Bioactive long chain N-acylethanolamines in five species of edible bivalve molluscs -: Possible implications for mollusc physiology and seafood industry

被引:58
作者
Sepe, N
De Petrocellis, L
Montanaro, F
Cimino, G
Di Marzo, V
机构
[1] CNR, Ist Chim Mol Interesse Biol, I-80072 Arco, Na, Italy
[2] CNR, Ist Cibernet, I-80072 Arco, Na, Italy
来源
BIOCHIMICA ET BIOPHYSICA ACTA-LIPIDS AND LIPID METABOLISM | 1998年 / 1389卷 / 02期
关键词
anandamide; palmitoylethanolamide; marine eicosanoid; cannabinoid receptor; fatty acid amide hydrolase; N-acylethanolamine;
D O I
10.1016/S0005-2760(97)00132-X
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
Several long chain N-acylethanolamines, including the proposed endogenous ligands of cannabinoid receptors, anandamide (N-arachidonoylethanolamine, C20:4 NAE) and N-palmitoylethanolamine (C16:0 NAE), as well as some of their putative biosynthetic precursors, the N-acyl-phosphatidylethanolamines, were found in lipid extracts of five species of bivalve molluscs, including Mytilus galloprovincialis, commonly used as sea food. The amounts of these metabolites, the most abundant being C16:0 NAE and N-stearoylethanolamine, appeared to increase considerably when mussels were extracted 24h post-mortem, but were not significantly affected by boiling the tissue prior to extraction. In particulate fractions of homogenates from Mytilus, where the existence of a highly selective cannabinoid receptor with an immunomodulatory function has been previously described, an enzymatic activity capable of catalyzing the hydrolysis of C20:4 NAE amide bond, and displaying similar pH dependency and inhibitor sensitivity profiles as the recently characterized 'fatty acid amide hydrolase' was found. The enzyme K-m and V-max for C20:4 NAE were 29.6 mu M and 73 pmol/mg protein/min, respectively. These findings support the hypothesis that C20:4 NAE, never reported before in the phylum Mollusca, may be a mollusc physiological mediator, and suggest that edible bivalves may be a dietary, albeit limited, source of C16:0 NAE, whose anti-inflammatory properties, when administered orally in amounts higher than those reported here, have been previously reported. (C) 1998 Elsevier Science B.V.
引用
收藏
页码:101 / 111
页数:11
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