ACTION OF PHOSPHOLIPASE-A2 AND PHOSPHOLIPASE-C ON FREE FATTY-ACID RELEASE DURING COMPLETE ISCHEMIA IN RAT NEOCORTEX - EFFECT OF PHOSPHOLIPASE-C INHIBITOR AND N-METHYL-D-ASPARTATE ANTAGONIST

被引:60
作者
UMEMURA, A
MABE, H
NAGAI, H
SUGINO, F
机构
[1] Department of Neurosurgery, Nagoya City University, Medical School, Mizuho-ku, Nagoya 467, 1 Kawasumi, Mizuho-cho
关键词
ISCHEMIA; FREE FATTY ACID; PHOSPHOLIPASE; CALCIUM; RAT;
D O I
10.3171/jns.1992.76.4.0648
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The levels of brain free fatty acids rapidly increase after the onset of ischemia. The purpose of this study was to investigate the action of phospholipases A2 and C during complete ischemia based on the effects of a phospholipase C inhibitor (phenylmethylsulfonyl fluoride) and the N-methyl-D-aspartate antagonist MK-801 on the release of free fatty acids in rat neocortex. Complete brain ischemia was induced in rats with cardiac arrest by intracardiac injection of KCl. Free fatty acid levels in the neocortex were measured 0, 2, 4, and 8 minutes after cardiac arrest. Phenylmethylsulfonyl fluoride inhibited the release of free fatty acids primarily from phosphatidylinositol during the first 2 minutes of ischemia and from phosphatidylcholine and phosphatidylethanolamine at 4 to 8 minutes of ischemia. Conversely, MK-801 inhibited free fatty acid release mainly from phosphatidylcholine and phosphatidylethanolamine at 2 to 4 minutes of ischemia. These, results indicate that the release of free fatty acids during the first 2 minutes of ischemia can be attributed mostly to the action of phospholipase C, and that the activation of phospholipase C further influences the activation of phospholipase A2 in the subsequent course, while phospholipase A2 predominantly acts after 2 minutes of ischemia.
引用
收藏
页码:648 / 651
页数:4
相关论文
共 14 条
[1]   MECHANISM OF ARACHIDONIC-ACID LIBERATION DURING ISCHEMIA IN GERBIL CEREBRAL-CORTEX [J].
ABE, K ;
KOGURE, K ;
YAMAMOTO, H ;
IMAZAWA, M ;
MIYAMOTO, K .
JOURNAL OF NEUROCHEMISTRY, 1987, 48 (02) :503-509
[2]  
AGRANOFF BW, 1989, BASIC NEUROCHEMISTRY, P333
[3]   POSITIONAL DISTRIBUTION AND TURNOVER OF FATTY-ACIDS IN PHOSPHATIDIC ACID, PHOSPHOINOSITIDES, PHOSPHATIDYLCHOLINE AND PHOSPHATIDYLETHANOLAMINE IN RAT-BRAIN IN-VIVO [J].
BAKER, RR ;
THOMPSON, W .
BIOCHIMICA ET BIOPHYSICA ACTA, 1972, 270 (04) :489-&
[4]   BRAIN FREE FATTY-ACID LEVELS IN RATS SACRIFICED BY DECAPITATION VERSUS FOCUSED MICROWAVE IRRADIATION [J].
CENEDELLA, RJ ;
GALLI, C ;
PAOLETTI, R .
LIPIDS, 1975, 10 (05) :290-293
[6]   DEVELOPMENT OF CYCLOOXYGENASE AND LIPOXYGENASE METABOLITES OF ARACHIDONIC-ACID AFTER TRANSIENT CEREBRAL-ISCHEMIA [J].
DEMPSEY, RJ ;
ROY, MW ;
MEYER, K ;
COWEN, DE ;
TAI, HH .
JOURNAL OF NEUROSURGERY, 1986, 64 (01) :118-124
[7]  
IKEDA M, 1986, J NEUROCHEM, V47, P123
[8]   NONCOMPETITIVE ANTAGONISTS OF EXCITATORY AMINO-ACID RECEPTORS [J].
KEMP, JA ;
FOSTER, AC ;
WONG, EHF .
TRENDS IN NEUROSCIENCES, 1987, 10 (07) :294-298
[9]  
SEISJO BK, 1989, J CEREB BLOOD FLOW M, V9, P127
[10]  
SUGIYAMA H, 1987, NATURE, V325, P331