Getting To The Heart Of Congenital Heart Disease

The acetylation of metabolic enzymes plays a key role in regulating heart muscle development in newborns, study says.

AsianScientist (Jun. 26, 2018) – Scientists in Japan and Canada have identified a metabolic pathway that is dysregulated in the hearts of newborns with congenital heart disease. They published their findings in the Journal of Clinical Investigation Insight.

Before birth, cardiac muscle cells use energy generated by breaking down glucose. Immediately after birth, they rapidly switch to breaking down fatty acids. This switch is hindered in hypertrophied newborn hearts.

To understand how this switch from glucose to fatty acids is regulated, Hokkaido University cardiologist Dr. Arata Fukushima, along with a team of University of Alberta scientists led by Dr. Gary Lopaschuk, examined the heart tissue of 84 newborns who had undergone surgery for congenital heart disease. Many patients with the disease develop thickened heart walls, or hypertrophy, which can lead to fatal heart failure even after the surgery.

Fukushima and his team compared the biopsy samples taken from normal and hypertrophied right ventricular walls. They found that two enzymes involved in fatty acid breakdown, called LCAD and βHAD, were hyperacetylated in normal right ventricles. This means that large amounts of acetyl groups were added to the enzyme proteins, increasing their activity levels. This, in turn, led to increased fatty acid metabolism.

In hypertrophied hearts, these two enzymes were not hyperacetylated, leading to reduced fatty acid metabolism in these newborns. The team detected reduced activity of an acetylation-promoting gene, called gcn5l1, in hypertrophied hearts.

When the team experimented on cultured hypertrophy-like cardiac muscle cells, they found that turning off the gcn5l1 gene led to decreased acetylation of LCAD and βHAD. This, in turn, reduced fatty acid oxidation in the cells. Moreover, the cells lacking gcn5l1 formed thicker muscle fibers compared to normal cells.

“Our findings show that acetylation of metabolic enzymes plays an important role in controlling the dramatic changes in energy metabolism that occur in newborn hearts immediately after birth,” said Fukushima.

“The findings also show how hypertrophy can perturb this process by delaying the maturation of fatty acid metabolism, which compromises the ability of the newborn heart to generate energy. Developing drugs that enhance acetylation of the metabolic enzymes could help treat patients with hypertrophy.”

The article can be found at: Fukushima et al. (2018) Acetylation Contributes to Hypertrophy-caused Maturational Delay of Cardiac Energy Metabolism.


Source: Hokkaido University; Photo: Shutterstock.
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