2022
DOI: 10.1016/j.jep.2021.114493
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Chamaecyparis obtusa (Siebold & Zucc.) Endl. leaf extracts prevent inflammatory responses via inhibition of the JAK/STAT axis in RAW264.7 cells

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Cited by 9 publications
(8 citation statements)
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“…In addition, it was confirmed that Platycodon grandifloras -fermented extracts showed an improved cell viability and reduced cytotoxicity compared to existing extracts [ 41 ]. In our previous study, we compared and evaluated the anti-inflammatory effects according to the COL extraction method in LPS-induced RAW264.7 cells and confirmed that COL EtOH extracts had excellent anti-inflammatory effects, but they show cytotoxicity at low concentrations [ 42 ]. In the present study, we confirmed that 70COLGA alleviated the high cytotoxicity of 70COL using bioconversion technology ( Figure 2 a).…”
Section: Discussionmentioning
confidence: 98%
“…In addition, it was confirmed that Platycodon grandifloras -fermented extracts showed an improved cell viability and reduced cytotoxicity compared to existing extracts [ 41 ]. In our previous study, we compared and evaluated the anti-inflammatory effects according to the COL extraction method in LPS-induced RAW264.7 cells and confirmed that COL EtOH extracts had excellent anti-inflammatory effects, but they show cytotoxicity at low concentrations [ 42 ]. In the present study, we confirmed that 70COLGA alleviated the high cytotoxicity of 70COL using bioconversion technology ( Figure 2 a).…”
Section: Discussionmentioning
confidence: 98%
“…NO concentration was determined by the Griess assay according to a previous report with minor modification . The RAW264.7 cells (3 × 10 4 cells/well) were plated into 96-well plates.…”
Section: Methodsmentioning
confidence: 99%
“…NO concentration was determined by the Griess assay according to a previous report with minor modification. 23 The RAW264.7 cells (3 × 10 4 cells/well) were plated into 96-well plates. After 12 h of incubation, the cells were pretreated with the sample drugs individually for 2 h and then co-treated with LPS (1 μg/ mL) for 24 h. Subsequently, the cells were discarded, and the aspirated medium was mixed with Griess reagent 1 and Griess reagent 2 in a 1:1:1 ratio.…”
Section: ■ Conclusionmentioning
confidence: 99%
“…NO concentration was determined by the Griess assay according to a previous report with some modification. 23 RAW264.7 cells (5 × 10 4 cells per well) were plated into 96-well plates. After an incubation period of 24 h, the cells were pre-treated with different drugs individually for 2 h and were cotreated with LPS (1 μg mL −1 ) for 12 h. Subsequently, the culture medium was mixed with the Griess reagent in a 1 : 1 ratio.…”
Section: Methodsmentioning
confidence: 99%