PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
2450590-3	1988	However, VIP and 8-bromo-cyclic AMP, when added in combination with carbamylcholine, potentiated the stimulation of amylase release to 170-180% of that caused by carbamylcholine alone.	Carbachol	162-177	vasoactive intestinal polypeptide	Mus musculus	9-12	
2450590-4	1988	As assessed by two-dimensional gel electrophoresis, VIP reproduced four of the ten changes in protein phosphorylation elicited by carbamylcholine, these changes being the increased phosphorylation of one soluble protein and the decreased phosphorylation of three soluble proteins.	Carbachol	130-145	vasoactive intestinal polypeptide	Mus musculus	52-55	
2450590-5	1988	VIP enhanced the carbamylcholine-induced changes in phosphorylation for three proteins.	Carbachol	17-32	vasoactive intestinal polypeptide	Mus musculus	0-3	
2450590-10	1988	Moreover, these effects appear to be mediated primarily by VIP-preferring receptors and may be involved in the synergistic action of VIP to promote carbamylcholine-induced amylase release.	Carbachol	148-163	vasoactive intestinal polypeptide	Mus musculus	59-62	
2450590-10	1988	Moreover, these effects appear to be mediated primarily by VIP-preferring receptors and may be involved in the synergistic action of VIP to promote carbamylcholine-induced amylase release.	Carbachol	148-163	vasoactive intestinal polypeptide	Mus musculus	133-136	
4070020-6	1985	Moreover, a high dose of carbachol could inhibit VIP-induced radioiodine secretion.	Carbachol	25-34	vasoactive intestinal polypeptide	Mus musculus	49-52	
4070020-7	1985	Methylatropine did not influence TSH- or VIP-stimulated radioiodine secretion, but counteracted the inhibitory action of carbachol on TSH- and VIP-induced radioiodine release.	Carbachol	121-130	vasoactive intestinal polypeptide	Mus musculus	143-146	
6204039-5	1984	VIP, IBMX and 8-Br-cyclic AMP, all of which act through or mimic the action of cyclic AMP, potentiated the secretory response to maximal concentrations of CCK, carbamylcholine and the ionophore A23187, all of which act via intracellular calcium.	Carbachol	160-175	vasoactive intestinal polypeptide	Mus musculus	0-3	
6175231-3	1982	Carbamylcholine and the C-terminal octapeptide of cholecystokinin also augmented the action of VIP on amylase secretion from mouse pancreatic acini.	Carbachol	0-15	vasoactive intestinal polypeptide	Mus musculus	95-98