Journal Article

Orientin Modulates Nrf2-ARE, PI3K/Akt, JNK-ERK1/2, and TLR4/NF-kB Pathways to Produce Neuroprotective Benefits in Parkinson's Disease

Thaggikuppe Krishnamurthy, Praveen, Vasudevan Sajini, Deepak, Chakkittukandiyil, Amritha, Mudavath, Ravi Naik

2024

Overview

Parkinson's disease (PD) is characterized by oxidative stress and neuroinflammation as key pathological features. Emerging evidence suggests that nuclear factor erythroid 2 related factor 2-antioxidant response element (Nrf2-ARE), phosphatidylinositol 3‑kinase-protein kinase B (PI3K-Akt), c-Jun N-terminal kinase-extracellular signal-regulated kinase 1/2 (JNK-ERK1/2), and toll-like receptor 4/nuclear factor-kappa B (TLR4/NF-kB) pathways play pivotal roles in PD pathogenesis. Orientin, a phenolic phytoconstituent, has demonstrated modulatory potential on these pathways in various experimental conditions other than PD. In this study, we aimed to evaluate the neuroprotective effects of Orientin against rotenone-induced neurodegeneration in SH-SY5Y cell lines and the Swiss albino mice model of PD. Orientin was administered at doses 10 and 20 µM in cell lines and 10 and 20 mg/kg in mice, and its effects on rotenone-induced neurodegeneration were investigated. Oxidative stress markers including mitochondrial membrane potential (ΔΨm), reactive oxygen species (ROS), superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GPx), as well as inflammatory markers including interleukin-1β (IL-1β), interleukin-6 (IL-6) and tumor necrosis factor-α (TNF-α), were measured. The expression levels of genes related to Nrf2-ARE (Nrf2), PI3K/Akt (Akt), JNK-ERK1/2 (TNF-α), and TLR4/NF-kB (TNF-α) pathways were measured to understand the modulatory effect of Orientin on these pathways. Additionally, behavioral studies assessing locomotor activity, muscle coordination, and muscle rigidity were conducted with mice. Our results indicate that Orientin dose-dependently attenuated rotenone-induced changes in oxidative stress markers, inflammatory markers, gene expression levels, and behavioral parameters. Therefore, our study concludes that Orientin exhibits significant neuroprotective benefits against rotenone-induced PD by modulating Nrf2-ARE, PI3K-Akt, JNK-ERK1/2, and TLR4/NF-kB pathways. Graphical Abstract

• Publisher: Springer US,Springer Nature B.V
• Subject: 1-Phosphatidylinositol 3-kinase / AKT protein / Animals / Biochemistry / Biomarkers / Biomedical and Life Sciences / Biomedicine / c-Jun protein / Catalase / Cell Biology / Cell Line, Tumor / Cytokines / Extracellular signal-regulated kinase / Flavonoids - pharmacology / Flavonoids - therapeutic use / Gene expression / Glucosides - pharmacology / Glucosides - therapeutic use / Glutathione / Glutathione peroxidase / Humans / Inflammation / Interleukin 6 / Interleukins / JNK protein / Kinases / Locomotor activity / MAP Kinase Signaling System - drug effects / MAP Kinase Signaling System - physiology / Membrane potential / Mice / Movement disorders / Muscles / Neurochemistry / Neurodegeneration / Neurodegenerative diseases / Neurology / Neuroprotection / Neuroprotective Agents - pharmacology / Neuroprotective Agents - therapeutic use / Neurosciences / NF-E2-Related Factor 2 - drug effects / NF-E2-Related Factor 2 - metabolism / NF-kappa B - drug effects / NF-kappa B - metabolism / NF-κB protein / Original Paper / Oxidative stress / Oxidative Stress - drug effects / Parkinson Disease - drug therapy / Parkinson Disease - metabolism / Parkinson's disease / Pathogenesis / Peroxidase / Phenolic compounds / Phenols / Phosphatidylinositol 3-Kinases - drug effects / Phosphatidylinositol 3-Kinases - metabolism / Proto-Oncogene Proteins c-akt - drug effects / Proto-Oncogene Proteins c-akt - metabolism / Reactive oxygen species / Rigidity / Rotenone / Rotenone - toxicity / Signal Transduction - drug effects / Superoxide dismutase / TLR4 protein / Toll-Like Receptor 4 - drug effects / Toll-Like Receptor 4 - metabolism / Toll-like receptors / Transcription factors / Tumor necrosis factor-TNF