Hepatoprotective effect of Nobiletin against 5-fluorouracil induce hepatotoxicity

Q2 Agricultural and Biological Sciences Current Research in Pharmacology and Drug Discovery Pub Date : 2024-01-01 DOI:10.1016/j.crphar.2024.100199
Safa A. Yahya, Nada N. Al-Shawi
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Abstract

5-florouracil is a widely used anticancer/anti-metabolite drug used to treat solid tumor like colon cancer, head and neck, rectum, stomach, pancreas and breast cancer; but, it can cause hepatotoxicity by induction of apoptosis through activation of caspases enzymes and oxidative stress. Nobiletin is a citrus fruit-derived flavonoid that possess significant biological activity, including anticancer, and anti-inflammatory. This study was design to investigate the effects of nobiletin against 5-florouracil-indcued hepatotoxicity in male rats through the measurement of selected -inflammatory, -apoptosis, and -oxidative stress markers. By use male Albino rats weighing 150-250gm around 28 animals; giving them tap water ad libitum and fed commercial pellets; and randomized into four groups (7animals/group) as following arrangement: Group I oral administered only corn oil for rats 1 ml for each kilogram for day by using of oral gavage for rat for 14 days. Group II: oral administered Nobiletin at dose 10 mg for each kilogram for each day (dissolved in corn oil) via oral gavage for 14 days. Group III: oral administered corn oil via oral gavage for 14 days after that single IP injection of 5-FU (150 mg/kg) on the day fourteenth (14). Group VI: Rats oral administered nobiletin dissolved in corn oil daily by oral gavage at a dose 10 mg/kg for each day for 14 days and a single IP injection of (150 mg/kg) 5-florouracil was given on day 14. All groups, seven animals of each group were sacrificed at day fifteenth (15); and, serum was collected to measure inflammatory and anti-inflammatory markers (interlukin-6 and interlukin-10) and liver function tests(ALT, LDH and AST); furthermore, liver tissue samples were collected to measure level of caspase-3, malondialdehyde and reduced form of glutathione, assessment of Hemeoxygenase-1 and NADPH quinone dehydrogenase-1 enzymes. In addition, histopathological study of the liver tissue of rats was perform to detect difference between architecture of liver cells in all rats’ groups. The protective effect of Nobiletin noted by decrease in apoptosis of hepatocytes by decreasing of caspase-3 and reduction on free radical through reduce in malondialdehyde level, also increase in Hemeoxygenase-1gene expression. Increase in NADPH quinone dehydrogenase-1 dehydrogenase enzyme. On histopath reduce in congestion and some inflammatory infiltration by using of nobiletin prior to give 5-florouracil.

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金雀花素对 5-氟尿嘧啶诱导的肝毒性的保护作用
5- 氟尿嘧啶是一种广泛使用的抗癌/抗代谢药物,用于治疗结肠癌、头颈部癌、直肠癌、胃癌、胰腺癌和乳腺癌等实体瘤;但它会通过激活 Caspases 酶和氧化应激诱导细胞凋亡,从而引起肝中毒。金霉素是一种源自柑橘类水果的黄酮类化合物,具有显著的生物活性,包括抗癌和抗炎。本研究旨在通过测量选定的炎症、细胞凋亡和氧化应激标记物,研究金没药对 5-氟尿嘧啶诱导的雄性大鼠肝毒性的影响。采用体重 150-250gm 的雄性白化大鼠 28 只,自由饮用自来水,喂食商品颗粒饲料,并按以下方法随机分为四组(每组 7 只):I 组:大鼠每天每公斤口服 1 毫升玉米油,连续 14 天。第二组:大鼠每天每公斤口服剂量为 10 毫克的诺比利汀(溶于玉米油中),连续口服 14 天。第三组:在第 14 天(14 日)IP 注射一次 5-FU(150 毫克/千克)后,口服玉米油,连续 14 天。第六组:大鼠每天口服 10 毫克/千克溶于玉米油的金霉素,连续 14 天,然后在第 14 天单次 IP 注射(150 毫克/千克)5-氟尿嘧啶。第 15 天,每组七只动物被处死;收集血清以测量炎症和抗炎标志物(interlukin-6 和 interlukin-10)以及肝功能测试(ALT、LDH 和 AST);此外,收集肝组织样本以测量 Caspase-3、丙二醛和还原型谷胱甘肽的水平,评估血氧合酶-1 和 NADPH 醌脱氢酶-1 的酶。此外,还对大鼠的肝组织进行了组织病理学研究,以检测各组大鼠肝细胞结构的差异。金没药的保护作用体现在通过降低 caspase-3 减少肝细胞凋亡,通过降低丙二醛水平减少自由基,以及增加血氧合酶-1 基因的表达。NADPH 醌脱氢酶-1 脱氢酶增加。在组织病理学方面,在使用 5-氟尿嘧啶之前,使用金霉素可减少充血和一些炎症浸润。
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来源期刊
Current Research in Pharmacology and Drug Discovery
Current Research in Pharmacology and Drug Discovery Agricultural and Biological Sciences-Animal Science and Zoology
CiteScore
6.40
自引率
0.00%
发文量
65
审稿时长
40 days
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