PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 10677633-1 2000 The present study investigated the effect of clonidine on the basal and inducible c-jun and c-fos mRNA expression in the nucleus tractus solitarius (middle, mNTS, and rostral, rNTS) and the rostral ventrolateral medulla (caudal, cRVLM, and rostral, rRVLM). Clonidine 45-54 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 92-97 10677633-5 2000 Clonidine attenuated the increases in c-fos in the mNTS and cRVLM and c-jun gene expression in the mNTS and rRVLM caused by NP-evoked hypotension and also reduced the basal expression of c-jun mRNA in the mNTS and rRVLM. Clonidine 0-9 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 38-43 10677633-6 2000 These findings establish a causal link between clonidine inhibition of c-fos expression in brainstem and its hypotensive action, and provide the first evidence that clonidine attenuates the expression of the closely linked c-jun gene in neurons implicated in centrally mediated hypotension. Clonidine 47-56 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 71-76 7624831-0 1995 NMDA antagonists and clonidine block c-fos expression during morphine withdrawal. Clonidine 21-30 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 37-42 9295196-0 1997 Atipamezole-precipitated clonidine withdrawal induces c-Fos expression in rat central nervous system. Clonidine 25-34 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 54-59 9295196-5 1997 The brains of the clonidine-atipamezole group showed massive c-Fos expression (especially in di- and telencephalon) while the other groups showed either background levels of c-Fos-immunopositive cells (saline-saline and clonidine-saline groups) or a slight increase over background in selected areas (saline-atipamezole group). Clonidine 18-27 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 61-66 8544995-0 1995 Effect of administration of high dose intrathecal clonidine or morphine prior to sciatic nerve section on c-Fos expression in rat lumbar spinal cord. Clonidine 50-59 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 106-111 8544995-1 1995 The effects of moderate and high intrathecal doses of clonidine, an alpha 2 adrenoceptor agonist, or a high dose of morphine on sciatic nerve section-induced expression of c-Fos-like immunoreactivity was studied in laminae I and II of the dorsal horn and laminae VIII and IX of the ventral horn of rat lumbar spinal cord. Clonidine 54-63 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 172-177 8544995-2 1995 c-Fos-like immunoreactivity was examined by immunohistochemistry in normal rats (group 1), rats implanted with an intrathecal catheter with its tip on the lumbar spinal cord (group 2), injected with 10 micrograms (group 3) or 50 micrograms (group 4) clonidine intrathecally 3 h before being killed. Clonidine 250-259 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 0-5 8544995-6 1995 The level of c-Fos-like immunoreactivity after 10 or 50 micrograms intrathecal clonidine was similar as in the intrathecal catheter group. Clonidine 79-88 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 13-18 8544995-8 1995 Pretreatment with 10 or 10 micrograms clonidine did not reduce sciatic nerve section-induced expression of c-Fos-like immunoreactivity, but instead caused a significant bilateral increase in c-Fos-like immunoreactivity. Clonidine 38-47 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 191-196 9295196-8 1997 In the three brainstem structures the number of c-Fos-positive cells was elevated 8-10-fold in the clonidine-atipamezole group compared to the other groups. Clonidine 99-108 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 48-53 9295196-10 1997 An increased number of c-Fos-positive neurons was also noted in the dorsal horn and intermediate layers of the thoracic spinal cord in the clonidine-atipamezole group compared to a sham-operated atipamezole-injected group. Clonidine 139-148 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 23-28 9295196-11 1997 In the RVL, 59% of c-Fos-positive cells contained alpha2A-adrenergic receptor-like immunoreactivity in clonidine-atipamezole treated (withdrawing) rats. Clonidine 103-112 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 19-24 9295196-12 1997 In addition, one-third of the tyrosine hydroxylase (TH)-immunopositive cells in RVL were also c-Fos-positive in clonidine withdrawing rats where no TH-positive cells were also c-Fos-positive in RVL of control groups. Clonidine 112-121 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 94-99 9295196-17 1997 In conclusion, administration of the selective alpha2-antagonist atipamezole to rats chronically treated with the alpha2-adrenergic agonist clonidine triggers a powerful withdrawal syndrome associated with massive CNS expression of c-Fos protein. Clonidine 140-149 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 232-237 7756634-4 1995 Coinjections of NPY and l-adrenaline or clonidine into the NTS reduced the NPY-induced increase in c-Fos IR. Clonidine 40-49 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 99-104 7542145-14 1995 C-Fos expression induced by naltrexone-precipitated withdrawal was examined in the brainstem of freely moving morphine-dependent rats pretreated with clonidine or saline before injection of the opioid antagonist. Clonidine 150-159 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 0-5 19120051-14 2009 Clonidine (60 microg/kg) or ethanol (1 g/kg) alone increased, but their combination decreased, c-Fos levels in LC, while inconsistent c-Fos responses were observed in cerebellum. Clonidine 0-9 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 95-100 1327843-0 1992 Expression of Fos-like immunoreactivity by yohimbine and clonidine in the rat brain. Clonidine 57-66 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 14-17 33188843-6 2021 The ingestive behavior was not significantly affected by PHE treatment in the DR. CLO treatment increased Fos expression in the arcuate nucleus (ARC) and paraventricular nucleus of the hypothalamus (PVN) in rats that were allowed to eat during the experimental recording (AF group). Clonidine 82-85 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 106-109 33188843-9 2021 However, double-labeled POMC/Fos cells were absent in the ARC of the WAF group, although an increase in Fos expression was observed in non-POMC cells after CLO injections in the WAF group. Clonidine 156-159 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 104-107 18838113-8 2008 Four experiments with unilateral clonidine injections into the A7 region and with Fos immunohistochemistry used as a marker of cell activity revealed that the percentage of Fos-positive A7 cells was significantly reduced on the injected side. Clonidine 33-42 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 173-176