Role of the vagus nerve in the development and treatment of diet‐induced obesity

Akufo and Ibarapa

Beckett, A. H., Rowland, M., & TURNER, P. (1965) · The Lancet · doi:10.1016/s0140-6736(65)91037-8 · Cited by 16,917 · see citing works

Saliency, switching, attention and control: a network model of insula function

Menon, V., & Uddin, L. Q. (2010) · Brain Structure and Function · doi:10.1007/s00429-010-0262-0 · Cited by 5,592 · see citing works

Food reward: brain substrates of wanting and liking

Berridge, K. C. (1996) · Neuroscience & Biobehavioral Reviews · doi:10.1016/0149-7634(95)00033-b · Cited by 1,901 · see citing works

Functional and chemical anatomy of the afferent vagal system

Berthoud, H.-R., & Neuhuber, W. L. (2000) · Autonomic Neuroscience · doi:10.1016/s1566-0702(00)00215-0 · Cited by 1,280 · see citing works

Efficacy of Liraglutide for Weight Loss Among Patients With Type 2 Diabetes: The SCALE Diabetes Randomized Clinical Trial

Davies, M. J., Bergenstal, R., Bode, B., Kushner, R. F., Lewin, A., Skjøth, T. V., Andreasen, A. H., Jensen, C. B., DeFronzo, R. A., & for the NN8022-1922 Study Group (2015) · JAMA · doi:10.1001/jama.2015.9676 · Cited by 1,198 · see citing works

Long-term Drug Treatment for Obesity: A Systematic and Clinical Review

Yanovski, S. Z., & Yanovski, J. A. (2014) · JAMA · doi:10.1001/jama.2013.281361 · Cited by 876 · see citing works

Long-term Follow-up After Bariatric Surgery: A Systematic Review

Puzziferri, N., Roshek, T. B., Mayo, H. G., Gallagher, R., Belle, S. H., & Livingston, E. H. (2014) · JAMA · doi:10.1001/jama.2014.10706 · Cited by 819 · see citing works

The UK Prospective Diabetes Study (UKPDS): clinical and therapeutic implications for type 2 diabetes

King, P., Peacock, I., & Donnelly, R. (1999) · British Journal of Clinical Pharmacology · doi:10.1046/j.1365-2125.1999.00092.x · Cited by 703 · 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

Anti-Obesity Drugs: A Review about Their Effects and Safety

Kang, J. G., & Park, C. (2012) · Diabetes & Metabolism Journal · doi:10.4093/dmj.2012.36.1.13 · Cited by 592 · see citing works

The taste reactivity test. II. Mimetic responses to gustatory stimuli in chronic thalamic and chronic decerebrate rats

Grill, H. J., & Norgren, R. (1978) · Brain Research · doi:10.1016/0006-8993(78)90569-3 · Cited by 588 · see citing works

Ado-trastuzumab Emtansine (T-DM1): An Antibody–Drug Conjugate (ADC) for HER2-Positive Breast Cancer

Lambert, J. M., & Chari, R. V. J. (2014) · Journal of Medicinal Chemistry · doi:10.1021/jm500766w · Cited by 545 · see citing works

Metabolic and hedonic drives in the neural control of appetite: who is the boss?

Berthoud, H. (2011) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2011.09.004 · Cited by 501 · see citing works

The central organization of the vagus nerve innervating the stomach of the rat

Shapiro, R. E., & Miselis, R. R. (1985) · The Journal of Comparative Neurology · doi:10.1002/cne.902380411 · Cited by 496 · see citing works

A Two-Year Randomized Trial of Obesity Treatment in Primary Care Practice

Wadden, T. A., Volger, S., Sarwer, D. B., Vetter, M. L., Tsai, A. G., Berkowitz, R. I., Kumanyika, S., Schmitz, K. H., Diewald, L. K., Barg, R., et al. (2011) · New England Journal of Medicine · doi:10.1056/nejmoa1109220 · Cited by 487 · see citing works

Neuroepithelial circuit formed by innervation of sensory enteroendocrine cells

Bohórquez, D. V., Shahid, R. A., Erdmann, A., Kreger, A. M., Wang, Y., Calakos, N., Wang, F., & Liddle, R. A. (2015) · Journal of Clinical Investigation · doi:10.1172/jci78361 · Cited by 484 · cited 1× · see citing works

Acute and Long-Term Suppression of Feeding Behavior by POMC Neurons in the Brainstem and Hypothalamus, Respectively

Zhan, C., Zhou, J., Feng, Q., Zhang, J.-E., Lin, S., Bao, J., Wu, P., & Luo, M. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2742-12.2013 · Cited by 444 · see citing works

Neuroimaging and neuromodulation approaches to study eating behavior and prevent and treat eating disorders and obesity

Val‐Laillet, D., Aarts, E., Weber, B., Ferrari, M., Quaresima, V., Stoeckel, L. E., Alonso‐Alonso, M., Audette, M. A., Malbert, C., & Stice, E. M. (2015) · NeuroImage Clinical · doi:10.1016/j.nicl.2015.03.016 · Cited by 443 · see citing works

Brain-gut axis and its role in the control of food intake.

Konturek, S. J., Konturek, J. W., Pawlik, T., & Brzozowski, T. (2004) · PubMed · Cited by 424 · see citing works

A spiral nerve cuff electrode for peripheral nerve stimulation

Naples, G. G., Mortimer, J. T., Scheiner, A., & Sweeney, J. D. (1988) · IEEE Transactions on Biomedical Engineering · doi:10.1109/10.8670 · Cited by 415 · see citing works

Effects of 12 Months of Vagus Nerve Stimulation in Treatment-Resistant Depression: A Naturalistic Study

Rush, A. J., Sackeïm, H. A., Marangell, L. B., George, M. S., Brannan, S. K., Thomas, S., Lavori, P., Howland, R. H., Kling, M. A., Rittberg, B. R., et al. (2005) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.05.024 · Cited by 399 · see citing works

Glucagon-like peptide-1, peptide YY, hunger, and satiety after gastric bypass surgery in morbidly obese subjects

Morínigo, R., Moizé, V., Musri, M., Lacy, A. M., Navarro, S., Marín, J. L., Delgado, S., Casamitjana, R., & Vidal, J. (2006) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2005-0904 · Cited by 397 · see citing works

Vagus Nerve and Vagus Nerve Stimulation, a Comprehensive Review: Part III

Yuan, H., & Silberstein, S. D. (2015) · Headache The Journal of Head and Face Pain · doi:10.1111/head.12649 · Cited by 381 · 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

Effects of Vagal Stimulation on Experimentally Induced Seizures in Rats

Woodbury, D. M., & Woodbury, J. W. (1990) · Epilepsia · doi:10.1111/j.1528-1157.1990.tb05852.x · Cited by 369 · see citing works

Brain Blood Flow Alterations Induced by Therapeutic Vagus Nerve Stimulation in Partial Epilepsy: I. Acute Effects at High and Low Levels of Stimulation

Henry, T. R., Bakay, R. A. E., Votaw, J. R., Pennell, P. B., Epstein, C. M., Faber, T. L., Grafton, S. T., & Hoffman, J. M. (1998) · Epilepsia · doi:10.1111/j.1528-1157.1998.tb01448.x · Cited by 367 · see citing works

Topography of efferent vagal innervation of the rat gastrointestinal tract

Berthoud, H., Carlson, N. R., & Powley, T. L. (1991) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1991.260.1.r200 · Cited by 363 · see citing works

The migrating motor complex: control mechanisms and its role in health and disease

Deloose, E., Janssen, P., Depoortere, I., & Tack, J. F. (2012) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/nrgastro.2012.57 · Cited by 350 · see citing works

Central distribution of subdiaphragmatic vagal branches in the rat

Norgren, R., & Smith, G. P. (1988) · The Journal of Comparative Neurology · doi:10.1002/cne.902730206 · Cited by 327 · see citing works

The vagus nerve, food intake and obesity

Berthoud, H.-R. (2008) · Regulatory Peptides · doi:10.1016/j.regpep.2007.08.024 · Cited by 316 · see citing works

Vagal and hormonal gut-brain communication: from satiation to satisfaction

Berthoud, H. ‐. (2008) · Neurogastroenterology & Motility · doi:10.1111/j.1365-2982.2008.01104.x · Cited by 307 · see citing works

Vagus Nerve and Vagus Nerve Stimulation, a Comprehensive Review: Part II

Yuan, H., & Silberstein, S. D. (2015) · Headache The Journal of Head and Face Pain · doi:10.1111/head.12650 · Cited by 304 · see citing works

Vagal afferent responses to fatty acids of different chain length in the rat

Lal, S., Kirkup, A. J., Brunsden, A. M., Thompson, D. G., & Grundy, D. (2001) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.2001.281.4.g907 · Cited by 303 · see citing works

Evidence that Intestinal Glucagon-Like Peptide-1 Plays a Physiological Role in Satiety

Williams, D. L., Baskin, D. G., & Schwartz, M. W. (2009) · Endocrinology · doi:10.1210/en.2008-1045 · Cited by 300 · see citing works

A Gut Lipid Messenger Links Excess Dietary Fat to Dopamine Deficiency

Téllez, L. A., Medina, S., Han, W., Ferreira, J. G. P., Licona-Limón, P., Ren, X., Lam, T. T., Schwartz, G. J., & de Araújo, I. E. (2013) · Science · doi:10.1126/science.1239275 · Cited by 298 · see citing works

Knockdown of GLP-1 Receptors in Vagal Afferents Affects Normal Food Intake and Glycemia

Krieger, J.-P., Arnold, M., Pettersen, K. G., Lossel, P., Langhans, W., & Lee, S. J. (2016) · Diabetes · doi:10.2337/db15-0973 · Cited by 269 · see citing works

Gastric volume rather than nutrient content inhibits food intake

Phillips, R. J., & Powley, T. L. (1996) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1996.271.3.r766 · Cited by 269 · see citing works

Cholecystokinin inhibits gastric motility and emptying via a capsaicin-sensitive vagal pathway in rats

Raybould, H. E., & Tache, Y. (1988) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1988.255.2.g242 · Cited by 267 · see citing works

Intraganglionic laminar endings are mechano‐transduction sites of vagal tension receptors in the guinea‐pig stomach

Zagorodnyuk, V. P., Chen, B. N., & Brookes, S. J. (2001) · The Journal of Physiology · doi:10.1111/j.1469-7793.2001.00255.x · Cited by 267 · see citing works

Gastrointestinal mechanisms of satiation for food

Ritter, R. C. (2004) · Physiology & Behavior · doi:10.1016/j.physbeh.2004.02.012 · Cited by 263 · see citing works

A review of functional neuroimaging studies of vagus nerve stimulation (VNS)

Chae, J.-H., Nahas, Z., Lomarev, M., Denslow, S., Lorberbaum, J. P., Bohning, D. E., & George, M. S. (2003) · Journal of Psychiatric Research · doi:10.1016/s0022-3956(03)00074-8 · Cited by 255 · see citing works

Reversible Nerve Conduction Block Using Kilohertz Frequency Alternating Current

Kilgore, K. L., & Bhadra, N. (2013) · Neuromodulation Technology at the Neural Interface · doi:10.1111/ner.12100 · Cited by 254 · see citing works

Gut chemosensing: Interactions between gut endocrine cells and visceral afferents

Raybould, H. E. (2010) · Autonomic Neuroscience · doi:10.1016/j.autneu.2009.07.007 · Cited by 254 · see citing works

Evidence of gender differences in the ability to inhibit brain activation elicited by food stimulation

Wang, G.-J., Volkow, N. D., Telang, F., Jayne, M., Ma, Y., Pradhan, K., Zhu, W., Wong, C. T., Thanos, P. K., Geliebter, A., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0807423106 · Cited by 242 · see citing works

High‐frequency electrical conduction block of mammalian peripheral motor nerve

Bhadra, N., & Kilgore, K. L. (2005) · Muscle & Nerve · doi:10.1002/mus.20428 · Cited by 239 · see citing works

Glucose‐sensitive afferent nerve fibres in the hepatic branch of the vagus nerve in the guinea‐pig.

Niijima, A. (1982) · The Journal of Physiology · doi:10.1113/jphysiol.1982.sp014415 · Cited by 236 · see citing works

The role of the autonomic nervous liver innervation in the control of energy metabolism

Yi, C., la Fleur, S. E., Fliers, E., & Kalsbeek, A. (2010) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2010.01.006 · Cited by 229 · see citing works

Obesity and Appetite Control

Suzuki, K., Jayasena, C. N., & Bloom, S. R. (2012) · Experimental Diabetes Research · doi:10.1155/2012/824305 · Cited by 227 · see citing works

Brain activity in hunger and satiety: an exploratory visually stimulated fMRI study

Führer, D., Zysset, S., & Stumvoll, M. (2008) · Obesity · doi:10.1038/oby.2008.33 · Cited by 218 · see citing works

Vagal sensors in the rat duodenal mucosa: distribution and structure as revealed by in vivo DiI-tracing

Berthoud, H., Kressel, M., Raybould, H., & Neuhuber, W. (1995) · Anatomy and Embryology · doi:10.1007/bf00187819 · Cited by 216 · see citing works

Effect of Reversible Intermittent Intra-abdominal Vagal Nerve Blockade on Morbid Obesity: The ReCharge Randomized Clinical Trial

Ikramuddin, S., Blackstone, R. P., Brancatisano, A., Toouli, J., Shah, S. N., Wolfe, B. M., Fujioka, K., Maher, J. W., Swain, J., Que, F. G., et al. (2014) · JAMA · doi:10.1001/jama.2014.10540 · Cited by 214 · see citing works

Caudal Brainstem Processing Is Sufficient for Behavioral, Sympathetic, and Parasympathetic Responses Driven by Peripheral and Hindbrain Glucagon-Like-Peptide-1 Receptor Stimulation

Hayes, M. R., Skibicka, K. P., & Grill, H. J. (2008) · Endocrinology · doi:10.1210/en.2007-1743 · Cited by 214 · see citing works

Vagal Mechanoreceptors and Chemoreceptors in Mouse Stomach and Esophagus

Page, A. J., Martin, C. M., & Blackshaw, L. A. (2002) · Journal of Neurophysiology · doi:10.1152/jn.00785.2001 · Cited by 214 · see citing works

Amygdalo-Hypothalamic Circuit Allows Learned Cues to Override Satiety and Promote Eating

Petrovich, G. D., Setlow, B., Holland, P. C., & Gallagher, M. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-19-08748.2002 · Cited by 205 · see citing works

Obesity and the four facets of impulsivity

Mobbs, O., Crépin, C., Thiéry, C., Golay, A., & der Linden, M. V. (2010) · Patient Education and Counseling · doi:10.1016/j.pec.2010.03.003 · Cited by 199 · see citing works

Proopiomelanocortin Neurons in Nucleus Tractus Solitarius Are Activated by Visceral Afferents: Regulation by Cholecystokinin and Opioids

Appleyard, S. M., Bailey, T. W., Doyle, M. W., Jin, Y., Smart, J. L., Low, M. J., & Andresen, M. C. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.4177-04.2005 · Cited by 195 · see citing works

Utility of HbA1c Levels for Diabetes Case Finding in Hospitalized Patients With Hyperglycemia

Greci, L. S., Kailasam, M. T., Malkani, S., Katz, D. L., Hulinsky, I., Ahmadi, R., & Nawaz, H. (2003) · Diabetes Care · doi:10.2337/diacare.26.4.1064 · Cited by 191 · see citing works

An anterograde tracing study of the vagal innervation of rat liver, portal vein and biliary system

Berthoud, H., Kressel, M., & Neuhuber, W. (1992) · Anatomy and Embryology · doi:10.1007/bf00185458 · Cited by 189 · see citing works

Impaired intestinal afferent nerve satiety signalling and vagal afferent excitability in diet induced obesity in the mouse

Daly, D., Park, S. J., Valinsky, W. C., & Beyak, M. J. (2011) · The Journal of Physiology · doi:10.1113/jphysiol.2010.204594 · Cited by 188 · see citing works

Vertical sleeve gastrectomy reduces hepatic steatosis while increasing serum bile acids in a weight-loss-independent manner

Myronovych, A., Kirby, M., Ryan, K. K., Zhang, W., Jha, P., Setchell, K. D. R., Dexheimer, P. J., Aronow, B. J., Seeley, R. J., & Kohli, R. (2013) · Obesity · doi:10.1002/oby.20548 · Cited by 182 · see citing works

Ghrelin receptors in rat and human nodose ganglia: putative role in regulating CB-1 and MCH receptor abundance

Burdyga, G., Varró, A., Dimaline, R., Thompson, D. G., & Dockray, G. J. (2006) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00543.2005 · Cited by 182 · 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

Diet-induced obesity leads to the development of leptin resistance in vagal afferent neurons

de Lartigue, G., Barbier de la Serre, C., Espero, E., Lee, J., & Raybould, H. E. (2011) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00056.2011 · Cited by 179 · see citing works

Peripheral administration of cholecystokinin activates c-fos expression in the locus coeruleus/subcoeruleus nucleus, dorsal vagal complex and paraventricular nucleus via capsaicin-sensitive vagal afferents and CCK-A receptors in the rat

Mönnikes, H., Lauer, G., & Arnold, R. (1997) · Brain Research · doi:10.1016/s0006-8993(97)00865-2 · Cited by 172 · see citing works

Cholecystokinin and gut–brain signalling

Dockray, G. J. (2009) · Regulatory Peptides · doi:10.1016/j.regpep.2009.03.015 · Cited by 168 · see citing works

Rats maintained on high-fat diets exhibit reduced satiety in response to CCK and bombesin

Covașă, M., & Ritter, R. C. (1998) · Peptides · doi:10.1016/s0196-9781(98)00096-5 · Cited by 164 · see citing works

Characterization of vagal pathways mediating gastric accommodation reflex in rats

Takahashi, T., & Owyang, C. (1997) · The Journal of Physiology · doi:10.1111/j.1469-7793.1997.479be.x · Cited by 163 · see citing works

Subjective feeling of appetite modulates brain activity

Porubská, K., Veit, R., Preissl, H. T., Fritsche, A., & Birbaumer, N. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.04.216 · Cited by 162 · see citing works

The EMPOWER Study: Randomized, Prospective, Double-Blind, Multicenter Trial of Vagal Blockade to Induce Weight Loss in Morbid Obesity

The EMPOWER Study Group, Sarr, M. G., Billington, C. J., Brancatisano, R., Brancatisano, A., Toouli, J., Kow, L., Nguyen, N. T., Blackstone, R., Maher, J. W., et al. (2012) · Obesity Surgery · doi:10.1007/s11695-012-0751-8 · Cited by 162 · see citing works

Intra-abdominal vagal blocking (VBLOC therapy): Clinical results with a new implantable medical device

Camilleri, M., Toouli, J., Herrera, M. F., Kulseng, B. E., Kow, L., Pantoja, J. P., Mårvik, R., Johnsen, G., Billington, C. J., Moody, F. G., et al. (2008) · Surgery · doi:10.1016/j.surg.2008.03.015 · Cited by 159 · see citing works

Vagus Nerve Stimulation Activates Central Nervous System Structures in Epileptic Patients During PET H215O Blood Flow Imaging

Ko, D., Heck, C., Grafton, S. T., Apuzzo, M. L. J., Couldwell, W. T., Chen, T., Day, J. D., Zelman, V., Thomas, S., & DeGiorgio, C. M. (1996) · Neurosurgery · doi:10.1097/00006123-199608000-00061 · Cited by 158 · see citing works

Hyperphagia and Increased Fat Accumulation in Two Models of Chronic CNS Glucagon-Like Peptide-1 Loss of Function

Barrera, J. G., Jones, K. R., Herman, J. P., D’Alessio, D. A., Woods, S. C., & Seeley, R. J. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.2212-10.2011 · Cited by 154 · see citing works

Leptin Resistance in Vagal Afferent Neurons Inhibits Cholecystokinin Signaling and Satiation in Diet Induced Obese Rats

de Lartigue, G., Serre, C. B. D. L., Espero, E., Lee, J., & Raybould, H. E. (2012) · PLoS ONE · doi:10.1371/journal.pone.0032967 · Cited by 150 · see citing works

Surgical treatment of obesity

Kral, J. G., & Näslund, E. B. (2007) · Nature Clinical Practice Endocrinology &#38 Metabolism · doi:10.1038/ncpendmet0563 · Cited by 149 · see citing works

Weight loss associated with vagus nerve stimulation

Burneo, J. G., Faught, E., Knowlton, R. C., Morawetz, R. B., & Kuzniecky, R. (2002) · Neurology · doi:10.1212/wnl.59.3.463 · Cited by 145 · see citing works

Weight loss during chronic, cervical vagus nerve stimulation in depressed patients with obesity: an observation

Pardo, J. V., Sheikh, S. A., Kuskowski, M. A., Surerus-Johnson, C., Hagen, M. C., Lee, J. T., Rittberg, B. R., & Adson, D. E. (2007) · International Journal of Obesity · doi:10.1038/sj.ijo.0803666 · Cited by 142 · see citing works

Medullary c-Fos activation in rats after ingestion of a satiating meal

Rinaman, L., Baker, E. A., Hoffman, G. E., Stricker, E. M., & Verbalis, J. G. (1998) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1998.275.1.r262 · Cited by 139 · see citing works

Mucosal receptors in the gastric antrum and small intestine of the rat with afferent fibres in the cervical vagus.

Clarke, G. D., & Davison, J. S. (1978) · The Journal of Physiology · doi:10.1113/jphysiol.1978.sp012527 · Cited by 139 · see citing works

Chronic exposure to Low dose bacterial lipopolysaccharide inhibits leptin signaling in vagal afferent neurons

Serre, C. B. D. L., de Lartigue, G., & Raybould, H. E. (2014) · Physiology & Behavior · doi:10.1016/j.physbeh.2014.10.032 · Cited by 136 · see citing works

Diet‐induced adaptation of vagal afferent function

Kentish, S. J., Li, H., Philp, L., O’Donnell, T. A., Isaacs, N. J., Young, R. L., Wittert, G., Blackshaw, L. A., & Page, A. J. (2011) · The Journal of Physiology · doi:10.1113/jphysiol.2011.222158 · Cited by 134 · see citing works

The Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications Study at 30 Years: Summary and Future Directions

Gubitosi‐Klug, R. (2013) · Diabetes Care · doi:10.2337/dc13-2148 · Cited by 131 · see citing works

Cocaine- and Amphetamine-Regulated Transcript: Stimulation of Expression in Rat Vagal Afferent Neurons by Cholecystokinin and Suppression by Ghrelin

de Lartigue, G., Dimaline, R., Varró, A., & Dockray, G. J. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.5508-06.2007 · Cited by 127 · see citing works

Integration of vagal afferent responses to gastric loads and cholecystokinin in rats

Schwartz, G. J., McHugh, P. R., & Moran, T. H. (1991) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1991.261.1.r64 · Cited by 127 · see citing works

Adaptation to a High-Fat Diet Leads to Hyperphagia and Diminished Sensitivity to Cholecystokinin in Rats

Savastano, D. M., & Covașă, M. (2005) · Journal of Nutrition · doi:10.1093/jn/135.8.1953 · Cited by 125 · see citing works

Anatomical Relationship between Vagal Afferent Fibers and CCK-Immunoreactive Entero-Endocrine Cells in the Rat Small Intestinal Mucosa

Berthoud, H. R., & Patterson, L. M. (1996) · Cells Tissues Organs · doi:10.1159/000147837 · Cited by 125 · see citing works

Chronic vagus nerve stimulation decreased weight gain, food consumption and sweet craving in adult obese minipigs

Val‐Laillet, D., Biraben, A., Randuineau, G., & Malbert, C. (2010) · Appetite · doi:10.1016/j.appet.2010.06.008 · Cited by 124 · see citing works

Gastric distension-induced c-fos expression in catecholaminergic neurons of rat dorsal vagal complex

Willing, A. E., & Berthoud, H. (1997) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1997.272.1.r59 · Cited by 124 · see citing works

Adaptation to high-fat diet reduces inhibition of gastric emptying by CCK and intestinal oleate

Covașă, M., & Ritter, R. C. (2000) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.2000.278.1.r166 · Cited by 122 · see citing works

The effects of amygdala lesions on conditioned stimulus- potentiated eating in rats.

Holland, P. C., Petrovich, G. D., & Gallagher, M. (2002) · Physiology & Behavior · doi:10.1016/s0031-9384(02)00688-1 · Cited by 117 · see citing works

Deletion of leptin signaling in vagal afferent neurons results in hyperphagia and obesity

de Lartigue, G., Ronveaux, C. C., & Raybould, H. E. (2014) · Molecular Metabolism · doi:10.1016/j.molmet.2014.06.003 · Cited by 117 · see citing works

Reflex Effects of Oral, Gastrointestinal and Hepatoportal Glutamate Sensors on Vagal Nerve Activity

Niijima, A. (2000) · Journal of Nutrition · doi:10.1093/jn/130.4.971s · Cited by 117 · see citing works

Control of gastrointestinal motility by the “gut brain” – the enteric nervous system

Schemann, M. (2005) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/01.scs.0000180285.51365.55 · Cited by 115 · see citing works

Vagovagal reflex control of digestion: afferent modulation by neural and "endoneurocrine" factors

Rogers, R. C., McTigue, D. M., & Hermann, G. E. (1995) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1995.268.1.g1 · Cited by 113 · see citing works

High-Frequency Stimulation Selectively Blocks Different Types of Fibers in Frog Sciatic Nerve

Joseph, L., & Butera, R. J. (2011) · IEEE Transactions on Neural Systems and Rehabilitation Engineering · doi:10.1109/tnsre.2011.2163082 · Cited by 108 · see citing works

Vagal Blocking Improves Glycemic Control and Elevated Blood Pressure in Obese Subjects with Type 2 Diabetes Mellitus

Shikora, S. A., Toouli, J., Herrera, M. F., Kulseng, B. E., Zulewski, H., Brancatisano, R., Kow, L., Pantoja, J. P., Johnsen, G., Brancatisano, A., et al. (2013) · Journal of Obesity · doi:10.1155/2013/245683 · Cited by 99 · see citing works

A review on gastric leptin: the exocrine secretion of a gastric hormone

Cammisotto, P., & Bendayan, M. (2012) · Anatomy & Cell Biology · doi:10.5115/acb.2012.45.1.1 · Cited by 99 · see citing works

Decreased intestinal nutrient response in diet-induced obese rats: role of gut peptides and nutrient receptors

Duca, F. A., Swartz, T. D., Sakar, Y., & Covașă, M. (2012) · International Journal of Obesity · doi:10.1038/ijo.2012.45 · Cited by 98 · see citing works

High fat maintenance diet attenuates hindbrain neuronal response to CCK

Covașă, M., Grahn, J. C., & Ritter, R. C. (2000) · Regulatory Peptides · doi:10.1016/s0167-0115(99)00084-1 · Cited by 97 · see citing works

Duodenal nutrient exposure elicits nutrient-specific gut motility and vagal afferent signals in rat

Schwartz, G. J., & Moran, T. H. (1998) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1998.274.5.r1236 · Cited by 95 · see citing works

Vagus Nerve Stimulation (VNS) and Treatment of Depression: To the Brainstem and Beyond.

O’Reardon, J. P., Cristancho, P., & Peshek, A. D. (2006) · PubMed Central · Cited by 94 · see citing works

Gastric vagal afferent modulation by leptin is influenced by food intake status

Kentish, S. J., O’Donnell, T. A., Isaacs, N. J., Young, R. L., Li, H., Harrington, A. M., Brierley, S. M., Wittert, G., Blackshaw, L. A., & Page, A. J. (2012) · The Journal of Physiology · doi:10.1113/jphysiol.2012.247577 · Cited by 93 · see citing works

Vagal nerve stimulator: Evolving trends

Ogbonnaya, S., & Kaliaperumal, C. (2013) · Journal of Natural Science Biology and Medicine · doi:10.4103/0976-9668.107254 · Cited by 91 · see citing works

Vagus Nerve Stimulation Increases Energy Expenditure: Relation to Brown Adipose Tissue Activity

Vijgen, G. H. E. J., Bouvy, N. D., Leenen, L. A. M., Rijkers, K., Cornips, E. M. J., Majoie, M., Brans, B. T., & Lichtenbelt, W. D. V. M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0077221 · Cited by 91 · see citing works

Cholecystokinin Regulates Expression of Y2 Receptors in Vagal Afferent Neurons Serving the Stomach

Burdyga, G., de Lartigue, G., Raybould, H. E., Morris, R., Dimaline, R., Varró, A., Thompson, D. G., & Dockray, G. J. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.2493-08.2008 · Cited by 91 · see citing works

A method for selective section of vagal afferent or efferent axons in the rat

Norgren, R., & Smith, G. P. (1994) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1994.267.4.r1136 · Cited by 90 · see citing works

Vagal afferent signaling of a gastric mucosal acid insult to medullary, pontine, thalamic, hypothalamic and limbic, but not cortical, nuclei of the rat brain

Michl, T., Jocič, M., Heinemann, Á., Schuligoi, R., & Holzer, P. D. (2001) · Pain · doi:10.1016/s0304-3959(00)00467-x · Cited by 88 · see citing works

Expression of cannabinoid CB1 receptors by vagal afferent neurons: kinetics and role in influencing neurochemical phenotype

Burdyga, G., Varró, A., Dimaline, R., et al. (2010) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00059.2010 · Cited by 85 · see citing works

Vagal control of canine postprandial upper gastrointestinal motility

Hall, K. E., El-Sharkawy, T. Y., & Diamant, N. E. (1986) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1986.250.4.g501 · Cited by 85 · see citing works

Roux‐en‐Y gastric bypass reverses the effects of diet‐induced obesity to inhibit the responsiveness of central vagal motoneurones

Browning, K. N., Fortna, S. R., & Hajnal, A. S. (2013) · The Journal of Physiology · doi:10.1113/jphysiol.2012.249268 · Cited by 84 · see citing works

Vagus nerve stimulation acutely alters food craving in adults with depression

Bodenlos, J. S., Köse, S., Borckardt, J. J., Nahas, Z. H., Shaw, D. L., O'Neil, P. M., & George, M. S. (2006) · Appetite · doi:10.1016/j.appet.2006.07.080 · Cited by 84 · see citing works

Sustained Weight Loss with Vagal Nerve Blockade but Not with Sham: 18-Month Results of the ReCharge Trial

Shikora, S. A., Wolfe, B. M., Apovian, C. M., Anvari, M., Sarwer, D. B., Gibbons, R. D., Ikramuddin, S., Miller, C. J., Knudson, M. B., Tweden, K. S., et al. (2015) · Journal of Obesity · doi:10.1155/2015/365604 · Cited by 83 · see citing works

EGR1 Is a Target for Cooperative Interactions between Cholecystokinin and Leptin, and Inhibition by Ghrelin, in Vagal Afferent Neurons

de Lartigue, G., Lür, G., Dimaline, R., Varró, A., Raybould, H. E., & Dockray, G. J. (2010) · Endocrinology · doi:10.1210/en.2010-0106 · Cited by 83 · see citing works

The hypothalamus and metabolism: integrating signals to control energy and glucose homeostasis

Coll, A. P., & Yeo, G. S. H. (2013) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2013.09.010 · Cited by 83 · see citing works

Feeding-dependent depression of melanin-concentrating hormone and melanin-concentrating hormone receptor-1 expression in vagal afferent neurones

Burdyga, G., Varró, A., Dimaline, R., Thompson, D. G., & Dockray, G. J. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.10.057 · Cited by 80 · see citing works

Selection of electrical algorithms to treat obesity with intermittent vagal block using an implantable medical device

Camilleri, M., Toouli, J., Herrera, M. F., et al. (2008) · Surgery for Obesity and Related Diseases · doi:10.1016/j.soard.2008.09.006 · Cited by 79 · see citing works

Effects of high-frequency alternating current on axonal conduction through the vagus nerve

Waataja, J. J., Tweden, K. S., & Honda, C. N. (2011) · Journal of Neural Engineering · doi:10.1088/1741-2560/8/5/056013 · Cited by 78 · see citing works

Reduced hindbrain and enteric neuronal response to intestinal oleate in rats maintained on high-fat diet

Covașă, M., Grahn, J. C., & Ritter, R. C. (2000) · Autonomic Neuroscience · doi:10.1016/s1566-0702(00)00176-4 · Cited by 78 · see citing works

Plasticity of vagal brainstem circuits in the control of gastrointestinal function

Browning, K. N., & Travagli, R. A. (2010) · Autonomic Neuroscience · doi:10.1016/j.autneu.2010.11.001 · Cited by 78 · see citing works

Surgical Treatment of Obesity

Kral, J. G. (1989) · Medical Clinics of North America · doi:10.1016/s0025-7125(16)30702-7 · Cited by 78 · see citing works

Visceral nerves: vagal and sympathetic innervation.

Teff, K. L. (2008) · Journal of Parenteral and Enteral Nutrition · doi:10.1177/0148607108321705 · Cited by 75 · see citing works

VAGOTOMY FOR TREATMENT OF SEVERE OBESITY

Kral, J. (1978) · The Lancet · doi:10.1016/s0140-6736(78)90074-0 · Cited by 71 · see citing works

Load-sensitive rat gastric vagal afferents encode volume but not gastric nutrients

Mathis, C., Moran, T. H., & Schwartz, G. J. (1998) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1998.274.2.r280 · Cited by 71 · see citing works

Attenuated satiation response to intestinal nutrients in rats that do not express CCK-A receptors

Covașă, M., & Ritter, R. C. (2001) · Peptides · doi:10.1016/s0196-9781(01)00461-2 · Cited by 68 · see citing works

Plasticity in vagal afferent neurones during feeding and fasting: mechanisms and significance*

Dockray, G. J., & Burdyga, G. (2010) · Acta Physiologica · doi:10.1111/j.1748-1716.2010.02219.x · Cited by 66 · see citing works

Effect of long-term vagal stimulation on food intake and body weight during diet induced obesity in rats.

Bugajski, A. J., Gil, K., Ziomber, A., Zurowski, D., Zaraska, W., & Thor, P. (2007) · PubMed · Cited by 65 · see citing works

Overnight food deprivation markedly attenuates hindbrain noradrenergic, glucagon-like peptide-1, and hypothalamic neural responses to exogenous cholecystokinin in male rats

Maniscalco, J. W., & Rinaman, L. (2013) · Physiology & Behavior · doi:10.1016/j.physbeh.2013.01.012 · Cited by 62 · see citing works

Design, fabrication and evaluation of a conforming circumpolar peripheral nerve cuff electrode for acute experimental use

Foldes, E. L., Ackermann, D. M., Bhadra, N., Kilgore, K. L., & Bhadra, N. (2011) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2010.12.020 · Cited by 61 · see citing works

The Use of Electrical Stimulation of the Vagus Nerve to Treat Morbid Obesity

Roslin, M. S., & Kurian, M. S. (2001) · Epilepsy & Behavior · doi:10.1006/ebeh.2001.0213 · Cited by 60 · see citing works

Cocaine- and Amphetamine-Regulated Transcript Mediates the Actions of Cholecystokinin on Rat Vagal Afferent Neurons

de Lartigue, G., Dimaline, R., Varró, A., Raybould, H. E., Serre, C. B. D. L., & Dockray, G. J. (2009) · Gastroenterology · doi:10.1053/j.gastro.2009.10.034 · Cited by 60 · see citing works

Reduced CCK signaling in obese-prone rats fed a high fat diet

Duca, F. A., Zhong, L., & Covașă, M. (2013) · Hormones and Behavior · doi:10.1016/j.yhbeh.2013.09.004 · Cited by 59 · see citing works

Electrical vagus nerve stimulation decreases food consumption and weight gain in rats fed a high-fat diet.

Gil, K., Bugajski, A. J., & Thor, P. (2011) · PubMed · Cited by 57 · see citing works

Putative roles of neuropeptides in vagal afferent signaling

de Lartigue, G. (2014) · Physiology & Behavior · doi:10.1016/j.physbeh.2014.03.011 · Cited by 56 · see citing works

Effects of vagal neuromodulation and vagotomy on control of food intake and body weight in rats.

Laskiewicz, J., Królczyk, G., Zurowski, G., Sobocki, J., Matyja, A., & Thor, P. (2003) · PubMed · Cited by 55 · see citing works

Dynamic Causal Modelling and physiological confounds: A functional MRI study of vagus nerve stimulation

Reyt, S., Picq, C. A., Sinniger, V., Clarençon, D., Bonaz, B. L., & Olivier David, A. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.05.021 · Cited by 55 · see citing works

Does vagal nerve stimulation affect body composition and metabolism? Experimental study of a new potential technique in bariatric surgery

Sobocki, J., Fourtanier, G., Estany, J., et al. (2006) · Surgery · doi:10.1016/j.surg.2005.06.025 · Cited by 55 · see citing works

Abdominal vagotomy decreases the satiating potency of CCK-8 in sham and real feeding

Joyner, K., Smith, G. P., & Gibbs, J. (1993) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1993.264.5.r912 · Cited by 55 · see citing works

A critical re‐evaluation of the specificity of action of perivagal capsaicin

Browning, K. N., Babic, T., Holmes, G. M., Swartz, E. M., & Travagli, R. A. (2013) · The Journal of Physiology · doi:10.1113/jphysiol.2012.246827 · Cited by 53 · see citing works

Effects and mechanisms of auricular vagus nerve stimulation on high-fat-diet—induced obese rats

Li, H., Zhang, J.-B., Xu, C., Tang, Q., Shen, W., Zhou, J., Chen, J., & Wang, Y. (2015) · Nutrition · doi:10.1016/j.nut.2015.05.007 · Cited by 53 · see citing works

Autonomic response and Fos expression in the NTS following intermittent vagal stimulation: Importance of pulse frequency

Osharina, V., Bagaev, V. A., Wallois, F., et al. (2006) · Autonomic Neuroscience · doi:10.1016/j.autneu.2006.03.011 · Cited by 51 · see citing works

Abrogation of peripheral cholecystokinin-satiety in the capsaicin treated rat

MacLean, D. B. (1985) · Regulatory Peptides · doi:10.1016/0167-0115(85)90204-6 · Cited by 51 · see citing works

Effect of lysine on afferent activity of the hepatic branch of the vagus nerve in normal and l-lysine-deficient rats

Torii, K., & Niijima, A. (2001) · Physiology & Behavior · doi:10.1016/s0031-9384(01)00426-7 · Cited by 50 · see citing works

Altered gastric vagal mechanosensitivity in diet-induced obesity persists on return to normal chow and is accompanied by increased food intake

Kentish, S. J., O’Donnell, T. A., Frisby, C. L., Li, H., Wittert, G., & Page, A. J. (2013) · International Journal of Obesity · doi:10.1038/ijo.2013.138 · Cited by 49 · see citing works

The ‘inhibitory’ effect of high‐frequency stimulation and the excitation state of nerve

Cattell, M., & Gerard, R. W. (1935) · The Journal of Physiology · doi:10.1113/jphysiol.1935.sp003238 · Cited by 49 · see citing works

Dopamine Depletion Reduces Food-Related Reward Activity Independent of BMI

Frank, S., Veit, R., Sauer, H., Enck, P., Friederich, H.-C., Unholzer, T., Bauer, U.-M., Linder, K., Heni, M., Fritsche, A., et al. (2016) · Neuropsychopharmacology · doi:10.1038/npp.2015.313 · Cited by 48 · see citing works

Small animal positron emission tomography during vagus nerve stimulation in rats: A pilot study

Dedeurwaerdere, S., Cornelissen, B. T., Laere, K. V., Vonck, K. E. J., Achten, E., Slegers, G., & Boon, P. (2005) · Epilepsy Research · doi:10.1016/j.eplepsyres.2005.09.008 · Cited by 45 · see citing works

Gastrointestinal Hormones and Their Targets

Rehfeld, J. F. (2014) · Advances in experimental medicine and biology · doi:10.1007/978-1-4939-0897-4_7 · Cited by 41 · see citing works

Intermittent Vagal Nerve Block for Improvements in Obesity, Cardiovascular Risk Factors, and Glycemic Control in Patients with Type 2 Diabetes Mellitus: 2-Year Results of the VBLOC DM2 Study

Shikora, S. A., Toouli, J., Herrera, M. F., Kulseng, B. E., Brancatisano, R., Kow, L., Pantoja, J. P., Johnsen, G., Brancatisano, A., Tweden, K. S., et al. (2015) · Obesity Surgery · doi:10.1007/s11695-015-1914-1 · Cited by 40 · see citing works

Vagus nerve stimulation does not lead to significant changes in body weight in patients with epilepsy

Koren, M. S., & Holmes, M. (2005) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2005.10.001 · Cited by 39 · see citing works

Magnetically induced vagus nerve stimulation and feeding behavior in rats.

Ziomber, A., Juszczak, K., Kaszuba-Zwoińska, J., et al. (2009) · PubMed · Cited by 38 · see citing works

Vagus Nerve Stimulation Affects Pain Perception in Depressed Adults

Borckardt, J. J., Kozel, F. A., Anderson, B. S., Walker, A., & George, M. S. (2005) · Pain Research and Management · doi:10.1155/2005/256472 · Cited by 37 · see citing works

Plasticity of gastro-intestinal vagal afferent endings

Kentish, S. J., & Page, A. J. (2014) · Physiology & Behavior · doi:10.1016/j.physbeh.2014.03.012 · Cited by 36 · see citing works

Truncal vagotomy in morbid obesity.

Kral, J. G., & Gortz, L. (1981) · PubMed · Cited by 36 · see citing works

Therapeutic Modalities for Treatment Resistant Depression: Focus on Vagal Nerve Stimulation and Ketamine

Shah, A. P., Carreno, F. R., & Frazer, A. (2014) · Clinical Psychopharmacology and Neuroscience · doi:10.9758/cpn.2014.12.2.83 · Cited by 35 · see citing works

Reduced Sensitivity to Cholecystokinin in Male Rats Fed a High-Fat Diet Is Reversible

Swartz, T. D., Savastano, D. M., & Covașă, M. (2010) · Journal of Nutrition · doi:10.3945/jn.110.124149 · Cited by 35 · see citing works

Effects of continuous microchip (MC) vagal neuromodulation on gastrointestinal function in rats.

Królczyk, G., Zurowski, D., Sobocki, J., et al. (2001) · PubMed · Cited by 35 · see citing works

Erratum to: Intermittent Vagal Nerve Block for Improvements in Obesity, Cardiovascular Risk Factors, and Glycemic Control in Patients with Type 2 Diabetes Mellitus: 2-Year Results of the VBLOC DM2 Study

Shikora, S. A., Toouli, J., Herrera, M. F., Kulseng, B. E., Brancatisano, R., Kow, L., Pantoja, J. P., Johnsen, G., Brancatisano, A., Tweden, K. S., et al. (2015) · Obesity Surgery · doi:10.1007/s11695-015-1951-9 · Cited by 33 · see citing works

Macronutrients act directly on the stomach to regulate gastric ghrelin release

Al–Massadi, O., Pardo, M., Roca-Rivada, A., Castelao, C., Casanueva, F. F., & Seoane, L. M. (2010) · Journal of Endocrinological Investigation · doi:10.1007/bf03346655 · Cited by 31 · see citing works

Vagotomy as a Treatment for Morbid Obesity

Kral, J. G. (1979) · Surgical Clinics of North America · doi:10.1016/s0039-6109(16)41991-2 · Cited by 31 · see citing works

Effects of truncal vagotomy on body weight and hyperinsulinemia in morbid obesity

Kral, J. G. (1980) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/33.2.416 · Cited by 29 · see citing works

Truncal vagotomy reduces food and liquid intake in man

Gortz, L., Bjorkman, A.-C., Andersson, H., & Kral, J. G. (1990) · Physiology & Behavior · doi:10.1016/0031-9384(90)90226-t · Cited by 27 · see citing works

Role of gastrin-releasing peptide in the neural control of pepsinogen secretion from the pig stomach

Skak‐Nielsen, T., Holst, J. J., & Nielsen, O. V. (1988) · Gastroenterology · doi:10.1016/0016-5085(88)90353-8 · Cited by 26 · see citing works

Loss of the liver X receptor LXRα/β in peripheral sensory neurons modifies energy expenditure

Mansuy‐Aubert, V., Gautron, L., Lee, S., Bookout, A. L., Kusminski, C. M., Sun, K., Zhang, Y., Scherer, P. E., Mangelsdorf, D. J., & Elmquist, J. K. (2015) · eLife · doi:10.7554/elife.06667 · Cited by 26 · see citing works

Microchip vagal pacing reduces food intake and body mass.

Sobocki, J., Pj, T., Usón, J., et al. (2002) · PubMed · Cited by 26 · see citing works

CCK inhibits real and sham feeding in gastric vagotomized rats

LeSauter, J., Goldberg, B., & Geary, N. (1988) · Physiology & Behavior · doi:10.1016/0031-9384(88)90314-9 · Cited by 24 · see citing works

Modulation of murine gastric vagal afferent mechanosensitivity by neuropeptide W

Li, H., Kentish, S. J., Kritas, S., Young, R. L., Isaacs, N. J., O’Donnell, T. A., Blackshaw, L. A., Wittert, G., & Page, A. J. (2013) · Acta Physiologica · doi:10.1111/apha.12154 · Cited by 24 · see citing works

Vagus Nerve Stimulation and Emotional Responses to Food among Depressed Patients

Bodenlos, J. S., Köse, S., Borckardt, J. J., Nahas, Z. H., Shaw, D. L., O'Neil, P. M., Pagoto, S., & George, M. S. (2007) · Journal of Diabetes Science and Technology · doi:10.1177/193229680700100524 · Cited by 23 · see citing works

Cholecystokinin regulates satiation independently of the abdominal vagal nerve in a pig model of total subdiaphragmatic vagotomy

Ripken, D., van der Wielen, N., van der Meulen, J., Schuurman, T., Witkamp, R. F., Hendriks, H., & Koopmans, S. J. (2014) · Physiology & Behavior · doi:10.1016/j.physbeh.2014.11.031 · Cited by 23 · see citing works

46

Tweden, K. S., Sarr, M. G., Camilleri, M., et al. (2006) · Surgery for Obesity and Related Diseases · doi:10.1016/j.soard.2006.04.050 · Cited by 21 · see citing works

Vagal efferent nerve-dependent inhibitory action of pancreatic polypeptide and peptide YY in conscious rats: comparison with somatostatin

Masuda, M., Tomita, H., Okubo, K., & Miyasaka, K. (1994) · Journal of the Autonomic Nervous System · doi:10.1016/0165-1838(94)90003-5 · Cited by 19 · see citing works

The effects of baclofen on the feeding behaviour and body weight of vagally stimulated rats.

Królczyk, G., Laskiewicz, J., Sobocki, J., et al. (2005) · PubMed · Cited by 16 · see citing works

Activation centrale à la suite d'une stimulation vagale chronique chez le porc : apports de l'imagerie fonctionnelle

Biraben, A., Guérin, S., Bobillier, É., et al. (2008) · Bulletin de l Académie vétérinaire de France · doi:10.4267/2042/48169 · Cited by 16 · see citing works

Fatty acid amide supplementation decreases impulsivity in young adult heavy drinkers

van Kooten, M. J., Veldhuizen, M. G., de Araújo, I. E., O’Malley, S. S., & Small, D. M. (2015) · Physiology & Behavior · doi:10.1016/j.physbeh.2015.11.032 · Cited by 16 · see citing works

Effects of vagal pacing on food intake and body mass in pigs.

Matyja, A., Thor, P. J., Sobocki, J., et al. (2004) · PubMed · Cited by 16 · see citing works

Histopathology of the stimulated Vagus nerve: primum non nocere

Cohen, M. L., & Georgievskaya, Z. (2010) · Heart Failure Reviews · doi:10.1007/s10741-010-9182-6 · Cited by 15 · see citing works

Relationship of postprandial motilin, gastrin, and pancreatic polypeptide release to intestinal motility during vagal interruption

Chung, S. A., Greenberg, G. R., & Diamant, N. E. (1992) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/y92-159 · Cited by 15 · see citing works

Electrical chronic vagus nerve stimulation activates the hypothalamic-pituitary-adrenal axis in rats fed high-fat diet.

Gil, K., Bugajski, A. J., Kurnik‐Łucka, M., & Thor, P. J. (2013) · PubMed · Cited by 14 · see citing works

Physiological and morphological effects of long-term vagal stimulation in diet induced obesity in rats.

Gil, K., Bugajski, A. J., Kurnik‐Łucka, M., Zaraska, W., & Thor, P. (2009) · PubMed · Cited by 14 · see citing works

The Cybergut. An Experimental Study on Permanent Microchip Neuromodulation for Control of Gut Function

Sobocki, J., Thor, P., Królczyk, G., et al. (2002) · Acta chirurgica Belgica · doi:10.1080/00015458.2002.11679268 · Cited by 13 · see citing works

Electric excitation of the fin nerve of sepia

Bugnard, L., & Hill, A. V. (1935) · The Journal of Physiology · doi:10.1113/jphysiol.1935.sp003240 · Cited by 13 · see citing works

Chronic vagus nerve stimulation reduces body fat, blood cholesterol and triglyceride levels in rats fed a high-fat diet.

Gil, K., Bugajski, A. J., Kurnik‐Łucka, M., et al. (2012) · PubMed · Cited by 13 · see citing works

Vagal plasticity the key to obesity

de Lartigue, G., Ronveaux, C. C., & Raybould, H. E. (2014) · Molecular Metabolism · doi:10.1016/j.molmet.2014.09.009 · Cited by 12 · see citing works

Vagal afferent controls of feeding: a possible role for gastrointestinal BDNF

Fox, E. A. (2012) · Clinical Autonomic Research · doi:10.1007/s10286-012-0170-x · Cited by 9 · see citing works

Vagus nerve stimulation confuses appetite: Comment on Bodenlos et al. (2007)

Gibson, E. L., & Mohiyeddini, C. (2007) · Appetite · doi:10.1016/j.appet.2007.10.001 · Cited by 5 · see citing works

Increased c-Fos expression in nodose ganglion in rats with electrical vagus nerve stimulation.

Gil, K., Bugajski, A. J., Skowron, B., et al. (2011) · PubMed · Cited by 2 · see citing works

Diseases, Disorders, and Comorbidities of Interoception

Bonaz, B., Lane, R. D., Oshinsky, M. L., Kenny, P. J., Sinha, R., Mayer, E. A., & Critchley, H. D. (2021) · Trends in Neurosciences · doi:10.1016/j.tins.2020.09.009 · Cited by 260 · see citing works

Role of the gut-brain axis in energy and glucose metabolism

Wachsmuth, H. R., Weninger, S. N., & Duca, F. A. (2022) · Experimental & Molecular Medicine · doi:10.1038/s12276-021-00677-w · Cited by 269 · see citing works

The metabolic role of vagal afferent innervation

Waise, T. M. Z., Dranse, H. J., & Lam, T. K. T. (2018) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-018-0062-1 · Cited by 140 · see citing works

Autonomic nervous system dysfunction in schizophrenia: impact on cognitive and metabolic health

Stogios, N., Gdanski, A., Gerretsen, P., Chintoh, A. F., Graff-Guerrero, A., Rajji, T. K., Remington, G., Hahn, M. K., & Agarwal, S. M. (2021) · npj Schizophrenia · doi:10.1038/s41537-021-00151-6 · Cited by 98 · see citing works

Recent progress on peripheral neural interface technology towards bioelectronic medicine

Cho, Y., Park, J., Lee, C., & Lee, S. (2020) · Bioelectronic Medicine · doi:10.1186/s42234-020-00059-z · Cited by 55 · see citing works

Intact vagal gut-brain signalling prevents hyperphagia and excessive weight gain in response to high-fat high-sugar diet

McDougle, M., Quinn, D., Diepenbroek, C., Singh, A., de la Serre, C., & de Lartigue, G. (2021) · Acta Physiologica · doi:10.1111/apha.13530 · Cited by 42 · see citing works

Chronic high fat diet impairs glucagon like peptide-1 sensitivity in vagal afferents

Al Helaili, A., Park, S. J., & Beyak, M. J. (2020) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2020.08.045 · Cited by 17 · see citing works

Cholecystokinin-octapeptide like immunoreactivity in the area postrema of the rat and cat

Newton, B. W., & Maley, B. E. (1985) · Regulatory Peptides · doi:10.1016/0167-0115(85)90084-9 · Cited by 15 · see citing works

A concise historical perspective of the area postrema structure and function

SOUZA, T. F. S. D. (2020) · Arquivos de Neuro-Psiquiatria · doi:10.1590/0004-282x20190118 · Cited by 7 · see citing works

Area postrema: site where cholecystokinin acts to decrease food intake

van der Kooy, D. (1984) · Brain Research · doi:10.1016/0006-8993(84)90982-x · Cited by 123 · see citing works

Evidence for cholinergic vagal afferents and vagal presynaptic M1 receptors in the ferret

Reynolds, D. J., Lowenstein, P. R., MOORMAN, J., GRAHAMESMITH, D., & Leslie, R. A. (1994) · Neurochemistry International · doi:10.1016/0197-0186(94)90022-1 · Cited by 10 · see citing works

A projection of vagus nerve to the area subpostrema in the cat

Gwyn, D. G., & Leslie, R. A. (1979) · Brain Research · doi:10.1016/0006-8993(79)90074-x · Cited by 36 · see citing works