Abstract

Background: Besides its well-known role as a peripheral chemical mediator of immune, vascular, and cellular responses, histamine plays major roles in the central nervous system, particularly in the mediation of arousal and cognition-enhancement. These central effects are mediated by the histamine-3 auto receptors, the modulation of which is thought to be beneficial for the treatment of disorders that impair cognition or manifest with excessive daytime sleepiness. Methods: A database search of PubMed, Google Scholar, and clinicaltrials.gov was performed in June 2020. Full-text articles were screened and reviewed to provide an update on pitolisant and other histamine-3 receptor antagonists. Results: A new class of drugs—histamine-3 receptor antagonists—has emerged with the approval of pitolisant for the treatment of narcolepsy with or without cataplexy. At the recommended dose, pitolisant is well tolerated and effective. It has also been evaluated for potential therapeutic benefit in Parkinson disease, epilepsy, attention deficit hyperactivity disorder, Alzheimer’s disease, and dementia. Limited studies have shown pitolisant to lack abuse potential which will be a major advantage over existing drug options for narcolepsy. Several histamine-3 receptor antagonists are currently in development for a variety of clinical indications. Conclusions: Although limited clinical studies have been conducted on this new class of drugs, the reviewed literature showed promising results for future additions to the clinical indications of pitolisant, and the expansion of the list of approved drugs in this class for a variety of indications.

Highlights

  • Histamine (2-(imidazol-4-yl) ethylamine), an endogenous monoamine, is one of the most studied chemical mediators in the biological systems involved in various physiological and pathological processes including cell proliferation and differentiation, tissues regeneration, wound healing, and immunomodulation [1,2,3]

  • The aim of the current review is to provide an update on histamine-3 receptor (H3R) receptor antagonists including pitolisant, which have been approved for clinical use, and others in development

  • Since the discovery of HR3, several studies have explored the clinical significance of its modulation with drugs

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Summary

Introduction

Histamine (2-(imidazol-4-yl) ethylamine), an endogenous monoamine, is one of the most studied chemical mediators in the biological systems involved in various physiological and pathological processes including cell proliferation and differentiation, tissues regeneration, wound healing, and immunomodulation [1,2,3]. Besides its well-known role as a peripheral chemical mediator of immune, vascular, and cellular responses, histamine plays major roles in the central nervous system, in the mediation of arousal and cognition-enhancement. These central effects are mediated by the histamine-3 auto receptors, the modulation of which is thought to be beneficial for the treatment of disorders that impair cognition or manifest with excessive daytime sleepiness. Conclusions: limited clinical studies have been conducted on this new class of drugs, the reviewed literature showed promising results for future additions to the clinical indications of pitolisant, and the expansion of the list of approved drugs in this class for a variety of indications

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