Literature DB >> 529072

Acid secretion from the completely isolated blood perfused canine stomach.

M A Pilot.   

Abstract

1. The canine gastric arterial supply was isolated and perfused by means of an extracorporeal circuit. The gastric venous blood was returned to the dog's venous system. Histamine acid phosphate (20 microgram min-1) infused intra-arterially gave a mean peak acid output of 2.3 m-mole per 10 min. 2. When a plateau of acid secretion was observed, the gastric venous blood was diverted to the oxygenator, by-passing the dog entirely (vascular isolation). This resulted in an immediate decrease in acid output which fell to or near zero by 90 min after isolation. 3. In three dogs, part of a lung was perfused in series with the stomach before total isolation of the gastric vasculature. With histamine stimulation, acid secretion was observed for about 1 hr with a peak acid output of 0.5 m-mole per 10 min during the period of total isolation. 4. Indomethacin (10 mg kg-1) was given to five dogs approximately 1 hr before vascular isolation. After acid secretion reached a plateau (mean peak acid output 2.3 m-mole per 10 minutes), the gastric circulation was isolated by diverting the gastric venous blood to the oxygenator. Acid secretion was maintained for 50 min, after which it gradually declined to reach 30% of the peak value after 2 hr. 5. Indomethacin (10 mg kg-1) and methysergide bimaleate (1 mg) were given I.V. to five dogs approximately 1 hr before vascular isolation. After acid secretion reached a plateau (peak output 3.0 m-mole per 10 min), the gastric circulation was isolated by diverting the gastric venous blood to the oxygenator. The plateau of secretion was maintained for a further 2 hr with no inhibition. 6. Methysergide bimaleate given alone did not prevent the inhibition of secretion caused by the total vascular isolation of the stomach. 7. These results suggest that in the isolated canine stomach preparation naturally occurring inhibitors of gastric acid secretion, which are normally metabolized at least in part in the lungs, accumulate in the circulation and may account for the observed suppression of acid secretion.

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Year:  1979        PMID: 529072      PMCID: PMC1279067          DOI: 10.1113/jphysiol.1979.sp012994

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  14 in total

1.  Acid secretion from the isolated perfused canine stomach.

Authors:  M A Pilot
Journal:  J Physiol       Date:  1975-02       Impact factor: 5.182

2.  5-Hydroxytryptamine; pharmacological action and destruction in perfused lungs.

Authors:  J H GADDUM; C O HEBB; A SILVER; A A SWAN
Journal:  Q J Exp Physiol Cogn Med Sci       Date:  1953

3.  The influence of variations in temperature and blood-pressure on the performance of the isolated mammalian heart.

Authors:  F P Knowlton; E H Starling
Journal:  J Physiol       Date:  1912-05-06       Impact factor: 5.182

Review 4.  Pharmacokinetic function of the pulmonary circulation.

Authors:  Y S Bakhle; J R Vane
Journal:  Physiol Rev       Date:  1974-10       Impact factor: 37.312

5.  Failure of ischemia to break the dog's gastric mucosal barrier.

Authors:  H W Davenport; L L Barr
Journal:  Gastroenterology       Date:  1973-10       Impact factor: 22.682

6.  Effect of intraarterial vasopressin on canine gastric mucosal permeability.

Authors:  N J Dorricott; H Eisenberg; W Silen
Journal:  Gastroenterology       Date:  1973-10       Impact factor: 22.682

7.  Prostaglandin synthetase activity in the rat stomach fundus. Activation by L-norepinephrine and related compounds.

Authors:  C Pace-Asciak
Journal:  Biochim Biophys Acta       Date:  1972-09-07

8.  Effect of humoral and cholinergic stimulants on secretory function of totally isolated canine stomach perfused by autologous and homologous blood.

Authors:  K Kowalewski; R Scharf
Journal:  Can J Surg       Date:  1972-05       Impact factor: 2.089

9.  Drugs which inhibit prostaglandin biosynthesis.

Authors:  R J Flower
Journal:  Pharmacol Rev       Date:  1974-03       Impact factor: 25.468

10.  The possible mechanism for the 'fade' in acid gastric secretion during continuous infusions of pentagastrin.

Authors:  A K Sanyal; N G Waton
Journal:  J Physiol       Date:  1976-10       Impact factor: 5.182

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  3 in total

1.  Hormonal control of the gastric motor response to feeding: cross-perfusion of an isolated stomach using a conscious donor dog.

Authors:  M A Pilot; P A Thomas; R E Gill; M A Knight; D H Ritchie
Journal:  World J Surg       Date:  1982-07       Impact factor: 3.352

2.  Vascular perfusion of the isolated rat stomach with a fluorocarbon emulsion.

Authors:  G A Van Huis; M F Kramer
Journal:  Gut       Date:  1981-09       Impact factor: 23.059

3.  Fade and tachyphylaxis of gastric acid secretory response to pentagastrin in rat isolated gastric mucosa.

Authors:  B H Hirst; J Holland; M E Parsons; C A Price
Journal:  Br J Pharmacol       Date:  1988-12       Impact factor: 8.739

  3 in total

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