2017
DOI: 10.1016/j.freeradbiomed.2017.04.156
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Taking up the cudgels for the traditional reactive oxygen and nitrogen species detection assays and their use in the cardiovascular system

Abstract: Keywords:Oxidative stress Redox signaling Fluorescence and chemiluminescence-based assays Dihydroethidium oxidative fluorescence microtopography Lucigenin-enhanced chemiluminescence L-012-enhanced chemiluminescence A B S T R A C T Reactive oxygen and nitrogen species (RONS such as H 2 O 2 , nitric oxide) confer redox regulation of essential cellular functions (e.g. differentiation, proliferation, migration, apoptosis), initiate and catalyze adaptive stress responses. In contrast, excessive formation of RONS ca… Show more

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Cited by 9 publications
(10 citation statements)
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“…Subsequently, hydrogen can be liberated, which accounts for the reduction in mitochondrial potential and disruption of ATP production (61,62). The mPTP opening can also facilitate leakage of the pro-apoptotic factor cyt-c into the cytoplasm or nucleus, where it activates the caspase-9-associated mitochondrial apoptotic pathway (63,64). Based on these data, the potential processes underlying mitochondrial injury induced by glucotoxicity were determined and these findings may further extend our understanding of hyperglycemia-mediated mitochondrial damage.…”
Section: Discussionmentioning
confidence: 99%
“…Subsequently, hydrogen can be liberated, which accounts for the reduction in mitochondrial potential and disruption of ATP production (61,62). The mPTP opening can also facilitate leakage of the pro-apoptotic factor cyt-c into the cytoplasm or nucleus, where it activates the caspase-9-associated mitochondrial apoptotic pathway (63,64). Based on these data, the potential processes underlying mitochondrial injury induced by glucotoxicity were determined and these findings may further extend our understanding of hyperglycemia-mediated mitochondrial damage.…”
Section: Discussionmentioning
confidence: 99%
“…Samples were lysed in RIPA buffer containing 1 mmol/L phenylmethylsulfonyl fluoride (PMSF) followed by centrifugation for 10 minutes at 4°C. A BCA Protein Quantification Kit was used to analyze the protein concentrations . A total of 50 μg of protein for each sample were loaded and transferred to a PVDF membrane.…”
Section: Methodsmentioning
confidence: 99%
“…A BCA Protein Quantification Kit was used to analyze the protein concentrations. 33 A total of 50 μg of protein for each sample were loaded and transferred to a PVDF membrane. Primary antibodies used for immunoblotting were as follows: Ripk3…”
Section: Immunoblottingmentioning
confidence: 99%
“…Briefly, cells ( 1x10 6 ) were treated with a MitoProbe™ JC-1 assay kit (Thermo Fisher Scientific Inc.) (10 mg/ml) at 37°C in the dark for 15-20 min [47]. Subsequently, PBS was used to wash the cells three times.…”
Section: Measurement Of Mitochondrial Permeability Transition Pore (Mmentioning
confidence: 99%