Solitary and Synergistic Effects of Different Hydrophilic and Hydrophobic Phospholipid Moieties on Rat Behaviors

Author:

Kikuchi Shuhei1,Iwasaki Yugo2ORCID,Yoshioka Mina1,Hino Kodai1,Morita Shin-ya3ORCID,Tada Ryu4,Uchimura Yasuhiro1,Kubo Yoshinori1ORCID,Kobayashi Tomoya1,Kinoshita Yusuke5,Hayashi Masahiro6,Furusho Yoshio7,Tamiaki Hitoshi5ORCID,Ishiyama Hiroaki1,Kuroda Minoru1,Udagawa Jun1ORCID

Affiliation:

1. Division of Anatomy and Cell Biology, Department of Anatomy, Shiga University of Medical Science, Otsu 520-2192, Shiga, Japan

2. College of Bioscience and Biotechnology, Chubu University, Kasugai 487-8501, Aichi, Japan

3. Department of Pharmacotherapeutics, Shiga University of Medical Science, Otsu 520-2192, Shiga, Japan

4. Molecular Engineering Institute, Shiga University of Medical Science, Otsu 520-2192, Shiga, Japan

5. Graduate School of Life Sciences, Ritsumeikan University, Kusatsu 525-8577, Shiga, Japan

6. Department of Marine Biology and Environmental Science, Faculty of Agriculture, University of Miyazaki, Miyazaki 889-2192, Miyazaki, Japan

7. Department of Chemistry, Shiga University of Medical Science, Otsu 520-2192, Shiga, Japan

Abstract

Glycerophospholipids have hydrophobic and hydrophilic moieties. Previous studies suggest that phospholipids with different moieties have different effects on rodent behavior; however, the relationship between chemical structures and behavioral effects remains unclear. To clarify the functions of phospholipid moieties, we injected male rats with phospholipids with different moieties and conducted behavioral tests. Exploratory activity was reduced by phosphatidylethanolamine (PE)(18:0/22:6) but not PE(18:0/18:0) or PE(18:0/20:4). Conversely, exploratory activity was increased by plasmanyl PE(16:0/22:6), which harbors an alkyl–ether linkage, but not by phosphatidylcholine (PC)(16:0/22:6) or plasmanyl PC(16:0/22:6). Docosahexaenoic acid (DHA)(22:6) and an alkyl–ether linkage in PE were thus postulated to be involved in exploratory activity. Anxiety-like behavior was reduced by plasmenyl PC(18:0/20:4), which harbors a vinyl–ether linkage, but not by PC(18:0/20:4) or plasmanyl PC(18:0/20:4), suggesting the anxiolytic effects of vinyl–ether linkage. The activation of social interaction was suppressed by PE(18:0/18:0), PE(18:0/22:6), PC(16:0/22:6), plasmanyl PE(16:0/22:6), and plasmanyl PC(16:0/22:6) but not by PE(18:0/20:4), plasmenyl PE(18:0/20:4), or plasmanyl PC(18:0/22:6). DHA may suppress social interaction, whereas arachidonic acid(20:4) or a combination of alkyl–ether linkage and stearic acid(18:0) may restore social deficits. Our findings indicate the characteristic effects of different phospholipid moieties on rat behavior, and may help to elucidate patterns between chemical structures and their effects.

Funder

Japan Society for the Promotion of Science KAKENHI

Publisher

MDPI AG

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