Physiological and histopathological investigations on the effects of alpha-lipoic acid in rats exposed to malathion
- PMID: 20454535
- PMCID: PMC2864892
- DOI: 10.1155/2010/203503
Physiological and histopathological investigations on the effects of alpha-lipoic acid in rats exposed to malathion
Abstract
The present study was designed to evaluate the influence of alpha-lipoic acid treatment in rats exposed to malathion. Forty adult male rats were used in this study and distributed into four groups. Animals of group 1 were untreated and served as control. Rats of group 2 were orally given malathion at a dose level of 100 mg/kg body weight (BW) for a period of one month. Experimental animals of group 3 were orally given alpha-lipoic acid at a dose level of 20 mg/kg BW and after 3 hours exposed to malathion at the same dose given to group 2. Rats of group 4 were supplemented with alpha-lipoic acid at the same dose given to group 3. The activities of serum glutamic oxaloacetic acid transaminase (GOT), glutamic pyruvic acid transaminase (GPT), alkaline phosphatase (ALP), and acid phosphatase (ACP), and the values of creatinine, urea, and uric acid were statistically increased, while the values of total protein and total albumin were significantly decreased in rats exposed to malathion. Moreover, administration of malathion for one month resulted in damage of liver and kidney structures. Administration of alpha-lipoic acid before malathion exposure to rat can prevent severe alterations of hemato-biochemical parameters and disruptions of liver and kidney structures. In conclusion, this study obviously demonstrated that pretreatment with alpha-lipoic acid significantly attenuated the physiological and histopathological alterations induced by malathion. Also, the present study identifies new areas of research for development of better therapeutic agents for liver, kidney, and other organs' dysfunctions and diseases.
Figures



Similar articles
-
Oxidative stress and alteration of biochemical markers in liver and kidney by malathion in rat pups.Toxicol Ind Health. 2015 Sep;31(9):783-8. doi: 10.1177/0748233713475507. Epub 2013 Jan 23. Toxicol Ind Health. 2015. PMID: 23344821
-
The potential protective role of alpha-lipoic acid against acetaminophen-induced hepatic and renal damage.Toxicology. 2008 Jan 20;243(3):261-70. doi: 10.1016/j.tox.2007.10.010. Epub 2007 Oct 23. Toxicology. 2008. PMID: 18068886
-
The effects of alpha-lipoic acid on breast of female albino rats exposed to malathion: Histopathological and immunohistochemical study.Pathol Res Pract. 2015 Jun;211(6):462-9. doi: 10.1016/j.prp.2015.02.006. Epub 2015 Mar 11. Pathol Res Pract. 2015. PMID: 25847504
-
The genotoxic, hepatotoxic, nephrotoxic, haematotoxic and histopathological effects in rats after aluminium chronic intoxication.Toxicol Ind Health. 2013 Oct;29(9):780-91. doi: 10.1177/0748233712440140. Epub 2012 Mar 15. Toxicol Ind Health. 2013. PMID: 22421584
-
Comparative evaluation of hepatotoxic and nephrotoxic effects of aroclors 1221 and 1254 in female rats.Cell Biochem Funct. 2007 Mar-Apr;25(2):167-72. doi: 10.1002/cbf.1289. Cell Biochem Funct. 2007. PMID: 16180246
Cited by
-
Organophosphate intermediate syndrome with neurological complications of extrapyramidal symptoms in clinical practice.J Neurosci Rural Pract. 2014 Jul;5(3):298-301. doi: 10.4103/0976-3147.133616. J Neurosci Rural Pract. 2014. PMID: 25002781 Free PMC article.
-
Chlorpyrifos and malathion have opposite effects on behaviors and brain size that are not correlated to changes in AChE activity.Neurotoxicology. 2015 Jul;49:50-8. doi: 10.1016/j.neuro.2015.05.002. Epub 2015 May 14. Neurotoxicology. 2015. PMID: 25983063 Free PMC article.
-
Oxidative macromolecular alterations in the rat central nervous system in response to experimentally co-induced chlorpyrifos and cold stress: a comparative assessment in aging rats.Neurochem Res. 2012 Feb;37(2):335-48. doi: 10.1007/s11064-011-0617-9. Epub 2011 Oct 13. Neurochem Res. 2012. PMID: 21993543
-
Arabica coffee and olive oils mitigate malathion-induced nephrotoxicity in rat: In silico, immunohistochemical and biochemical evaluation.Saudi J Biol Sci. 2022 Jun;29(6):103307. doi: 10.1016/j.sjbs.2022.103307. Epub 2022 May 13. Saudi J Biol Sci. 2022. PMID: 35602869 Free PMC article.
-
Malathion, an organophosphate insecticide, provokes metabolic, histopathologic and molecular disorders in liver and kidney in prepubertal male mice.Toxicol Rep. 2018 Jan 9;5:189-195. doi: 10.1016/j.toxrep.2017.12.021. eCollection 2018. Toxicol Rep. 2018. PMID: 29854588 Free PMC article.
References
-
- Chaudhuri K, Selvaraj S, Pal AK. Studies on the genotoxicity of endosulfan in bacterial systems. Mutation Research. 1999;439(1):63–67. - PubMed
-
- Davis JE. Neurotoxic concerns of human pesticide exposures. American Journal of Industrial Medicine. 1991;18(3):327–331. - PubMed
-
- Mason HJ. The recovery of plasma cholinesterase and erythrocyte acetylcholinesterase activity in workers after over-exposure to dichlorvos. Occupational Medicine. 2000;50(5):343–347. - PubMed
-
- Nigg HN, Knaak JB. Blood cholinesterases as human biomarkers of organophosphorus pesticide exposure. Reviews of Environmental Contamination & Toxicology. 2000;163:29–111. - PubMed
MeSH terms
Substances
LinkOut - more resources
Full Text Sources