氯氰菊酯毒性对雄性白化大鼠肝线粒体影响的评价

IF 1.8 4区 医学 Q4 PHARMACOLOGY & PHARMACY
Venkataramanaiah Poli , Srinivasulu Reddy Motireddy
{"title":"氯氰菊酯毒性对雄性白化大鼠肝线粒体影响的评价","authors":"Venkataramanaiah Poli ,&nbsp;Srinivasulu Reddy Motireddy","doi":"10.1016/j.vascn.2025.108388","DOIUrl":null,"url":null,"abstract":"<div><div>The purpose of this study is to look into the toxic effects of giving male albino rats cypermethrin (CPM). In order to achieve this, three groups of rats were formed. Every group received the same amount of saline, including the control group, while the experimental groups received 4.5 and 5.5 mg/kg body weight of cypermethrin. After that, the rats are sacrificed, and tissue samples are pooled. In all the treatments, rats were administered orally for an experimental period of 30 days. Every week, the body weight of every individual rat was recorded. In order to achieve this goal, indicators of toxicity such as body and organic weight, ATP and ATP/ADP ratio, antioxidant enzymes and oxidative stress, complex activity (complex I–IV), plasma biochemical parameters, and levels of pro-inflammatory cytokines are utilized. Rats injected with cypermethrin showed a substantial (<em>p</em> &lt; 0.05) drop in their ultimate weight and organ weight when compared to control rats. The administration of cypermethrin resulted in a significant (<em>p</em> &lt; 0.05) drop in adenosine triphosphate (ATP) and the ATP/ADP ratio, indicating the involvement of activity of liver mitochondria. The administration of cypermethrin oxidative stress biomarkers resulted in a substantial increase (<em>p</em> &lt; 0.05) in malondialdehyde (MDA), glutathione (GSH), reactive oxygen species (ROS), and protein carbonylated content (PCC). Nevertheless, there was a significant (<em>p</em> &lt; 0.05) drop in the antioxidant enzymes catalase (CAT), superoxide dismutase (SOD), glutathione peroxidase (GPx), and glutathione S-transferase (GST) in the mitochondria of rat liver. In the present study, the complex activity (complex I–IV) and mitochondrial membrane potential (MMP) of rat liver mitochondria decreased significantly (<em>p</em> &lt; 0.05). The administration of Cypermethrin resulted in a significant (p &lt; 0.05) increase in plasma levels of triglycerides (TAG), alanine aminotransferase (ALT), aspartate aminotransferase (AST), bilirubin (BIL), total cholesterol (TC), high-density lipoprotein (HDL-C), low-density lipoprotein (LDL-C), and alkaline phosphatase (ALP). Pro-inflammatory cytokines (TNF-α, IL-1β, IL-6, and IL-10) were observed to have higher plasma levels after cypermethrin injection (<em>p</em> &lt; 0.05) when compared to the control. The current study's findings demonstrated that rat liver tissue suffered mitochondrial damage as a result of cypermethrin intoxication.</div></div>","PeriodicalId":16767,"journal":{"name":"Journal of pharmacological and toxicological methods","volume":"135 ","pages":"Article 108388"},"PeriodicalIF":1.8000,"publicationDate":"2025-07-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Evaluation of the Effects of cypermethrin Toxicity on Liver Mitochondria of Male Albino Rats\",\"authors\":\"Venkataramanaiah Poli ,&nbsp;Srinivasulu Reddy Motireddy\",\"doi\":\"10.1016/j.vascn.2025.108388\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The purpose of this study is to look into the toxic effects of giving male albino rats cypermethrin (CPM). In order to achieve this, three groups of rats were formed. Every group received the same amount of saline, including the control group, while the experimental groups received 4.5 and 5.5 mg/kg body weight of cypermethrin. After that, the rats are sacrificed, and tissue samples are pooled. In all the treatments, rats were administered orally for an experimental period of 30 days. Every week, the body weight of every individual rat was recorded. In order to achieve this goal, indicators of toxicity such as body and organic weight, ATP and ATP/ADP ratio, antioxidant enzymes and oxidative stress, complex activity (complex I–IV), plasma biochemical parameters, and levels of pro-inflammatory cytokines are utilized. Rats injected with cypermethrin showed a substantial (<em>p</em> &lt; 0.05) drop in their ultimate weight and organ weight when compared to control rats. The administration of cypermethrin resulted in a significant (<em>p</em> &lt; 0.05) drop in adenosine triphosphate (ATP) and the ATP/ADP ratio, indicating the involvement of activity of liver mitochondria. The administration of cypermethrin oxidative stress biomarkers resulted in a substantial increase (<em>p</em> &lt; 0.05) in malondialdehyde (MDA), glutathione (GSH), reactive oxygen species (ROS), and protein carbonylated content (PCC). Nevertheless, there was a significant (<em>p</em> &lt; 0.05) drop in the antioxidant enzymes catalase (CAT), superoxide dismutase (SOD), glutathione peroxidase (GPx), and glutathione S-transferase (GST) in the mitochondria of rat liver. In the present study, the complex activity (complex I–IV) and mitochondrial membrane potential (MMP) of rat liver mitochondria decreased significantly (<em>p</em> &lt; 0.05). The administration of Cypermethrin resulted in a significant (p &lt; 0.05) increase in plasma levels of triglycerides (TAG), alanine aminotransferase (ALT), aspartate aminotransferase (AST), bilirubin (BIL), total cholesterol (TC), high-density lipoprotein (HDL-C), low-density lipoprotein (LDL-C), and alkaline phosphatase (ALP). Pro-inflammatory cytokines (TNF-α, IL-1β, IL-6, and IL-10) were observed to have higher plasma levels after cypermethrin injection (<em>p</em> &lt; 0.05) when compared to the control. The current study's findings demonstrated that rat liver tissue suffered mitochondrial damage as a result of cypermethrin intoxication.</div></div>\",\"PeriodicalId\":16767,\"journal\":{\"name\":\"Journal of pharmacological and toxicological methods\",\"volume\":\"135 \",\"pages\":\"Article 108388\"},\"PeriodicalIF\":1.8000,\"publicationDate\":\"2025-07-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of pharmacological and toxicological methods\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1056871925008081\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of pharmacological and toxicological methods","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1056871925008081","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

摘要

本研究的目的是观察雄性白化大鼠给予氯氰菊酯(CPM)的毒性作用。为了达到这个目的,我们将老鼠分成了三组。包括对照组在内的各组均给予等量生理盐水,实验组给予4.5、5.5 mg/kg体重的氯氰菊酯。之后,处死大鼠,收集组织样本。在所有治疗中,大鼠口服30天的实验期。每周记录每只大鼠的体重。为了实现这一目标,毒性指标如体重和有机质量、ATP和ATP/ADP比值、抗氧化酶和氧化应激、复合体活性(复合体I-IV)、血浆生化参数和促炎细胞因子水平被利用。注射氯氰菊酯的大鼠表现出显著的(p <;0.05),与对照大鼠相比,其最终体重和器官重量下降。施用氯氰菊酯可显著降低(p <;0.05),三磷酸腺苷(ATP)和ATP/ADP比值下降,提示肝脏线粒体活性受到影响。氯氰菊酯氧化应激生物标志物显著增加(p <;0.05)丙二醛(MDA)、谷胱甘肽(GSH)、活性氧(ROS)和蛋白羰基化含量(PCC)。然而,有显著的(p <;0.05)降低大鼠肝脏线粒体抗氧化酶过氧化氢酶(CAT)、超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GPx)和谷胱甘肽s -转移酶(GST)。在本研究中,大鼠肝脏线粒体复合体活性(复合体I-IV)和线粒体膜电位(MMP)显著降低(p <;0.05)。施用氯氰菊酯可显著降低(p <;0.05)血浆甘油三酯(TAG)、丙氨酸转氨酶(ALT)、天冬氨酸转氨酶(AST)、胆红素(BIL)、总胆固醇(TC)、高密度脂蛋白(HDL-C)、低密度脂蛋白(LDL-C)、碱性磷酸酶(ALP)水平升高。注射氯氰菊酯后,血浆中促炎细胞因子(TNF-α、IL-1β、IL-6和IL-10)水平升高(p <;0.05)。目前的研究结果表明,由于氯氰菊酯中毒,大鼠肝脏组织遭受线粒体损伤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Evaluation of the Effects of cypermethrin Toxicity on Liver Mitochondria of Male Albino Rats

Evaluation of the Effects of cypermethrin Toxicity on Liver Mitochondria of Male Albino Rats
The purpose of this study is to look into the toxic effects of giving male albino rats cypermethrin (CPM). In order to achieve this, three groups of rats were formed. Every group received the same amount of saline, including the control group, while the experimental groups received 4.5 and 5.5 mg/kg body weight of cypermethrin. After that, the rats are sacrificed, and tissue samples are pooled. In all the treatments, rats were administered orally for an experimental period of 30 days. Every week, the body weight of every individual rat was recorded. In order to achieve this goal, indicators of toxicity such as body and organic weight, ATP and ATP/ADP ratio, antioxidant enzymes and oxidative stress, complex activity (complex I–IV), plasma biochemical parameters, and levels of pro-inflammatory cytokines are utilized. Rats injected with cypermethrin showed a substantial (p < 0.05) drop in their ultimate weight and organ weight when compared to control rats. The administration of cypermethrin resulted in a significant (p < 0.05) drop in adenosine triphosphate (ATP) and the ATP/ADP ratio, indicating the involvement of activity of liver mitochondria. The administration of cypermethrin oxidative stress biomarkers resulted in a substantial increase (p < 0.05) in malondialdehyde (MDA), glutathione (GSH), reactive oxygen species (ROS), and protein carbonylated content (PCC). Nevertheless, there was a significant (p < 0.05) drop in the antioxidant enzymes catalase (CAT), superoxide dismutase (SOD), glutathione peroxidase (GPx), and glutathione S-transferase (GST) in the mitochondria of rat liver. In the present study, the complex activity (complex I–IV) and mitochondrial membrane potential (MMP) of rat liver mitochondria decreased significantly (p < 0.05). The administration of Cypermethrin resulted in a significant (p < 0.05) increase in plasma levels of triglycerides (TAG), alanine aminotransferase (ALT), aspartate aminotransferase (AST), bilirubin (BIL), total cholesterol (TC), high-density lipoprotein (HDL-C), low-density lipoprotein (LDL-C), and alkaline phosphatase (ALP). Pro-inflammatory cytokines (TNF-α, IL-1β, IL-6, and IL-10) were observed to have higher plasma levels after cypermethrin injection (p < 0.05) when compared to the control. The current study's findings demonstrated that rat liver tissue suffered mitochondrial damage as a result of cypermethrin intoxication.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Journal of pharmacological and toxicological methods
Journal of pharmacological and toxicological methods PHARMACOLOGY & PHARMACY-TOXICOLOGY
CiteScore
3.60
自引率
10.50%
发文量
56
审稿时长
26 days
期刊介绍: Journal of Pharmacological and Toxicological Methods publishes original articles on current methods of investigation used in pharmacology and toxicology. Pharmacology and toxicology are defined in the broadest sense, referring to actions of drugs and chemicals on all living systems. With its international editorial board and noted contributors, Journal of Pharmacological and Toxicological Methods is the leading journal devoted exclusively to experimental procedures used by pharmacologists and toxicologists.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信