Bimoclomol: A nontoxic, hydroxylamine derivative with stress protein-inducing activity and cytoprotective effects View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1997-10

AUTHORS

László Vígh, Péter N. Literáti, Ibolya Horváth, Zsolt Török, Gábor Balogh, Attila Glatz, Eszter Kovács, Imre Boros, Péter Ferdinándy, Beatrix Parkas, László Jaszlits, Andrea Jednákovits, László Korányi, Bruno Maresca

ABSTRACT

Preservation of the chemical architecture of a cell or of an organism under changing and perhaps stressful conditions is termed homeostasis. An integral feature of homeostasis is the rapid expression of genes whose products are specifically dedicated to protect cellular functions against stress. One of the best known mechanisms protecting cells from various stresses is the heat-shock response which results in the induction of the synthesis of heat-shock proteins (HSPs or stress proteins)1–3. A large body of information supports that stress proteins — many of them molecular chaperones4–8 — are crucial for the maintenance of cell integrity during normal growth as well as during patho-physiological conditions9–11, and thus can be considered “homeostatic proteins.” Recently emphasis is being placed on the potential use of these proteins in preventing and/or treating diseases12–14. Therefore, it would be of great therapeutic benefit to discover compounds that are clinically safe yet able to induce the accumulation of HSPs in patients with chronic disorders such as diabetes mellitus, heart disease or kidney failure. Here we show that a novel cytoprotective hydroxylamine derivative, [2-hydroxy-3-(1-piperidinyl) propoxy]-3-pyridinecarboximidoil-chloride maleate, Bimoclomol15, facilitates the formation of chaperone molecules in eukaryotic cells by inducing or amplifying expression of heat-shock genes. The cytoprotective effects observed under several experimental conditions, including a murine model of ischemia and wound healing in the diabetic rat, are likely mediated by the coordinate expression of all major HSPs. This nontoxic drug, which is under Phase II clinical trials, has enormous potential therapeutic applications. More... »

PAGES

1150-1154

Journal

TITLE

Nature Medicine

ISSUE

10

VOLUME

3

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/nm1097-1150

DOI

http://dx.doi.org/10.1038/nm1097-1150

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1024254744

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/9334730


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