Whey Protein Complexes with Green Tea Polyphenols: Antimicrobial, Osteoblast-Stimulatory, and Antioxidant Activities
Language English Country Switzerland Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
30677765
DOI
10.1159/000494732
PII: 000494732
Knihovny.cz E-resources
- Keywords
- Antibacterial properties, Antioxidant, Osteoblast, Polyphenol, Whey protein isolate,
- MeSH
- Anti-Bacterial Agents chemistry pharmacology MeSH
- Antioxidants chemistry pharmacology MeSH
- Bacteria drug effects MeSH
- Cell Differentiation drug effects MeSH
- Cell Line MeSH
- Tea chemistry MeSH
- Adult MeSH
- Fibroblasts cytology drug effects MeSH
- Catechin analogs & derivatives chemistry pharmacology MeSH
- Cells, Cultured MeSH
- Humans MeSH
- Young Adult MeSH
- Osteoblasts cytology drug effects MeSH
- Osteogenesis drug effects MeSH
- Polyphenols chemistry pharmacology MeSH
- Cell Proliferation drug effects MeSH
- Whey Proteins chemistry pharmacology MeSH
- Check Tag
- Adult MeSH
- Humans MeSH
- Young Adult MeSH
- Male MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Anti-Bacterial Agents MeSH
- Antioxidants MeSH
- Tea MeSH
- epigallocatechin gallate MeSH Browser
- Catechin MeSH
- Polyphenols MeSH
- Whey Proteins MeSH
Polyphenols are known for their antimicrobial activity, whilst both polyphenols and the globular protein β-lactoglobulin (bLG) are suggested to have antioxidant properties and promote cell proliferation. These are potentially useful properties for a tissue-engineered construct, though it is unknown if they are retained when both compounds are used in combination. In this study, a range of different microbes and an osteoblast-like cell line (human fetal osteoblast, hFOB) were used to assess the combined effect of: (1) green tea extract (GTE), rich in the polyphenol epigallocatechin gallate (EGCG), and (2) whey protein isolate (WPI), rich in bLG. It was shown that approximately 20-48% of the EGCG in GTE reacted with WPI. GTE inhibited the growth of Gram-positive bacteria, an effect which was potentiated by the addition of WPI. GTE alone also significantly inhibited the growth of hFOB cells after 1, 4, and 7 days of culture. Alternatively, WPI significantly promoted hFOB cell growth in the absence of GTE and attenuated the effect of GTE at low concentrations (64 µg/mL) after 4 and 7 days. Low concentrations of WPI (50 µg/mL) also promoted the expression of the early osteogenic marker alkaline phosphatase (ALP) by hFOB cells, whereas GTE inhibited ALP activity. Therefore, the antioxidant effects of GTE can be boosted by WPI, but GTE is not suitable to be used as part of a tissue-engineered construct due to its cytotoxic effects which negate any positive effect WPI has on cell proliferation.
Engineering Department Lancaster University Lancaster United Kingdom
Laboratory of Pharmaceutical Microbiology Ghent University Ghent Belgium
Materials Science Institute Lancaster University Lancaster United Kingdom
School of Nursing and Midwifery Queen's University Belfast Belfast United Kingdom
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