Saint-Petersburg Institute of Pharmacy, Leningrad Region, Vsevolozhsky District, Kuzmolovo P 245, 188663 Saint-Petersburg, Russia
Division of Pharmaceutical Biosciences, Faculty of Pharmacy, University of Helsinki, P.O. Box 56 (Viikinkaari 5E), FI-00014 Helsinki, Finland
Mar Drugs. 2017 Nov 24;15(12):365. doi: 10.3390/md15120365.
The lipids from gonads and polyhydroxynaphthoquinone pigments from body walls of sea urchins are intensively studied. However, little is known about the body wall (BW) lipids. Ethanol extract (55 °C) contained about equal amounts of saturated (SaFA) and monounsaturated fatty acids (MUFA) representing 60% of total fatty acids, with myristic, palmitic and eicosenoic acids as major SaFAs and MUFAs, respectively. Non-methylene-interrupted dienes (13%) were composed of eicosadienoic and docosadienoic acids. Long-chain polyunsaturated fatty acids (LC-PUFA) included two main components, n6 arachidonic and n3 eicosapentaenoic acids, even with equal concentrations (15 μg/mg) and a balanced n6/n3 PUFA ratio (0.86). The UPLC-ELSD analysis showed that a great majority of the lipids (80%) in the ethanolic extract were phosphatidylcholine (60 μg/mg) and phosphatidylethanolamine (40 μg/mg), while the proportion of neutral lipids remained lower than 20%. In addition, alkoxyglycerol derivatives-chimyl, selachyl, and batyl alcohols-were quantified. We have assumed that the mechanism of action of body wall lipids in the present study is via the inhibition of MAPK p38, COX-1, and COX-2. Our findings open the prospective to utilize this lipid fraction as a source for the development of drugs with anti-inflammatory activity.
性腺中的脂质和海胆体壁中的多羟基萘醌类色素受到了广泛的研究。然而,对于体壁(BW)脂质的研究却知之甚少。55°C 的乙醇提取物中含有等量的饱和脂肪酸(SaFA)和单不饱和脂肪酸(MUFA),分别占总脂肪酸的 60%,其中肉豆蔻酸、棕榈酸和二十碳烯酸分别为主要的 SaFA 和 MUFA。非亚甲基中断的二烯(13%)由二十碳二烯酸和二十二碳二烯酸组成。长链多不饱和脂肪酸(LC-PUFA)包括两种主要成分,n6 花生四烯酸和 n3 二十碳五烯酸,即使浓度相等(15μg/mg)且 n6/n3 PUFA 比值也平衡(0.86)。UPLC-ELSD 分析表明,乙醇提取物中绝大多数脂质(80%)为磷脂酰胆碱(60μg/mg)和磷脂乙醇胺(40μg/mg),而中性脂质的比例仍低于 20%。此外,还定量了烷氧基甘油衍生物——鲨烯、角鲨烯和姥鲛醇。我们假设,本研究中体壁脂质的作用机制是通过抑制 MAPK p38、COX-1 和 COX-2。我们的发现为利用这种脂质部分作为开发具有抗炎活性的药物的来源开辟了前景。