Nimgampalle Mallikarjuna, Bhat Anoop Ramachandra, Perumal Muthuraja, Ganesh Pothapragada S K Prabhakar, Purushothaman Gopinath, Devanathan Vasudharani
Department of Biology, Indian Institute of Science Education and Research Tirupati (IISER T), Srinivasapuram, Venkatagiri Road, Jangalapalli Village, Panguru (G.P), Yerpedu Mandal, Tirupati, 517619, Andhra Pradesh, India.
Institute for Drug Research, School of Pharmacy, Faculty of Medicine, The Hebrew University of Jerusalem, 91120, Jerusalem, Israel.
Mol Neurobiol. 2025 Apr 6. doi: 10.1007/s12035-025-04854-0.
Neuroinflammation and altered neurite outgrowth are pivotal pathological characteristic features of neurodegenerative disorders. Our research aims to explore the potential anti-neuroinflammatory activity of palmitic acid derived from Cissus quadrangularis. Our results reveal that palmitic acid at low concentrations significantly attenuates neuroinflammation in Neuro-2a cells by suppressing the expression of TNF-α and RhoA GTPase. Palmitic acid also modulates the activity of the small GTPase RhoA, a crucial regulator of cytoskeletal dynamics, thereby facilitating cytoskeletal rearrangements essential for neurite outgrowth. Our study also identifies those low concentrations of palmitic acid have a positive regulatory influence on cellular prion protein (PrP) and reelin, which are known for their roles in neuronal migration, differentiation, and synaptic plasticity. It maintains optimal neurite formation in LPS + PA (1 ng/ml)-Neuro-2a cells compared to LPS-treated cells, demonstrating a dose-dependent promotion of neurite extensions and branching. In conclusion, our findings elucidate the molecular pathways that palmitic acid exhibits anti-neuroinflammatory activity, highlighting its potential as a regulatory molecule at low concentrations under neuroinflammation. The palmitic acid modulates the functional activities of Rho small GTPases, and their regulation by transmembrane proteins, PrP, and reelin under neuroinflammation contribute to the optimum neurite outgrowth in the neurons.
神经炎症和神经突生长改变是神经退行性疾病的关键病理特征。我们的研究旨在探索来源于四角葡萄的棕榈酸的潜在抗神经炎症活性。我们的结果显示,低浓度的棕榈酸通过抑制TNF-α和RhoA GTP酶的表达,显著减轻Neuro-2a细胞中的神经炎症。棕榈酸还调节小GTP酶RhoA的活性,RhoA是细胞骨架动力学的关键调节因子,从而促进神经突生长所必需的细胞骨架重排。我们的研究还发现,低浓度的棕榈酸对细胞朊蛋白(PrP)和Reelin有正向调节作用,它们在神经元迁移、分化和突触可塑性中发挥作用。与LPS处理的细胞相比,它在LPS + PA(1 ng/ml)-Neuro-2a细胞中维持最佳的神经突形成,显示出对神经突延伸和分支的剂量依赖性促进作用。总之,我们的研究结果阐明了棕榈酸发挥抗神经炎症活性的分子途径,突出了其在神经炎症下作为低浓度调节分子的潜力。棕榈酸调节Rho小GTP酶的功能活性,以及它们在神经炎症下受跨膜蛋白、PrP和Reelin的调节,有助于神经元中最佳的神经突生长。