1. β-asarone protects against age-related motor decline via activation of SKN-1/Nrf2 and subsequent induction of GST-4.
- Author
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Lei M, Wu J, Tan Y, Shi Y, Yang W, Tu H, and Tan W
- Subjects
- Animals, Mitochondria drug effects, Mitochondria metabolism, Motor Activity drug effects, Signal Transduction drug effects, Glutathione Transferase metabolism, Longevity drug effects, Insulin-Like Growth Factor I metabolism, Caenorhabditis elegans drug effects, Allylbenzene Derivatives pharmacology, Aging drug effects, Caenorhabditis elegans Proteins metabolism, Caenorhabditis elegans Proteins genetics, NF-E2-Related Factor 2 metabolism, Anisoles pharmacology, DNA-Binding Proteins metabolism, Transcription Factors metabolism
- Abstract
Decelerating motor decline is important for promoting healthy aging in the elderly population. Acorus tatarinowii Schott is a traditional Chinese medicine that contains β-asarone as a pharmacologically active constituent. We found that β-asarone can decelerate motor decline in various age groups of Caenorhabditis elegans, while concurrently prolonging their lifespan and modulating synaptic transmission. To understand the mechanisms of its efficacy in motor improvement, we investigated and discovered that mitochondrial fragmentation, a marker for aging, is delayed after β-asarone treatment. Moreover, their efficacy is blocked by dysfunctional mitochondria. Corresponding to their role in regulating mitochondrial homeostasis, we found that SKN-1/Nrf2 and GST-4 are critical in the β-asarone treatment, and they appear to be activated via the insulin/IGF-1 signaling pathway. Well-developed intestinal microvilli are required for this process. Our study demonstrates the efficacy and mechanism of β-asarone treatment in age-related motor decline, contributing to the discovery of drugs for achieving healthy aging., Competing Interests: Declaration of Competing Interest The authors declare no competing interests., (Copyright © 2024 The Authors. Published by Elsevier Ltd.. All rights reserved.)
- Published
- 2024
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