Affiliations 

  • 1 Food Science and Technology Research Centre, Malaysia Agriculture Research and Development Institute (MARDI), Persiaran MARDI-UPM, 43400 Serdang Selangor Malaysia. anisj@mardi.gov.my
  • 2 Faculty of Science and Technology, Universiti Kebangsaan Malaysia, 43650 Bangi Selangor Malaysia. muneerah6r@gmail.com
  • 3 Food Science and Technology Research Centre, Malaysia Agriculture Research and Development Institute (MARDI), Persiaran MARDI-UPM, 43400 Serdang Selangor Malaysia. bakri@mardi.gov.my
  • 4 Food Science and Technology Research Centre, Malaysia Agriculture Research and Development Institute (MARDI), Persiaran MARDI-UPM, 43400 Serdang Selangor Malaysia. danglela@mardi.gov.my
  • 5 Food Science and Technology Research Centre, Malaysia Agriculture Research and Development Institute (MARDI), Persiaran MARDI-UPM, 43400 Serdang Selangor Malaysia. yuhas@mardi.gov.my
  • 6 Food Science and Technology Research Centre, Malaysia Agriculture Research and Development Institute (MARDI), Persiaran MARDI-UPM, 43400 Serdang Selangor Malaysia. amsal@mardi.gov.my
  • 7 Faculty of Science and Technology, Universiti Kebangsaan Malaysia, 43650 Bangi Selangor Malaysia. yuziana@ukm.edu.my
Cell Mol Biol (Noisy-le-grand), 2023 Nov 15;69(11):9-16.
PMID: 38015547 DOI: 10.14715/cmb/2023.69.11.2

Abstract

In this study, UVA- and UVB-irradiated human fibroblasts were used to investigate the anti-photoaging efficacy of two aqueous extracts from Aspergillus oryzae-fermented broken rice (FBR) and brewers' rice (FBrR). As UVA and UVB can damage the dermal and epidermal layers, respectively, two UV radiation approaches were utilised: i) direct UVA irradiation on fibroblasts, and ii) UVB-irradiated keratinocytes indirectly co-cultured with fibroblasts to observe their epithelial-mesenchymal interaction during UVB-induced photoaging. The anti-photoaging properties were tested utilising biochemical tests and quantitative polymerase chain reaction (qPCR). The treatment of UV-irradiated human fibroblasts with FBR and FBrR dramatically downregulates MMP-1 and SFE gene expression. Nonetheless, MMP-1 secretion was inhibited by FBR and FBrR, with more substantial decreases in UVB-treated co-cultures, ranging from 0.76- to 1.89-fold relative to the untreated control. In UVA-treated fibroblasts, however, the elastase-inhibiting activity of FBR and FBrR is up to 1.63-fold and 2.13-fold more potent, respectively. In addition, post-UV irradiation treatment with FBR and FBrR was able to repair and enhance collagen formation in UVA-irradiated fibroblasts. Both FBR and FBrR were able to upregulate elastin gene expression in fibroblasts under both culture conditions, especially at 50 µg/mL. The pro-inflammatory cytokines TNF-, IL-1ß, and IL-6 were likewise lowered by FBR and FBrR, which may have contributed to the anti-photoaging effect of the UVB-treated co-culture. These results reveal that FBR and FBrR inhibit photoaging in human fibroblasts under both UV induction conditions. In conclusion, FBR and FBrR may be attractive bio-ingredients for usage in the cosmetic sector as cosmeceuticals.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.