New cytokinin derivatives possess UVA and UVB photoprotective effect on human skin cells and prevent oxidative stress
Language English Country France Media print-electronic
Document type Journal Article
PubMed
29604584
DOI
10.1016/j.ejmech.2018.03.043
PII: S0223-5234(18)30286-1
Knihovny.cz E-resources
- Keywords
- Aromatic cytokinins, Caenorhabditis elegans, Kinetin derivatives, Oxidative stress, UVA/UVB photoprotectivity,
- MeSH
- Cytokinins chemical synthesis chemistry pharmacology MeSH
- Skin drug effects MeSH
- Humans MeSH
- Molecular Structure MeSH
- Protective Agents chemical synthesis chemistry pharmacology MeSH
- Oxidative Stress drug effects MeSH
- Ultraviolet Rays * MeSH
- Dose-Response Relationship, Drug MeSH
- Structure-Activity Relationship MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Cytokinins MeSH
- Protective Agents MeSH
Eleven 6-furfurylaminopurine (kinetin, Kin) derivatives were synthesized to obtain biologically active compounds. The prepared compounds were characterized using 1H NMR, mass spectrometry combined with HPLC purity determination and elemental C, H, N analyses. The biological activity of new derivatives was tested on plant cells and tissues in cytokinin bioassays, such as tobacco callus, detached wheat leaf chlorophyll retention bioassay and Amaranthus bioassay. The selected compounds were subsequently tested on normal human dermal fibroblasts (NHDF) and keratinocyte cell lines (HaCaT) to exclude possible phototoxic effects and, on the other hand, to reveal possible UVA and UVB photoprotective activity. The protective antioxidant activity of the prepared cytokinin derivatives was further studied and compared to previously prepared antisenescent compound 6-furfurylamino-9-(tetrahydrofuran-2-yl)purine (Kin-THF) using induced oxidative stress (OS) on nematode Caenorhabditis elegans damaged by 5-hydroxy-1,4-naphthoquinone (juglone), a generator of reactive oxygen species. The observed biological activity was interpreted in relation to the structure of the prepared derivatives. The most potent oxidative stress protection of all the prepared compounds was shown by 6-(thiophen-2-ylmethylamino)-9-(tetrahydrofuran-2-yl)purine (6) and 2-chloro-6-furfurylamino-9-(tetrahydrofuran-2-yl)purine (9) derivatives and the results were comparable to Kin-THF. Compounds 6 and 9 were able to significantly protect human skin cells against UV radiation in vitro. Both the derivatives 6 and 9 showed higher protective activity in comparison to previously known structurally similar compounds Kin and Kin-THF. The obtained results are surprising due to the fact that the prepared compounds showed to be inactive in the ORAC assay which proved that the compounds did not act as direct antioxidants as they were unable to directly scavenge oxygen radicals.
References provided by Crossref.org
Photoprotective properties of new derivatives of kinetin
Role of Cytokinins in Senescence, Antioxidant Defence and Photosynthesis