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Pharmacological Modulation and (Patho)Physiological Roles of TRPM4 Channel-Part 1: Modulation of TRPM4.

Authors :
Kovács ZM
Dienes C
Hézső T
Almássy J
Magyar J
Bányász T
Nánási PP
Horváth B
Szentandrássy N
Source :
Pharmaceuticals (Basel, Switzerland) [Pharmaceuticals (Basel)] 2022 Jan 10; Vol. 15 (1). Date of Electronic Publication: 2022 Jan 10.
Publication Year :
2022

Abstract

Transient receptor potential melastatin 4 is a unique member of the TRPM protein family and, similarly to TRPM5, is Ca <superscript>2+</superscript> -sensitive and permeable to monovalent but not divalent cations. It is widely expressed in many organs and is involved in several functions by regulating the membrane potential and Ca <superscript>2+</superscript> homeostasis in both excitable and non-excitable cells. This part of the review discusses the pharmacological modulation of TRPM4 by listing, comparing, and describing both endogenous and exogenous activators and inhibitors of the ion channel. Moreover, other strategies used to study TRPM4 functions are listed and described. These strategies include siRNA-mediated silencing of TRPM4, dominant-negative TRPM4 variants, and anti-TRPM4 antibodies. TRPM4 is receiving more and more attention and is likely to be the topic of research in the future.

Details

Language :
English
ISSN :
1424-8247
Volume :
15
Issue :
1
Database :
MEDLINE
Journal :
Pharmaceuticals (Basel, Switzerland)
Publication Type :
Academic Journal
Accession number :
35056138
Full Text :
https://doi.org/10.3390/ph15010081