Related Experiment Video
Updated: Jul 6, 2026

07:00
Mechanisms Underlying Gut Hormone Secretion Using the Isolated Perfused Rat Small Intestine
Published on: February 26, 2019
A new look at an old hormone gastrin
Trends in Endocrinology and Metabolism: TEM
|March 1, 1993
Summary
Gastrin
Area of Science:
- Gastroenterology and Molecular Biology
- Endocrinology
- Cell Biology
Background:
- Gastrin, a key peptide hormone, regulates gastric acid secretion and gastrointestinal tissue growth.
- While G cell origin and some regulatory mechanisms are known, intracellular processing and secretion regulation remain unclear.
- Gastrin receptors have been identified and cloned, with ongoing research into their relationship with cholecystokinin receptors.
Purpose of the Study:
- To elucidate the complex molecular mechanisms underlying gastrin's regulation of gastric function.
- To explore the intracellular regulation of gastrin processing and secretion.
- To investigate the role of gastrin in gastric acid secretion and gastrointestinal trophic effects.
Main Methods:
- Gene sequencing of the gastrin peptide.
- Identification of gastrin gene promoters and regulatory sequences.
- Analysis of gastrin's action on gastric parietal cells and enterochromaffin-like cells.
Main Results:
- The gastrin gene and its regulatory elements have been sequenced, revealing interrelationships with epidermal growth factor and somatostatin.
- Gastrin's dynamic role in regulating acid secretion through multiple cellular targets has been detailed.
- Gastrin's trophic effects contribute to gastric fundic hyperplasia and microcarcinoid development in hypergastrinemia.
Conclusions:
- A complex, gastric-based molecular regulatory system involving gastrin has been identified.
- Gastrin plays a critical role in both acid secretion and the trophic regulation of the gastrointestinal tract.
- Understanding gastrin's intricate functions is crucial for comprehending conditions like gastric hyperplasia and microcarcinoid evolution.
Related Concept Videos
GTPases and their Regulation
Guanine nucleotide-binding proteins (G-proteins), also known as GTPases, are a superfamily of proteins that regulate many cellular processes, such as cell signaling, vesicular transport, and the regulation of cell shape and motility. Mutation or dysfunction of these proteins can lead to disease. There are around 40,000 known G-proteins that can broadly be classified into two groups ‒ small G-proteins consisting of a single domain and large multi-domain G-proteins.
Large G-proteins, also known...
Large G-proteins, also known...
GTPases and their Regulation
Guanine nucleotide-binding proteins (G-proteins), also known as GTPases, are a superfamily of proteins that regulate many cellular processes, such as cell signaling, vesicular transport, and the regulation of cell shape and motility. Mutation or dysfunction of these proteins can lead to disease. There are around 40,000 known G-proteins that can broadly be classified into two groups ‒ small G-proteins consisting of a single domain and large multi-domain G-proteins.
Large G-proteins, also known...
Large G-proteins, also known...
Activation and Inactivation of G Proteins
Heterotrimeric G proteins are guanine nucleotide-binding proteins. As the name suggests, heterotrimeric G proteins are composed of three subunits: alpha, beta, and gamma. They remain GDP-bound or GTP-bound inside the cells and switch between inactive/active states. The Gα subunit possesses the nucleotide-binding pocket that binds guanine nucleotides and switches between GDP or GTP-bound states. In contrast, the Gꞵ and Gγ subunits are always bound together with high affinity and are together...
Transducer Mechanism: Enzyme-Linked Receptors
Enzyme-linked receptors are cell-surface receptors acting as an enzyme or associating with an enzyme intracellularly. They make excellent drug targets. Drugs can bind to the extracellular ligand-binding domain or directly affect their enzymatic domain and alter their activity.
Major types that are helpful drug targets include:
Major types that are helpful drug targets include:
GPCRs Regulate Adenylyl Cylase Activity
Some GPCRs transmit signals through adenylyl cyclase (AC), a transmembrane enzyme. AC helps synthesize second messenger cyclic adenosine monophosphate (cAMP). AC catalyzes cyclization reaction and converts ATP to cAMP by releasing a pyrophosphate. The pyrophosphate is further hydrolyzed to phosphate by the enzyme pyrophosphatase, which drives cAMP synthesis to completion. However, cAMP is rapidly degraded to 5′ AMP by the enzymes phosphodiesterase (PDE), preventing overstimulation of cells.
Two...
Two...
Secondary Messengers in Hormone Action
Water-soluble hormones cannot cross the plasma membrane, so they rely on protein receptors that span the membrane to trigger intracellular signaling pathways. These pathways then activate second messengers inside the cell, including cAMP or calcium ions.
Many hormones bind to transmembrane G protein-coupled receptors that connect to regulatory G proteins. These G proteins can then activate enzymes such as adenylyl cyclase or phospholipase C. Adenylyl cyclase converts ATP to cAMP, activating...
Many hormones bind to transmembrane G protein-coupled receptors that connect to regulatory G proteins. These G proteins can then activate enzymes such as adenylyl cyclase or phospholipase C. Adenylyl cyclase converts ATP to cAMP, activating...

