PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
8386213-5	1993	5-HT, 8-OH-DPAT (both at 10 nmol/l) and DOI (at higher concentrations) blunted the stimulatory effect of CRH.	8-Hydroxy-2-(di-n-propylamino)tetralin	6-15	corticotropin releasing hormone	Rattus norvegicus	105-108	
8945958-8	1996	The CRH antagonist alpha-helical CRH-(9-41) attenuated the increases in metabolic rate induced by DOI and 8-OH-DPAT.	8-Hydroxy-2-(di-n-propylamino)tetralin	106-115	corticotropin releasing hormone	Rattus norvegicus	4-7	
8945958-8	1996	The CRH antagonist alpha-helical CRH-(9-41) attenuated the increases in metabolic rate induced by DOI and 8-OH-DPAT.	8-Hydroxy-2-(di-n-propylamino)tetralin	106-115	corticotropin releasing hormone	Rattus norvegicus	33-36	
8386213-6	1993	The suppressive effects of 8-OH-DPAT and DOI on CRH-stimulated ACTH release were antagonized by (-)propranolol, a beta-adrenergic receptor antagonist which binds the 5-HT1A receptor with elevated affinity, and ketanserin, a 5-HT2 receptor antagonist respectively.	8-Hydroxy-2-(di-n-propylamino)tetralin	27-36	corticotropin releasing hormone	Rattus norvegicus	48-51	
1369587-6	1992	This same dose of 8-OH-DPAT also induced a decrease of hypothalamic CRH concentration, which was completely antagonized as well by pretreatment injection of (+/-)-pindolol into the PVN.	8-Hydroxy-2-(di-n-propylamino)tetralin	18-27	corticotropin releasing hormone	Rattus norvegicus	68-71	
2150776-5	1990	Pituitary stalk transection (PST), as well as pretreatment with rabbit serum hyperimmune against rat corticotropin-releasing hormone (CRH, TS-6) completely abolished beta-End-LI response to 8-OH-DPAT and attenuated the responses by about 60% to DOI.	8-Hydroxy-2-(di-n-propylamino)tetralin	190-199	corticotropin releasing hormone	Rattus norvegicus	101-132	
2150776-5	1990	Pituitary stalk transection (PST), as well as pretreatment with rabbit serum hyperimmune against rat corticotropin-releasing hormone (CRH, TS-6) completely abolished beta-End-LI response to 8-OH-DPAT and attenuated the responses by about 60% to DOI.	8-Hydroxy-2-(di-n-propylamino)tetralin	190-199	corticotropin releasing hormone	Rattus norvegicus	134-137