Is the mechanism of nitroglycerin tolerance associated with aldehyde dehydrogenase activity? A contribution to the ongoing discussion.
Journal
Acta biochimica Polonica
ISSN: 1734-154X
Titre abrégé: Acta Biochim Pol
Pays: Poland
ID NLM: 14520300R
Informations de publication
Date de publication:
28 Dec 2019
28 Dec 2019
Historique:
received:
08
11
2019
accepted:
16
12
2019
pubmed:
29
12
2019
medline:
19
5
2020
entrez:
29
12
2019
Statut:
ppublish
Résumé
The aim of the study presented here was an attempt to answer the question posed in the title: Is the mechanism of nitroglycerin tolerance associated with aldehyde dehydrogenase (ALDH) activity? Here, we investigated the effect of administration (separately or jointly) of lipoic acid (LA), nitroglycerin (GTN), and disulfiram (DSF; an irreversible in vivo inhibitor of all ALDH isozymes (including ALDH2)), on the development of tolerance to GTN. We also assessed the total activity of ALDH in the rat liver homogenates. Our data revealed that not only DSF and GTN inhibited the total ALDH activity in the rat liver, but LA also proved to be an inhibitor of this enzyme. At the same time, the obtained results demonstrated that the GTN tolerance did not develop in GTN, DSF and LA jointly treated rats, but did develop in GTN and DSF jointly treated rats. This means that the ability of LA to prevent GTN tolerance is not associated with the total ALDH activity in the rat liver. In this context, the fact that animals jointly receiving GTN and DSF developed tolerance to GTN, and in animals that in addition to GTN and DSF also received LA such tolerance did not develop, is - in our opinion - a sufficient premise to conclude that the nitrate tolerance certainly is not caused by a decrease in the activity of any of the ALDH isoenzymes present in the rat liver, including ALDH2. However, many questions still await an answer, including the basic one: What is the mechanism of tolerance to nitroglycerin?
Identifiants
pubmed: 31883320
pii: 2908
doi: 10.18388/abp.2019_2908
doi:
Substances chimiques
Thioctic Acid
73Y7P0K73Y
Aldehyde Dehydrogenase 1 Family
EC 1.2.1
Aldehyde Dehydrogenase, Mitochondrial
EC 1.2.1.3
Aldh2 protein, rat
EC 1.2.1.3
Aldh1a1 protein, rat
EC 1.2.1.36
Nitroglycerin
G59M7S0WS3
Disulfiram
TR3MLJ1UAI
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM