Banana peel extract alleviate inflammation and oxidative stress via modulation of the Nrf2/Hmox-1 and NF-κB pathways in thyroid of heavy metal mixture exposed female rats

Boma F. Eddie-Amadi, A. Ezejiofor, C. Orish, A. Ćirović, Aleksandar Cirovic, O. Orisakwe
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Abstract

This is an evaluation of the effects of banana peel BP extract on the heavy metals’ mixture HMM mediated oxido-inflammatory effects in the thyroid of female albino rats. Five groups (5 female rats/group) were treated as follows for 60 days: Group 1: Deionized water only; Group 2: (Pb, Hg, Mn and Al); Group 3: 200 mg/kg BP extract + HMM; Group 4: 400 mg/kg BP extract + HMM; Group 5: 800 mg/kg BP extract + HMM. On day 60 animals were euthanized, thyroid was harvested and used for, malondialdehyde MDA, nitric oxide NO, antioxidants, tumor necrosis factor alpha (TNF – α), interleukin 6 (IL – 6), Caspase-3, Nuclear factor erythroid 2- related factor 2 (Nrf2), Nuclear factor kappa B (NfkB) and Heme Oxygynase – 1 (Hmox-1) and histopathology. There was significant bioaccumulation of Pb, Al, Hg and MN; elevated IL-6 and Tnf-α, MDA and NO, caspase-3 and Nrf2, NF-κB and Hmox-1 in the HMM only group in comparison to the control. There was significant ( p < 0.05) decrease in SOD, CAT GSH activities in HMM only exposed group in comparison to the control deionized water group, whereas BP co-treatment with HMM significantly ( p < 0.05) increased SOD, CAT GSH activities. Co-treatment with BP extract also reversed most of these effects. BP extract may ameliorate HMM -induced thyrotoxicity in female albino rats by blunting oxido-inflammatory activities.
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香蕉皮提取物通过调节重金属混合物暴露雌性大鼠甲状腺Nrf2/Hmox-1和NF-κB通路减轻炎症和氧化应激
本文研究了香蕉皮BP提取物对重金属混合物HMM介导的雌性白化大鼠甲状腺氧化炎症的影响。5组(雌鼠5只/组)按以下方法治疗60 d:第1组:只给去离子水;第2组:(Pb、Hg、Mn和Al);第三组:200 mg/kg BP提取物+ HMM;第4组:400mg /kg BP提取物+ HMM;第5组:800 mg/kg BP提取物+ HMM。第60天处死动物,取甲状腺用于丙二醛MDA、一氧化氮NO、抗氧化剂、肿瘤坏死因子α (TNF - α)、白细胞介素6 (IL - 6)、Caspase-3、核因子红细胞2相关因子2 (Nrf2)、核因子κ B (NfkB)和血红素氧合酶-1 (Hmox-1)和组织病理学检查。Pb、Al、Hg、MN的生物富集显著;与对照组相比,单纯HMM组IL-6、Tnf-α、MDA、NO、caspase-3、Nrf2、NF-κB、Hmox-1均升高。与去离子水对照组相比,HMM单独处理组SOD、CAT - GSH活性显著(p < 0.05)降低,BP与HMM共处理组SOD、CAT - GSH活性显著(p < 0.05)升高。与BP提取物共同治疗也逆转了大部分这些影响。BP提取物可能通过减弱氧化炎症活性来改善HMM诱导的雌性白化大鼠甲状腺毒性。
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