ACUTE AND CHRONİC DEGREE OF TOXICITY IN TRAMADOL CONSUMPTİON ON PLASMA PROTEIN, ASPARTATE AMİNOTRANSFERASE (AST), ALANİNE AMİNOTRANSFERASE (ALT) AND ALKALİNE PHOSPHATASE (ALP) İN ADULT WISTAR RATS

Nduka Richard Ossai, T.M.E. Daubry, A. Ojieh
{"title":"ACUTE AND CHRONİC DEGREE OF TOXICITY IN TRAMADOL CONSUMPTİON ON PLASMA PROTEIN, ASPARTATE AMİNOTRANSFERASE (AST), ALANİNE AMİNOTRANSFERASE (ALT) AND ALKALİNE PHOSPHATASE (ALP) İN ADULT WISTAR RATS","authors":"Nduka Richard Ossai, T.M.E. Daubry, A. Ojieh","doi":"10.59287/icpis.874","DOIUrl":null,"url":null,"abstract":"Although the mechanism of hepatotoxicity from tramadol overdoses is unknown, it is most likelycaused by direct hepatocellular injury, either as a result of ischemia or mitochondrial toxicity. Overdosingon tramadol has been reported to cause acute liver failure. Tramadol-related minor enzyme increases areoften asymptomatic, self-limited, and resolve even when medication is continued. This investigationexamines the short- and long-term effects of tramadol use on liver enzymes in an animal model. The studyinvolved sixty (60) mature Wistar rats of both sexes. Tramadol (300g) were administered to the animals inthe experimental and control groups in the following ways: Before being sacrificed, Group A (n = 5 Malesand 5 Females) received no treatment within the study's time frame. Group B (n = 5 Males and 5 Females)received tramadol 30 mg/kg body weight for 7 days and were sacrificed; Group C (n = 5 Males and 5Females) received tramadol 30 mg/kg body weight for 14 days and were sacrifice; Group D (n = 5 Malesand 5 Females) received tramadol 30 mg/kg body weight for 21 days and were sacrifice, Group E (n = 5Male and 5 Female) received tramadol 30 mg/kg body weight for 42 days and were sacrificed, while GroupF (n = 5 Male and 5 Female) withdrew for 3 weeks after receiving tramadol 30 mg/kg for three weeksbefore sacrificing. Liver was removed from the animals for biochemical examination. The findings of theSPSS analysis on the generated data were expressed as mean SEM. After three and six weeks of tramadoladministration, the results obtained demonstrated a progressive increase in weight and an increase in theactivities of ALT, ALP, and AST in the plasma while decreasing the level of total protein, albumin, directbilirubin as well as indirect bilirubin as compared to the control rats. Therefore, this study comes to theconclusion that tramadol has harmful effects, both acute and chronic, on the structure and operation ofhepatic tissue in wistar rats. As a result, tramadol use needs to be monitored.","PeriodicalId":292916,"journal":{"name":"International Conference on Pioneer and Innovative Studies","volume":"43 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-06-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Conference on Pioneer and Innovative Studies","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.59287/icpis.874","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Although the mechanism of hepatotoxicity from tramadol overdoses is unknown, it is most likelycaused by direct hepatocellular injury, either as a result of ischemia or mitochondrial toxicity. Overdosingon tramadol has been reported to cause acute liver failure. Tramadol-related minor enzyme increases areoften asymptomatic, self-limited, and resolve even when medication is continued. This investigationexamines the short- and long-term effects of tramadol use on liver enzymes in an animal model. The studyinvolved sixty (60) mature Wistar rats of both sexes. Tramadol (300g) were administered to the animals inthe experimental and control groups in the following ways: Before being sacrificed, Group A (n = 5 Malesand 5 Females) received no treatment within the study's time frame. Group B (n = 5 Males and 5 Females)received tramadol 30 mg/kg body weight for 7 days and were sacrificed; Group C (n = 5 Males and 5Females) received tramadol 30 mg/kg body weight for 14 days and were sacrifice; Group D (n = 5 Malesand 5 Females) received tramadol 30 mg/kg body weight for 21 days and were sacrifice, Group E (n = 5Male and 5 Female) received tramadol 30 mg/kg body weight for 42 days and were sacrificed, while GroupF (n = 5 Male and 5 Female) withdrew for 3 weeks after receiving tramadol 30 mg/kg for three weeksbefore sacrificing. Liver was removed from the animals for biochemical examination. The findings of theSPSS analysis on the generated data were expressed as mean SEM. After three and six weeks of tramadoladministration, the results obtained demonstrated a progressive increase in weight and an increase in theactivities of ALT, ALP, and AST in the plasma while decreasing the level of total protein, albumin, directbilirubin as well as indirect bilirubin as compared to the control rats. Therefore, this study comes to theconclusion that tramadol has harmful effects, both acute and chronic, on the structure and operation ofhepatic tissue in wistar rats. As a result, tramadol use needs to be monitored.
曲马多consumptİon对成年wistar大鼠血浆蛋白、天冬氨酸amİnotransferase (ast)、alanİne amİnotransferase (alt)和alkalİne磷酸酶(alp) İn的急性和chronİc毒性程度
虽然曲马多过量引起肝毒性的机制尚不清楚,但它很可能是由直接肝细胞损伤引起的,要么是缺血,要么是线粒体毒性。据报道,曲马多服用过量可引起急性肝衰竭。曲马多相关的轻微酶升高通常是无症状的,自限性的,即使继续用药也会消退。本研究在动物模型中考察了曲马多对肝酶的短期和长期影响。这项研究涉及60只成年雌雄Wistar大鼠。实验组和对照组分别给予曲马多300g: A组(雄性5只,雌性5只)在实验时间内未接受任何治疗。B组(男5名,女5名)给予曲马多30 mg/kg体重,连续7 d处死;C组(男5名,女5名)给予曲马多30 mg/kg体重治疗14 d后处死;D组(男5只,女5只)接受曲马多30 mg/kg体重治疗21 D后处死,E组(男5只,女5只)接受曲马多30 mg/kg体重治疗42 D后处死,f组(男5只,女5只)接受曲马多30 mg/kg治疗3周后退出治疗3周后处死。从动物身上取下肝脏进行生化检查。生成数据的espss分析结果表示为平均SEM。在曲马多给药3周和6周后,结果显示,与对照大鼠相比,体重逐渐增加,血浆中ALT、ALP和AST活性增加,同时总蛋白、白蛋白、直接胆红素和间接胆红素水平降低。因此,本研究得出结论,曲马多对wistar大鼠肝组织的结构和运作有急性和慢性的有害影响。因此,曲马多的使用需要监控。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
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