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Anti-Aging Properties of Cannabis sativa Leaf Extract against UVA Irradiation
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Hemp extract has garnered interest as a potential cosmeceutical agent with multifunctional activities, particularly in protecting against UV-induced skin cell aberrations and restoring aged skin cells. The ethanolic extract of Cannabis sativa leaves was prepared into an aqueous solution (CLES) to investigate its anti-photoaging ability. HPLC analysis revealed that the CLES contained 1.64 ± 0.01% w/w of cannabidiol and 0.11% w/w of ∆9-tetrahydrocannabinol. Additionally, the total phenolic content was found to be 4.08 ± 0.30 mg gallic acid equivalent per g of solution using the Folin–Ciocalteu method. The CLES exhibited potent scavenging activity using a DPPH assay, with an EC50 value of 277.9 ± 2.41 μg/mL, comparable to L-ascorbic acid, with 2.19 ± 0.28 μg/mL. The anti-photoaging potential of the CLES was evaluated using UVA-irradiated and in vitro-aged fibroblasts as a model. Pre-treatment with 20 μg/mL CLES for 24 h significantly alleviated the reduction in type I procollagen and suppressed the overproduction of MMP-1 and IL-6 induced by UVA. Moreover, the percentage of senescence-associated β-galactosidase-expressing cells decreased significantly to 11.9 ± 0.5% in the aged cells treated with CLES compared with untreated cells (18.8 ± 3.8%). These results strongly indicate the cosmeceutical potential of the CLES as an effective active agent for the anti-photoaging prevention and/or treatment.
Title: Anti-Aging Properties of Cannabis sativa Leaf Extract against UVA Irradiation
Description:
Hemp extract has garnered interest as a potential cosmeceutical agent with multifunctional activities, particularly in protecting against UV-induced skin cell aberrations and restoring aged skin cells.
The ethanolic extract of Cannabis sativa leaves was prepared into an aqueous solution (CLES) to investigate its anti-photoaging ability.
HPLC analysis revealed that the CLES contained 1.
64 ± 0.
01% w/w of cannabidiol and 0.
11% w/w of ∆9-tetrahydrocannabinol.
Additionally, the total phenolic content was found to be 4.
08 ± 0.
30 mg gallic acid equivalent per g of solution using the Folin–Ciocalteu method.
The CLES exhibited potent scavenging activity using a DPPH assay, with an EC50 value of 277.
9 ± 2.
41 μg/mL, comparable to L-ascorbic acid, with 2.
19 ± 0.
28 μg/mL.
The anti-photoaging potential of the CLES was evaluated using UVA-irradiated and in vitro-aged fibroblasts as a model.
Pre-treatment with 20 μg/mL CLES for 24 h significantly alleviated the reduction in type I procollagen and suppressed the overproduction of MMP-1 and IL-6 induced by UVA.
Moreover, the percentage of senescence-associated β-galactosidase-expressing cells decreased significantly to 11.
9 ± 0.
5% in the aged cells treated with CLES compared with untreated cells (18.
8 ± 3.
8%).
These results strongly indicate the cosmeceutical potential of the CLES as an effective active agent for the anti-photoaging prevention and/or treatment.
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