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Oral batyl alcohol supplementation rescues decreased cardiac conduction in ether phospholipid-deficient mice.

Authors :
Todt H
Dorninger F
Rothauer PJ
Fischer CM
Schranz M
Bruegger B
Lüchtenborg C
Ebner J
Hilber K
Koenig X
Erdem FA
Gawali VS
Berger J
Source :
Journal of inherited metabolic disease [J Inherit Metab Dis] 2020 Sep; Vol. 43 (5), pp. 1046-1055. Date of Electronic Publication: 2020 Jun 05.
Publication Year :
2020

Abstract

Plasmalogens (Pls) are a class of membrane phospholipids which serve a number of essential biological functions. Deficiency of Pls is associated with common disorders such as Alzheimer's disease or ischemic heart disease. A complete lack of Pls due to genetically determined defective biosynthesis gives rise to rhizomelic chondrodysplasia punctata (RCDP), characterized by a number of severe disabling pathologic features and death in early childhood. Frequent cardiac manifestations of RCDP include septal defects, mitral valve prolapse, and patent ductus arteriosus. In a mouse model of RCDP, reduced nerve conduction velocity was partially rescued by dietary oral supplementation of the Pls precursor batyl alcohol (BA). Here, we examine the impact of Pls deficiency on cardiac impulse conduction in a similar mouse model (Gnpat KO). In-vivo electrocardiographic recordings showed that the duration of the QRS complex was significantly longer in Gnpat KO mice than in age- and sex-matched wild-type animals, indicative of reduced cardiac conduction velocity. Oral supplementation of BA for 2 months resulted in normalization of cardiac Pls levels and of the QRS duration in Gnpat KO mice but not in untreated animals. BA treatment had no effect on the QRS duration in age-matched wild-type mice. These data suggest that Pls deficiency is associated with increased ventricular conduction time which can be rescued by oral BA supplementation.<br /> (© 2020 The Authors. Journal of Inherited Metabolic Disease published by John Wiley & Sons Ltd on behalf of SSIEM.)

Details

Language :
English
ISSN :
1573-2665
Volume :
43
Issue :
5
Database :
MEDLINE
Journal :
Journal of inherited metabolic disease
Publication Type :
Academic Journal
Accession number :
32441337
Full Text :
https://doi.org/10.1002/jimd.12264