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Details

Autor(en) / Beteiligte
Titel
Antioxidant and anti-aging potential of a peptide formulation (Gal-Pep) conjugated with gallic acid
Ist Teil von
  • RSC advances, 2021-09, Vol.11 (47), p.2947-29415
Ort / Verlag
England: Royal Society of Chemistry
Erscheinungsjahr
2021
Link zum Volltext
Quelle
Elektronische Zeitschriftenbibliothek (Open access)
Beschreibungen/Notizen
  • Skin is highly vulnerable to premature aging due to external stress, therefore, in this study, a peptide formulation, (galloyl) 2 -KTPPTTP (Gal 2 -Pep) was synthesized by combining TPPTTP peptide, and gallic acid (GA). All peptides were synthesized on 2-chlorotrityl chloride resin using solid-phase peptide synthesis (SPPS), and analyzed on an electrospray ionization (ESI)/quadrupole-time-of-flight (Q-TOF) tandem mass spectroscopy (MS) system. Initially, Gal 2 -Pep showed no toxicity below the concentration 100 μM with cell survival rate of 88% for keratinocytes and fibroblasts. The reactive oxygen species (ROS) scavenging activity of Gal 2 -Pep was more stable compared to GA alone; and after four weeks at room temperature, its ROS scavenging activity remained higher than 50%. Moreover, the peptide formulation, Gal 2 -Pep also exhibited elastase inhibitory effect in CCD-1064Sk fibroblast cells. Based on the results of RT-qPCR, it was proved in this study that Gal 2 -Pep increased the expression of PGC-1α to prevent oxidative stress, and validated its potential as an anti-aging agent through increasing the expression of type I collagen and by decreasing the expression of matrix metalloproteinase-1 (MMP1). The findings obtained reinforce the suggestion that the peptide formulation synthesized in this study could be used as a natural antioxidant and anti-aging agent for its cosmetic applications. Skin is highly vulnerable to premature aging due to external stress, therefore, in this study, a peptide formulation, (galloyl) 2 -KTPPTTP (Gal 2 -Pep) was synthesized by combining TPPTTP peptide, and gallic acid (GA).
Sprache
Englisch
Identifikatoren
ISSN: 2046-2069
eISSN: 2046-2069
DOI: 10.1039/d1ra03421a
Titel-ID: cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9040627

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