Abstract

Macamides are very important secondary metabolites produced by Lepidium meyenii Walp, which possess multiple bioactivities, especially in the neuronal system. In a previous study, we observed that macamides exhibited excellent effects in the recovery of injured nerves after 1-methyl-4-phenylpyridinium (MPP+)-induced dopaminergic neuronal damage in zebrafish. However, the mechanism underlying this effect remains unclear. In the present study, we observed that N-benzylhexadecanamide (XA), which is a typical constituent of macamides, improved the survival rate of neurons in vitro. We determined the concentration of neurotransmitters in MN9D cells and used it in conjunction with an integrated proteomics and lipidomics approach to investigate the mechanism underlying the neuroprotective effects of XA in an MPP+-induced neurodegeneration cell model using QqQ MS, Q-TOF MS, and Orbitrap MS. The statistical analysis of the results led to the identification of differentially-expressed biomarkers, including 11 proteins and 22 lipids, which may be responsible for the neuron-related activities of XA. All these potential biomarkers were closely related to the pathogenesis of neurodegenerative diseases, and their levels approached those in the normal group after treatment with XA. Furthermore, seven lipids, including five phosphatidylcholines, one lysophosphatidylcholine, and one phosphatidylethanolamine, were verified by a relative quantitative approach. Moreover, four proteins (Scarb2, Csnk2a2, Vti1b, and Bnip2) were validated by ELISA. The neurotransmitters taurine and norepinephrine, and the cholinergic constituents, correlated closely with the neuroprotective effects of XA. Finally, the protein–lipid interaction network was analyzed. Based on our results, the regulation of sphingolipid metabolism and mitochondrial function were determined to be the main mechanisms underlying the neuroprotective effect of XA. The present study should help us to better understand the multiple effects of macamides and their use in neurodegenerative diseases.

Highlights

  • Macamides are representative lipophilic constituents of Lepidium meyenii (Maca), with various promising pharmacological properties, including neuroprotective, anti-fatigue, and fertility improving effects [1,2,3,4,5]

  • Node proteins related to energy metabolism

  • The results indicated that XA could regulate the differential biomarkers support that the neuroprotective mechanism of XA which is mainly involved in the regulation of sphingolipid metabolism and mitochondrial function

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Summary

Introduction

Macamides are representative lipophilic constituents of Lepidium meyenii (Maca), with various promising pharmacological properties, including neuroprotective, anti-fatigue, and fertility improving effects [1,2,3,4,5]. In previous reports, they were demonstrated to act on CB1 receptor for their neuroprotective activity against Mn-induced mitochondrial depolarization and toxicity in U-87 cells [5]. The inhibition of fatty acid amide hydrolase (FAAH) was regarded as another mechanism for the Molecules 2018, 23, 2929; doi:10.3390/molecules23112929 www.mdpi.com/journal/molecules. An in vitro evaluation using AChE and BuChE inhibition assays supported this result [7]

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