Large scale toxicological evaluation of lead acetate in broiler chicken

Among heavy metals, lead is one of the very toxic pollutants of the environment. Its accumulating nature in the body makes it a great threat to public health particularly when humans consume lead intoxicated foods like chickens. The main purpose of the conducted research was to elucidate the bioaccumulation of lead in different organs of chickens and its toxicological effects on various organs and biochemical parameters. An experimental study on the effect of lead acetate toxicity in chicks was conducted by orally administration for consecutive thirty days. Thirty-chicks were categorized into A, B, C, D, E, and F groups with lead acetate dose rate 0, 71, 142, 213, and 284 mg/kg body weight, correspondingly. During the experiment, various biochemical parameters (uric acid, GPT, creatinine, ALP, LDH, ASAT, ALT, glutathione, superoxide dismutase) were measured employing commercially available kits. At the end of experimentation, and lead accumulation in liver, kidney and brain was estimated by absorption spectrophotometer. Some biochemical parameters like uric acid, GPT, creatinine, ALP, LDH, AST, and ALT were increased while the level of glutathione and superoxide dismutase, was found to be decreased after exposure to lead acetate. In present study, the pattern of metal accumulation in different organs directly related with concentration of metal. The order of metal accumulation in organs is; liver > kidney > brain. In the present study, supplementation of lead acetate has affected the exposed chicken. Mostly the blood profile and chemistry are perturbed. These effects might be due to the accumulation of lead in the brain, kidneys, and liver which may result in neurotoxicity, nephrotoxicity, and hepatotoxicity. To refine such outcomes, further studies in the future are recommended.

[1]  X. Teng,et al.  Energy metabolism disorder mediated ammonia gas-induced autophagy via AMPK/mTOR/ULK1-Beclin1 pathway in chicken livers. , 2021, Ecotoxicology and environmental safety.

[2]  M. Ashraf,et al.  The effects of some heavy metals on some fish species , 2021, Environmental Science and Pollution Research.

[3]  A. Golian,et al.  Effect of replacement different methionine levels and sources with betaine on blood metabolites, breast muscle morphology and immune response in heat-stressed broiler chickens , 2021, Italian Journal of Animal Science.

[4]  Q. Han,et al.  Oxidative stress and mitochondrial dysfunction involved in ammonia-induced nephrocyte necroptosis in chickens. , 2020, Ecotoxicology and environmental safety.

[5]  You Tang,et al.  The effect of ammonia exposure on energy metabolism and mitochondrial dynamic proteins in chicken thymus: Through oxidative stress, apoptosis, and autophagy. , 2020, Ecotoxicology and environmental safety.

[6]  H. A. Shakir,et al.  Abnormal steroidogenesis, oxidative stress, and reprotoxicity following prepubertal exposure to butylparaben in mice and protective effect of Curcuma longa , 2020, Environmental Science and Pollution Research.

[7]  Hongfu Zhang,et al.  The involvement of miR-6615-5p/Smad7 axis and immune imbalance in ammonia-caused inflammatory injury via NF-κB pathway in broiler kidneys , 2020, Poultry science.

[8]  I. Baranowska-Bosiacka,et al.  The Effect of Whole Blood Lead (Pb-B) Levels on Changes in Peripheral Blood Morphology and Selected Biochemical Parameters, and the Severity of Depression in Peri-Menopausal Women at Risk of Metabolic Syndrome or with Metabolic Syndrome , 2020, International journal of environmental research and public health.

[9]  J. Wan,et al.  Salidroside protects mice against CCl4-induced acute liver injury via down-regulating CYP2E1 expression and inhibiting NLRP3 inflammasome activation. , 2020, International immunopharmacology.

[10]  H. M. Tahir,et al.  Cardiac toxicity of heavy metals (cadmium and mercury) and pharmacological intervention by vitamin C in rabbits , 2020, Environmental Science and Pollution Research.

[11]  Jichang Li,et al.  Mycoplasma gallisepticum triggers immune damage in the chicken thymus by activating the TLR-2/MyD88/NF-κB signaling pathway and NLRP3 inflammasome , 2020, Veterinary Research.

[12]  O. Eidelman,et al.  Liver Function Enzymes are Potential Predictive Markers for Kidney Allograft Dysfunction. , 2020, Advancements in journal of urology and nephrology.

[13]  H. M. Tahir,et al.  Dose and duration-dependent toxicological evaluation of lead acetate in chicks , 2020, Environmental Science and Pollution Research.

[14]  E. Abd-Elhady,et al.  The Protective Effect of Seeds and Sprouts of Fenugreek and Alfalfa on Rats Exposed to Lead Poisoning , 2020 .

[15]  N. Akhtar,et al.  Evaluation of chemopreventive and chemotherapeutic effect of Artemisia vulgaris extract against diethylnitrosamine induced hepatocellular carcinogenesis in Balb C mice. , 2020, Brazilian journal of biology = Revista brasleira de biologia.

[16]  Q. Han,et al.  Ammonia inhalation impaired immune function and mitochondrial integrity in the broilers bursa of fabricius: Implication of oxidative stress and apoptosis. , 2019, Ecotoxicology and environmental safety.

[17]  The protective effect of Zataria Multiflora on the embryotoxicity induced by bisphenol A in the brain of chicken embryos , 2019, Biointerface Research in Applied Chemistry.

[18]  J. Mutić,et al.  Subchronic Oral Cadmium Exposure Exerts both Stimulatory and Suppressive Effects on Pulmonary Inflammation/Immune Reactivity in Rats. , 2019, Biomedical and environmental sciences : BES.

[19]  O. Orisakwe,et al.  Natural antidotes and management of metal toxicity , 2019, Environmental Science and Pollution Research.

[20]  Hyeon Seok Choi,et al.  Prediction of Lead Intake and Tissue Lead Concentrations in Broiler Chickens Using Feather Lead Concentrations , 2019, Biological Trace Element Research.

[21]  H. M. Tahir,et al.  Toxicological effects of toxic metals (cadmium and mercury) on blood and the thyroid gland and pharmacological intervention by vitamin C in rabbits , 2019, Environmental Science and Pollution Research.

[22]  H. A. Shakir,et al.  The protective role of ascorbic acid in the hepatotoxicity of cadmium and mercury in rabbits , 2019, Environmental Science and Pollution Research.

[23]  M. Rashid,et al.  Assessing the prevalence and economic significance of coccidiosis individually and in combination with concurrent infections in Pakistani commercial poultry farms , 2019, Poultry science.

[24]  F. Babiker,et al.  Lead exposure induces oxidative stress, apoptosis, and attenuates protection of cardiac myocytes against ischemia–reperfusion injury , 2019, Drug and chemical toxicology.

[25]  M. Khan,et al.  In vivo induction of hepatocellular carcinoma by diethylnitrosoamine and pharmacological intervention in Balb C mice using Bergenia ciliata extracts. , 2019, Brazilian journal of biology = Revista brasleira de biologia.

[26]  Arun J. Patil,et al.  Impact of Occupational Lead Exposure on Liver and Kidney Function Tests on Silver Jewellery Workers , 2019, JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH.

[27]  Amandeep,et al.  Pathomorphological Changes during Amelioration of Lead Induced Toxicity in Chickens by Withania somnifera , 2019, Journal of Immunology and Immunopathology.

[28]  M. Babar,et al.  Evaluation of Hepatotoxicity of Carbon Tetrachloride and Pharmacological Intervention by Vitamin E in Balb C Mice , 2019, Pakistan Journal of Zoology.

[29]  H. M. Tahir,et al.  Renal toxicity of heavy metals (cadmium and mercury) and their amelioration with ascorbic acid in rabbits , 2018, Environmental Science and Pollution Research.

[30]  M. Ashrafizadeh,et al.  Histological Changes in the Liver and Biochemical Parameters of Chickens Treated with Lead Acetate II , 2018, Iranian Journal of Toxicology.

[31]  M. Tomczyk,et al.  Complexation of Bioelements and Toxic Metals by Polyphenolic Compounds - Implications for Health. , 2018, Current drug targets.

[32]  M. Ashrafizadeh,et al.  Expression of Collagen Type II and Osteocalcin Genes in Mesenchymal Stem Cells from Rats Treated with Lead acetate II , 2018, Iranian Journal of Toxicology.

[33]  P. Jeandet,et al.  The Role of Heavy Metals in Plant Response to Biotic Stress , 2018, Molecules.

[34]  A. Mathee,et al.  Is There a Relationship between Lead Exposure and Aggressive Behavior in Shooters? , 2018, International journal of environmental research and public health.

[35]  C. Oh,et al.  Antioxidant Responses, Neurotoxicity, and Metallothionein Gene Expression in Juvenile Korean Rockfish Sebastes schlegelii under Dietary Lead Exposure. , 2017, Journal of aquatic animal health.

[36]  O. Orisakwe,et al.  Lead Induced Hepato-renal Damage in Male Albino Rats and Effects of Activated Charcoal , 2017, Front. Pharmacol..

[37]  B. Fauconneau,et al.  Ultrastructural study of liver and lead tissue concentrations in young mallard ducks (Anas platyrhynchos) after ingestion of single lead shot , 2017, Journal of toxicology and environmental health. Part A.

[38]  Kai Yang,et al.  Alleviation of lead-induced oxidative stress and immune damage by selenium in chicken bursa of Fabricius , 2017, Environmental Science and Pollution Research.

[39]  P. Hasanein,et al.  Effects of isoquinoline alkaloid berberine on lipid peroxidation, antioxidant defense system, and liver damage induced by lead acetate in rats , 2017, Redox report : communications in free radical research.

[40]  A. Anjum,et al.  Effects of experimental lead toxicity on hematology and biochemical parameters in Lohi sheep , 2017 .

[41]  A. Muhammad,et al.  Evaluation of Changes in Liver Enzymes in Broiler Chicks (Gallous domesticus) , 2016 .

[42]  A. A. Abou-Rawash,et al.  Protective Role of an Aqueous Extract of Punica Granatum (Pomegranate) Peel on Lead-Induced Anemia In Rats - , 2016 .

[43]  Pourkhabbaz Hamid Reza,et al.  SYNERGISTIC EFFECTS OF SUB-LETHAL CONCENTRATIONS OF DELTAMETHRIN ON LEAD ACETATE TOXICITY IN JAPANESE QUAIL (COTURNIX JAPONICA) , 2016 .

[44]  Q. J. Zhao,et al.  The relationship between chemical‐induced kidney weight increases and kidney histopathology in rats , 2015, Journal of applied toxicology : JAT.

[45]  A. Winiarska-Mieczan,et al.  The Effect of Exposure to Cd and Pb in the Form of a Drinking Water or Feed on the Accumulation and Distribution of These Metals in the Organs of Growing Wistar Rats , 2015, Biological Trace Element Research.

[46]  J. Qazi,et al.  Metal bioaccumulation levels in different organs of three edible fish species from the river Ravi, Pakistan , 2015 .

[47]  M. Salim Evaluation of Performance of Date Palm Pollen on Urea and Creatinine Levels in Adult Female Rats Exposed to Lead Acetate Intoxication , 2015 .

[48]  H. Abdou,et al.  Protective Role of Omega-3 Polyunsaturated Fatty Acid against Lead Acetate-Induced Toxicity in Liver and Kidney of Female Rats , 2014, BioMed research international.

[49]  A. Oyagbemi,et al.  Failure of recovery from lead induced hepatoxicity and disruption of erythrocyte antioxidant defence system in Wistar rats. , 2014, Environmental toxicology and pharmacology.

[50]  N. Osman The role of antioxidant properties of Celery against lead acetate induced hepatotoxicity and oxidative stress in irradiated rats , 2013 .

[51]  A. Khan,et al.  Effect of lead acetate administered orally at different dosage levels in broiler chicks , 2011 .

[52]  A. Saxena,et al.  Impact of different doses of lead on internal organs of quails. , 2008, Journal of environmental biology.