<b><i>Background/Objective:</i></b> In recent years, herbal extracts are becoming increasingly popular ingredients added in cosmetics; however, the assessment of their potential adverse effects on the skin remains unclear. As <i>Coptis</i>, <i>Phellodendron amurense</i>, curcumin, and shikonin are herbs currently used in cosmetic ingredients, the aim of this study was to assess their skin photoallergy (PA) potential and the concentrations at which they could safely be used. <b><i>Methods:</i></b> In the patch test, <i>Coptis</i>, <i>P. amurense</i>, curcumin, and shikonin with 5, 10, 25, and 50% concentration were applied on 33 healthy Chinese subjects using the T.R.U.E. TEST® patch test system for 48 h. Photopatch testing was performed on 206 Chinese subjects with predisposed photosensitivity history using the Scandinavian photopatch series, and subjects were irradiated by 50% UVA minimum erythema dose. Photopatch testing of herbal extracts was then performed on subjects diagnosed with PA. <b><i>Results:</i></b> Thirty-three subjects (14 with type III skin and 19 with type IV skin) completed contact patch testing of herbal extracts. <i>Coptis</i> induced a contact allergy (CA) reaction on 2 subjects at 25% concentration and on 2 subjects at 10% concentration. <i>P. amurense</i> induced a CA reaction on 1 subject at 10% concentration and on 1 subject at 5% concentration. Shikonin induced a stimulating reaction on 1 subject at 10% concentration. Curcumin induced a stimulating reaction on 1 subject at 10% concentration. Of the 206 Chinese subjects predisposed for photosensitivity, 10.19% had PA, 16.5% showed CA, and 1.45% had both PA + CA. PA-induced substances were promethazine hydrochloride (15%, <i>n</i> = 31), chlorpromazine hydrochloride (10.84%, <i>n</i> = 19), perfume mix (5.82%, <i>n</i> = 12), atranorin (3.39%, <i>n</i> = 7), 6-methyl coumarine (3.39%, <i>n</i> = 7), balsam Peru (1.94%, <i>n</i> = 4), fentichlor (1.94%, <i>n</i> = 4), 3,3′,4′,5-tetrachloro salicylanilide (0.97%, <i>n</i> = 2), hexachlorophene (0.97%, <i>n</i> = 2), chlorhexidine digluconate (0.97%, <i>n</i> = 2), and 4-aminobenzoic acid 2-hydroxy-4-methoxybenzophenone (0.97%, <i>n</i> = 2). <i>Coptis</i> at 25, 10, and 5% concentration and <i>P. amurense</i>, shikonin, and curcumin each at 10 and 5% concentration induced negative photopatch test results in all 10 photosensitive subjects. <b><i>Conclusion:</i></b> We have shown that <i>Coptis</i>, shikonin, or curcumin at 5% concentration in cosmetics could be applied safely without inducing contact allergic and photosensitive reactions on the skin. These findings advance the understanding of herbal extract use in cosmetic ingredients as related to the fields of dermatopharmacology and dermatotoxicology.
Background/purpose: Skin photoaging, main causes of skin aging, is induced by chronic UV irradiation. LncSPRY4-IT1, a broadly expressed lncRNA, takes part in various biological functions by combining with functional protein molecules. However, the role of LncSPRY4-IT1 in skin photoaging process has not been characterized. This study is to investigate the interacting proteins of LncSPRY4-IT1 by combining RNA pull-down, high-throughput, and bioinformatic analysis.Methods: Human skin fibroblasts (HDFs) were exposed to 10 J/cm 2 UVA irradiation, once a day for 14 days. LncSPRY4-IT1 expression was qualified via RT-PCR. In vitro RNA pull-down assays and liquid chromatography-mass spectrometry analysis were used to identify the LncSPRY4-IT1-related proteins. Functional annotation analysis and pathway enrichment were preformed via Gene Ontology and KEGG.Results: LncSPRY4-IT1 expression in photoaging fibroblasts was increased 1.66 ± 0.23 folds. 181 LncSPRY4-IT1-interacting proteins in UVA-induced photoaging skin fibroblast irradiation were identified, of which 56 proteins with two or more unique peptides, 73 proteins related to RNA processing, and 5 proteins related to DNA processing. High-throughput and bioinformatic analysis showed that LncSPRY4-IT1-targeting proteins were involved in cellular process, metabolic process, biological regulation, and cell part in skin photoaging process. The KEGG revealed that LncSPRY4-IT1-targeting proteins were mainly enriched in metabolic pathways. Conclusion:The results of our studies illuminate how LncSPRY4-IT1 formed a LncRNA-protein regulatory network in skin photoaging mechanisms and suggest that LncSPRY4-IT1 may serve as a novel upstream intervention target for the prevention and treatment of photoaging and related skin diseases.
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