J K Akintunde, J A Ajiboye, E O Siemuri, O O Olabisi
{"title":"芬司达药物诱导大鼠模型中某些重要组织的细胞毒性:硒和锌胶囊的联合防御作用。","authors":"J K Akintunde, J A Ajiboye, E O Siemuri, O O Olabisi","doi":"10.1177/20420986211027101","DOIUrl":null,"url":null,"abstract":"<p><strong>Aim: </strong>Fansidar (FAN) is widely used as an antimalarial drug, but it may cause hepatoxicity, nephrotoxicity, and neurotoxicity. Hence, the study examines the cytoprotection of selenium (Se) and zinc (Zn) tablets against FAN induced toxicity.</p><p><strong>Method: </strong>Group I was given distilled water. Groups II, III, IV, and V received 50 mg/kg FAN by gavage. Group III was co-treated with a 50 mg/kg Se tablet. Group IV was co-treated with a 50 mg/kg Zn tablet. Group V was co-treated with a 50 mg/kg Se tablet + 50 mg/kg Zn tablet. The exposure lasted for 7 days (sub-acute exposure).</p><p><strong>Result: </strong>FAN causes cytotoxicity through significant (<i>p</i> < 0.05) alteration of antioxidant molecules and hepatic enzymes. It also significantly (<i>p</i> < 0.05) induces renal, hepatocyte, and purkinje cell damage, but no visible lesion on testicular cells. The FAN induced cytotoxicity was significantly (<i>p</i> < 0.05) reversed on treatment with both single and combined antioxidant tablets.</p><p><strong>Conclusion: </strong>Our study supports the view that antioxidant micronutrient (Se and Zn) tablets may be a useful modulator in alleviating FAN induced oxidative stress and cytotoxicity in male rats.</p><p><strong>Plain language summary: </strong><b>Combined selenium and zinc capsules: better therapy against cytotoxicity</b> Fansidar was approved by United States' Food and Drug Administration as an anti-malarial drug to treat acute and complicated malaria fever among patients in West Africa; however, its usage elicits toxicity to several organs of the body. It was elucidated that the combination of selenium and zinc capsules promotes organ wellness on co-treatment with Fansidar.</p>","PeriodicalId":23012,"journal":{"name":"Therapeutic Advances in Drug Safety","volume":"12 ","pages":"20420986211027101"},"PeriodicalIF":3.4000,"publicationDate":"2021-07-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/fe/ad/10.1177_20420986211027101.PMC8287264.pdf","citationCount":"0","resultStr":"{\"title\":\"Fansidar drug induces cytotoxicity in some vital tissues in a rat model: combination defensive effect of selenium and zinc capsules.\",\"authors\":\"J K Akintunde, J A Ajiboye, E O Siemuri, O O Olabisi\",\"doi\":\"10.1177/20420986211027101\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Aim: </strong>Fansidar (FAN) is widely used as an antimalarial drug, but it may cause hepatoxicity, nephrotoxicity, and neurotoxicity. Hence, the study examines the cytoprotection of selenium (Se) and zinc (Zn) tablets against FAN induced toxicity.</p><p><strong>Method: </strong>Group I was given distilled water. Groups II, III, IV, and V received 50 mg/kg FAN by gavage. Group III was co-treated with a 50 mg/kg Se tablet. Group IV was co-treated with a 50 mg/kg Zn tablet. Group V was co-treated with a 50 mg/kg Se tablet + 50 mg/kg Zn tablet. The exposure lasted for 7 days (sub-acute exposure).</p><p><strong>Result: </strong>FAN causes cytotoxicity through significant (<i>p</i> < 0.05) alteration of antioxidant molecules and hepatic enzymes. It also significantly (<i>p</i> < 0.05) induces renal, hepatocyte, and purkinje cell damage, but no visible lesion on testicular cells. The FAN induced cytotoxicity was significantly (<i>p</i> < 0.05) reversed on treatment with both single and combined antioxidant tablets.</p><p><strong>Conclusion: </strong>Our study supports the view that antioxidant micronutrient (Se and Zn) tablets may be a useful modulator in alleviating FAN induced oxidative stress and cytotoxicity in male rats.</p><p><strong>Plain language summary: </strong><b>Combined selenium and zinc capsules: better therapy against cytotoxicity</b> Fansidar was approved by United States' Food and Drug Administration as an anti-malarial drug to treat acute and complicated malaria fever among patients in West Africa; however, its usage elicits toxicity to several organs of the body. 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引用次数: 0
摘要
目的:芬斯达(FAN)作为一种抗疟药物被广泛使用,但它可能会引起肝中毒、肾中毒和神经中毒。因此,本研究探讨了硒(Se)和锌(Zn)片对 FAN 引起的毒性的细胞保护作用:方法:I 组给予蒸馏水。方法:I 组给予蒸馏水,II、III、IV 和 V 组灌胃 50 mg/kg FAN。第三组同时服用 50 毫克/千克 Se 片剂。第四组同时服用每公斤 50 毫克的锌片。第五组同时服用 50 毫克/千克硒片剂和 50 毫克/千克锌片剂。暴露持续 7 天(亚急性暴露):结果:FAN 通过显著的细胞毒性(p p p p 结论:抗氧化剂对细胞毒性的影响很小:我们的研究支持这样一种观点,即抗氧化微量营养素(硒和锌)片剂可能是一种有效的调节剂,可减轻 FAN 对雄性大鼠诱导的氧化应激和细胞毒性。研究表明,硒和锌胶囊的组合可促进与 Fansidar 同时治疗的器官的健康。
Fansidar drug induces cytotoxicity in some vital tissues in a rat model: combination defensive effect of selenium and zinc capsules.
Aim: Fansidar (FAN) is widely used as an antimalarial drug, but it may cause hepatoxicity, nephrotoxicity, and neurotoxicity. Hence, the study examines the cytoprotection of selenium (Se) and zinc (Zn) tablets against FAN induced toxicity.
Method: Group I was given distilled water. Groups II, III, IV, and V received 50 mg/kg FAN by gavage. Group III was co-treated with a 50 mg/kg Se tablet. Group IV was co-treated with a 50 mg/kg Zn tablet. Group V was co-treated with a 50 mg/kg Se tablet + 50 mg/kg Zn tablet. The exposure lasted for 7 days (sub-acute exposure).
Result: FAN causes cytotoxicity through significant (p < 0.05) alteration of antioxidant molecules and hepatic enzymes. It also significantly (p < 0.05) induces renal, hepatocyte, and purkinje cell damage, but no visible lesion on testicular cells. The FAN induced cytotoxicity was significantly (p < 0.05) reversed on treatment with both single and combined antioxidant tablets.
Conclusion: Our study supports the view that antioxidant micronutrient (Se and Zn) tablets may be a useful modulator in alleviating FAN induced oxidative stress and cytotoxicity in male rats.
Plain language summary: Combined selenium and zinc capsules: better therapy against cytotoxicity Fansidar was approved by United States' Food and Drug Administration as an anti-malarial drug to treat acute and complicated malaria fever among patients in West Africa; however, its usage elicits toxicity to several organs of the body. It was elucidated that the combination of selenium and zinc capsules promotes organ wellness on co-treatment with Fansidar.
期刊介绍:
Therapeutic Advances in Drug Safety delivers the highest quality peer-reviewed articles, reviews, and scholarly comment on pioneering efforts and innovative studies pertaining to the safe use of drugs in patients.
The journal has a strong clinical and pharmacological focus and is aimed at clinicians and researchers in drug safety, providing a forum in print and online for publishing the highest quality articles in this area. The editors welcome articles of current interest on research across all areas of drug safety, including therapeutic drug monitoring, pharmacoepidemiology, adverse drug reactions, drug interactions, pharmacokinetics, pharmacovigilance, medication/prescribing errors, risk management, ethics and regulation.