Nitric Oxide Attenuates Oxidative Stress Induced by Arsenic in Lettuce (Lactuca sativa) Leaves

Water, Air, and Soil Pollution

Volumn 226, Issue 11, 2015, Pages 226-379

  Silveira, Neidiquele M ^a   De Oliveira, Juraci A ^a   Ribeiro, Cleberson ^a   Canatto, Regiane A ^a   Siman, Luhan ^a   Cambraia, José ^a   Farnese, Fernanda ^b  

^a FEDERAL UNIVERSITY OF VIÇOSA   (Brazil)

^b INSTITUTO FEDERAL GOIANO   (Brazil)

Author keywords

Antioxidative enzymes; Arsenic contaminated food; Plant physiology; Public health; Reactive oxygen species

Indexed keywords

ALDEHYDES; ARSENIC; ENZYMES; METABOLITES; NITRIC OXIDE; OXIDATIVE STRESS; PLANTS (BOTANY); PUBLIC HEALTH; REDUCTION;

ANTI-OXIDATIVE ENZYMES; ENZYMATIC ACTIVITIES; OXIDATIVE STRESS RESPONSE; PLANT PHYSIOLOGY; REACTIVE OXYGEN SPECIES; SODIUM NITROPRUSSIDE; SUPEROXIDE ANIONS; TOXIC METABOLITES;

CHEMICAL CONTAMINATION;

ARSENIC; ASCORBATE PEROXIDASE; CATALASE; GLUTATHIONE PEROXIDASE; GLUTATHIONE REDUCTASE; HYDROGEN PEROXIDE; MALONALDEHYDE; NITRIC OXIDE; NITROPRUSSIDE SODIUM; PEROXIDASE; REACTIVE OXYGEN METABOLITE; SUPEROXIDE; SUPEROXIDE DISMUTASE;

ANNUAL PLANT; ARSENIC; BIOACCUMULATION; ENZYME ACTIVITY; FOOD CONSUMPTION; LEAF; NITRIC OXIDE; PHYSIOLOGY; PUBLIC HEALTH; SHOOT; VEGETABLE;

ABSORPTION; ANTIOXIDANT ACTIVITY; ARTICLE; CONTROLLED STUDY; ENZYME ACTIVITY; LETTUCE; LIPID PEROXIDATION; MEMBRANE DAMAGE; NONHUMAN; OXIDATIVE STRESS; PLANT LEAF; SHOOT;

LACTUCA; LACTUCA SATIVA;

EID: 84945139589     PISSN: 00496979     EISSN: 15732932     Source Type: Journal    
DOI: 10.1007/s11270-015-2630-0     Document Type: Article

References (44)

1. Anderson, J. V., & Davis, D. G. (2004). Abiotic stress alters transcript profiles and activity of glutathione S-transferase, glutathione peroxidase, and glutathione reductase in Euphorbia esula. Physiologia Plantarum, 120, 421-433.
2. Anderson, M. D., Prasad, T. K., & Stewart, C. R. (1995). Changes in isozyme profiles of catalase, peroxidase, and glutathione reductase during acclimation to chilling in mesocotylus of maize seedlings. Plant Physiology, 109, 1247-1257.
3. Andrade, H. M. A., Silva, C. S., Mattos, G., & Arantes, R. (2013). Oxidative stress and antioxidant responses in four aquatic plants exposed to arsenic. Duc in Altum, 13, 21-26.
4. Beauchamp, C., & Fridovich, I. (1971). Superoxide dismutase: improved assays and an assay aplicable to acrylamide gels. Analytical Biochemistry, 44, 276-287.
5. Berridge, M. J., Bootman, M. D., & Roderick, H. L. (2003). Calcium signaling: dynamics, homeostasis and remodeling. Nature Reviews Molecular Cell Biology, 4, 517-529.
6. Bradford, M. M. (1976). A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein dye binding. Analytical Biochemistry, 72, 248-254.
7. Carlberg, I., & Mannervik, B. (1985). Glutathione reductase. Methods in Enzymology, 113, 484-495.
8. Chance, B., & Maehley, A. C. (1955). Assay of catalases and peroxidases. Methods in Enzymology, 2, 764-775.
9. Clark, R. B. (1975). Characterization of phosphatase of intact maize roots. Journal of Agricultural and Food Chemistry, 23, 458-460.
10. Del Longo, O. T., González, A., Pastori, G. M., & Trippi, V. S. (1993). Antioxidant defenses under hyperoxygenic and hyperosmotic conditions in leaves of two lines of maize with differential sensitivity to drought. Plant Cell Physiology, 34, 1023-1028.
11. Farid, A. T. M., Roy, K. C., Hossain, K. M., & Sen, R. (2003). A study of arsenic contaminated irrigation water and its carried over effect on vegetable (pp. 113-121). Dhaka: BUET-UNU, International Symposium of Fate of Arsenic in the Environment.
12. Farnese, F. S., Oliveira, J. A., Gusman, G. S., Leão, G. A., Ribeiro, C., Siman, L. I., & Cambraia, J. (2013). Plant responses to arsenic: the role of nitric oxide. Water, Air, and Soil Pollution, 224, 1660-1667.
13. Farnese, F. S., Oliveira, J. A., Gusman, G. S., Leao, G. A., Silveira, N. M., Silva, P. E. M., Ribeiro, C., & Cambraia, J. (2014a). Effects of adding nitroprusside on arsenic stressed response of Pistia stratiotes L. under hydroponic conditions. International Journal of Phytoremediation, 16, 123-137.
14. Farnese, F. S., Oliveira, J. A., Lima, F. S., Leão, G. A., Gusman, G. S., & Silva, L. C. (2014b). Evaluation of the potential of Pistia stratiotes L. (water lettuce) for bioindication and phytoremediation of aquatic environments contaminated with arsenic. Brazilian Journal of Biology, 74(4), 25-31.
15. Foyer, C. H., & Halliwell, B. (1976). The presence of glutathione and glutathione reductase in chloroplasts: a proposed role in ascorbic acid metabolism. Planta, 133, 21-25.
16. Gay, C., & Gebicki, J. M. (2000). A critical evaluation of the effect of sorbitol on the ferric-xylenol orange hydroperoxide assay. Analytical Biochemistry, 284, 217-220.
17. Giannopolitis, C. N., & Ries, S. K. (1977). Superoxide dismutases. Plant Physiology, 59, 309-314.
18. Gomes, M. P., Carvalho, M., Carvalho, G. S., Marques, T. C., Garcia, Q. S., Guilherme, L. R., & Soares, A. M. (2013). Phosphorus improves arsenic phytoremediation by Anadenanthera peregrina by alleviating induced oxidative stress. International Journal of Phytoremediation, 15, 633-646.
19. Gusman, G. S., Oliveira, J. A., Farnese, F. S., & Cambraia, J. (2013a). Mineral nutrition and enzymatic adaptation induced by arsenate and arsenite exposure in lettuce plants. Plant Physiology and Biochemistry, 71, 307-314.
20. Gusman, G. S., Oliveira, J. A., Farnese, F. S., & Cambraia, J. (2013b). Arsenate and arsenite: the toxic effects on photosynthesis and growth of lettuce plants. Acta Physiologiae Plantarum, 35, 1201-1209.
21. Havir, E. A., & McHale, N. A. (1987). Biochemical and developmental characterization of multiple forms of catalase in tobacco leaves. Plant Physiology, 84, 450-455.
22. Heath, R. L., & Packer, L. (1968). Photoperoxidation in isolated chloroplast. I. kinetics and stoichiometry of fatty acid peroxidation. Archives of Biochemistry and Biophysics, 125, 189-198.
23. Koshiba, T. (1993). Cytosolic ascorbato peroxidase in seedlings and leaves of maize (Zea mays). Plant Cell Physiology, 34, 713-721.
24. Kuo, M. C., & Kao, C. H. (2003). Aluminum effects on lipid peroxidation and antioxidative enzyme activities in rice leaves. Biologia Plantarum, 46, 149-152.
25. Leão, G. A., Oliveira, J. A., Farnese, F. S., Gusman, G. S., & Felipe, R. T. A. (2014a). Sulfur metabolism: different tolerances of two aquatic macrophytes exposed to arsenic. Ecotoxicology and Environmental Safety, 105, 36-42.
26. Leão, G. A., Oliveira, J. A., Felipe, R. T. A., Farnese, F. S., & Gusman, G. S. (2014b). Anthocyanins, thiols, and antioxidant scavenging enzymes are involved in Lemna gibba tolerance to arsenic. Journal of Plant Interactions, 9, 143-151.
27. Liu, S., Yang, R., Pan, Y., Ma, M., Pan, J., Zhao, Y., Cheng, Q., Wu, M., Wang, M., & Zhang, L. (2015). Nitric oxide contributes to minerals absorption, proton pumps and hormone equilibrium under cadmium excess in Trifolium repens L. plants. Ecotoxicology and Environmental Safety, 119, 35-46.
28. Marin, A. R., Pezeshki, S. R., Masscheleyn, P. H., & Choi, H. S. (1993). Effect of dimethylarsenic acid (DMAA) on growth, tissue arsenic and photosynthesis in rice plants. Journal of Plant Nutrition, 16, 865-880.
29. Meier, S., Madeo, L., Ederli, L., Donaldson, L., Pasqualini, S., & Gehring, C. (2009). Deciphering cGMP signatures and cGMP-dependent pathways in plant defence. Plant Signaling & Behavior, 4, 307-309.
30. Mizuno, M., Kamei, M., & Tsuchida, H. (1998). Ascorbate peroxidase and catalase cooperate for protection against hydrogen peroxide generated in potato tubers during low-temperature storage. Biochemistry and Molecular Biology International, 44, 717-725.
31. Mohammadi, M., & Karr, A. L. (2001). Superoxide anion generation in effective and ineffective soybean root nodules. Journal of Plant Physiology, 158, 1023-1029.
32. Mulabagal, V., Ngouajio, M., Nair, A., Zhang, Y., Gottumukkala, A. L., & Nair, M. G. (2010). In vitro evaluation of red and green lettuce (Lactuca sativa) for functional food properties. Food Chemistry, 118, 300-306.
33. Nagalakshmi, N., & Prasad, M. N. V. (2001). Responses of glutathione cycle enzymes and glutathione metabolism to copper stress in Scenedesmus bijugatus. Plant Science, 160, 291-299.
34. Nakano, Y., & Asada, K. (1981). Hydrogen peroxide is scavenged by ascorbate specific peroxidase in spinach chloroplasts. Plant Cell Physiology, 22, 867-880.
35. Päivöke, K. E., & Simola, L. K. (2001). Arsenate toxicity to Pisum sativum: mineral nutrients, chlorophyll content, and phytase activity. Ecotoxicology and Environmental Safety, 49, 111-121.
36. Peixoto, P. H. P., Cambraia, J., Sant'ana, R., Mosquim, P. R., & Moreira, M. A. (1999). Aluminum effects on lipid peroxidation and on activities of enzymes of oxidative metabolism in sorghum. Revista Brasileira de Fisiologia Vegetal, 11, 137-143.
37. Peto, A., Lehotai, N., Juste, J. L., León, J., Tari, I., & Erdei, L. (2011). Involvement of nitric oxide and auxin in signal transduction of copper-induced morphological responses in Arabidopsis seedlings. Annals of Botany, 108, 449-457.
38. SAS Institute. (1999). SAS/STAT user's guide 8.0. Cary: SAS Institute Inc.
39. Singh, H. P., Kaur, S., Batish, D. R., Sharma, V. P., Sharma, N., & Kohli, R. K. (2009). Nitric oxide alleviates arsenic toxicity by reducing oxidative damage in the roots of Oryza sativa (rice). Nitric Oxide, 20, 289-297.
40. Srivastava, S., Mishra, S., Tripathi, R. D., Dwivedi, S., Trivedi, P. K., & Tandon, P. K. (2007). Phytochelatins and antioxidant systems respond differentially during arsenite and arsenate stress in Hydrilla verticillata (L.f.) Royle. Environmental and Science Technology, 41, 2930-2936.
41. Wang, Y., Loake, G. J., & Chu, C. (2013). Cross-talk of nitric oxide and reactive oxygen species in plant programmed cell death. Frontiers in Plant Science, 4, 1-7.
42. Wang, J., Yu, S. X., Zhang, M., & Cui, X. M. (2015). Exogenous nitric oxide mediated GSH-PC synthesis pathway in tomato under copper stress. Russian Journal of Plant Physiology, 3, 349-359.
43. Xiong, J., An, L., Lu, H., & Zhu, C. (2009). Exogenous nitric oxide enhances cadmium tolerance of rice by increasing pectin and hemicellulose contents in root cell wall. Planta, 230, 755-765.
44. Zhang, M., Jiang, C., & Cui, X.-M. (2013). Effects of exogenous nitric oxide donor snp on physiological and biochemical indexes in tomato seedlings under copper stress. Plant Physiology Journal, 49, 144-152.