Acta Veterinaria Brno

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• Bojarski Bartosz, Osikowski Artur, Rombel-Bryzek Agnieszka, Hofman Sebastian, Sza\u0142a Leszek: The Influence of Clomazone-Based Herbicide Formulation on Common Carp (Cyprinus carpio) \u2013 A Laboratory Study Including Pathophysiological and Histopathological Assessment. Annals of Animal Science 2024, 24, 1179. <https://doi.org/10.2478/aoas-2024-0061>
• Maimuna A., Isiyaku Mohammed Sani, Laurat H. T., Iorhiin R. M., Shaibu A. L.: TOXICITY AND HAEMATOLOGICAL CHANGES OF Datura innoxia STEM ON Clarias gariepinus JUVENILES. FJS 2024, 8, 255. <https://doi.org/10.33003/fjs-2024-0804-2536>
• Kumar Reddy C. Prabhanjan, Manikandavelu D., Arisekar Ulaganathan, Ahilan B., Uma A., Jayakumar N., Kim Woong, Govarthanan Muthusamy, Harini C., Vidya R. Sri, Madhavan N., Kumar Reddy D. Ravindra: Toxicological effect of endocrine disrupting insecticide (deltamethrin) on enzymatical, haematological and histopathological changes in the freshwater iridescent shark, Pangasius hypothalamus. Environmental Toxicology and Pharmacology 2023, 101, 104201. <https://doi.org/10.1016/j.etap.2023.104201>
• Khan Mursalin, Mortuza Asif, Blumenthal Elliott, Mustafa Ahmed: Role of elderberry (Sambucus nigra) on the modulation of stress and immune response of Nile tilapia, Oreochromis niloticus. Journal of Applied Aquaculture 2023, 35, 765. <https://doi.org/10.1080/10454438.2022.2026269>
• Sahoo P. K., Sahoo S. K., Mohanty B. R., Das A., Giri S., Paramanik M.: Haematological and Innate Immunological Reference Intervals for Farmed Yellow Catfish Horabagrus brachysoma and Their Seasonal Variations. joa 2023, 1. <https://doi.org/10.61885/joa.v23.2015.91>
• Sahota Charanveer, Hayek Kassia, Surbey Brady, Kennedy Christopher J.: Lethal and sublethal effects in Pink salmon (Oncorhynchus gorbuscha) following exposure to five aquaculture chemotherapeutants. Ecotoxicology 2022, 31, 33. <https://doi.org/10.1007/s10646-021-02473-8>
• Shahjahan Md, Islam Md Jakiul, Hossain Md Tahmeed, Mishu Moshiul Alam, Hasan Jabed, Brown Christopher: Blood biomarkers as diagnostic tools: An overview of climate-driven stress responses in fish. Science of The Total Environment 2022, 843, 156910. <https://doi.org/10.1016/j.scitotenv.2022.156910>
• Hassan Marwa E., El-Sayed Abo El-Khair B., Abdel-Wahhab Mosaad A.: Screening of the bioactive compounds in Amphora coffeaeformis extract and evaluating its protective effects against deltamethrin toxicity in rats. Environ Sci Pollut Res 2021, 28, 15185. <https://doi.org/10.1007/s11356-020-11745-5>
• Jan Kousar, Ahmed Imtiaz: The influence of sex and season on some hematological and biochemical parameters of snow trout Schizothorax labiatus in the Indian Himalayan Region. Fish Sci 2021, 87, 39. <https://doi.org/10.1007/s12562-020-01469-3>
• Bej Suman, Ghosh Koushik, Chatterjee Arnab, Saha Nimai Chandra: Assessment of biochemical, hematological and behavioral biomarkers of Cyprinus carpio on exposure to a type-II pyrethroid insecticide Alpha-cypermethrin. Environmental Toxicology and Pharmacology 2021, 87, 103717. <https://doi.org/10.1016/j.etap.2021.103717>
• Amiri Resketi Maryam, Yeganeh Sakineh, Jani Khalili Khosro: Dietary sour lemon (Citrus limon) peel essential oil supplementation for reduction of deltamethrin‐induced stress in rainbow trout (Oncorhynchus mykiss). J World Aquaculture Soc 2021, 52, 105. <https://doi.org/10.1111/jwas.12749>
• Taysı Mehmet Reşit, Kırıcı Muammer, Kırıcı Mahinur, Ulusal Hasan, Söğüt Bünyamin, Taysı Seyithan: The role of nitrosative and oxidative stress in rainbow trout (Oncorhynchus mykiss) liver tissue applied mercury chloride (HgCl2). EgeJFAS 2021, 38, 269. <https://doi.org/10.12714/egejfas.38.3.02>
• Bojarski Bartosz, Witeska Małgorzata: Blood biomarkers of herbicide, insecticide, and fungicide toxicity to fish—a review. Environ Sci Pollut Res 2020, 27, 19236. <https://doi.org/10.1007/s11356-020-08248-8>
• Bhattacharjee Parmita, Borah Anupom, Das Suchismita: Quercetin-induced amelioration of deltamethrin stress in freshwater teleost, Channa punctata: Multiple biomarker analysis. Comparative Biochemistry and Physiology Part C: Toxicology & Pharmacology 2020, 227, 108626. <https://doi.org/10.1016/j.cbpc.2019.108626>
• Dawood Mahmoud A.O., Abdel‐Tawwab Mohsen, Abdel‐Latif Hany M.R.: Lycopene reduces the impacts of aquatic environmental pollutants and physical stressors in fish. Reviews in Aquaculture 2020, 12, 2511. <https://doi.org/10.1111/raq.12455>
• Petrovici Adriana, Strungaru Stefan-Adrian, Nicoara Mircea, Robea Madalina Andreea, Solcan Carmen, Faggio Caterina: Toxicity of Deltamethrin to Zebrafish Gonads Revealed by Cellular Biomarkers. JMSE 2020, 8, 73. <https://doi.org/10.3390/jmse8020073>
• Lutnicka Hanna, Bojarski Bartosz, Witeska Małgorzata, Tombarkiewicz Barbara, Formicki Grzegorz: Exposure to herbicide linuron results in alterations in hematological profile and stress biomarkers of common carp (Cyprinus carpio). Ecotoxicology 2019, 28, 69. <https://doi.org/10.1007/s10646-018-2000-y>
• Strungaru Stefan-Adrian, Plavan Gabriel, Ciobica Alin, Nicoara Mircea, Robea Madalina Andreea, Solcan Carmen, Petrovici Adriana: Toxicity and chronic effects of deltamethrin exposure on zebrafish (Danio rerio) as a reference model for freshwater fish community. Ecotoxicology and Environmental Safety 2019, 171, 854. <https://doi.org/10.1016/j.ecoenv.2019.01.057>
• Stara Alzbeta, Bellinvia Roberto, Velisek Josef, Strouhova Alzbeta, Kouba Antonin, Faggio Caterina: Acute exposure of common yabby (Cherax destructor) to the neonicotinoid pesticide. Science of The Total Environment 2019, 665, 718. <https://doi.org/10.1016/j.scitotenv.2019.02.202>
• Prodhan Mohammad Dalower Hossain, Papadakis Emmanouil‐Nikolaos, Papadopoulou‐Mourkidou Euphemia: Variability of pesticide residues in eggplant units collected from a field trial and marketplaces in Greece. J Sci Food Agric 2018, 98, 2277. <https://doi.org/10.1002/jsfa.8716>
• Özok Necati, OĞuz Ahmet R., Kankaya Ertuğrul, Yeltekin Aslı Çilingir: Hemato-biochemical responses of Van fish (Alburnus tarichi Guldenstadt, 1814) during sublethal exposure to cypermethrin. Human and Ecological Risk Assessment: An International Journal 2018, 24, 2240. <https://doi.org/10.1080/10807039.2018.1443389>
• Verep Bülent, Mutlu Tanju, Yüksek Turan, Gürdal Aydın Aytaç: Yumuşak ve Sert Su Koşullarinda Karadeniz alabaliği (Salmo coruhensis) Dokularinda Civa (Hg) Birikiminin Belirlenmesi. Journal of Anatolian Environmental and Animal Sciences 2018, 3, 19. <https://doi.org/10.35229/jaes.387681>
• Esmaeili Noah, Kenari Abdolmohamad Abedian, Rombenso Artur: Immunohematological status under acute ammonia stress of juvenile rainbow trout (Oncorhynchus mykiss Walbaum, 1792) fed garlic (Allium sativum) powder-supplemented meat and bone meal-based feeds. Comp Clin Pathol 2017, 26, 853. <https://doi.org/10.1007/s00580-017-2457-8>
• Forouhar Vajargah Mohammad, Hedayati Aliakbar: Acute Toxicity of Butachlor to Rutilus rutilus caspicus and Sander lucioperca in Vivo Condition. Transylvanian Review of Systematical and Ecological Research 2017, 19, 85. <https://doi.org/10.1515/trser-2017-0023>
• JA Vega: Putative Mechanoproteins in Vertebrate Cutaneous Mechanoreceptors-Are they at the Basis of the Mechanotransduction?. MOJAP 2017, 4. <https://doi.org/10.15406/mojap.2017.04.00126>
• Shahbazi Naserabad Saeid, Mirvaghefi Alireza, Rashidiyan Ghasem, Rostamian Narges, Ghafari Farsani Hamed: Investigating the Agent of Temperature into Acute Toxicity (LC50 96h) of Edifenphos in Rutilus Frisii Kutum (Kamensky, 1901). IJT 2017, 11, 39. <https://doi.org/10.29252/arakmu.11.2.39>
• Shirani Mahboube, Haddadi Hedayat, Rezaee Mohammad, Semnani Abolfazl, Habibollahi Saeed: Solid-Phase Extraction Combined with Dispersive Liquid–Liquid Microextraction for the Simultaneous Determination of Deltamethrin and Permethrin in Honey by Gas Chromatography–Mass Spectrometry. Food Anal. Methods 2016, 9, 2613. <https://doi.org/10.1007/s12161-016-0455-0>
• Ren Qing, Zhang Tingting, Li Shangge, Ren Zongming, Yang Meiyi, Pan Hongwei, Xu Shiguo, Qi Li, Chon Tae-Soo: Integrative Characterization of Toxic Response of Zebra Fish (Danio rerio) to Deltamethrin Based on AChE Activity and Behavior Strength. BioMed Research International 2016, 2016, 1. <https://doi.org/10.1155/2016/7309184>
• VEREP Bülent, BEŞLİ Evrim Sibel, AKIN Şenol: Effect of Water Salinity on the Acute Toxicity of Mercuric Chloride on Rainbow Trout (Oncorhynchus mykiss, Walbaum 1792). El-Cezeri Fen ve Mühendislik Dergisi 2016, 3. <https://doi.org/10.31202/ecjse.264185>
• Prusty A. K., Meena D. K., Mohapatra S., Panikkar P., Das P., Gupta S. K., Behera B. K.: Synthetic pyrethroids (Type II) and freshwater fish culture: Perils and mitigations. Int Aquat Res 2015, 7, 163. <https://doi.org/10.1007/s40071-015-0106-x>
• Suvetha Lenin, Saravanan Manoharan, Hur Jang-Hyun, Ramesh Mathan, Krishnapriya Kalliappan: Acute and sublethal intoxication of deltamethrin in an Indian major carp, Labeo rohita: Hormonal and enzymological responses. The Journal of Basic & Applied Zoology 2015, 72, 58. <https://doi.org/10.1016/j.jobaz.2015.04.005>
• Suvetha Lenin, Saravanan Manoharan, Hur Jang-Hyun, Ramesh Mathan, Bindu F. Clara: Responses of the Indian major carp Labeo rohita to deltamethrin at acute and sublethal concentrations. Toxicological & Environmental Chemistry 2015, 97, 186. <https://doi.org/10.1080/02772248.2015.1031666>
• Saeid Shahbazi Naserabad, Alireza Mirvaghefi, Mohammad Hasan Gerami, Hamed Ghafari Farsani: Acute toxicity and behavioral changes of Caspian kutum (Rutilus frisii Kutum Kamensky, 1991) and Caspian roach (Rutilus rutilus caspicus Jakowlew, 1870) exposed to the fungicide hinosan. Afr. J. Biotechnol. 2015, 14, 1737. <https://doi.org/10.5897/AJB2015.14494>
• Hassaan Mohamed S., Goda Ashraf M. A.-S., Mahmoud Soaad A., Tayel Safaa I.: Protective effect of dietary vitamin E against fungicide copperoxychloride stress on Nile tilapia, Oreochromis niloticus (L.) fingerlings. Int Aquat Res 2014, 6. <https://doi.org/10.1007/s40071-014-0058-6>
• Marques Ana, Custódio Marco, Guilherme Sofia, Gaivão Isabel, Santos Maria Ana, Pacheco Mário: Assessment of chromosomal damage induced by a deltamethrin-based insecticide in fish (Anguilla anguilla L.) – A follow-up study upon exposure and post-exposure periods. Pesticide Biochemistry and Physiology 2014, 113, 40. <https://doi.org/10.1016/j.pestbp.2014.06.003>
• Fawole Olatunde Olubanjo, Yekeen Taofeek Akangbe: Alterations in haematological and biochemical parameters of African catfishClarias gariepinusexposed to sublethal concentrations of deltamethrin. Zoology and Ecology 2014, 24, 355. <https://doi.org/10.1080/21658005.2014.980551>
• Hassaan Mohamed S, Goda Ashraf M, Mahmoud Soaad A, Tayel Safaa I: Protective effect of dietary vitamin E against fungicide copperoxychloride stress on Nile tilapia, Oreochromis niloticus (L.), fingerlings. Int Aquat Res 2014, 6, 1. <https://doi.org/10.1186/2008-6970-6-1>
• Kubrak Olga I., Atamaniuk Tetiana M., Storey Kenneth B., Lushchak Volodymyr I.: Goldfish can recover after short-term exposure to 2,4-dichlorophenoxyacetate: Use of blood parameters as vital biomarkers. Comparative Biochemistry and Physiology Part C: Toxicology & Pharmacology 2013, 157, 259. <https://doi.org/10.1016/j.cbpc.2012.12.005>
• Abdul-Hamid Manal, Salah Marwa: Lycopene reduces deltamethrin effects induced thyroid toxicity and DNA damage in albino rats. The Journal of Basic & Applied Zoology 2013, 66, 155. <https://doi.org/10.1016/j.jobaz.2013.08.001>
• Sarma Kamal, Pal A. K., Sahu N. P., Dalvi R. S., Chatterjee Nirupama, Mukherjee S. C., Baruah Kartik: Acute and chronic effects of endosulfan on the haemato-immunological and histopathological responses of a threatened freshwater fish, spotted murrel, Channa punctatus. Fish Physiol Biochem 2012, 38, 499. <https://doi.org/10.1007/s10695-011-9530-z>
• Amin Kamal A, Hashem Khalid S: Deltamethrin-induced oxidative stress and biochemical changes in tissues and blood of catfish (Clarias gariepinus): antioxidant defense and role of alpha-tocopherol. BMC Vet Res 2012, 8, 45. <https://doi.org/10.1186/1746-6148-8-45>
• Ait Ayad Mohamed, Ait Fdil Mohamed, Mouabad Abdelfattah: Effects of Cypermethrin (Pyrethroid Insecticide) on the Valve Activity Behavior, Byssal Thread Formation, and Survival in Air of the Marine Mussel Mytilus galloprovincialis. Arch Environ Contam Toxicol 2011, 60, 462. <https://doi.org/10.1007/s00244-010-9549-7>
• Li Zhi-Hua, Zlabek Vladimir, Velisek Josef, Grabic Roman, Machova Jana, Kolarova Jitka, Li Ping, Randak Tomas: Acute toxicity of carbamazepine to juvenile rainbow trout (Oncorhynchus mykiss): Effects on antioxidant responses, hematological parameters and hepatic EROD. Ecotoxicology and Environmental Safety 2011, 74, 319. <https://doi.org/10.1016/j.ecoenv.2010.09.008>
• Yonar M. Enis, Sakin Fatih: Ameliorative effect of lycopene on antioxidant status in Cyprinus carpio during pyrethroid deltamethrin exposure. Pesticide Biochemistry and Physiology 2011, 99, 226. <https://doi.org/10.1016/j.pestbp.2010.12.008>
• Vani T., Saharan N., Mukherjee S.C., Ranjan Ritesh, Kumar Rajesh, Brahmchari R.K.: Deltamethrin induced alterations of hematological and biochemical parameters in fingerlings of Catla catla (Ham.) and their amelioration by dietary supplement of vitamin C. Pesticide Biochemistry and Physiology 2011, 101, 16. <https://doi.org/10.1016/j.pestbp.2011.05.007>
• Siwicki Andrzej K., Terech‐Majewska Elzbieta, Grudniewska Joanna, Malaczewska Joanna, Kazun Krzysztof, Lepa Agnieszka: Influence of deltamethrin on nonspecific cellular and humoral defense mechanisms in rainbow trout (Oncorhynchus mykiss). Enviro Toxic and Chemistry 2010, 29, 489. <https://doi.org/10.1002/etc.75>
• Singh Narendra Nath, Srivastava Anil Kumar: Haematological parameters as bioindicators of insecticide exposure in teleosts. Ecotoxicology 2010, 19, 838. <https://doi.org/10.1007/s10646-010-0465-4>
• Chukwu L.O., Lawal O.S.: Joint Action Response and Haematological Profile of Macrobrachium vollenhoevenii (Herklots, 1857) Exposed to Binary Mixtures of Spent Lubricant Oil and Dispersant. Research J. of Environmental Sciences 2010, 4, 115. <https://doi.org/10.3923/rjes.2010.115.126>
• Velisek J., Svobodova Z., Machova J.: Effects of bifenthrin on some haematological, biochemical and histopathological parameters of common carp (Cyprinus carpio L.). Fish Physiol Biochem 2009, 35, 583. <https://doi.org/10.1007/s10695-008-9258-6>
• Velisek J., Svobodova Z., Piackova V.: Effects of acute exposure to bifenthrin on some haematological, biochemical and histopathological parameters of rainbow trout (Oncorhynchus mykiss). Vet. Med. 2009, 54, 131. <https://doi.org/10.17221/15/2009-VETMED>
• Köprücü K., Seker E.: Acute Toxicity of Deltamethrin for Freshwater Mussel, Unio elongatulus eucirrus Bourguignat. Bull Environ Contam Toxicol 2008, 80, 1. <https://doi.org/10.1007/s00128-007-9254-z>
• El‐Sayed Yasser Said, Saad Talaat Talaat: Subacute Intoxication of a Deltamethrin‐Based Preparation (Butox® 5% EC) in Monosex Nile Tilapia, Oreochromis niloticus L. Basic Clin Pharma Tox 2008, 102, 293. <https://doi.org/10.1111/j.1742-7843.2007.00157.x>
• Borges Adriana, Scotti Luciana V., Siqueira Daniele R., Zanini Rebeca, Amaral Fernanda do, Jurinitz Daiane F., Wassermann Guillermo F.: Changes in hematological and serum biochemical values in jundiá Rhamdia quelen due to sub-lethal toxicity of cypermethrin. Chemosphere 2007, 69, 920. <https://doi.org/10.1016/j.chemosphere.2007.05.068>
• Velíšek J., Jurčíková J., Dobšíková R., Svobodová Z., Piačková V., Máchová J., Novotný L.: Effects of deltamethrin on rainbow trout (Oncorhynchus mykiss). Environmental Toxicology and Pharmacology 2007, 23, 297. <https://doi.org/10.1016/j.etap.2006.11.006>
• El-Sayed Y.S., Saad T.T., El-Bahr S.M.: Acute intoxication of deltamethrin in monosex Nile tilapia, Oreochromis niloticus with special reference to the clinical, biochemical and haematological effects. Environmental Toxicology and Pharmacology 2007, 24, 212. <https://doi.org/10.1016/j.etap.2007.05.006>
• Verep Bulent, Sibel Besl E., Altinok Ilhan, Mutlu Cengiz: Assessment of Mercuric Chloride Toxicity on Rainbow Trouts(Oncorhynchus mykiss) and Chubs (Alburnoides bipunctatus). Pakistan J. of Biological Sciences 2007, 10, 1098. <https://doi.org/10.3923/pjbs.2007.1098.1102>
• Cengiz Elif Ipek: Gill and kidney histopathology in the freshwater fish Cyprinus carpio after acute exposure to deltamethrin. Environmental Toxicology and Pharmacology 2006, 22, 200. <https://doi.org/10.1016/j.etap.2006.03.006>
• Ural M. Şener, Sağlam Naim: A study on the acute toxicity of pyrethroid deltamethrin on the fry rainbow trout (Oncorhynchus mykiss Walbaum, 1792). Pesticide Biochemistry and Physiology 2005, 83, 124. <https://doi.org/10.1016/j.pestbp.2005.04.004>
• de Pedro Nuria, Guijarro Ana Isabel, Lopez-Patino Marcos Antonio, Martinez-Alvarez Rosa, Delgado Maria Jesus: Daily and seasonal variations in haematological and blood biochemical parameters in the tench, Tinca tinca Linnaeus, 1758. Aquaculture Res 2005, 36, 1185. <https://doi.org/10.1111/j.1365-2109.2005.01338.x>
• Köprücü Kenan, Aydın Rahmi: The toxic effects of pyrethroid deltamethrin on the common carp (Cyprinus carpio L.) embryos and larvae. Pesticide Biochemistry and Physiology 2004, 80, 47. <https://doi.org/10.1016/j.pestbp.2004.05.004>
• Bouboulis D., Athanassopoulou F., Tyrpenou A.: Experimental treatments with diflubenzuron and deltamethrin of sea bass, Dicentrarchus labrax L., infected with the isopod, Ceratothoa oestroides. J Appl Ichthyol 2004, 20, 314. <https://doi.org/10.1111/j.1439-0426.2004.00579.x>