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丁香酚对雄性小鼠分离的胰岛中过氧化氢诱导的氧化应激的抗氧化作用。

Antioxidant Effects of Eugenol on Oxidative Stress Induced by Hydrogen Peroxide in Islets of Langerhans Isolated from Male Mouse.

作者信息

Oroojan Ali Akbar, Chenani Narges, An'aam Marzieh

机构信息

Department of Physiology, Faculty of Medicine, Student Research Committee, Dezful University of Medical Sciences, Dezful, Iran.

Student Research Committee, Faculty School of Paramedical Sciences, Dezful University of Medical Sciences, Dezful, Iran.

出版信息

Int J Hepatol. 2020 Dec 30;2020:5890378. doi: 10.1155/2020/5890378. eCollection 2020.

Abstract

BACKGROUND

The antioxidant system in islets of Langerhans is weak, which can lead to diabetes. Meanwhile, the main component of cloves that produce antioxidant effects is eugenol. Accordingly, the present study was conducted to investigate the antioxidant effect of eugenol on oxidative stress induced by hydrogen peroxide (HO) in islets of Langerhans isolated from the male mice.

MATERIALS AND METHODS

In this experimental study, adult Naval Medical Research Institute (NMRI) mice (20-25 g) were prepared. The collagenase digestion method was used for dissecting the islets of Langerhans. HO 50 M was administered for 30 min to induce oxidative stress, with 50, 100, and 200 M of eugenol employed for 2 hours before the administration of HO. The experimental groups were divided into five groups: (control, HO, and HO+eugenol 50, 100, and 200 M). Finally, the islet's lipid peroxidation and antioxidants levels were measured by the ELISA assay method.

RESULTS

Malondialdehyde (MDA), total antioxidant capacity (TAC), superoxide dismutase (SOD), and catalase (CAT) increased in all groups when compared to the control ( < 0.05). MDA diminished in HO+eugenol 50, 100, and 200 M ( < 0.01) groups versus the HO. TAC was elevated when eugenol 50, 100, and 200 M was administered in oxidative stress-induced islets ( < 0.001). Also, CAT increased in the HO+eugenol 50 ( < 0.05) group in comparison with the HO group.

CONCLUSIONS

In conclusion, HO induced oxidative stress and lipid peroxidation in the islets, and administration of eugenol recovered these alterations by raising the level of TAC and CAT, while reducing MDA as a lipid peroxidation biomarker.

摘要

背景

胰岛中的抗氧化系统较弱,这可能导致糖尿病。同时,丁香产生抗氧化作用的主要成分是丁香酚。因此,本研究旨在探讨丁香酚对雄性小鼠分离的胰岛中过氧化氢(H₂O₂)诱导的氧化应激的抗氧化作用。

材料与方法

在本实验研究中,制备了成年海军医学研究所(NMRI)小鼠(20 - 25克)。采用胶原酶消化法分离胰岛。给予50μM H₂O₂ 30分钟以诱导氧化应激,在给予H₂O₂前2小时使用50、100和200μM丁香酚。实验组分为五组:(对照组、H₂O₂组以及H₂O₂ + 50、100和200μM丁香酚组)。最后,通过酶联免疫吸附测定(ELISA)法测量胰岛的脂质过氧化和抗氧化剂水平。

结果

与对照组相比,所有组的丙二醛(MDA)、总抗氧化能力(TAC)、超氧化物歧化酶(SOD)和过氧化氢酶(CAT)均升高(P < 0.05)。与H₂O₂组相比,H₂O₂ + 50、100和200μM丁香酚组的MDA降低(P < 0.01)。在氧化应激诱导的胰岛中给予50、100和200μM丁香酚时,TAC升高(P < 0.001)。此外,与H₂O₂组相比,H₂O₂ + 50μM丁香酚组的CAT升高(P < 0.05)。

结论

总之,H₂O₂诱导胰岛氧化应激和脂质过氧化,而给予丁香酚通过提高TAC和CAT水平,同时降低作为脂质过氧化生物标志物的MDA,恢复了这些改变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3afc/7787786/9f77d46141cd/IJH2020-5890378.001.jpg

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