Literature DB >> 35367225

Metformin to treat Huntington disease: A pleiotropic drug against a multi-system disorder.

C Trujillo-Del Río1, J Tortajada-Pérez1, A P Gómez-Escribano2, F Casterá3, C Peiró3, J M Millán2, M J Herrero4, R P Vázquez-Manrique5.   

Abstract

Huntington disease (HD) is a neurodegenerative disorder produced by an expansion of CAG repeats in the HTT gene. Patients of HD show involuntary movements, cognitive decline and psychiatric impairment. People carrying abnormally long expansions of CAGs (more than 35 CAG repeats) produce mutant huntingtin (mHtt), which encodes tracks of polyglutamines (polyQs). These polyQs make the protein prone to aggregate and cause it to acquire a toxic gain of function. Principally affecting the frontal cortex and the striatum, mHtt disrupts many cellular functions. In addition, this protein is expressed ubiquitously, and some reports show that many other cell types are affected by the toxicity of mHtt. Several studies reported that metformin, a widely-used anti-diabetic drug, is neuroprotective in models of HD. Here, we provide a review of the benefits of this substance to treat HD. Metformin is a pleiotropic drug, modulating different targets such as AMPK, insulin signalling and many others. These molecules regulate autophagy, chaperone expression, and more, which in turn reduce mHtt toxicity. Moreover, metformin alters gut microbiome and its metabolic processes. The study of potential targets, interactions between the drug, host and microbiome, or genomic and pharmacogenomic approaches may allow us to design personalised medicine to treat HD.
Copyright © 2022 Elsevier B.V. All rights reserved.

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Keywords:  AMPK; Gut microbiome; Huntington disease; Metformin; Pharmacogenetics; Pleiotropic effects

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Year:  2022        PMID: 35367225     DOI: 10.1016/j.mad.2022.111670

Source DB:  PubMed          Journal:  Mech Ageing Dev        ISSN: 0047-6374            Impact factor:   5.432


  1 in total

1.  Mn(II) Quinoline Complex (4QMn) Restores Proteostasis and Reduces Toxicity in Experimental Models of Huntington's Disease.

Authors:  Marián Merino; María Dolores Sequedo; Ana Virginia Sánchez-Sánchez; Mª Paz Clares; Enrique García-España; Rafael P Vázquez-Manrique; José L Mullor
Journal:  Int J Mol Sci       Date:  2022-08-11       Impact factor: 6.208

  1 in total

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