3,4-diaminopyridine reverses paralysis in botulinum neurotoxin-intoxicated diaphragms through two functionally distinct mechanisms.

Abstract

Botulinum neurotoxins (BoNTs) are exceedingly potent neurological poisons that prevent neurotransmitter release from peripheral nerve terminals by cleaving presynaptic proteins required for synaptic vesicle fusion. The ensuing neuromuscular paralysis causes death by asphyxiation. Although no antidotal treatments exist to block toxin activity within the nerve terminal, aminopyridine antagonists of voltage-gated potassium channels have been proposed as symptomatic treatments for botulism toxemia. However, clinical evaluation of aminopyridines as symptomatic treatments for botulism has been inconclusive, in part because mechanisms responsible for reversal of paralysis in BoNT-poisoned nerve terminals are not understood. Here we measured the effects of 3,4-diaminopyridine (DAP) on phrenic nerve-elicited diaphragm contraction and end-plate potentials at various times after intoxication with BoNT serotypes A, B, or E. We found that DAP-mediated increases in quantal content promote neurotransmission from intoxicated nerve terminals through two functionally distinguishable mechanisms. First, DAP increases the probability of neurotransmission at non-intoxicated release sites. This mechanism is serotype-independent, becomes less effective as nerve terminals become progressively impaired, and remains susceptible to ongoing intoxication. Second, DAP elicits persistent production of toxin-resistant endplate potentials from nerve terminals fully intoxicated by BoNT/A, but not serotypes B or E. Since this effect appears specific to BoNT/A intoxication, we propose that DAP treatment enables BoNT/A-cleaved SNAP-25 to productively engage in fusogenic release by increasing the opportunity for low-efficiency fusion events. These findings have important implications for DAP as a botulism therapeutic by defining conditions under which DAP may be clinically effective in reversing botulism symptoms.

• Authors: Aaron B Bradford, James B Machamer, Trisha M Russo, Patrick M McNutt
• Journal: Toxicology and applied pharmacology (Toxicol Appl Pharmacol) Vol. 341 Pg. 77-86 (02 15 2018) ISSN: 1096-0333 [Electronic] United States
• PMID: 29366638 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, U.S. Gov't, Non-P.H.S.)
• Copyright: Published by Elsevier Inc.

Chemical References

• Potassium Channel Blockers
• 4-Aminopyridine
• Botulinum Toxins, Type A
• Amifampridine

Topics

• 4-Aminopyridine (analogs & derivatives, pharmacology, therapeutic use)
• Amifampridine
• Animals
• Botulinum Toxins, Type A (toxicity)
• Diaphragm (drug effects, physiology)
• Male
• Mice
• Mice, Inbred C57BL
• Organ Culture Techniques
• Potassium Channel Blockers (pharmacology, therapeutic use)
• Respiratory Paralysis (chemically induced, drug therapy, physiopathology)