Crocin Possesses Excellent Hepatoprotective Effects Against Acetaminophen-Induced Hepatotoxicity in Mice

IF 1 Q4 PHARMACOLOGY & PHARMACY Jundishapur Journal of Natural Pharmaceutical Products Pub Date : 2021-12-31 DOI:10.5812/JJNPP.115165
Leila Fouladi, H. Kalantar, M. Khodayar, M. Shirani, L. Khorsandi, Masoud Mahdavinia
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引用次数: 1

Abstract

Background: Acetaminophen (APAP) is a common analgesic and antipyretic medicine that can lead to acute liver injury at high doses. Crocin, a Crocus sativus’ ingredient, has potent antioxidant effects. Objectives: This study examined the protective effects of crocin against APAP-induced oxidative stress in mice. Methods: In this study, 56 mice were randomly divided into seven groups (n = 8 per group), including the negative (normal saline, 10 mL/kg) and positive (oral normal saline for five days + a single dose of APAP (300 mg/kg) on day 6th) control groups. The third group (NAC) received normal saline for up to five days, and on the 6th day, immediately after the administration of acetaminophen, received NAC (50 mg/kg). Groups fourth to sixth received respectively 12.5, 25, and 50 mg/kg of crocin (orally for six days), followed by a single dose of APAP (300 mg/kg) on 6th day. The last group received crocin (50 mg/kg) for six days. Then 24 h after the last injection, the animals were sacrificed, and samples were collected for biochemical and histopathological evaluations. Results: The levels of ALT, AST, and MDA increased, and the activity of CAT, GSH, and GPX decreased in the APAP-treated group compared to the control group. In APAP-treated groups, the administration of crocin decreased the serum levels of AST, ALT, and MDA and increased the activity of CAT, GSH, and GPX. Histopathological evaluations confirmed the above findings. Conclusions: According to our results, it seems that crocin has a protective effect against acetaminophen-induced liver toxicity and can be used as a therapeutic agent to treat APAP-induced hepatotoxicity.
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藏红花素对对乙酰氨基酚所致小鼠肝毒性具有良好的保护作用
背景:对乙酰氨基酚(APAP)是一种常见的镇痛退热药,大剂量使用可导致急性肝损伤。番红花素是番红花的一种成分,具有强大的抗氧化作用。目的:研究番红花苷对APAP诱导的小鼠氧化应激的保护作用。方法:本研究将56只小鼠随机分为7组(每组n=8),包括阴性(生理盐水,10mL/kg)和阳性(口服生理盐水5天+第6天单剂量APAP(300mg/kg))对照组。第三组(NAC)接受生理盐水长达5天,第6天,在给予对乙酰氨基酚后立即接受NAC(50mg/kg)。第4至第6组分别接受12.5、25和50 mg/kg番红花苷(口服6天),然后在第6天接受单剂量APAP(300 mg/kg)。最后一组接受番红花苷(50mg/kg)治疗6天。最后一次注射后24小时,处死动物,收集样本进行生化和组织病理学评估。结果:与对照组相比,APAP治疗组的ALT、AST和MDA水平升高,CAT、GSH和GPX活性降低。在APAP治疗组中,服用番红花苷降低了血清AST、ALT和MDA水平,并增加了CAT、GSH和GPX的活性。组织病理学评估证实了上述发现。结论:根据我们的研究结果,番红花苷似乎对对乙酰氨基酚诱导的肝毒性具有保护作用,可以作为治疗APAP诱导的肝中毒的药物。
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CiteScore
1.40
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26
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