author_facet Chan, Y. L.
Malnic, G.
Giebisch, G.
Chan, Y. L.
Malnic, G.
Giebisch, G.
author Chan, Y. L.
Malnic, G.
Giebisch, G.
spellingShingle Chan, Y. L.
Malnic, G.
Giebisch, G.
American Journal of Physiology-Renal Physiology
Passive driving forces of proximal tubular fluid and bicarbonate transport: gradient dependence of H+ secretion
Physiology
author_sort chan, y. l.
spelling Chan, Y. L. Malnic, G. Giebisch, G. 1931-857X 1522-1466 American Physiological Society Physiology http://dx.doi.org/10.1152/ajprenal.1983.245.5.f622 <jats:p> The effect of oncotic pressure changes on fluid (Jv) and net bicarbonate transport (JHCO-3) and the transepithelial bicarbonate permeability (PHCO-3) were measured by an improved luminal and capillary microperfusion method that allows paired experiments on the same tubule. Rat proximal tubules were pump-perfused and Jv and [HCO-3] measured with [14C]inulin and a pH glass electrode. Raising peritubular protein (0-8-15 g/100 ml bovine serum albumin) stimulated Jv and HCO-3 reabsorption. The response to oncotic pressure changes was asymmetrical since changes of the luminal protein concentration had no significant effects. Whereas transepithelial solvent drag effects on HCO-3 must be minimal, peritubular protein most likely stimulates translocation of fluid and bicarbonate from intercellular spaces into peritubular capillaries. PHCO-3 was measured from HCO-3 net flux along a lumen-to-capillary-directed electrochemical potential gradient. In these experiments active H+ transport and Jv were minimized by 10(-4) M acetazolamide and luminal raffinose. PHCO-3 was 1.77 X 10(-5) cm X s-1 and was unaffected by increasing luminal flow rate from 10 to 45 nl X min-1. Since bicarbonate backflux is only a small fraction of physiological rates of JHCO-3, net transport alterations at varying [HCO-3] in the lumen must be due to changes in active HCO-3 (H+) transport. Thus, active H+ ion secretion across the luminal membrane of the proximal tubule is gradient dependent. </jats:p> Passive driving forces of proximal tubular fluid and bicarbonate transport: gradient dependence of H+ secretion American Journal of Physiology-Renal Physiology
doi_str_mv 10.1152/ajprenal.1983.245.5.f622
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series American Journal of Physiology-Renal Physiology
source_id 49
title Passive driving forces of proximal tubular fluid and bicarbonate transport: gradient dependence of H+ secretion
title_unstemmed Passive driving forces of proximal tubular fluid and bicarbonate transport: gradient dependence of H+ secretion
title_full Passive driving forces of proximal tubular fluid and bicarbonate transport: gradient dependence of H+ secretion
title_fullStr Passive driving forces of proximal tubular fluid and bicarbonate transport: gradient dependence of H+ secretion
title_full_unstemmed Passive driving forces of proximal tubular fluid and bicarbonate transport: gradient dependence of H+ secretion
title_short Passive driving forces of proximal tubular fluid and bicarbonate transport: gradient dependence of H+ secretion
title_sort passive driving forces of proximal tubular fluid and bicarbonate transport: gradient dependence of h+ secretion
topic Physiology
url http://dx.doi.org/10.1152/ajprenal.1983.245.5.f622
publishDate 1983
physical F622-F633
description <jats:p> The effect of oncotic pressure changes on fluid (Jv) and net bicarbonate transport (JHCO-3) and the transepithelial bicarbonate permeability (PHCO-3) were measured by an improved luminal and capillary microperfusion method that allows paired experiments on the same tubule. Rat proximal tubules were pump-perfused and Jv and [HCO-3] measured with [14C]inulin and a pH glass electrode. Raising peritubular protein (0-8-15 g/100 ml bovine serum albumin) stimulated Jv and HCO-3 reabsorption. The response to oncotic pressure changes was asymmetrical since changes of the luminal protein concentration had no significant effects. Whereas transepithelial solvent drag effects on HCO-3 must be minimal, peritubular protein most likely stimulates translocation of fluid and bicarbonate from intercellular spaces into peritubular capillaries. PHCO-3 was measured from HCO-3 net flux along a lumen-to-capillary-directed electrochemical potential gradient. In these experiments active H+ transport and Jv were minimized by 10(-4) M acetazolamide and luminal raffinose. PHCO-3 was 1.77 X 10(-5) cm X s-1 and was unaffected by increasing luminal flow rate from 10 to 45 nl X min-1. Since bicarbonate backflux is only a small fraction of physiological rates of JHCO-3, net transport alterations at varying [HCO-3] in the lumen must be due to changes in active HCO-3 (H+) transport. Thus, active H+ ion secretion across the luminal membrane of the proximal tubule is gradient dependent. </jats:p>
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author Chan, Y. L., Malnic, G., Giebisch, G.
author_facet Chan, Y. L., Malnic, G., Giebisch, G., Chan, Y. L., Malnic, G., Giebisch, G.
author_sort chan, y. l.
container_issue 5
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container_title American Journal of Physiology-Renal Physiology
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description <jats:p> The effect of oncotic pressure changes on fluid (Jv) and net bicarbonate transport (JHCO-3) and the transepithelial bicarbonate permeability (PHCO-3) were measured by an improved luminal and capillary microperfusion method that allows paired experiments on the same tubule. Rat proximal tubules were pump-perfused and Jv and [HCO-3] measured with [14C]inulin and a pH glass electrode. Raising peritubular protein (0-8-15 g/100 ml bovine serum albumin) stimulated Jv and HCO-3 reabsorption. The response to oncotic pressure changes was asymmetrical since changes of the luminal protein concentration had no significant effects. Whereas transepithelial solvent drag effects on HCO-3 must be minimal, peritubular protein most likely stimulates translocation of fluid and bicarbonate from intercellular spaces into peritubular capillaries. PHCO-3 was measured from HCO-3 net flux along a lumen-to-capillary-directed electrochemical potential gradient. In these experiments active H+ transport and Jv were minimized by 10(-4) M acetazolamide and luminal raffinose. PHCO-3 was 1.77 X 10(-5) cm X s-1 and was unaffected by increasing luminal flow rate from 10 to 45 nl X min-1. Since bicarbonate backflux is only a small fraction of physiological rates of JHCO-3, net transport alterations at varying [HCO-3] in the lumen must be due to changes in active HCO-3 (H+) transport. Thus, active H+ ion secretion across the luminal membrane of the proximal tubule is gradient dependent. </jats:p>
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spelling Chan, Y. L. Malnic, G. Giebisch, G. 1931-857X 1522-1466 American Physiological Society Physiology http://dx.doi.org/10.1152/ajprenal.1983.245.5.f622 <jats:p> The effect of oncotic pressure changes on fluid (Jv) and net bicarbonate transport (JHCO-3) and the transepithelial bicarbonate permeability (PHCO-3) were measured by an improved luminal and capillary microperfusion method that allows paired experiments on the same tubule. Rat proximal tubules were pump-perfused and Jv and [HCO-3] measured with [14C]inulin and a pH glass electrode. Raising peritubular protein (0-8-15 g/100 ml bovine serum albumin) stimulated Jv and HCO-3 reabsorption. The response to oncotic pressure changes was asymmetrical since changes of the luminal protein concentration had no significant effects. Whereas transepithelial solvent drag effects on HCO-3 must be minimal, peritubular protein most likely stimulates translocation of fluid and bicarbonate from intercellular spaces into peritubular capillaries. PHCO-3 was measured from HCO-3 net flux along a lumen-to-capillary-directed electrochemical potential gradient. In these experiments active H+ transport and Jv were minimized by 10(-4) M acetazolamide and luminal raffinose. PHCO-3 was 1.77 X 10(-5) cm X s-1 and was unaffected by increasing luminal flow rate from 10 to 45 nl X min-1. Since bicarbonate backflux is only a small fraction of physiological rates of JHCO-3, net transport alterations at varying [HCO-3] in the lumen must be due to changes in active HCO-3 (H+) transport. Thus, active H+ ion secretion across the luminal membrane of the proximal tubule is gradient dependent. </jats:p> Passive driving forces of proximal tubular fluid and bicarbonate transport: gradient dependence of H+ secretion American Journal of Physiology-Renal Physiology
spellingShingle Chan, Y. L., Malnic, G., Giebisch, G., American Journal of Physiology-Renal Physiology, Passive driving forces of proximal tubular fluid and bicarbonate transport: gradient dependence of H+ secretion, Physiology
title Passive driving forces of proximal tubular fluid and bicarbonate transport: gradient dependence of H+ secretion
title_full Passive driving forces of proximal tubular fluid and bicarbonate transport: gradient dependence of H+ secretion
title_fullStr Passive driving forces of proximal tubular fluid and bicarbonate transport: gradient dependence of H+ secretion
title_full_unstemmed Passive driving forces of proximal tubular fluid and bicarbonate transport: gradient dependence of H+ secretion
title_short Passive driving forces of proximal tubular fluid and bicarbonate transport: gradient dependence of H+ secretion
title_sort passive driving forces of proximal tubular fluid and bicarbonate transport: gradient dependence of h+ secretion
title_unstemmed Passive driving forces of proximal tubular fluid and bicarbonate transport: gradient dependence of H+ secretion
topic Physiology
url http://dx.doi.org/10.1152/ajprenal.1983.245.5.f622