Nitric oxide (nitrogen monoxide, NO) stimulates insulin secretion by inducing calcium release from mitochondria
Abstract
Nitric oxide (nitrogen monoxide, NO) acts as messenger molecule in a variety of cells and may also be involved in the insulin secretory pathway of islet beta-cells. We report here that NO at a low micromolar concentration stimulates epinephrine-sensitive insulin secretion from cells of the beta-cell line, INS-1. Insulin secretion is paralleled by a reversible decrease of the mitochondrial membrane potential and by an increase of the cytosolic calcium. Chelation of intracellular, but not of extracellular calcium prevents the NO-induced insulin secretion. These data indicate that NO can stimulate insulin secretion by deenergizing mitochondria and thereby triggering mitochondrial calcium release.
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Insulin resistance is improved by NO at various levels including insulin secretion, mitochondrial function, modulation of inflammation, insulin signaling, and glucose uptake.
“Insulin resistance is improved by NO at various levels including insulin secretion [54,55], mitochondrial function [56], modulation of inflammation [57], insulin signaling [58] and glucose uptake [59].”
From NO-Rich Diet for Lifestyle-Related Diseases (2015) · cites this paper as [54]
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Brown, G. C. (1999) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/s0005-2728(99)00025-0 · Cited by 702 · see citing works
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Ghafourifar, P., & Richter, C. (1997) · FEBS Letters · doi:10.1016/s0014-5793(97)01397-5 · Cited by 567 · see citing works
Self-citationOxidative stress and beta-cell dysfunction
Drews, G., Krippeit-Drews, P., & Düfer, M. (2010) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-010-0862-9 · Cited by 315 · see citing works
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BackgroundThe Exercise-Induced Growth Hormone Response in Athletes
Godfrey, R., Madgwick, Z., & Whyte, G. P. (2003) · Sports Medicine · doi:10.2165/00007256-200333080-00005 · Cited by 297 · see citing works
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Sansbury, B. E., & Hill, B. G. (2014) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2014.05.016 · Cited by 274 · see citing works
“However, NO is suggested to stimulate islet cell insulin secretion by inducing calcium release from mitochondria [315], which may be due to NO-mediated inhibition of”
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Bahadoran, Z., Mirmiran, P., & Ghasemi, A. (2019) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2019.10.001 · Cited by 162 · see citing works
Lajoix, A., Reggio, H., Chardès, T., Péraldi‐Roux, S., Tribillac, F., Roye, M., Dietz, S., Broca, C., Manteghetti, M., Ribes, G., et al. (2001) · Diabetes · doi:10.2337/diabetes.50.6.1311 · Cited by 139 · see citing works
“Likewise exogenous NO has been shown to stimulate insulin secretion, suggested to be due to Ca(21) release from mitochondria in the insulin-secreting b-cell line INS-1 (24) or from endoplasmic reticulum in rat pancreatic b-cells (25).”
BackgroundKinetics of the inhibition of mitochondrial respiration by NO
Koivisto, A., Matthias, A., Bronnikov, G. E., & Nedergaard, J. (1997) · FEBS Letters · doi:10.1016/s0014-5793(97)01258-1 · Cited by 126 · see citing works
Simpson, P. B., & Russell, J. T. (1998) · Brain Research Reviews · doi:10.1016/s0165-0173(97)00056-8 · Cited by 113 · see citing works
Nitric oxide as a competitive inhibitor of oxygen consumption in the mitochondrial respiratory chain
Brown, G. C. (2000) · Acta Physiologica Scandinavica · doi:10.1046/j.1365-201x.2000.00718.x · Cited by 108 · see citing works
Brown, G. C. (1997) · Springer eBooks · doi:10.1007/978-1-4615-6111-8_29 · Cited by 105 · see citing works
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The Chemical Biology of Nitric Oxide
Wink, D. A., Feelisch, M., Yoram Vodovotz, B., Fukuto, J. M., & Grisham, M. B. (2006) · Kluwer Academic Publishers eBooks · doi:10.1007/0-306-46806-9_10 · Cited by 102 · see citing works
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Richter, C. (1997) · Bioscience Reports · doi:10.1023/a:1027387301845 · Cited by 96 · see citing works
Self-citationThe Dual Role of Nitric Oxide in Islet β-Cells
Spinas, G. A. (1999) · Physiology · doi:10.1152/physiologyonline.1999.14.2.49 · Cited by 98 · see citing works
Self-citationBrown, G. C. (1997) · Molecular and Cellular Biochemistry · doi:10.1023/a:1006800322719 · Cited by 95 · see citing works
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Kobayashi, J., Ohtake, K., & Uchida, H. (2015) · Nutrients · doi:10.3390/nu7064911 · Cited by 94 · see citing works
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Nyström, T., Ortsäter, H., Huang, Z., Zhang, F., Larsen, F. J., Weitzberg, E., Lundberg, J. O., & Sjöholm, Å. (2012) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2012.06.031 · Cited by 94 · see citing works
Role of nitric oxide in the control of renin secretion
Kurtz, A., & Wagner, C. (1998) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.1998.275.6.f849 · Cited by 88 · see citing works
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Spinas, G. A., Laffranchi, R., Francoys, I., David, I., Richter, C., & Reinecke, M. (1998) · Diabetologia · doi:10.1007/s001250050906 · Cited by 83 · see citing works
“stimulates insulin secretion from INS-1 cells by inducing calcium release from mitochondria [11].”
BackgroundSelf-citationKandanur, S. G. S., Tamang, N., Golakoti, N. R., et al. (2019) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2019.05.022 · Cited by 83 · see citing works
Nitric oxide and cellular respiration
Brunori, M., Giuffr�, A., Sarti, P., Stubauer, G., & Wilson, M. T. (1999) · Cellular and Molecular Life Sciences · doi:10.1007/s000180050452 · Cited by 81 · see citing works
Regulation of astrocyte gap junctions by hypoxia–reoxygenation
Martı́nez, A. D., & Sáez, J. C. (2000) · Brain Research Reviews · doi:10.1016/s0165-0173(99)00086-7 · Cited by 78 · see citing works
Nitric oxide promotes intracellular calcium release from mitochondria in striatal neurons
Horn, T. F. W., Wolf, G. L., Duffy, S. N., Weiss, S., Keilhoff, G., & MacVicar, B. A. (2002) · The FASEB Journal · doi:10.1096/fj.02-0126com · Cited by 71 · see citing works
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Cheng, K., Delghingaro‐Augusto, V., Nolan, C. J., Turner, N. A., Hallahan, N., Andrikopoulos, S., & Gunton, J. E. (2012) · PLoS ONE · doi:10.1371/journal.pone.0040868 · Cited by 70 · see citing works
“L-arginine stimulates insulin by inducing Ca release from mitochondria via the actions of nitrogen oxides in the presence of glucose [28,29].”
BackgroundSarti, P., Lendaro, E., Ippoliti, R., Bellelli, A., Benedetti, P. A., & Brunori, M. (1999) · The FASEB Journal · doi:10.1096/fasebj.13.1.191 · Cited by 65 · see citing works
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Utoguchi, N., Watanabe, Y., Shida, T., et al. (1998) · Pharmaceutical Research · doi:10.1023/a:1011920530771 · Cited by 54 · see citing works
Islet constitutive nitric oxide synthase and glucose regulation of insulin release in mice
Akesson, B., Henningsson, R. N., Salehi, A. A., & Lundquist, I. (1999) · Journal of Endocrinology · doi:10.1677/joe.0.1630039 · Cited by 54 · see citing works
Kaneko, Y. K., Ishikawa, T., Amano, S., et al. (2003) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00223.2002 · Cited by 51 · see citing works
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Mohseni, M. M., Tabatabaei‐Malazy, O., Hasani‐Ranjbar, S., et al. (2011) · Diabetes Research and Clinical Practice · doi:10.1016/j.diabres.2010.12.030 · Cited by 46 · see citing works
“[8] Laffranchi R, Gogvadze V, Richter C, Spinas GA.”
BackgroundThe Chemical Biology of Nitric Oxide
Miranda, K. M., Espey, M. G., Jourd’heuil, D., Grisham, M. B., Fukuto, J. M., Feelisch, M., & Wink, D. A. (2000) · Elsevier eBooks · doi:10.1016/b978-012370420-7/50004-6 · Cited by 56 · see citing works
Pinilla, L., González, D., Tena‐Sempere, M., et al. (1998) · Neuroendocrinology · doi:10.1159/000054364 · Cited by 42 · see citing works
“Considering that Ca 2p in the end-point signal for several elicitors of gonadotropin release (see above), and that some cellular responses induced by NO, as NO-stimulated insulin and serotonin release by pancreatic β-cells, are mediated by increases in Ca 2p release from mitochondrial stores [”
BackgroundReversible inhibition of cellular respiration by nitric oxide in vascular inflammation
Borutaitė, V., Matthias, A., Harris, H., Moncada, S., & Brown, G. C. (2001) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.2001.281.6.h2256 · Cited by 42 · see citing works
Pinilla, L., Tena‐Sempere, M., & Aguilar, E. (1999) · Hormone Research in Paediatrics · doi:10.1159/000023378 · Cited by 42 · see citing works
“Since previous studies have shown that NO stimulates insulin and serotonin secretion in rat pancreatic β-cells by inducing calcium release from mitochondria [”
ResultRao, V. S. N., Santos, F. A., Silva, R. M., & Teixiera, M. G. (2002) · Vascular Pharmacology · doi:10.1016/s1537-1891(02)00212-4 · Cited by 38 · see citing works
Nitric oxide and neuronal and pancreatic beta cell death
Adeghate, E., & Parvez, S. (2000) · Toxicology · doi:10.1016/s0300-483x(00)00310-3 · Cited by 37 · see citing works
Nitric oxide inhibits capacitative Ca2+ entry by suppression of mitochondrial Ca2+ handling
Thyagarajan, B., Malli, R., Schmidt, K., Graier, W. F., & Groschner, K. (2002) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0704949 · Cited by 36 · see citing works
eNOS gene polymorphism association with retinopathy in type 1 diabetes
Tavakkoly‐Bazzaz, J., Amoli, M. M., Pravica, V., et al. (2010) · Ophthalmic Genetics · doi:10.3109/13816810.2010.482553 · Cited by 35 · see citing works
Insulin secretion: The nitric oxide controversy
Gheibi, S., & Ghasemi, A. (2020) · EXCLI journal · doi:10.17179/excli2020-2711 · Cited by 34 · see citing works
“Nitric oxide through increasing intracellular Ca2+ levels or via S-nitrosylation of glucokinase and syntaxin 4, as well as vasodilation of islet vasculature, increases insulin secretion (Laffranchi et al., 1995; Rizzo and Piston, 2003; Wiseman et al., 2011; Nystrom et al., 2012; Kruszelnicka, 2014).”
BackgroundGasotransmitter signaling in energy homeostasis and metabolic disorders
Ali, A., Wang, Y., Wu, L., & Yang, G. (2020) · Free Radical Research · doi:10.1080/10715762.2020.1862827 · Cited by 32 · see citing works
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Nakata, M., Uto, N., Maruyama, I., et al. (1999) · Cell Structure and Function · doi:10.1247/csf.24.451 · Cited by 32 · see citing works
Maccario, M., Oleandri, S. E., Massimo, P., et al. (1997) · Journal of Endocrinological Investigation · doi:10.1007/bf03348006 · Cited by 31 · see citing works
Nakada, S., Ishikawa, T., Yamamoto, Y. T., et al. (2003) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-003-1176-y · Cited by 31 · see citing works
“suggested an insulinotropic effect of exogenous NO [6, 16, 18, 19, 25, 29, 34], whereas others have shown an”
ResultNitric Oxide Induces Synchronous Ca 2+ Transients in Pancreatic β Cells Lacking Contact
Grapengiesser, E., Gylfe, E., Dansk, H., et al. (2001) · Pancreas · doi:10.1097/00006676-200111000-00009 · Cited by 30 · see citing works
“Both tumor-derived (28) and normal (29) rat cells have previously been reported to respond to 2 M gaseous NO with mobilization of intracellular calcium.”
BackgroundModulation of Cav1 and Cav2.2 channels induced by nitric oxide via cGMP-dependent protein kinase
Grassi, C., D’Ascenzo, M., & Azzena, G. B. (2004) · Neurochemistry International · doi:10.1016/j.neuint.2004.03.019 · Cited by 27 · see citing works
Smith, P. A., Proks, P., & Moorhouse, A. J. (1999) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s004240050820 · Cited by 27 · see citing works
“In further support of this argument, nitric oxide, an inhibitor of oxidative respiration, has been demonstrated to also depolarize Δψm and release mitochondrial Ca 2+ in single βcells [ 20 ].”
BackgroundInfluentialCitrulline-Argininosuccinate-Arginine Cycle Coupled to Ca2+-Signaling in Rat Pancreatic β-Cells
Nakata, M., Yada, T., Nakagawa, S., et al. (1997) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1997.6854 · Cited by 25 · see citing works
Huang, Z., Liu, L., Chen, J., et al. (2018) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2018.08.142 · Cited by 24 · see citing works
Ding, Y., & Rana, R. S. (1998) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1998.9536 · Cited by 23 · see citing works
Gross, R., Roye, M., Manteghetti, M., Broca, C., Hillaire‐Buys, D., Masiello, P., & Ribes, G. (1997) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0700911 · Cited by 21 · see citing works
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Campbell, S. C., Richardson, H., Ferris, W. F., et al. (2007) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.12.127 · Cited by 20 · see citing works
Dual effect of nitric oxide on ATP-sensitive K+ channels in rat pancreatic β cells
Sunouchi, T., Suzuki, K., Nakayama, K., et al. (2008) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-008-0463-z · Cited by 20 · see citing works
“Several research groups have suggested that NO serves to increase insulin secretion [5, 13, 16, 24], whereas others have proposed that the main effect of NO is to suppress insulin secretion [2, 3, 6, 22, 26, 27].”
BackgroundRahman, F. U., Park, D., Joe, Y., et al. (2018) · Antioxidants and Redox Signaling · doi:10.1089/ars.2017.7380 · Cited by 19 · see citing works
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Ataie, Z., Dastjerdi, M., Farrokhfall, K., & Ghiravani, Z. (2021) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2021/9970678 · Cited by 19 · see citing works
Enhanced expression of neuronal nitric oxide synthase in islets of exercise-trained rats
Ueda, H., Urano, Y., Sakurai, T., Kizaki, T., Hitomi, Y., Ohno, H., & Izawa, T. (2003) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2003.10.189 · Cited by 18 · see citing works
Drews, G., Krämer, C., & Krippeit-Drews, P. (2000) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/s0005-2736(99)00242-4 · Cited by 18 · see citing works
Nitric oxide and insulin resistance
(2015) · Immunoendocrinology · doi:10.14800/ie.657 · Cited by 16 · see citing works
“Recent evidence suggests that NO plays suppressive roles in the development of insulin resistance at various levels, including effects on insulin secretion ([60,61]), mitochondrial function ([62]), modulation of inflammation ([63]), insulin signaling ([64]), and glucose uptake ([65]).”
BackgroundGónzalez, D., & Aguilar, E. (1999) · Journal of Endocrinological Investigation · doi:10.1007/bf03343643 · Cited by 16 · see citing works
Arranz-Paraíso, D., Solá, Y., Moyano, D. B., Martínez, M. B., Melero-Tur, S., & González‐Lezcano, R. A. (2022) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/j.jphotobiol.2022.112614 · Cited by 13 · see citing works
Modulation of presynaptic calcium homeostasis by nitric oxide
Martı́nez-Serrano, A., Börner, C., Pereira, R., et al. (1996) · Cell Calcium · doi:10.1016/s0143-4160(96)90035-4 · Cited by 8 · see citing works
Red-light photons on skin cells and the mechanism of photobiomodulation
Herrera, M. A., Ribas, A. P., da Costa, P. E., & Baptista, M. S. (2024) · Frontiers in Photonics · doi:10.3389/fphot.2024.1460722 · Cited by 9 · see citing works
Akarte, A. S., Srinivasan, B. P., & Gandhi, S. (2011) · European Journal of Pharmaceutical Sciences · doi:10.1016/j.ejps.2011.11.016 · Cited by 7 · see citing works
Schroeder, T., Carattino, M. D., Frontera, M., et al. (1998) · Brazilian Journal of Medical and Biological Research · doi:10.1590/s0100-879x1998000500004 · Cited by 7 · see citing works
“(10) postulated that NO can stimulate insulin secretion by deenergizing mitochondria, thereby triggering mitochondrial calcium release.”
BackgroundJun, H., Lim, D., Andukuri, A., et al. (2014) · International Journal of Nanomedicine · doi:10.2147/ijn.s50873 · Cited by 6 · see citing works
Impaired Nitric Oxide Metabolism in Type 2 Diabetes: At a Glance
Bahadoran, Z., Carlström, M., Mirmiran, P., & Ghasemi, A. (2022) · BENTHAM SCIENCE PUBLISHERS eBooks · doi:10.2174/9789815079814122010006 · Cited by 6 · see citing works
In vitro vascular toxicity assessment of NitDOX, a novel NO-releasing doxorubicin
Durante, M., Frosini, M., Fusi, F., Gamberucci, A., Chegaev, K. Y., Rolando, B., Riganti, C., Fruttero, R., & Saponara, S. (2020) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2020.173164 · Cited by 6 · see citing works
Nitric oxide stimulates insulin release in liver cells expressing human insulin
Qian, Q., Williams, J. P., Karounos, D. G., et al. (2005) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2005.02.111 · Cited by 5 · see citing works
Insulin-secreting INS-1 cells generate a novel type of poorly synchronized transients
Dorff, G., Grapengiesser, E., & Hellman, B. (2002) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(02)00311-x · Cited by 5 · see citing works
The Role of NO-cGMP Signaling Pathway in Pancreatic Beta-cell Function
Lazo-de-la-Vega-Monroy, M.-L., & Vilches‐Flores, A. (2014) · Immunology Endocrine & Metabolic Agents - Medicinal Chemistry · doi:10.2174/1871522214666140116213815 · Cited by 4 · see citing works
Asari, H., & Sugiyanta, S. (2021) · Folia Medica Indonesiana · doi:10.20473/fmi.v56i3.24528 · Cited by 4 · see citing works
Effect of nitric oxide on the somatostatinergic system in the rat exocrine pancreas
Rodríguez‐Martín, E., Muñoz-Acedo, G., Puebla, L., et al. (1999) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/s0167-4889(99)00032-4 · Cited by 3 · see citing works
Nitric Oxide Bioavailability and Insulin Resistance: An Overview
Kobayashi, J. (2022) · Book Publisher International (a part of SCIENCEDOMAIN International) · doi:10.9734/bpi/capr/v8/4440a · Cited by 2 · see citing works
Nitric Oxide Signaling Through Mitochondrial Calcium Release
Richter, C., & Laffranchi, R. (1997) · Springer eBooks · doi:10.1007/978-1-4615-5981-8_3 · Cited by 1 · see citing works
Self-citationNitric Oxide and Voltage-Gated Ca2+ Channels
Grassi, C., D’Ascenzo, M., & Azzena, G. B. (2004) · Humana Press eBooks · doi:10.1007/978-1-59259-806-9_7 · Cited by 1 · see citing works
A neural entero-pancreatic pathway that regulates insulin secretion and glucose tolerancePreprint
Sokolov, M., Tamayo, A., Levi, N., Seeley, R. J., & Caicedo, A. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.08.14.670343 · Cited by 1 · see citing works
Kurtz, A., & Schricker, K. (1997) · Springer eBooks · doi:10.1007/978-1-4615-6039-5_12
Mitochondrial impact on nerve growth factor production in vascular smooth muscle-derived cells
Sherer, T., Neff, P. S., Parks, J. K., & Tuttle, J. B. (1999) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/s0304-4165(99)00194-4
The anti-obesogenic effects of nitric oxide.
Sansbury, B. E. (2014) · doi:10.18297/etd/1262
Does Citrulline Malate Enhance Physical Performance
Walker, T. B., Zupan, M. F., Rutter, M. J., & Vojta, C. N. (2010) · doi:10.21236/ada532948
“NO has been demonstrated to stimulate insulin release (Laffranchi et al., 1995).”
BackgroundInvolvement of Nitric Oxide in Insulin Secretion to Carbohydrate Metabolism
Khatua, S., Bank, S., & Acharya, K. (2023) · Advances in biochemistry in health and disease · doi:10.1007/978-3-031-24778-1_10
Thomas, D. D., Miranda, K. M., Citrin, D. E., Espey, M. G., & Wink, D. A. (2003) · Humana Press eBooks · doi:10.1007/978-1-59259-407-8_2 · Cited by 2 · see citing works
No synthase neuronale pancréatique et musculaire dans la pathogénie des états prédiabétiques
Mezghenna, K. (2010) · theses.fr (ABES) · doi:10.70675/ee8948b3z1c69z4ea5zbe52zfaa318ae3a10
- Authors
- Laffranchi, R., Gogvadze, V., Richter, C., & Spinas, G. A.
- Affiliations
- University of Zurich (CH)
- Venue
- Biochemical and Biophysical Research Communications
- Publisher
- Elsevier BV
- Published
- 1995-12
- Volume
- 217
- Issue
- 2
- Pages
- 584-591
- ISSN
- 0006-291X (ISSN-L)
- OpenAlex
- W2066215218
- Cited by
- 87
- References
- 0
- Citations by year
- 2025: 1 · 2024: 1 · 2023: 1 · 2022: 4 · 2021: 2 · 2020: 3 · 2019: 2 · 2018: 2 · 2015: 2 · 2014: 4 · 2012: 2
- FWCI
- 8.18
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Biochemical and Biophysical Research Communications (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Surgery › Pancreatic function and diabetes
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Physiology › Calcium signaling and nucleotide metabolism
- Health Sciences › Medicine › Physiology › Nitric Oxide and Endothelin Effects
- Keywords
- nitric oxide, insulin secretion, pancreatic beta cells, mitochondrial calcium release, mitochondrial membrane potential, intracellular calcium, epinephrine, INS-1 cells, calcium chelation
- MeSH terms
- Insulin Secretion, Animals, Calcium, Carbonyl Cyanide m-Chlorophenyl Hydrazone, Cell Line, Epinephrine, Insulin, Intracellular Membranes, Islets of Langerhans, Membrane Potentials, Mitochondria, Nitric Oxide, Secretory Rate, Uncoupling Agents, Signal Transduction, Rats
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 ›
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