Wednesday, January 08, 2020

Researchers discover a way to restore strength of cardiac muscles in aging fruit flies

Researchers may have discovered a way to turn back the clock on aging heart muscles in fruit flies, a development that could lead to new therapies for older humans with heart disease.

Hua Bai, an assistant professor of genetics, development and cell biology at Iowa State University, led a study, published recently in the academic journal Autophagy, that explores the genetic mechanism that causes fly cardiac muscles to deteriorate with age. Bai said the research team restored much of the cardiac function in middle-aged flies, which experience many of the same heart maladies as middle-aged humans.

The researchers' approach starts with autophagy, a cellular "cleanup process" that removes and recycles damaged proteins and organelles. The autophagy process slows with age, which can lead to the weakening of cardiac muscles. Bai's research team looked at a key genetic pathway conserved in virtually all organisms on Earth related to autophagy that balances organism growth with nutrient intake. This pathway, called mechanistic target of rapamycin (or mTOR), has long been linked to tissue aging, Bai said. One of two complexes that underlie the mTOR pathway, referred to as mTORC2, decreases with age as autophagy declines. But the researchers found that transgenically boosting mTORC2 strengthens heart muscles of older fruit flies.
"Boosting the complex almost fully restored heart function," Bai said.


Implications for treatment in humans
The discovery that enhancing mTORC2 slows the decline of the critical autophagy process could have big implications for how doctors treat patients with heart disease, one of the leading causes of the death in the United States. While flies and humans might seem to be worlds apart evolutionarily, Bai said the two species' hearts age in a similar fashion. By middle age, cardiac muscles in both species tend to contract with less strength and regularity.

The fly model can be useful for developing drug target discoveries that could have a big impact on human health."     Hua Bai, assistant professor of genetics, development and cell biology at Iowa State University

The researchers arrived at their conclusions after conducting thousands of video recordings on cardiac muscles in fruit flies of various ages. High-resolution, high-speed cameras measured the activity of the flies' cardiac muscles. The experiments showed that boosting mTORC2 could restore a five-to-six-week-old fly's heart function to that of a fly between one and two weeks old. That's like restoring a middle-aged heart to how it functioned during young adulthood, Bai said.

Because flies live only between two and three months, it's much easier for scientists to study aging and longevity in flies than in more long-lived species, he said. And the ability to manipulate the fly genome also makes them ideal for genetic study and a common model organism, he said.



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Sunday, January 07, 2018

Diabetics with excess fat around heart at increased risk of heart failure

A team of researchers has revealed that excess fat around the heart can increase the risk of heart failure in people with diabetes by two to five times.

According to the researchers, excess fat in the heart, may contribute to the two- to five-fold increased risk of heart failure in people with diabetes. The heart is the most energy-hungry organ in the body. Just like a combustion engine burning fuel to power the pistons, healthy heart cells consume fuel molecules to create the necessary energy to keep the heart pumping.
 
This essential energy production takes place inside mitochondria, the self-contained 'powerplant' organelles inside cells. Diabetes, however, reduces the heart muscle's metabolic adaptability and causes heart cells to overuse fat as a metabolic fuel.

The study found that this cardiac lipid overload leads to numerous small, misshapen mitochondria that don't produce energy as efficiently as normal mitochondria. Previous research suggested that problems with mitochondrial energy production may play a role in heart failure associated with diabetes.

Lead study author said, "Diabetes, significantly increases the risk of heart failure, and one of the cardinal manifestations of the hearts of people with diabetes is the tendency to overuse fat as a metabolic fuel, which ultimately leads to mitochondrial and cardiac damage".

The team used genetically modified mice that mimic the increased fatty acid uptake (lipid overload) that characterizes diabetes to investigate the consequences of cardiac lipid overload on mitochondria. In the mouse model, lipid uptake to heart is doubled. This modest increase resulted in mitochondria that became thinner and more twisted than mitochondria in healthy heart cells.

These structural changes (almost like a noodle snaking through the heart) lead to an appearance of mitochondrial fragmentation when imaged by conventional electron microscopy. The study also revealed the molecular cause of the change in mitochondrial structure.

Prolonged lipid overload leads to increased levels of damaging substances called reactive oxygen species (ROS). The findings suggest that cardiac lipid overload disrupts normal mitochondrial structure, which may impair energy production and compromise heart function.

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