Literature DB >> 4646586

The control of the plasma choline concentration in the cat.

J E Gardiner, W D Paton.   

Abstract

1. Changes in choline concentration of the blood after injections or infusions of choline were studied in cats anaesthetized with chloralose.2. Single I.V. injections of choline 10-100 mumole/kg produced arterial plasma levels 1 min later corresponding to an apparent volume of initial distribution of 430 ml./kg. The concentration then declined rapidly (half-time, 1-2 min), with a later slower decline after large doses.3. Infusions of choline at a rate of 0.8 mumole/kg.min or greater produced steady rises in plasma level, corresponding to a clearance of 28.6 ml. plasma/kg.min. The half time of rate of approach to steady state was 7 min or less. Infusions at rates of 0.40 mumole/kg.min or less produced much smaller or negligible rises, suggesting mechanisms for disposal which were saturated at higher concentration. At low rates, little infused choline appeared in urine. At the end of an infusion, the plasma choline level usually fell without delay.4. Portal blood contained about 50% of the arterial level, renal venous blood 15-70%, caval blood 30-60%, and amniotic fluid 2.5%. Occlusion of renal coeliac or mesenteric arteries raised plasma choline, but relatively rapid choline removal still occurred in the eviscerate animal.5. After infusions of [methyl-(14)C]choline, the level of radioactivity retained in the circulation amounted to only a few per cent of the total dose infused. At low rates of infusion (0.0125-0.1 mumole/kg.min) the radioactivity represented only a small fraction of bio-assayable choline; but at 0.40 mumole/kg.min it came to exceed the concentration of free choline, indicating metabolic conversion. Only traces of (14)C were found in expired air, and only 1-1.5% of total infused radioactivity in the urine. After infusion of 150 mumole over 3 hr, high levels of radioactivity were found in liver, kidney, lung, brain and heart, but levels in muscle and spleen were comparable to that of blood.6. It was concluded that choline is rapidly lost from the blood, that the abdominal viscera, liver, kidney and lung are important extraction sites, that some partial metabolism occurs, the metabolites also being rapidly lost from blood, and that it is probable that choline lost to the tissues becomes bound in some form.

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Year:  1972        PMID: 4646586      PMCID: PMC1331263          DOI: 10.1113/jphysiol.1972.sp010020

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


  14 in total

1.  The mechanism of action of the hemicholiniums.

Authors:  F W SCHUELER
Journal:  Int Rev Neurobiol       Date:  1960       Impact factor: 3.230

2.  Effect of HC-3 on acetylcholine turnover.

Authors:  F C MACINTOSH
Journal:  Fed Proc       Date:  1961-07

3.  Improved automatic apparatus for pharmacological assays on isolated preparations.

Authors:  A BOURA; J L MONGAR; H O SCHILD
Journal:  Br J Pharmacol Chemother       Date:  1954-03

4.  The role of the liver and the kidneys in the maintenance of the level of free choline in plasma.

Authors:  J BLIGH
Journal:  J Physiol       Date:  1953-04-28       Impact factor: 5.182

5.  The level of free choline in plasma.

Authors:  J BLIGH
Journal:  J Physiol       Date:  1952-06       Impact factor: 5.182

6.  Movement of choline between the blood and cerebrospinal fluid in the cat.

Authors:  J E Gardiner; F R Domer
Journal:  Arch Int Pharmacodyn Ther       Date:  1968-10

7.  A p-terphenyl hemicholinium compound.

Authors:  J E Gardiner; L H Sung
Journal:  Br J Pharmacol       Date:  1969-05       Impact factor: 8.739

8.  The incorporation of L-[Me-14C]methionine and [Me-3H]choline into lung phosphatides.

Authors:  H L Spitzer; K Morrison; J R Norman
Journal:  Biochim Biophys Acta       Date:  1968-05-01

9.  Choline metabolism in brain. The role of choline transport and the effects of phenobarbital.

Authors:  I Diamond
Journal:  Arch Neurol       Date:  1971-04

10.  Concentrative accumulation of choline by human erythrocytes.

Authors:  K Martin
Journal:  J Gen Physiol       Date:  1968-04       Impact factor: 4.086

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  7 in total

1.  Effect of two hemicholiniums on the disposition and distribution of endogenous free choline in anaesthetized rabbits.

Authors:  J E Gardiner; M C Gwee
Journal:  Br J Pharmacol       Date:  1977-07       Impact factor: 8.739

2.  Uptake of free choline by isolated perfused rat liver.

Authors:  S H Zeisel; D L Story; R J Wurtman; H Brunengraber
Journal:  Proc Natl Acad Sci U S A       Date:  1980-08       Impact factor: 11.205

3.  Steady-state concentrations of choline and acetylcholine in rat brain parts during a constant rate infusion of deuterated choline.

Authors:  G Racagni; M Trabucchi; D L Cheney
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1975       Impact factor: 3.000

4.  Renal tubular excretion of triethylcholine (TEC) in the chicken: enhancement and inhibition of renal excretion of choline and acetylcholine by TEC.

Authors:  M Acara; M Kowalski; B Rennick; B Hemsworth
Journal:  Br J Pharmacol       Date:  1975-05       Impact factor: 8.739

5.  Arterio-venous differences of choline and choline lipids across the brain of rat and rabbit.

Authors:  S Spanner; R C Hall; G B Ansell
Journal:  Biochem J       Date:  1976-01-15       Impact factor: 3.857

6.  The distribution in the rabbit of choline administered by injection or infusion.

Authors:  J E Gardiner; M C Gwee
Journal:  J Physiol       Date:  1974-06       Impact factor: 5.182

7.  No up-regulation of the phosphatidylethanolamine N-methyltransferase pathway and choline production by sex hormones in cats.

Authors:  Chiara Valtolina; Arie B Vaandrager; Robert P Favier; Joris H Robben; Maidina Tuohetahuntila; Anne Kummeling; Isabelle Jeusette; Jan Rothuizen
Journal:  BMC Vet Res       Date:  2015-11-09       Impact factor: 2.741

  7 in total

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