PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
20592767-11	2009	These results suggest that there is a direct relationship between the lipid peroxidation and nitrite contents during epileptic activity that can be responsible for the superoxide dismutase and catalase enzymatic activity changes observed during the establishment of seizures and SE induced by pilocarpine.	Nitrites	93-100	catalase	Rattus norvegicus	193-201	
12690103-1	2003	A significant increase in the induction of inducible nitric-oxide synthase (iNOS) protein expression and in the levels of nitrite plus nitrate was observed in rat aortic smooth muscle cells (RASMCs) stably transfected with catalase (RASMC-2C2) as compared with empty vector-transfected RASMC-V4 cells after exposure to cytokines and lipopolysaccharide.	Nitrites	122-129	catalase	Rattus norvegicus	223-231	
16632127-9	2006	A line of evidence including inhibitor studies, EPR spectroscopy, and nitrite/nitrate detection identifies catalase as a possible oxidant for the conversion of hydroxyurea to NO.	Nitrites	70-77	catalase	Rattus norvegicus	107-115	
7833830-2	1994	It reduced the rate of methemoglobin formation from oxyhemoglobin exposed to nitric oxide generated from the reaction of hydroxylamine with Complex I of catalase and it decreased the amount of nitrite formed in the reaction of oxygen with nitric oxide generated from sodium nitroprusside.	Nitrites	193-200	catalase	Rattus norvegicus	153-161	
3220326-0	1988	Interaction of nitrite with catalase in the perfused rat liver.	Nitrites	15-22	catalase	Rattus norvegicus	28-36	
3220326-1	1988	The interaction of nitrite with catalase was investigated spectrophotometrically in the perfused rat liver.	Nitrites	19-26	catalase	Rattus norvegicus	32-40	
3220326-6	1988	It was concluded that relatively low concentrations of nitrite caused decomposition of catalase compound I in the physiologically functioning liver cell.	Nitrites	55-62	catalase	Rattus norvegicus	87-95	
31251976-7	2019	While 2K1C hypertension decreased nuclear Nrf2 accumulation, both doses of nitrite increased nuclear Nrf2 accumulation and mRNA expression of Nrf2-regulated genes including superoxide dismutase-1 (SOD1), catalase (CAT), glutathione peroxidase (GPX), thioredoxin-1(TRDX-1) and -2 (TRDX-2).	Nitrites	75-82	catalase	Rattus norvegicus	204-212	
29609494-7	2019	Diminution of SOD, GPx, GR and CA activity was congruent with elevated nitrite levels and upregulation of iNOS and UCP-2 expression, without any DNA damage.	Nitrites	71-78	catalase	Rattus norvegicus	31-33	
31251976-7	2019	While 2K1C hypertension decreased nuclear Nrf2 accumulation, both doses of nitrite increased nuclear Nrf2 accumulation and mRNA expression of Nrf2-regulated genes including superoxide dismutase-1 (SOD1), catalase (CAT), glutathione peroxidase (GPX), thioredoxin-1(TRDX-1) and -2 (TRDX-2).	Nitrites	75-82	catalase	Rattus norvegicus	214-217	
27670067-7	2016	Among the doses of nitrite evaluated, the 50 nM was proved efficient: it significantly reduced cytolysis, mitochondrial damage, and lipid peroxidation, and enhanced antioxidant enzyme activity (superoxide dismutase, catalase, and glutathione peroxidase activity) and hepatic function parameters (portal resistance, bile flow, and bromosulfophthalein clearance).	Nitrites	19-26	catalase	Rattus norvegicus	216-224	
27992114-13	2017	CONCLUSIONS: The increase in total nitrite/nitrotyrosine in DM promoted significant compensatory increases in antioxidant activities of SOD, catalase and glutathione peroxidase/reductase probably to prevent cardiac oxidative damage.	Nitrites	35-42	catalase	Rattus norvegicus	141-149