Literature DB >> 33465376

A high-affinity, partial antagonist effect of 3,4-diaminopyridine mediates action potential broadening and enhancement of transmitter release at NMJs.

Kristine S Ojala1, Scott P Ginebaugh1, Man Wu1, Evan W Miller2, Gloria Ortiz2, Manuel Covarrubias3, Stephen D Meriney4.   

Abstract

3,4-Diaminopyridine (3,4-DAP) increases transmitter release from neuromuscular junctions (NMJs), and low doses of 3,4-DAP (estimated to reach ∼1 μM in serum) are the Food and Drug Administration (FDA)-approved treatment for neuromuscular weakness caused by Lambert-Eaton myasthenic syndrome. Canonically, 3,4-DAP is thought to block voltage-gated potassium (Kv) channels, resulting in prolongation of the presynaptic action potential (AP). However, recent reports have shown that low millimolar concentrations of 3,4-DAP have an off-target agonist effect on the Cav1 subtype ("L-type") of voltage-gated calcium (Cav) channels and have speculated that this agonist effect might contribute to 3,4-DAP effects on transmitter release at the NMJ. To address 3,4-DAP's mechanism(s) of action, we first used the patch-clamp electrophysiology to characterize the concentration-dependent block of 3,4-DAP on the predominant presynaptic Kv channel subtypes found at the mammalian NMJ (Kv3.3 and Kv3.4). We identified a previously unreported high-affinity (1-10 μM) partial antagonist effect of 3,4-DAP in addition to the well-known low-affinity (0.1-1 mM) antagonist activity. We also showed that 1.5-μM DAP had no effects on Cav1.2 or Cav2.1 current. Next, we used voltage imaging to show that 1.5- or 100-μM 3,4-DAP broadened the AP waveform in a dose-dependent manner, independent of Cav1 calcium channels. Finally, we demonstrated that 1.5- or 100-μM 3,4-DAP augmented transmitter release in a dose-dependent manner and this effect was also independent of Cav1 channels. From these results, we conclude that low micromolar concentrations of 3,4-DAP act solely on Kv channels to mediate AP broadening and enhance transmitter release at the NMJ.
Copyright © 2021 The Authors. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Lambert–Eaton myasthenic syndrome (LEMS); action potential (AP); neurological disease; neuromuscular junction (NMJ); neurotransmitter release; voltage-gated calcium (Cav) channel; voltage-gated potassium (Kv) channel

Mesh:

Substances:

Year:  2021        PMID: 33465376      PMCID: PMC7949096          DOI: 10.1016/j.jbc.2021.100302

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  80 in total

1.  Requirement for the synaptic protein interaction site for reconstitution of synaptic transmission by P/Q-type calcium channels.

Authors:  Sumiko Mochida; Ruth E Westenbroek; Charles T Yokoyama; Huijun Zhong; Scott J Myers; Todd Scheuer; Kanako Itoh; William A Catterall
Journal:  Proc Natl Acad Sci U S A       Date:  2003-02-24       Impact factor: 11.205

2.  Alternative splicing contributes to K+ channel diversity in the mammalian central nervous system.

Authors:  C J Luneau; J B Williams; J Marshall; E S Levitan; C Oliva; J S Smith; J Antanavage; K Folander; R B Stein; R Swanson
Journal:  Proc Natl Acad Sci U S A       Date:  1991-05-01       Impact factor: 11.205

3.  Distinct Kv channel subtypes contribute to differences in spike signaling properties in the axon initial segment and presynaptic boutons of cerebellar interneurons.

Authors:  Matthew J M Rowan; Elizabeth Tranquil; Jason M Christie
Journal:  J Neurosci       Date:  2014-05-07       Impact factor: 6.167

4.  Lambert-Eaton myasthenic syndrome IgG depletes presynaptic membrane active zone particles by antigenic modulation.

Authors:  A Nagel; A G Engel; B Lang; J Newsom-Davis; T Fukuoka
Journal:  Ann Neurol       Date:  1988-10       Impact factor: 10.422

5.  Non-linear summation of end-plate potentials in the frog and mouse.

Authors:  E M McLachlan; A R Martin
Journal:  J Physiol       Date:  1981-02       Impact factor: 5.182

6.  Rapid State-Dependent Alteration in Kv3 Channel Availability Drives Flexible Synaptic Signaling Dependent on Somatic Subthreshold Depolarization.

Authors:  Matthew J M Rowan; Jason M Christie
Journal:  Cell Rep       Date:  2017-02-21       Impact factor: 9.423

7.  4-aminopyridine in the treatment of patients with multiple sclerosis. Long-term efficacy and safety.

Authors:  C H Polman; F W Bertelsmann; A C van Loenen; J C Koetsier
Journal:  Arch Neurol       Date:  1994-03

8.  Enhanced brain motor activity in patients with MS after a single dose of 3,4-diaminopyridine.

Authors:  C Mainero; M Inghilleri; P Pantano; A Conte; D Lenzi; V Frasca; L Bozzao; C Pozzilli
Journal:  Neurology       Date:  2004-06-08       Impact factor: 9.910

9.  Effect of 3,4-diaminopyridine at the murine neuromuscular junction.

Authors:  Fiona Ng; Diana C Lee; Leah A Schrumpf; Mary E Mazurek; Victoria Lee Lo; Sharleen K Gill; Ricardo A Maselli
Journal:  Muscle Nerve       Date:  2016-08-17       Impact factor: 3.217

10.  Novel truncating RAPSN mutations causing congenital myasthenic syndrome responsive to 3,4-diaminopyridine.

Authors:  Brenda L Banwell; Kinji Ohno; Joern P Sieb; Andrew G Engel
Journal:  Neuromuscul Disord       Date:  2004-03       Impact factor: 4.296

View more
  3 in total

1.  Antidotal treatment of botulism in rats by continuous infusion with 3,4-diaminopyridine.

Authors:  James B Machamer; Edwin J Vazquez-Cintron; Sean W O'Brien; Kyle E Kelly; Amber C Altvater; Kathleen T Pagarigan; Parker B Dubee; Celinia A Ondeck; Patrick M McNutt
Journal:  Mol Med       Date:  2022-06-03       Impact factor: 6.376

Review 2.  Microphysiological Modeling of the Structure and Function of Neuromuscular Transmitter Release Sites.

Authors:  Rozita Laghaei; Stephen D Meriney
Journal:  Front Synaptic Neurosci       Date:  2022-06-13

Review 3.  Neuromuscular Active Zone Structure and Function in Healthy and Lambert-Eaton Myasthenic Syndrome States.

Authors:  Scott P Ginebaugh; Yomna Badawi; Tyler B Tarr; Stephen D Meriney
Journal:  Biomolecules       Date:  2022-05-24
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.