Literature DB >> 6865926

Inhibition of [3H]acetylcholine active transport by tetraphenylborate and other anions.

D C Anderson, S C King, S M Parsons.   

Abstract

The effects of tetraphenylborate and other anions on the active uptake of [3H]acetylcholine by synaptic vesicles isolated from Torpedo californica electric organ were studied. Tetraphenylborate completely inhibits active uptake with a half-inhibitory concentration of 0.3 microM. Dipicrylaminate also half-inhibits at 0.3 microM, phenyldicarbaundecaborane at 14 microM, fluoride at 2 mM, thiocyanate at 3 mM, and azide at 16 mM. Tetraphenylborate had no effect on the vesicle ATPase activity or the transmembrane electric potential at low concentrations where it inhibits [3H]acetylcholine active transport. The mechanism for tetraphenylborate inhibition is uncertain, but it might be similar to that of its action as a mitochondrial uncoupler. Solubility products for the acetylcholine, choline, and potassium salts of the tetraphenylborate and dipicrylaminate anions also were measured. The inhibition results confirm the hypothesis of Marshall and Parsons [Br. J. Pharmacol. 54:333-338 (1975)] that tetraphenylborate acts on intact neuromuscular preparations to inhibit transmitter storage, and constitute new pharmacological evidence that evoked release of acetylcholine is mediated by synaptic vesicles.

Entities:  

Mesh:

Substances:

Year:  1983        PMID: 6865926

Source DB:  PubMed          Journal:  Mol Pharmacol        ISSN: 0026-895X            Impact factor:   4.436


  11 in total

1.  Accounting for the shapes and size distributions of miniature endplate currents.

Authors:  W Van der Kloot; L A Naves
Journal:  Biophys J       Date:  1996-05       Impact factor: 4.033

2.  Release of acetylcholine from embryonic myocytes in Xenopus cell cultures.

Authors:  W M Fu; H C Liou; Y H Chen; S M Wang
Journal:  J Physiol       Date:  1998-06-01       Impact factor: 5.182

3.  Activity increases quantal size at the frog neuromuscular junction.

Authors:  W Van der Kloot; T E Van der Kloot
Journal:  Experientia       Date:  1985-01-15

4.  Bromoacetylcholine and acetylcholinesterase introduced via liposomes into motor nerve endings block increases in quantal size.

Authors:  E Brailoiu; W V der Kloot
Journal:  Pflugers Arch       Date:  1996-07       Impact factor: 3.657

5.  2-(4-phenylpiperidino) cyclohexanol (AH5183) decreases quantal size at the frog neuromuscular junction.

Authors:  W Van der Kloot
Journal:  Pflugers Arch       Date:  1986-01       Impact factor: 3.657

6.  The packing of acetylcholine into quanta at the frog neuromuscular junction is inhibited by increases in intracellular sodium.

Authors:  W Van der Kloot
Journal:  Pflugers Arch       Date:  1988-08       Impact factor: 3.657

7.  Calcitonin gene-related peptide acts presynaptically to increase quantal size and output at frog neuromuscular junctions.

Authors:  W Van der Kloot; W B Benjamin; O P Balezina
Journal:  J Physiol       Date:  1998-03-15       Impact factor: 5.182

8.  The nature and origin of calcium-insensitive miniature end-plate potentials at rodent neuromuscular junctions.

Authors:  M T Lupa; N Tabti; S Thesleff; F Vyskocil; S P Yu
Journal:  J Physiol       Date:  1986-12       Impact factor: 5.182

9.  Increasing quantal size at the mouse neuromuscular junction and the role of choline.

Authors:  S P Yu; W Van der Kloot
Journal:  J Physiol       Date:  1991-02       Impact factor: 5.182

10.  Is an acetylcholine transport system responsible for nonquantal release of acetylcholine at the rodent myoneural junction?

Authors:  C Edwards; V Dolezal; S Tucek; H Zemková; F Vyskocil
Journal:  Proc Natl Acad Sci U S A       Date:  1985-05       Impact factor: 11.205

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.