The hepatic vagal reception of intraportal GLP-1 is via receptor different from the pancreatic GLP-1 receptor (Q73608186)

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5 November 2019

title

The hepatic vagal reception of intraportal GLP-1 is via receptor different from the pancreatic GLP-1 receptor (English)

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5 November 2019

author name string

M Nishizawa

1

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5 November 2019

H Nakabayashi

2

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5 November 2019

K Kawai

3

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5 November 2019

T Ito

4

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5 November 2019

S Kawakami

5

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5 November 2019

A Nakagawa

6

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5 November 2019

A Niijima

7

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5 November 2019

K Uchida

8

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5 November 2019

publication date

1 April 2000

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Journal of the autonomic nervous system

5 November 2019

published in

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5 November 2019

volume

80

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5 November 2019

page(s)

14-21

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5 November 2019

issue

1-2

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Glucagon-like peptide-1-(7-36)amide increases pulmonary surfactant secretion through a cyclic adenosine 3',5'-monophosphate-dependent protein kinase mechanism in rat type II pneumocytes

5 November 2019

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

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Divergent tissue-specific and developmental expression of receptors for glucagon and glucagon-like peptide-1 in the mouse.

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Glucagon-like peptide-1 binding to rat skeletal muscle

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Glucagon-like peptide 1 has a physiological role in the control of postprandial glucose in humans: studies with the antagonist exendin 9-39

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7 January 2021

Inositolphosphoglycans and diacyglycerol are possible mediators in the glycogenic effect of GLP-1(7-36)amide in BC3H-1 myocytes

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Sympathetic pathways mediate GLP-1 actions in the gastrointestinal tract of the rat.

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Once daily injection of exendin-4 to diabetic mice achieves long-term beneficial effects on blood glucose concentrations

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Truncated glucagon-like peptide I, an insulin-releasing hormone from the distal gut

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Comparison of the effects of glucagon-like peptide-1-(1-37) and -(7-37) and glucagon on islet hormone release from isolated perfused canine and rat pancreases

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Glucagon-like peptide-1 7-36: a physiological incretin in man.

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Insulinotropin: glucagon-like peptide I (7-37) co-encoded in the glucagon gene is a potent stimulator of insulin release in the perfused rat pancreas

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7 January 2021

Neural monitoring system for circulating somatostatin in the hepatoportal area

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Somatostatin receptor on the afferent nerve terminals in the rat hepatoportal area

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7 January 2021

Somatostatin-sensitive neural system in the liver

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A unique receptor-mediated mechanism in vagal chemoreception of somatostatin in the hepatoportal area

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7 January 2021

Monoclonal Antibodies to Somatostatin Receptor of Rat Brain

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7 January 2021

Afferent impulse discharges from glucoreceptors in the liver of the guinea pig

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7 January 2021

The hepatic vagal nerve is receptive to incretin hormone glucagon-like peptide-1, but not to glucose-dependent insulinotropic polypeptide, in the portal vein

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7 January 2021

Exendin-4 and exendin-(9–39)NH2: agonist and antagonist, respectively, at the rat parietal cell receptor for glucagon-like peptide-1-(7–36)NH2

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7 January 2021

Expression cloning of the pancreatic beta cell receptor for the gluco-incretin hormone glucagon-like peptide 1

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7 January 2021

Cloning and functional expression of the human islet GLP-1 receptor. Demonstration that exendin-4 is an agonist and exendin-(9-39) an antagonist of the receptor

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7 January 2021

Glucagon-like peptide 1: a potent glycogenic hormone

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7 January 2021

Potent glycogenic effect of GLP-1(7-36)amide in rat skeletal muscle

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7 January 2021

Glucagon-like peptide-1 is a physiological incretin in rat

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7 January 2021

Glucagon-like peptide-1 7-36 amide and peptide YY from the L-cell of the ileal mucosa are potent inhibitors of vagally induced gastric acid secretion in man.

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7 January 2021

The inhibitory effect of glucagon-like peptide-1 (GLP-1) 7-36 amide on gastric acid secretion in humans depends on an intact vagal innervation

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7 January 2021

Functional expression of the rat glucagon-like peptide-I receptor, evidence for coupling to both adenylyl cyclase and phospholipase-C.

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7 January 2021

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Identifiers

DOI

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5 November 2019

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