Involvement of the Nrf2-Keap1 signaling pathway in protection against thallium-induced oxidative stress and mitochondrial dysfunction in primary hippocampal neurons
Autor: | Jun Yang, Huanhuan He, Guodong Lin, Qian Wang, Yawei Sun, Yuan Luo, Jianhai Long, Sui Xin, Zewu Qiu, Yongan Wang, Shuai Wang |
---|---|
Rok vydání: | 2020 |
Předmět: |
0301 basic medicine
NF-E2-Related Factor 2 Primary Cell Culture MFN2 Hippocampal formation Toxicology medicine.disease_cause Hippocampus Neuroprotection GTP Phosphohydrolases Mitochondrial Proteins 03 medical and health sciences 0302 clinical medicine medicine Animals Rats Wistar Thallium Neurons Brain Diseases Kelch-Like ECH-Associated Protein 1 Chemistry Neurotoxicity Membrane Proteins General Medicine medicine.disease KEAP1 Mitochondria Rats Cell biology Oxidative Stress 030104 developmental biology mitochondrial fusion Female Signal transduction Reactive Oxygen Species 030217 neurology & neurosurgery Oxidative stress Signal Transduction |
Zdroj: | Toxicology Letters. 319:66-73 |
ISSN: | 0378-4274 |
DOI: | 10.1016/j.toxlet.2019.11.008 |
Popis: | Thallium ion (Tl+) and its neurotoxic products are widely known to cause severe neurological complications. However, the exact mechanism of action remains unknown, with limited therapeutic options available. This study aims to examine the toxic effects of Thallium (I) Nitrate (TlNO3) on primary hippocampal neurons of E17-E18 Wistar rat embryos, and the potential neuroprotective role of Nrf2- Keap1 signaling pathway against thallium-induced oxidative stress and mitochondrial dysfunction. TlNO3 induces a significant increase in reactive oxygen species levels and mitochondrial dysfunction in primary hippocampal neurons. Furthermore, the Nrf2-Keap1 signaling pathway played a protective role against TlNO3-induced hippocampal neuronal cytotoxicity. Moreover, mitochondrial fusion protein Mitofusin 2 (Mfn2) levels significantly decreased in hippocampal neurons when exposed to TlNO3, indicating that Mfn2 protein levels are linked to TlNO3-induced neurotoxicity. t-BHQ, a Nrf2 and phase II detoxification enzyme inducer, counteracted the oxidative damage in hippocampal neurons by activating the Nrf2-Keap1 signaling pathway after TlNO3 exposure; the activated Nrf2-Keap1 pathway could then maintain Mfn2 function by regulating Mfn2 protein expression. Thus, Nrf2-Keap1 pathway activation plays a protective role in Tl+-induced brain damage, and specific agonists have been identified to have great potential for treating thallium poisoning. |
Databáze: | OpenAIRE |
Externí odkaz: |