PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
8103010-9	1993	The somatostatin analogue exerts a long-lasting inhibitory action on gastric acid, pancreatic enzyme and bicarbonate secretion as well as on bile flow.	Bicarbonates	105-116	somatostatin	Homo sapiens	4-16	
2888607-6	1987	Bicarbonate concentration was slightly but significantly reduced only by the two highest doses of somatostatin.	Bicarbonates	0-11	somatostatin	Homo sapiens	98-110	
2888607-9	1987	The results demonstrate that: (1) the administration of somatostatin at a low dose level does not affect human exocrine pancreatic secretion, at least under the experimental conditions of this study; and (2) the administration of larger doses of somatostatin inhibits pancreatic secretion of both protein and bicarbonate dose-dependently.	Bicarbonates	309-320	somatostatin	Homo sapiens	246-258	
6131942-1	1983	Somatostatin-producing cerebral cortical cell cultures were grown in either high- (33 mM) or low-glucose (5 mM) medium and then exposed to short repetitive changes of high- or low-glucose Krebs-Ringer"s bicarbonate buffer.	Bicarbonates	203-214	somatostatin	Homo sapiens	0-12	
7907564-4	1994	Somatostatin probably inhibits pancreatic exocrine secretion by a variety of mechanisms which depend on the species and the type of secretion studied (postprandial vs. interdigestive secretion, protein vs. bicarbonate secretion): Somatostatin may act via inhibition of the release of circulating hormones such as cholecystokinin (CCK) and secretin or via intrapancreatic inhibition of the release or action of CCK.	Bicarbonates	206-217	somatostatin	Homo sapiens	0-12	
1351858-2	1992	To evaluate the possibility that the increased levels of S-28 post cibum might modulate the release of enzymes and bicarbonate from the exocrine pancreas, S-28 was infused intravenously into healthy volunteers to levels seen after food intake.	Bicarbonates	115-126	somatostatin	Homo sapiens	57-61	
1351858-3	1992	During S-28 infusion, the output of lipase, trypsin, amylase, and bicarbonate stimulated by either exogenous cholecystokinin octapeptide or endogenous signals from intraduodenal administration of tryptophan or a mixture of amino acids was significantly reduced.	Bicarbonates	66-77	somatostatin	Homo sapiens	7-11	
1967642-8	1990	Mucosal lsc responses to SS-14 were absent in tissues bathed in HCO3-free media.	Bicarbonates	64-68	somatostatin	Homo sapiens	25-30