Figure_6.tif (550.26 kB)
Circadian desynchronization not only disrupts rhythms but also reduces the expression levels of clock and metabolic genes in the heart of C57BL/6J mice with PE-induced cardiomyopathy.
figure
posted on 2014-11-12, 03:18 authored by Akira Kohsaka, Partha Das, Izumi Hashimoto, Tomomi Nakao, Yoko Deguchi, Sabine S. Gouraud, Hidefumi Waki, Yasuteru Muragaki, Masanobu Maeda(A-C) Relative expression levels of genes regulating (A) clock machinery as well as (B) glucose and (C) lipid metabolism in heart. All heart tissues used were from PE-infused animals subjected to either a fixed or a disrupted LD cycle as described in Figure 5A (n = 4 per group per time point). To provide a 24-h overall mean expression level, the data over a 24-h time period in each group were also averaged and are expressed using a bar graph format. Data are the mean ± SEM. *P<0.05, **P<0.01, unpaired two-tailed Student's t-test.
History
Usage metrics
Categories
Keywords
Mice Cardiac functionacid oxidative pathwaymitochondrial functionMitochondrial RespirationC 57BL micemitochondrial metabolismcircadian clock gene Bmal 1 resultsgene expressiontricarboxylic acid cyclemitochondrial oxidative metabolismmitochondrial defectsBmal 1 function showcircadian rhythmicityRegulating Mitochondrial MetabolismHeart failureoxidative energyCircadian Clock Maintains Cardiac Functioncircadian clock system
Licence
Exports
RefWorks
BibTeX
Ref. manager
Endnote
DataCite
NLM
DC