PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
10617146-7	2000	Exposure of raphe cells to 5-HT, (+/-)-8 hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT; a 5-HT1A agonist), or citalopram induced a significant decrease in number of GR binding sites.	8-Hydroxy-2-(di-n-propylamino)tetralin	33-77	nuclear receptor subfamily 3, group C, member 1	Rattus norvegicus	167-169