Eicosanoide und Phospholipasen |
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Authors: | M. Goerig A. J. R. Habenicht G. Schettler |
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Affiliation: | (1) Medizinische Klinik der Universität Heidelberg (Ludolf-Krehl-Klinik), Germany |
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Abstract: | Summary Prostaglandins, thromboxanes, and leukotrienes have been implicated to play an important role in physiology as well as in a growing list of pathophysiologic conditions. These oxidation products of 8.11.14.-eicosatrienoic-,5.8.11.14.-eicosatetraenoic-, and 5.8.11.14.17.-pentaenoic acids have been collectively designated eicosanoids. Many clinically important diseases are associated with altered eicosanoid biosynthesis. Furthermore, a series of hormones are known to induce acutely formation of eicosanoids, suggesting a crucial role in a multitude of tissue responses including phenomena such as secretion, platelet aggregation, chemotaxis, and smooth muscle contraction. The major precursor for the eicosanoids seems to be 5.8.11.14.-eicosatetraneoic acid or arachidonic acid. Virtually all of arachidonic acid however is present in esterified form in complex glycerolipids. Since cyclooxygenase and the lipoxygenases utilize arachidonic acid in its free form, a set of acylhydrolases is required to liberate arachidonic acid from membrane lipids before eicosanoid formation can occur. It became only recently apparent that a minor acidic phospholipid, phosphatidylinositol, comprising only 5%–10% of the phospholipid mass in mammalian cells, plays an important role in arachidonic acid metabolism. Phosphatidylinositol — after phosphorylation to phosphatidylinositolphosphate and phosphatidylinositolbisphosphate — appears to be hydrolyzed by specific phospholipases C generating 1-stearoyl-2-arachidonoyl-diglyceride. Diglyceride serves as substrate for diglyceride lipase to form monoglyceride and free fatty acid. Alternatively diglyceride is phosphorylated by diglyceride kinase yielding phosphatidic acid, which is believed to be reincorporated into phosphatidylinositol. In addition to phosphatidylinositol phosphatidylcholine, phosphatidylethanolamine and phosphatidic acid may contribute to arachidonic acid release. These phospholipids are substrates for phospholipases A2 generating free arachidonic acid and the respective lysophospholipid. Understanding of the biochemistry of arachidonic acid liberation may be critical in developing strategies of pharmacological intervention in a variety of pathological conditions. Abkürzungen AA Arachidonsäure - CDP-DG Cytidindiphosphodiglycerid - DG Diglycerid - DPI Phosphatidylinositoldiphosphat - FA freie Fettsäure - GSH Glutathion - HETE Hydroxyeicosatetraensäure - HPETE Hydroperoxyeicosatetraensäure - MDA Malondialdehyd - MG Monoglycerid - MI Myoinositol - Lyso-PA Lysophosphatidsäure - Lyso-PC Lysophosphatidylcholin - Lyso-Pl Lysophosphatidylinositol - LT Leukotrien - PA Phosphatidsäure - PC Phosphatidylcholin - PG Prostaglandin - Pl Phosphatidylinositol - THETE Tetrahydroxyeicosatetraensäure - TX ThromboxanDiese Arbeit wurde von der Deutschen Forschungsgemeinschaft (HA-1083/2-2) und dem Forschungsrat Rauchen und Gesundheit (Hamburg) unterstütztHerrn Professor Hans Neurath zum 75. Geburtstag gewidmet |
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Keywords: | Eicosanoids Leukotrienes Prostaglandins Phospholipases Arachidonic acid |
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