Refine your search
Collections
Co-Authors
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z All
Singla, Saloni
- Alterations in Hematological Profile of Experimentally Induced Subchronic Thiacloprid Toxicosis in Gallus domesticus
Abstract Views :185 |
PDF Views:1
Authors
Affiliations
1 Department of Veterinary Pharmacology and Toxicology, College of Veterinary Science, GADVASU, Ludhiana, Punjab, IN
1 Department of Veterinary Pharmacology and Toxicology, College of Veterinary Science, GADVASU, Ludhiana, Punjab, IN
Source
Toxicology International (Formerly Indian Journal of Toxicology), Vol 22, No 1 (2015), Pagination: 147-151Abstract
Objectives: Thiacloprid, a novel neonicotinoid insecticide is chiefly used as a crop protectant therefore it is likely to cause indirect exposure to poultry through contaminated feed and water because this species is occasionally supplied with feed that is, declared unfit for human consumption. The current study was performed to explore the nonlethal toxic effects of thiacloprid in Gallus domesticus on hematological parameters. Materials and Methods: Fifty‑two birds were randomly divided into nine groups. Groups I to IV of four birds each were kept as healthy control. The Groups V, VI, VII, VIII, IX, and X contained six birds each and were administered thiacloprid at 1 mg/kg/day for 15, 30, 45, 60, 75, and 90 days, respectively. Results: Thiacloprid caused variable changes in the hematological parameters. There was a significant decline in the packed cell volume (PCV), hemoglobin (Hb) concentration, and total erythrocyte count (TEC). The PCV declined to the extent of 23.33 ± 0.76% on day 90 from the 0 day value of 29.75 ± 1.26% of experiment. The Hb concentration decreased from 9.93 ± 0.57 g/dl (0 day) to 7.52 ± 0.62 g/dl (90 days). The TEC declined from the 0 day value of 2.41 ± 0.08 × 106/mm3 to 90 days value of 2.08 ± 0.05 × 106/mm3. The total leukocyte count on 0 day was 12.50 ± 0.76 × 103/mm3 and it showed a significant increase from day 45 (17.80 ± 2.67 × 103/mm3) to day 90 (21.33 ± 1.48 × 103/mm3) of thiacloprid treatment. There was a significant rise in value of erythrocyte sedimentation rate to 19.25 ± 1.22 mm/24 h on day 90 of treatment from the 14.42 ± 1.09 mm/24 h on 0 day. The long‑term oral administration of thiacloprid produced no significant alterations in the values of erythrocytic indices. Conclusions: The repeated oral toxicity on thiacloprid in present investigation suggested that it has an adverse effect on health of birds and is moderately risk insecticide in G. domesticus.Keywords
Gallus domesticus, Insecticide, Neonicotinoid, Thiacloprid, Toxicity.- Evaluation of Aldrin-Induced Oxidative Stress and Apoptosis in J774 Macrophages
Abstract Views :490 |
PDF Views:0
Authors
Affiliations
1 Department of Veterinary Pharmacology and Toxicology, College of Veterinary Science, Guru Angad Dev Veterinary and Animal Sciences University, Ludhiana-141004, IN
1 Department of Veterinary Pharmacology and Toxicology, College of Veterinary Science, Guru Angad Dev Veterinary and Animal Sciences University, Ludhiana-141004, IN
Source
Toxicology International (Formerly Indian Journal of Toxicology), Vol 22, No 2 (2015), Pagination: 88-96Abstract
The present study was carried out to evaluate the aldrin-induced oxidative stress and apoptosis in murine macrophage (J774A.1) cells. Acute exposure of aldrin for 2 hrs was given to the J774A.1 cells cultured in DMEM with 10% FBS at 37oC and 5% CO2 in air with 95% relative humidity under in vitro system. Lethal concentration-50 (LC50) was calculated after exposure period as 7.24 μg/ml. Further, cells were exposed with three different concentration of aldrin (1.81, 3.65 and 7.24 μg/ml) and 0.1% DMSO was used as negative control. The antioxidant enzymes and non-enzymes were determined along with G6pDH, LDH and ALP enzymes in J774A.1 cells. Cells were monitored for cell morphology and apoptosis. Exposure of aldrin to J774A.1cells resulted in increase in lipid peroxidation and decrease in antioxidant enzyme/ nonenzymes system. Further it caused decrease in G6PDH enzymes activity and excess leakage of LDH and ALP enzymes. The aldrin-treated cells showed higher number of apoptotic cells with alteration in cell morphology indicating apoptotic and necrotic changes. These effects were noticed in dose dependant manner. In conclusion, the result of in vitro study suggests that the aldrin can induced the process of apoptosis and cell death through the generation of ROS and thereof oxidative insult in J774A.1 cells.Keywords
Aldrin, Apoptosis, Antioxidant Enzymes, J774A.1 Cells, Oxidative Stress.References
- Chaiyarat R, Sookjam C, Eiam-Ampai K, Damrongphol P. Organochlorine pesticide levels in the food web in rice paddies of Bueng Boraphet wetland, Thailand. Environ Monit Assess. 2015; 187(5):4469.
- Badr A, Elkington TT. Antimitotic and chromo, toxic effects of isoproturon in A. cepa and H. vulgare. Environ Exp Bot. 1982; 22:265–70.
- Gui D, Yu R, He X, Tu Q, Wu Y. Tissue distribution and fate of persistent organic pollutants in Indo-Pacific humpback dolphins from the Pearl River Estuary, China. Mar Pollut Bull. 2014; 86(1-2):266–73.
- Iyer P. Developmental and reproductive toxicology of pesticides. In: Krieger R editor. Handbook of Pesticide Toxicology, Academic Press, San Diego, 2010; 1:375–420.
- Parron T, Requena M, Hernández AF, Alarcon R. Association between environmental exposure to pesticides and neurodegenerative diseases. Toxicol Appl Pharmacol 2011; 256: 379–85.
- Hernandez AF, Lacasana M, Gil F, Rodriguez-Barranco M, Pla A, Lopez-Guarnido O. Evaluation of pesticide-induced oxidative stress from a gene–environment interaction perspective. Toxicol. 2013; 307:95–102.
- Lonare M, Kumar M, Raut S, Badgujar P, Doltade S, Telang A. Evaluation of imidacloprid-induced neurotoxicity in male rats: A protective effect of curcumin. Neurochem Inter. 2014; 78:122–9
- Bedia C, Dalmau N, Jaumot J, Tauler R. Phenotypic malignant changes and untargeted lipidomic analysis of longterm exposed prostate cancer cells to endocrine disruptors. Environ Res. 2015; 140:18–31.
- Abdollahi M, Ranjbar A, Shadnia S, Nikfar S, Rezaiee A. Pesticides and oxidative stress: a review. Med Sci Monit. 2004; 10:RA141–7.
- Raina R, Verma PK, Pankaj NK, Prawez S. Induction of oxidative stress and lipid peroxidation in rats chronically exposed to cypermethrin through dermal application. J Vet Sci. 2009; 10:257–9.
- Gao LY, Abu Kwaik Y. Hijacking of apoptotic pathways by bacterial athogens. Microb Infect. 2000; 2:1705–19.
- Sharma H, Zhang P, Barber DS, Liu B. Organochlorine pesticides dieldrin and lindane induce cooperative toxicity in dopaminergic neurons: Role of oxidative stress NeuroToxicol. 2010; 31(2):215–22
- Tobiszewski M, Orlowski A. Multicriteria decision analysis in ranking of analytical procedures for aldrin determination in water. J Chromatogr A. 2015; 1387:116–22.
- Wrobel MH, Grzeszczyk M, Mlynarczuk J, Kotwica J. The adverse effects of aldrin and dieldrin on both myometrial contractions and the secretory functions of bovine ovaries and uterus in vitro. Toxicol Appl Pharmacol. 2015; 85(1):23–31.
- Koner BC, Banerjee BD, Ray A. Organochlorine pesticide-induced oxidative stress and immune suppression in rats. Indian J Exp Biol. 1998; 36(4):395–8.
- Naqvi S, Samim M, Abdin MZ, Ahmed FJ, Maitra AN, Prashant CK, Dinda AK. Concentration-dependent toxicity of iron oxide nanoparticles mediated by increased oxidative stress; Inter J Nanomed. 2010; 5:983–9.
- Mahajan S, Prashant CK, Koul V, Choudhary V, Dinda AK. Receptor specific macrophage targeting by mannose-conjugated gelatin nanoparticles: An in-vitro and in-vivo study. Curr Nanosci. 2010; 6(4):413–21.
- Borenfreund E, Puerner J. Toxicity determined in vitro by morphological alterations and neutral red absorption. Toxicol Lett. 1985; 24:119–24.
- Spector DL, Goldman RD, Leinwand LA. Morphological assessment of cell death. In: Spector DL, Goldman RD, Leinwand LA editors. Cells, a laboratory manual, in culture and biochemical analysis of cells. NY: Cold Spring Harbor Laboratory Press; 1997; 2:15.3–15.10.
- Bergmeyer H. Methods of enzymatic analysis. New York: Academic Press. 1974.
- Aebi H. Catalase in vitro. Methods Enzymol. 1984 ; 105:121–6.
- Paglia DE, Valentine WN. Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase. J Lab Clin Med. 1967; 70:158–69.
- Madesh J, Balasubramanian KA. Microtitre plate assay for superoxide dismutase using MTT reduction by superoxide. Indian J Biochem Biophys 1998; 35: 184–8.
- Habig WH, Pabst MJ, Jakoby WB. Glutathione S-transferases. The first enzymatic step in mercapturic acid formation. J Biol Chem. 1974; 249:7130–9.
- Sedlak J, Lindsay RH. Estimation of total, protein-bound, and nonprotein sulfhydryl groups in tissue with Ellman’s reagent. Anal Biochem. 1968; 25:192–205.
- Ohkawa H, Ohishi N, Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem. 1979; 95:351–8.
- Lowry, OH, Rosebrough NJ, Farr AL, Randall RJ. Protein measurement with Folin- Phenol reagent. J Biol Chem. 1951; 193:265–75.
- Bachowski S, Xu Y, Stevenson DE, Walborg EF Jr, Klaunig JE. Role of oxidative stress in the selective toxicity of dieldrin in the mouse liver. Toxicol Appl Pharmacol. 1998; 150(2):301–9.
- Kitazawa M, Anantharam V, Kanthasamy AG. Dieldrin-induced oxidative stress and neurochemical changes contribute to apoptotic cell death in dopaminergic cells. Free Radic Biol Med. 2001; 31:1473–85.
- Hincal F, Gurbay A, Giray, B. Induction of lipid peroxidation and alteration of glutathione redox status by endosulfan. Biol Trace Elem Res. 1995; 47(1-3):321–6.
- Dorval J, Leblond VS, Hontela A. Oxidative stress and loss of cortisol secretion in adrenocortical cells of rainbow trout (Oncorhynchus mykiss) exposed in vitro to endosulfan, an organochlorine pesticide. Aquat Toxicol. 2002; 63(3):229–41.
- Pandey S, Ahmad I, Parvez S, Bin-Hafeez B, Haque R, Raisuddin S. Effect of endosulfan on antioxidants of freshwater fish Channa punctatus Bloch: 1. Protection against lipid peroxidation in liver by copper preexposure. Arch Environ Contam Toxicol. 2001; 41(3):345–52.
- Lonare M, Kumar M, Raut S, More A, Doltade S, Badgujar P, Telang A. Evaluation of ameliorative effect of curcumin on imidacloprid-induced male reproductive toxicity in wistar rats. Environ Toxicol. 2015. Doi: 10.1002/tox.22132.
- Lopez O, Hernandez AF, Rodrigo L et al. Changes in antioxidant enzymes in humans with long-term exposure to pesticides. Toxicol Lett. 2007; 171:146–53.
- Kannan K, Jain SK. Oxidative stress and apoptosis. Pathophysiology. 2000; 7(3):153–63.
- Simon HU, Haj-Yehia A, Levi-Schaffer F. Role of reactive oxygen species (ROS) in apoptosis induction. Apoptosis. 2000; 5:415–8.
- Junn E, Mouradian MM. Apoptotic signaling in dopamineinduced cell death: the role of oxidative stress, p38 mitogen-activated protein kinase, cytochrome c and caspases. J Neurochem. 2001; 78:374–83.
- Akbarsha MA, Sivasamy P. Apoptosis in male germinal line cells of rat in vivo: caused by phosphamidon. Cytobios. 1997; 91:33–44.
- Tian WN, Braunstein LD, Pang J, Stuhlmeier KM, Xi QC, Tian X, Stanton RC. Importance of glucose-6-phosphate dehydrogenase activity for cell growth. J Biol Chem. 1998; 273:10609–17.
- Cho SW, Joshi JG. Inactivation of glucose-6-phosphate 11. dehydrogenase isozymes from human and pig brain by aluminum. J Neurochem. 1989; 53:616–21.
- Manna S, Bhattacharyya D, Mandal TK, Das S. Sub-chronic toxicity study of alfa-cypermethrin in rats. Iranian J Pharmacol Therapeutics. 2006; 5:163–6.
- Kale M, Rathore N, John S, Bhatnagar D. Lipid peroxidative damage on pyrethroid exposure and alterations in antioxidant status in rat erythrocytes: A possible involvement of reactive oxygen species. Toxicol Lett. 1999; 105(3):197–205.
- Ranjbar A, Pasalar P, Sedighi A, Abdollahi M. Induction of oxidative stress in paraquat formulating workers. Toxicol Lett. 2002; 131:191–4.
- Ronald WT, Malcolm RS, John WL. Mechanism of action and fate of the fungicide chlorothalonil (2,4,5,6-tetrachloroisophthalonitrile) in biological systems: I. Reactions with cells and subcellular components of Saccharomyces pastorianus. Pest Biochem Physiol. 2004; 3(2):160–7.
- Kostaropoulos I, Papadopoulos AI, Metaxakis A et al. The role of glutathione S-transferases in the detoxification of some organophosphorus insecticides in larvae and pupae of the yellow mealworm, Tenebrio molitor (Coleoptera: Tenebrionidae). Pest Manag Sci. 2001; 57:501–8.
- Vina J. Glutathione: Metabolism and Physiological Functions. CRC Press, Boston. 1990; 222–8.
- Perez-Maldonado IN, Herrera C, Batres LE, Gonzalez-Amaroa R, Diaz-Barriga F, Yanez L. DDT-induced oxidative damage in human blood mononuclear cells. Environ Res. 2005; 98:177–84.
- Kannan K, Holcombe RF, Jain SK, Alvarez-Hernandez X, Chervenak R, Wolf RE, Glass J. Evidence for the induction of apoptosis by endosulfan in a human T-cell leukemic line. Mol Cell Biochem. 2000; 205:53–66.
- Slim R, Toborek M, Robertson LW, Lehmler HJ, Henning B. Cellular glutathione status modulates polychlorinated biphenyl-induced stress response and apoptosis in vascular endothelial cells. Toxicol Appl Pharmacol. 2000; 166:36–42.
- Kitizawa M, Anantharam V, Kanthasamy AG. Dieldrininducedoxidative stress and neurochemical changes contribute to apoptotic cell death in dopaminergic cells. Free Radical Biol. Med. 2001; 31:1473–85.
- Immune Response to Sub Acute Toxicity of Thiacloprid Insecticide in Gallus domesticus
Abstract Views :296 |
PDF Views:0
Authors
Saloni Singla
1,
V. K. Dumka
1
Affiliations
1 Department of Veterinary Pharmacology and Toxicology, Guru Angad Dev Veterinary and Animal Science University, Ludhiana, IN
1 Department of Veterinary Pharmacology and Toxicology, Guru Angad Dev Veterinary and Animal Science University, Ludhiana, IN
Source
Toxicology International (Formerly Indian Journal of Toxicology), Vol 24, No 3 (2017), Pagination: 249-253Abstract
Thiacloprid is fairly a new chemical, but it has established itself as key component in insecticides because of its selectivity and low toxicity. It is effective on contact and via stomach action and bind agonistically to the nicotinic acetylcholine receptors in the CNS of insects, affecting synaptic transmission and leading to disruption of the nervous system. The immune system is a host defense system comprising many biological structures and processes within an organism that protects against disease. It can be the target of many chemicals, with potentially severe adverse effects on the host’s health. The health implications of these immune dysfunctions are increased risk of infectious diseases; development of neoplasia; autoimmune disorders and allergies. Estimation of total immunoglobulins and enumeration of B and T lymphocytes in blood after repeated oral administration of thiacloprid at the dose rate of 10 mg/kg/day revealed no significant alterations in Gallus domesticus. The observed findings in the present study indicated that repeated thiacloprid exposure in poultry birds did not adversely affect the immune status of Gallus domesticus and thus is immunologically safer insecticide.Keywords
Toxicity, Gallus domesticus, Thiacloprid, Insecticide, Immune System.References
- Uok K. Neonicotinoid Insecticides. Microbiology and Molecular Genetics. 2006; 2: 46-52.
- National Registration Authority for Agricultural and Veterinary Chemicals. ISSN 1443-1335, Evaluation of the new active Thiacloprid in the new product Calypos 480 SC Insecticide. 2001.
- Tomizawa M and Casida JE. Neonicotinoid insecticide toxicology: mechanisms of selective action. Annu. Rev. Pharmacol. Toxicol. 2005; 45: 247-268.
- Felsot AS and Ruppert JR. Imidacloprid Residues in Willapa Bay (Washington State) Water and Sediment Following Application for Control of Burrowing Shrimp J. Agric. Food Chem. 2002; 50(15): 4417-23.
- Ware GW and Whitacre DM. An Introduction to Insecticides fourth ed., MeisterPro Information Resources, A division of Meister Media Worldwide, Willoughby, Ohio, USA. 2004.
- Anatra-M. and Durkin P. Imidacloprid. Human health assessment and ecological risk assessment Final report. Syracuse Environmental Research Associates, Inc., New York, SERA TR 2005; 5- 43-24-03.
- Karabaym NUand Oguz, MG. Cytogenetic and genotoxic effects of the insecticides, imidacloprid and methamidophos Genet. Mol. Res. 2005; 4: 653-62.
- Demsia G, Vlastos D, Goumenou M, Mathopoulos DP. Assesment of the genotoxicity of imidacloprid and metalaxyl in cultured human lymphocytes and rat bone marrow Mutat. Res. 2007; 634: 32-39.
- Abou-Donia MB, Goldstein LB, Bulman S, Tu T, Khan WA, Dechkovskaia.AM and Abdel-Rahman AA. Imidacloprid induces neurobehavioral deficits an increase expression of glial fibrillary acidic protein in the motor cortex and hippocampus in offspring rats following in utero exposure. J.Toxicol. Environ. Health. 2008;. 71: 119–130.
- Holsapple MP. Developmental immunotoxicity testing: a review.Toxicolology. 2003; 185: 193-203.
- Meguire TC, Pfeiffer NE, Weikel JM, Bartsch, RC. Failure of cloistral immunoglobulin transfer in calves dying from infectious disease. JAVMA 1976; 169: 713-71.
- Mcewan AD, Fisher EW, Selman IE Penhale WJ. A turbidity test for the estimation of immunoglobulin levels in neonatal calf serum. Clin. Chim. Acta, 1970; 27: 155-63.
- Pfeiffer NE, Mcguire TC, Bendel RB. Quantitation of bovine immunoglobulins: comparison of single radial immunodiffusion, zinc sulfate turbidity, serum electrophoresis, and refractometer methods. Am J Vet Res, 1977; 38:693-698.
- Boyum A. Separation of leukocytes from blood and bone marrow with special reference to factors which influence and modify redimentation properties of hematopoietic cells. Scandinavian Journal of Clinical and Laboratory Investigation 1968; 21: 1.
- Julius MH, Simpson E, Herzenberg LA. A rapid method for the isolation of functional thymus-derived murine lymphocytes European Journal of Immunology. 1973; 3: 645-49.
- Street JC. and Sharma RP. Alteration of induced cellular and humoral responses by pesticide and chemicals of environmental concern: Quantitative studies of immunosuppression by DDT, Aroclor 1254, carbaryl, carbofuran and Methylparathion. Toxicology and Applied Pharmacology 1995; 32: 58.
- Goyal S and Sandhu HS. Immunological effects of sub chronic exposure to Thiacloprid insecticide in Gallus domesticus. The Veterinary Practitioner 2012; 13(2) 226-28.
- Saha S. and Banerjee D. Effect of sub-chronic lindane exposure on humoral and cell-mediated immune responses in albino rats. Bulletin of Environmental Contamination and Toxicology.1993; 51: 795.
- Khurana R and Chauhan RS. Immunopathological effects of lindane on humoral immune response in sheep. Journal of Immunology and Immunopathology1999; 1: 67-70.
- Kumar S. Immunotoxic effects of endosulfan and cypermethrin in chickens. M.V.Sc. Thesis, CCS Haryana Agricultural University, Hisar. 1994.
- Burns LA, Meade BJ and Murson AE. Toxic responses of the immune system. In: Klaassen C D.(ed) Casarett and Doull’s Toxicology: The Basic Science of Poisons. 5th edn. 1996; p 355-402. McGraw Hill, New York.
- Ringer RK. PBB fed to immature chickens: Its effects on organ weights and function and on the cardiovascular system. Environmental Health Perspectives. 1978; 23: 247-55.
- Sharma RP. Immunotoxicity. In: Gupta R C (ed) Veterinary Toxicology Basic and Clinical Principles. 2007; p 289-301. Academic Press Inc. San Diego.
- Tamang RK, Gupta G and Chauhan H. In vivo immunosuppression by synthetic pyrethroid (cypermethrin) pesticide in mice and goats. Veterinary Immunology and Immunopathology. 1988; 19: 299-305.
- Blaylock RL. Suppression of cellular immune responses in BALB/c mice following oral exposure to permethrin. Bulletin of Environmental Contamination and Toxicology. 1995; 54: 768-74.
- Casale GP, Cohen SD and DiCapua RA. The effects of organophosphate-induced cholinergic stimulation on the antibody response to sheep erythrocytes in inbred mice. Toxicology and Applied Pharmacology.1983; 68: 198-205.
- Chauhan RS and Tripathi BN. In: Veterinary Immunology Pathology Theory and Practice. International Book Distributing Co. Lucknow. 2002.
- Parham P. The Immune System, Garland Science Publishing, New York. 2005.
- Holtmeier W and Kabelitz D. Gamma delta T cells link innate and adaptive immune responses. Chemistry of Immunology Allergy 1990; 86: 151–83.
- Katsenovich LA, Ruzybakiev, RM and Fedorin LA. T-and B-immunity in patients with pesticide poisoning. Gig. Tr. Prof Zabo. 1981; 4: 17.
- Safety Assessment of Marbofloxacin Following Repeated Intramuscular Administration in Goats
Abstract Views :278 |
PDF Views:0
Authors
Affiliations
1 Dept. of Vety. Pharmacology and Toxicology, GADVASU, Ludhiana, Punjab, IN
2 Dept. of Vety. Physiology and Biochemistry, COVAS, CSKHPKV, Palampur, H.P, IN
1 Dept. of Vety. Pharmacology and Toxicology, GADVASU, Ludhiana, Punjab, IN
2 Dept. of Vety. Physiology and Biochemistry, COVAS, CSKHPKV, Palampur, H.P, IN
Source
Toxicology International (Formerly Indian Journal of Toxicology), Vol 24, No 3 (2017), Pagination: 288-291Abstract
Marbofloxacin (MB) is an extended spectrum, third generation fluoroquinolone, developed exclusively for the use in veterinary medicine. The safety assessment was done to evaluate the clinical impact of marbofloxacin after repeated intramuscular administration in goats. Safety of drugs is important and changes in serum biochemical and/or hematological markers could provide an early indication of cellular toxicity. The drug was administered at the dose of 2 mg/kg for 5 days by intramuscular route in six healthy, non-lactating Beetal goats, 1.5-2 yrs of age. Haematological (TLC, TEC, Hb, PCV, MCV, MCH and MCHC) and serum biochemical parameters viz. liver function test (LFT) and kidney function test (KFT) (ALT, AST, ALP, GGT, BUN, creatinine, total proteins and albumin) were determined and analyzed to establish the safety profile of marbofloxacin. The hematological and biochemical parameters were found to fluctuate within normal range during treatment period and no significant alterations (p < 0.05) were found in the mean values. The results indicated that intramuscular administration of marbofloxacin in goats at the dose of 2 mg/kg for 5 days seems to be safe.Keywords
Marbofloxacin, Repeated Administration, Safety Assessment, Goats.References
- Schneider M, Thomas V, Boisrame B, Deleforge J. Pharmacokinetics of marbofloxacin in dogs after oral and parenteral administration. Journal of Veterinary Pharmacology and Therapeutics 1996;19:56-61.
- Spreng M, Deleforge J, Thomas V, Boisrame B, Drugeon H. Antibacterial activity of marbofloxacin. A new fluoroquinolone for veterinary use against canine and feline isolates. Journal of Veterinary Pharmacology and Therapeutics 1995;18:284-89.
- Brown SA. Fluoroquinolones in animal health. Journal of Veterinary Pharmacology and Therapeutics 1996;19:1-14.
- Thomas A, Nicolas C, Dizier I, Mainil J, Linden A. Antibiotic susceptibilities of recent isolates of Mycoplasma bovis in Belgium. Veterinary Record 2003;153:428-31.
- Aliabadi FS and Lees P. Pharmacokinetics and pharmacokinetic/pharmacodynamic integration of marbofloxacin in calf serum, exudate and transudate. Journal of Veterinary Pharmacology and Therapeutics 2002;25:161-74.
- Thomas E, Madelenat A, Davot JL, Boisrame B. Clinical efficacy and tolerance of marbofloxacin and tetracycline in the treatment of bovine respiratory disease. Revue MedecineVeterinaire1998; 174:21-27.
- Thomas E, Caldow GL, Borell D, Davot JL. A field comparison of the efficacy and tolerance of marbofloxacin in the treatment of bovine respiratory disease. Journal of Veterinary Pharmacology and Therapeutics 2001;24:353-58.
- Stass H, Dalhoff A, Kubitza D, Schuhly U. Pharmacokinetics, Safety, and Tolerability of, Ascending Single Doses of Moxifloxacin, a New 8-Methoxy Quinolone, Administered to Healthy Subjects. Antimicrobial agents and Chemotherapy 1998;42(8):2060-65.
- Bhavsar SK, Verma MP, Thaker AM. Pharmacokinetics, tissue concentration and safety of multiple dose Intravenous administration of ciprofloxacin in cow calves. J. Vet. Pharmacol. Toxicol.2004;3(1):27-34.
- Khargharia S, Barua CC, Nath N, Bhattachrya M. Blood Biochemical Studies of Enrofloxacin in Yak after Intravenous Administration. Iranian J.Pharmacol.Therap. 2007;6:137-38.
- Patel JH, Varia RD, Patel UD, Vihol PD, Bhavsar SK and Thaker AM. Safety level of levofloxacin following repeated oral administration in White Leg Horn layer birds. Veterinary world2009;2(4):137-39.
- Sadariya KA, Gothi AK, Patel SD, Bhavsar SK and Thaker AM. Safety of Moxifloxacin following repeated intramuscular administration in Wistar rat. Veterinary World 2010;3(10):449-52
- Kim JC, Shin DH, Ahn TH, Kang SS, Song SW, Han J, Kim CY, Ha CS, Chung MK. 26-week repeated oral dose toxicity study of the new quinolone antibacterial DW 116 in prague–Dawley rats. Food and Chem. Toxicol.2003;41(5):637-45.
- Keutz EV and Schluter G. Preclinical safety evalution of Moxifloxacin, a novel fluoroquinolones. Journal of antimicrobial Chemotherapy1999;43:91-100.
- Lu GC, She JH, Jiang H, Li ZY, Yuan BJ. Sixty-day repeated dose toxicity of sinafloxacin in rats and dogs. Food and chemical toxicology2008;46(2):575-80.
- Zhao B, Chingnell CF, Rammal M, Smith F, Hamilton MG, Roberts JE. Detection and prevention of ocular phototoxicity of ciprofloxacin and other fluoroquinolone antibiotics. Phototoxicity and Photobiology 2010;86(4):798-805
- Wiebe V and Hamilton P. Fluoroquinolone-induced retinal degeneration in cats. Journal of the American Veterinary Medical Association 2002;221:1568-71
- Ford MM, Dubielzig RR, Giuliano EA, Moore CP and Narfstrom KL. Ocular and systemic manifestations after oral administration of a high dose of enrofloxacin in cats. American Journal of Veterinary research 2007;68(2):190-202
- Rampal S, Kaur R, Sethi R, Singh O, Sood N. Ofloxacin-associated retinopathy in rabbits: role of oxidative stress. Human and Experimental Toxicology 2008;27:409-15
- FrydmanAM, Roux YL, Lefebrre MA, Djebbai F, Foartfflan JB,Gafflof J. Pharmacokinetics of pefloxacin after repeated intravenons and oral administration (400 mg bid) in young healthy volunteers. Journal of Antimicrobial Chemotherapy 1986;17(B):65-79.
- Schneider M, Valle M, Woehrle F, Boisrame B. Pharmacokinetics of marbofloxacin in lactating cows after repeated intramuscular administrations and pharmacodynamics against mastitis isolated strains. Journal of Dairy Science 2004;87:202-11
- Shimoda K, Okawara S, Kato M. Phototoxic retinal degeneration and toxicokinetics of sitafloxacin, a quinolone antibacterial agent, in mice. Archives of Toxicology 2001;75: 395-99
- Nix D E and Schentag JJ. The quinolones: an overview and comparative appraisal of their pharmacokinetics and pharmacodynamics. Journal of Clinical Pharmacology 1988;28:169-78.
- Chang T, Black A, Dunkey A, Wolf R, Sedman A, Latts J, Welling PG. Pharmacokinetics of intravenous and oral enoxacin in healthy volunteers. Journal of Antimicrobial Chemotherapy 1988;21(B):49-56.
- Sarkozy G. Quinolones: a class of antimicrobial agents. Veterinary Medicine-Czech 2001;46(9-10):257-74.e