Techaniyom Peerapa, Korsirikoon Chawin, Rungruang Thanaporn, Pakaprot Narawut, Prombutara Pinidphon, Mukda Sujira, Kettawan Aurawan Kringkasemsee, Kettawan Aikkarach
Doctor of Philosophy Program in Nutrition, Faculty of Medicine Ramathibodi Hospital and Institute of Nutrition Mahidol University Bangkok Thailand.
Department of Anatomy, Faculty of Medicine Siriraj Hospital Mahidol University Bangkok Thailand.
Food Sci Nutr. 2024 Jun 14;12(9):6259-6283. doi: 10.1002/fsn3.4265. eCollection 2024 Sep.
Perilla seed oil, derived from a regional plant native to northern Thailand, undergoes cold-pressing to analyze its bioactive components, notably alpha-linolenic acid (ALA). ALA, constituting approximately 61% of the oil, serves as a precursor for therapeutic omega-3 fatty acids, EPA and DHA, with neurodegenerative disease benefits and anti-inflammatory responses. This study administered different concentrations of perilla seed oil to male C57BL/6 mice, categorized as low dose (LP 5% w/w), middle dose (MP 10% w/w), and high dose (HP 20% w/w), along with a fish oil (FP 10% w/w) diet. An experimental group received soybean oil (5% w/w). Over 42 days, these diets were administered while inducing Parkinson's disease (PD) with rotenone injections. Mice on a high perilla seed oil dose exhibited decreased Cox-2 expression in the colon, suppressed Iba-1 microglia activation, reduced alpha-synuclein accumulation in the colon and hippocampus, prevented dopaminergic cell death in the substantia nigra, and improved motor and non-motor symptoms. Mice on a middle dose showed maintenance of diverse gut microbiota, with an increased abundance of short-chain fatty acid (SCFA)-producing bacteria (, , and ). A reduction in bacteria correlated with PD (, , and ) was observed. Results suggest the potential therapeutic efficacy of high perilla seed oil doses in mitigating both intestinal and neurological aspects linked to the gut-brain axis in PD.
紫苏籽油源自泰国北部的一种本土植物,通过冷榨来分析其生物活性成分,尤其是α-亚麻酸(ALA)。ALA约占该油的61%,是治疗性ω-3脂肪酸二十碳五烯酸(EPA)和二十二碳六烯酸(DHA)的前体,对神经退行性疾病有益且具有抗炎反应。本研究将不同浓度的紫苏籽油给予雄性C57BL/6小鼠,分为低剂量组(LP 5% w/w)、中剂量组(MP 10% w/w)和高剂量组(HP 20% w/w),同时设置了鱼油(FP 10% w/w)饮食组作为对照。一个实验组给予大豆油(5% w/w)。在42天的时间里,在通过注射鱼藤酮诱导帕金森病(PD)的同时给予这些饮食。高剂量紫苏籽油组的小鼠结肠中Cox-2表达降低,小胶质细胞Iba-1激活受到抑制,结肠和海马中α-突触核蛋白积累减少,黑质中多巴胺能细胞死亡得到预防,运动和非运动症状得到改善。中剂量组的小鼠多种肠道微生物群得以维持,产生短链脂肪酸(SCFA)的细菌(如 、 和 )丰度增加。观察到与PD相关的细菌(如 、 和 )数量减少。结果表明,高剂量紫苏籽油在减轻与PD中肠脑轴相关的肠道和神经方面具有潜在的治疗效果。