PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
1369587-3	1992	In this report, microinjection of 8-hydroxy-2-(di-n-propylamino) tetralin (8-OH-DPAT), a selective 5-HT1A agonist, into the PVN increased rat plasma ACTH concentration in a dose-related manner.	8-Hydroxy-2-(di-n-propylamino)tetralin	34-73	5-hydroxytryptamine receptor 1A	Rattus norvegicus	99-105	
1369587-3	1992	In this report, microinjection of 8-hydroxy-2-(di-n-propylamino) tetralin (8-OH-DPAT), a selective 5-HT1A agonist, into the PVN increased rat plasma ACTH concentration in a dose-related manner.	8-Hydroxy-2-(di-n-propylamino)tetralin	75-84	5-hydroxytryptamine receptor 1A	Rattus norvegicus	99-105	
1369587-4	1992	Similar responses were observed when two other 5-HT1A agonists, busipirone and gepirone, were used.	busipirone	64-74	5-hydroxytryptamine receptor 1A	Rattus norvegicus	47-53	
1369587-5	1992	(+/-)-Pindolol, known to have 5-HT1A antagonist properties, blocked the effect induced by an optimal dose of 8-OH-DPAT after injection into the PVN.	Pindolol	0-14	5-hydroxytryptamine receptor 1A	Rattus norvegicus	30-36	
1369587-5	1992	(+/-)-Pindolol, known to have 5-HT1A antagonist properties, blocked the effect induced by an optimal dose of 8-OH-DPAT after injection into the PVN.	8-Hydroxy-2-(di-n-propylamino)tetralin	109-118	5-hydroxytryptamine receptor 1A	Rattus norvegicus	30-36	
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	
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.	Pindolol	157-171	corticotropin releasing hormone	Rattus norvegicus	68-71