Matches in SemOpenAlex for { <https://semopenalex.org/work/W2890832579> ?p ?o ?g. }
- W2890832579 endingPage "123" @default.
- W2890832579 startingPage "123" @default.
- W2890832579 abstract "Oxidative stress has been implicated in pathophysiology of different human stress- and age-associated disorders, including osteoporosis for which antioxidants could be considered as therapeutic remedies as was suggested recently. The 1,4-dihydropyridine (DHP) derivatives are known for their pleiotropic activity, with some also acting as antioxidants. To find compounds with potential antioxidative activity, a group of 27 structurally diverse DHPs, as well as one pyridine compound, were studied. A group of 11 DHPs with 10-fold higher antioxidative potential than of uric acid, were further tested in cell model of human osteoblast-like cells. Short-term combined effects of DHPs and 50 µM H2O2 (1-h each), revealed better antioxidative potential of DHPs if administered before a stressor. Indirect 24-h effect of DHPs was evaluated in cells further exposed to mild oxidative stress conditions induced either by H2O2 or tert-butyl hydroperoxide (both 50 µM). Cell growth (viability and proliferation), generation of ROS and intracellular glutathione concentration were evaluated. The promotion of cell growth was highly dependent on the concentrations of DHPs used, type of stressor applied and treatment set-up. Thiocarbatone III-1, E2-134-1 III-4, Carbatone II-1, AV-153 IV-1, and Diethone I could be considered as therapeutic agents for osteoporosis although further research is needed to elucidate their bioactivity mechanisms, in particular in respect to signaling pathways involving 4-hydroxynoneal and related second messengers of free radicals." @default.
- W2890832579 created "2018-09-27" @default.
- W2890832579 creator A5006569192 @default.
- W2890832579 creator A5012374133 @default.
- W2890832579 creator A5019638802 @default.
- W2890832579 creator A5020088694 @default.
- W2890832579 creator A5029869475 @default.
- W2890832579 creator A5033025859 @default.
- W2890832579 creator A5057419608 @default.
- W2890832579 creator A5064169547 @default.
- W2890832579 creator A5070918468 @default.
- W2890832579 creator A5071500690 @default.
- W2890832579 creator A5078930677 @default.
- W2890832579 date "2018-09-19" @default.
- W2890832579 modified "2023-10-17" @default.
- W2890832579 title "Antioxidative 1,4-Dihydropyridine Derivatives Modulate Oxidative Stress and Growth of Human Osteoblast-Like Cells In Vitro" @default.
- W2890832579 cites W1515194322 @default.
- W2890832579 cites W1649220013 @default.
- W2890832579 cites W1968194419 @default.
- W2890832579 cites W1975510427 @default.
- W2890832579 cites W1981593314 @default.
- W2890832579 cites W1990845078 @default.
- W2890832579 cites W1991690086 @default.
- W2890832579 cites W1992933488 @default.
- W2890832579 cites W2001045834 @default.
- W2890832579 cites W2020077166 @default.
- W2890832579 cites W2022431707 @default.
- W2890832579 cites W2024361822 @default.
- W2890832579 cites W2032155041 @default.
- W2890832579 cites W2034038543 @default.
- W2890832579 cites W2037555973 @default.
- W2890832579 cites W2038912017 @default.
- W2890832579 cites W2041590030 @default.
- W2890832579 cites W2050379759 @default.
- W2890832579 cites W2057907582 @default.
- W2890832579 cites W2064828659 @default.
- W2890832579 cites W2066024445 @default.
- W2890832579 cites W2067780422 @default.
- W2890832579 cites W2068009821 @default.
- W2890832579 cites W2079512039 @default.
- W2890832579 cites W2084478798 @default.
- W2890832579 cites W2095008955 @default.
- W2890832579 cites W2097857551 @default.
- W2890832579 cites W2110498771 @default.
- W2890832579 cites W2128534910 @default.
- W2890832579 cites W2128635872 @default.
- W2890832579 cites W2145605021 @default.
- W2890832579 cites W2150428981 @default.
- W2890832579 cites W2181843155 @default.
- W2890832579 cites W2223404154 @default.
- W2890832579 cites W2277461376 @default.
- W2890832579 cites W2406994491 @default.
- W2890832579 cites W2419646961 @default.
- W2890832579 cites W2518822993 @default.
- W2890832579 cites W2563719958 @default.
- W2890832579 cites W2563773664 @default.
- W2890832579 cites W2569651681 @default.
- W2890832579 cites W2570879331 @default.
- W2890832579 cites W2580135764 @default.
- W2890832579 cites W2604361851 @default.
- W2890832579 cites W2604612121 @default.
- W2890832579 cites W2720632745 @default.
- W2890832579 cites W2761949123 @default.
- W2890832579 cites W2766380710 @default.
- W2890832579 cites W2766985559 @default.
- W2890832579 cites W2772373988 @default.
- W2890832579 cites W2783761503 @default.
- W2890832579 cites W2788079625 @default.
- W2890832579 cites W4236652389 @default.
- W2890832579 cites W4290295972 @default.
- W2890832579 cites W4293247451 @default.
- W2890832579 doi "https://doi.org/10.3390/antiox7090123" @default.
- W2890832579 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6162383" @default.
- W2890832579 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30235855" @default.
- W2890832579 hasPublicationYear "2018" @default.
- W2890832579 type Work @default.
- W2890832579 sameAs 2890832579 @default.
- W2890832579 citedByCount "20" @default.
- W2890832579 countsByYear W28908325792018 @default.
- W2890832579 countsByYear W28908325792019 @default.
- W2890832579 countsByYear W28908325792020 @default.
- W2890832579 countsByYear W28908325792021 @default.
- W2890832579 countsByYear W28908325792022 @default.
- W2890832579 countsByYear W28908325792023 @default.
- W2890832579 crossrefType "journal-article" @default.
- W2890832579 hasAuthorship W2890832579A5006569192 @default.
- W2890832579 hasAuthorship W2890832579A5012374133 @default.
- W2890832579 hasAuthorship W2890832579A5019638802 @default.
- W2890832579 hasAuthorship W2890832579A5020088694 @default.
- W2890832579 hasAuthorship W2890832579A5029869475 @default.
- W2890832579 hasAuthorship W2890832579A5033025859 @default.
- W2890832579 hasAuthorship W2890832579A5057419608 @default.
- W2890832579 hasAuthorship W2890832579A5064169547 @default.
- W2890832579 hasAuthorship W2890832579A5070918468 @default.
- W2890832579 hasAuthorship W2890832579A5071500690 @default.
- W2890832579 hasAuthorship W2890832579A5078930677 @default.
- W2890832579 hasBestOaLocation W28908325791 @default.
- W2890832579 hasConcept C1491633281 @default.