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Synaptic lipid signaling
Open accessAbstract
Neuronal cellular and intracellular membranes are rich in specialized phospholipids that are reservoirs of lipid messengers released by specific phospholipases and stimulated by neurotransmitters, neurotrophic factors, cytokines, membrane depolarization, ion channel activation, etc. Secretory phospholipases A2 may be both intercellular messengers and generators of lipid messengers. The highly networked nervous system includes cells (e.g., astrocytes, oligodendrocytes, microglial cells, endothelial microvascular cells) that extensively interact with neurons; several lipid messengers participate in these interactions. This review highlights modulation of postsynaptic membrane excitability and long-term synaptic plasticity by cyclooxygenase-2-generated prostaglandin E2, arachidonoyldiacylcylglycerol, and arachidonic acid-containing endocannabinoids. The peroxidation of docosahexaenoic acid (DHA), a critical component of excitable membranes in brain and retina, is promoted by oxidative stress. DHA is also the precursor of enzyme-derived, neuroprotective docosanoids. The phospholipid platelet-activating factor is a retrograde messenger of long-term potentiation, a modulator of glutamate release, and an upregulator of memory formation. Lipid messengers modulate signaling cascades and contribute to cellular differentiation, function, protection, and repair in the nervous system. Lipidomic neurobiology will advance our knowledge of the brain, spinal cord, retina, and peripheral nerve function and diseases that affect them, and new discoveries on networks of signaling in health and disease will likely lead to novel therapeutic interventions.
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“Intracellular processing of the transmembrane glycoprotein βAPP through a sequential β- and γ- secretase–catalyzed proteolysis generates Aβ peptides that are subsequently shuttled to the plasma membrane and secreted (Bazan, 2003; Stein and Johnson, 2003).”
From Docosanoids and elovanoids from omega-3 fatty acids are pro-homeostatic modulators of inflammatory responses, cell damage and neuroprotection (2018) · cites this paper as Bazan, 2003
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“sAPPα generated via the α-secretase pathway does not give rise to the shorter amyloidogenic Aβ peptides;”
From Docosanoids and elovanoids from omega-3 fatty acids are pro-homeostatic modulators of inflammatory responses, cell damage and neuroprotection (2018) · cites this paper as Bazan, 2003
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Cites
Regulation of Synaptic Efficacy by Coincidence of Postsynaptic APs and EPSPs
Markram, H., Lübke, J., Frotscher, M., & Sakmann, B. (1997) · Science · doi:10.1126/science.275.5297.213 · Cited by 3,832
Chandrasekharan, N. V., Dai, H., Roos, K. L. T., Evanson, N. K., Tomsik, J., Elton, T. S., & Simmons, D. L. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.162468699 · Cited by 1,989
The molecular logic of endocannabinoid signalling
Piomelli, D. (2003) · Nature Reviews Neuroscience · doi:10.1038/nrn1247 · Cited by 1,957
Morrow, J. D., Hill, K. E., Burk, R. F., Nammour, T., Badr, K. F., & Roberts, L. J. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.23.9383 · Cited by 1,898
Serhan, C. N., Hong, S., Gronert, K., Colgan, S. P., Devchand, P. R., Mirick, G., & Moussignac, R.-L. (2002) · The Journal of Experimental Medicine · doi:10.1084/jem.20020760 · Cited by 1,650
Endogenous cannabinoids mediate retrograde signalling at hippocampal synapses
Wilson, R. I., & Nicoll, R. A. (2001) · Nature · doi:10.1038/35069076 · Cited by 1,607
Synaptic Modification by Correlated Activity: Hebb's Postulate Revisited
Bi, G., & Poo, M. (2001) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.24.1.139 · Cited by 1,525
Neuron-to-astrocyte signaling is central to the dynamic control of brain microcirculation
Zonta, M., Angulo, M. C., Gobbo, S., Rosengarten, B., Hossmann, K.-A., Pozzan, T., & Carmignoto, G. (2002) · Nature Neuroscience · doi:10.1038/nn980 · Cited by 1,446
Diversity of group types, regulation, and function of phospholipase A2.
Dennis, E. A. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)36794-7 · Cited by 1,435
The expanding superfamily of phospholipase A2 enzymes: classification and characterization
Six, D. A., & Dennis, E. A. (2000) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/s1388-1981(00)00105-0 · Cited by 1,359
Research works printed but not linked: 2
- Bazan, N. G., and E. B. Rodriguez de Turco. 1996. Alterations in plasma lipoproteins and DHA transport in progressive rod-cone degeneration (prcd). Retinal Degeneration and Regeneration, Proceedings of an International Symposium in Kanazawa, Japan. 1995.
- Bazan, 1997, Bioactive lipids in excitatory neurotransmission and neuronal plasticity, Neurochem. Int., 30, 225, 10.1016/S0197-0186(96)00020-4 · DOI
Cited by
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Items 101–200 of 247
Viola, A., Saywell, V., Villard, L., Cozzone, P. J., & Lutz, N. W. (2007) · PLoS ONE · doi:10.1371/journal.pone.0000157 · Cited by 49
Lin, L. E., Chen, C. T., Hildebrand, K. D., Liu, Z., Hopperton, K. E., & Bazinet, R. P. (2014) · Journal of Lipid Research · doi:10.1194/jlr.m055590 · Cited by 48
Differential distribution of DHA-phospholipids in rat brain after feeding: A lipidomic approach
Lamazière, A., Richard, D., Barbe, U., Kefi, K., Bausero, P., Wolf, C., & Visioli, F. (2010) · Prostaglandins Leukotrienes and Essential Fatty Acids · doi:10.1016/j.plefa.2010.11.001 · Cited by 49
Integrated Pathways of COX-2 and mTOR: Roles in Cell Sensing and Alzheimer’s Disease
Tyagi, A., Kamal, M. A., & Poddar, N. K. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00693 · Cited by 50
He, J. (2006) · Archives of Ophthalmology · doi:10.1001/archopht.124.1.70 · Cited by 48
Microglial Lipid Biology in the Hypothalamic Regulation of Metabolic Homeostasis
Folick, A., Koliwad, S. K., & Valdearcos, M. (2021) · Frontiers in Endocrinology · doi:10.3389/fendo.2021.668396 · Cited by 48
Akaneya, Y., & Tsumoto, T. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.3028-06.2006 · Cited by 43
Cyclooxygenase‐2, Prostaglandin E2, and Microglial Activation in Prion Diseases
Minghetti, L., & Pocchiari, M. (2007) · International review of neurobiology · doi:10.1016/s0074-7742(07)82014-9 · Cited by 45
Eady, T. N., Khoutorova, L., Obenaus, A., Mohd‐Yusof, A., Bazan, N. G., & Belayev, L. (2013) · Neurobiology of Disease · doi:10.1016/j.nbd.2013.09.008 · Cited by 44
Self-citationShalini, S.-M., Ho, C. F., Ng, Y., Tong, J. X., Ong, E. S., Herr, D. R., Dawe, G. S., & Ong, W. (2017) · Molecular Neurobiology · doi:10.1007/s12035-017-0413-x · Cited by 43
Lipid-Mediated Cell Signaling Protects against Injury and Neurodegeneration
Zhang, C., & Bazan, N. G. (2010) · Journal of Nutrition · doi:10.3945/jn.109.114884 · Cited by 44
Self-citationMass‐Spectrometric Identification of Anandamide and 2‐Arachidonoylglycerol in Nematodes
Lehtonen, M., Reisner, K., Auriola, S. O. K., Wong, G., & Callaway, J. C. (2008) · Chemistry & Biodiversity · doi:10.1002/cbdv.200890208 · Cited by 41
Berra‐Romani, R., Faris, P. S., Negri, S., Botta, L., Genova, T., & Moccia, F. D. (2019) · Cells · doi:10.3390/cells8070689 · Cited by 42
German, O. L., Monaco, S., Agnolazza, D. L., Rotstein, N. P., & Politi, L. E. (2013) · Journal of Lipid Research · doi:10.1194/jlr.m039040 · Cited by 40
Blood-brain barrier breakdown by PAF and protection by XQ-1H due to antagonism of PAF effects
Deng, Y., Fang, W., Li, Y., Cen, J., Fang, F., Lv, P., Gong, S., & Mao, L. (2009) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2009.06.017 · Cited by 39
Regional changes in CNS and retinal glycerophospholipid profiles with age: a molecular blueprint
Hopiavuori, B. R., Agbaga, M., Brush, R. S., Sullivan, M. T., Sonntag, W. E., & Anderson, R. E. (2017) · Journal of Lipid Research · doi:10.1194/jlr.m070714 · Cited by 38
Belayev, L., Khoutorova, L., Atkins, K. D., Gordon, W. C., Álvarez‐Buílla, J., & Bazan, N. G. (2008) · Experimental Neurology · doi:10.1016/j.expneurol.2008.08.009 · Cited by 37
Self-citationHamza, R. Z., Al‐Salmi, F. A., & El‐Shenawy, N. S. (2019) · PeerJ · doi:10.7717/peerj.7460 · Cited by 36
Bazan, N. G., Calandria, J. M., & Gordon, W. C. (2013) · Nestlé Nutrition Institute Workshop series · doi:10.1159/000351395 · Cited by 37
Self-citationModulation of T-type calcium channels by bioactive lipids
Chemin, J., Cazade, M., & Lory, P. (2014) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-014-1467-5 · Cited by 35
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Farooqui, A. A. (2012) · Journal of Alzheimer s Disease · doi:10.3233/jad-2011-111085 · Cited by 34
Andrade, C., Singh, N. M., Thyagarajan, S., Nagaraja, N., Rao, N. S. K., & Chandra, J. S. (2007) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2007.08.009 · Cited by 34
Belayev, L., Hong, S., Freitas, R. S., Menghani, H., Marcell, S. J., Khoutorova, L., Mukherjee, P. K., Reid, M. M., Oriá, R. B., & Bazan, N. G. (2020) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.13444 · Cited by 34
Self-citationSanfeliu, A., Hokamp, K., Gill, M., & Tropea, D. (2019) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2019.00278 · Cited by 35
Wang, D., Hu, X., Jiang, J., Sun, L., Qing, Y., Yang, X., Gao, Y., Cui, G., Li, M., Wang, P.-K., et al. (2021) · Schizophrenia Research · doi:10.1016/j.schres.2021.02.009 · Cited by 33
Shen, Y., Kishimoto, K., Linden, D. J., & Sapirstein, A. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0605427104 · Cited by 32
Trofimiuk, E., & Braszko, J. J. (2011) · Lipids · doi:10.1007/s11745-011-3551-3 · Cited by 32
Fontaine, D., Figiel, S., Félix, R., Kouba, S., Fromont, G., Mahéo, K., Potier‐Cartereau, M., Chantôme, A., & Vandier, C. (2020) · Journal of Lipid Research · doi:10.1194/jlr.ra120000634 · Cited by 31
Mattacks, C. A., Sadler, D., & Pond, C. M. (2004) · Lymphatic Research and Biology · doi:10.1089/1539685042564363 · Cited by 30
Eady, T. N., Khoutorova, L., Atkins, K. D., Bazan, N. G., & Belayev, L. (2012) · Experimental & Translational Stroke Medicine · doi:10.1186/2040-7378-4-19 · Cited by 30
Self-citationLeikin-Frenkel, A. I., Beeri, M. S., & Cooper, I. (2022) · Nutrients · doi:10.3390/nu14235091 · Cited by 31
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Musto, A. E., & Bazan, N. G. (2006) · Epilepsia · doi:10.1111/j.1528-1167.2006.00418.x · Cited by 29
Self-citationNomura, D. K., Fujioka, K., Issa, R. S., Ward, A. M., Cravatt, B. F., & Casida, J. E. (2007) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2007.11.021 · Cited by 28
Cazade, M., Bidaud, I., Hansen, P., Lory, P., & Chemin, J. (2013) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-013-1411-0 · Cited by 28
Fang, W., Zhang, R., Sha, L., Lv, P., Shang, E., Han, D., Wei, J., Geng, X., Yang, Q., & Li, Y. (2013) · Journal of Neurochemistry · doi:10.1111/jnc.12507 · Cited by 27
Eady, T. N., Khoutorova, L., Anzola, D., Hong, S., Obenaus, A., Mohd‐Yusof, A., Bazan, N. G., & Belayev, L. (2013) · PLoS ONE · doi:10.1371/journal.pone.0077237 · Cited by 27
Self-citationDing, S., Wang, C., Wang, W., Yu, H., Chen, B., Liu, L., Zhang, M., & Yan, L. (2021) · Cell Biology and Toxicology · doi:10.1007/s10565-021-09674-1 · Cited by 26
Omega–3 Fatty Acid Docosahexaenoic Acid Is the Precursor of Neuroprotectin D1 in the Nervous System
Niemoller, T. D., Stark, D. T., & Bazan, N. G. (2008) · World review of nutrition and dietetics · doi:10.1159/000192994 · Cited by 28
Self-citationXu, Y., Zhang, B., Hua, Z., Johns, R. A., Bredt, D. S., & Tao, Y. (2004) · Experimental Neurology · doi:10.1016/j.expneurol.2004.05.013 · Cited by 26
Harada, S., Haruna, Y., Aizawa, F., Matsuura, W., Nakamoto, K., Yamashita, T., Kasuya, F., & Tokuyama, S. (2014) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2014.09.036 · Cited by 25
Bozlu, G., Atıcı, A., Turhan, A. H., Polat, A., Naycı, A., Okuyaz, Ç., & Taşkınlar, H. (2007) · Brain Research · doi:10.1016/j.brainres.2007.01.094 · Cited by 25
Kelly, P. T., MacKinnon, R. L., Dietz, R. V., Maher, B. J., & Wang, J. (2005) · Molecular Brain Research · doi:10.1016/j.molbrainres.2004.12.018 · Cited by 24
Taoro‐González, L., Pereda, D., Valdés‐Baizabal, C., González‐Gómez, M., Pérez, J. A., Mesa-Herrera, F., Canerina‐Amaro, A., Perez-Gonzalez, H., Rodríguez, C., Díaz, M. L., et al. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23137430 · Cited by 26
Cieślik, M., Pyszko, J., & Strosznajder, J. B. (2013) · Neurochemistry International · doi:10.1016/j.neuint.2013.02.016 · Cited by 23
Yan-Jia, F., Zhou, M.-H., Gao, X.-F., Gu, H., & Mei, Y. (2011) · Biochemical Journal · doi:10.1042/bj20110569 · Cited by 22
Connor, S., Tenorio, G., Clandinin, M. T., & Sauvé, Y. (2012) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/h2012-062 · Cited by 27
Campello‐Costa, P., Fosse-Júnior, A. M., Oliveira-Silva, P., & Serfaty, C. A. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2005.12.039 · Cited by 21
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Kolko, M., Christoffersen, N. R., Varoqui, H., & Bazan, N. G. (2005) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-005-8221-7 · Cited by 22
Self-citationHillard, C. J. (2005) · Life Sciences · doi:10.1016/j.lfs.2005.05.004 · Cited by 21
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Wang, C., Liu, S., Liu, F., Bhutta, A. T., Patterson, T. A., & Slikker, W. (2022) · Anesthesia & Analgesia · doi:10.1213/ane.0000000000005926 · Cited by 20
Katzen-Luchenta, J. (2007) · Nutrition and Health · doi:10.1177/026010600701900212 · Cited by 20
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Sliz, E., Shin, J., Syme, C. A., Patel, Y., Parker, N., Richer, L., Gaudet, D., Bennett, S. A. L., Paus, T., & Pausová, Z. (2020) · Molecular Psychiatry · doi:10.1038/s41380-019-0640-9 · Cited by 20
Challet, É., Denis, I., Rochet, V., Aı̈oun, J., Gourmelen, S., Lacroix, H., Goustard, B., Papillon, C., Alessandri, J., & Lavialle, M. (2012) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-012-1241-9 · Cited by 17
Wong, L., Hirst, S. M., Pye, Q. N., Reilly, C. M., Seal, S., & McGinnis, J. F. (2013) · PLoS ONE · doi:10.1371/annotation/569989ba-586e-468d-bba3-d9a737b15459 · Cited by 17
Tissue-Specific Content of Polyunsaturated Fatty Acids in (n-3) Deficiency State of Rats
Kulkarni, A., Zhao, A., Yang, B., Zhang, Y., & Linderborg, K. M. (2022) · Foods · doi:10.3390/foods11020208 · Cited by 16
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Fonteh, A. N., Chung, R., Sharma, T. L., Fisher, R. D., Pogoda, J. M., Cowan, R. P., & Harrington, M. G. (2010) · Cephalalgia · doi:10.1177/0333102410383589 · Cited by 16
Label-free quantitative proteomics of rat hypothalamus under fever induced by LPS and PGE2
Firmino, M., Weis, S. N., de Souza, J. M. F., Gomes, B. R. B., Mól, A. R., Mortari, M. R., de Souza, G. E. P., Coca, G. C., Williams, T. C. R., Fontes, W., et al. (2018) · Journal of Proteomics · doi:10.1016/j.jprot.2018.07.018 · Cited by 16
Belayev, L., Khoutorova, L., Atkins, K. D., Cherqui, A., Álvarez‐Buílla, J., & Bazan, N. G. (2008) · Brain Research · doi:10.1016/j.brainres.2008.11.074 · Cited by 15
Self-citationQuiescence induced by iron challenge protects neuroblastoma cells from oxidative stress
Mura, C. V., Delgado, R., Aguirre, P., Bacigalupo, J., & Núñez, M. T. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.03798.x · Cited by 15
Chen, S., & Li, K. W. (2008) · Chemistry and Physics of Lipids · doi:10.1016/j.chemphyslip.2008.01.001 · Cited by 14
Belayev, L., Bazan, N. G., Obenaus, A., Mukherjee, P., Knott, E. J., Khoutorova, L., Reid, M. M., Roque, C. R., Nguyen, L., Lee, J., et al. (2020) · Brain Circulation · doi:10.4103/bc.bc_36_20 · Cited by 15
Self-citationMetabolism and Functions of Platelet-Activating Factor (PAF) in the Nervous Tissue
Goracci, G., Balestrieri, M. L., & Nardicchi, V. (2009) · Springer eBooks · doi:10.1007/978-0-387-30378-9_13 · Cited by 14
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Liou, J., Kang, K., Chang, L., & Ho, S. (2006) · Neuropharmacology · doi:10.1016/j.neuropharm.2006.05.016 · Cited by 14
Wang, X., Ilarraza, R., Tancowny, B. P., Alam, S. B., & Kulka, M. (2020) · Frontiers in Nutrition · doi:10.3389/fnut.2020.597809 · Cited by 15
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Heusler, P., & Boehmer, G. (2007) · Brain Research · doi:10.1016/j.brainres.2006.12.016 · Cited by 11
Zhao, Z.-G., Zhang, M., Zeng, X., Fei, X., Liu, L., Zhang, Z.-H., & Mei, Y. (2007) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.106.117556 · Cited by 11
Benjamins, J. A., Murphy, E. J., & Seyfried, T. N. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-374947-5.00005-5 · Cited by 14
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Farooqui, A. A., Horrocks, L. A., & Farooqui, T. (2009) · Springer eBooks · doi:10.1007/978-0-387-30378-9_2 · Cited by 11
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Self-citationWang, C., Han, X., Liu, F., Patterson, T. A., Hanig, J. P., Paule, M. G., & Slikker, W. (2018) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2018.03.017 · Cited by 8
Zhang, M., Shi, W., Fei, X., Liu, Y., Zeng, X., & Mei, Y. (2007) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2007.09.008 · Cited by 8
Machová, E., Málková, B., Lisá, V., Nováková, J., & Doležal, V. (2006) · Neurochemical Research · doi:10.1007/s11064-006-9156-1 · Cited by 8
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Wang, C., Wang, C., Liu, F., Rainosek, S. W., Patterson, T. A., Slikker, W., & Han, X. (2018) · Chemical Research in Toxicology · doi:10.1021/acs.chemrestox.8b00186 · Cited by 7
LaManna, J. C., Sun, X., Ivy, A., & Ward, N. L. (2006) · Springer eBooks · doi:10.1007/0-387-29540-2_47 · Cited by 8
COX-2 pathway is upregulated in ultra-high risk individuals for psychosis
Pereira, C. A. C., Costa, A. C., Joaquim, H. P. G., Talib, L. L., van de Bilt, M. T., Loch, A. A., & Gattaz, W. F. (2021) · The World Journal of Biological Psychiatry · doi:10.1080/15622975.2021.1961501 · Cited by 6
Dileep, K. V., Remya, C., Tintu, I., & Sadasivan, C. (2013) · Frontiers in Life Science · doi:10.1080/21553769.2014.901924 · Cited by 7
Immunomodulatory effects of lactate dehydrogenase in vitro and in vivo
Daifuku, M., Nishi, K., Okamoto, T., Nishimoto, S., & Sugahara, T. (2012) · Journal of Functional Foods · doi:10.1016/j.jff.2012.07.005 · Cited by 6
Zheng, G., Xiong, S.-Q., Chen, H., Mei, L.-J., & Wang, T. (2017) · Chinese Journal of Integrative Medicine · doi:10.1007/s11655-017-2802-4 · Cited by 6
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Self-citation
Metadata
- Authors
- Bazan, N. G.
- Affiliations
- Louisiana State University (US)
- Corresponding author
- Bazan, Nicolas G.
- ORCID
- Bazan, Nicolas G.
- Venue
- Journal of Lipid Research
- Publisher
- Elsevier BV
- Published
- 2003-12
- Volume
- 44
- Issue
- 12
- Pages
- 2221-2233
- ISSN
- 0022-2275 (ISSN-L)
- OpenAlex
- W2168480206
- Cited by
- 247
- References
- 154
- Citations by year
- 2026: 3 · 2025: 3 · 2024: 3 · 2022: 7 · 2021: 5 · 2020: 13 · 2019: 7 · 2018: 6 · 2017: 6 · 2015: 3 · 2014: 8 · 2013: 12 · 2012: 12
- FWCI
- 2.46
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Lipid Research (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- National Eye Institute (R01 EY 05121, R01EY005121)
- National Institute of Neurological Disorders and Stroke (R01NS023002, R01NS23002)
- National Center for Research Resources (P20RR-16816, P20RR016816)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Health Sciences › Nursing › Nutrition and Dietetics › Fatty Acid Research and Health
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Sphingolipid Metabolism and Signaling
- Keywords
- secretory phospholipase A2, prostaglandin E2, cyclooxygenase-2, endocannabinoids, arachidonic acid, docosanoids, platelet-activating factor, retrograde signaling, long-term potentiation, synaptic plasticity, lipidomics, neuroprotection, astrocytes, microglia, memory formation
- MeSH terms
- Animals, Fatty Acids, Unsaturated, Humans, Nervous System, Synaptic Transmission, Neuronal Plasticity, Platelet Activating Factor, Lipid Metabolism
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