Fat-induced satiety factor oleoylethanolamide enhances memory consolidation

The rat brain in stereotaxic coordinates

Palkovits, M. (1983) · Neuropeptides · doi:10.1016/0143-4179(83)90049-5 · Cited by 28,959 · see citing works

The Rat Brain in Stereotaxic Coordinates

Paxinos, G., & Watson, C. (1983) · Elsevier eBooks · doi:10.1016/c2009-0-63235-9 · Cited by 28,585 · see citing works

Validation of open:closed arm entries in an elevated plus-maze as a measure of anxiety in the rat

Pellow, S., Chopin, P., File, S. E., & Briley, M. (1985) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(85)90031-7 · Cited by 5,822 · see citing works

AChE-stained horizontal sections of the rat brain in stereotaxic coordinates

Paxinos, G., WATSON, C. R. R., & Emson, P. C. (1980) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(80)90021-7 · Cited by 4,497 · see citing works

Memory - A century of consolidation

McGaugh, J. L. (2000) · Science · doi:10.1126/science.287.5451.248 · Cited by 4,250 · see citing works

THE AMYGDALA MODULATES THE CONSOLIDATION OF MEMORIES OF EMOTIONALLY AROUSING EXPERIENCES

McGaugh, J. L. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.27.070203.144157 · Cited by 2,296 · see citing works

PPARs and the complex journey to obesity

Evans, R. M., Barish, G. D., & Wang, Y.-X. (2004) · Nature Medicine · doi:10.1038/nm1025 · Cited by 1,621 · see citing works

Oleylethanolamide regulates feeding and body weight through activation of the nuclear receptor PPAR-α

Fu, J., Gaetani, S., Oveisi, F., Verme, J., Serrano, A., de Fonseca, F. D., Rosengarth, A., Luecke, H., Giacomo, B. D., Tarzia, G., et al. (2003) · Nature · doi:10.1038/nature01921 · Cited by 1,113 · see citing works

Anatomical profiling of nuclear receptor expression reveals a hierarchical transcriptional network

Bookout, A. L., Jeong, Y., Downes, M., Yu, R. T., Evans, R. M., & Mangelsdorf, D. J. (2006) · Cell · doi:10.1016/j.cell.2006.06.049 · Cited by 1,015 · see citing works

Sorting out the roles of PPAR  in energy metabolism and vascular homeostasis

Lefebvre, P. (2006) · Journal of Clinical Investigation · doi:10.1172/jci27989 · Cited by 962 · see citing works

Role of adrenal stress hormones in forming lasting memories in the brain

McGaugh, J. L., & Roozendaal, B. (2002) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(02)00306-9 · Cited by 818 · see citing works

An anorexic lipid mediator regulated by feeding

de Fonseca, F. R., Navarro, M. A., de Heras, R. G., Escuredo, L., Nava, F. A., Fu, J., Murillo‐Rodríguez, E., Giuffrida, A., LoVerme, J., Gaetani, S., et al. (2001) · Nature · doi:10.1038/35102582 · Cited by 695 · see citing works

The Brain, Appetite, and Obesity

Berthoud, H., & Morrison, C. D. (2007) · Annual Review of Psychology · doi:10.1146/annurev.psych.59.103006.093551 · Cited by 661 · see citing works

Immunolocalization of peroxisome proliferator-activated receptors and retinoid x receptors in the adult rat CNS

Moreno, S., Vecchioli, S. F., & Cerù, M. P. (2003) · Neuroscience · doi:10.1016/j.neuroscience.2003.08.064 · Cited by 581 · see citing works

Physiological workload reactions to increasing levels of task difficulty

VELTMAN, J. A., & GAILLARD, A. W. K. (1998) · Ergonomics · doi:10.1080/001401398186829 · Cited by 433 · see citing works

The Lipid Messenger OEA Links Dietary Fat Intake to Satiety

Schwartz, G. J., Fu, J., Astarita, G., Li, X., Gaetani, S., Campolongo, P., Cuomo, V., & Piomelli, D. (2008) · Cell Metabolism · doi:10.1016/j.cmet.2008.08.005 · Cited by 370 · see citing works

Oleoylethanolamide Stimulates Lipolysis by Activating the Nuclear Receptor Peroxisome Proliferator-activated Receptor α (PPAR-α)

Guzmán, M., Lo Verme, J., Fu, J., Oveisi, F., Blázquez, C., & Piomelli, D. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m404087200 · Cited by 328 · see citing works

The hippocampus mediates glucocorticoid-induced impairment of spatial memory retrieval: Dependence on the basolateral amygdala

Roozendaal, B., Griffith, Q. K., Buranday, J., de Quervain, D. J.-F., & McGaugh, J. L. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0337480100 · Cited by 291 · see citing works

Involvement of stress-released corticotropin-releasing hormone in the basolateral amygdala in regulating memory consolidation

Roozendaal, B., Brunson, K. L., Holloway, B. L., McGaugh, J. L., & Baram, T. Z. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.212504599 · Cited by 258 · see citing works

Activation of TRPV1 by the Satiety Factor Oleoylethanolamide

Ahern, G. P. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m305051200 · Cited by 256 · see citing works

Food Intake Regulates Oleoylethanolamide Formation and Degradation in the Proximal Small Intestine

Fu, J., Astarita, G., Gaetani, S., Kim, J., Cravatt, B. F., Mackie, K., & Piomelli, D. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m607809200 · Cited by 244 · see citing works

Episodic-like memory in rats: is it based on when or how long ago?

Roberts, W. A., Feeney, M. C., MacPherson, K., Petter, M., McMillan, N., & Musolino, E. (2008) · Science · doi:10.1126/science.1152709 · Cited by 191 · see citing works

Mechanisms of CCK signaling from gut to brain

Raybould, H. E. (2007) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2007.09.006 · Cited by 151 · see citing works

What–Where–When memory in magpies (Pica pica)

Zinkivskay, A., Nazir, F., & Smulders, T. V. (2009) · Animal Cognition · doi:10.1007/s10071-008-0176-x · Cited by 139 · see citing works

Targeted enhancement of oleoylethanolamide production in proximal small intestine induces across-meal satiety in rats

Fu, J., Kim, J., Oveisi, F., Astarita, G., & Piomelli, D. (2008) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00126.2008 · Cited by 106 · see citing works

Oleoylethanolamide inhibits food intake in free-feeding rats after oral administration

Oveisi, F. (2004) · Pharmacological Research · doi:10.1016/j.phrs.2003.12.006 · Cited by 100 · see citing works

Pharmacological Characterization of Hydrolysis-Resistant Analogs of Oleoylethanolamide with Potent Anorexiant Properties

Astarita, G., Giacomo, B. D., Gaetani, S., Oveisi, F., Compton, T. R., Rivara, S., Tarzia, G., Mor, M., & Piomelli, D. (2006) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.106.105221 · Cited by 91 · see citing works

Mechanism of oleoylethanolamide on fatty acid uptake in small intestine after food intake and body weight reduction

Yang, Y., Chen, M., Georgeson, K. E., & Harmon, C. M. (2006) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00270.2006 · Cited by 82 · see citing works

Oleylethanolamide impairs glucose tolerance and inhibits insulin-stimulated glucose uptake in rat adipocytes through p38 and JNK MAPK pathways

González-Yanes, C., Serrano, A., Bermúdez‐Silva, F. J., Hernández-Dominguez, M., Páez-Ochoa, M. A., de Fonseca, F. R., & Sánchez‐Margalet, V. (2005) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00555.2004 · Cited by 52 · see citing works

Ontogenetic and pharmacological dissociation of various components of locomotor activity and habituation in the rat

Giovanni Laviola, A., Renna, G., Bignami, G., & Cuomo, V. (1988) · International Journal of Developmental Neuroscience · doi:10.1016/0736-5748(88)90049-4 · Cited by 45 · see citing works

The endocannabinoid system and the brain.

Mechoulam, R., & Parker, L. A. (2013) · Annual Review of Psychology · doi:10.1146/annurev-psych-113011-143739 · Cited by 1,090 · see citing works

An update on PPAR activation by cannabinoids

O’Sullivan, S. E. (2016) · British Journal of Pharmacology · doi:10.1111/bph.13497 · Cited by 469 · see citing works

Memory modulation.

Roozendaal, B., & McGaugh, J. L. (2011) · Behavioral Neuroscience · doi:10.1037/a0026187 · Cited by 445 · see citing works

Differential role of anandamide and 2-arachidonoylglycerol in memory and anxiety-like responses

Busquets-Garcia, A., Puighermanal, E., Pastor, A., de la Torre, R., Maldonado, R., & Ozaita, A. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.04.022 · Cited by 273 · see citing works

Consolidating memories

McGaugh, J. L. (2015) · Annual Review of Psychology · doi:10.1146/annurev-psych-010814-014954 · Cited by 271 · see citing works

Mechanisms Mediating the Regulation of Peroxisomal Fatty Acid Beta-Oxidation by PPARα

Tahri-Joutey, M., Andreoletti, P., Surapureddi, S., Nasser, B., Cherkaoui‐Malki, M., & Latruffe, N. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22168969 · Cited by 258 · see citing works

Cannabinoid activation of peroxisome proliferator-activated receptors: Potential for modulation of inflammatory disease

O’Sullivan, S. E., & Kendall, D. A. (2009) · Immunobiology · doi:10.1016/j.imbio.2009.09.007 · Cited by 247 · see citing works

Disruption of fatty acid amide hydrolase activity prevents the effects of chronic stress on anxiety and amygdalar microstructure

Hill, M. N., Kumar, S. A., Filipski, S. B., Iverson, M., Stuhr, K. L., Keith, J. M., Cravatt, B. F., Hillard, C. J., Chattarji, S., & McEwen, B. S. (2013) · Molecular Psychiatry · doi:10.1038/mp.2012.90 · Cited by 222 · see citing works

Effects of endocannabinoid system modulation on cognitive and emotional behavior

Zanettini, C. (2011) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2011.00057 · Cited by 214 · see citing works

Plasma concentrations of endocannabinoids and related primary fatty acid amides in patients with post-traumatic stress disorder

Hauer, D., Schelling, G., Gola, H., Campolongo, P., Morath, J., Roozendaal, B., Hamuni, G., Karabatsiakis, A., Atsak, P., Vogeser, M., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0062741 · Cited by 200 · see citing works

A fatty gut feeling

Piomelli, D. (2013) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2013.03.001 · Cited by 185 · see citing works

Alterations in the endocannabinoid system in the rat valproic acid model of autism

Kerr, D. M., Downey, L., Conboy, M., Finn, D. P., & Roche, M. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.04.043 · Cited by 183 · see citing works

Regulation of Cyclic AMP Response Element Binding and Hippocampal Plasticity-Related Genes by Peroxisome Proliferator-Activated Receptor α

Roy, A., Jana, M., Corbett, G. T., Ramaswamy, S., Kordower, J. H., Gonzalez, F. J., & Pahan, K. (2013) · Cell Reports · doi:10.1016/j.celrep.2013.07.028 · Cited by 166 · see citing works

Palmitoylethanolamide in CNS health and disease

Raso, G. M., Russo, R., Calignano, A., & Meli, R. (2014) · Pharmacological Research · doi:10.1016/j.phrs.2014.05.006 · Cited by 148 · see citing works

Endogenous cannabinoid release within prefrontal-limbic pathways affects memory consolidation of emotional training

Morena, M., Roozendaal, B., Trezza, V., Ratano, P., Peloso, A., Hauer, D., Atsak, P., Trabace, L., Cuomo, V., McGaugh, J. L., et al. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1420285111 · Cited by 146 · see citing works

The endocannabinoid system: An emotional buffer in the modulation of memory function

Morena, M., & Campolongo, P. (2014) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2013.12.010 · Cited by 143 · see citing works

From Surface to Nuclear Receptors: The Endocannabinoid Family Extends its Assets

Pistis, M., & Melis, M. (2010) · Current Medicinal Chemistry · doi:10.2174/092986710790980014 · Cited by 142 · see citing works

Palmitoylethanolamide and other anandamide congeners. Proposed role in the diseased brain

Hansen, H. S. (2010) · Experimental Neurology · doi:10.1016/j.expneurol.2010.03.022 · Cited by 136 · see citing works

The Fat-Induced Satiety Factor Oleoylethanolamide Suppresses Feeding through Central Release of Oxytocin

Gaetani, S., Fu, J., Cassano, T., Dipasquale, P., Romano, A., Righetti, L., Cianci, S., Laconca, L., Giannini, E., Scaccianoce, S., et al. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.0036-10.2010 · Cited by 124 · see citing works

Blockade of Nicotine Reward and Reinstatement by Activation of Alpha-Type Peroxisome Proliferator-Activated Receptors

Mascia, P., Pistis, M., Justinová, Z., Panlilio, L. V., Luchicchi, A., Lecca, S., Scherma, M., Fratta, W., Fadda, P., Barnes, C., et al. (2010) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.07.009 · Cited by 118 · see citing works

Endocannabinoid concentrations in hair are associated with PTSD symptom severity

Wilker, S., Pfeiffer, A., Elbert, T. R., Ovuga, E., Karabatsiakis, A., Krumbholz, A., Thieme, D., Schelling, G., & Kolassa, I. (2016) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2016.02.010 · Cited by 116 · see citing works

Stress Related Shift Toward Inflammaging in Cosmonauts After Long-Duration Space Flight

Buchheim, J., Matzel, S., Петровна, Р. М., Vassilieva, G. Y., Ponomarev, S. A., Ничипорук, И. А., Hoerl, M., Moser, D., Biere, K., Feuerecker, M., et al. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.00085 · Cited by 119 · see citing works

Inhibition of FAAH and activation of PPAR: New approaches to the treatment of cognitive dysfunction and drug addiction

Panlilio, L. V., Justinová, Z., & Goldberg, S. R. (2013) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2013.01.003 · Cited by 106 · see citing works

Amygdala-hippocampal interactions in synaptic plasticity and memory formation

Roesler, R., Parent, M. B., LaLumiere, R. T., & McIntyre, C. K. (2021) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2021.107490 · Cited by 108 · see citing works

Satiety factor oleoylethanolamide recruits the brain histaminergic system to inhibit food intake

Provensi, G., Coccurello, R., Umehara, H., Munari, L., Giacovazzo, G., Galeotti, N., Nosi, D., Gaetani, S., Romano, A., Moles, A., et al. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1322016111 · Cited by 104 · see citing works

Role of the endocannabinoid system in regulating glucocorticoid effects on memory for emotional experiences

Atsak, P., Roozendaal, B., & Campolongo, P. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2011.08.047 · Cited by 98 · see citing works

Intestinal lipid–derived signals that sense dietary fat

DiPatrizio, N. V., & Piomelli, D. (2015) · Journal of Clinical Investigation · doi:10.1172/jci76302 · Cited by 97 · see citing works

Peroxisome Proliferator‐Activated Receptorsαandγare Linked with Alcohol Consumption in Mice and Withdrawal and Dependence in Humans

Blednov, Y. A., Benavidez, J. M., Black, M., Ferguson, L. B., Schoenhard, G. L., Goate, A., Edenberg, H. J., Wetherill, L. F., HESSELBROCK, V. M., Foroud, T., et al. (2014) · Alcoholism Clinical and Experimental Research · doi:10.1111/acer.12610 · Cited by 96 · see citing works

Oleoylethanolamide, Neuroinflammation, and Alcohol Abuse

Orío, L., Alén, F., Pavón, F. J., Serrano, A., & García‐Bueno, B. (2019) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00490 · Cited by 90 · see citing works

Dietary Triacylglycerols with Palmitic Acid in the sn-2 Position Modulate Levels of N-Acylethanolamides in Rat Tissues

Carta, G., Murru, E., Lisai, S., Sirigu, A., Piras, A., Collu, M., Batetta, B., Gambelli, L., & Banni, S. (2015) · PLoS ONE · doi:10.1371/journal.pone.0120424 · Cited by 84 · see citing works

Obesity surgery and gut–brain communication

Berthoud, H., Shin, A. C., & Zheng, H. (2011) · Physiology & Behavior · doi:10.1016/j.physbeh.2011.01.023 · Cited by 84 · see citing works

Amygdala activity and amygdala-hippocampus connectivity: Metabolic diseases, dementia, and neuropsychiatric issues

Song, J. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.114647 · Cited by 84 · see citing works

Identification and characterization of PPARα ligands in the hippocampus

Roy, A., Kundu, M., Jana, M., Mishra, R. K., Yung, Y. P., Luan, C.-H., Gonzalez, F. J., & Pahan, K. (2016) · Nature Chemical Biology · doi:10.1038/nchembio.2204 · Cited by 83 · see citing works

Age-dependent roles of peroxisomes in the hippocampus of a transgenic mouse model of Alzheimer’s disease

Fanelli, F., Sepe, S., D’Amelio, M., Bernardi, C., Cristiano, L., Cimini, A., Cecconi, F., Cerù, M. P., & Moreno, S. (2013) · Molecular Neurodegeneration · doi:10.1186/1750-1326-8-8 · Cited by 76 · see citing works

Fatty-Acid Binding Proteins Modulate Sleep and Enhance Long-Term Memory Consolidation in Drosophila

Gerstner, J. R., Vanderheyden, W. M., Shaw, P. J., Landry, C. F., & Yin, J. C. P. (2011) · PLoS ONE · doi:10.1371/journal.pone.0015890 · Cited by 71 · see citing works

Omega 3 fatty acids in the elderly

Úbeda, N., Achón, M., & Varela‐Moreiras, G. (2012) · British Journal Of Nutrition · doi:10.1017/s0007114512001535 · Cited by 71 · see citing works

Training-Associated Emotional Arousal Shapes Endocannabinoid Modulation of Spatial Memory Retrieval in Rats

Morena, M., Castro, V. D., Gray, J. M., Palmery, M., Trezza, V., Roozendaal, B., Hill, M. N., & Campolongo, P. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.1983-15.2015 · Cited by 70 · see citing works

Altering endocannabinoid neurotransmission at critical developmental ages: impact on rodent emotionality and cognitive performance

Trezza, V., Campolongo, P., Manduca, A., Morena, M., Palmery, M., Vanderschuren, L. J. M. J., & Cuomo, V. (2012) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2012.00002 · Cited by 69 · see citing works

Propofol Enhances Memory Formation via an Interaction with the Endocannabinoid System

Hauer, D., Ratano, P., Morena, M., Scaccianoce, S., Briegel, I., Palmery, M., Cuomo, V., Roozendaal, B., Schelling, G., & Campolongo, P. (2011) · Anesthesiology · doi:10.1097/aln.0b013e31821c120e · Cited by 68 · see citing works

Role of the satiety factor oleoylethanolamide in alcoholism

Bilbao, A., Serrano, A., Cippitelli, A., Pavón, F. J., Giuffrida, A., Suárez, J., García‐Marchena, N., Baixerás, E., de Heras, R. G., Orío, L., et al. (2015) · Addiction Biology · doi:10.1111/adb.12276 · Cited by 67 · see citing works

Extinction of avoidance behavior by safety learning depends on endocannabinoid signaling in the hippocampus

Micale, V., Stepan, J., Jurik, A., Pamplona, F. A., Marsch, R., Drago, F., Eder, M., & Wotjak, C. T. (2017) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2017.02.002 · Cited by 62 · see citing works

PPARα Signaling in the Hippocampus: Crosstalk Between Fat and Memory

Roy, A., & Pahan, K. (2015) · Journal of Neuroimmune Pharmacology · doi:10.1007/s11481-014-9582-9 · Cited by 61 · see citing works

Oleoylethanolamide: The role of a bioactive lipid amide in modulating eating behaviour

Sihag, J., & Jones, P. J. H. (2017) · Obesity Reviews · doi:10.1111/obr.12630 · Cited by 59 · see citing works

The Role of Nuclear Hormone Receptors in Cannabinoid Function

Pistis, M., & O’Sullivan, S. E. (2017) · Advances in pharmacology · doi:10.1016/bs.apha.2017.03.008 · Cited by 56 · see citing works

The omega-3 hydroxy fatty acid 7( S )-HDHA is a high-affinity PPARα ligand that regulates brain neuronal morphology

Liu, J., Sahin, C., Ahmad, S., Magomedova, L., Zhang, M., Jia, Z., Metherel, A. H., Orellana, A. J., Poda, G. I., Bazinet, R. P., et al. (2022) · Science Signaling · doi:10.1126/scisignal.abo1857 · Cited by 48 · see citing works

Post-training disruption of Arc protein expression in the anterior cingulate cortex impairs long-term memory for inhibitory avoidance training

Holloway-Erickson, C. M., & McIntyre, C. K. (2011) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2011.02.002 · Cited by 48 · see citing works

A Postnatal Diet Containing Phospholipids, Processed to Yield Large, Phospholipid-Coated Lipid Droplets, Affects Specific Cognitive Behaviors in Healthy Male Mice

Schipper, L., van Dijk, G., Broersen, L. M., Loos, M., Bartke, N., Scheurink, A. J. W., & van der Beek, E. M. (2016) · Journal of Nutrition · doi:10.3945/jn.115.224998 · Cited by 48 · see citing works

Oleoylethanolamide treatment reduces neurobehavioral deficits and brain pathology in a mouse model of Gulf War Illness

Joshi, U., Evans, J. E., Joseph, R. A., Emmerich, T., Saltiel, N. A., Lungmus, C., Oberlin, S., Langlois, H., Ojo, J. O., Mouzon, B., et al. (2018) · Scientific Reports · doi:10.1038/s41598-018-31242-7 · Cited by 48 · see citing works

Understanding Peroxisome Proliferator-Activated Receptors: From the Structure to the Regulatory Actions on Metabolism

Bervejillo, M. L., & Ferreira, A. M. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-11488-6_3 · Cited by 46 · see citing works

The endocannabinoid transport inhibitor AM404 differentially modulates recognition memory in rats depending on environmental aversiveness

Campolongo, P., Ratano, P., Manduca, A., Scattoni, M. L., Palmery, M., Trezza, V., & Cuomo, V. (2012) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2012.00011 · Cited by 48 · see citing works

Low brain endocannabinoids associated with persistent non-goal directed nighttime hyperactivity after traumatic brain injury in mice

Vogel, A., Wilken‐Schmitz, A., Hummel, R., Lang, M., Gurke, R., Schreiber, Y., Schäfer, M. K. E., & Tegeder, I. (2020) · Scientific Reports · doi:10.1038/s41598-020-71879-x · Cited by 43 · see citing works

Computational insights into function and inhibition of fatty acid amide hydrolase

Palermo, G., Röthlisberger, U., Cavalli, A., & Vivo, M. D. (2014) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2014.09.037 · Cited by 41 · see citing works

Cannabinoid Modulation of Memory Consolidation in Rats: Beyond the Role of Cannabinoid Receptor Subtype 1

Ratano, P., Palmery, M., Trezza, V., & Campolongo, P. (2017) · Frontiers in Pharmacology · doi:10.3389/fphar.2017.00200 · Cited by 41 · see citing works

Oleoylethanolamide dose‐dependently attenuates cocaine‐induced behaviours through a PPARα receptor‐independent mechanism

Bilbao, A., Blanco, E., Rojas, M. J. L., Suárez, J., Palomino, A., Vida, M., Araos, P. F., Bermúdez‐Silva, F. J., Fernández‐Espejo, E., Spanagel, R., et al. (2012) · Addiction Biology · doi:10.1111/adb.12006 · Cited by 39 · see citing works

Systemic Administration of Substance P Recovers Beta Amyloid-Induced Cognitive Deficits in Rat: Involvement of Kv Potassium Channels

Campolongo, P., Ratano, P., Ciotti, M. T., Florenzano, F., Nori, S. L., Marolda, R., Palmery, M., Rinaldi, A. M., Zona, C., Possenti, R., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0078036 · Cited by 37 · see citing works

Oleoylethanolamide: A Novel Potential Pharmacological Alternative to Cannabinoid Antagonists for the Control of Appetite

Romano, A., Coccurello, R., Giacovazzo, G., Bedse, G., Moles, A., & Gaetani, S. (2014) · BioMed Research International · doi:10.1155/2014/203425 · Cited by 37 · see citing works

Revealing the role of the endocannabinoid system modulators, SR141716A, URB597 and VDM-11, in sleep homeostasis

Murillo‐Rodríguez, E., Machado, S. E. D. C., Rocha, N., Budde, H., Yuan, T., & Arias-Carrión, Ó. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.10.011 · Cited by 36 · see citing works

Inhibition of fatty acid amide hydrolase by chlorpyrifos in juvenile rats results in altered exploratory and social behavior as adolescents

Carr, R. L., Alugubelly, N., de Leon, K., Loyant, L., Mohammed, A. N., Patterson, M. E., Ross, M. K., & Rowbotham, N. E. (2020) · NeuroToxicology · doi:10.1016/j.neuro.2020.01.002 · Cited by 36 · see citing works

Cannabinoid receptor as a potential therapeutic target for Parkinson’s Disease

Baul, H. S., Manikandan, C., & Sen, D. (2019) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2019.01.016 · Cited by 32 · see citing works

Interference with acute nausea and anticipatory nausea in rats by fatty acid amide hydrolase (FAAH) inhibition through a PPARα and CB1 receptor mechanism, respectively: a double dissociation

Rock, E. M., Limebeer, C. L., Ward, J. M., Cohen, A., Grove, K., Niphakis, M. J., Cravatt, B. F., & Parker, L. A. (2015) · Psychopharmacology · doi:10.1007/s00213-015-4050-7 · Cited by 30 · see citing works

Wagging the Tail: Essential Role of Substrate Flexibility in FAAH Catalysis

Palermo, G., Campomanes, P., Neri, M., Piomelli, D., Cavalli, A., Röthlisberger, U., & Vivo, M. D. (2013) · Journal of Chemical Theory and Computation · doi:10.1021/ct300611q · Cited by 27 · see citing works

Selected bioactives from callus cultures of olives (Olea europaea L. Var. Coratina) by LC-MS

Gentile, L., & Uccella, N. (2013) · Food Research International · doi:10.1016/j.foodres.2013.10.046 · Cited by 27 · see citing works

Milk lipid composition and structure; The relevance for infant brain development

Schipper, L., van Dijk, G., & van der Beek, E. M. (2020) · OCL · doi:10.1051/ocl/2020001 · Cited by 28 · see citing works

On making (and turning adaptive to) maladaptive aversive memories in laboratory rodents

Gazarini, L., Stern, C. A. J., & Bertoglio, L. J. (2023) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105101 · Cited by 25 · see citing works

Modulations of Neuroendocrine Stress Responses During Confinement in Antarctica and the Role of Hypobaric Hypoxia

Strewe, C., Thieme, D., Dangoisse, C., Fiedel, B., van den Berg, F., Bauer, H., Salam, A. P., Gössmann-Lang, P., Campolongo, P., Moser, D., et al. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.01647 · Cited by 24 · see citing works

Engineering yeast phospholipid metabolism for de novo oleoylethanolamide production

Liu, Y., Liu, Q., Krivoruchko, A., Khoomrung, S., & Nielsen, J. (2019) · Nature Chemical Biology · doi:10.1038/s41589-019-0431-2 · Cited by 24 · see citing works

Brain region‐specific changes in N‐acylethanolamine contents with time of day

Liedhegner, E. S., Sasman, A., & Hillard, C. J. (2013) · Journal of Neurochemistry · doi:10.1111/jnc.12495 · Cited by 24 · see citing works

Brain histamine and oleoylethanolamide restore behavioral deficits induced by chronic social defeat stress in mice

Rani, B., Santangelo, A., Romano, A., Koczwara, J. B., Friuli, M., Provensi, G., Blandina, P., Casarrubea, M., Gaetani, S., Passani, M. B., et al. (2021) · Neurobiology of Stress · doi:10.1016/j.ynstr.2021.100317 · Cited by 22 · see citing works

Cannabinoid modulation of mother-infant interaction: is it just about milk?

Manduca, A., Campolongo, P., & Trezza, V. (2012) · Reviews in the Neurosciences · doi:10.1515/revneuro-2012-0074 · Cited by 22 · see citing works

Brain Molecules and Appetite: The Case of Oleoylethanolamide

Sarro-Ramírez, A., Sanchez-Lopez, D., Tejeda-Padrón, A., Frias, C., Rae, J. Z., & Murillo‐Rodríguez, E. (2013) · Central Nervous System Agents in Medicinal Chemistry · doi:10.2174/1871524911313010010 · Cited by 23 · see citing works

Palmitoylethanolamide prevents neuroinflammation, reduces astrogliosis and preserves recognition and spatial memory following induction of neonatal anoxia-ischemia

Holubiec, M. I., Romero, J. I., Suárez, J., Portavella, M., Fernández‐Espejo, E., Blanco, E., Galeano, P., & de Fonseca, F. R. (2018) · Psychopharmacology · doi:10.1007/s00213-018-4982-9 · Cited by 23 · see citing works

Chronic Oleoylethanolamide Treatment Decreases Hepatic Triacylglycerol Level in Rat Liver by a PPARγ/SREBP-Mediated Suppression of Fatty Acid and Triacylglycerol Synthesis

Romano, A., Friuli, M., Coco, L. D., Longo, S., Vergara, D., Boccio, P. D., Valentinuzzi, S., Cicalini, I., Fanizzi, F. P., Gaetani, S., et al. (2021) · Nutrients · doi:10.3390/nu13020394 · Cited by 24 · see citing works

Vasorelaxation toN‐oleoylethanolamine in rat isolated arteries: mechanisms of action and modulation via cyclooxygenase activity

Wheal, A., Alexander, S., & Randall, M. (2010) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2010.00770.x · Cited by 23 · see citing works

Cannabinoids in Health and Disease

Meccariello, R., & Chianese, R. (2016) · InTech eBooks · doi:10.5772/61595 · Cited by 21 · see citing works

Histaminergic Neurotransmission as a Gateway for the Cognitive Effect of Oleoylethanolamide in Contextual Fear Conditioning

Provensi, G., Fabbri, R., Munari, L., Costa, A., Baldi, E., Bucherelli, C., Blandina, P., & Passani, M. B. (2016) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyw110 · Cited by 20 · see citing works

Environmental Enrichment, Age, and PPARα Interact to Regulate Proliferation in Neurogenic Niches

Pérez‐Martín, M., Rivera, P., Blanco, E., Lorefice, C., Decara, J. M., Pavón, F. J., Serrano, A., de Fonseca, F. R., & Suárez, J. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2016.00089 · Cited by 19 · see citing works

Ketamine anesthesia enhances fear memory consolidation via noradrenergic activation in the basolateral amygdala

Morena, M., Colucci, P., Mancini, G. F., Castro, V. D., Peloso, A., Schelling, G., & Campolongo, P. (2020) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2020.107362 · Cited by 19 · see citing works

Oleoylethanolamide: a new player in energy metabolism control. Role in food intake

Dipasquale, P., Romano, A., Cianci, S., Righetti, L., & Gaetani, S. (2010) · Drug Discovery Today Disease Mechanisms · doi:10.1016/j.ddmec.2011.01.004 · Cited by 19 · see citing works

N-Palmitoylethanolamine Maintains Local Lipid Homeostasis to Relieve Sleep Deprivation–Induced Dry Eye Syndrome

Chen, Q., Ji, C., Zheng, R., Yang, L., Ren, J., Li, Y., Han, Y., Zhou, P., Liu, Z., & Qiu, Y. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2019.01622 · Cited by 18 · see citing works

Role of oleoylethanolamide as a feeding regulator in goldfish

Tinoco, A. B., Armirotti, A., Isorna, E., Delgado, M. J., Piomelli, D., & de Pedro, N. (2014) · Journal of Experimental Biology · doi:10.1242/jeb.106161 · Cited by 18 · see citing works

Positive and negative emotional arousal increases duration of memory traces: common and independent mechanisms

Cruciani, F. (2011) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2011.00086 · Cited by 18 · see citing works

Eating disorders: from bench to bedside and back

Gaetani, S., Romano, A., Provensi, G., Ricca, V., Lutz, T. A., & Passani, M. B. (2016) · Journal of Neurochemistry · doi:10.1111/jnc.13848 · Cited by 17 · see citing works

The hypophagic factor oleoylethanolamide differentially increases c-fos expression in appetite regulating centres in the brain of wild type and histamine deficient mice

Umehara, H., Fabbri, R., Provensi, G., & Passani, M. B. (2016) · Pharmacological Research · doi:10.1016/j.phrs.2016.08.020 · Cited by 16 · see citing works

Oleoylethanolamide restores alcohol-induced inhibition of neuronal proliferation and microglial activity in striatum

Rivera, P., Silva‐Peña, D., Blanco, E., Vargas, A., Arrabal, S., Serrano, A., Pavón, F. J., Bîndilă, L., Lutz, B., de Fonseca, F. R., et al. (2018) · Neuropharmacology · doi:10.1016/j.neuropharm.2018.11.037 · Cited by 16 · see citing works

Persistent proteomic changes in glutamatergic and GABAergic signaling in the amygdala of adolescent rats exposed to chlorpyrifos as juveniles

Alugubelly, N., Mohammed, A. N., & Carr, R. L. (2021) · NeuroToxicology · doi:10.1016/j.neuro.2021.05.012 · Cited by 15 · see citing works

Circadian regulation of memory under stress: Endocannabinoids matter

Morena, M., Santori, A., & Campolongo, P. (2022) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2022.104712 · Cited by 14 · see citing works

“To brain or not to brain”: evaluating the possible direct effects of the satiety factor oleoylethanolamide in the central nervous system

Romano, A., Friuli, M., Eramo, B., Gallelli, C. A., Koczwara, J. B., Azari, E. K., Paquot, A., Arnold, M., Langhans, W., Muccioli, G. G., et al. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1158287 · Cited by 14 · see citing works

Mammalian Fatty Acid Amides of the Brain and CNS

Waluk, D. P., Battistini, M. R., Dempsey, D. R., Farrell, E. K., Jeffries, K. A., Mitchell, P. R., Hernandez, L. W., McBride, J. C., Merkler, D. J., & Hunt, M. C. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-410527-0.00009-0 · Cited by 15 · see citing works

Transcriptional regulation of human and murine short-chain dehydrogenase/reductases (SDRs) – an in silico approach

Ebert, B., Kisiela, M., & Maser, E. (2016) · Drug Metabolism Reviews · doi:10.3109/03602532.2016.1167902 · Cited by 14 · see citing works

Cerebellar and cortical TLR4 activation and behavioral impairments in Wernicke-Korsakoff Syndrome: Pharmacological effects of oleoylethanolamide

Moya, M., Felipe, D. S., Ballesta, A., Alén, F., de Fonseca, F. R., García‐Bueno, B., Marco, E. M., & Orío, L. (2020) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2020.110190 · Cited by 14 · see citing works

Pharmacological Blockade of PPARα Exacerbates Inflammatory Pain-Related Impairment of Spatial Memory in Rats

Gaspar, J. C., Healy, C. R., Ferdousi, M. I., Roche, M., & Finn, D. P. (2021) · Biomedicines · doi:10.3390/biomedicines9060610 · Cited by 14 · see citing works

Oleoylethanolamide Delays the Dysfunction and Death of Purkinje Cells and Ameliorates Behavioral Defects in a Mouse Model of Cerebellar Neurodegeneration

Pérez-Martín, E., Muñoz-Castañeda, R., Moutin, M., Ávila-Zarza, C. A., Munõz-Castañeda, J. M., del Pilar, C., Alonso, J. R., Andrieux, A., Díaz, D., & Weruaga, E. (2021) · Neurotherapeutics · doi:10.1007/s13311-021-01044-3 · Cited by 12 · see citing works

High energy diets prevent the enhancing effects of emotional arousal on memory.

Ross, A. P., Darling, J. N., & Parent, M. B. (2013) · Behavioral Neuroscience · doi:10.1037/a0033732 · Cited by 12 · see citing works

Roles of N-Acylethanolamines in Brain Functions and Neuropsychiatric Diseases

Pistis, M., & Muntoni, A. L. (2017) · Springer eBooks · doi:10.1007/978-3-319-57371-7_11 · Cited by 12 · see citing works

Cannabinoid activation of peroxisome proliferator‐activated receptors: an update and review of the physiological relevance

O’Sullivan, S. E. (2012) · Wiley Interdisciplinary Reviews Membrane Transport and Signalling · doi:10.1002/wmts.73 · Cited by 11 · see citing works

Pharmacological Blockade of PPAR Isoforms Increases Conditioned Fear Responding in the Presence of Nociceptive Tone

Gaspar, J. C., Okine, B. N., Llorente‐Berzal, A., Roche, M., & Finn, D. P. (2020) · Molecules · doi:10.3390/molecules25041007 · Cited by 11 · see citing works

Memory Consolidation Depends on Endogenous Hippocampal Levels of Anandamide: CB1 and M4, but Possibly not TRPV1 Receptors Mediate AM404 effects

Scienza-Martin, K., Lotz, F. N., Zanona, Q. K., Santana, F., Crestani, A. P., Boos, F. Z., Calcagnotto, M. E., & Quillfeldt, J. A. (2022) · Neuroscience · doi:10.1016/j.neuroscience.2022.04.009 · Cited by 10 · see citing works

Profound Modification of Fatty Acid Profile and Endocannabinoid-Related Mediators in PPARα Agonist Fenofibrate-Treated Mice

Murru, E., Muntoni, A. L., Manca, C., Aroni, S., Pistis, M., Banni, S., & Carta, G. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms24010709 · Cited by 10 · see citing works

Effects of Intra-BLA Administration of PPAR Antagonists on Formalin-Evoked Nociceptive Behaviour, Fear-Conditioned Analgesia, and Conditioned Fear in the Presence or Absence of Nociceptive Tone in Rats

Gaspar, J. C., Okine, B. N., Dinneen, D., Roche, M., & Finn, D. P. (2022) · Molecules · doi:10.3390/molecules27062021 · Cited by 8 · see citing works

Relationship between sex, APOE genotype, endocannabinoids and cognitive change in older adults with metabolic syndrome during a 3-year Mediterranean diet intervention

Soldevila‐Domenech, N., Fagundo, A. B., Cuenca‐Royo, A., Forcano, L., Gomis‐González, M., Boronat, A., Pastor, A., Castañer, O., Zomeño, M. D., Goday, A., et al. (2024) · Nutrition Journal · doi:10.1186/s12937-024-00966-w · Cited by 9 · see citing works

Satiety Signal and Memory Enhancer

Gough, N. R. (2009) · Science Signaling · doi:10.1126/scisignal.271ec165

Histaminergic Neurotransmission as a Gateway for the Cognitive Effect of Oleoylethanolamide in Contextual Fear Conditioning

Provensi, G., Fabbri, R., Munari, L., Costa, A., Baldi, E., Bucherelli, C., Blandina, P., & Passani, M. B. (2016) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyw110 · Cited by 20 · see citing works

Orphanin FQ/nociceptin interacts with the basolateral amygdala noradrenergic system in memory consolidationPreprint

Roozendaal, B., Lengvilas, R., McGaugh, J. L., Civelli, O., & Reinscheid, R. K. (2007) · Learning & Memory · doi:10.1101/lm.403607 · Cited by 52 · see citing works

The satiety signal oleoylethanolamide stimulates oxytocin neurosecretion from rat hypothalamic neurons

Romano, A., Cassano, T., Tempesta, B., Cianci, S., Dipasquale, P., Coccurello, R., Cuomo, V., & Gaetani, S. (2013) · Peptides · doi:10.1016/j.peptides.2013.08.006 · Cited by 43 · see citing works

Histamine in the basolateral amygdala contributes to oleoylethanolamide-induced precognitive effects

Provensi, G., Munari, L., BALDI, E., Bucherelli, C., Blandina, P., & PASSANI, M. B. (2015) · Florence Research (University of Florence)