{"title":"Toxicological assessment of exposure to pharmaceutical effluents in rats for 28 days by repeated oral dose.","authors":"Sudhakar Chatakondu, Naresh Dumala, Rekhadevi Perumalla Venkata","doi":"10.1007/s00210-025-03948-9","DOIUrl":null,"url":null,"abstract":"<p><p>The widespread presence of contaminants in various zones of the environment raises an alarming signal for the need of assessing their ability in causing deleterious health effects in humans and degradation of environment. This investigation mainly aims at evaluation of the genotoxicity and oxidative damage induced by the pharmaceutical industry wastes in Hyderabad, India. Pollution load in effluents was determined by water quality assessment and heavy metal analysis. Wistar rats were orally administered low, medium, and high doses of effluents for a 28-day period, collected from two private and one government pharmaceuticals' manufacturing units. DNA damage quantification in peripheral blood lymphocytes and liver was done using comet assay and micronucleus test in bone marrow cells. Oxidative stress assessment was done by estimation of reduced glutathione, catalase, and malondialdehyde levels. Effluent-induced histopathological changes were reported in the liver and kidney tissues of rats treated that received a high dose of effluent. Significant induction of genotoxicity and alterations in antioxidant enzymes and serum biochemistry parameters were documented. Results of this study reveal altered levels of various physicochemical parameters, above permissible limits in pharmaceutical industry treated effluent indicating their potential role as a disastrous contaminant. The study innovatively evaluates the chronic effects of pharmaceutical effluents on rat health, providing critical insights into systemic toxicity, biochemical alterations, and potential health risks after 28-day repeated oral exposure.</p>","PeriodicalId":18876,"journal":{"name":"Naunyn-Schmiedeberg's archives of pharmacology","volume":" ","pages":""},"PeriodicalIF":3.1000,"publicationDate":"2025-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Naunyn-Schmiedeberg's archives of pharmacology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s00210-025-03948-9","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0
Abstract
The widespread presence of contaminants in various zones of the environment raises an alarming signal for the need of assessing their ability in causing deleterious health effects in humans and degradation of environment. This investigation mainly aims at evaluation of the genotoxicity and oxidative damage induced by the pharmaceutical industry wastes in Hyderabad, India. Pollution load in effluents was determined by water quality assessment and heavy metal analysis. Wistar rats were orally administered low, medium, and high doses of effluents for a 28-day period, collected from two private and one government pharmaceuticals' manufacturing units. DNA damage quantification in peripheral blood lymphocytes and liver was done using comet assay and micronucleus test in bone marrow cells. Oxidative stress assessment was done by estimation of reduced glutathione, catalase, and malondialdehyde levels. Effluent-induced histopathological changes were reported in the liver and kidney tissues of rats treated that received a high dose of effluent. Significant induction of genotoxicity and alterations in antioxidant enzymes and serum biochemistry parameters were documented. Results of this study reveal altered levels of various physicochemical parameters, above permissible limits in pharmaceutical industry treated effluent indicating their potential role as a disastrous contaminant. The study innovatively evaluates the chronic effects of pharmaceutical effluents on rat health, providing critical insights into systemic toxicity, biochemical alterations, and potential health risks after 28-day repeated oral exposure.
期刊介绍:
Naunyn-Schmiedeberg''s Archives of Pharmacology was founded in 1873 by B. Naunyn, O. Schmiedeberg and E. Klebs as Archiv für experimentelle Pathologie und Pharmakologie, is the offical journal of the German Society of Experimental and Clinical Pharmacology and Toxicology (Deutsche Gesellschaft für experimentelle und klinische Pharmakologie und Toxikologie, DGPT) and the Sphingolipid Club. The journal publishes invited reviews, original articles, short communications and meeting reports and appears monthly. Naunyn-Schmiedeberg''s Archives of Pharmacology welcomes manuscripts for consideration of publication that report new and significant information on drug action and toxicity of chemical compounds. Thus, its scope covers all fields of experimental and clinical pharmacology as well as toxicology and includes studies in the fields of neuropharmacology and cardiovascular pharmacology as well as those describing drug actions at the cellular, biochemical and molecular levels. Moreover, submission of clinical trials with healthy volunteers or patients is encouraged. Short communications provide a means for rapid publication of significant findings of current interest that represent a conceptual advance in the field.