author_facet Gilfillan, A.M.
Hollingsworth, M.
Jones, A.W.
Gilfillan, A.M.
Hollingsworth, M.
Jones, A.W.
author Gilfillan, A.M.
Hollingsworth, M.
Jones, A.W.
spellingShingle Gilfillan, A.M.
Hollingsworth, M.
Jones, A.W.
British Journal of Pharmacology
The pharmacological modulation of [3H]‐disaturated phosphatidylcholine overflow from perifused lung slices of adult rats: a new method for the study of lung surfactant secretion
Pharmacology
author_sort gilfillan, a.m.
spelling Gilfillan, A.M. Hollingsworth, M. Jones, A.W. 0007-1188 1476-5381 Wiley Pharmacology http://dx.doi.org/10.1111/j.1476-5381.1983.tb11008.x <jats:p><jats:list list-type="explicit-label"> <jats:list-item><jats:p>Lung slices from adult rats incubated in [methyl‐<jats:sup>3</jats:sup>H]‐choline chloride formed [<jats:sup>3</jats:sup>H]‐disaturated phosphatidylcholine ([<jats:sup>3</jats:sup>H]‐DSPC) which was used as an index of lung surfactant.</jats:p></jats:list-item> <jats:list-item><jats:p>The slices were perifused after 3 h incubation in [methyl‐<jats:sup>3</jats:sup>H]‐choline chloride and the overflow of [<jats:sup>3</jats:sup>H]‐DSPC, as a rate coefficient, was used as a measure of surfactant secretion. The basal overflow of [<jats:sup>3</jats:sup>H]‐DSPC rapidly declined over the first 30 min of perifusion and then declined slowly.</jats:p></jats:list-item> <jats:list-item><jats:p>Salbutamol induced a prolonged, and sometimes delayed, increase in [<jats:sup>3</jats:sup>H]‐DSPC overflow, which was reduced by (±)‐propranolol. Potassium chloride produced an immediate, and usually transient, increase in [<jats:sup>3</jats:sup>H]‐DSPC overflow which was not modified by atropine or (±)‐propranolol. Adenosine 5′‐triphosphate, but not phenylephrine, also increased [<jats:sup>3</jats:sup>H]‐DSPC overflow.</jats:p></jats:list-item> <jats:list-item><jats:p>This method can measure the magnitude and time‐course of lung surfactant secretion induced by drugs.</jats:p></jats:list-item> </jats:list></jats:p> The pharmacological modulation of [<sup>3</sup>H]‐disaturated phosphatidylcholine overflow from perifused lung slices of adult rats: a new method for the study of lung surfactant secretion British Journal of Pharmacology
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series British Journal of Pharmacology
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title The pharmacological modulation of [3H]‐disaturated phosphatidylcholine overflow from perifused lung slices of adult rats: a new method for the study of lung surfactant secretion
title_unstemmed The pharmacological modulation of [3H]‐disaturated phosphatidylcholine overflow from perifused lung slices of adult rats: a new method for the study of lung surfactant secretion
title_full The pharmacological modulation of [3H]‐disaturated phosphatidylcholine overflow from perifused lung slices of adult rats: a new method for the study of lung surfactant secretion
title_fullStr The pharmacological modulation of [3H]‐disaturated phosphatidylcholine overflow from perifused lung slices of adult rats: a new method for the study of lung surfactant secretion
title_full_unstemmed The pharmacological modulation of [3H]‐disaturated phosphatidylcholine overflow from perifused lung slices of adult rats: a new method for the study of lung surfactant secretion
title_short The pharmacological modulation of [3H]‐disaturated phosphatidylcholine overflow from perifused lung slices of adult rats: a new method for the study of lung surfactant secretion
title_sort the pharmacological modulation of [<sup>3</sup>h]‐disaturated phosphatidylcholine overflow from perifused lung slices of adult rats: a new method for the study of lung surfactant secretion
topic Pharmacology
url http://dx.doi.org/10.1111/j.1476-5381.1983.tb11008.x
publishDate 1983
physical 363-371
description <jats:p><jats:list list-type="explicit-label"> <jats:list-item><jats:p>Lung slices from adult rats incubated in [methyl‐<jats:sup>3</jats:sup>H]‐choline chloride formed [<jats:sup>3</jats:sup>H]‐disaturated phosphatidylcholine ([<jats:sup>3</jats:sup>H]‐DSPC) which was used as an index of lung surfactant.</jats:p></jats:list-item> <jats:list-item><jats:p>The slices were perifused after 3 h incubation in [methyl‐<jats:sup>3</jats:sup>H]‐choline chloride and the overflow of [<jats:sup>3</jats:sup>H]‐DSPC, as a rate coefficient, was used as a measure of surfactant secretion. The basal overflow of [<jats:sup>3</jats:sup>H]‐DSPC rapidly declined over the first 30 min of perifusion and then declined slowly.</jats:p></jats:list-item> <jats:list-item><jats:p>Salbutamol induced a prolonged, and sometimes delayed, increase in [<jats:sup>3</jats:sup>H]‐DSPC overflow, which was reduced by (±)‐propranolol. Potassium chloride produced an immediate, and usually transient, increase in [<jats:sup>3</jats:sup>H]‐DSPC overflow which was not modified by atropine or (±)‐propranolol. Adenosine 5′‐triphosphate, but not phenylephrine, also increased [<jats:sup>3</jats:sup>H]‐DSPC overflow.</jats:p></jats:list-item> <jats:list-item><jats:p>This method can measure the magnitude and time‐course of lung surfactant secretion induced by drugs.</jats:p></jats:list-item> </jats:list></jats:p>
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author Gilfillan, A.M., Hollingsworth, M., Jones, A.W.
author_facet Gilfillan, A.M., Hollingsworth, M., Jones, A.W., Gilfillan, A.M., Hollingsworth, M., Jones, A.W.
author_sort gilfillan, a.m.
container_issue 2
container_start_page 363
container_title British Journal of Pharmacology
container_volume 79
description <jats:p><jats:list list-type="explicit-label"> <jats:list-item><jats:p>Lung slices from adult rats incubated in [methyl‐<jats:sup>3</jats:sup>H]‐choline chloride formed [<jats:sup>3</jats:sup>H]‐disaturated phosphatidylcholine ([<jats:sup>3</jats:sup>H]‐DSPC) which was used as an index of lung surfactant.</jats:p></jats:list-item> <jats:list-item><jats:p>The slices were perifused after 3 h incubation in [methyl‐<jats:sup>3</jats:sup>H]‐choline chloride and the overflow of [<jats:sup>3</jats:sup>H]‐DSPC, as a rate coefficient, was used as a measure of surfactant secretion. The basal overflow of [<jats:sup>3</jats:sup>H]‐DSPC rapidly declined over the first 30 min of perifusion and then declined slowly.</jats:p></jats:list-item> <jats:list-item><jats:p>Salbutamol induced a prolonged, and sometimes delayed, increase in [<jats:sup>3</jats:sup>H]‐DSPC overflow, which was reduced by (±)‐propranolol. Potassium chloride produced an immediate, and usually transient, increase in [<jats:sup>3</jats:sup>H]‐DSPC overflow which was not modified by atropine or (±)‐propranolol. Adenosine 5′‐triphosphate, but not phenylephrine, also increased [<jats:sup>3</jats:sup>H]‐DSPC overflow.</jats:p></jats:list-item> <jats:list-item><jats:p>This method can measure the magnitude and time‐course of lung surfactant secretion induced by drugs.</jats:p></jats:list-item> </jats:list></jats:p>
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spelling Gilfillan, A.M. Hollingsworth, M. Jones, A.W. 0007-1188 1476-5381 Wiley Pharmacology http://dx.doi.org/10.1111/j.1476-5381.1983.tb11008.x <jats:p><jats:list list-type="explicit-label"> <jats:list-item><jats:p>Lung slices from adult rats incubated in [methyl‐<jats:sup>3</jats:sup>H]‐choline chloride formed [<jats:sup>3</jats:sup>H]‐disaturated phosphatidylcholine ([<jats:sup>3</jats:sup>H]‐DSPC) which was used as an index of lung surfactant.</jats:p></jats:list-item> <jats:list-item><jats:p>The slices were perifused after 3 h incubation in [methyl‐<jats:sup>3</jats:sup>H]‐choline chloride and the overflow of [<jats:sup>3</jats:sup>H]‐DSPC, as a rate coefficient, was used as a measure of surfactant secretion. The basal overflow of [<jats:sup>3</jats:sup>H]‐DSPC rapidly declined over the first 30 min of perifusion and then declined slowly.</jats:p></jats:list-item> <jats:list-item><jats:p>Salbutamol induced a prolonged, and sometimes delayed, increase in [<jats:sup>3</jats:sup>H]‐DSPC overflow, which was reduced by (±)‐propranolol. Potassium chloride produced an immediate, and usually transient, increase in [<jats:sup>3</jats:sup>H]‐DSPC overflow which was not modified by atropine or (±)‐propranolol. Adenosine 5′‐triphosphate, but not phenylephrine, also increased [<jats:sup>3</jats:sup>H]‐DSPC overflow.</jats:p></jats:list-item> <jats:list-item><jats:p>This method can measure the magnitude and time‐course of lung surfactant secretion induced by drugs.</jats:p></jats:list-item> </jats:list></jats:p> The pharmacological modulation of [<sup>3</sup>H]‐disaturated phosphatidylcholine overflow from perifused lung slices of adult rats: a new method for the study of lung surfactant secretion British Journal of Pharmacology
spellingShingle Gilfillan, A.M., Hollingsworth, M., Jones, A.W., British Journal of Pharmacology, The pharmacological modulation of [3H]‐disaturated phosphatidylcholine overflow from perifused lung slices of adult rats: a new method for the study of lung surfactant secretion, Pharmacology
title The pharmacological modulation of [3H]‐disaturated phosphatidylcholine overflow from perifused lung slices of adult rats: a new method for the study of lung surfactant secretion
title_full The pharmacological modulation of [3H]‐disaturated phosphatidylcholine overflow from perifused lung slices of adult rats: a new method for the study of lung surfactant secretion
title_fullStr The pharmacological modulation of [3H]‐disaturated phosphatidylcholine overflow from perifused lung slices of adult rats: a new method for the study of lung surfactant secretion
title_full_unstemmed The pharmacological modulation of [3H]‐disaturated phosphatidylcholine overflow from perifused lung slices of adult rats: a new method for the study of lung surfactant secretion
title_short The pharmacological modulation of [3H]‐disaturated phosphatidylcholine overflow from perifused lung slices of adult rats: a new method for the study of lung surfactant secretion
title_sort the pharmacological modulation of [<sup>3</sup>h]‐disaturated phosphatidylcholine overflow from perifused lung slices of adult rats: a new method for the study of lung surfactant secretion
title_unstemmed The pharmacological modulation of [3H]‐disaturated phosphatidylcholine overflow from perifused lung slices of adult rats: a new method for the study of lung surfactant secretion
topic Pharmacology
url http://dx.doi.org/10.1111/j.1476-5381.1983.tb11008.x