The DOI matches its Crossref record; 54 of the 54 references it cites were found in a registry or an index.
The Cephalic Insulin Response to Meal Ingestion in Humans Is Dependent on Both Cholinergic and Noncholinergic Mechanisms and Is Important for Postprandial Glycemia
Open accessAbstract
We studied the mechanisms and physiological relevance of the cephalic insulin response to meal ingestion in 12 healthy women (age 63 ± 0.4 years; BMI 27.7 ± 1.7 kg/m2). The ganglionic antagonist, trimethaphan, which impairs neurotransmission across parasympathetic and sympathetic autonomic ganglia, or atropine or saline was given intravenously during the first 15 min after ingestion of a standard meal (350 kcal). During saline infusion, insulin levels increased during the first 10 min after meal ingestion, whereas the first increase in glucose was evident at 15 min. The preabsorptive 10-min insulin response was reduced by 73 ± 11% by trimethaphan (P = 0.009), accompanied by impaired reduction of glucose levels from 25 to 60 min after meal ingestion (Δglucose = –1.27 ± 0.5 [with saline] vs. 0.1 ± 0.4 mmol/l [with trimethaphan]; P = 0.008). This reduction at 25–60 min in glucose levels correlated significantly to the 10-min insulin response (r = 0.65, P = 0.024). The 10-min insulin response to meal ingestion was also reduced by atropine, but only by 20 ± 9% (P = 0.045), which was lower than the reduction with trimethaphan (P = 0.004). The preabsorptive insulin response was not accompanied by any increase in circulating levels of gastric inhibitory polypeptide (GIP) or glucagon-like peptide 1 (GLP-1). In conclusion, 1) the early preabsorptive insulin response to meal ingestion in humans can be largely attributed to autonomic activation mediated by noncholinergic and cholinergic mechanisms, 2) this cephalic insulin response is required for a normal postprandial glucose tolerance, and 3) GIP and GLP-1 do not contribute to the preabsorptive cephalic phase insulin response to meal ingestion.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The cited source says what the claim attributes to it.
In the citing paper
“The neural mechanism underlying cephalic phase insulin response was found to include cholinergic and non-cholinergic processes136 as well as the dorsal vagal complex located in the medulla oblongata.137”
From Pancreatic regulation of glucose homeostasis. (2016) · cites this paper as [136]
The cited source says what the claim attributes to it.
In the citing paper
“Moreover, cephalic phase insulin response is pivotal for ensuring normal postprandial glucose management.136”
From Pancreatic regulation of glucose homeostasis. (2016) · cites this paper as [136]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
The Pharmacological Basis of Therapeutics
(1976) · American Journal of Health-System Pharmacy · doi:10.1093/ajhp/33.4.373a · Cited by 9,216
The pharmacological basis of therapeutics
Starr, I. (1941) · American Heart Journal · doi:10.1016/s0002-8703(41)90958-4 · Cited by 1,907
Kieffer, T. J., & Habener, J. F. (1999) · Endocrine Reviews · doi:10.1210/edrv.20.6.0385 · Cited by 1,062
Autonomic regulation of islet hormone secretion - Implications for health and disease
Åhrén, B. (2000) · Diabetologia · doi:10.1007/s001250051322 · Cited by 929
Tissue and Plasma Concentrations of Amidated and Glycine-Extended Glucagon-Like Peptide I in Humans
Ørskov, C., Rabenhøj, L., Wettergren, A., Kofod, H., & Holst, J. J. (1994) · Diabetes · doi:10.2337/diab.43.4.535 · Cited by 916
Self-citationScrocchi, L. A., Brown, T. J., Maclusky, N., Brubaker, P. L., Auerbach, A. B., Joyner, A. L., & Drucker, D. J. (1996) · Nature Medicine · doi:10.1038/nm1196-1254 · Cited by 793
Mitrakou, A., Kelley, D., Mokan, M., Veneman, T., Pangburn, T., Reilly, J., & Gerich, J. (1992) · New England Journal of Medicine · doi:10.1056/nejm199201023260104 · Cited by 595
Miyawaki, K., Yamada, Y., Yano, H., Niwa, H., Ban, N., Ihara, Y., Kubota, A., Fujimoto, S., Kajikawa, M., Kuroe, A., et al. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.26.14843 · Cited by 454
Avignon, A., Radauceanu, A., & Monnier, L. (1997) · Diabetes Care · doi:10.2337/diacare.20.12.1822 · Cited by 363
Cephalic phase, reflex insulin secretion neuroanatomical and physiological characterization
Berthoud, H. R., Bereiter, D. A., Trimble, E. R., Siegel, E. G., & Jeanrenaud, B. (1981) · Diabetologia · doi:10.1007/bf00254508 · Cited by 231
Cited by
Sorted by citations
Items 101–200 of 290
Cephalic phase insulin release: A review of its mechanistic basis and variability in humans
Pullicin, A. J., Glendinning, J. I., & Lim, J. (2021) · Physiology & Behavior · doi:10.1016/j.physbeh.2021.113514 · Cited by 39
Zhu, Y., Hsu, W. H., & Hollis, J. (2014) · Physiology & Behavior · doi:10.1016/j.physbeh.2014.06.009 · Cited by 35
Dimitriadis, G., Boutati, E. I., Lambadiari, V., Mitrou, P., Maratou, E., Brunel, P., & Raptis, S. (2004) · European Journal of Clinical Investigation · doi:10.1111/j.1365-2362.2004.01377.x · Cited by 35
Neuronal glucose sensing mechanisms and circuits in the control of insulin and glucagon secretion
Thorens, B. (2024) · Physiological Reviews · doi:10.1152/physrev.00038.2023 · Cited by 37
“This anticipatory insulin secretion plays an important role to ensure normal postprandial glucose tolerance (98, 99).”
BackgroundCholinergic Regulation of Ghrelin and Peptide YY Release May Be Impaired in Obesity
Maier, C., Riedl, M., Vila, G., Nowotny, P., Wolzt, M., Clodi, M., Ludvik, B. H., & Luger, A. (2008) · Diabetes · doi:10.2337/db07-0758 · Cited by 35
“It has been shown that cholinergic regulation is an important part of meal-induced insulin release (38).”
Backgroundde Courten, B. V., Weyer, C., Stefan, N., Horton, M. B., DelParigi, A., Havel, P. J., Bogardus, C., & Tataranni, P. A. (2004) · Diabetes · doi:10.2337/diabetes.53.3.663 · Cited by 34
“The significant contribution of the PNS to insulin secretion in response to meal ingestion has been demonstrated in both animals (28,30) and humans (29,31).”
BackgroundGrowth Hormone-Releasing Hormone in Diabetes
Fridlyand, L. E., Tamarina, N. A., Schally, A. V., & Philipson, L. H. (2016) · Frontiers in Endocrinology · doi:10.3389/fendo.2016.00129 · Cited by 33
“The subsequent cholinergic stimulation via the muscarinic (acetylcholine) GPCR leads to an activation of the phospholipase C (PLC) pathway (48, 49).”
BackgroundEmerging Role of Lymphatics in the Regulation of Intestinal Lipid Mobilization
Xiao, C., Stahel, P., Nahmias, A., & Lewis, G. F. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2019.01604 · Cited by 34
“, 2005), and both cholinergic and non-cholinergic autonomic activations mediate cephalic phase response of insulin secretion (Ahrén and Holst, 2001).”
BackgroundInfluentialPaschetta, E., Hvalryg, M., & Musso, G. (2011) · Obesity Reviews · doi:10.1111/j.1467-789x.2011.00897.x · Cited by 34
“vagal innervation may, in part, be involved (56).”
BackgroundActivation of the dorsal vagal nucleus increases pancreatic exocrine secretion in the rat
Mussa, B. M., & Verberne, A. J. M. (2007) · Neuroscience Letters · doi:10.1016/j.neulet.2007.12.048 · Cited by 32
“The ‘cephalic’ r pre-digestive phase of insulin secretion occurs via the vagus nd appears to be important for normal glucose tolerance [1].”
BackgroundHypothalamic insulin responsiveness is associated with pancreatic insulin secretion in humans
Kullmann, S., Fritsche, A., Wagner, R. J., Schwab, S., Häring, H., Preissl, H. T., & Heni, M. (2017) · Physiology & Behavior · doi:10.1016/j.physbeh.2017.03.036 · Cited by 31
“This conditioned reflex originates in the brain and probably reaches pancreatic beta cells via both branches of the autonomic nervous system [11,14,15].”
TRPV1 neurons regulate β-cell function in a sex-dependent manner
Karam, J. B., Cai, W.-K., Mohamed, R., Huang, T., Meng, L., Homan, E. P., Dirice, E., Kahn, C. R., & Ouaamari, A. E. (2018) · Molecular Metabolism · doi:10.1016/j.molmet.2018.10.002 · Cited by 33
Glucose Activates Vagal Control of Hyperglycemia and Inflammation in Fasted Mice
Joseph, B., Shimojo, G. L., Li, Z., Thompson-Bonilla, M. D. R., Shah, R., Kanashiro, A., Salgado, H. C., & Ulloa, L. (2019) · Scientific Reports · doi:10.1038/s41598-018-36298-z · Cited by 30
Insulin Transport into the Brain and Cerebrospinal Fluid
Begg, D. P. (2015) · Vitamins and hormones · doi:10.1016/bs.vh.2014.12.007 · Cited by 31
Lundberg, M., Lindqvist, A., Wierup, N., Krogvold, L., Dahl-Jørgensen, K., & Skog, O. (2017) · PLoS ONE · doi:10.1371/journal.pone.0179911 · Cited by 24
The Role of Taste in Cephalic Phase of Insulin Secretion
Dušková, M., Macourek, M., Šrámková, M., Hill, M., & Stárka, L. (2013) · Prague Medical Report · doi:10.14712/23362936.2014.11 · Cited by 30
Cummings, B. P., Bremer, A. A., Kieffer, T. J., D’Alessio, D. A., & Havel, P. J. (2012) · Journal of Endocrinology · doi:10.1530/joe-12-0459 · Cited by 29
“…polypeptide is an islet hormone known to be closely regulated by parasympathetic input to the islet in response to feeding and during insulin-induced hypoglycemia in rhesus macaques and humans (Schwartz 1988, Havel & Valverde 1996, Havel & Ahren 1997, Ahren & Holst 2001, D’Alessio et al. 2001).”
BackgroundPapakonstantinou, E., Triantafillidou, D., Panagiotakos, D. B., Iraklianou, S., Berdanier, C. D., & Zampelas, A. (2010) · Journal of Human Nutrition and Dietetics · doi:10.1111/j.1365-277x.2009.01020.x · Cited by 29
Chowdhury, S., Reeds, D. N., Crimmins, D. L., Patterson, B. W., Laciny, E., Wang, S., Tran, H. D., Griest, T. A., Rometo, D. A., Dunai, J., et al. (2013) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00383.2013 · Cited by 28
Åhrén, B. (2008) · Diabetologia · doi:10.1007/s00125-008-0995-y · Cited by 31
“We have previously used this approach to study the contribution of autonomic mechanisms to counter regulatory responses to hypoglycaemia [21] and to the cephalic phase of insulin secretion after meal ingestion [22].”
BackgroundMethodVahl, T. P., & D’Alessio, D. A. (2003) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/01.mco.0000078991.96795.84 · Cited by 28
Montaner, M., Denom, J., Jiang, W., Magnan, C., Trapp, S., & Gurden, H. (2023) · Molecular Metabolism · doi:10.1016/j.molmet.2023.101738 · Cited by 27
Obesity, Metabolic Syndrome and Disorders of Energy Balance
Han, J. C., & Weiss, R. (2021) · Elsevier eBooks · doi:10.1016/b978-0-323-62520-3.00024-5 · Cited by 27
Novel findings in the cephalic phase of digestion: A role for microcirculation?
Buss, C., Kraemer‐Aguiar, L. G., Maranhao, P. A., Marinho, C., de Souza, M. D. G. C., Wiernsperger, N. F., & Bouskela, E. (2011) · Physiology & Behavior · doi:10.1016/j.physbeh.2011.12.004 · Cited by 27
“Physiologically, this period is fundamental for nutrient metabolism due to the early supply of insulin to tissues priming its receptors and allowing further glucose metabolization [8,12].”
Vagal pathways for systemic regulation of glucose metabolism
Borgmann, D., & Fenselau, H. (2023) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2023.07.010 · Cited by 27
Plamboeck, A., Veedfald, S., Deacon, C. F., Hartmann, B., Vilsbøll, T., Knop, F. K., & Holst, J. J. (2015) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00123.2015 · Cited by 24
“In humans, a selective block of afferent vagal transmission is not easily accomplished, but efferent activity may be blocked by using either a ganglionic blocker or atropine (2, 4, 44, 46).”
BackgroundMethodSelf-citationChien, H.-J., Peng, S.-J., Hua, T.-E., Kuo, C.-H., Juang, J.-H., & Tang, S.-C. (2015) · International Journal of Obesity · doi:10.1038/ijo.2015.224 · Cited by 25
Molecular regulation of insulin granule biogenesis and exocytosis
Röder, P. V., Wong, X. M., Hong, W., & Han, W. (2016) · Biochemical Journal · doi:10.1042/bcj20160291 · Cited by 25
Adipose stem cell-based regenerative medicine for reversal of diabetic hyperglycemia
Paek, H. J. (2014) · World Journal of Diabetes · doi:10.4239/wjd.v5.i3.235 · Cited by 26
Vosseler, A., Zhao, D., Fritsche, L., Lehmann, R., Kantartzis, K., Small, D. M., Peter, A., Häring, H., Birkenfeld, A. L., Fritsche, A., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-77430-2 · Cited by 24
Miguel, J. C., Abdel‐Wahab, Y. H. A., Green, B. D., Mathias, P. C. D. F., & Flatt, P. R. (2002) · Biochemical Pharmacology · doi:10.1016/s0006-2952(02)01482-x · Cited by 25
Mechanism of rapid-phase insulin response to elevation of portal glucose concentration
Fukaya, M., Mizuno, A., Arai, H., Muto, K., Uebanso, T., Matsuo, K., Yamamoto, H., Taketani, Y., Doi, T., & Takeda, E. (2007) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00536.2006 · Cited by 26
“Ahrén and Holst (1) suggested that the cephalicphase insulin response was more closely correlated with glucose tolerance than was the 30-min insulin response to an oral glucose load.”
BackgroundInfluentialNeural Control of the Pancreas
Travagli, T. B. A. R. A. (2016) · doi:10.3998/panc.2016.27 · Cited by 24
“Calcitonin gene-related peptide has been reported to either stimulate or inhibit glucagon release (1, 35).”
BackgroundThe Role of Accessory Cells in Islet Homeostasis
Tang, S., Jessup, C. F., & Campbell‐Thompson, M. (2018) · Current Diabetes Reports · doi:10.1007/s11892-018-1096-z · Cited by 24
An alternative pathway for sweet sensation: possible mechanisms and physiological relevance
von Molitor, E., Riedel, K., Krohn, M., Rudolf, R., Hafner, M., & Cesetti, T. (2020) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-020-02467-1 · Cited by 28
“CPIR needs the oral component and is independent of digestion in humans [2, 3] and animals [100, 101, 321].”
BackgroundBenetti, A., Martins, F. L., Sene, L. D. B., Shimizu, M. H. M., Seguro, A. C., Luchi, W. M., & Girardi, A. C. C. (2020) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00288.2020 · Cited by 23
The House Economist and the Eating Paradox
Woods, S. C. (2002) · Appetite · doi:10.1006/appe.2001.0468 · Cited by 23
Technosphere insulin: inhaled prandial insulin
Setji, T. L., Hong, B. D., & Feinglos, M. N. (2015) · Expert Opinion on Biological Therapy · doi:10.1517/14712598.2016.1121230 · Cited by 22
“This initial spike in insulin is important for subsequent glucose tolerance and is impaired in patients with diabetes.[27] SC insulin therapy with rapid-acting analogs does not mimic the cephalic insulin response, and instead provides a slow increase in insulin concentration peaking around 40 minutes after injection,…”
BackgroundPorcellati, F., Pampanelli, S., Rossetti, P., Cordoni, C., Marzotti, S., Scionti, L., Bolli, G. B., & Fanelli, C. G. (2003) · Diabetes · doi:10.2337/diabetes.52.11.2774 · Cited by 23
“This is likely due to the early neural stimulation of a meal on pancreatic polypeptide secretion (30).”
BackgroundLoutseiko, M., Voskanyan, G. R., Keenan, D. B., & Steil, G. M. (2011) · Journal of Diabetes Science and Technology · doi:10.1177/193229681100500605 · Cited by 22
Effects of Nutrient Intake during Pregnancy and Lactation on the Endocrine Pancreas of the Offspring
Moullé, V. S., & Parnet, P. (2019) · Nutrients · doi:10.3390/nu11112708 · Cited by 24
“This corresponds to the pre-absorptive secretion of insulin in response to neural signals triggered by meal olfactory clues rather than changes in plasma glucose concentrations after meal intake [29,30].”
Background48-h Glucose infusion in humans: Effect on hormonal responses, hunger and food intake
Teff, K. L., Petrova, M., Havel, P. J., & Townsend, R. R. (2007) · Physiology & Behavior · doi:10.1016/j.physbeh.2006.12.013 · Cited by 20
Barber, T. M., Bhatti, A. A., Elder, P. J. D., Ball, S., Calvez, R., Ramsden, D. B., Cuthbertson, D. J., Pfeiffer, A. F. H., Burnett, D. A., & Weickert, M. O. (2020) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/clinem/dgaa473 · Cited by 19
de Laat, M. A., & Fitzgerald, D. M. (2023) · The Veterinary Journal · doi:10.1016/j.tvjl.2023.105967 · Cited by 20
Alberti, G., Parada, J., Cataldo, L. R., Vega, J., Aguilera, C. M., Álvarez‐Mercado, A. I., Hodgson, M. I., López, A. J., Angellotti, I., Gil, Á., et al. (2015) · doi:10.12691/jfnr-3-8-11 · Cited by 19
“Then, it was proposed that the release of starch digestion products in the oral cavity may signal the body to prepare for incoming starch through vagal activation, resulting in an early insulin release termed preabsorptive insulin or cephalic phase of insulin secretion [9,17,18,19].”
BackgroundEliasson, B., Rawshani, A., Axelsen, M., Hammarstedt, A., & Smith, U. (2017) · PLoS ONE · doi:10.1371/journal.pone.0173654 · Cited by 18
Moullé, V. S. (2021) · Peptides · doi:10.1016/j.peptides.2021.170709 · Cited by 22
Chen, L.-H., Yang, Z.-M., Chen, W.-W., Lin, J., Zhang, M., Yang, X.-R., & Zhao, L.-B. (2015) · British Journal of Nutrition · doi:10.1017/s0007114515000446 · Cited by 17
“CPIR plays an extremely important role in glycaemic homeostasis((32)), and thus can affect individual nutrition.”
BackgroundLustig, R. H., & Weiss, R. (2008) · Elsevier eBooks · doi:10.1016/b978-141604090-3.50024-7 · Cited by 17
The Different Faces of the Pancreatic Islet
Abdulreda, M. H., Rodriguez‐Diaz, R., Cabrera, O., Caicedo, A., & Berggren, P. (2016) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-39824-2_2 · Cited by 18
Dunning, B. E., Moore, M. C., Ikeda, T., Neal, D. W., Scott, M. F., & Cherrington, A. D. (2002) · Metabolism · doi:10.1053/meta.2002.34712 · Cited by 17
Yavropoulou, M. P., Kotsa, K., Κεσίσογλου, Ι., Anastasiou, O. E., & Yovos, J. G. (2008) · Peptides · doi:10.1016/j.peptides.2008.08.024 · Cited by 17
“Human studies, have revealed that although basal GIP levels were not altered by atropine, the early post-absorptive GIP-induced response was reduced, suggesting that vagal mediation may be involved [1].”
BackgroundHuman pancreatic capillaries and nerve fibers persist in type 1 diabetes despite beta cell loss
Richardson, T. M., Saunders, D. C., Haliyur, R., Shrestha, S., Cartailler, J., Reinert, R. B., Petronglo, J. R., Bottino, R., Aramandla, R., Bradley, A. M., et al. (2023) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00246.2022 · Cited by 17
Scigliano, G., Ronchetti, G., & Girotti, F. (2008) · Neurological Sciences · doi:10.1007/s10072-008-0853-1 · Cited by 16
“Dino Ferrari Centre Department of Neurological Sciences University of Milan, IRCCS Foundation Ospedale Maggiore Policlinico, Mangiagalli and Regina Elena Milan, Italy secretory response is associated with increased parasympathetic activity and inhibition of the sympathetic splanchnic and adrenal nerves [ 3 ], while st…”
BackgroundPediatric Endocrine Disorders of Energy Balance
Lustig, R. H. (2005) · Reviews in Endocrine and Metabolic Disorders · doi:10.1007/s11154-005-6183-1 · Cited by 16
Vella, A. V., Sathananthan, M., Ikramuddin, S., Swain, J. M., Shah, M., Piccinini, F., Man, C. D., Cobelli, C., Rizza, R. A., & Camilleri, M. (2014) · Diabetes Metabolic Syndrome and Obesity · doi:10.2147/dmso.s65733 · Cited by 15
Mastracci, T. L., Apte, M. V., Amundadottir, L. T., Alvarsson, A., Artandi, S. E., Bellin, M. D., Bernal‐Mizrachi, E., Caicedo, A., Campbell‐Thompson, M., Cruz‐Monserrate, Z., et al. (2023) · Diabetes · doi:10.2337/db22-0942 · Cited by 15
Morey, S., Shafat, A., & Clegg, M. (2015) · Appetite · doi:10.1016/j.appet.2015.11.002 · Cited by 14
CD36 Modulates Fasting and Preabsorptive Hormone and Bile Acid Levels
Shibao, C. A., Celedonio, J. E., Tamboli, R. A., Sidani, R. M., Love-Gregory, L. D., Pietka, T., Xiong, Y., Yan, W., Abumrad, N. N., Abumrad, N. A., et al. (2018) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2017-01982 · Cited by 16
Role of GLP-1 induced glucagon suppression in type 2 diabetes mellitus.
Hare, K. J. (2010) · PubMed · Cited by 14
Charlot, K., Pichon, A., & Chapelot, D. (2011) · Nutrition & Metabolism · doi:10.1186/1743-7075-8-66 · Cited by 14
“Thus, the effect of prior exercise on postprandial metabolism could involve postprandial vagal withdrawal and sympathetic activation, both of which would result in a transiently blunted glucose tolerance mediated by reduced insulin secretion [21,66].”
BackgroundVosseler, A., Zhao, D., Hummel, J., Gholamrezaei, A., Hudak, S., Kantartzis, K., Peter, A., Birkenfeld, A. L., Häring, H., Wagner, R. J., et al. (2021) · Scientific Reports · doi:10.1038/s41598-021-99183-2 · Cited by 13
Expecting to Eat: Glucagon-Like Peptide-1 and the Anticipation of Meals
Williams, D. L. (2010) · Endocrinology · doi:10.1210/en.2009-1372 · Cited by 13
Food perception and postprandial lipid metabolism
Robertson, M. D. (2006) · Physiology & Behavior · doi:10.1016/j.physbeh.2006.01.030 · Cited by 13
Tasyurek, H. M., Ekşi, Y. E., Şanlioğlu, A. D., Altunbaş, H., Balcı, M. K., Griffith, T. S., & Şanlıoğlu, S. (2018) · Gene Therapy · doi:10.1038/s41434-018-0011-1 · Cited by 13
Nutritional Implications of Taste and Smell Dysfunction
Lee, J. C. L., Tucker, R. M., Tan, S., Running, C. A., Jones, J. B., & Mattes, R. D. (2015) · Wiley eBooks · doi:10.1002/9781118971758.ch37 · Cited by 13
Comparison of aspartame- and sugar-sweetened soft drinks on postprandial metabolism
Pearson, R. C., Green, E. S., Olenick, A. A., & Jenkins, N. T. (2023) · Nutrition and Health · doi:10.1177/02601060211057415 · Cited by 12
“Additionally, the CPIR only accounts for a very small percentage of total postprandial AUC after a mixed meal test (Ahren and Holst, 2001).”
BackgroundIntracerebroventricular infusion of bombesin modulates GIP secretion in conscious dogs
Yavropoulou, M. P., Kotsa, K., Anastasiou, O. E., O’Dorisio, T. M., Pappas, T. N., & Yovos, J. G. (2009) · Neuropharmacology · doi:10.1016/j.neuropharm.2009.06.025 · Cited by 12
Modeling the effect of the cephalic phase of insulin secretion on glucose metabolism
Güemes, A., Herrero, P., Bondia, J., & Georgiou, P. (2019) · Medical and Biological Engineering and Computing · doi:10.1007/s11517-019-01950-x · Cited by 12
The Efferent Arm of the Energy Balance Regulatory Pathway: Neuroendocrinology and Pathology
Lustig, R. H. (2007) · Humana Press eBooks · doi:10.1007/978-1-60327-139-4_5 · Cited by 12
“This is the “cephalic” phase of insulin secretion, described above ( 42 ).”
BackgroundA novel, rapid, inhibitory effect of insulin on α1β2γ2s γ-aminobutyric acid type A receptors
Williams, D. B. (2008) · Neuroscience Letters · doi:10.1016/j.neulet.2008.07.038 · Cited by 12
A NATURAL BODY WINDOW TO STUDY HUMAN PANCREATIC ISLET CELL FUNCTION AND SURVIVAL.
Abdulreda, M. H., Caicedo, A., & Berggren, P.-O. (2013) · PubMed · Cited by 12
Lechner, A. (2004) · Pediatric Diabetes · doi:10.1111/j.1399-543x.2004.00084.x · Cited by 12
Zhan, F., Chen, J., Yan, H., Wang, S., Zhao, M., Zhang, S., Lan, X., & Maekawa, M. (2021) · Diabetes Metabolic Syndrome and Obesity · doi:10.2147/dmso.s339604 · Cited by 11
Effects of artificial and natural sweeteners on host metabolic health: A double-edged sword
Xue, H., Kang, X., Hong, K., Gao, Y., Tang, Y., Lin, Y., Liu, X., Huang, W., Zhan, J., & You, Y. (2025) · Food Research International · doi:10.1016/j.foodres.2025.117158 · Cited by 14
Glucagon-like peptide 1 and dysglycemia: Conflict in incretin science
Singh, A. K. (2014) · Indian Journal of Endocrinology and Metabolism · doi:10.4103/2230-8210.146881 · Cited by 13
Veedfald, S., Rehfeld, J. F., van Hall, G., Svendsen, L. B., & Holst, J. J. (2021) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/clinem/dgab610 · Cited by 11
Self-citationShort-term oral exposure to white wine transiently lowers serum free fatty acids
Joosten, M. M., de Graaf, C., Rietman, A., Witkamp, R. F., & Hendriks, H. (2010) · Appetite · doi:10.1016/j.appet.2010.04.217 · Cited by 11
Effects of nateglinide on the secretion of glycated insulin and glucose tolerance in type 2 diabetes
Lindsay, J. R., McKillop, A. M., Mooney, M. H., O'Harte, F. P. M., Flatt, P. R., & Bell, P. M. (2003) · Diabetes Research and Clinical Practice · doi:10.1016/s0168-8227(03)00107-4 · Cited by 11
Potential Role of Yoga in Management of the Ominous Octet
Vijayakumar, V., Mavathur, R. N., Raguram, N., Ranjani, H., Anjana, R. M., & Mohan, V. (2021) · Journal of Diabetology · doi:10.4103/jod.jod_6_18 · Cited by 12
Al-Akl, N. S., Thompson, I. R., & Arredouani, A. (2022) · PLoS ONE · doi:10.1371/journal.pone.0264692 · Cited by 10
Integrated Physiology of the Exocrine and Endocrine Compartments in Pancreatic Diseases
Mastracci, T. L., Apte, M. V., Amundadottir, L. T., Alvarsson, A., Artandi, S. E., Bellin, M. D., Bernal‐Mizrachi, E., Caicedo, A., Campbell‐Thompson, M., Cruz‐Monserrate, Z., et al. (2022) · Pancreas · doi:10.1097/mpa.0000000000002170 · Cited by 10
Postprandial increase in glucagon-like peptide-1 is blunted in severe heart failure
Arruda-Junior, D. F., Martins, F. L., Salles, T. A., Jensen, L., Dariolli, R., Antônio, E. L., dos SANTOS, L., Crajoinas, R. O., Tucci, P. J. F., Gowdak, L. H. W., et al. (2020) · Clinical Science · doi:10.1042/cs20190946 · Cited by 10
Lipid-Induced Peroxidation in the Intestine Is Involved in Glucose Homeostasis Imbalance in Mice
Sérino, M., Waget, A., Marsollier, N., Masseboeuf, M., Payros, G., Gallou‐Kabani, C., Denom, J., Lacombe, A., Thiers, J., Nègre‐Salvayre, A., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0021184 · Cited by 10
“Particularly, a study by Ahren and Holst showed that the pre-absorptive insulin response to meal ingestion in humans was largely attributed to autonomic activation [27].”
BackgroundInfluentialCentral Regulation of Glucose-Dependent Insulinotropic Polypeptide Secretion
Yavropoulou, M. P., & Yovos, J. G. (2010) · Vitamins and hormones · doi:10.1016/b978-0-12-381517-0.00006-0 · Cited by 10
Current literature in diabetes
Nazlıel, B., Yetkin, İ., İrkeç, C., & Koçer, B. (2001) · Diabetes/Metabolism Research and Reviews · doi:10.1002/dmrr.173 · Cited by 10
Huang, Y., Wang, W., Zheng, X.-M., Yang, L., Wang, L., Qiu, X., Chen, L., Li, R., & Lin, C.-Q. (2022) · PLoS ONE · doi:10.1371/journal.pone.0269621 · Cited by 9
“CPIR plays a crucial role in glucose homeostasis [42], and thus can influence individual nutrition.”
BackgroundGlendinning, J. I., Drimmer, Z., & Isber, R. (2024) · Physiology & Behavior · doi:10.1016/j.physbeh.2024.114476 · Cited by 9
Blood glucose monitoring as a teaching tool for endocrinology: a new perspective
Moats, R. K. (2009) · AJP Advances in Physiology Education · doi:10.1152/advan.00009.2009 · Cited by 9
“Pharmacological blockade of the autonomic nervous system (ANS) prevents a slight but significant elevation in insulin levels at the onset of meal ingestion (2).”
BackgroundUse of c-peptide as a measure of cephalic phase insulin release in humans
Pullicin, A. J., Newsom, S. A., Robinson, M. M., & Lim, J. (2022) · Physiology & Behavior · doi:10.1016/j.physbeh.2022.113940 · Cited by 9
Tang, M. W., van Nierop, F. S., Koopman, F. A., Eggink, H. M., Gerlag, D. M., Chan, M. W., Zitnik, R. J., Vaz, F. M., Romijn, J. A., Tak, P. P., et al. (2017) · Clinical Rheumatology · doi:10.1007/s10067-017-3618-5 · Cited by 9
Obesity, metabolic syndrome, and disorders of energy balance
Weiss, R., & Lustig, R. H. (2014) · Elsevier eBooks · doi:10.1016/b978-1-4557-4858-7.00031-7 · Cited by 9
Chen, C., Peng, S.-J., Wu, P.-Y., Chien, H., Lee, C., Chung, M., & Tang, S. (2021) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00605.2020 · Cited by 9
Yavropoulou, M. P., Kotsa, K., Anastasiou, O. E., O’Dorisio, T. M., Pappas, T. N., & Yovos, J. G. (2009) · Neuroscience Letters · doi:10.1016/j.neulet.2009.05.052 · Cited by 11
Yavropoulou, M. P., Kotsa, K., Κεσίσογλου, Ι., Gotzamani-Psarakou, A., & Yovos, J. G. (2009) · Peptides · doi:10.1016/j.peptides.2009.09.029 · Cited by 9
Chai, J., Zhang, G., Liu, S., Hu, C., Han, H., Hu, S., & Zhang, Z. (2015) · Obesity Surgery · doi:10.1007/s11695-015-1745-0 · Cited by 8
Evidence for neural contribution to islet effects of DPP-4 inhibition in mice
Ahlkvist, L., Omar, B. A., Pacini, G., & Åhrén, B. (2016) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2016.03.030 · Cited by 8
Pharmacogenetics of insulin secretagogue antidiabetics
Winkler, G., & Gerő, L. (2011) · Orvosi Hetilap · doi:10.1556/oh.2011.29175 · Cited by 8
Irwin, N., Francis, J. M. E., & Flatt, P. R. (2011) · Biological Chemistry · doi:10.1515/bc.2011.176 · Cited by 8
“However, the early meal-induced GIP response is reduced by atropine in humans (Ahrén and Holst, 2001), highlighting potential species differences.”
BackgroundThe vagus is inhibitory of the late postprandial insulin secretion in conscious pigs
Blat, S., Guérin, S., Chauvin, A., Sève, B., Morgan, L., Cuber, J.-C., & Malbert, C. (2002) · Autonomic Neuroscience · doi:10.1016/s1566-0702(02)00184-4 · Cited by 8
Metadata
- Authors
- Ahrén, B., & Holst, J. J.
- Affiliations
- Department of Medicine, Lund University, Lund, Sweden, and
- University of Copenhagen (DK)
- ORCID
- Holst, Jens J.
- Venue
- Diabetes
- Publisher
- American Diabetes Association
- Published
- 2001-05-01
- Volume
- 50
- Issue
- 5
- Pages
- 1030-1038
- ISSN
- 0012-1797 (ISSN-L)
- 1939-327X
- OpenAlex
- W2168149788
- Cited by
- 292
- References
- 52
- Citations by year
- 2026: 7 · 2025: 6 · 2024: 11 · 2023: 9 · 2022: 9 · 2021: 15 · 2020: 12 · 2019: 14 · 2018: 17 · 2017: 13 · 2016: 16 · 2015: 22 · 2014: 14 · 2013: 9 · 2012: 11
- FWCI
- 8.58
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Diabetes (publishedVersion)
- PubMed (publishedVersion)
- Research at the University of Copenhagen (University of Copenhagen) (submittedVersion)
- Topics
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Pancreatic function and diabetes
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Regulation of Appetite and Obesity
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Management and Research
- Keywords
- meal ingestion, postprandial blood glucose, cholinergic mechanisms, trimethaphan, atropine, autonomic nervous system, glucose-dependent insulinotropic polypeptide, glucagon-like peptide-1, glucose tolerance
- MeSH terms
- Insulin Secretion, Blood Glucose, Blood Pressure, Eating, Female, Ganglionic Blockers, Gastric Inhibitory Polypeptide, Glucagon, Humans, Insulin, Middle Aged, Peptide Fragments, Protein Precursors, Reference Values, Time Factors, Trimethaphan, Body Mass Index, Postmenopause, Postprandial Period, Area Under Curve, Glucagon-Like Peptide 1
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review