2018
DOI: 10.1016/j.jgr.2018.02.007
|View full text |Cite
|
Sign up to set email alerts
|

Antimelanogenesis and skin-protective activities of Panax ginseng calyx ethanol extract

Abstract: BackgroundThe antioxidant effects of Panax ginseng have been reported in several articles; however, little is known about the antimelanogenesis effect, skin-protective effect, and cellular mechanism of Panax ginseng, especially of P. ginseng calyx. To understand how an ethanol extract of P. ginseng berry calyx (Pg-C-EE) exerts skin-protective effects, we studied its activities in activated melanocytes and reactive oxygen species (ROS)–induced keratinocytes.MethodsTo confirm the antimelanogenesis effect of Pg-C… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

0
30
0

Year Published

2019
2019
2024
2024

Publication Types

Select...
9

Relationship

4
5

Authors

Journals

citations
Cited by 51 publications
(30 citation statements)
references
References 48 publications
0
30
0
Order By: Relevance
“…This process is characterized by formation of coarse wrinkles, thickening of skin, and dryness [7][8][9][10]. In melanocytes, ROS regulate melanogenesis [11,12], and UVB irradiation stimulates keratinocytes to induce α-melanocyte-stimulating hormone (α-MSH) secretion, which triggers cell signaling in response to melanocortin 1 receptor (MC1R) of melanocytes [6]. In melanogenesis, the tyrosinase protein is regulated by the MC1R signaling pathway.…”
Section: Introductionmentioning
confidence: 99%
“…This process is characterized by formation of coarse wrinkles, thickening of skin, and dryness [7][8][9][10]. In melanocytes, ROS regulate melanogenesis [11,12], and UVB irradiation stimulates keratinocytes to induce α-melanocyte-stimulating hormone (α-MSH) secretion, which triggers cell signaling in response to melanocortin 1 receptor (MC1R) of melanocytes [6]. In melanogenesis, the tyrosinase protein is regulated by the MC1R signaling pathway.…”
Section: Introductionmentioning
confidence: 99%
“…Before UVB irradiation, culture medium was replaced with 1 ml of phosphate-buffered saline (PBS) per well. After removing the plate lid, cells were irradiated at 30 mJ/cm 2 [25]. After UVB irradiation, PBS was replaced with complete culture medium with the appropriate compound treatments prior to harvesting.…”
Section: Cell Viability Assaymentioning
confidence: 99%
“…The nuclear fraction was prepared as described previously [25]. Immunoblotting of both nuclear fraction and whole-cell lysate were performed as previously described [24,26]. β-actin and lamin A/C were used as a loading control for the whole cell lysate and nuclear fraction, respectively.…”
Section: Preparation Of Whole-cell Lysates Nuclear Fraction and Immmentioning
confidence: 99%