Anti-cyclooxygenase effects of lipid extracts from the New Zealand green-lipped mussel, Perna canaliculus

被引:51
作者
McPhee, S.
Hodges, L. D.
Wright, P. F. A.
Wynne, P. M.
Kalafatis, N.
Harney, D. W.
Macrides, T. A.
机构
[1] RMIT Univ, Nat Prod Res Grp, Sch Med Sci, Div Lab Med, Bundoora, Vic 3083, Australia
[2] RMIT Univ, Toxicol Key Ctr, Sch Med Sci, Bundoora, Vic 3083, Australia
[3] SGE Int Pty Ltd, Ringwood, Vic, Australia
来源
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY | 2007年 / 146卷 / 03期
基金
澳大利亚研究理事会;
关键词
anti-inflammatory; cyclooxygenase; Lyprinol (R); Perna canaliculus; polyunsaturated fatty acids;
D O I
10.1016/j.cbpb.2006.11.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Total lipid extracts of P. canaliculus (a bivalve marine mollusc native to New Zealand, commonly called the green-ripped mussel) and Mytilus edulis (commonly called the common blue mussel) moderately inhibited ovine COX-1 and COX-2 pure enzymes in vitro. The inhibition was increased after the mussel extracts were saponified by KOH hydrolysis. Protease- and protease-lipase-hydrolysed lipid extracts of P. canaliculus exhibited similarly strong COX inhibition as the KOH-hydrolysed extract. Lyprinol (R) (a commercial extract from P. canaliculus) also exhibited strong inhibition of both COX isoforms, an effect that was increased 10-fold upon subsequent hydrolysis. In contrast, fish oil was not as anti-COX active as Lyprinol. The Lyprinol free fatty acid fraction, and to a lesser extent the Lyprinol triglyceride fraction, were the only lipid classes of Lyprinol to exhibit strong inhibition of the COX isoforms. The purified PUFA extracts were all bioactive, potently inhibiting COX-1 and COX-2. Incubation of Lyprinol in the absence of exogenous arachidonic acid (AA) showed the appearance of alternate prostaglandin metabolites, confirming Lyprinol PUFA as a competitive substrate inhibitor of AA metabolism. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:346 / 356
页数:11
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