Electrical stimulation of the suprachiasmatic nucleus of the hypothalamus causes hyperglycemia

Acute stimulation of glucose metabolism in mice by leptin treatment

Kamohara, S., Burcelin, R., Halaas, J. L., Friedman, J. M., & Charron, M. J. (1997) · Nature · doi:10.1038/38717 · Cited by 708 · see citing works

Circadian control of glucose metabolism

Kalsbeek, A., la Fleur, S., & Fliers, E. (2014) · Molecular Metabolism · doi:10.1016/j.molmet.2014.03.002 · Cited by 338 · see citing works

Chemically modified, carbon-based electrodes and their application as electrochemical sensors for the analysis of biologically important compounds. A review

Wring, S. A., & Hart, J. P. (1992) · The Analyst · doi:10.1039/an9921701215 · Cited by 308 · see citing works

A Suprachiasmatic Nucleus Generated Rhythm In Basal Glucose Concentrations

Fleur, L., Kalsbeek, Wortel, & Buijs (1999) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.1999.00373.x · Cited by 256 · see citing works

Suprachiasmatic GABAergic inputs to the paraventricular nucleus control plasma glucose concentrations in the rat via sympathetic innervation of the liver

Kalsbeek, A., La Fleur, S., Van Heijningen, C., & Buijs, R. M. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.5328-03.2004 · Cited by 244 · see citing works

Circadian rhythms in glucose and lipid metabolism in nocturnal and diurnal mammals

Kumar Jha, P., Challet, E., & Kalsbeek, A. (2015) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2015.01.024 · Cited by 235 · 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

Bipolar disorder and diabetes mellitus: epidemiology, etiology, and treatment implications

Mcintyre, R., Konarski, J., Misener, V., & Kennedy, S. (2005) · Annals of Clinical Psychiatry · doi:10.1080/10401230590932380 · Cited by 203 · see citing works

The suprachiasmatic nucleus controls the daily variation of plasma glucose via the autonomic output to the liver: are the clock genes involved?

Cailotto, C., La Fleur, S. E., Van Heijningen, C., Wortel, J., Kalsbeek, A., Feenstra, M., Pévet, P., & Buijs, R. M. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04439.x · Cited by 191 · see citing works

Polysynaptic neural pathways between the hypothalamus, including the suprachiasmatic nucleus, and the liver

la Fleur, S. E., Kalsbeek, A., Wortel, J., & Buijs, R. M. (2000) · Brain Research · doi:10.1016/s0006-8993(00)02423-9 · Cited by 160 · see citing works

Circadian Control of Insulin Secretion Is Independent of the Temporal Distribution of Feeding

Kalsbeek, A., & Strubbe, J. H. (1998) · Physiology & Behavior · doi:10.1016/s0031-9384(97)00493-9 · Cited by 142 · see citing works

SCN output drives the autonomic nervous system: with special reference to the autonomic function related to the regulation of glucose metabolism.

Nagai, K., Nagai, N., Shimizu, K., Chun, S.-J., Nakagawa, H., & Niijima, A. (1996) · Progress in Brain Research · doi:10.1016/s0079-6123(08)60413-6 · Cited by 135 · see citing works

Daily Rhythms in Glucose Metabolism: Suprachiasmatic Nucleus Output to Peripheral Tissue

la Fleur, S. (2003) · Journal of neuroendocrinology · doi:10.1046/j.1365-2826.2003.01019.x · Cited by 86 · see citing works

Evidence for subdivisions in the human suprachiasmatic nucleus

Mai, J. K., Kedziora, O., Teckhaus, L., & Sofroniew, M. V. (1991) · The Journal of Comparative Neurology · doi:10.1002/cne.903050312 · Cited by 132 · see citing works

The hypothalamic clock and its control of glucose homeostasis

Kalsbeek, A., Yi, C., la Fleur, S. E., & Fliers, E. (2010) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2010.02.005 · Cited by 106 · see citing works

Epigenetic control and the circadian clock: Linking metabolism to neuronal responses

Orozco-Solis, R., & Sassone-Corsi, P. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.01.043 · Cited by 94 · see citing works

Bishomoaromatische Dianionen von 1,2,4-Triboracyclopentanen: starke Dreizentren-Zweielektronen-Bindungen zwischen drei Boratomen

Scheschkewitz, D., Ghaffari, A., Amseis, P., Unverzagt, M., Subramanian, G., Hofmann, M., Schleyer, P. V. R., Schaefer, H. F., Geiseler, G., Massa, W., et al. (2000) · Angewandte Chemie · doi:10.1002/(sici)1521-3757(20000403)112:7 · Cited by 17 · see citing works

Light enhances sympathetic and suppresses vagal outflows and lesions including the suprachiasmatic nucleus eliminate these changes in rats

Niijima, A., Nagai, K., Nagai, N., & Nakagawa, H. (1992) · Journal of the Autonomic Nervous System · doi:10.1016/0165-1838(92)90026-d · Cited by 86 · see citing works

Effects of light stimulation on the activity of the autonomic nerves in anesthetized rats

Niijima, A., Nagai, K., Nagai, N., & Akagawa, H. (1993) · Physiology & Behavior · doi:10.1016/0031-9384(93)90249-f · Cited by 85 · see citing works

Polyferrocenes as mediators in amperometric biosensors for glucose

Hendry, S. P., Cardosi, M. F., Turner, A. P. F., et al. (1993) · Analytica Chimica Acta · doi:10.1016/0003-2670(93)85002-2 · Cited by 78 · see citing works

Review of the role of the nervous system in glucose homoeostasis and future perspectives towards the management of diabetes

Güemes, A., & Georgiou, P. (2018) · Bioelectronic Medicine · doi:10.1186/s42234-018-0009-4 · Cited by 74 · see citing works

Redox electrodeposition polymers: adaptation of the redox potential of polymer-bound Os complexes for bioanalytical applications

Guschin, D. A., Castillo, J. J., Dimcheva, N. D., et al. (2010) · Analytical and Bioanalytical Chemistry · doi:10.1007/s00216-010-3982-3 · Cited by 60 · see citing works

Coordinated regulation of circadian rhythms and homeostasis by the suprachiasmatic nucleus

Nakagawa, H., & OKUMURA, N. (2010) · Proceedings of the Japan Academy Series B · doi:10.2183/pjab.86.391 · Cited by 53 · see citing works

Circadian rhythms and energy metabolism with special reference to the suprachiasmatic nucleus

Nagai, K., Nagai, N., Sugahara, K., Niijima, A., & Nakagawa, H. (1994) · Neuroscience & Biobehavioral Reviews · doi:10.1016/0149-7634(94)90014-0 · Cited by 48 · see citing works

An ormosil-based peroxide biosensor — a comparative study on direct electron transport from horseradish peroxidase

Pandey, P. C., Upadhyay, S., Tiwari, I., et al. (2001) · Sensors and Actuators B Chemical · doi:10.1016/s0925-4005(00)00669-9 · Cited by 45 · see citing works

Fundamentals of Glucose Sensors

Fischer, U. (1991) · Diabetic Medicine · doi:10.1111/j.1464-5491.1991.tb01603.x · Cited by 45 · see citing works

Clock gene defect disrupts light-dependency of autonomic nerve activity

Ikeda, H., Yong, Q., Kurose, T., Todo, T., Mizunoya, W., Fushiki, T., Seino, Y., & Yamada, Y. (2007) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2007.10.058 · Cited by 44 · see citing works

Electrochemical and quartz crystal microbalance evidence for mediation and direct electrochemical reactions of small molecules at tetrathiafulvalene-te

Freund, M. S., Brajter‐Toth, A., & Ward, M. D. (1990) · Journal of Electroanalytical Chemistry · doi:10.1016/0022-0728(90)87211-2 · Cited by 43 · see citing works

An Enzyme Electrode for Glucose Consisting of Glucose Oxidase Immobilised at a Benzoquinone-Modified Carbon Electrode

Hu, J., & Turner, A. P. F. (1991) · Analytical Letters · doi:10.1080/00032719108052880 · Cited by 41 · see citing works

Amperometric enzyme sensor for glucose based on graphite paste-modified electrodes

Pandey, P. C., Kayastha, A. M., & Pandey, V. (1992) · Applied Biochemistry and Biotechnology · doi:10.1007/bf02950782 · Cited by 40 · see citing works

Enzyme Electrode Biosensors: Theory and Applications

Kauffmann, J., & Guilbault, G. G. (1992) · Methods of biochemical analysis · doi:10.1002/9780470110577.ch3 · Cited by 37 · see citing works

Effect of glucagon in macronutrient self-selection: Glucagon-enhanced protein intake

Nagai, K., Thibault, L., Nishikawa, K., Hashida, A., Ootani, K., & Nakagawa, H. (1991) · Brain Research Bulletin · doi:10.1016/0361-9230(91)90134-6 · Cited by 33 · see citing works

The hypothalamic clock and its control of glucose homeostasis

Kalsbeek, A., Ruiter, M., la Fleur, S. E., Cailotto, C., Kreier, F., & Buijs, R. M. (2006) · Progress in brain research · doi:10.1016/s0079-6123(06)53017-1 · Cited by 33 · see citing works

Electrochemical studies on tetrathiafulvalene-tetracyanoquinodimethane modified acetylcholine/choline sensor

Pandey, P. C., Tran‐Minh, C., & Lantreibecq, F. (1991) · Applied Biochemistry and Biotechnology · doi:10.1007/bf02921785 · Cited by 32 · see citing works

Circadian rhythms and metabolism: from the brain to the gut and back again

Cribbet, M. R., Logan, R. W., Edwards, M. D., Hanlon, E. C., Peek, C. B., Stubblefield, J. J., Vasudevan, S. R., Ritchey, F. C., & Frank, E. (2016) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.13188 · Cited by 28 · see citing works

NADH sensor with electrochemically modified TCNQ electrode

Murthy, A. S. N., & Gupta, A. R. L. (1994) · Analytica Chimica Acta · doi:10.1016/0003-2670(94)80006-5 · Cited by 26 · see citing works

Tetracyanoquinodimethane (TCNQ) modified electrode for NADH oxidation

Surya, A., Murthy, N., & Anita, A. (1994) · Bioelectrochemistry and Bioenergetics · doi:10.1016/0302-4598(94)87035-7 · Cited by 26 · see citing works

Time-dependent involvement of autonomic nervous system in hyperglycemia due to 2-deoxy-D-glucose

Yamamoto, H., Nagai, K., & Nakagawa, H. (1988) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1988.255.6.e928 · Cited by 26 · see citing works

Little or no induction of hyperglycemia by 2-deoxy-d-glucose in hereditary blind microphthalmic rats

Nagai, K., Sekitani, M., Otani, K., et al. (1988) · Life Sciences · doi:10.1016/0024-3205(88)90528-0 · Cited by 24 · see citing works

Sensitivity, Selectivity and Reproducibility of Some Mediated Electrochemical Biosensors/sensors

Pandey, P. C., Upadhyay, S., Pathak, H. C., et al. (1998) · Analytical Letters · doi:10.1080/00032719808005310 · Cited by 24 · see citing works

Neuroscience of glucose homeostasis

la Fleur, S. E., Fliers, E., & Kalsbeek, A. (2014) · Handbook of clinical neurology · doi:10.1016/b978-0-444-53480-4.00026-6 · Cited by 21 · see citing works

Chronic Light Cycle Disruption Alters Central Insulin and Leptin Signaling as well as Metabolic Markers in Male Mice

Skinner, N. J., Rizwan, M. Z., Grattan, D. R., & Tups, A. (2019) · Endocrinology · doi:10.1210/en.2018-00935 · Cited by 21 · see citing works

Hormones and the Autonomic Nervous System are Involved in Suprachiasmatic Nucleus Modulation of Glucose Homeostasis

Ruiter, M., Buijs, R. M., & Kalsbeek, A. (2006) · Current Diabetes Reviews · doi:10.2174/157339906776818596 · Cited by 21 · see citing works

Biosensors

Lowe, C. R., Hin, B. F. Y. Y., Cullen, D. C., et al. (1990) · Journal of Chromatography A · doi:10.1016/s0021-9673(01)93769-0 · Cited by 21 · see citing works

An Introduction to Biosensors

Turner, A. P. F., & Newman, J. D. (2005) · Elsevier eBooks · doi:10.1533/9781845698157.1.13 · Cited by 15 · see citing works

Revisited: The Conception of Lability of Metal Complexes

van Leeuwen, H. P. (2001) · Electroanalysis · doi:10.1002/1521-4109(200106)13:10 · Cited by 72 · see citing works

Employing Heterocyclic Dihydropolyazines for Amperometric Glucose Sensing

Kulys, J. J., PALAIMA, A. I., & Urbelis, G. (1998) · Analytical Letters · doi:10.1080/00032719808001862 · Cited by 11 · see citing works

Benzoquinone-mediated enzyme biosensor for amperometric determination of glucose

Murthy, A. S. N., & Sharma, J. (1997) · Journal of Chemical Sciences · doi:10.1007/bf02872567 · Cited by 9 · see citing works

Reduced increase in plasma renin activity on water-deprivation in blind hereditary microphthalmic rats

Nagai, K., Stoynev, A. G., Nagai, N., et al. (1993) · Neuroscience Letters · doi:10.1016/0304-3940(93)90775-g · Cited by 9 · see citing works

Morphological Changes in the Hypothalamic Suprachiasmatic Nucleus and Circadian Rhythm of Locomotor Activity in Hereditary Microphthalmic Rats.

Sugita, S., Minematsu, S., Nagai, K., & Sugahara, K. (1996) · EXPERIMENTAL ANIMALS · doi:10.1538/expanim.45.115 · Cited by 9 · see citing works

The Electrochemical and Photochemical Activation of Redox Enzymes

Katz, E. Y., Shipway, A. N., & Willner, I. (2001) · doi:10.1002/9783527618248.ch50 · Cited by 9 · see citing works

Gold-thioglucose-induced hypothalamic lesions inhibit metabolic modulation of light-induced circadian phase shifts in mice

Challet, É., Bernard, D. J., & Turek, F. W. (1999) · Brain Research · doi:10.1016/s0006-8993(99)01192-0 · Cited by 6 · see citing works

Role of VIP-neurons in the hypothalamic suprachiasmatic nucleus in the control of blood glucose

Nagai, K. (2004) · Folia Pharmacologica Japonica · doi:10.1254/fpj.123.253 · Cited by 4 · see citing works

Suprachiasmatic hypothalamic nuclei (SCN) in regulation of homeostasis: a role beyond circadian control?

Stoynev, A. G., Ikonomov, O. C., & Stoynev, N. (2021) · Biological Rhythm Research · doi:10.1080/09291016.2021.1920125 · Cited by 2 · see citing works

Increased Risk of Diabetes due to Obesity: Does Chronodisruption Play a Role?

la Fleur, S. E., & Kalsbeek, A. (2012) · Springer eBooks · doi:10.1007/978-1-4614-5082-5_7 · Cited by 1 · see citing works

Hypothalamic neural networks in control of glucose homeostasis

Yi, C. (2010) · UvA-DARE (University of Amsterdam) · Cited by 1 · see citing works

The suprachiasmatic nucleus organizes daily physiology : an analysis of the role of the autonomic nervous system and peripheral clock genes

Cailotto, C. (2006) · UvA-DARE (University of Amsterdam)

Sleep deprivation and its impact on circadian rhythms and glucose metabolism

Jha, P. K. (2016) · doi:10.70675/090a1809z3e96z4876zbbcez4a3609e56272

Biological Clock Control of Glucose Metabolism

Ruiter, M., Buijs, R. M., & Kalsbeek, A. (2006) · Springer eBooks · doi:10.1007/0-387-23692-9_5

Glycogen metabolism in the liver of the developing rat

Watts, C., & Gain, E. R. (1976) · Biochemical Journal · doi:10.1042/bj1600263 · Cited by 45 · see citing works

The control of glycogen metabolism in yeast

François, J., Villanueva, M., & Hers, H. G. (1988) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1988.tb14134.x · Cited by 96 · see citing works

Correlations of glycogen synthase and phosphorylase activities with glycogen concentration in human muscle biopsies. Evidence for a double-feedback mechanism regulating glycogen synthesis and breakdown

Munger, R., Temler, E., Jallut, D., Haesler, E., & Jp, F. (1993) · Metabolism · doi:10.1016/0026-0495(93)90169-o · Cited by 40 · see citing works

Glucose 6‐phosphate plays a central role in the regulation of glycogen synthesis in a glycogen‐storing liver cell line

Mayer, D., & Letsch, I. (1989) · Cell Biochemistry and Function · doi:10.1002/cbf.290070403 · Cited by 16 · see citing works

Particulate glycogen of mammalian liver: specificity in binding phosphorylase and glycogen synthase

Vardanis, A. (1992) · Biochemistry and Cell Biology · doi:10.1139/o92-081 · Cited by 16 · see citing works