PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
20442823-1	2009	OBJECTIVE: To study the mechanism involved in hydrogen peroxide (H(2)O(2)) or tert-butyl hydroperoxide (t-BHP)-induced potentiation of the Ang II-mediated contraction of isolated rat thoracic aorta.	tert-Butylhydroperoxide	78-102	angiogenin	Rattus norvegicus	139-142	
20442823-1	2009	OBJECTIVE: To study the mechanism involved in hydrogen peroxide (H(2)O(2)) or tert-butyl hydroperoxide (t-BHP)-induced potentiation of the Ang II-mediated contraction of isolated rat thoracic aorta.	tert-Butylhydroperoxide	104-109	angiogenin	Rattus norvegicus	139-142	
20442823-3	2009	To explore the probable mechanism of H(2)O(2) and t-BHP-induced potentiation of Ang II-mediated contractile response, different blockers such as losartan (AT(1) receptor blocker; 1 muM), catalase (H(2)O(2) scavenger; 500 U/ml), lercanidipine (L-type calcium channel blocker; 1 muM), geinistein (tyrosine kinase inhibitor; 100 muM), and indomethacin (cyclo-oxygenase inhibitor; 10 muM) were used.	tert-Butylhydroperoxide	50-55	angiogenin	Rattus norvegicus	80-83	
20442823-11	2009	CONCLUSION: From the above-mentioned results, we can reasonably conclude that H(2)O(2) and t-BHP potentiated the contraction induced by the Ang II.	tert-Butylhydroperoxide	91-96	angiogenin	Rattus norvegicus	140-143	
20442823-12	2009	H(2)O(2)-induced potentiation of Ang II response may be mediated through tyrosine kinase activation and t-BHP through the activation of cyclo-oxygenase enzyme.	tert-Butylhydroperoxide	104-109	angiogenin	Rattus norvegicus	33-36