PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 8873559-0 1996 Halothane and diazepam inhibit ketamine-induced c-fos expression in the rat cingulate cortex. Halothane 0-9 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 48-53 14689487-9 2004 Anesthesia with halothane induced the strongest c-Fos expression in a restricted pool of pmXII located in the pons at the level of the Kolliker-Fuse nucleus and the intertrigeminal region. Halothane 16-25 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 48-53 12587265-0 2002 [C-fos gene expression in the rat spinal cord and brain cells during stress and the use of different types of halothane anesthesia]. Halothane 110-119 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 1-6 12587265-2 2002 Using of 1.5% light halothane narcosis allowed the detection of c-Fos-like proteins expression in the spinal cord cells only. Halothane 20-29 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 64-69 12587265-3 2002 Under initial 1.5% halothane narcosis, c-Fos-like proteins expression in the rat spinal cord (lumbar segments) and the brain cells was observed after placing the rats into the hammock, noxious mechanical stimulation (NMS) or high frequency electromagnetic irradiation of the skin (EHF). Halothane 19-28 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 39-44 11561259-8 2001 Halothane inhalation affected the results of both the behavior and the c-fos immunoreactivity, especially in the 10% formalin (3.7% formaldehyde) group. Halothane 0-9 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 71-76 10513171-0 1999 [The study of the anesthetic action of halothane on the rat spinal cord by fos immunoreactivity]. Halothane 39-48 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 75-78 10513171-1 1999 This study was performed to examine the anesthetic action of halothane on the spinal cord of rats by using fos immunoreactivity, a marker for neuronal activity following noxious stimulation. Halothane 61-70 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 107-110 10513171-9 1999 The number of fos immunoreactive cells decreased in the cord of rats that showed no response to noxious stimulation by halothane 1 or 1.5 MAC. Halothane 119-128 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 14-17 15341219-0 2004 Expression of the c-fos gene in spinal cord and brain cells in rats subjected to stress in conditions of exposure to various types of halothane anesthesia. Halothane 134-143 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 18-23 15341219-2 2004 Synthesis of c-Fos-like proteins occurred only in the spinal cord in conditions of constant 1.5% halothane anesthesia. Halothane 97-106 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 13-18 15341219-3 2004 Use of induction anesthesia with 1.5% halothane allowed detection of c-Fos-like protein expression in cells of the rat spinal cord (lumbar segments) and brain, both when animals were placed in a hammock and when mechanical pain stimulation or electromagnetic irradiation of the skin with UHF currents were applied. Halothane 38-47 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 69-74 12749994-0 2003 The effects of dexmedetomidine and halothane on Fos expression in the spinal dorsal horn using a rat postoperative pain model. Halothane 35-44 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 48-51 12749994-1 2003 We investigated the effect of an intrathecal injection of a selective alpha2 adrenergic receptor agonist, dexmedetomidine (Dex), and halothane anesthesia on Fos expression in the lumbar spinal dorsal horn after skin incision of the plantar surface of the hind paw, a postoperative pain model using rats. Halothane 133-142 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 157-160 12749994-3 2003 Halothane anesthesia (0.5-1.5%) partially reversed Fos induction, but not in a dose-dependent manner. Halothane 0-9 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 51-54 10930210-8 2000 Sustained noxious stimulation to the hindpaw in halothane-anesthetized animals was associated with an increase in c-fos immunoreactivity in the dorsal horn of the lumbar spinal cord ipsilateral to the stimulation (P < 0.001). Halothane 48-57 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 114-119 9098575-1 1997 The effects of inhalation anesthetics, nitrous oxide (N2O) and halothane, on the expression of c-Fos protein evoked by formalin injection were studied in the spinal cord in the rat. Halothane 63-72 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 95-100 9098575-8 1997 Both N2O and halothane suppressed the expression of c-Fos in the neck of the dorsal horn and ventral gray in a dose-dependent manner, but no effects were seen at the superficial layer or nucleus proprius. Halothane 13-22 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 52-57 9098575-9 1997 Suppression of c-Fos expression was greater under N2O than halothane anesthesia. Halothane 59-68 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 15-20 8873559-4 1996 METHODS: The effects of diazepam and halothane on c-Fos expression induced by ketamine were studied. Halothane 37-46 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 50-55 8873559-11 1996 Halothane suppressed the ketamine-induced c-Fos-like immunoreactivity in the cingulate and retrosplenial cortices and the neocortex in a dose-dependent manner, leaving the thalamus relatively unaffected. Halothane 0-9 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 42-47 8873559-12 1996 CONCLUSION: Halothane and diazepam inhibited ketamine-induced c-Fos expression in the cingulate and retrosplenial cortices, leaving the thalamus relatively unaffected. Halothane 12-21 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 62-67 8907361-1 1996 Immunohistochemical detection of the protein product (Fos) of the c-fos immediate early gene was used to study neuronal activation in the rostral pons and midbrain of halothane-anesthetised rats following noxious deep somatic or noxious visceral stimulation. Halothane 167-176 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 54-57 8907361-1 1996 Immunohistochemical detection of the protein product (Fos) of the c-fos immediate early gene was used to study neuronal activation in the rostral pons and midbrain of halothane-anesthetised rats following noxious deep somatic or noxious visceral stimulation. Halothane 167-176 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 66-71 8907361-2 1996 In animals exposed only to halothane anesthesia, Fos-like immunoreactive (IR) neurons were located in the midbrain periaqueductal gray matter, tectum, and parabrachial nucleus. Halothane 27-36 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 49-52 8907361-3 1996 Following noxious stimulation of hindlimb muscle, knee joint, vagal cardiopulmonary, or peritoneal nociceptors, there was, compared to halothane-only animals, a significant increase in the numbers of Fos-like (IR) cells in the caudal ventrolateral periaqueductal gray and the intermediate gray lamina of the superior colliculus. Halothane 135-144 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 200-203 8063876-1 1994 Middle cerebral artery (MCA) occlusion in halothane-anesthetized rats induced c-fos, junB, and c-jun immediate early gene mRNAs and hsp70 heat shock gene mRNA in brain. Halothane 42-51 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 78-83 1642355-0 1992 Selective effects of pentobarbital and halothane on c-fos and jun-B gene expression in rat brain. Halothane 39-48 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 52-57 1642355-1 1992 The effects of pentobarbital and halothane anesthesia on the expression in brain of the immediate-early genes c-fos and jun-B were investigated. Halothane 33-42 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 110-115