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Gastrin

Summary

Gastrin is a peptide hormone that stimulates secretion of gastric acid (HCl) by the parietal cells of the stomach and aids in gastric motility. It is released by G cells in the pyloric antrum of the stomach, duodenum, and the pancreas.

GAST
Identifiers
AliasesGAST, GAS, gastrin
External IDsOMIM: 137250 MGI: 104768 HomoloGene: 628 GeneCards: GAST
Orthologs
SpeciesHumanMouse
Entrez

2520

14459

Ensembl

ENSG00000184502

ENSMUSG00000017165

UniProt

P01350

P48757

RefSeq (mRNA)

NM_000805

NM_010257

RefSeq (protein)

NP_000796

NP_034387

Location (UCSC)Chr 17: 41.71 – 41.72 MbChr 11: 100.23 – 100.23 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse
Gastrin
Identifiers
SymbolGastrin
PfamPF00918
InterProIPR001651
PROSITEPDOC00232
Available protein structures:
Pfam  structures / ECOD  
PDBRCSB PDB; PDBe; PDBj
PDBsumstructure summary

Gastrin binds to cholecystokinin B receptors to stimulate the release of histamines in enterochromaffin-like cells, and it induces the insertion of K+/H+ ATPase pumps into the apical membrane of parietal cells (which in turn increases H+ release into the stomach cavity). Its release is stimulated by peptides in the lumen of the stomach.

Physiology edit

Genetics edit

In humans, the GAS gene is located on the long arm of the seventeenth chromosome (17q21).[5]

Synthesis edit

Gastrin is a linear peptide hormone produced by G cells of the duodenum and in the pyloric antrum of the stomach. It is secreted into the bloodstream. The encoded polypeptide is preprogastrin, which is cleaved by enzymes in posttranslational modification to produce progastrin (an intermediate, inactive precursor) and then gastrin in various forms, primarily the following three:

Also, pentagastrin is an artificially synthesized, five amino acid sequence identical to the last five amino acid sequence at the C-terminus end of gastrin. The numbers refer to the amino acid count.

Release edit

Gastrin is released in response to certain stimuli. These include:

Gastrin release is inhibited by:[8][9]

Function edit

 
G cell is visible near bottom left, and gastrin is labeled as the two black arrows leading from it. Note: this diagram does not illustrate gastrin's stimulatory effect on ECL cells.

The presence of gastrin stimulates parietal cells of the stomach to secrete hydrochloric acid (HCl)/gastric acid. This is done both directly on the parietal cell [failed verification] and indirectly via binding onto CCK2/gastrin receptors on ECL cells in the stomach, which respond by releasing histamine, which in turn acts in a paracrine manner on parietal cells stimulating them to secrete H+ ions. This is the major stimulus for acid secretion by parietal cells.[10]

Along with the above-mentioned function, gastrin has been shown to have additional functions as well:

Factors influencing secretion edit

Factors influencing secretion of gastrin can be divided into 2 categories:[16]

Physiologic edit

Gastric lumen edit
  • Stimulatory factors: dietary protein and amino acids (meat), hypercalcemia. (i.e. during the gastric phase)
  • Inhibitory factor: acidity (pH below 3) - a negative feedback mechanism, exerted via the release of somatostatin from δ cells in the stomach, which inhibits gastrin and histamine release.
Paracrine edit
  • Stimulatory factor: bombesin or gastrin-releasing peptide (GRP)
  • Inhibitory factor: somatostatin - acts on somatostatin-2 receptors on G cells. in a paracrine manner via local diffusion in the intercellular spaces, but also systemically through its release into the local mucosal blood circulation; it inhibits acid secretion by acting on parietal cells.
Nervous edit
Circulation edit

Pathophysiologic edit

Paraneoplastic edit

Role in disease edit

In the Zollinger–Ellison syndrome, gastrin is produced at excessive levels, often by a gastrinoma gastrin-producing tumor, mostly benign of the duodenum or the pancreas. To investigate for hypergastrinemia high blood levels of gastrin, a "pentagastrin test" can be performed.[17]

In autoimmune gastritis, the immune system attacks the parietal cells leading to hypochlorhydria low stomach acid secretion. This results in an elevated gastrin level in an attempt to compensate for increased pH in the stomach. Eventually, all the parietal cells are lost and achlorhydria results leading to a loss of negative feedback on gastrin secretion. Plasma gastrin concentration is elevated in virtually all individuals with mucolipidosis type IV (mean 1507 pg/mL; range 400-4100 pg/mL) (normal 0-200 pg/mL) secondary to a constitutive achlorhydria. This finding facilitates the diagnosis of patients with this neurogenetic disorder.[18] Additionally, elevated gastrin levels may be present in chronic gastritis resulting from H pylori infection.[19]

History edit

Its existence was first suggested in 1905 by the British physiologist John Sydney Edkins,[20][21] and gastrins were isolated in 1964 by Hilda Tracy and Roderic Alfred Gregory at the University of Liverpool.[22] In 1964 the structure of gastrin was determined.[23]

References edit

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000184502 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000017165 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Lund T, Geurts van Kessel AH, Haun S, Dixon JE (May 1986). "The genes for human gastrin and cholecystokinin are located on different chromosomes". Human Genetics. 73 (1): 77–80. doi:10.1007/BF00292669. PMID 3011648. S2CID 32216320.
  6. ^ Blanco, Antonio; Blanco, Gustavo (2017), "Biochemical Bases of Endocrinology (II) Hormones and Other Chemical Intermediates", Medical Biochemistry, Elsevier, pp. 573–644, doi:10.1016/b978-0-12-803550-4.00026-4, ISBN 9780128035504
  7. ^ Feng J, Petersen CD, Coy DH, Jiang JK, Thomas CJ, Pollak MR, Wank SA (October 2010). "Calcium-sensing receptor is a physiologic multimodal chemosensor regulating gastric G-cell growth and gastrin secretion". Proceedings of the National Academy of Sciences of the United States of America. 107 (41): 17791–6. Bibcode:2010PNAS..10717791F. doi:10.1073/pnas.1009078107. PMC 2955134. PMID 20876097.
  8. ^ Holst JJ, Orskov C, Seier-Poulsen S (1992). "Somatostatin is an essential paracrine link in acid inhibition of gastrin secretion". Digestion. 51 (2): 95–102. doi:10.1159/000200882. PMID 1354190.
  9. ^ Johnson LR (March 1984). "Effects of somatostatin and acid on inhibition of gastrin release in newborn rats". Endocrinology. 114 (3): 743–6. doi:10.1210/endo-114-3-743. PMID 6141932. Archived from the original on 2008-09-05. Retrieved 2011-05-17.
  10. ^ Lindström, E.; Chen, D.; Norlén, P.; Andersson, K.; Håkanson, R. (2001). "Control of gastric acid secretion:the gastrin-ECL cell-parietal cell axis". Comparative Biochemistry and Physiology. Part A, Molecular & Integrative Physiology. 128 (3): 505–514. doi:10.1016/s1095-6433(00)00331-7. ISSN 1095-6433. PMID 11246041.
  11. ^ Tortora, G. J., & Grabowski, S. R. (1996). Principles of anatomy and physiology. New York, NY: HarperCollins College. 14th Ed. Pg 906
  12. ^ Vadokas B, Lüdtke FE, Lepsien G, Golenhofen K, Mandrek K (December 1997). "Effects of gastrin-releasing peptide (GRP) on the mechanical activity of the human ileocaecal region in vitro". Neurogastroenterology and Motility. 9 (4): 265–70. doi:10.1046/j.1365-2982.1997.d01-59.x. PMID 9430795. S2CID 31858033.
  13. ^ Valenzuela JE, Walsh JH, Isenberg JI (September 1976). "Effect of gastrin on pancreatic enzyme secretion and gallbladder emptying in man". Gastroenterology. 71 (3): 409–11. doi:10.1016/S0016-5085(76)80445-3. PMID 950091.
  14. ^ Castell DO (February 1978). "Gastrin and lower esophageal sphincter tone". Archives of Internal Medicine. 138 (2): 196. doi:10.1001/archinte.138.2.196. PMID 626547.
  15. ^ Henderson JM, Lidgard G, Osborne DH, Carter DC, Heading RC (February 1978). "Lower oesophageal sphincter response to gastrin--pharmacological or physiological?". Gut. 19 (2): 99–102. doi:10.1136/gut.19.2.99. PMC 1411818. PMID 631634.
  16. ^ Indu Khurana (2006). Textbook medical physiology. New Delhi: Reed Elsevier India. p. 605. ISBN 978-8181478504. OCLC 968478170.
  17. ^ Baron, J. H. (1978). Clinical Tests of Gastric Secretion. doi:10.1007/978-1-349-03188-7. ISBN 978-1-349-03190-0.
  18. ^ Schiffmann R, Dwyer NK, Lubensky IA, Tsokos M, Sutliff VE, Latimer JS, Frei KP, Brady RO, Barton NW, Blanchette-Mackie EJ, Goldin E (February 1998). "Constitutive achlorhydria in mucolipidosis type IV". Proceedings of the National Academy of Sciences of the United States of America. 95 (3): 1207–12. Bibcode:1998PNAS...95.1207S. doi:10.1073/pnas.95.3.1207. PMC 18720. PMID 9448310.
  19. ^ "Review Article: Strategies to Determine Whether Hypergastrinaemia Is Due to Zollinger-Ellison Syndrome Rather Than a More Common Benign Cause". www.medscape.com. Archived from the original on 2023-05-22. Retrieved 2016-12-02.
  20. ^ Edkins JS (March 1906). "The chemical mechanism of gastric secretion". The Journal of Physiology. 34 (1–2): 133–44. doi:10.1113/jphysiol.1906.sp001146. PMC 1465807. PMID 16992839.
  21. ^ Modlin IM, Kidd M, Marks IN, Tang LH (February 1997). "The pivotal role of John S. Edkins in the discovery of gastrin". World Journal of Surgery. 21 (2): 226–34. doi:10.1007/s002689900221. PMID 8995084. S2CID 28243696.
  22. ^ Gregory RA, Tracy HJ (1964). "The constitution and properties of two gastrins extracted from hog antral mucosa: Part I the isolation of two gastrins from hog antral mucosa". Gut. 5 (2): 103–107. doi:10.1136/gut.5.2.103. PMC 1552180. PMID 14159395.
  23. ^ Gregory H, Hardy PM, Jones DS, Kenner GW, Sheppard RC (December 1964). "The antral hormone gastrin. Structure of gastrin". Nature. 204 (4962): 931–3. Bibcode:1964Natur.204..931G. doi:10.1038/204931a0. PMID 14248711. S2CID 4262131.

Further reading edit

  • Rozengurt E, Walsh JH (2001). "Gastrin, CCK, signaling, and cancer". Annual Review of Physiology. 63: 49–76. doi:10.1146/annurev.physiol.63.1.49. PMID 11181948.
  • Dockray GJ (December 2004). "Clinical endocrinology and metabolism. Gastrin". Best Practice & Research. Clinical Endocrinology & Metabolism. 18 (4): 555–68. doi:10.1016/j.beem.2004.07.003. PMID 15533775.
  • Anlauf M, Garbrecht N, Henopp T, Schmitt A, Schlenger R, Raffel A, Krausch M, Gimm O, Eisenberger CF, Knoefel WT, Dralle H, Komminoth P, Heitz PU, Perren A, Klöppel G (September 2006). "Sporadic versus hereditary gastrinomas of the duodenum and pancreas: distinct clinico-pathological and epidemiological features". World Journal of Gastroenterology. 12 (34): 5440–6. doi:10.3748/wjg.v12.i34.5440. PMC 4088224. PMID 17006979.
  • Polosatov MV, Klimov PK, Masevich CG, Samartsev MA, Wünsch E (April 1979). "Interaction of synthetic human big gastrin with blood proteins of man and animals". Acta Hepato-Gastroenterologica. 26 (2): 154–9. PMID 463490.
  • Fritsch WP, Hausamen TU, Scholten T (April 1977). "[Gastrointestinal hormones. I. Hormones of the gastrin group]". Zeitschrift für Gastroenterologie. 15 (4): 264–76. PMID 871064.
  • Higashimoto Y, Himeno S, Shinomura Y, Nagao K, Tamura T, Tarui S (May 1989). "Purification and structural determination of urinary NH2-terminal big gastrin fragments". Biochemical and Biophysical Research Communications. 160 (3): 1364–70. doi:10.1016/S0006-291X(89)80154-8. PMID 2730647.
  • Pauwels S, Najdovski T, Dimaline R, Lee CM, Deschodt-Lanckman M (June 1989). "Degradation of human gastrin and CCK by endopeptidase 24.11: differential behaviour of the sulphated and unsulphated peptides". Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology. 996 (1–2): 82–8. doi:10.1016/0167-4838(89)90098-8. PMID 2736261.
  • Lund T, Geurts van Kessel AH, Haun S, Dixon JE (May 1986). "The genes for human gastrin and cholecystokinin are located on different chromosomes". Human Genetics. 73 (1): 77–80. doi:10.1007/BF00292669. PMID 3011648. S2CID 32216320.
  • Kariya Y, Kato K, Hayashizaki Y, Himeno S, Tarui S, Matsubara K (1986). "Expression of human gastrin gene in normal and gastrinoma tissues". Gene. 50 (1–3): 345–52. doi:10.1016/0378-1119(86)90338-0. PMID 3034736.
  • Gregory RA, Tracy HJ, Agarwal KL, Grossman MI (August 1969). "Aminoacid constitution of two gastrins isolated from Zollinger-Ellison tumour tissue". Gut. 10 (8): 603–8. doi:10.1136/gut.10.8.603. PMC 1552899. PMID 5822140.
  • Bentley PH, Kenner GW, Sheppard RC (February 1966). "Structures of human gastrins I and II". Nature. 209 (5023): 583–5. doi:10.1038/209583b0. PMID 5921183. S2CID 4200721.
  • Ito R, Sato K, Helmer T, Jay G, Agarwal K (August 1984). "Structural analysis of the gene encoding human gastrin: the large intron contains an Alu sequence". Proceedings of the National Academy of Sciences of the United States of America. 81 (15): 4662–6. Bibcode:1984PNAS...81.4662I. doi:10.1073/pnas.81.15.4662. PMC 391550. PMID 6087340.
  • Wiborg O, Berglund L, Boel E, Norris F, Norris K, Rehfeld JF, Marcker KA, Vuust J (February 1984). "Structure of a human gastrin gene". Proceedings of the National Academy of Sciences of the United States of America. 81 (4): 1067–9. Bibcode:1984PNAS...81.1067W. doi:10.1073/pnas.81.4.1067. PMC 344765. PMID 6322186.
  • Kato K, Hayashizaki Y, Takahashi Y, Himeno S, Matsubara K (December 1983). "Molecular cloning of the human gastrin gene". Nucleic Acids Research. 11 (23): 8197–203. doi:10.1093/nar/11.23.8197. PMC 326575. PMID 6324077.
  • Boel E, Vuust J, Norris F, Norris K, Wind A, Rehfeld JF, Marcker KA (May 1983). "Molecular cloning of human gastrin cDNA: evidence for evolution of gastrin by gene duplication". Proceedings of the National Academy of Sciences of the United States of America. 80 (10): 2866–9. Bibcode:1983PNAS...80.2866B. doi:10.1073/pnas.80.10.2866. PMC 393933. PMID 6574456.
  • Kato K, Himeno S, Takahashi Y, Wakabayashi T, Tarui S, Matsubara K (December 1983). "Molecular cloning of human gastrin precursor cDNA". Gene. 26 (1): 53–7. doi:10.1016/0378-1119(83)90035-5. PMID 6689486.
  • Koh TJ, Wang TC (November 1995). "Molecular cloning and sequencing of the murine gastrin gene". Biochemical and Biophysical Research Communications. 216 (1): 34–41. doi:10.1006/bbrc.1995.2588. PMID 7488110.
  • Rehfeld JF, Hansen CP, Johnsen AH (January 1995). "Post-poly(Glu) cleavage and degradation modified by O-sulfated tyrosine: a novel post-translational processing mechanism". The EMBO Journal. 14 (2): 389–96. doi:10.1002/j.1460-2075.1995.tb07013.x. PMC 398093. PMID 7530658.
  • Rehfeld JF, Johnsen AH (August 1994). "Identification of gastrin component I as gastrin-71. The largest possible bioactive progastrin product". European Journal of Biochemistry. 223 (3): 765–73. doi:10.1111/j.1432-1033.1994.tb19051.x. PMID 8055952.
  • Varro A, Dockray GJ (November 1993). "Post-translational processing of progastrin: inhibition of cleavage, phosphorylation and sulphation by brefeldin A". The Biochemical Journal. 295 (Pt 3): 813–9. doi:10.1042/bj2950813. PMC 1134634. PMID 8240296.

External links edit

  • Overview at colostate.edu
  • Nosek, Thomas M. "Section 6/6ch4/s6ch4_14". Essentials of Human Physiology. Archived from the original on 2016-03-24.

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