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Modulating effect of graphine oxide loaded Hesperidin nanocomposite on 1,2-dimethylhydrazine provoked primary tumorabrasion, oxidative strain and alterations in biological enzymes, in tentative model of rat colon carcinogenesis via inhibition iNOs,COX-2 pathway
Arabian Journal of Chemistry ( IF 5.3 ) Pub Date : 2020-08-01 , DOI: 10.1016/j.arabjc.2020.06.025
Jin Liu , Xiaoyan Ma , LingWang

Abstract Hesperidin is a flavonoid derived from citrus plant peels. It have convinced biological actions, which includes antioxidant possessions, anti-inflammatory outcome, and thus we investigate that hesperidin will encompass chemopreventive probable next to 1,2-dimethylhydrazine (DMH)-provoked experimental colon carcinogenesis in male Wistar rats. Rats were randomly alienated into six groups. Group I rats were considered as control. Group II rats received only DMH. Groups III&IV animals received 20 mg/kg b.w of DMH subcutaneous one time a week, for initial 4 weeks. In adding, groups III & IV animals given DMH along with hesperidin at the dose of 5&10mg/kg b.w., correspondingly for about 16 weeks. In present study we optimized hesperidin loaded with graphine oxide as a result achieved and was itemized and illustrated by UV Visible spectroscopy (876.25 nm), X-Ray diffraction, Fourier Transform Infrared Spectroscopy and Dynamic light scattering (45.50nm). Hesperidin to the DMH induced rats drastically diminished the incidence of polyps as contrast to the DMH alone animals. Additionally in hesperidin management over DMH exposed experimental rats, we observed elevated actions of the oxidation inhibitors and diminished planes of LPO in liver and passage along with improved stage of lipids and antioxidants in colon tissues, which be distorted in the DMH unaided rats. Moreover, we experiential tainted actions of Interleukins, tumor necrosis factor and bioactive enzymes in DMH only rats, which are upturned in hesperidin treatment. All remarks are sustained in our histological conclusion. Ultimately, hesperidin might worned as effectual chemopreventive agent adjacent to DMH tempted colon cancer.

中文翻译:

氧化石墨烯负载橙皮苷纳米复合材料对 1,2-二甲基肼引起的原发性肿瘤磨损、氧化应变和生物酶改变的调节作用,在大鼠结肠癌的初步模型中通过抑制 iNOs、COX-2 途径

摘要 橙皮苷是一种来源于柑橘类植物皮的黄酮类化合物。它已经证实了生物学作用,包括抗氧化物质、抗炎结果,因此我们研究橙皮苷将包括可能与 1,2-二甲基肼 (DMH) 诱发的雄性 Wistar 大鼠实验性结肠癌发生相邻的化学预防。将大鼠随机分为六组。I组大鼠被认为是对照。II组大鼠仅接受DMH。在最初的 4 周内,III 和 IV 组动物每周一次皮下注射 20 毫克/千克体重的 DMH。此外,第 III 组和 IV 组动物以 5 和 10 毫克/千克体重的剂量给予 DMH 和橙皮苷,相应地持续约 16 周。在本研究中,我们优化了载有氧化石墨的橙皮苷,并通过紫外可见光谱 (876.25 nm)、X 射线衍射、傅里叶变换红外光谱和动态光散射 (45.50 nm) 逐项列出和说明。与单独使用 DMH 的动物相比,橙皮苷对 DMH 诱导的大鼠显着降低了息肉的发生率。此外,在对 DMH 暴露实验大鼠的橙皮苷管理中,我们观察到氧化抑制剂的作用升高,肝脏和通道中的 LPO 平面减少,以及结肠组织中脂质和抗氧化剂的改善阶段,这些在 DMH 独立大鼠中被扭曲。此外,我们在仅 DMH 的大鼠中体验了白细胞介素、肿瘤坏死因子和生物活性酶的受污染作用,这些作用在橙皮苷治疗中被逆转。我们的组织学结论支持所有评论。最终,橙皮苷可能作为有效的化学预防剂与 DMH 诱发的结肠癌相邻。
更新日期:2020-08-01
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