Neuropeptides and the Microbiota-Gut-Brain Axis
Open accessAbstract
Neuropeptides are important mediators both within the nervous system and between neurons and other cell types. Neuropeptides such as substance P, calcitonin gene-related peptide and neuropeptide Y (NPY), vasoactive intestinal polypeptide, somatostatin and corticotropin-releasing factor are also likely to play a role in the bidirectional gut-brain communication. In this capacity they may influence the activity of the gastrointestinal microbiota and its interaction with the gut-brain axis. Current efforts in elucidating the implication of neuropeptides in the microbiota-gut-brain axis address four information carriers from the gut to the brain (vagal and spinal afferent neurons; immune mediators such as cytokines; gut hormones; gut microbiota-derived signalling molecules) and four information carriers from the central nervous system to the gut (sympathetic efferent neurons; parasympathetic efferent neurons; neuroendocrine factors involving the adrenal medulla; neuroendocrine factors involving the adrenal cortex). Apart from operating as neurotransmitters, many biologically active peptides also function as gut hormones. Given that neuropeptides and gut hormones target the same cell membrane receptors (typically G protein-coupled receptors), the two messenger roles often converge in the same or similar biological implications. This is exemplified by NPY and peptide YY (PYY), two members of the PP-fold peptide family. While PYY is almost exclusively expressed by enteroendocrine cells, NPY is found at all levels of the gut-brain and brain-gut axis. The function of PYY-releasing enteroendocrine cells is directly influenced by short chain fatty acids generated by the intestinal microbiota from indigestible fibre, while NPY may control the impact of the gut microbiota on inflammatory processes, pain, brain function and behaviour. Although the impact of neuropeptides on the interaction between the gut microbiota and brain awaits to be analysed, biologically active peptides are likely to emerge as neural and endocrine messengers in orchestrating the microbiota-gut-brain axis in health and disease.
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The gastrointestinal tract responds to stress in an endocrine manner by releasing hormones such as GABA, neuropeptide Y and dopamine.
“Additionally, gastrointestinal tract responds to stress in an endocrine manner by releasing hormones such as Gamma-amino butyric acid (GABA), neuropeptide Y and dopamine that have been purported to be involved in the gastrointestinal disturbances, anxiety, depression, reduced food intake and less stress coping.”
From Exercise-induced stress behavior, gut-microbiota-brain axis and diet: a systematic review for athletes (2016) · cites this paper as [37]
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Cites
Molecular Mechanisms of Depression: Perspectives on New Treatment Strategies
Lang, U. E., & Borgwardt, S. (2013) · Cellular Physiology and Biochemistry · doi:10.1159/000350094 · Cited by 8,501 · see citing works
From inflammation to sickness and depression: when the immune system subjugates the brain
Dantzer, R., O'Connor, J. C., Freund, G. G., Johnson, R. W., & Kelley, K. W. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2297 · Cited by 7,395 · see citing works
Host-gut microbiota metabolic interactions
Nicholson, J. K., Holmes, E., Kinross, J., Burcelin, R., Gibson, G., Jia, W., & Pettersson, S. (2012) · Science · doi:10.1126/science.1223813 · Cited by 4,760 · see citing works
Physiology of the Gastrointestinal Tract
Johnson, L. R. (2006) · Elsevier eBooks · doi:10.1016/b978-0-12-088394-3.x5000-4 · Cited by 4,611 · see citing works
Mind-altering microorganisms: the impact of the gut microbiota on brain and behaviour
Cryan, J. F., & Dinan, T. G. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3346 · Cited by 4,572 · see citing works
Functional interactions between the gut microbiota and host metabolism
Tremaroli, V., & Bäckhed, F. (2012) · Nature · doi:10.1038/nature11552 · Cited by 4,387 · see citing works
Bravo, J. A., Forsythe, P., Chew, M. V., Escaravage, E., Savignac, H. M., Dinan, T. G., Bienenstock, J., & Cryan, J. F. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1102999108 · Cited by 3,888 · see citing works
The Physiology of Glucagon-like Peptide 1
Holst, J. J. (2007) · Physiological Reviews · doi:10.1152/physrev.00034.2006 · Cited by 3,371 · see citing works
Gut microbiota composition correlates with diet and health in the elderly
Claesson, M. J., Jeffery, I. B., Conde, S., Power, S. E., O’Connor, E. M., Cusack, S., Harris, H. M. B., Coakley, M., Lakshminarayanan, B., O’Sullivan, O., et al. (2012) · Nature · doi:10.1038/nature11319 · Cited by 3,314 · see citing works
Normal gut microbiota modulates brain development and behavior
Heijtz, R. D., Wang, S., Anuar, F., Qian, Y., Björkholm, B., Samuelsson, A., Hibberd, M. L., Forssberg, H., & Pettersson, S. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1010529108 · Cited by 3,228 · see citing works
Sudo, N., Chida, Y., Aiba, Y., Sonoda, J., Oyama, N., Yu, X., Kubo, C., & Koga, Y. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2004.063388 · Cited by 2,735 · see citing works
Metabolomics analysis reveals large effects of gut microflora on mammalian blood metabolites
Wikoff, W. R., Anfora, A. T., Liu, J., Schultz, P. G., Lesley, S. A., Peters, E. C., & Siuzdak, G. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0812874106 · Cited by 2,677 · see citing works
Cani, P. D., Possemiers, S., Van de Wiele, T., Guiot, Y., Everard, A., Rottier, O., Geurts, L., Naslain, D., Neyrinck, A., Lambert, D. M., et al. (2009) · Gut · doi:10.1136/gut.2008.165886 · Cited by 2,518 · see citing works
Guide to receptors and channels (GRAC), 5th edition
Alexander, S., Mathie, A., & Peters, J. (2011) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2011.01649_1.x · Cited by 1,947 · see citing works
Clarke, G., Grenham, S., Scully, P., Fitzgerald, P., Moloney, R. D., Shanahan, F., Dinan, T. G., & Cryan, J. F. (2013) · Molecular Psychiatry · doi:10.1038/mp.2012.77 · Cited by 1,893 · see citing works
Bercik, P., Denou, E., Collins, J., Jackson, W., Lu, J., Jury, J., Deng, Y., Blennerhassett, P., Macri, J., McCoy, K. D., et al. (2011) · Gastroenterology · doi:10.1053/j.gastro.2011.04.052 · Cited by 1,748 · see citing works
Pearse, A. G. E. (1969) · Journal of Histochemistry & Cytochemistry · doi:10.1177/17.5.303 · Cited by 1,681 · see citing works
The interplay between the intestinal microbiota and the brain
Collins, S. M., Surette, M., & Bercik, P. (2012) · Nature Reviews Microbiology · doi:10.1038/nrmicro2876 · Cited by 1,611 · cited 1× · see citing works
“• microbial factors that may directly reach the brain via the blood stream but can also interact with the other 3 transmission pathways [6-8].”
Samuel, B. S., Shaito, A., Motoike, T., Rey, F. E., Backhed, F., Manchester, J. K., Hammer, R. E., Williams, S. C., Crowley, J., Yanagisawa, M., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0808567105 · Cited by 1,564 · see citing works
Neufeld, K. M., Kang, N., Bienenstock, J., & Foster, J. A. (2011) · Neurogastroenterology & Motility · doi:10.1111/j.1365-2982.2010.01620.x · Cited by 1,392 · see citing works
Proinflammatory T-cell responses to gut microbiota promote experimental autoimmune encephalomyelitis
Lee, Y. K., Menezes, J. S., Umesaki, Y., & Mazmanian, S. K. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1000082107 · Cited by 1,323 · see citing works
Abreu, M. T. (2010) · Nature Reviews Immunology · doi:10.1038/nri2707 · Cited by 1,288 · see citing works
Commensal microbiota and myelin autoantigen cooperate to trigger autoimmune demyelination
Berer, K., Mues, M., Koutrolos, M., Rasbi, Z. A., Boziki, M., Johner, C., Wekerle, H., & Krishnamoorthy, G. (2011) · Nature · doi:10.1038/nature10554 · Cited by 1,251 · see citing works
Immune system to brain signaling: Neuropsychopharmacological implications
Capuron, L., & Miller, A. H. (2011) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2011.01.014 · Cited by 1,195 · see citing works
γ-Aminobutyric acid production by culturable bacteria from the human intestine
Barrett, E., Ross, R. P., O'Toole, P. W., Fitzgerald, G. F., & Stanton, C. (2012) · Journal of Applied Microbiology · doi:10.1111/j.1365-2672.2012.05344.x · Cited by 1,156 · see citing works
Recognition of peptidoglycan from the microbiota by Nod1 enhances systemic innate immunity
Clarke, T. B., Davis, K. M., Lysenko, E. S., Zhou, A. Y., Yu, Y., & Weiser, J. N. (2010) · Nature Medicine · doi:10.1038/nm.2087 · Cited by 1,154 · see citing works
Peripheral education of the immune system by colonic commensal microbiota
Lathrop, S. K., Bloom, S. M., Rao, S. M., Nutsch, K., Lio, C.-W., Santacruz, N., Peterson, D. A., Stappenbeck, T. S., & Hsieh, C.-S. (2011) · Nature · doi:10.1038/nature10434 · Cited by 1,034 · see citing works
Bercik, P., Park, A. J., Sinclair, D., Khoshdel, A., Lu, J., Huang, X., Deng, Y., Blennerhassett, P. A., Fahnestock, M., Moine, D., et al. (2011) · Neurogastroenterology & Motility · doi:10.1111/j.1365-2982.2011.01796.x · Cited by 1,018 · see citing works
Bacterial infection causes stress-induced memory dysfunction in mice
Gareau, M. G., Wine, E., Rodrigues, D. M., Cho, J. H., Whary, M. T., Philpott, D. J., MacQueen, G., & Sherman, P. M. (2011) · Gut · doi:10.1136/gut.2009.202515 · Cited by 909 · cited 2× · see citing works
“At the behavioural level, germ-free animals exhibit reduced anxiety in three [43,58,59] but one study [60].”
Lactobacillus acidophilus modulates intestinal pain and induces opioid and cannabinoid receptors
Rousseaux, C., Thuru, X., Gelot, A., Barnich, N., Neut, C., Dubuquoy, L., Dubuquoy, C., Merour, E., Geboes, K., Chamaillard, M., et al. (2007) · Nature Medicine · doi:10.1038/nm1521 · Cited by 793 · see citing works
Cani, P. D., Lecourt, E., Dewulf, E. M., Sohet, F. M., Pachikian, B. D., Naslain, D., Backer, F. D., Neyrinck, A. M., & Delzenne, N. M. (2009) · American Journal of Clinical Nutrition · doi:10.3945/ajcn.2009.28095 · Cited by 763 · see citing works
Handbook of Biologically Active Peptides
(2006) · Elsevier eBooks · doi:10.1016/b978-0-12-369442-3.x5001-6 · Cited by 720 · see citing works
The endocannabinoid system links gut microbiota to adipogenesis
Muccioli, G. G., Naslain, D., Bäckhed, F., Reigstad, C. S., Lambert, D. M., Delzenne, N. M., & Cani, P. D. (2010) · Molecular Systems Biology · doi:10.1038/msb.2010.46 · Cited by 691 · see citing works
Asano, Y., Hiramoto, T., Nishino, R., Aiba, Y., Kimura, T., Yoshihara, K., Koga, Y., & Sudo, N. (2012) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00341.2012 · Cited by 659 · see citing works
The orexigenic hormone ghrelin defends against depressive symptoms of chronic stress
Lutter, M., Sakata, I., Osborne-Lawrence, S., Rovinsky, S. A., Anderson, J. G., Jung, S., Birnbaum, S., Yanagisawa, M., Elmquist, J. K., Nestler, E. J., et al. (2008) · Nature Neuroscience · doi:10.1038/nn.2139 · Cited by 644 · see citing works
Regulation of the stress response by the gut microbiota: implications for psychoneuroendocrinology
Dinan, T. G., & Cryan, J. F. (2012) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2012.03.007 · Cited by 577 · see citing works
Lyte, M. (2011) · BioEssays · doi:10.1002/bies.201100024 · Cited by 549 · see citing works
The brain-gut axis in abdominal pain syndromes.
Mayer, E. A., & Tillisch, K. (2011) · Annual Review of Medicine · doi:10.1146/annurev-med-012309-103958 · Cited by 511 · see citing works
Neuropeptide, Y, peptide YY and pancreatic polypeptide in the gut-brain axis
Holzer, P., Reichmann, F., & Farzi, A. (2012) · Neuropeptides · doi:10.1016/j.npep.2012.08.005 · Cited by 501 · see citing works
Self-citationQueipo-Ortuño, M. I., Seoane, L. M., Murri, M., Pardo, M., Gomez-Zumaquero, J. M., Cardona, F., Casanueva, F., & Tinahones, F. J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0065465 · Cited by 497 · see citing works
PYY modulation of cortical and hypothalamic brain areas predicts feeding behaviour in humans
Batterham, R. L., Ffytche, D. H., Rosenthal, J., Zelaya, F. O., Barker, G. J., Withers, D. J., & Williams, S. (2007) · Nature · doi:10.1038/nature06212 · Cited by 474 · see citing works
Genetic variation in human NPY expression affects stress response and emotion
Zhou, Z., Zhu, G., Hariri, A. R., Enoch, M.-A., Scott, D., Sinha, R., Virkkunen, M., Mash, D. C., Lipsky, R. H., Hu, X.-Z., et al. (2008) · Nature · doi:10.1038/nature06858 · Cited by 455 · see citing works
Specific probiotic therapy attenuates antibiotic induced visceral hypersensitivity in mice
Verdú, E. F., Bercik, P., Verma-Gandhu, M., Huang, X.-X., Blennerhassett, P., Jackson, W., Mao, Y., Wang, L., Rochat, F., & Collins, S. M. (2006) · Gut · doi:10.1136/gut.2005.066100 · Cited by 448 · see citing works
Maes, M., Kubera, M., Leunis, J.-C., & Berk, M. (2012) · Journal of Affective Disorders · doi:10.1016/j.jad.2012.02.023 · Cited by 446 · see citing works
The role of the vagal nerve in peripheral PYY3-36-induced feeding reduction in rats
Koda, S., Date, Y., Murakami, N., Shimbara, T., Hanada, T., Toshinai, K., Niijima, A., Furuya, M., Inomata, N., Osuye, K., et al. (2005) · Endocrinology · doi:10.1210/en.2004-1266 · Cited by 431 · see citing works
Immune–neural connections: how the immune system’s response to infectious agents influences behavior
McCusker, R. H., & Kelley, K. W. (2013) · Journal of Experimental Biology · doi:10.1242/jeb.073411 · Cited by 429 · see citing works
Handbook of Biologically Active Peptides
(2013) · Elsevier eBooks · doi:10.1016/c2010-0-66490-x · Cited by 403 · see citing works
Gut microbial products regulate murine gastrointestinal motility via Toll-like receptor 4 signaling
Anitha, M., Vijay–Kumar, M., Sitaraman, S. V., Gewirtz, A. T., & Srinivasan, S. (2012) · Gastroenterology · doi:10.1053/j.gastro.2012.06.034 · Cited by 397 · see citing works
MacFabe, D. F., Cain, N. E., Boon, F., Ossenkopp, K.-P., & Cain, D. P. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.10.005 · Cited by 365 · see citing works
The neurocircuitry and receptor subtypes mediating anxiolytic-like effects of neuropeptide Y
Kask, A., Harro, J., von Hörsten, S., Redrobe, J. P., Dumont, Y., & Quirion, R. (2002) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(01)00066-5 · Cited by 358 · see citing works
Marcobal, A. M., Kashyap, P., Nelson, T. A., Aronov, P. A., Donia, M. S., Spormann, A. M., Fischbach, M. A., & Sonnenburg, J. L. (2013) · The ISME Journal · doi:10.1038/ismej.2013.89 · Cited by 351 · see citing works
The gut microbiome as therapeutic target
Cani, P. D., & Delzenne, N. M. (2011) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2011.01.012 · Cited by 350 · see citing works
Voices from within: gut microbes and the CNS
Forsythe, P., & Kunze, W. A. (2013) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-012-1028-z · Cited by 336 · see citing works
Commensal microbiota is fundamental for the development of inflammatory pain
Amaral, F. A., Sachs, D., Costa, V. V., Fagundes, C. T., Cisalpino, D., Cunha, T. M., Ferreira, S. H., Cunha, F. Q., Silva, T. A., Nicoli, J. R., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0711891105 · Cited by 289 · see citing works
Toll-like Receptors 3, 4, and 7 Are Expressed in the Enteric Nervous System and Dorsal Root Ganglia
Barajon, I., Serrao, G., Arnaboldi, F., Opizzi, E., Ripamonti, G., Balsari, A., & Rumio, C. (2009) · Journal of Histochemistry & Cytochemistry · doi:10.1369/jhc.2009.953539 · Cited by 287 · see citing works
Effect of Antibiotic Treatment on the Intestinal Metabolome
Antunes, L. C. M., Han, J., Ferreira, R. B. R., Lolić, P., Borchers, C. H., & Finlay, B. B. (2011) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01664-10 · Cited by 271 · see citing works
Yehuda, R., Brand, S. R., & Yang, R.-K. (2005) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.08.027 · Cited by 244 · see citing works
Colonic endocrine cells in inflammatory bowel disease
El‐Salhy, M., Danielsson, Å., Stenling, R., & Grimelius, L. (1997) · Journal of Internal Medicine · doi:10.1046/j.1365-2796.1997.00237.x · Cited by 235 · see citing works
Cerebral low-molecular metabolites influenced by intestinal microbiota: a pilot study
Matsumoto, M., Kibe, R., Ooga, T., Aiba, Y., Sawaki, E., Koga, Y., & Benno, Y. (2013) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2013.00009 · Cited by 227 · see citing works
Kinzig, K. P., D’Alessio, D. A., Herman, J. P., Sakai, R. R., Vahl, T. P., Figueiredo, H. F., Murphy, E. K., & Seeley, R. J. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-15-06163.2003 · Cited by 219 · see citing works
Neuropeptides: Regulators of Physiological Processes
Strand, F. L. (1999) · Medical Entomology and Zoology · Cited by 219 · see citing works
A possible role of neuropeptide Y in depression and stress
Morales‐Medina, J. C., Dumont, Y., & Quirion, R. (2009) · Brain Research · doi:10.1016/j.brainres.2009.09.077 · Cited by 217 · see citing works
Horvath, A., Dziechciarz, P., & Szajewska, H. (2011) · Alimentary Pharmacology & Therapeutics · doi:10.1111/j.1365-2036.2011.04665.x · Cited by 201 · cited 2× · see citing works
“While these studies have primarily focused on somatic pain, it remains to be investigated whether the NPY/Y receptor system also plays a role in the impact of the gut microbiota on visceral pain sensitivity [66-70].”
Central nervous system pharmacology of neuropeptide Y
Wettstein, J. G., Earley, B., & Junien, J. (1995) · Pharmacology & Therapeutics · doi:10.1016/0163-7258(95)98598-k · Cited by 200 · see citing works
Thomas, R. H., Meeking, M. M., Mepham, J. R., Tichenoff, L., Possmayer, F., Liu, S., & MacFabe, D. F. (2012) · Journal of Neuroinflammation · doi:10.1186/1742-2094-9-153 · Cited by 200 · see citing works
Sensory neuro-immune interactions differ between Irritable Bowel Syndrome subtypes
Hughes, P. A., Harrington, A. M., Castro, J., Liebregts, T., Adam, B., Grasby, D. J., Isaacs, N. J., Maldeniya, L., Martin, C. M., Persson, J., et al. (2012) · Gut · doi:10.1136/gutjnl-2011-301856 · Cited by 195 · see citing works
A fundamental bimodal role for neuropeptide Y1 receptor in the immune system
Wheway, J., Mackay, C. R., Newton, R. A., Sainsbury, A., Boey, D., Herzog, H., & Mackay, F. (2005) · The Journal of Experimental Medicine · doi:10.1084/jem.20051971 · Cited by 194 · see citing works
Karim, I. A. E., Linden, G. J., Orr, D. F., & Lundy, F. T. (2008) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2008.05.014 · Cited by 185 · see citing works
Increased oral detection, but decreased intestinal signaling for fats in mice lacking gut microbiota
Duca, F. A., Swartz, T. D., Sakar, Y., & Covasa, M. (2012) · PLoS ONE · doi:10.1371/journal.pone.0039748 · Cited by 181 · see citing works
Peptide YY abnormalities in gastrointestinal diseases
Adrian, T. E., Savage, A. P., Bacarese-Hamilton, A. J., Wolfe, K., Besterman, H. S., & Bloom, S. R. (1986) · Gastroenterology · doi:10.1016/0016-5085(86)90936-4 · Cited by 176 · see citing works
Fetissov, S. O., Hamze Sinno, M., Coëffier, M., Bole-Feysot, C., Ducrotté, P., Hökfelt, T., & Déchelotte, P. (2008) · Nutrition · doi:10.1016/j.nut.2007.12.006 · Cited by 175 · see citing works
Bowels control brain: gut hormones and obesity
Field, B. C. T., Chaudhri, O. B., & Bloom, S. R. (2010) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2010.93 · Cited by 171 · see citing works
Moreau, M. M., André, C., O’Connor, J. C., Dumich, S. A., Woods, J. A., Kelley, K. W., Dantzer, R., Lestage, J., & Castanon, N. (2008) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2008.04.001 · Cited by 168 · see citing works
NPY and Stress 30 Years Later: The Peripheral View
Hirsch, D., & Żukowska, Z. (2012) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-011-9793-z · Cited by 163 · see citing works
Maes, M. H. J., Song, C., & Yirmiya, R. (2012) · Expert Opinion on Therapeutic Targets · doi:10.1517/14728222.2012.718331 · Cited by 156 · see citing works
Autoantibodies against neuropeptides are associated with psychological traits in eating disorders
Fetissov, S. O., Harro, J., Jaanisk, M., Järv, A., Podar, I., Allik, J., Nilsson, I., Sakthivel, P., Lefvert, A. K., & Hökfelt, T. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0507204102 · Cited by 152 · see citing works
Ji, R., Zhang, X., Wiesenfeld‐Hallin, Z., et al. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-11-06423.1994 · Cited by 152 · see citing works
Relevance of Neuropeptide Y (NPY) in Psychiatry
Eaton, K., Sallee, F. R., & Sah, R. (2007) · Current Topics in Medicinal Chemistry · doi:10.2174/156802607782341037 · Cited by 148 · see citing works
Low Cerebrospinal Fluid Neuropeptide Y Concentrations in Posttraumatic Stress Disorder
Sah, R., Ekhator, N. N., Strawn, J. R., Sallee, F. R., Baker, D. G., Horn, P. S., & Geracioti, T. D. (2009) · Biological Psychiatry · doi:10.1016/j.biopsych.2009.04.037 · Cited by 145 · see citing works
NPY receptors as potential targets for anti‐obesity drug development
Yulyaningsih, E., Zhang, L., Herzog, H., & Sainsbury, A. (2011) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2011.01363.x · Cited by 142 · see citing works
Tonic inhibition of chronic pain by neuropeptide Y
Solway, B., Bose, S. C., Corder, G. F., Donahue, R. R., & Taylor, B. K. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1017719108 · Cited by 139 · see citing works
Biosynthesis, synthesis, and biological activities of pyrrolobenzodiazepines
Gerratana, B. (2010) · Medicinal Research Reviews · doi:10.1002/med.20212 · Cited by 137 · see citing works
Alterations in the Colonic Microbiota in Response to Osmotic Diarrhea
Gorkiewicz, G., Thallinger, G., Trajanoski, S., Lackner, S., Stocker, G., Hinterleitner, T. A., Gülly, C., & Högenauer, C. (2013) · PLoS ONE · doi:10.1371/journal.pone.0055817 · Cited by 129 · see citing works
Neuropeptides from concept to online database www.neuropeptides.nl
Burbach, J. P. H. (2010) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2009.10.015 · Cited by 123 · see citing works
Neuropeptide tyrosine and pain
Brumovsky, P. R., Shi, T.-J. S., Landry, M., Villar, M. J., & Hökfelt, T. G. M. (2007) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2006.12.003 · Cited by 121 · see citing works
NPY and Receptors in Immune and Inflammatory Diseases
Wheway, J., Herzog, H., & Mackay, F. (2007) · Current Topics in Medicinal Chemistry · doi:10.2174/156802607782341046 · Cited by 119 · see citing works
Toll-like receptors in the CNS: implications for neurodegeneration and repair
van Noort, J. M., & Bsibsi, M. (2009) · Progress in brain research · doi:10.1016/s0079-6123(09)17509-x · Cited by 118 · see citing works
Toll-like receptors are key players in neurodegeneration
Arroyo, D. S., Soria, J. A., Gaviglio, E. A., Rodriguez‐Galán, M. C., & Iribarren, P. (2011) · International Immunopharmacology · doi:10.1016/j.intimp.2011.05.006 · Cited by 117 · see citing works
Straub, R. H., Herfarth, H., Falk, W., Andus, T., & Schölmerich, J. (2002) · Journal of Neuroimmunology · doi:10.1016/s0165-5728(02)00047-4 · Cited by 115 · see citing works
Emotion Processing, Major Depression, and Functional Genetic Variation of Neuropeptide Y
Mickey, B. J., Zhou, Z., Heitzeg, M. M., Heinz, E., Hodgkinson, C. A., Hsu, D. T., Langenecker, S. A., Love, T. M., Peciña, M., Shafir, T., et al. (2011) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2010.197 · Cited by 115 · see citing works
Kubera, M., Curzytek, K., Duda, W., Leśkiewicz, M., Basta‐Kaim, A., Budziszewska, B., Roman, A., Zajı́cová, A., Holáň, V., Szczęsny-Małysiak, E., et al. (2013) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2013.01.001 · Cited by 114 · see citing works
Effects of the histone deacetylase inhibitor sodium butyrate in models of depression and anxiety
Gundersen, B. B., & Blendy, J. A. (2009) · Neuropharmacology · doi:10.1016/j.neuropharm.2009.04.008 · Cited by 112 · see citing works
Domschke, K., Dannlowski, U., Hohoff, C., Ohrmann, P., Bauer, J., Kugel, H., Zwanzger, P., Heindel, W. L., Deckert, J., Arolt, V., et al. (2009) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2009.09.006 · Cited by 110 · see citing works
Maes, M. H. J., Twisk, F., Kubera, M., Ringel, K., Leunis, J., & Geffard, M. (2011) · Journal of Affective Disorders · doi:10.1016/j.jad.2011.09.010 · Cited by 108 · see citing works
The role of PYY in feeding regulation
Ueno, H., Yamaguchi, H., Mizuta, M., & Nakazato, M. (2008) · Regulatory Peptides · doi:10.1016/j.regpep.2007.09.011 · Cited by 105 · see citing works
Kiank, C., Taché, Y., & Larauche, M. H. (2009) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2009.08.006 · Cited by 104 · see citing works
Neuropeptide Y blocks and reverses interleukin-1β-induced anorexia in rats
Sonti, G., Ilyin, S. E., & Plata‐Saláman, C. R. (1996) · Peptides · doi:10.1016/0196-9781(96)00016-2 · Cited by 103 · see citing works
Neuropeptides: Regulators of Physiological Processes
Phillips, M. I. (2000) · Regulatory Peptides · doi:10.1016/s0167-0115(00)00102-6 · Cited by 98 · see citing works
Benzodiazepine Biosynthesis in Streptomyces refuineus
Hu, Y., Phelan, V. V., Ntai, I., Farnet, C. M., Zazopoulos, E., & Bachmann, B. O. (2007) · Chemistry & Biology · doi:10.1016/j.chembiol.2007.05.009 · Cited by 97 · see citing works
Reolon, G. K., Maurmann, N., Werenicz, A., Garcia, V. A., Schröder, N., Wood, M. A., & Roesler, R. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.03.033 · Cited by 94 · see citing works
Ma, X., Mao, Y., Wang, B., Huizinga, J. D., Bienenstock, J., & Kunze, W. (2009) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.90511.2008 · Cited by 93 · see citing works
Painsipp, E., Herzog, H., Sperk, G., & Holzer, P. (2011) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2011.01326.x · Cited by 93 · see citing works
Self-citationThe intriguing mission of neuropeptide Y in the immune system
Dimitrijević, M., & Stanojević, S. (2011) · Amino Acids · doi:10.1007/s00726-011-1185-7 · Cited by 86 · see citing works
Microbiota and AutoimmunityPreprint
Chervonsky, A. V. (2013) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a007294 · Cited by 85 · see citing works
Innate Immune Regulation by Toll-Like Receptors in the Brain
Mallard, C. E. (2012) · ISRN Neurology · doi:10.5402/2012/701950 · Cited by 82 · see citing works
Spinal mechanisms of NPY analgesia
Smith, P. A., Moran, T. D., Abdulla, F. A., Tumber, K. K., & Taylor, B. K. (2006) · Peptides · doi:10.1016/j.peptides.2006.09.029 · Cited by 82 · see citing works
Yurdaydın, C., Walsh, T. J., Engler, H. D., Ha, J., Li, Y., Jones, E. A., & Basile, A. S. (1995) · Brain Research · doi:10.1016/0006-8993(95)00241-h · Cited by 82 · see citing works
Painsipp, E., Köfer, M. J., Sinner, F. M., & Holzer, P. D. (2011) · PLoS ONE · doi:10.1371/journal.pone.0020719 · Cited by 77 · see citing works
Self-citationExpression and functional importance of innate immune receptors by intestinal epithelial cells
Marques, R., & Boneca, I. G. (2011) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-011-0829-9 · Cited by 76 · see citing works
Tasan, R. O., Lin, S., Hetzenauer, A., Singewald, N., Herzog, H., & Sperk, G. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2008.11.048 · Cited by 71 · cited 1× · see citing works
“The major receptor subtypes which NPY acts on are the Y1 and Y2 receptors, which are widely distributed in the central nervous system, while the localization of Y4 and Y5 receptors is restricted to particular regions of the brain [82-85].”
Targeted deletion of neuropeptide Y (NPY) modulates experimental colitis
Chandrasekharan, B., Bala, V., Kolachala, V. L., Vijay-Kumar, M., Jones, D., Gewirtz, A. T., Sitaraman, S. V., & Srinivasan, S. (2008) · PLoS ONE · doi:10.1371/journal.pone.0003304 · Cited by 70 · see citing works
Emerging role of autoantibodies against appetite-regulating neuropeptides in eating disorders
Fetissov, S. O., Sinno, M. H., Coquerel, Q., do-Rego, J.-C., Coëffier, M., Gilbert, D., Hökfelt, T. G. M., & Déchelotte, P. (2008) · Nutrition · doi:10.1016/j.nut.2008.06.021 · Cited by 66 · see citing works
Morgan, C. A., Rasmusson, A. M., Winters, B., Hauger, R. L., Morgan, J., Hazlett, G. A., & Southwick, S. M. (2003) · Biological Psychiatry · doi:10.1016/s0006-3223(03)00433-5 · Cited by 65 · see citing works
Attenuation of acute experimental colitis by preventing NPY Y1 receptor signaling
Hassani, H., Lucas, G., Rozell, B., & Ernfors, P. (2004) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00182.2004 · Cited by 65 · see citing works
Chee, M. J. S., & Colmers, W. F. (2008) · Nutrition · doi:10.1016/j.nut.2008.06.007 · Cited by 64 · see citing works
Painsipp, E., Herzog, H., & Holzer, P. D. (2008) · Neuropharmacology · doi:10.1016/j.neuropharm.2008.05.004 · Cited by 57 · see citing works
Self-citationThe Y1 receptor for NPY: A key modulator of the adaptive immune system
Wheway, J., Herzog, H., & Mackay, F. (2007) · Peptides · doi:10.1016/j.peptides.2006.09.030 · Cited by 57 · see citing works
Ghrelin and PYY in the regulation of energy balance and metabolism: lessons from mouse mutants
Kirchner, H., Tong, J., Tschöp, M. H., & Pfluger, P. T. (2010) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00191.2009 · Cited by 57 · see citing works
A role for neuropeptide Y (NPY) in phagocytosis: Implications for innate and adaptive immunity
Bedoui, S., von Hörsten, S., & Gebhardt, T. (2007) · Peptides · doi:10.1016/j.peptides.2006.07.029 · Cited by 56 · see citing works
McMahon, C. D., Buxton, D. F., Elsasser, T. H., Gunter, D. R., Sanders, L., Steele, B., & Sartin, J. L. (1999) · Journal of Endocrinology · doi:10.1677/joe.0.1610333 · Cited by 55 · see citing works
Schmidt, P. T., Ljung, T., Hartmann, B., Hare, K. J., Holst, J. J., & Hellstr??m, P. M. (2005) · European Journal of Gastroenterology & Hepatology · doi:10.1097/00042737-200502000-00012 · Cited by 52 · see citing works
Interleukin-1 beta-induced anorexia and pyrexia in rat: relationship to hypothalamic neuropeptide Y
McCarthy, H. D., Dryden, S. D., & Williams, G. (1995) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1995.269.5.e852 · Cited by 45 · see citing works
Neural and behavioral responses to low-grade inflammation
Tarr, A. J., Chen, Q., Wang, Y., Sheridan, J. F., & Quan, N. (2012) · Behavioural Brain Research · doi:10.1016/j.bbr.2012.07.038 · Cited by 45 · see citing works
Anxiogenic-like action of centrally administered glucagon-like peptide-1 in a punished drinking test
Møller, C. H., Sommer, W. H., Thorsell, A., Rimondini, R., & Heilig, M. A. (2002) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/s0278-5846(01)00223-8 · Cited by 44 · see citing works
Antidepressant-like effects of glucagon-like peptide-2 in mice occur via monoamine pathways
Iwai, T., Hayashi, Y., Narita, S., Kasuya, Y., Jin, K., Tsugane, M., & Oka, J. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2009.06.020 · Cited by 39 · see citing works
Experimental gastritis in mice enhances anxiety in a gender-related manner
Painsipp, E., Wultsch, T., Shahbazian, A., Edelsbrunner, M., Kreissl, M. C., Schirbel, A., Bock, E., Pabst, M. A., Thoeringer, C. K., Huber, H., et al. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.09.024 · Cited by 39 · see citing works
Self-citationForbes, S. C., Herzog, H., & Cox, H. M. (2012) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2012.01939.x · Cited by 34 · see citing works
Batičić, L., Detel, D., Kučić, N., Buljević, S., Pugel, E. P., & Varljen, J. (2011) · Journal of Cellular Biochemistry · doi:10.1002/jcb.23261 · Cited by 34 · see citing works
Süyen, G. G., Işbil-Büyükcoşkun, N., & Kahveci, N. (2010) · Neuropeptides · doi:10.1016/j.npep.2010.02.002 · Cited by 32 · see citing works
Painsipp, E., Herzog, H., & Holzer, P. D. (2009) · Journal of Psychopharmacology · doi:10.1177/0269881109348171 · Cited by 31 · see citing works
Self-citationShibata, M., Hisajima, T., Nakano, M., Goris, R. C., & Funakoshi, K. (2007) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2007.08.013 · Cited by 30 · see citing works
Plasma Hormones Facilitated the Hypermotility of the Colon in a Chronic Stress Rat Model
Liang, C., Luo, H., Liu, Y., Cao, J., & Xia, H. (2012) · PLoS ONE · doi:10.1371/journal.pone.0031774 · Cited by 29 · see citing works
Peptide YY abnormalities in patients with ulcerative colitis.
Tari, A., TESHIMA, H., Sumii, K., et al. (1988) · Japanese Journal of Medicine · doi:10.2169/internalmedicine1962.27.49 · Cited by 26 · see citing works
Hirotani, Y., MIKAJIRI, K., Ikeda, K., et al. (2008) · YAKUGAKU ZASSHI · doi:10.1248/yakushi.128.1347 · Cited by 26 · see citing works
Pang, X. H., Li, T. K., Xie, Q., He, F. Q., Cui, D. J., Chen, Y. Q., Huang, X. L., & Gan, H. T. (2010) · International Journal of Colorectal Disease · doi:10.1007/s00384-010-0964-z · Cited by 25 · see citing works
Neural Regulation of Gastrointestinal Blood Flow
Holzer, P. D. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-382026-6.00029-4 · Cited by 24 · see citing works
Self-citationWultsch, T., Painsipp, E., Thoeringer, C. K., Herzog, H., Sperk, G., & Holzer, P. D. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.08.038 · Cited by 22 · see citing works
Self-citationPainsipp, E., Sperk, G., Herzog, H., & Holzer, P. D. (2009) · Journal of Psychopharmacology · doi:10.1177/0269881109104851 · Cited by 21 · see citing works
Self-citationBallinger, A., Williams, G., Corder, R., et al. (2001) · Clinical Science · doi:10.1042/cs1000221 · Cited by 21 · see citing works
Holzer, P. D., Danzer, M., Schicho, R., Samberger, C., Painsipp, E., & Lippe, I. T. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.07.040 · Cited by 20 · see citing works
Self-citationFriendly pathogens: prevent or provoke autoimmunity
Sathyabama, S., Khan, N., & Agrewala, J. N. (2013) · Critical Reviews in Microbiology · doi:10.3109/1040841x.2013.787043 · Cited by 18 · see citing works
Probiotic Lactobacillus reuteri Alleviates the Response to Gastric Distension in Rats,
Duncker, S. C., Kamiya, T., Wang, L., Yang, P., & Bienenstock, J. (2011) · Journal of Nutrition · doi:10.3945/jn.110.136689 · Cited by 18 · see citing works
Redrobe, J. P., Carvajal, C., Kask, A., Dumont, Y., & Quirion, R. (2004) · Handbook of experimental pharmacology · doi:10.1007/978-3-642-18764-3_5 · Cited by 17 · see citing works
Neuropeptide Y and peptide YY protect from weight loss caused by B acille C almette– G uérin in mice
Painsipp, E., Köfer, M. J., Farzi, A., Dischinger, U., Sinner, F. M., Herzog, H., & Holzer, P. D. (2013) · British Journal of Pharmacology · doi:10.1111/bph.12354 · Cited by 16 · see citing works
Self-citationThe Role of the Vagus Nerve in Afferent Signaling and Homeostasis During Visceral Inflammation
Holzer, P. D. (2008) · Neuroimmune biology · doi:10.1016/s1567-7443(08)10414-8 · Cited by 14 · see citing works
Self-citationKlompus, M., Ho, W., Sharkey, K. A., et al. (2010) · Regulatory Peptides · doi:10.1016/j.regpep.2010.05.014 · Cited by 14 · see citing works
Ballinger, A., Williams, G., Corder, R., et al. (2001) · Clinical Science · doi:10.1042/cs20000211 · Cited by 9 · see citing works
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Research works printed but not linked: 3
- [112]Painsipp E Köfer MJ Farzi A Dischinger US Sinner F Sperk G Herzog H Holzer P Neuropeptide Y and peptide YY protect from weight loss caused by Bacille Calmette-Guérin in mice Br J Pharmacol 2013 in press PMC3949650 23992467
- [132]Field BC Chaudhri OB Bloom SR Bowels control brain: gut hormones and obesity Nat Rev Endocrinol 2010 6 8 444 453 20585346
- [137]Chee MJ Colmers WF Y eat? Nutrition 2008 24 9 869 877 18662858
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- Authors
- Holzer, P., & Farzi, A.
- Affiliations
- Medical University of Graz (AT)
- Corresponding author
- Holzer, Peter
- Venue
- Advances in Experimental Medicine and Biology
- Publisher
- Springer New York
- Published
- 2014
- Volume
- 817
- Pages
- 195-219
- ISSN
- 0065-2598 (ISSN-L)
- 2214-8019
- PMC
- PMC4359909
- OpenAlex
- W1925671842
- Cited by
- 451
- References
- 147
- Citations by year
- 2026: 13 · 2025: 40 · 2024: 35 · 2023: 54 · 2022: 53 · 2021: 49 · 2020: 44 · 2019: 41 · 2018: 39 · 2017: 34 · 2016: 28 · 2015: 17 · 2014: 3
- FWCI
- 32.11
- Type
- book chapter
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- Locations
- Advances in experimental medicine and biology (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Health Sciences › Medicine › Gastroenterology › Gastrointestinal motility and disorders
- Keywords
- neuropeptides, microbiota-gut-brain axis, gut-brain signaling, gastrointestinal hormones, neuropeptide Y, peptide YY, enteroendocrine cells, short-chain fatty acids, G protein-coupled receptors, substance P, calcitonin gene-related peptide, vasoactive intestinal peptide, somatostatin, corticotropin-releasing factor, vagal afferent neurons, neuroendocrine regulation, gut microbiota, inflammation, pain, behavior
- MeSH terms
- Animals, Behavior, Brain, Humans, Neuropeptides, Signal Transduction, Gastrointestinal Tract, Host-Pathogen Interactions, Microbiota
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