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J. Biol. Chem., Vol. 263, Issue 32, 16591-16596, Nov, 1988

Formation and biological activity of 12-ketoeicosatetraenoic acid in the nervous system of Aplysia

D Piomelli, SJ Feinmark, E Shapiro and JH Schwartz
Howard Hughes Medical Institute, Center for Neurobiology and Behavior, Columbia University, New York, New York 10032.

12-Hydroperoxy-5,8,10,14-eicosatetraenoic acid (12-HPETE), a lipoxygenase product, simulates the synaptic responses produced by the modulatory transmitter, histamine, and the neuroactive peptide, Phe-Met- Arg-Phe-amide (FMRFamide), in identified neurons of the marine mollusk, Aplysia californica (Piomelli, D., Shapiro, E., Feinmark, S. J., and Schwartz, J. H. (1987) J. Neurosci. 7, 3675-3886; Shapiro, E., Piomelli, D., Feinmark, S., Vogel, S., Chin, G., and Schwartz, J. H. (1988) Cold Spring Harbor Symp. Quant. Biol. 53, in press). The 12- lipoxygenase pathway has not yet been fully characterized, but 12-HPETE is known to be metabolized further. We therefore began to search for other metabolites in order to investigate whether the actions of 12- HPETE might require its conversion to other active products. Here we report the identification of 12-keto-5,8,10,14-eicosatetraenoic acid (12-KETE), a metabolite of 12-HPETE formed by Aplysia nervous tissue. This product was identified in incubations of the tissue with arachidonic acid using high performance liquid chromatography, UV spectrometry, and gas chromatography/mass spectrometry. [3H]12-KETE was formed from endogenous lipid stores in nervous tissue, labeled by incubation with [3H]arachidonic acid, when stimulated by application of histamine. In L14 and L10 cells, identified neurons in the abdominal ganglion, applications of 12-KETE elicit changes in membrane potential similar to those evoked by histamine. 12(S)-Hydroxy-5,8,10,14- eicosatetraenoic acid, another metabolite of 12-HPETE, is inactive. These results support the hypothesis that 12-HPETE and its metabolite, 12-KETE, participate in transduction of histamine responses in Aplysia neurons.
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This article has been cited by other articles:


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J. Neurophysiol.Home page
T. L. Tieman, D. J. Steel, Y. Gor, J. Kehoe, J. H. Schwartz, and S. J. Feinmark
A Pertussis Toxin-Sensitive 8-Lipoxygenase Pathway Is Activated by a Nicotinic Acetylcholine Receptor in Aplysia Neurons
J Neurophysiol, May 1, 2001; 85(5): 2150 - 2158.
[Abstract] [Full Text] [PDF]


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J. Biol. Chem.Home page
D. J. Steel, T. L. Tieman, J. H. Schwartz, and S. J. Feinmark
Identification of an 8-Lipoxygenase Pathway in Nervous Tissue of Aplysia californica
J. Biol. Chem., July 25, 1997; 272(30): 18673 - 18681.
[Abstract] [Full Text] [PDF]




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