Elimination of heavy metals from contaminated water is a significant issue. Algae can be used as the detoxifying agent of these metals. This study was achieved to assess the efficacy of red marine alga (Jania Rubens) opposed to the initial modifications that may be concerning the toxicity of heavy metal-polluted water on male rats. 45 male Wistar rats were separated into 3 groups (15 rat/ group): Group I (control); Group II (Heavy metal group) and Group III (Treated group). There were significant increases in the levels of SGPT, SGOT, ALP, creatinine, urea, UA, malondialdehyde (MDA), glutathione peroxidase (GPx), protein carbonyl (PC) and significant decrease of body weights& levels of blood hemoglobin, total protein, albumin, catalase, SOD, and GSH in the heavy metal group in comparison with control. Meanwhile, the administration of treated water to rats restores all parameters to normal level in the treated group. Highly significant increase in Metallothionein (MT) levels in hepatic and renal tissue of heavy metal group compared to control, that restored to normal in the treated group. Also, Ni, Cd and Pb metals accumulated in liver, kidney and brain tissues were measured in all studied groups. Our results suggested the ameliorative effect of red marine algae treated water opposed to the toxicity of heavy metals in liver, kidney and brain tissues.
Published in | Science, Technology & Public Policy (Volume 2, Issue 2) |
DOI | 10.11648/j.stpp.20180202.13 |
Page(s) | 38-46 |
Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
Copyright |
Copyright © The Author(s), 2019. Published by Science Publishing Group |
Heavy Metals, Water Treatment, Red Marine Algae, Metallothionein, Oxidative Stress
[1] | Filote, C., Ungureanu, G., Boaventura, R., Santos, S., Volf, I., & Botelho, C. (2017). Green macroalgae from the Romanian coast of Black Sea: Physico-chemical characterization and future perspectives on their use as metal anions biosorbents. Process Safety and Environmental Protection, 108, 34-43. |
[2] | Nweke, O. C., & Sanders III, W. H. (2009). Modern environmental health hazards: a public health issue of increasing significance in Africa. Environmental Health Perspectives, 117 (6), 863. |
[3] | Fernandez-Luqueno, F., López-Valdez, F., Gamero-Melo, P., Luna-Suárez, S., Aguilera-González, E. N., Martínez, A. I.,... & Pérez-Velázquez, I. R. (2013). Heavy metal pollution in drinking water-a global risk for human health: A review. African Journal of Environmental Science and Technology, 7 (7), 567-584. |
[4] | Markiewicz-Górka, I., Januszewska, L., Michalak, A., Prokopowicz, A., Januszewska, E., Pawlas, N., & Pawlas, K. (2015). Effects of chronic exposure to lead, cadmium, and manganese mixtures on oxidative stress in rat liver and heart/Utjecaj kronične istodobne izloženosti olovu, kadmiju i manganu na oksidativni stres u jetri i srcu štakora. Archives of Industrial Hygiene and Toxicology, 66 (1), 51-62. |
[5] | Alissa, E. M., & Ferns, G. A. (2011). Heavy metal poisoning and cardiovascular disease. Journal of toxicology, 2011. |
[6] | Jomova, K., & Valko, M. (2011). Advances in metal-induced oxidative stress and human disease. Toxicology, 283 (2-3), 65-87. |
[7] | Flora, S. J. (2009). Structural, chemical and biological aspects of antioxidants for strategies against metal and metalloid exposure. Oxidative medicine and cellular longevity, 2 (4), 191-206. |
[8] | Patra, R. C.; Rautray, A. K and Swarup, D. (2011). Oxidative stress in lead and cadmium toxicity and its amelioration. Veterinary Medicine International. 457327: 1–9. |
[9] | Gunatilake, S. K. (2015). Methods of removing heavy metals from industrial wastewater. Methods, 1 (1). |
[10] | Carolin, C. F., Kumar, P. S., Saravanan, A., Joshiba, G. J., & Naushad, M. (2017). Efficient techniques for the removal of toxic heavy metals from aquatic environment: A review. Journal of Environmental Chemical Engineering, 5 (3), 2782-2799. |
[11] | Ibrahim, W. M. (2011). Biosorption of heavy metal ions from aqueous solution by red macroalgae. Journal of Hazardous Materials, 192 (3), 1827-1835. |
[12] | Trinelli, M. A., Areco, M. M., & dos Santos Afonso, M. (2013). Co-biosorption of copper and glyphosate by Ulva lactuca. Colloids and Surfaces B: Biointerfaces, 105, 251-258. |
[13] | He, J., & Chen, J. P. (2014). A comprehensive review on biosorption of heavy metals by algal biomass: materials, performances, chemistry, and modeling simulation tools. Bioresource technology, 160, 67-78. |
[14] | Gella, F. J., Olivella, T., Pastor, M. C., Arenas, J., Moreno, R., Durban, R., & Gomez, J. A. (1985). A simple procedure for the routine determination of aspartate aminotransferase and alanine aminotransferase with pyridoxal phosphate. Clinica chimica acta, 153 (3), 241-247. |
[15] | Tietz, N. W., Rinker, A. D., & Shaw, L. M. (1983). IFCC methods for the measurement of catalytic concentration of enzymes Part 5. IFCC method for alkaline phosphatase (orthophosphoric-monoester phosphohydrolase, alkaline optimum, EC 3.1. 3.1). Journal of clinical chemistry and clinical biochemistry. Zeitschrift fur klinische Chemie und klinische Biochemie, 21 (11), 731. |
[16] | Gornall, A. G., Bardawill, C. J., & David, M. M. (1949). Determination of serum proteins by means of the biuret reaction. Journal of biological chemistry, 177 (2), 751-766. |
[17] | Doumas, B. T., Watson, W. A., & Biggs, H. G. (1971). Albumin standards and the measurement of serum albumin with bromcresol green. Clinica chimica acta, 31 (1), 87-96. |
[18] | Betke, I. and Savelsberg, W. (1950). Stufen photometrische hemoglobin best immung mittels cyanhamiglobin. Biochemische Zeitschrift. 320: 431–439. |
[19] | Fabiny, D. L., & Ertingshausen, G. (1971). Automated reaction-rate method for determination of serum creatinine with the CentrifiChem. Clinical chemistry, 17 (8), 696-700. |
[20] | Tabacco, A., Meiattini, F., Moda, E., & Tarli, P. (1979). Simplified enzymic/colorimetric serum urea nitrogen determination. Clinical chemistry, 25 (2), 336-337. |
[21] | Fossati, P., Prencipe, L., & Berti, G. (1980). Use of 3, 5-dichloro-2-hydroxybenzenesulfonic acid/4-aminophenazone chromogenic system in direct enzymic assay of uric acid in serum and urine. Clinical chemistry, 26 (2), 227-231. |
[22] | Ohkawa, H., Ohishi, N., & Yagi, K. (1979). Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Analytical biochemistry, 95 (2), 351-358. |
[23] | Reznick, A. Z., & Packer, L. (1994). Oxidative damage to proteins: spectrophotometric method for carbonyl assay. In Methods in enzymology (Vol. 233, pp. 357-363). Academic Press. |
[24] | Aebi, H. (1984). Catalase in vitro. In Methods in enzymology (Vol. 105, pp. 121-126). Academic Press. |
[25] | Nishikimi, M., Rao, N. A., & Yagi, K. (1972). The occurrence of superoxide anion in the reaction of reduced phenazine methosulfate and molecular oxygen. Biochemical and biophysical research communications, 46 (2), 849-854. |
[26] | Paglia, D. E., & Valentine, W. N. (1967). Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase. The Journal of laboratory and clinical medicine, 70 (1), 158-169. |
[27] | Beutler, E. (1963). Improved method for the determination of blood glutathione. J. lab. clin. Med., 61, 882-888. |
[28] | Aggarwal, B. B. (2000). Tumour necrosis factors receptor associated signalling molecules and their role in activation of apoptosis, JNK and NF-κB. Annals of the rheumatic diseases, 59 (suppl 1), i6-i16. |
[29] | Viarengo, A.; Ponzano, E.; Donderob, F and Fabbrih, R (1977). A simple spectrophotometric method for metallothionein evaluation in marine organisms: an application to mediterranean and antarctic molluscs. Marine Environmental Research. 44 (1): 69–84. |
[30] | IAEA (1980). Elemental analysis of biological materials. International Atomic Energy Agency, Veinna. Technical Reports Series. 197: 317–345. |
[31] | Delafield, F. (1984). Haematoxylin and eosin for general staining. Staining of the animal tissues practical and theoretical. |
[32] | Nowrouzi, M., Mansouri, B., Nabizadeh, S., & Pourkhabbaz, A. (2014). Analysis of heavy metals concentration in water and sediment in the Hara biosphere reserve, southern Iran. Toxicology and industrial health, 30 (1), 64-72. |
[33] | Singh, R., Gautam, N., Mishra, A., & Gupta, R. (2011). Heavy metals and living systems: An overview. Indian journal of pharmacology, 43 (3), 246. |
[34] | Malik, A. (2004). Metal bioremediation through growing cells. Environment international, 30 (2), 261-278. |
[35] | Jadhav, S. H., Sarkar, S. N., Patil, R. D., & Tripathi, H. C. (2007). Effects of subchronic exposure via drinking water to a mixture of eight water-contaminating metals: a biochemical and histopathological study in male rats. Archives of environmental contamination and toxicology, 53 (4), 667-677. |
[36] | Otitoloju, A. A., & Igwo-Ezikpe, M. N. (2014). Usefulness of liver and kidney function parameters as biomarkers of heavy metals exposure in a mammalian model Mus musculus. African Journal of Biochemistry Research, 8 (3), 65-73. |
[37] | El-Boshy, M. E., Risha, E. F., Abdelhamid, F. M., Mubarak, M. S., & Hadda, T. B. (2015). Protective effects of selenium against cadmium induced hematological disturbances, immunosuppressive, oxidative stress and hepatorenal damage in rats. Journal of Trace Elements in Medicine and Biology, 29, 104-110. |
[38] | Bhattacharjee, T., Bhattacharjee, S., & Choudhuri, D. (2016). HEPATOTOXIC AND NEPHROTOXIC EFFECTS OF CHRONIC LOW DOSE EXPOSURE TO A MIXTURE OF HEAVY METALS-LEAD, CADMIUM AND ARSENIC. International Journal of Pharmaceutical, Chemical & Biological Sciences, 6 (1). |
[39] | Apaydın, F. G., Baş, H., Kalender, S., & Kalender, Y. (2016). Subacute effects of low dose lead nitrate and mercury chloride exposure on kidney of rats. Environmental toxicology and pharmacology, 41, 219-224. |
[40] | Yuan, G., Dai, S., Yin, Z., Lu, H., Jia, R., Xu, J.,... & Zhao, X. (2014). Toxicological assessment of combined lead and cadmium: acute and sub-chronic toxicity study in rats. Food and chemical toxicology, 65, 260-268. |
[41] | Hussein, S. A., Hassanein, M. R. R., Amin, A., & Hussein, A. H. M. (2016). Alpha-lipoic acid protects rat kidney against oxidative stress-mediated DNA damage and apoptosis induced by lead. Am J Biochem Mol Biol, 6, 1-14. |
[42] | Moniuszko-Jakoniuk, J., Jurczuk, M., & Gałażyn-Sidorczuk, M. (2009). Evaluation of Some Immunoregulatory Cytokines in Serum of Rats Exposed to Cadmium and Ethanol. Polish Journal of Environmental Studies, 18 (4). |
[43] | Kim, H. S., Kim, Y. J., & Seo, Y. R. (2015). An overview of carcinogenic heavy metal: molecular toxicity mechanism and prevention. Journal of cancer prevention, 20 (4), 232. |
[44] | Reckziegel, P., Dias, V. T., Benvegnú, D. M., Boufleur, N., Barcelos, R. C. S., Segat, H. J.,... & Bürger, M. E. (2016). Antioxidant protection of gallic acid against toxicity induced by Pb in blood, liver and kidney of rats. Toxicology reports, 3, 351-356. |
[45] | Padma, V. V., Baskaran, R., Divya, S., Priya, L. B., & Saranya, S. (2016). Modulatory effect of Tinospora cordifolia extract on Cd-induced oxidative stress in Wistar rats. Integrative medicine research, 5 (1), 48-55. |
[46] | Hussein, S. A., Mohammed, R. R., & Ali, A. H. (2014). Protective effects of alpha-lipoic acid against lead-induced oxidative stress in erythrocytes of rats. Benha Vet Med J, 27, 382-395. |
[47] | Antonio-García, M. T., & Massó-Gonzalez, E. L. (2008). Toxic effects of perinatal lead exposure on the brain of rats: involvement of oxidative stress and the beneficial role of antioxidants. Food and chemical toxicology, 46 (6), 2089-2095. |
[48] | Reddy, U. A., Prabhakar, P. V., Rao, G. S., Rao, P. R., Sandeep, K., Rahman, M. F.,... & Mahboob, M. (2015). Biomarkers of oxidative stress in rat for assessing toxicological effects of heavy metal pollution in river water. Environmental science and pollution research, 22 (17), 13453-13463. |
[49] | Das, K. K., Gupta, A. D., Dhundasi, S. A., Patil, A. M., Das, S. N., & Ambekar, J. G. (2007). Protective role of L-ascorbic acid on antioxidant defense system in erythrocytes of albino rats exposed to nickel sulfate. Biometals, 20 (2), 177-184. |
[50] | Wang, M., Song, H., Chen, W. Q., Lu, C., Hu, Q., Ren, Z.,... & Ling, W. (2011). Cancer mortality in a Chinese population surrounding a multi-metal sulphide mine in Guangdong province: an ecologic study. BMC public health, 11 (1), 319. |
[51] | Abdelmigid, H. M., Hassan, A. M., & El-Rab, S. M. G. (2014). Expression of metallothionein as a biomarker in response to various stress factors in different organisms. International Journal, 2 (10), 683-695. |
[52] | Šveikauskaitė, I., Šulinskienė, J., Sadauskienė, I., & Ivanov, L. (2014). The effects of lead and nickel ions on total proteins and metallothioneins synthesis in mice liver. Biologija, 60 (1). |
[53] | Ryvolova, M., Krizkova, S., Adam, V., Beklova, M., Trnkova, L., Hubalek, J., & Kizek, R. (2011). Analytical methods for metallothionein detection. Current Analytical Chemistry, 7 (3), 243-261. |
[54] | Li, X., Chen, Z., Chen, Z., & Zhang, Y. (2013). A human health risk assessment of rare earth elements in soil and vegetables from a mining area in Fujian Province, Southeast China. Chemosphere, 93 (6), 1240-1246. |
[55] | Bajpai, R., & Upreti, D. K. (2012). Accumulation and toxic effect of arsenic and other heavy metals in a contaminated area of West Bengal, India, in the lichen Pyxine cocoes (Sw.) Nyl. Ecotoxicology and environmental safety, 83, 63-70. |
[56] | Steuerwald, A. J., Blaisdell, F. S., Geraghty, C. M., & Parsons, P. J. (2014). Regional distribution and accumulation of lead in caprine brain tissues following a long-term oral dosing regimen. Journal of Toxicology and Environmental Health, Part A, 77 (12), 663-678. |
[57] | Samir, D., & Zine, K. (2013). Preventive effect of zinc on nickel-induced oxidative liver injury in rats. African Journal of Biotechnology, 12 (51), 7112-7119. |
[58] | Cobbina, S. J., Chen, Y., Zhou, Z., Wu, X., Zhao, T., Zhang, Z.,... & Yang, L. (2015). Toxicity assessment due to sub-chronic exposure to individual and mixtures of four toxic heavy metals. Journal of Hazardous materials, 294, 109-120. |
APA Style
Soha Mohamed Hamdy, Amany Mohamed Shaban, Yasmeen Saeid Abdel Aziz, Atef Mohamed Mahmoud, Leqaa Abdel Aziz Moemen, et al. (2019). Ameliorative Role of Jania Rubens Alga Against Toxicity of Heavy Metal Polluted Water in Male Rats. Science, Technology & Public Policy, 2(2), 38-46. https://doi.org/10.11648/j.stpp.20180202.13
ACS Style
Soha Mohamed Hamdy; Amany Mohamed Shaban; Yasmeen Saeid Abdel Aziz; Atef Mohamed Mahmoud; Leqaa Abdel Aziz Moemen, et al. Ameliorative Role of Jania Rubens Alga Against Toxicity of Heavy Metal Polluted Water in Male Rats. Sci. Technol. Public Policy 2019, 2(2), 38-46. doi: 10.11648/j.stpp.20180202.13
AMA Style
Soha Mohamed Hamdy, Amany Mohamed Shaban, Yasmeen Saeid Abdel Aziz, Atef Mohamed Mahmoud, Leqaa Abdel Aziz Moemen, et al. Ameliorative Role of Jania Rubens Alga Against Toxicity of Heavy Metal Polluted Water in Male Rats. Sci Technol Public Policy. 2019;2(2):38-46. doi: 10.11648/j.stpp.20180202.13
@article{10.11648/j.stpp.20180202.13, author = {Soha Mohamed Hamdy and Amany Mohamed Shaban and Yasmeen Saeid Abdel Aziz and Atef Mohamed Mahmoud and Leqaa Abdel Aziz Moemen and Wael Mohamed Ibrahim and Nahed Shafik Gad}, title = {Ameliorative Role of Jania Rubens Alga Against Toxicity of Heavy Metal Polluted Water in Male Rats}, journal = {Science, Technology & Public Policy}, volume = {2}, number = {2}, pages = {38-46}, doi = {10.11648/j.stpp.20180202.13}, url = {https://doi.org/10.11648/j.stpp.20180202.13}, eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.stpp.20180202.13}, abstract = {Elimination of heavy metals from contaminated water is a significant issue. Algae can be used as the detoxifying agent of these metals. This study was achieved to assess the efficacy of red marine alga (Jania Rubens) opposed to the initial modifications that may be concerning the toxicity of heavy metal-polluted water on male rats. 45 male Wistar rats were separated into 3 groups (15 rat/ group): Group I (control); Group II (Heavy metal group) and Group III (Treated group). There were significant increases in the levels of SGPT, SGOT, ALP, creatinine, urea, UA, malondialdehyde (MDA), glutathione peroxidase (GPx), protein carbonyl (PC) and significant decrease of body weights& levels of blood hemoglobin, total protein, albumin, catalase, SOD, and GSH in the heavy metal group in comparison with control. Meanwhile, the administration of treated water to rats restores all parameters to normal level in the treated group. Highly significant increase in Metallothionein (MT) levels in hepatic and renal tissue of heavy metal group compared to control, that restored to normal in the treated group. Also, Ni, Cd and Pb metals accumulated in liver, kidney and brain tissues were measured in all studied groups. Our results suggested the ameliorative effect of red marine algae treated water opposed to the toxicity of heavy metals in liver, kidney and brain tissues.}, year = {2019} }
TY - JOUR T1 - Ameliorative Role of Jania Rubens Alga Against Toxicity of Heavy Metal Polluted Water in Male Rats AU - Soha Mohamed Hamdy AU - Amany Mohamed Shaban AU - Yasmeen Saeid Abdel Aziz AU - Atef Mohamed Mahmoud AU - Leqaa Abdel Aziz Moemen AU - Wael Mohamed Ibrahim AU - Nahed Shafik Gad Y1 - 2019/01/03 PY - 2019 N1 - https://doi.org/10.11648/j.stpp.20180202.13 DO - 10.11648/j.stpp.20180202.13 T2 - Science, Technology & Public Policy JF - Science, Technology & Public Policy JO - Science, Technology & Public Policy SP - 38 EP - 46 PB - Science Publishing Group SN - 2640-4621 UR - https://doi.org/10.11648/j.stpp.20180202.13 AB - Elimination of heavy metals from contaminated water is a significant issue. Algae can be used as the detoxifying agent of these metals. This study was achieved to assess the efficacy of red marine alga (Jania Rubens) opposed to the initial modifications that may be concerning the toxicity of heavy metal-polluted water on male rats. 45 male Wistar rats were separated into 3 groups (15 rat/ group): Group I (control); Group II (Heavy metal group) and Group III (Treated group). There were significant increases in the levels of SGPT, SGOT, ALP, creatinine, urea, UA, malondialdehyde (MDA), glutathione peroxidase (GPx), protein carbonyl (PC) and significant decrease of body weights& levels of blood hemoglobin, total protein, albumin, catalase, SOD, and GSH in the heavy metal group in comparison with control. Meanwhile, the administration of treated water to rats restores all parameters to normal level in the treated group. Highly significant increase in Metallothionein (MT) levels in hepatic and renal tissue of heavy metal group compared to control, that restored to normal in the treated group. Also, Ni, Cd and Pb metals accumulated in liver, kidney and brain tissues were measured in all studied groups. Our results suggested the ameliorative effect of red marine algae treated water opposed to the toxicity of heavy metals in liver, kidney and brain tissues. VL - 2 IS - 2 ER -