Abstract

In this review are described the preclinical and clinical pharmacological data as well as new therapeutic indications for the use of 4-aminopyridine. 4-aminopyridine is a potassium (K+) channel blocker that has a long history and various application areas. It is a chemical agent developed in 1963 as a bird poison. The first approval for clinical application of 4-aminopyridine was in 70’s in Bulgaria, since anesthetists in that country have confirmed its effect as reversal agent for nondepolarizing myorelaxants. The Bulgarian pharmaceutical company Sopharma commersialized 4-aminopyridine under the trade name Pymadin. Since then 4-aminopyridine was extensively studied and in 2010 is approved in the USA for the treatment of walking disabilities in patients with multiple sclerosis. In recent years, data from clinical trials indicated that K-channel blockade may prove to be an appropriate strategy to overcome disturbances in nerve impulses conduction associated with demyelination of the central nervous system.

Highlights

  • Multiple sclerosis (MS) is the most frequent cause of neurological deficit in young adults (Solari et al 2002)

  • There is no effective cure for MS, but there are available therapies approved for reduction of the symptoms and progression of the disease

  • Some of the pharmacological effects of aminopyridines have been known for many years, but only since Bulgarian pharmacologists and anesthetists, based on their experimental and clinical studies, recommended the use of 4-aminopyridine hydrochloride (Pymadin, Sopharma, Bulgaria) for facilitation of neuromuscular transmission

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Summary

Research Article

4-aminopyridine – the new old drug for the treatment of neurodegenerative diseases. Citation: Kostadinova I, Danchev N (2019) Evaluation of kidney function parameters in diabetic rats following virgin coconut oil diet. 4-aminopyridine – the new old drug for the treatment of neurodegenerative diseases

Introduction
Chemical properties
Single dose toxicity
Preclinical pharmacology
Effects on neuromuscular transmission
Clinical trials
Pharmacokinetic properties in humans
Pharmacokinetic data for special populations
Interaction with other medicinal products and other forms of interaction
Findings
Conclusion
Full Text
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