Related Experiment Video
Updated: Jan 14, 2026

Analysis of Raw and Processed Cyperi Rhizoma Samples Using Liquid Chromatography-Tandem Mass Spectrometry in Rats with Primary Dysmenorrhea
Published on: December 23, 2022
Oxidation of the Unsaturated Fatty Acid Linoleic Acid Generates Highly Potent TRPA1 Agonists
Anna Kaneko1, Yuko Terada1, Hiroyoshi Yamamoto2
1Department of Food and Nutritional Sciences, Graduate School of Integrated Pharmaceutical and Nutritional Sciences, University of Shizuoka, Suruga-ku, Shizuoka, Japan.
Abstract:
Polyunsaturated fatty acids (PUFAs) play important roles in health and biological functions. However, their high susceptibility to oxidation leads to the formation of unpleasant astringent sensations, posing a significant challenge in food production. In this study, to elucidate the molecular mechanisms underlying astringency induced by oxidized PUFAs, linoleic acid (LA), a representative PUFA, was used as a model. The effects of its oxidation products on two key human astringency-related receptors, transient receptor potential ankyrin 1 (TRPA1) and transient receptor potential vanilloid 1 (TRPV1), were analyzed. Ten oxidation products were identified from oxidized LA, among which 9-HpODE and 13-HpODE exhibited 5- to 10-fold higher TRPA1 activity than LA. This study is the first to demonstrate that PUFA oxidation generates highly potent TRPA1 agonists. Our findings propose a novel mechanism for astringency induced by oxidized PUFAs, wherein PUFA oxidation products activate TRPA1. PRACTICAL APPLICATIONS: This study is the first to demonstrate that oxidation of linoleic acid, a model polyunsaturated fatty acid (PUFA), produces potent agonists of the pungency receptor TRPA1. Part of the molecular mechanism underlying pungent sensation induced by oxidized PUFAs was elucidated. These findings may contribute to the development of novel strategies for controlling the pungency of oxidized PUFAs by combining TRPA1 response suppression with conventional approaches such as oxidation inhibition.
More Related Videos
Related Concept Videos
Radical Autoxidation
Structure of Lipids
Oxidation of Alkenes: Anti Dihydroxylation with Peroxy Acids
Formation of Lipopolysaccharides
Antiasthma Drugs: Leukotriene Modifiers
Leukotriene modifiers work through two distinct mechanisms:
Adrenergic Agonists: Chemistry and Structure-Activity Relationship
Aromatic ring substitutions: Substituting the aromatic ring with –OH groups at positions 3 and 4 yields catecholamines (e.g., epinephrine), which have a high affinity for adrenoceptors. Hydrogen bonding between –OH groups and receptors enhances adrenergic activity.
Separation of...

