Fujino Minoru, Fukuda Jun, Isogai Hirohisa, Ogaki Tetsuro, Mawatari Shiro, Takaki Atsushi, Wakana Chikako, Fujino Takehiko
BOOCS Clinic Fukuoka, Fukuoka, Japan.
Faculty of Human Sciences, Kyushu Sangyo University, Fukuoka, Japan.
Front Cell Dev Biol. 2022 Jun 2;10:894734. doi: 10.3389/fcell.2022.894734. eCollection 2022.
Plasmalogens have been shown to improve neurodegenerative pathology and cognitive function. We hypothesized that plasmalogens work in small amounts as a kind of hormone interacting with a G protein-coupled receptor, and then explored the effects of scallop-derived purified plasmalogens on psychobehavioral conditions in a randomized placebo-controlled trial of college athletes in Japan. Eligible participants were male students aged 18-22 years who belonged to university athletic clubs. They were randomly allocated to either plasmalogen (2 mg per day) or placebo treatment of 4 weeks' duration. The primary outcome was the T-score of the Profile of Mood States (POMS) 2-Adult Short, and the secondary outcomes included the seven individual scales of the POMS 2, other psychobehavioral measures, physical performance, and laboratory measurements. The trial was registered at the Japan Registry of Clinical Trials (jRCTs071190028). Forty participants (20 in the plasmalogen group and 20 in the placebo group) completed the 4-week treatment. The Total Mood Disturbance (TMD) score of the plasmalogen group showed a greater decrease at 4 weeks than that of the placebo group while the between-group difference was marginally significant ( = 0.07). The anger-hostility and fatigue-inertia scores of the POMS 2 decreased significantly in the plasmalogen group, but not in the placebo group, at 4 weeks. Between-group differences in those scores were highly significant ( = 0.003 for anger-hostility and = 0.005 for fatigue-inertia). The plasmalogen group showed a slight decrease in the Athens Insomnia Scale at 2 weeks, and the between-group difference was near-significant ( = 0.07). The elapsed time in minute patterns on the Uchida-Kraepelin test, which is a marker of mental concentration, revealed significantly greater performance in the plasmalogen group than in the placebo group. There were no between-group differences in physical and laboratory measurements. It is suggested that orally administered plasmalogens alleviate negative mood states and sleep problems, and also enhance mental concentration.
已证明缩醛磷脂可改善神经退行性病变和认知功能。我们推测缩醛磷脂作为一种与G蛋白偶联受体相互作用的激素,少量即可发挥作用,随后在日本一项针对大学生运动员的随机安慰剂对照试验中,探究了扇贝来源的纯化缩醛磷脂对心理行为状况的影响。符合条件的参与者为年龄在18至22岁、隶属于大学体育俱乐部的男学生。他们被随机分配接受缩醛磷脂(每日2毫克)或安慰剂治疗,为期4周。主要结局指标是情绪状态量表(POMS)2成人简版的T分数,次要结局指标包括POMS 2的七个单项量表、其他心理行为指标、身体表现和实验室测量指标。该试验已在日本临床试验注册中心(jRCTs071190028)注册。40名参与者(缩醛磷脂组20名,安慰剂组20名)完成了为期4周的治疗。缩醛磷脂组的总情绪紊乱(TMD)分数在4周时比安慰剂组有更大幅度的下降,而组间差异接近显著(P = 0.07)。4周时,缩醛磷脂组POMS 2的愤怒 - 敌意和疲劳 - 惰性分数显著下降,而安慰剂组未下降。这些分数的组间差异非常显著(愤怒 - 敌意P = 0.003,疲劳 - 惰性P = 0.005)。缩醛磷脂组在2周时雅典失眠量表得分略有下降,组间差异接近显著(P = 0.07)。作为精神集中度指标的内田 - 克雷佩林测验中,缩醛磷脂组按分钟模式计算的耗时显示出比安慰剂组显著更好的表现。身体和实验室测量指标在组间没有差异。研究表明,口服缩醛磷脂可缓解负面情绪状态和睡眠问题,还可提高精神集中度。