Physical exercise improves the elimination of toxic proteins from muscles
September 26, 2018
By André Julião | Agência FAPESP – The health benefits of physical activity are well known, but the cellular processes responsible for those benefits have begun to become clearer only relatively recently.
One such finding is the link between exercise and the prevention of muscle dysfunction. A fairly frequent type of muscle dysfunction occurs when skeletal muscle cells, which make up most of the body’s mass, stop receiving stimuli.
This happens, for example, when the sciatic nerve is injured, as it sometimes is in bus drivers, other individuals who spend long hours sitting or bedridden patients. Intervention to minimize or even reverse muscle dysfunction due to the lack of stimulus is necessary to improve the quality of life for these people.
In a study published in Scientific Reports by researchers at the University of São Paulo (USP) in Brazil, in partnership with colleagues in the United States and Norway, the lack of muscle stimulus due to a surgically induced sciatic nerve injury in rats resulted in a buildup of inadequately processed proteins in muscle cells and consequently led to muscle weakness or wasting.
The researchers found that this buildup was caused by the impairment of autophagy, the cellular machinery responsible for identifying and removing damaged proteins and toxins. They demonstrated that physical exercise can keep the autophagic system primed and facilitate its activity when necessary, as in the case of muscle dysfunction due to the lack of stimulus. The degenerative processes caused by a lack of muscle stimulus were found to be delayed in rats that had been subjected to a prior regime of aerobic exercise training.
“Daily exercise sensitizes the autophagic system, facilitating the elimination of proteins and organelles that aren’t functional in the muscles. Removal of these dysfunctional components is very important; when they accumulate, they become toxic and contribute to muscle cell impairment and death,” said Julio Cesar Batista Ferreira, a professor in the university’s Biomedical Science Institute (ICB-USP) and principal investigator for the study.
Ferreira offered an analogy to help explain muscle cell autophagy. “Imagine the muscles working in a similar manner to a refrigerator, which needs electricity to run. If this signal ceases because you pull the plug on the fridge or block the neurons that innervate the muscles, before long, you find that the food in the fridge and the proteins in the muscles will start to spoil at different speeds according to their composition,” he told Agência FAPESP.
“At this point, an early warning mechanism, present in cells but not yet in fridges, activates the autophagic system, which identifies, isolates and ‘incinerates’ the defective material, preventing propagation of the damage. However, if the muscle does not receive the right electric signal for long periods, the early warning mechanism stops working properly, and this contributes to cell collapse.”
Spoiled food in a broken fridge corresponds to proteins that instead of performing their proper function form toxic aggregates, which start killing cells. Autophagy can isolate these proteins and destroy them in lysosomes, intracellular organelles that degrade and recycle waste.
“Without autophagy, a cascade effect occurs, leading to cell death,” said Juliane Cruz Campos, first author of the article, who is currently engaged in postdoctoral research under Ferreira’s supervision with a scholarship from FAPESP.
In the latest study, rats were submitted to sciatic nerve ligation surgery, creating an effect equivalent to that of sciatic nerve compression in humans. The pain it causes prevents the individual from using the affected leg, and eventually the muscles concerned weaken and atrophy.
Before the surgical procedure, the rats were divided into two groups. One remained sedentary, and the other was given exercise training that consisted of running at 60% of maximum aerobic capacity for an hour a day, five days a week.
After four weeks of exercise training, the surgery was performed, and the muscular dysfunction induced by sciatic nerve injury was found to be less aggressive in the aerobic exercise group than in the sedentary group. Functional and biochemical parameters in the affected muscles were also evaluated at that time.
“The exercise training increased autophagic flux and hence reduced dysfunctional protein levels in the muscles of the animals. At the same time, the exercise improved the muscle tissue’s contractility properties,” Campos said.
“Exercise is a transient stress that leaves a memory in the organism, in this case via the autophagic system,” Ferreira explained. “When the organism is subjected to other kinds of stress, it’s better prepared to respond and combat the effects.”
Proof of concept
The researchers performed two other experiments designed to investigate the link between exercise and autophagy more deeply. One experiment used mice in which the autophagy-related gene ATG7 was silenced in the skeletal muscle.
ATG7 encodes a protein responsible for synthesizing a vesicle called the autophagosome that forms around dysfunctional organelles and transports them to the lysosome, where they are broken down and digested.
This experiment validated the importance of autophagy in muscle biology because ATG7 knockout mice that had not been subjected to sciatic nerve ligation nevertheless displayed muscular dysfunction.
In the other experiment, muscles from rats with sciatic nerve injury and control rats (without the injury) were treated with a drug called chloroquine, which inhibits autophagy by raising the lysosomal pH (alkalinity) and hence prevents the degradation of defective proteins.
“The tests showed less muscle strength in the control animals treated with the drug than in the untreated group. Chloroquine had no effect on the muscles of rats with sciatic nerve injury, proving that the inhibition of autophagy is critical to muscular dysfunction caused by the lack of stimulus,” Ferreira said.
The researchers stress that their studies do not aim to find a treatment for sciatica, one of the most common types of pain. The idea is to use the experimental model in further research to understand the cellular processes involved in muscle dysfunction. This will facilitate the development of new drugs and nonpharmacological interventions capable of minimizing or reversing an increasingly serious problem in contemporary societies, namely, muscle weakness and atrophy due to a lack of movement, especially among the elderly.
“If we can identify a molecule that selectively keeps the autophagic system on alert, in a similar manner to what happens during physical exercise, we may be able to develop a drug that can be given to people with muscle dysfunction due to a lack of stimulus, such as patients with immobilized limbs, people who are bedridden for long periods, and even patients with [degenerative] muscular diseases,” Ferreira said.
The article “Exercise prevents impaired autophagy and proteostasis in a model of neurogenic myopathy” (doi: 10.1038/s41598-018-30365-1) by Juliane C. Campos, Leslie M. Baehr, Kátia M. S. Gomes, Luiz R. G. Bechara, Vanessa A. Voltarelli, Luiz H. M. Bozi, Márcio A. C. Ribeiro, Nikolas D. Ferreira, José B. N. Moreira, Patricia C. Brum, Sue C. Bodine and Julio C. B. Ferreira can be read at: nature.com/articles/s41598-018-30365-1.
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