曼氏黄瓜籽油通过减轻大鼠炎症和氧化应激来保护大鼠免受双酚a诱导的肝毒性

Patrick Maduabuchi Aja, Chinecherem Adanna Chukwu, Ugwu Okechukwu Paul-Chima, Boniface Anthony Ale, Peter Chinedu Agu, Tusubira Deusdedi, Darlington C Chukwu, Onyedika Gabriel Ani, Ezebuilo Ugbala Ekpono, Hilary Akobi Ogwoni, Joshua Nonso Awoke, Patience N Ogbu, Lucy Aja, Oliver Ugochukwu Ukachi, Obasi Uche Orji, Chinoso Peter Nweke, Chinedu Egwu, Ejike Ugbala Ekpono, Gift Onyinyechi Ewa, Ikechuku Okorie Igwenyi, Esther Ugo Alum, Daniel Ejim Uti, Christian Emeka Offor, Josiah E Ifie, Amaobichukwu Njoku, Maduagwunna Ekenechukwu Kenneth, Ejike Daniel Eze
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引用次数: 0

摘要

【摘要】目的观察双酚a对雄性Wistar白化大鼠肝损伤的影响。方法采用高效液相色谱法测定双酚a对雄性Wistar白化大鼠肝损伤的影响。然后,六组(n = 8) 48只雄性Wistar大鼠(150 - 20克)分别接受CMSO或橄榄油,然后暴露于BPA 42天。组:A(1毫升橄榄油,不论重量)、B (BPA 100毫克/公斤体重)、C (CMSO 7.5毫克/公斤体重)、D (CMSO 7.5毫克/公斤体重+ BPA 100毫克/公斤体重)、E (CMSO 5.0毫克/公斤体重+ BPA 100毫克/公斤体重)、F (CMSO 2.5毫克/公斤体重+ BPA 100毫克/公斤体重)。HPLC数据显示,黄酮类化合物的含量高达17.800 ~ 10.95 g/100 g。双酚a组丙二醛、肝酶、活性氧、总胆红素和直接胆红素水平均显著升高(p 0.05)。此外,核因子- b、白细胞介素-6、白细胞介素-1、肿瘤坏死因子及组织学改变均显著(p < 0.05)。然而,通过CMSO,改变的生化标志物和组织学明显恢复到与对照组相当的水平。结论丁香精油中含有丰富的黄酮类成分,可通过降低氧化应激和炎症反应,保护肝脏免受bpa诱导的肝毒性。
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Cucumeropsis mannii seed oil protects against bisphenol A-induced hepatotoxicity by mitigating inflammation and oxidative stress in rats
Abstract OBJECTIVES This study looked at how CMSO affected male Wistar albino rats' liver damage caused by bisphenol A. METHODS The standard HPLC method was used to assess the CMSO's phenolic content. Then, six (n = 8) groups of forty-eight (48) male Wistar rats (150 20 g) each received either CMSO or olive oil before being exposed to BPA for 42 days. Groups: A (one milliliter of olive oil, regardless of weight), B (BPA 100 mg/kg body weight (BW)), C (CMSO 7.5 mg/kg BW), D (CMSO 7.5 mg/kg BW + BPA 100 mg/kg BW), E (CMSO 5.0 mg/kg BW + BPA 100 mg/kg BW), and F (CMSO 2.5 mg/kg BW + BPA 100 mg/kg BW). KEY FINDINGS A surprising abundance of flavonoids, totaling 17.8006 10.95 g/100 g, were found in the HPLC data. Malondialdehyde, liver enzymes, reactive oxygen species, total bilirubin, and direct bilirubin levels were all significantly elevated by BPA (p 0.05). Additionally, nuclear factor-B, interleukin-6, interleukin-1, tumor necrosis factor, and histological alterations were all considerably (p 0.05) caused by BPA. The altered biochemical markers and histology were, however, noticeably recovered by CMSO to a level that was comparable to the control. CONCLUSION Due to the abundance of flavonoid components in the oil, CMSO protects the liver from BPA-induced hepatotoxicity by lowering oxidative stress and inflammatory reactions.
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