PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 30125791-7 2018 Independent of group, DEX and GTS-21 dose-dependently inhibited TNF-alpha and IL-10 production, whereas TERB inhibited TNF-alpha and upregulated IL-10 production. Terbutaline 104-108 tumor necrosis factor Homo sapiens 119-128 17112600-3 2007 METHODS: We analyzed the in vitro effects of the beta-adrenergic agonist terbutaline and the glucocorticoid agonist dexamethasone on TNF-alpha and IL-10 production by LPS-stimulated monocytes in whole cell blood cultures in patients with inflammatory bowel diseases in remission (N=10), diarrhoea-predominant irritable bowel syndrome (IBS, N=12), patients with a recent gastroenteritis (post-infectious group, N=10), and healthy controls (N=15). Terbutaline 73-84 tumor necrosis factor Homo sapiens 133-142 21901530-13 2011 The cells will respond to the beta-adrenergic receptor agonist terbutaline resulting in reduced TNF-alpha and increased IL-10 and IL-6 production following CEA activation. Terbutaline 63-74 tumor necrosis factor Homo sapiens 96-105 17112600-5 2007 In contrast, terbutaline resulted in a concentration-dependent suppression of TNF-alpha production, which was comparable in all groups. Terbutaline 13-24 tumor necrosis factor Homo sapiens 78-87 12417450-0 2002 Oral terbutaline differentially affects cytokine (IL-10, IL-12, TNF, IFNg) release in multiple sclerosis patients and controls. Terbutaline 5-16 tumor necrosis factor Homo sapiens 64-67 12538816-6 2003 In the same manner, salbutanol and terbutaline as well as norepinephrine, epinephrine, and isoproterenol regulated the IL-18-induced cytokine production, including IL-12, tumor necrosis factor-alpha or interferon-gamma through the stimulation of beta 2-AR. Terbutaline 35-46 tumor necrosis factor Homo sapiens 171-198 11193379-7 2000 A beta-adrenoceptor agonists (beta-agonist), procaterol, clenbuterol, fenoterol and terbutaline suppressed the production of TNF- and IL-1 beta. Terbutaline 84-95 tumor necrosis factor Homo sapiens 125-128 11675405-9 2001 Terbutaline (10(-6) M to 10(-8) M) suppressed MAPK (p42/p44, p38), NF-kappa B (p50, p65), and TNF-alpha promoter activity in a dose-dependent way that was prevented by the beta(2)-adrenoceptor antagonist, ICI118,551. Terbutaline 0-11 tumor necrosis factor Homo sapiens 94-103 11675405-12 2001 In summary, the downregulation of TNF-alpha transcription by terbutaline was mediated by an inhibitory effect of beta(2)-adrenoceptor activation on MAPK (p42/p44, p38) and NF-kappa B (p50/p65), which were exerted through a cAMP-PKA pathway and a cAMP-independent mechanism. Terbutaline 61-72 tumor necrosis factor Homo sapiens 34-43 10469353-5 1999 Furthermore, the time course effects of terbutaline on cAMP, MAPK (p42/p44), and TNF-alpha release were evaluated in the cells. Terbutaline 40-51 tumor necrosis factor Homo sapiens 81-90 10469353-10 1999 The terbutaline-induced down-regulation of IL-6 gene production was mediated by an inhibitory effect of terbutaline on TNF-alpha, which was exerted through the MAPK and cAMP pathways, whereas the up-regulation appeared to be due to a direct action of intracellular cAMP. Terbutaline 4-15 tumor necrosis factor Homo sapiens 119-128 10469353-10 1999 The terbutaline-induced down-regulation of IL-6 gene production was mediated by an inhibitory effect of terbutaline on TNF-alpha, which was exerted through the MAPK and cAMP pathways, whereas the up-regulation appeared to be due to a direct action of intracellular cAMP. Terbutaline 104-115 tumor necrosis factor Homo sapiens 119-128 9127437-2 1997 The beta-agonists, procaterol, clenbuterol, fenoterol and terbutaline, inhibited TNF-alpha and IL-1 beta production in a concentration-dependent manner, whereas they had no effect on IL-8 production. Terbutaline 58-69 tumor necrosis factor Homo sapiens 81-90