Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/13398
Full metadata record
DC FieldValueLanguage
dc.contributor.authorKapuscinski, Men
dc.contributor.authorShulkes, Arthuren
dc.date.accessioned2015-05-16T03:14:29Z
dc.date.available2015-05-16T03:14:29Z
dc.date.issued1995-07-08en
dc.identifier.citationJournal of Gastroenterology and Hepatology; 10(4): 405-12en
dc.identifier.govdoc8527706en
dc.identifier.otherPUBMEDen
dc.identifier.urihttp://ahro.austin.org.au/austinjspui/handle/1/13398en
dc.description.abstractThe activity of gastric parietal cells in terms of hydrochloric acid (HCl) secretion is regulated by the interaction of stimulatory substances (e.g. gastrin) and inhibitors (e.g. somatostatin) acting in an endocrine and paracrine mode, as well as luminal factors. In the present study the following parameters were measured: the synthesis (mRNA), storage (tissue peptide concentration) and secretion (plasma peptide concentration) of somatostatin and gastrin following short-term treatment of rats with pentagastrin (acid stimulant), secretin, omeprazole (reduces gastric acidity by inactivating gastric H/K ATPase) and the somatostatin analogue octreotide (reduces gastric acidity by inhibiting both the parietal cell and gastrin). The mRNA coding for H/K ATPase and carbonic anhydrase II (CA II), the two enzymes responsible for the generation of hydrogen ions from the parietal cell, were also quantitated. In response to octreotide, somatostatin peptide and mRNA levels in the fundus rose to 180 +/- 16% (P < 0.001) and 1073 +/- 356% (P < 0.05) of control, respectively. In contrast, octreotide caused a decrease in antral somatostatin peptide and its mRNA did not change significantly. No significant changes in synthesis, secretion or storage of gastrin were observed except for omeprazole induced hypergastrinaemia (580 +/- 76%, P < 0.001). H/K ATPase and CA II mRNA were largely unaffected except for an increase in CA II mRNA following octreotide and a decrease in H/K ATPase mRNA after pentagastrin. These data support the concept of the differential control of antral and fundic somatostatin synthesis and provide evidence for a regulatory loop by which somatostatin can influence its own synthesis.(ABSTRACT TRUNCATED AT 250 WORDS)en
dc.language.isoenen
dc.subject.otherAdenosine Triphosphatases.drug effects.genetics.metabolismen
dc.subject.otherAnimalsen
dc.subject.otherCarbonic Anhydrases.drug effects.genetics.metabolismen
dc.subject.otherEnzyme Inhibitors.pharmacologyen
dc.subject.otherFemaleen
dc.subject.otherGastric Acid.metabolismen
dc.subject.otherGastric Mucosa.drug effects.secretionen
dc.subject.otherGastrins.biosynthesis.drug effects.geneticsen
dc.subject.otherGene Expression Regulationen
dc.subject.otherHydrogen-Ion Concentrationen
dc.subject.otherOmeprazole.pharmacologyen
dc.subject.otherRNA, Messenger.metabolismen
dc.subject.otherRatsen
dc.subject.otherRats, Sprague-Dawleyen
dc.subject.otherSomatostatin.biosynthesis.drug effects.geneticsen
dc.titleSecretory and biosynthetic responses of gastrin and somatostatin to acute changes in gastric acidity.en
dc.typeJournal Articleen
dc.identifier.journaltitleJournal of Gastroenterology and Hepatologyen
dc.identifier.affiliationUniversity of Melbourne Department of Surgery, Austin Hospital, Heidelberg, Victoria, Australiaen
dc.description.pages405-12en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/8527706en
dc.type.austinJournal Articleen
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.languageiso639-1en-
item.openairetypeJournal Article-
Appears in Collections:Journal articles
Show simple item record

Page view(s)

2
checked on Feb 5, 2023

Google ScholarTM

Check


Items in AHRO are protected by copyright, with all rights reserved, unless otherwise indicated.