2020
DOI: 10.1002/tox.23069
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Seven traditional Chinese herbal extracts fermented by Lactobacillus rhamnosus provide anti‐pigmentation effects by regulating the CREB/MITF/tyrosinase pathway

Abstract: Skin pigmentation is resulted from several processes, such as melanin synthesis transportation and abnormal melanin accumulation in keratinocytes. Various studies have suggested that seven traditional Chinese herbal extracts from Atractylodes macrocephala, Paeonia lactiflora, Bletilla striata, Poria cocos, Dictamnus dasycarpus, Ampelopsis japonica and Tribulus terrestris (which we collectively named ChiBai), show several protective effects toward skin‐related diseases. Lactobacillus rhamnosus, a lactic acid ba… Show more

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Cited by 12 publications
(7 citation statements)
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“…The slides were immunostained with anti-PGC-1α, anti-Sirt1, and anti-β-gal antibodies using an UltraVision LP detection system (Vector Laboratories, Burlingame, CA, USA), according to the manufacturer's instructions [27]. Tissue biopsies were dried overnight at 60 • C. The following day, tissues were deparaffinized in xylene for 40 min and rehydrated with a graded series of ethanol.…”
Section: Immunohistochemistrymentioning
confidence: 99%
“…The slides were immunostained with anti-PGC-1α, anti-Sirt1, and anti-β-gal antibodies using an UltraVision LP detection system (Vector Laboratories, Burlingame, CA, USA), according to the manufacturer's instructions [27]. Tissue biopsies were dried overnight at 60 • C. The following day, tissues were deparaffinized in xylene for 40 min and rehydrated with a graded series of ethanol.…”
Section: Immunohistochemistrymentioning
confidence: 99%
“…Ultraviolet type B (UVB) radiation is a critical factor in inducing abnormal melanogenesis and dendrite formation in B16F10 cells [ 25 ]. The previous study supports that UVB radiation is a factor that promotes cellular oxidative stress.…”
Section: Discussionmentioning
confidence: 99%
“…Melanin content in B16F10 cells was performed according to the manufacturer's instructions 29 . B16F10 cells were cultured at a density of 2 × 10 5 cells/well in 6‐well plates overnight, following treatment with different concentrations of α‐MSH and paeoniflorin for 48 h. The cells were treated with 2 N NaOH (S5881, Sigma), followed by heating at 80°C for 30 min, and the melanin content was measured at an absorbance of 405 nm using a spectrophotometer.…”
Section: Methodsmentioning
confidence: 99%
“…Tyrosinase activity in B16F10 cells was performed according to the manufacturer's instructions 29 . B16F10 cells were cultured at a density of 2 × 10 5 cells/well in 6‐well plates overnight, following treatment with different concentrations of α‐MSH and paeoniflorin for 48 h. Following washing, the cells were treated with 1% Triton X‐100 prepared in PBS.…”
Section: Methodsmentioning
confidence: 99%