4.7 Article

Lipoamide Ameliorates Oxidative Stress via Induction of Nrf2/ARE Signaling Pathway in PC12 Cells

Journal

JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
Volume 67, Issue 29, Pages 8227-8234

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jafc.9b02680

Keywords

lipoamide; oxidative stress; antioxidant; Nrf2; neuroprotective effect

Funding

  1. National Natural Science Foundation of China [21572093, 21778028]
  2. 111 project

Ask authors/readers for more resources

The mechanisms underlying neurodegenerative diseases are not fully understood yet. However, an increasing amount of evidence has suggested that these disorders are related to oxidative stress. We reported herein that lipoamide (LM), a neutral amide derivative of lipoic acid (LA), could resist oxidative stress-mediated neuronal cell damage. LM is more potent than LA in alleviating hydrogen peroxide- or 6-hydroxydopamine-induced PC12 cell injury. Our results reveal that LM promotes the nuclear accumulation of NFE2-related factor 2 (Nrf2), following with the activation of expression of Nrf2-governed antioxidant and detoxifying enzymes. Notably, silencing Nrf2 gene annuls the protection of LM, which demonstrates that Nrf2 is engaged in this cytoprotection. Our findings suggest that LM might be used as a potential therapeutic candidate for oxidative stress-related neurological disorders.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

Review Chemistry, Medicinal

Small molecules regulating reactive oxygen species homeostasis for cancer therapy

Junmin Zhang, Dongzhu Duan, Zi-Long Song, Tianyu Liu, Yanan Hou, Jianguo Fang

Summary: Regulating intracellular ROS levels may be an effective strategy for cancer prevention or treatment. This can be achieved through chemoprevention to reduce ROS production pathways, or through ROS-mediated anticancer therapy to stimulate ROS clearance, ultimately inhibiting tumor growth.

MEDICINAL RESEARCH REVIEWS (2021)

Article Chemistry, Multidisciplinary

Fluorescent Probes for Imaging Protein Disulfides in Live Organisms

Guodong Hu, Miao Zhong, Jintao Zhao, Hao Gao, Lu Gan, Hong Zhang, Shengxiang Zhang, Jianguo Fang

Summary: Cellular redox homeostasis is primarily regulated by the ratio of thiols and disulfides, with reversible thioldisulfide exchange reactions being crucial. Detecting protein disulfides (PDS) poses challenges due to dynamic exchanges of thiols and disulfides. Researchers have designed a probe that selectively recognizes PDS in live organisms, revealing an increase of PDS in mouse brains of a stroke model.

ACS SENSORS (2021)

Article Biochemistry & Molecular Biology

Activation of Cellular Antioxidant Defense System by Naturally Occurring Dibenzopyrone Derivatives Confers Neuroprotection against Oxidative Insults

Yanan Hou, Jie Li, Jun-Chen Wu, Quan-Xiang Wu, Jianguo Fang

Summary: Seven dibenzopyrone phenolic derivatives were isolated from endophytic fungi Alternaria alternata extract, with compound 3 determined as a new compound. Compounds 3, 4, 6, and 7 showed significant neuroprotective effects in PC12 cells through activating Nrf2, promoting the expression of Nrf2-governed genes, and enhancing cellular antioxidant capacity. The genetic silence of Nrf2 expression eliminated the observed cytoprotection, emphasizing the crucial role of Nrf2 in the protection offered by these compounds.

ACS CHEMICAL NEUROSCIENCE (2021)

Article Plant Sciences

Fusaricide is a Novel Iron Chelator that Induces Apoptosis through Activating Caspase-3

Yaling Hui, Ting Tang, Jing Wang, Huanhuan Zhao, Hong-Ying Yang, Junmin Xi, Baoxin Zhang, Jianguo Fang, Kun Gao, Yueting Wu

Summary: The study isolated a natural product FDC from an endophytic fungus of Lycium barbarum, which significantly inhibited proliferation in various human NSCLC cell lines through binding to intracellular iron to induce apoptosis.

JOURNAL OF NATURAL PRODUCTS (2021)

Article Agriculture, Multidisciplinary

Cynaropicrin Induces Cell Cycle Arrest and Apoptosis by Inhibiting PKM2 to Cause DNA Damage and Mitochondrial Fission in A549 Cells

Zhenjiang Ding, Junmin Xi, Miao Zhong, Fan Chen, Huanhuan Zhao, Baoxin Zhang, Jianguo Fang

Summary: The research demonstrates that CYN inhibits PKM2 activity and induces cell cycle arrest, oxidative stress, and mitochondrial damage. However, overexpression of PKM2 attenuates the effects of CYN on cells.

JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY (2021)

Article Chemistry, Medicinal

Integration of a Diselenide Unit Generates Fluorogenic Camptothecin Prodrugs with Improved Cytotoxicity to Cancer Cells

Jintao Zhao, Zihua Wang, Miao Zhong, Qianhe Xu, Xinming Li, Bingbing Chang, Jianguo Fang

Summary: In this study, a diselenide/disulfide unit was introduced into camptothecin, leading to the identification of two selenoprodrugs with improved efficacy in treating cancer. These selenoprodrugs can be activated by glutathione, accompanied by the generation of selenol intermediates that catalyze oxidation reactions. The discovery of the fluorescence quenching property of the diselenide/disulfide bond provides insights into developing novel theranostic agents.

JOURNAL OF MEDICINAL CHEMISTRY (2021)

Article Chemistry, Medicinal

Structural Modification of Aminophenylarsenoxides Generates Candidates for Leukemia Treatment via Thioredoxin Reductase Inhibition

Zi-Long Song, Junmin Zhang, Qianhe Xu, Danfeng Shi, Xiaojun Yao, Jianguo Fang

Summary: The study prepared different amino-substituted phenylarsine oxides and found that the o-substituted molecule exhibited higher potency in inhibiting cellular TrxR activity, leading to oxidative stress-mediated apoptosis. These findings suggest the promising potential of TrxR inhibitors as cancer therapeutic agents.

JOURNAL OF MEDICINAL CHEMISTRY (2021)

Article Chemistry, Medicinal

Baylis-Hillman Adducts as a Versatile Module for ConstructingFluorogenic Release System

Lanning Zhao, Yuan Qu, Fang Zhang, Di Ma, Hao Gao, Lu Gan, Hong Zhang, Shengxiang Zhang, Jianguo Fang

Summary: We report a versatile thiol-triggered fluorogenic release system that can rapidly release a molecule of interest and has been validated for its therapeutic potential in live cells and animal models.

JOURNAL OF MEDICINAL CHEMISTRY (2022)

Review Chemistry, Medicinal

Progress and perspective on hydrogen sulfide donors and their biomedical applications

Zi-Long Song, Lanning Zhao, Tao Ma, Alsiddig Osama, Tong Shen, Yilin He, Jianguo Fang

Summary: This review categorizes and describes H2S donors and comprehensively discusses their release mechanisms, biological applications, and therapeutic values. It also analyzes the drawbacks of typical H2S donors and proposes future development directions.

MEDICINAL RESEARCH REVIEWS (2022)

Article Agriculture, Multidisciplinary

Isolation and Identification of Novel Antioxidant Polyketides from an Endophytic Fungus Ophiobolus cirsii LZU-1509

Xiao-Wei Guo, Zhen-Qing Yu, Junmin Xi, Hao Ren, Xin-Yu Xiang, Jia Wu, Jianguo Fang, Quan-Xiang Wu

Summary: Sixteen new polyketides, including four novel carbon skeletons, were isolated from an endophytic fungus. The structures of these polyketides were determined using X-ray diffraction analysis and electric circular dichroism spectra comparison. The polyketides showed low toxicity and exhibited excellent antioxidant activity, with one compound showing greater efficacy than resveratrol in scavenging free radicals. These findings suggest that the novel polyketides could be potential antioxidant agents for neuroprotection.

JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY (2023)

Article Chemistry, Analytical

Naphthalimide Fluorescent Skeleton for Facile and Accurate Quantification of Glutathione

Fang Zhang, Fan Chen, Ruipeng Shen, Ya-xiong Chen, Zhengjia Zhao, Baoxin Zhang, Jianguo Fang

Summary: This study reports the construction of a probe library based on the naphthalimide skeleton to detect glutathione (GSH). Compound R13 was identified as a highly efficient GSH fluorescent probe and could be used to quantify GSH in cells and tissues. The probe was applied to study the alteration of GSH level in mouse livers after X-ray irradiation and Parkinson's mouse brains, providing valuable insights into the fluctuation of GSH/GSSG ratio in diseases.

ANALYTICAL CHEMISTRY (2023)

Article Chemistry, Multidisciplinary

Hemin as a General Static Dark Quencher for Constructing Heme Oxygenase-1 Fluorescent Probes

Fan Chen, Baoxin Zhang, Zhenjiang Ding, Miao Zhong, Yanan Hou, Fang Zhang, Guodong Hu, Jianguo Fang

Summary: We report a new fluorescent probe, RBH, for imaging HO-1 activity in live cells, utilizing hemin as a universal static quencher. RBH has favorable properties such as long excitation/emission wavelengths, fast response rate, and high signal increase, enabling its use for determining HO-1 activity in complex biological samples. The discovery of hemin as a general static dark quencher provides a straightforward strategy for constructing novel fluorescent probes.

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2023)

Article Chemistry, Analytical

Imaging of Carbonic Anhydrase Level in Epilepsy with an Environment-Sensitive Fluorescent Probe

Fang Zhang, Fan Chen, Miao Zhong, Ruipeng Shen, Zhengjia Zhao, Haopai Wei, Baoxin Zhang, Jianguo Fang

Summary: This study reports a fluorescent probe for detecting carbonic anhydrases (CAs), which demonstrates excellent selectivity, favorable biocompatibility, and desirable blood-brain barrier (BBB) penetration. The probe enables imaging of CA fluctuations in cells and mice, providing insights into the role of CA in disease pathogenesis.

ANALYTICAL CHEMISTRY (2023)

Article Chemistry, Multidisciplinary

A β-allyl carbamate fluorescent probe for vicinal dithiol proteins

Lanning Zhao, Feifei Bai, Fan Chen, Menghuan Guo, Lu Gan, Hong Zhang, Jianguo Fang

CHEMICAL COMMUNICATIONS (2020)

Article Biochemistry & Molecular Biology

Onopordopicrin from the new genus Shangwua as a novel thioredoxin reductase inhibitor to induce oxidative stress-mediated tumor cell apoptosis

Junmin Zhang, Zai-Qin Zheng, Qianhe Xu, Ya Li, Kun Gao, Jianguo Fang

Summary: The study identifies a new natural product, onopordopicrin (ONP), which inhibits thioredoxin reductase leading to disruption of cellular redox balance and promotion of oxidative stress. ONP shows the highest potency in killing cancer cells, with its inhibitory effect on TrxR closely correlated with cytotoxicity.

JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY (2021)

No Data Available