Complex interactions between nicotine and resveratrol in the Drosophila melanogaster wing spot test
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Author
Velázquez-Ulloa, N.A.Heres-Pulido, M.E.
Santos-Cruz, L.F.
Durán-Díaz, A.
Castañeda-Partida, L.
Browning, A.
Carmona-Alvarado, C.
Estrada-Guzmán, J.C.
Ferderer, G.
Garfias, M.
Gómez-Loza, B.
Magaña-Acosta, M.J.
Perry, H.H.
Dueñas-García, I.E.
Affiliation
Animal and Comparative Biomedical Sciences, University of ArizonaIssue Date
2022
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Elsevier LtdCitation
Velázquez-Ulloa, N. A., Heres-Pulido, M. E., Santos-Cruz, L. F., Durán-Díaz, A., Castañeda-Partida, L., Browning, A., Carmona-Alvarado, C., Estrada-Guzmán, J. C., Ferderer, G., Garfias, M., Gómez-Loza, B., Magaña-Acosta, M. J., Perry, H. H., & Dueñas-García, I. E. (2022). Complex interactions between nicotine and resveratrol in the Drosophila melanogaster wing spot test. Heliyon, 8(6).Journal
HeliyonRights
Copyright © 2022 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Nicotine (NIC) and resveratrol (RES) are chemicals in tobacco and wine, respectively, that are widely consumed concurrently worldwide. NIC is an alkaloid known to be toxic, addictive and to produce oxidative stress, while RES is thought of as an antioxidant with putative health benefits. Oxidative stress can induce genotoxic damage, yet few studies have examined whether NIC is genotoxic in vivo. In vitro studies have shown that RES can ameliorate deleterious effects of NIC. However, RES has been reported to have both antioxidant and pro-oxidant effects, and an in vivo study reported that 0.011 mM RES was genotoxic. We used the Drosophila melanogaster wing spot test to determine whether NIC and RES, first individually and then in combination, were genotoxic and/or altered the cell division. We hypothesized that RES would modulate NIC's effects. NIC was genotoxic in the standard (ST) cross in a concentration-independent manner, but not genotoxic in the high bioactivation (HB) cross. RES was not genotoxic in either the ST or HB cross at the concentrations tested. We discovered a complex interaction between NIC and RES. Depending on concentration, RES was protective of NIC's genotoxic damage, RES had no interaction with NIC, or RES had an additive or synergistic effect, increasing NIC's genotoxic damage. Most NIC, RES, and NIC/RES combinations tested altered the cell division in the ST and HB crosses. Because we used the ST and HB crosses, we demonstrated that genotoxicity and cell division alterations were modulated by the xenobiotic metabolism. These results provide evidence of NIC's genotoxicity in vivo at specific concentrations. Moreover, NIC's genotoxicity can be modulated by its interaction with RES in a complex manner, in which their interaction can lead to either increasing NIC's damage or protecting against it. © 2022 The Author(s)Note
Open access journalISSN
2405-8440Version
Final published versionae974a485f413a2113503eed53cd6c53
10.1016/j.heliyon.2022.e09744
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Except where otherwise noted, this item's license is described as Copyright © 2022 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).