Santos Peterson Alves, Pflüger Pricila, Rott Marilise Brittes, Gómez-Couso Hipólito, Rodrigues Ionara, Pereira Patricia, Fontenla José Ángel
Laboratory of Neuropharmacology and Preclinical Toxicology, Institute of Basic Health Sciences, Federal University of Rio Grande do Sul, Porto Alegre, 90050-170, Brazil; GI-1684 Laboratory of Central Nervous System Pharmacology (Faculty of Pharmacy), Department of Pharmacology, Pharmacy and Pharmaceutical Technology, University of Santiago de Compostela, Santiago de Compostela, 15782, Spain.
GI-1684 Laboratory of Central Nervous System Pharmacology (Faculty of Pharmacy), Department of Pharmacology, Pharmacy and Pharmaceutical Technology, University of Santiago de Compostela, Santiago de Compostela, 15782, Spain; Center for Research in Molecular Medicine and Chronic Diseases (CIMUS). University of Santiago de Compostela, Santiago de Compostela, 15782, Spain.
J Ethnopharmacol. 2025 Sep 25;353(Pt A):120335. doi: 10.1016/j.jep.2025.120335. Epub 2025 Jul 31.
Achyrocline satureioides (Lam.) DC is traditionally used as an infusion in several South American countries to treat various health conditions, including those affecting the central nervous system. Recent studies indicate its potential neuroprotective effects and suggest possible benefits in alleviating neurological symptoms in COVID-19 patients. However, its direct impact on the central nervous system remains underexplored.
This study aimed to assess the Achyrocline satureioides effects infusion on dopaminergic and cholinergic neurodegeneration patterns induced by reserpine or manganese in Caenorhabditis elegans (C. elegans), and to perform in silico analysis of the primary bioactive compounds in the Achyrocline satureioides aqueous extract (ASAE).
Using C. elegans as an experimental model, we evaluated the neuroprotective effects of the aqueous extract of Achyrocline satureioides on dopaminergic and/or cholinergic neurodegeneration induced by reserpine or manganese. Behavioral assays evaluated the preservation of motor function and pharyngeal pumping in nematodes. In addition, in silico studies were performed with the bioactive compounds identified in the extract and compared with drugs currently used for Parkinson's and Alzheimer's diseases.
In the studies with C. elegans, neurodegeneration induced by reserpine (60 μM) was attenuated at the highest extract concentration (25 mg/ml) tested. Additionally, animals previously exposed to the extract exhibited improved behavior at both concentrations (10 and 25 mg/ml). When neurodegeneration was induced by manganese (50 mM), both concentrations of the ASAE reduced neurodegeneration and improved behavior. In silico studies evaluated the absorption, distribution, metabolism, and elimination (ADME) properties and molecular docking of identified compounds against established targets associated with neurodegenerative diseases.
The Achyrocline satureioides bioactive compounds appear to influence pathways targeted by current therapies for Parkinson's and Alzheimer's diseases. The aqueous extract demonstrated promising neuroprotective potential and modulation of the dopaminergic and cholinergic systems, reducing neurodegenerative damage and enhancing behavior.