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Chlorin E6-Curcumin-Mediated Photodynamic Therapy Promotes an Anti-Photoaging Effect in UVB-Irradiated Fibroblasts.
Thapa Magar, Til Bahadur; Mallik, Shyam Kumar; Gurung, Pallavi; Lim, Junmo; Kim, Young-Tak; Shrestha, Rajeev; Kim, Yong-Wan.
Afiliación
  • Thapa Magar TB; Dongsung Cancer Center, Dongsung Biopharmaceutical, Daegu 41061, Republic of Korea.
  • Mallik SK; Dongsung Cancer Center, Dongsung Biopharmaceutical, Daegu 41061, Republic of Korea.
  • Gurung P; Dongsung Cancer Center, Dongsung Biopharmaceutical, Daegu 41061, Republic of Korea.
  • Lim J; Dongsung Cancer Center, Dongsung Biopharmaceutical, Daegu 41061, Republic of Korea.
  • Kim YT; Dongsung Cancer Center, Dongsung Biopharmaceutical, Daegu 41061, Republic of Korea.
  • Shrestha R; Dongsung Cancer Center, Dongsung Biopharmaceutical, Daegu 41061, Republic of Korea.
  • Kim YW; Dongsung Cancer Center, Dongsung Biopharmaceutical, Daegu 41061, Republic of Korea.
Int J Mol Sci ; 24(17)2023 Aug 30.
Article en En | MEDLINE | ID: mdl-37686273
ABSTRACT
Skin photoaging due to ultraviolet B (UVB) exposure generates reactive oxygen species (ROS) that increase matrix metalloproteinase (MMP). Chlorin e6-photodynamic therapy (Ce6-PDT), in addition to being the first-line treatment for malignancies, has been shown to lessen skin photoaging, while curcumin is well known for reducing the deleterious effects of ROS. In the current study, PDT with three novel Ce6-curcumin derivatives, a combination of Ce6 and curcumin with various linkers, including propane-1,3-diamine for Ce6-propane-curcumin; hexane-1,6-diamine for Ce6-hexane-curcumin; and 3,3'-((oxybis(ethane-2,1-diyl))bis(oxy))bis(propan-1-amine) for Ce6-dipolyethylene glycol (diPEG)-curcumin, were studied for regulation of UVB-induced photoaging on human skin fibroblast (Hs68) and mouse embryonic fibroblast (BALB/c 3T3) cells. We assessed the antiphotoaging effects of Ce6-curcumin derivatives on cell viability, antioxidant activity, the mechanism of matrix metalloproteinase-1 and 2 (MMP-2) expression, and collagen synthesis in UVB-irradiated in vitro models. All three Ce6-curcumin derivatives were found to be non-phototoxic in the neutral red uptake phototoxicity test. We found that Ce6-hexane-curcumin-PDT and Ce6-propane-curcumin-associated PDT exhibited less cytotoxicity in Hs68 and BALB/c 3T3 fibroblast cell lines compared to Ce6-diPEG-curcumin-PDT. Ce6-diPEG-curcumin and Ce6-propane-curcumin-associated PDT showed superior antioxidant activity in Hs68 cell lines. Further, in UVB-irradiated in vitro models, the Ce6-diPEG-curcumin-PDT greatly attenuated the expression levels of MMP-1 and MMP-2 by blocking mitogen-activated protein kinases (MAPKs), activator protein 1 (AP-1), and tumor necrosis factor-α (NF-κB) signaling. Moreover, Ce6-diPEG-curcumin effectively inhibited inflammatory molecules, such as cyclooxygenase-2 (COX-2) and inducible nitric oxide synthase (iNOS) expression, while accelerating collagen synthesis. These results demonstrate that Ce6-diPEG-curcumin may be a potential therapy for treating skin photoaging.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Fotoquimioterapia / Dermatitis Fototóxica / Curcumina Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Int J Mol Sci Año: 2023 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Fotoquimioterapia / Dermatitis Fototóxica / Curcumina Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Int J Mol Sci Año: 2023 Tipo del documento: Article