Literature DB >> 7397111

Electrogenic epinephrine transport in chromaffin granule ghosts.

J Knoth, K Handloser, D Njus.   

Abstract

An ATP-dependent proton pump drives epinephrine transport in chromaffin granule ghosts. When ghosts are suspended in a medium free of permeant anions, ATP addition leads to an increase in membrane potential (interior positive) and epinephrine uptake but not to a change in intravesicular pH. Since ATP does not affect the pH gradient, the energy for transport must be drawn from the membrane potential (delta psi), and epinephrine uptake must result in a net efflux of positive charge. This can be achieved by an antiport (exchange diffusion) mechanism in which each catecholamine cation is taken up in exchange for more than one H+. Measurements indicate that the stoichiometry is close to 2 H+/epinephrine cation, so the equilibrium epinephrine gradient is theoretically [E]in/[E]out = ([H+]in/[H+]out)2eFdelta psi/(RT). In deenergized ghosts, the epinephrine concentration gradient equals the [H+] gradient. This is consistent with a situation in which the H+ concentration gradient is in equilibrium with the membrane potential as described by the Nernst equation. Then, in the equation above, the membrane potential term (eFdelta psi/(RT)) will exactly cancel one power of the [H+] gradient, leaving [E]in/[E]out equal to [H+]in/[H+]out.

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Year:  1980        PMID: 7397111     DOI: 10.1021/bi00554a019

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  7 in total

Review 1.  A molecular description of nerve terminal function.

Authors:  L F Reichardt; R B Kelly
Journal:  Annu Rev Biochem       Date:  1983       Impact factor: 23.643

2.  Uptake of norepinephrine and related catecholamines by cultured chromaffin cells: characterization of cocaine-sensitive and -insensitive plasma membrane transport sites.

Authors:  D K Banerjee; R A Lutz; M A Levine; D Rodbard; H B Pollard
Journal:  Proc Natl Acad Sci U S A       Date:  1987-04       Impact factor: 11.205

3.  Does the carrier of chromaffin granules transport the protonated or the uncharged species of catecholamines?

Authors:  G Kobold; R Langer; A Burger
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1985-11       Impact factor: 3.000

4.  Characterization of the monoamine carrier of chromaffin granule membrane by binding of [2-3H]dihydrotetrabenazine.

Authors:  D Scherman; P Jaudon; J P Henry
Journal:  Proc Natl Acad Sci U S A       Date:  1983-01       Impact factor: 11.205

5.  Chemical evidence that catecholamines are transported across the chromaffin granule membrane as noncationic species.

Authors:  A Ramu; M Levine; H Pollard
Journal:  Proc Natl Acad Sci U S A       Date:  1983-04       Impact factor: 11.205

6.  Alternative modes of enkephalin biosynthesis regulation by reserpine and cyclic AMP in cultured chromaffin cells.

Authors:  L E Eiden; P Giraud; H U Affolter; E Herbert; A J Hotchkiss
Journal:  Proc Natl Acad Sci U S A       Date:  1984-07       Impact factor: 11.205

7.  Effects of changes in osmolality on the stability and function of cultured chromaffin cells and the possible role of osmotic forces in exocytosis.

Authors:  R Y Hampton; R W Holz
Journal:  J Cell Biol       Date:  1983-04       Impact factor: 10.539

  7 in total

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