1991
DOI: 10.1016/0047-6374(91)90079-f
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Aging in brown fat: Antioxidant defenses and oxidative stress

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Cited by 7 publications
(8 citation statements)
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“…Another component of the anti−/pro-oxidant system as it may relate to WNS involves the extreme fluctuations in oxygen consumption of bats while they periodically transition from deep torpor to euthermia [65]. During arousals, the rapid rates of oxygen consumption in brown adipose tissue (BAT) promote the generation of reactive oxygen species [66], which easily oxidize lipid molecules [67].…”
Section: Discussionmentioning
confidence: 99%
“…Another component of the anti−/pro-oxidant system as it may relate to WNS involves the extreme fluctuations in oxygen consumption of bats while they periodically transition from deep torpor to euthermia [65]. During arousals, the rapid rates of oxygen consumption in brown adipose tissue (BAT) promote the generation of reactive oxygen species [66], which easily oxidize lipid molecules [67].…”
Section: Discussionmentioning
confidence: 99%
“…For example, Lopez‐Torres et al . have reported a significant increase in the antioxidant enzymes in the BAT of 3–9‐month‐old rats. However, direct evidence of oxidative stress impairing brown adipocyte function has not been reported.…”
Section: Discussionmentioning
confidence: 96%
“…There is a large body of research suggesting that there is a causal relationship between oxidative stress and BAT dysfunction. For example, Lopez-Torres et al [15] have reported a significant increase in the antioxidant enzymes in the BAT of 3-9-monthold rats. However, direct evidence of oxidative stress impairing brown adipocyte function has not been reported.…”
Section: Discussionmentioning
confidence: 99%
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“…Changes in absorbance were read on a SPECTRAmax Plus microplate spectrophotometer (Molecular Devices Corp. Sunnyvale, CA, USA). Additionally, the GSH-Px was assayed at 25°C as described by Paglia and Valentine (1967) and Lopez-Torres et al (1991), wherein NADPH oxidation was followed by spectrophotometry at 340 nm in the presence of reduced glutathione (GSH) and hydrogen peroxide (H 2 O 2 ). To correct spontaneous reactions in the absence of enzyme, blanks were run without samples and then subtracted from the assay values.…”
Section: Methodsmentioning
confidence: 99%