diazepam treatment. Diazepam 106-114 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 16-19 24797330-8 2014 The diazepam treatment significantly reduced the stress-induced Fos expression in many brain regions including the prefrontal, sensory and motor cortices, septum, medial amygdaloid nucleus, medial and lateral preoptic areas, parvicellular paraventricular hypothalamic nucleus, dorsomedial hypothalamus, perifornical nucleus, tuberomammillary nucleus, association, midline and intralaminar thalami, and median and dorsal raphe nuclei. Diazepam 4-12 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 64-67 24797330-9 2014 In contrast, diazepam increased Fos-IR cells in the central amygdaloid nucleus, medial habenular nucleus, ventromedial hypothalamic nucleus and magnocellular lateral hypothalamus. Diazepam 13-21 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 32-35 1668366-4 1991 Administration of the anxiogenic beta-carboline FG 7142 also increased the total number of VTA DA neurons expressing Fos protein, whereas pretreatment with an anxiolytic benzodiazepine (diazepam) partially prevented the stress-induced increase in Fos expression. Diazepam 186-194 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 247-250 20514481-5 2010 Ultrasound-induced c-Fos expression was measured in different periaqueductal gray (PAG) and amygdala subregions after treatment with diazepam or Ro 64-6198. Diazepam 133-141 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 19-24 21636214-9 2011 Hyperalgesia and c-Fos overexpression were blocked only by prestress treatment with diazepam and post-stress treatment with ketamine, whereas changes in GABA and glutamate release were reversed by prestress treatment with diazepam. Diazepam 84-92 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 17-22 20514481-8 2010 Diazepam, but not Ro 64-6198, reduced c-Fos expression in the dPAG/dlPAG, while Ro 64-6198, but not diazepam, reduced c-Fos expression in the central amygdala. Diazepam 0-8 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 38-43 17669374-0 2007 Brainstem areas activated by diazepam withdrawal as measured by Fos-protein immunoreactivity in rats. Diazepam 29-37 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 64-67 18255166-8 2008 In FS rats, diazepam did not have effect on GABA release but reduced pain scores and overexpression of c-Fos whereas flumazenil (0.1 mg/kg, i.p. Diazepam 12-20 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 103-108 8873559-0 1996 Halothane and diazepam inhibit ketamine-induced c-fos expression in the rat cingulate cortex. Diazepam 14-22 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 48-53 15714225-0 2005 Stress-induced c-Fos expression is differentially modulated by dexamethasone, diazepam and imipramine. Diazepam 78-86 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 15-20 15714225-12 2005 We conclude that dexamethasone, diazepam and imipramine differentially modulate stress-induced Fos expression. Diazepam 32-40 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 95-98 9404938-0 1997 Modulation of c-fos expression in the rat striatum by diazepam. Diazepam 54-62 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 14-19 9404938-3 1997 Intraperitoneal administration of diazepam increased Fos protein levels in the striatum, but not in the hippocampus. Diazepam 34-42 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 53-56 9404938-6 1997 The possible mechanisms underlying the modulatory effects of diazepam on c-fos expression in the brain are discussed. Diazepam 61-69 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 73-78 9140695-10 1997 On the other hand, the increase in c-fos mRNA produced by the stress of the injection was inhibited in the cerebral cortex by diazepam or propranolol and in the hippocampus only by diazepam. Diazepam 126-134 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 35-40 9140695-10 1997 On the other hand, the increase in c-fos mRNA produced by the stress of the injection was inhibited in the cerebral cortex by diazepam or propranolol and in the hippocampus only by diazepam. Diazepam 181-189 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 35-40 8873559-4 1996 METHODS: The effects of diazepam and halothane on c-Fos expression induced by ketamine were studied. Diazepam 24-32 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 50-55 8873559-10 1996 Diazepam suppressed the ketamine-induced c-Fos-like immunoreactivity in the cingulate and retrosplenial cortices in a dose-dependent manner, leaving the thalamus and neocortex less affected. Diazepam 0-8 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 41-46 8873559-12 1996 CONCLUSION: Halothane and diazepam inhibited ketamine-induced c-Fos expression in the cingulate and retrosplenial cortices, leaving the thalamus relatively unaffected. Diazepam 26-34 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 62-67 8728564-0 1996 Expression of Fos protein in various rat brain areas following acute nicotine and diazepam. Diazepam 82-90 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 14-17 8728564-7 1996 In diazepam- and nicotine-treated rats Fos IS was increased in PVN and SON as well as in MT and i.p.. Diazepam 3-11 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 39-42 8728564-9 1996 of diazepam and nicotine-treated rats Fos IS was similar to that induced by nicotine alone, and in PVN and SON of these rats Fos IS in ACe. Diazepam 3-11 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 38-41 8728564-10 1996 Taken together, diazepam induced Fos IS in all stress-related areas studied (PVN, SON, ACe), but not in central visual structures, where nicotine induces Fos IS (MT, i.p.). Diazepam 16-24 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 33-36 8728564-10 1996 Taken together, diazepam induced Fos IS in all stress-related areas studied (PVN, SON, ACe), but not in central visual structures, where nicotine induces Fos IS (MT, i.p.). Diazepam 16-24 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 154-157 8728564-6 1996 Diazepam alone increased Fos IS in PVN and in SON as well as in ACe. Diazepam 0-8 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 25-28 7823174-9 1995 Diazepam also produced dose-related decreases in conditioned stress-induced c-fos expression in all but one structure, the effects being statistically significant in 38 of 60 sampled structures. Diazepam 0-8 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 76-81 7823174-10 1995 Diazepam dose dependently increased fear-induced c-fos expression in the central nucleus of the amygdala. Diazepam 0-8 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 49-54 7823174-13 1995 The extent to which diazepam decreased conditioned stress-induced c-fos expression was unrelated to previous estimates of benzodiazepine receptor density in the sampled structures. Diazepam 20-28 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 66-71