TOXIC EFFECTS OF LEAD ON FISH AND HUMAN

Authors

  • A Ishaque Institute of Molecular Biology & Biotechnology, University of Lahore, Lahore, Pakistan
  • S Ishaque Department of Biotechnology, Kinnaird College for Women, Lahore, Pakistan
  • A Arif Institute of Molecular Biology & Biotechnology, University of Lahore, Lahore, Pakistan
  • HG Abbas Cotton Research Institute, Ayub Agricultural Research Institute Faisalabad, Pakistan

DOI:

https://doi.org/10.54112/bcsrj.v2020i1.47

Keywords:

lead, heavy metal, toxicity, antioxidant, biochemical, physiological

Abstract

Bioaccumulation is a characteristic aspect in toxicity caused by Pb exposure. Toxic effects are induced in fish due to Pb exposure effecting its biochemical and physiological functions. Exposure pathway (dietary and waterborne), environmental factors (salt-water or fresh water) and Pb binding capacity with protein, SH and sulfur group decide accumulation pattern of Pb exposure. Activation of antioxidant responses like TBARS, GSH, GST, CAT and SOD occurs in fish for its protection in response to the oxidative stresses induced in fish due to Pb accumulation. Disruption of neurotransmitter function also occurs due to Pb accumulation which causes neurotoxicity in fish. Pb interaction also disturbs immune system responses. In fish, various systems are affected due to Pb toxic exposure which can be used as an indicator of toxicity in aquatic environment.

Downloads

Download data is not yet available.

References

Adeyemo, O., Adedeji, O., and Offor, C. (2010). Blood lead level as biomarker of environmental lead pollution in feral and cultured African catfish (Clarias gariepinus). Nigerian veterinary journal 31.

Al-Balawi, H. F. A., Al-Akel, A. S., Al-Misned, F., Suliman, E. A. M., Al-Ghanim, K. A., Mahboob, S., and Ahmad, Z. (2013). Effects of sub-lethal exposure of lead acetate on histopathology of gills, liver, kidney and muscle and its accumulation in these organs of Clarias gariepinus. Brazilian archives of biology and technology 56, 293-302.

Alsop, R. J., Schober, R. M., and Rheinstädter, M. C. (2016). Swelling of phospholipid membranes by divalent metal ions depends on the location of the ions in the bilayers. Soft Matter 12, 6737-6748.

Alvares, A. P., Fischbein, A., Sassa, S., Anderson, K. E., and Kappas, A. (1976). Lead intoxication: Effects on cytochrome P‐450‐mediated hepatic oxidations. Clinical Pharmacology & Therapeutics 19, 183-190.

Alves, L., Glover, C., and Wood, C. (2006). Dietary Pb accumulation in juvenile freshwater rainbow trout (Oncorhynchus mykiss). Archives of environmental contamination and toxicology 51, 615.

Apostoli, P., Kiss, P., Porru, S., Bonde, J. P., and Vanhoorne, M. (1998). Male reproductive toxicity of lead in animals and humans. ASCLEPIOS Study Group. Occupational and environmental medicine 55, 364-374.

Assennato, G., Paci, C., Baser, M. E., Molinini, R., Candela, R. G., Altamura, B. M., and Giorgino, R. (1987). Sperm count suppression without endocrine dysfunction in lead-exposed men. Archives of Environmental Health: An International Journal 42, 124-127.

Audesirk, G. (1993). Electrophysiology of lead intoxication: effects on voltage-sensitive ion channels. Neurotoxicology 14, 137-147.

Bernard, A., and Lauwerys, R. (1984). Cadmium in human population. Experientia 40, 143-152.

Braunstein, G. D., Dahlgren, J., and Loriaux, D. L. (1978). HYPOGONADISl• f IN CHRONICALLY LEAD-POISONED!•! Etl. Infertility 1, 33-51.

Campara, P., D'andrea, F., Micciolo, R., Savonitto, C., Tansella, M., and Zimmermann-Tansella, C. (1984). Psychological performance of workers with blood-lead concentration below the current threshold limit value. International archives of occupational and environmental health 53, 233-246.

Castro-González, M., and Méndez-Armenta, M. (2008). Heavy metals: Implications associated to fish consumption. Environmental toxicology and pharmacology 26, 263-271.

Chain, E. P. o. C. i. t. F. (2010). Scientific Opinion on lead in food. EFSA Journal 8, 1570.

Chang, L.-F., Jiang, S.-J., and Sahayam, A. (2007). Speciation analysis of mercury and lead in fish samples using liquid chromatography–inductively coupled plasma mass spectrometry. Journal of Chromatography A 1176, 143-148.

Chen, Y., Huang, L., Wu, W., Ruan, Y., Wu, Z., Xue, Z., and Fu, F. (2014). Speciation analysis of lead in marine animals by using capillary electrophoresis couple online with inductively coupled plasma mass spectrometry. Electrophoresis 35, 1346-1352.

Cheng, H., and Hu, Y. (2010). Municipal solid waste (MSW) as a renewable source of energy: Current and future practices in China. Bioresource technology 101, 3816-3824.

Coscia, G., Discalzi, G., and Ponzetti, C. (1987). Immunological aspects of occupational lead exposure. La Medicina del lavoro 78, 360.

Dai, J., Zhang, L., Du, X., Zhang, P., Li, W., Guo, X., and Li, Y. (2018). Effect of lead on antioxidant ability and immune responses of crucian carp. Biological trace element research 186, 546-553.

Dunier, M. (1996). Water pollution and immunosuppression of freshwater fish. Italian Journal of Zoology 63, 303-309.

Dural, M., Göksu, M. Z. L., and Özak, A. A. (2007). Investigation of heavy metal levels in economically important fish species captured from the Tuzla lagoon. Food chemistry 102, 415-421.

Ehrlich, R., Robins, T., Jordaan, E., Miller, S., Mbuli, S., Selby, P., Wynchank, S., Cantrell, A., De Broe, M., and D'Haese, P. (1998). Lead absorption and renal dysfunction in a South African battery factory. Occupational and Environmental medicine 55, 453-460.

Eroglu, A., Dogan, Z., Kanak, E., Atli, G., and Canli, M. (2015). Effects of heavy metals (Cd, Cu, Cr, Pb, Zn) on fish glutathione metabolism. Environmental Science and Pollution Research 22, 3229-3237.

Evis, M. J., Dhaliwal, K., Kane, K. A., Moore, M. R., and Parratt, J. R. (1987). The effects of chronic lead treatment and hypertension on the severity of cardiac arrhythmias induced by coronary artery occlusion or by noradrenaline in anaesthetised rats. Archives of toxicology 59, 336-340.

Ewers, U., Stiller-Winkler, R., and Idel, H. (1982). Serum immunoglobulin, complement C3, and salivary IgA levels in lead workers. Environmental research 29, 351-357.

Farkas, A., Salánki, J., and Specziár, A. (2003). Age-and size-specific patterns of heavy metals in the organs of freshwater fish Abramis brama L. populating a low-contaminated site. Water research 37, 959-964.

Flegal, A. R. (1986). Lead in tropical marine systems: a review. Science of the Total Environment 58, 1-8.

Gerhardsson, L., Chettle, D., Englyst, V., Nordberg, G., Nyhlin, H., Scott, M., Todd, A., and Vesterberg, O. (1992). Kidney effects in long term exposed lead smelter workers. Occupational and Environmental Medicine 49, 186-192.

Gidlow, D. A. (2015). Lead toxicity. Occupational medicine 65, 348-356.

Goering, P. (1993). Lead-protein interactions as a basis for lead toxicity. Neurotoxicology 14, 45.

Goyer, R. (1989). Mechanisms of lead and cadmium nephrotoxicity. Toxicology letters 46, 153-162.

Grosell, M., Gerdes, R., and Brix, K. (2006). Influence of Ca, humic acid and pH on lead accumulation and toxicity in the fathead minnow during prolonged water-borne lead exposure. Comparative Biochemistry and Physiology Part C: Toxicology & Pharmacology 143, 473-483.

Gurer, H., and Ercal, N. (2000). Can antioxidants be beneficial in the treatment of lead poisoning? Free Radical Biology and Medicine 29, 927-945.

Hogstedt, C., Hane, M., Agrell, A., and Bodin, L. (1983). Neuropsychological test results and symptoms among workers with well-defined long-term exposure to lead. Occupational and Environmental Medicine 40, 99-105.

Hsu, P.-C., and Guo, Y. L. (2002). Antioxidant nutrients and lead toxicity. Toxicology 180, 33-44.

IARC, W. (2006). IARC monographs on the evaluation of carcinogenic risks to humans: inorganic and organic lead compounds. Vol. 87. World Health Organization, Lyon, France.

Jaishankar, M., Tseten, T., Anbalagan, N., Mathew, B. B., and Beeregowda, K. N. (2014). Toxicity, mechanism and health effects of some heavy metals. Interdisciplinary toxicology 7, 60-72.

Javed, M. (2012). Effects of zinc and lead toxicity on the growth and their bioaccumulation in fish. Pak. Vet. J 32, 357-362.

Kalay, M., Ay, Ö., and Canli, M. (1999). Heavy metal concentrations in fish tissues from the Northeast Mediterranean Sea. Bulletin of environmental contamination and toxicology 63, 673-681.

Khalil-Manesh, F., Gonick, H. C., and Cohen, A. H. (1993). Experimental model of lead nephropathy. III. Continuous low-level lead administration. Archives of Environmental Health: An International Journal 48, 271-278.

Kim, J.-H., and Kang, J.-C. (2014). The selenium accumulation and its effect on growth, and haematological parameters in red sea bream, Pagrus major, exposed to waterborne selenium. Ecotoxicology and environmental safety 104, 96-102.

Kim, J.-H., and Kang, J.-C. (2015a). The arsenic accumulation and its effect on oxidative stress responses in juvenile rockfish, Sebastes schlegelii, exposed to waterborne arsenic (As3+). Environmental Toxicology and Pharmacology 39, 668-676.

Kim, J.-H., and Kang, J.-C. (2015b). The lead accumulation and hematological findings in juvenile rock fish Sebastes schlegelii exposed to the dietary lead (II) concentrations. Ecotoxicology and environmental safety 115, 33-39.

Kim, J.-H., and Kang, J.-C. (2016a). The chromium accumulation and its physiological effects in juvenile rockfish, Sebastes schlegelii, exposed to different levels of dietary chromium (Cr6+) concentrations. Environmental toxicology and pharmacology 41, 152-158.

Kim, J.-H., and Kang, J.-C. (2016b). The immune responses in juvenile rockfish, Sebastes schlegelii for the stress by the exposure to the dietary lead (II). Environmental toxicology and pharmacology 46, 211-216.

Kim, J.-H., and Kang, J.-C. (2016c). The toxic effects on the stress and immune responses in juvenile rockfish, Sebastes schlegelii exposed to hexavalent chromium. Environmental Toxicology and Pharmacology 43, 128-133.

Kim, J.-H., and Kang, J.-C. (2017a). Effects of dietary chromium exposure to rockfish, Sebastes schlegelii are ameliorated by ascorbic acid. Ecotoxicology and environmental safety 139, 109-115.

Kim, J.-H., and Kang, J.-C. (2017b). Effects of sub-chronic exposure to lead (Pb) and ascorbic acid in juvenile rockfish: antioxidant responses, MT gene expression, and neurotransmitters. Chemosphere 171, 520-527.

Lai, B., Murthy, R., Anand, M., Chandra, S., Kumar, R., Tripathi, O., and Srimal, R. (1991). Cardiotoxicity and hypertension in rats after oral lead exposure. Drug and chemical toxicology 14, 305-318.

Lead, W. I. (1995). Environmental health criteria 165. International Programme on Chemical Safety. Geneva: World Health Organization.

Lee, T.-h., and Jiang, S.-J. (2005). Speciation of lead compounds in fish by capillary electrophoresis-inductively coupled plasma mass spectrometry. Journal of Analytical Atomic Spectrometry 20, 1270-1274.

Lerda, D. (1992). Study of sperm characteristics in persons occupationally exposed to lead. American journal of industrial medicine 22, 567-571.

Loghman-Adham, M. (1997). Renal effects of environmental and occupational lead exposure. Environmental health perspectives 105, 928-939.

Mantere, P., Hänninen, H., Hernberg, S., and Luukkonen, R. (1984). A prospective follow-up study on psychological effects in workers exposed to low levels of lead. Scandinavian journal of work, environment & health, 43-50.

Marchetti, C. (2003). Molecular targets of lead in brain neurotoxicity. Neurotoxicity research 5, 221-235.

Nunes, B., Brandão, F., Sérgio, T., Rodrigues, S., Gonçalves, F., and Correia, A. T. (2014). Effects of environmentally relevant concentrations of metallic compounds on the flatfish Scophthalmus maximus: biomarkers of neurotoxicity, oxidative stress and metabolism. Environmental Science and Pollution Research 21, 7501-7511.

Oflaherty, E. J. (1995). Physiologically based models for bone-seeking elements: V. Lead absorption and disposition in childhood. Toxicology and applied pharmacology 131, 297-308.

Patra, R., Swarup, D., and Dwivedi, S. (2001). Antioxidant effects of α tocopherol, ascorbic acid and L-methionine on lead induced oxidative stress to the liver, kidney and brain in rats. Toxicology 162, 81-88.

Paul, N., Chakraborty, S., and Sengupta, M. (2014). Lead toxicity on non-specific immune mechanisms of freshwater fish Channa punctatus. Aquatic Toxicology 152, 105-112.

Philip, A. T., and Gerson, B. (1994). Lead Poisoning-Part II: Effects and Assay. Clinics in laboratory medicine 14, 651-670.

Ponka, P. (1999). Cell biology of heme. The American journal of the medical sciences 318, 241-256.

Richetti, S. K., Rosemberg, D. B., Ventura-Lima, J., Monserrat, J. M., Bogo, M. R., and Bonan, C. D. (2011). Acetylcholinesterase activity and antioxidant capacity of zebrafish brain is altered by heavy metal exposure. Neurotoxicology 32, 116-122.

Rogers, J., Richards, J., and Wood, C. (2003). Ionoregulatory disruption as the acute toxic mechanism for lead in the rainbow trout (Oncorhynchus mykiss). Aquatic toxicology 64, 215-234.

Sakai, T. (2000). Biomarkers of lead exposure. Industrial health 38, 127-142.

Savan, R., and Sakai, M. (2006). Genomics of fish cytokines. Comparative Biochemistry and Physiology Part D: Genomics and Proteomics 1, 89-101.

Senger, M. R., Rico, E. P., de Bem Arizi, M., Frazzon, A. P. G., Dias, R. D., Bogo, M. R., and Bonan, C. D. (2006). Exposure to Hg2+ and Pb2+ changes NTPDase and ecto-5′-nucleotidase activities in central nervous system of zebrafish (Danio rerio). Toxicology 226, 229-237.

Small, B. C. (2004). Effect of isoeugenol sedation on plasma cortisol, glucose, and lactate dynamics in channel catfish Ictalurus punctatus exposed to three stressors. Aquaculture 238, 469-481.

Somero, G. N., Chow, T. J., Yancey, P. H., and Snyder, C. B. (1977). Lead accumulation rates in tissues of the estuarine teleost fish, Gillichthys mirabilis: salinity and temperature effects. Archives of environmental Contamination and Toxicology 6, 337-348.

Souid, G., Souayed, N., Yaktiti, F., and Maaroufi, K. (2015). Lead accumulation pattern and molecular biomarkers of oxidative stress in seabream (Sparus aurata) under short-term metal treatment. Drug and chemical toxicology 38, 98-105.

Sures, B., Dezfuli, B. S., and Krug, H. F. (2003). The intestinal parasite Pomphorhynchus laevis (Acanthocephala) interferes with the uptake and accumulation of lead (210Pb) in its fish host chub (Leuciscus cephalus). International Journal for Parasitology 33, 1617-1622.

Sures, B., and Siddall, R. (1999). Pomphorhynchus laevis: the intestinal acanthocephalan as a lead sink for its fish host, chub (Leuciscus cephalus). Experimental Parasitology 93, 66-72.

Telisman, S., Cvitković, P., Jurasović, J., Pizent, A., Gavella, M., and Rocić, B. (2000). Semen quality and reproductive endocrine function in relation to biomarkers of lead, cadmium, zinc, and copper in men. Environmental health perspectives 108, 45-53.

Verstraeten, S. V., Aimo, L., and Oteiza, P. I. (2008). Aluminium and lead: molecular mechanisms of brain toxicity. Archives of toxicology 82, 789-802.

Vinodhini, R., and Narayanan, M. (2008). Bioaccumulation of heavy metals in organs of fresh water fish Cyprinus carpio (Common carp). International Journal of Environmental Science & Technology 5, 179-182.

Westerink, R. H., and Vijverberg, H. P. (2002). Vesicular catecholamine release from rat PC12 cells on acute and subchronic exposure to polychlorinated biphenyls. Toxicology and applied pharmacology 183, 153-159.

Witeska, M. (2005). Stress in fish-hematological and immunological effects of heavy metals. Electronic journal of ichthyology 1, 35-41.

Zhai, Q., Wang, H., Tian, F., Zhao, J., Zhang, H., and Chen, W. (2017). Dietary Lactobacillus plantarum supplementation decreases tissue lead accumulation and alleviates lead toxicity in Nile tilapia (Oreochromis niloticus). Aquaculture Research 48, 5094-5103.

Zhu, B., Wang, Q., Shi, X., Guo, Y., Xu, T., and Zhou, B. (2016). Effect of combined exposure to lead and decabromodiphenyl ether on neurodevelopment of zebrafish larvae. Chemosphere 144, 1646-1654.

Zizza, M., Giusi, G., Crudo, M., Canonaco, M., and Facciolo, R. M. (2013). Lead-induced neurodegenerative events and abnormal behaviors occur via ORXRergic/GABAARergic mechanisms in a marine teleost. Aquatic toxicology 126, 231-241.

Downloads

Published

2020-12-28

How to Cite

Ishaque, A., Ishaque, S., Arif, A., & Abbas, H. (2020). TOXIC EFFECTS OF LEAD ON FISH AND HUMAN. Biological and Clinical Sciences Research Journal, 2020(1). https://doi.org/10.54112/bcsrj.v2020i1.47

Issue

Section

Minireview Article