EVALUATING PESTICIDE-INDUCED TOXICITY IN CYPRINUS CARPIO: CYHALOTHRIN AS A CASE STUDY

Authors

  • Dr Umme Habeeba Habeeba Assistant Professor, Government First Grade College, Rajnagar, Hubli, Karnataka
  • Dr M David Professor, Department of studies in Zoology, karnatak University, Dharwad, Karnataka

DOI:

https://doi.org/10.53555/eijmhs.v9i2.271

Keywords:

Lambda-cyhalothrin, Cyprinus carpio, sublethal toxicity, oxidative stress, reproductive disruption

Abstract

The widespread agricultural application of synthetic pyrethroids has created environmental issues because they harm aquatic organisms that are not the target of treatment. This research examines the sublethal toxicity of lambda-cyhalothrin (LCH) on Cyprinus carpio's physiological, biochemical, and reproductive functions by subjecting the fish to controlled LCH exposure for 20 days. The 96-hour LC₅₀ value for LCH was established at 1.6 µg/L, while sublethal doses of LCH caused fish to become progressively hyperactive and produce mucus, and become lethargic. The biochemical analysis revealed protein content reductions of all variants, including structural and soluble proteins, while showing study concentrations enhanced protease activity with rising free amino acid levels, which indicated proteolysis along with metabolic disorder. Oxidative stress developed due to the significant reduction of antioxidant enzymes (CAT, SOD, GPx, GST) and accompanying MDA level increase. ATPase activity declined along with tissue ion concentrations because osmoregulatory paths and energy-dependent transport pathways lost their functionality. The fish showed reproductive problems through decreased gonado-somatic index and hormonal levels (testosterone, estradiol, 11-ketotestosterone) and gonad tissue degeneration. The blood tests showed reduced RBC numbers and decreased hemoglobin and PCV levels, and increased WBC counts, which indicated both anemic and immunological reactions. The research shows that C. carpio suffers multi-organ dysfunction when exposed to any amount of LCH below lethal levels, which creates significant ecological threats. According to this research, scientists need to tighten regulations regarding pesticide application while emphasizing how C. carpio functions as an excellent indicator for freshwater toxicology investigations.

References

Stanley, J., Preetha, G., Stanley, J., & Preetha, G. (2016). Pesticide toxicity to fishes: exposure, toxicity and risk assessment methodologies. Pesticide Toxicity to Non-target Organisms: Exposure, Toxicity and Risk Assessment Methodologies, 411-497.

Sabra, F. S., & Mehana, E. S. E. D. (2015). Pesticides toxicity in fish with particular reference to insecticides. Asian Journal of Agriculture and Food Sciences, 3(1).

Ullah, S., & Zorriehzahra, M. J. (2015). Ecotoxicology: a review of pesticides induced toxicity in fish. Advances in Animal and Veterinary Sciences, 3(1), 40-57.

Dey, C., & Saha, S. K. (2014). A comparative study on the acute toxicity bioassay of dimethoate and lambda-cyhalothrin and effects on thyroid hormones of freshwater teleost fish Labeo rohita (Hamilton). International journal of environmental research, 8(4), 1085-1092.

Ullah, R., Zuberi, A., Ullah, S., Ullah, I., & Dawar, F. U. (2014). Cypermethrin induced behavioral and biochemical changes in mahseer, Tor putitora. The Journal of toxicological sciences, 39(6), 829-836.

Bhavan, P. S., Srinivasan, V., Satgurunathan, T., & Deepthi, P. (2015). Lethal and sub-lethal toxic effects of a pyrethroid insecticide, λ-cyhalothrin on activities of acetylcholinesterase, glutamic oxaloacetic transaminase, glutamic pyruvic transaminase and catalase in the post-larvae of the prawn Macrobrachium rosenbergii. Advances in Bioresearch, 6(5).

Srivastava, P., Singh, A., & Pandey, A. K. (2016). Pesticides toxicity in fishes: biochemical, physiological and genotoxic aspects. Biochemical and cellular archives, 16(2), 199-218.

Köprücü, K., Yonar, S. M., & Şeker, E. (2010). Effects of cypermethrin on antioxidant status, oxidative stress biomarkers, behavior, and mortality in the freshwater mussel Unio elongatulus eucirrus. Fisheries science, 76, 1007-1013.

Banaee, M. (2013). Physiological dysfunction in fish after insecticides exposure. In Insecticides-Development of safer and more effective technologies. IntechOpen.

Sana Ullah, S. U., & Zorriehzahra, M. J. (2015). Ecotoxicology: a review of pesticides induced toxicity in fish.

Elbialy, Z. I., Ismail, T., Abdelhady, D. H., & El-Asely, A. M. (2015). Assessment of Genotoxic Effects of Pesticide Residues and Related Haemato-Biochemical Parameters on Farmed Nile Tilapia (Oreochromis Niloticus L.) in Kafrelsheikh Governorate, Egypt. Alexandria Journal of Veterinary Sciences, 44(1).

Kartheek, R., & David, M. (2016). Fipronil induced modulations in biochemical and histopathological aspects of male Wistar albino rats: a subchronic study. World, 5(2), 26-32.

Chaâbane, M., Ghorbel, I., Elwej, A., Mnif, H., Boudawara, T., Chaâbouni, S. E., ... & Soudani, N. (2017). Penconazole alters redox status, cholinergic function, and membrane-bound ATPases in the cerebrum and cerebellum of adult rats. Human & experimental toxicology, 36(8), 854-866.

Khan, A., Ahmad, L., & Khan, M. Z. (2012). Hemato-Biochemical Changes Induced by Pyrethroid Insecticides in Avian, Fish and Mammalian Species. International journal of agriculture & biology, 14(5).

Hernández-Moreno, D., Soler, F., Míguez, M. P., & Pérez-López, M. (2010). Brain acetylcholinesterase, malondialdehyde and reduced glutathione as biomarkers of continuous exposure of tench, Tinca tinca, to carbofuran or deltamethrin. Science of the Total Environment, 408(21), 4976-4983.

Yekeen, T. A., Fawole, O. O., Bakare, A. A., & Emikpe, B. O. (2016). Alteration in haematological, biochemical and reproductive indices of Rattus norvegicus treated with lambdacyhalothrin. Zoology and Ecology, 26(1), 47-56.

Mani, V. M., Gokulakrishnan, A., & Sadiq, A. M. (2017). Molecular mechanism of Neu-rodevelopmental toxicity risks of Occupational exposure of Pyrethroid Pesticide with reference to Deltamethrin-A critical review. BAOJ Pathology, 1(008).

El-Gerbed, M. S. (2014). Protective effect of lycopene on deltamethrin-induced histological and ultrastructural changes in kidney tissue of rats. Toxicology and industrial health, 30(2), 160-173.

Qayoom, I., Balkhi, M. H., Mukhtar, M., Bhat, F. A., & Shah, F. A. (2014). Biochemical toxicity of organophosphate compounds in fishes. SKUAST Journal of Research, 16(1), 1-13.

Mani, V. M., & Sadiq, A. M. M. (2014). Naringin modulates the impairment of memory, anxiety, locomotor, and emotionality behaviors in rats exposed to deltamethrin; a possible mechanism association with oxidative stress, acetylcholinesterase and ATPase. Biomedicine & Preventive Nutrition, 4(4), 527-533.

Oliveira, C. A. V. (2010). Behavioural Alterations and Biomarker Responses of Palaemon Serratus Exposed to Pesticides (Master's thesis, Universidade de Aveiro (Portugal)).

Nwani, C. D., Agrawal, N. D., Raghuvanshi, S., Jaswal, A., Shrivastava, S., Sinha, N., ... & Shukla, S. (2016). Toxicological effects of carbosulfan in rats: Antioxidant, enzymological, biochemical, and hematological responses. Toxicology and industrial health, 32(7), 1335-1343.

Xing, H., Li, S., Wang, Z., Gao, X., Xu, S., & Wang, X. (2012). Oxidative stress response and histopathological changes due to atrazine and chlorpyrifos exposure in common carp. Pesticide biochemistry and physiology, 103(1), 74-80.

Qureshi, I. Z., Bibi, A., Shahid, S., & Ghazanfar, M. (2016). Exposure to sub-acute doses of fipronil and buprofezin in combination or alone induces biochemical, hematological, histopathological and genotoxic damage in common carp (Cyprinus carpio L.). Aquatic toxicology, 179, 103-114.

Ural, M. Ş. (2013). Chlorpyrifos-induced changes in oxidant/antioxidant status and haematological parameters of Cyprinus carpio carpio: ameliorative effect of lycopene. Chemosphere, 90(7), 2059-2064.

Downloads

Published

2023-04-22