2021
DOI: 10.3390/antiox10121932
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Powdered Green Tea (Matcha) Attenuates the Cognitive Dysfunction via the Regulation of Systemic Inflammation in Chronic PM2.5-Exposed BALB/c Mice

Abstract: This study was conducted to evaluate the anti-amnesic effect of the aqueous extract of powdered green tea (matcha) (EM) in particulate matter (PM)2.5-induced systemic inflammation in BALB/c mice. EM ameliorated spatial learning and memory function, short-term memory function, and long-term learning and memory function in PM2.5-induced mice. EM protected against antioxidant deficit in pulmonary, dermal, and cerebral tissues. In addition, EM improved the cholinergic system through the regulation of acetylcholine… Show more

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Cited by 20 publications
(25 citation statements)
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“…PM 2.5 induces mitochondrial dysfunction, resulting in cellular oxidative stress and cellular energy supply inhibition [ 21 ]. In addition, oxidative stress causes DNA damage and arrests the cell cycle in the G 0 /G 1 phase [ 22 , 23 ].…”
Section: Resultsmentioning
confidence: 99%
“…PM 2.5 induces mitochondrial dysfunction, resulting in cellular oxidative stress and cellular energy supply inhibition [ 21 ]. In addition, oxidative stress causes DNA damage and arrests the cell cycle in the G 0 /G 1 phase [ 22 , 23 ].…”
Section: Resultsmentioning
confidence: 99%
“…The mixture was centrifuged at 13,000 × g , for 15 min at 4°C. The pellet was mixed with MI buffer, and mitochondrial function was evaluated using the mixture [ 28 ].…”
Section: Methodsmentioning
confidence: 99%
“…To assess the amount of ROS in mitochondria, KCl-based respiration buffer (125 mM potassium chloride, 2 mM potassium phosphate monobasic, 2.5 mM malate, 20 mM HEPES, 1 mM magnesium chloride, 5 mM pyruvate, and 500 μM EGTA, pH 7.0) was mixed with DCF-DA for 20 min. This reaction solution was measured at excitation wave 485 nm and emission wave 535 nm using a microplate reader (Epoch2, BioTek, Winooski, VT, USA) [ 33 ].…”
Section: Methodsmentioning
confidence: 99%
“…To investigate the MMP, the mitochondrial extract was mixed with MI buffer containing 5 mM pyruvate and 5 mM malate, and then 1 μM JC-1 was reacted in the dark for 20 min. The reaction solution was measured at excitation wave 530 nm and emission wave 590 nm using a fluorescence photometer (Infinite F200, Tecan, Männedorf, Switzerland) [ 33 ].…”
Section: Methodsmentioning
confidence: 99%