小管柏稳定脂质提取物的抗炎作用。

Allergie et immunologie Pub Date : 2000-09-01
G M Halpern
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引用次数: 0

摘要

通过超临界流体(CO2)提取冻干稳定的NZ绿唇贻贝粉(Lyprinol)制备的富含脂质的提取物,在给动物和人类时显示出显著的抗炎(AI)活性。当用来普利醇处理p.o.时,Wistar和Dark Agouti大鼠既没有发生佐剂诱导的多关节炎,也没有发生胶原(II)诱导的自身过敏性关节炎。这是在非甾体抗炎药剂量< 200倍其他种子油或鱼油<的情况下实现的。赖丙醇亚组分抑制PMN体外合成LTB4,抑制活化巨噬细胞产生PGE2。这种AI活动大部分与omega-3 PUFAs和天然抗氧化剂(如类胡萝卜素)有关。与非甾体抗炎药相比,在疾病应激大鼠中,300 mg/kg / o的Lyprinol没有胃毒性,并且不影响血小板聚集[人,大鼠]。临床研究,无论是对照研究还是随机研究,都表明AI在骨关节炎(OA)、类风湿性关节炎(RA)、哮喘和其他炎症疾病患者中具有非常显著的活性。赖丙醇是一种可再生的、稳定的生物活性脂质来源,其效力比目前用作改善炎症迹象的营养补充剂的植物/海洋油大得多。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anti-inflammatory effects of a stabilized lipid extract of Perna canaliculus (Lyprinol).

A lipid-rich extract, prepared by supercritical fluid (CO2) extraction of freeze-dried stabilized NZ green-lipped mussel powder (Lyprinol) has shown significant anti-inflammatory (AI) activity when given to animals and humans. When treated p.o. with Lyprinol, Wistar and Dark Agouti rats developed neither adjuvant-induced polyarthritis or collagen(II)-induced auto-allergic arthritis. This was achieved with doses < NSAIDs, and 200 times < of other seed or fish oils. Lyprinol subfractions inhibited LTB4 biosynthesis by PMN in vitro, and PGE2 production by activated macrophages. Much of this AI activity was associated with omega-3 PUFAs and natural antioxidants [e.g. carotenoids]. In contrast to NSAIDs, Lyprinol is non-gastro toxic in disease-stressed rats at 300 mg/kg p.o., and does not affect platelet aggregation [human, rat]. Clinical studies, either controlled or randomized, have demonstrated very significant AI activity in patients with osteoarthritis (OA), rheumatoid arthritis (RA), asthma, and other inflammatory conditions. Lyprinol is a reproducible, stable source of bioactive lipids with much greater potency than plant/marine oils currently used as nutritional supplements to ameliorate signs of inflammation.

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