Pentagastrin
Overview
A synthetic pentapeptide containing the C-terminal tetrapeptide sequence of gastrin (Trp-Met-Asp-Phe-NH2) linked to beta-alanine. Pentagastrin stimulates gastric acid secretion by binding to cholecystokinin-2 (CCK2) receptors on parietal cells, and stimulates calcitonin release from thyroid C-cells.
Mechanism of Action
It has been used as a diagnostic agent for both gastric acid secretory capacity testing and provocative testing for medullary thyroid carcinoma (MTC).
Research Summary & Key Findings
Historically used for gastric acid analysis (pentagastrin stimulation test) to assess maximal acid output. Pentagastrin-stimulated calcitonin test was a standard screening tool for MTC and MEN2 kindreds before genetic testing became available. Product availability has been limited in recent years in many countries. Largely superseded by genetic RET mutation testing for MTC screening and proton pump inhibitor trials for acid-related disorders.
Clinical Status
Pentagastrin has received FDA approval and is available for clinical use under appropriate medical supervision. Consult a qualified healthcare provider for prescribing information.
Administration Routes
References
Primary literature
- PubMed — "Pentagastrin"
Peer-reviewed literature indexed by the National Library of Medicine.
- ClinicalTrials.gov — "Pentagastrin"
Registered interventional and observational studies, including status and phase.
- PubChem — "Pentagastrin"
Chemical structure, molecular properties, and bioactivity data.
Study-level citations for this compound are being verified against the primary sources before publication. The database queries above return the current indexed literature in the meantime.
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