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氧化应激标志物F2-异前列腺素和早老素-1在临床诊断的阿尔茨海默病中的作用

Role of Oxidative Stress Markers F2-Isoprostanes and Presenilin-1 in Clinical Diagnosed Alzheimer's Diseases.

作者信息

Timalsina Dilip Raj, Abichandani Leela, Ambad Ranjit

机构信息

Department of Biochemistry, Datta Meghe Medical College, Nagpur, Datta Meghe Institute of Higher Education and Research (DU) Sawangi Wardha, Maharashtra, India.

Department of Biochemistry, Jawaharlal Nehru Medical College, Wardha, Datta Meghe Institute of Higher Education and Research (DU) Sawangi Wardha, Maharashtra, India.

出版信息

J Pharm Bioallied Sci. 2025 May;17(Suppl 1):S384-S387. doi: 10.4103/jpbs.jpbs_1786_24. Epub 2025 Apr 25.

Abstract

INTRODUCTION

Oxidative stress is an important component in the pathogenesis of Alzheimer's disease (AD).

MATERILS AND METHODS

A comparative cross-sectional study was conducted on 140 participants who made up 70 subjects diagnosed with AD and 70 controls. Serum levels of F2-isoprostanes and Presenilin 1 were estimated using ELISA. These markers were significantly elevated in the serum of AD patients, suggesting them to be potential biomarkers for early diagnosis and disease progression.

AIM AND OBJECTIVE

In this study, the level of F2-isoprostanes and Presenilin 1 was determined in patients clinically diagnosed with AD, thus establishing a possible relationship between heightened markers for oxidative stress and progression of AD.

RESULTS

The results showed significantly elevated levels of F2-isoprostanes (179.38 ± 3.01 pg/mL vs 85.89 ± 0.97 pg/mL, < 0.0001) and Presenilin 1 (93.26 ± 2.39 ng/mL vs 49.46 ± 0.78 ng/mL, < 0.0001) in AD patients compared to controls. Additionally, markers of lipid peroxidation, such as malondialdehyde (MDA), were elevated in AD patients, while antioxidant defense mechanisms, including glutathione (GSH) and superoxide dismutase (SOD), were significantly impaired ( < 0.0001).

CONCLUSION

This study provides compelling evidence that oxidative stress, as shown by elevated levels of F2-isoprostanes and Presenilin 1, plays a crucial role in the onset of AD.

摘要

引言

氧化应激是阿尔茨海默病(AD)发病机制中的一个重要组成部分。

材料与方法

对140名参与者进行了一项比较横断面研究,其中包括70名被诊断为AD的受试者和70名对照者。使用酶联免疫吸附测定法(ELISA)评估血清中F2-异前列腺素和早老素1的水平。这些标志物在AD患者血清中显著升高,表明它们可能是早期诊断和疾病进展的潜在生物标志物。

目的

在本研究中,测定了临床诊断为AD的患者中F2-异前列腺素和早老素1的水平,从而确定氧化应激标志物升高与AD进展之间的可能关系。

结果

结果显示,与对照组相比,AD患者的F2-异前列腺素水平(179.38±3.01 pg/mL对85.89±0.97 pg/mL,<0.0001)和早老素1水平(93.26±2.39 ng/mL对49.46±0.78 ng/mL,<0.0001)显著升高。此外,AD患者中脂质过氧化标志物如丙二醛(MDA)升高,而包括谷胱甘肽(GSH)和超氧化物歧化酶(SOD)在内的抗氧化防御机制显著受损(<0.0001)。

结论

本研究提供了有力证据,表明F2-异前列腺素和早老素1水平升高所显示的氧化应激在AD发病中起关键作用。

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