Hanan Sabry Abd El-Shafi Ahmed, Ashraf A. A.Elkomy, Enas A.H. Farag
{"title":"评价南瓜籽油对环丙沙星诱导的雄性白化大鼠肝肾毒性的保护作用","authors":"Hanan Sabry Abd El-Shafi Ahmed, Ashraf A. A.Elkomy, Enas A.H. Farag","doi":"10.14419/ijpt.v10i1.31908","DOIUrl":null,"url":null,"abstract":"Background: Ciprofloxacin increased the production of reactive oxygen species, As a result of its intracellular accumulation, which leads to extracellular membrane damage, resulting in the release of apoptotic components into the bloodstream, a condition known as apoptosis.Objective: The goal of this study is to investigate the protective effect of pumpkin seeds oil (PSO), a well-known natural antioxidant against Ciprofloxacin-induced liver and kidney impairment (CPFX[i]).Material and methods: Forty-Four male albino rats weighing approximately 180–200 gm were formed. (n = 10): (1) control saline, (2) PSO [ii] (4ml/kg/day orally for 4 weeks), (3) CPFX (80mg/kg/day orally for 2 weeks), and (4) PSO (4ml/kg/day orally for 4 weeks) + CPFX (80mg/kg/day orally for 2 weeks), starting on the first day of the third week. Finally, Serum and tissue specimens are collected at the conclusion of the experiment for biochemical and histopathological examination. Results: It ended up being found in the CPFX-treated group. ALT [iii], AST [iv], and TNFα[v] levels were all significantly elevated in the serum. While this medication reduced the hepatocellular content of GSH [vi], it increased the tissue content of MDA [vii], which clearly shows oxidative stress Reduced BCL2[viii] levels also indicate the presence of apoptosis. CPFX causes an increase in kidney-specific markers such as creatinine and urea, indicating kidney disease. When PSO was combined with CPFX BAX [ix], MDA, AST, ALT, and TNFα levels were considerably reduced, while GSH and BCL2 levels increased, indicating that PSO has antioxidant action and reduces apoptosis. Additionally, the renal function parameters improved, as seen by lower serum creatinine and urea levels.Conclusion: In rats, employing PSO as a concurrent prophylactic therapy while administering CPFX effectively reduced CPFX-induced oxidative stress and apoptotic damage. PSO could be used as a preventive medication to prevent CPFX-induced cellular damage to the kidneys and liver.   ","PeriodicalId":13897,"journal":{"name":"International journal of clinical pharmacology, therapy and toxicology","volume":"96 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-02-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Evaluating the protective impact of pumpkin seeds oil against ciprofloxacin induced hepatorenal toxicity in the male albino rats\",\"authors\":\"Hanan Sabry Abd El-Shafi Ahmed, Ashraf A. A.Elkomy, Enas A.H. Farag\",\"doi\":\"10.14419/ijpt.v10i1.31908\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Background: Ciprofloxacin increased the production of reactive oxygen species, As a result of its intracellular accumulation, which leads to extracellular membrane damage, resulting in the release of apoptotic components into the bloodstream, a condition known as apoptosis.Objective: The goal of this study is to investigate the protective effect of pumpkin seeds oil (PSO), a well-known natural antioxidant against Ciprofloxacin-induced liver and kidney impairment (CPFX[i]).Material and methods: Forty-Four male albino rats weighing approximately 180–200 gm were formed. (n = 10): (1) control saline, (2) PSO [ii] (4ml/kg/day orally for 4 weeks), (3) CPFX (80mg/kg/day orally for 2 weeks), and (4) PSO (4ml/kg/day orally for 4 weeks) + CPFX (80mg/kg/day orally for 2 weeks), starting on the first day of the third week. Finally, Serum and tissue specimens are collected at the conclusion of the experiment for biochemical and histopathological examination. Results: It ended up being found in the CPFX-treated group. ALT [iii], AST [iv], and TNFα[v] levels were all significantly elevated in the serum. While this medication reduced the hepatocellular content of GSH [vi], it increased the tissue content of MDA [vii], which clearly shows oxidative stress Reduced BCL2[viii] levels also indicate the presence of apoptosis. CPFX causes an increase in kidney-specific markers such as creatinine and urea, indicating kidney disease. When PSO was combined with CPFX BAX [ix], MDA, AST, ALT, and TNFα levels were considerably reduced, while GSH and BCL2 levels increased, indicating that PSO has antioxidant action and reduces apoptosis. Additionally, the renal function parameters improved, as seen by lower serum creatinine and urea levels.Conclusion: In rats, employing PSO as a concurrent prophylactic therapy while administering CPFX effectively reduced CPFX-induced oxidative stress and apoptotic damage. 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引用次数: 0
摘要
背景:环丙沙星增加活性氧的产生,由于其在细胞内积聚,导致胞外膜损伤,导致凋亡成分释放到血液中,这种情况称为细胞凋亡。目的:探讨南瓜籽油(PSO)对环丙沙星所致肝肾损害(CPFX)的保护作用[i]。材料与方法:取体重约180 ~ 200gm的雄性白化大鼠44只。(n = 10):(1)对照生理盐水,(2)PSO [ii] (4ml/kg/天口服,持续4周),(3)CPFX (80mg/kg/天口服,持续2周),(4)PSO (4ml/kg/天口服,持续4周)+ CPFX (80mg/kg/天口服,持续2周),从第三周第一天开始。最后,在实验结束时采集血清和组织标本进行生化和组织病理学检查。结果:cpfx治疗组均有出现。血清ALT [iii]、AST [iv]、TNFα[v]水平均显著升高。该药物在降低肝细胞GSH含量[vi]的同时,增加了组织MDA含量[vii],这清楚地表明氧化应激降低的BCL2[viii]水平也表明细胞凋亡的存在。CPFX引起肾脏特异性标志物如肌酐和尿素的增加,表明肾脏疾病。当PSO联合CPFX BAX [ix]时,MDA、AST、ALT和TNFα水平明显降低,GSH和BCL2水平升高,表明PSO具有抗氧化作用,减少细胞凋亡。此外,肾功能参数得到改善,如血清肌酐和尿素水平降低。结论:大鼠在给予CPFX的同时采用PSO进行预防治疗,可有效降低CPFX诱导的氧化应激和细胞凋亡损伤。PSO可作为预防药物,预防cpfx引起的肾、肝细胞损伤。  Â
Evaluating the protective impact of pumpkin seeds oil against ciprofloxacin induced hepatorenal toxicity in the male albino rats
Background: Ciprofloxacin increased the production of reactive oxygen species, As a result of its intracellular accumulation, which leads to extracellular membrane damage, resulting in the release of apoptotic components into the bloodstream, a condition known as apoptosis.Objective: The goal of this study is to investigate the protective effect of pumpkin seeds oil (PSO), a well-known natural antioxidant against Ciprofloxacin-induced liver and kidney impairment (CPFX[i]).Material and methods: Forty-Four male albino rats weighing approximately 180–200 gm were formed. (n = 10): (1) control saline, (2) PSO [ii] (4ml/kg/day orally for 4 weeks), (3) CPFX (80mg/kg/day orally for 2 weeks), and (4) PSO (4ml/kg/day orally for 4 weeks) + CPFX (80mg/kg/day orally for 2 weeks), starting on the first day of the third week. Finally, Serum and tissue specimens are collected at the conclusion of the experiment for biochemical and histopathological examination. Results: It ended up being found in the CPFX-treated group. ALT [iii], AST [iv], and TNFα[v] levels were all significantly elevated in the serum. While this medication reduced the hepatocellular content of GSH [vi], it increased the tissue content of MDA [vii], which clearly shows oxidative stress Reduced BCL2[viii] levels also indicate the presence of apoptosis. CPFX causes an increase in kidney-specific markers such as creatinine and urea, indicating kidney disease. When PSO was combined with CPFX BAX [ix], MDA, AST, ALT, and TNFα levels were considerably reduced, while GSH and BCL2 levels increased, indicating that PSO has antioxidant action and reduces apoptosis. Additionally, the renal function parameters improved, as seen by lower serum creatinine and urea levels.Conclusion: In rats, employing PSO as a concurrent prophylactic therapy while administering CPFX effectively reduced CPFX-induced oxidative stress and apoptotic damage. PSO could be used as a preventive medication to prevent CPFX-induced cellular damage to the kidneys and liver.  Â