Literature DB >> 8653556

Glucose-responsive neurons in the brainstem.

A Adachi1, M Kobashi, M Funahashi.   

Abstract

AREA POSTREMA: The influence on feeding behavior caused by ablation of the area postrema (AP) in rodents indicates the participation of this structure in the control of ingestion. Two types of glucose responsive neurons were identified in the AP: one is characterized by increasing the discharge rate in response to glucose (glucoreceptor type) and the other by decreasing the discharge rates in response to glucose (glucose sensitive type). These glucose responsive neurons may participate in glycemic homeostasis. NUCLEUS OF SOLITARY TRACT: The glucose responsive neurons exist within the caudal portion of nucleus of the solitary tract (NTS), a relay station in visceral afferents. Two types similar to the AP were also recognized. It is confirmed that hepatic glucose sensitive afferents terminate on some of the glucose sensitive neurons. This convergence may serve as a fail-safe mechanism. In addition, the NTS involving complex neural networks of excitatory and inhibitory interneurons may be concerned with integration of glycemic information. DORSAL MOTOR NUCLEUS OF VAGUS: Some neurons within the dorsal motor nucleus of the vagus (DMV) were identified as the glucose responsive ones. Both types were also recognized. It is confirmed by antidromic activation that these glucose responsive DMV neurons send their axons toward the gastric or coeliac branch that innervates either the stomach, intestine or pancreas. Some of the DMV neurons may subserve an enteroceptor function by themselves. They may also play a role in the brainstem neural control of glycemic homeostasis as the fail-safe mechanism.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 8653556     DOI: 10.1002/j.1550-8528.1995.tb00493.x

Source DB:  PubMed          Journal:  Obes Res        ISSN: 1071-7323


  28 in total

Review 1.  Multiple hypothalamic circuits sense and regulate glucose levels.

Authors:  Mahesh Karnani; Denis Burdakov
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2010-11-03       Impact factor: 3.619

Review 2.  Brain Glucose-Sensing Mechanism and Energy Homeostasis.

Authors:  A J López-Gambero; F Martínez; K Salazar; M Cifuentes; F Nualart
Journal:  Mol Neurobiol       Date:  2018-05-24       Impact factor: 5.590

3.  Glucose increases synaptic transmission from vagal afferent central nerve terminals via modulation of 5-HT3 receptors.

Authors:  Shuxia Wan; Kirsteen N Browning
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2008-09-18       Impact factor: 4.052

Review 4.  Central nervous system control of gastrointestinal motility and secretion and modulation of gastrointestinal functions.

Authors:  Kirsteen N Browning; R Alberto Travagli
Journal:  Compr Physiol       Date:  2014-10       Impact factor: 9.090

5.  Glucose effects on gastric motility and tone evoked from the rat dorsal vagal complex.

Authors:  M Ferreira; K N Browning; N Sahibzada; J G Verbalis; R A Gillis; R A Travagli
Journal:  J Physiol       Date:  2001-10-01       Impact factor: 5.182

6.  Characterization of the role of endogenous cholecystokinin on the activity of the paraventricular nucleus of the hypothalamus in rats.

Authors:  Victoria Cano; Laura Ezquerra; M Pilar Ramos; Mariano Ruiz-Gayo
Journal:  Br J Pharmacol       Date:  2003-09-29       Impact factor: 8.739

Review 7.  Astrocytes in the hindbrain detect glucoprivation and regulate gastric motility.

Authors:  David H McDougal; Edouard Viard; Gerlinda E Hermann; Richard C Rogers
Journal:  Auton Neurosci       Date:  2013-01-10       Impact factor: 3.145

8.  Adaptation of glucokinase gene expression in the rat dorsal vagal complex in a model for recurrent intermediate insulin-induced hypoglycemia: impact of gender.

Authors:  Naresh K Genabai; Kamlesh V Vavaiya; Karen P Briski
Journal:  J Mol Neurosci       Date:  2008-07-09       Impact factor: 3.444

9.  Hindbrain glucoprivation effects on gastric vagal reflex circuits and gastric motility in the rat are suppressed by the astrocyte inhibitor fluorocitrate.

Authors:  Gerlinda E Hermann; Edouard Viard; Richard C Rogers
Journal:  J Neurosci       Date:  2014-08-06       Impact factor: 6.167

10.  Decreased GABAA receptor function in the brain stem during pancreatic regeneration in rats.

Authors:  S Balarama Kaimal; G Gireesh; C S Paulose
Journal:  Neurochem Res       Date:  2007-08-14       Impact factor: 3.996

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.