Muscle contraction increases insulin sensitivity and your body’s ability to burn fat, not only in muscle tissue but also all over the body. How this happens remained a mystery for years. Until it was recently discovered that muscle also functions as an endocrine organ producing a number of myokines. These myokines are released into the circulatory system and influence metabolism.
Think of myokines as special chemical messengers sent from muscle tissue to coordinate metabolic changes all over the body in response to exercise.
Myokines activate glucose disposal, potentiate the effects of insulin and increase the use of fat for energy production. A number of myokines have been discovered, but interleukin-6 (IL-6) in particular has emerged as one of the most important.
With many leptin-like properties, IL-6 can be considered the “leptin” of muscle tissue. Released in response to intense training, IL-6 increases insulin sensitivity and fat-burning, while at the same time decreases inflammation. Like leptin, IL-6 activity and release can be influenced by training and nutritional variables, so read on to learn more about this powerful myokine – what it does, how it works and what we can do to harness its power.
EXERCISE. THE IMMUNE SYSTEM AND THE DISCOVERY OF MYOKINES
For most of the last century scientists have scratched their heads over the link between muscle contraction and exercise-induced metabolic changes. Because training a muscle hard causes metabolic changes all over the body, researchers reasoned that there must be some kind of “exercise factor” that is released in response to muscle contraction. This mystery “exercise factor” would then somehow communicate with other tissues, increasing insulin sensitivity and fat-burning all over the body. The problem is, the source of this exercise factor was completely unknown, let alone how it might work.
One clue as to the identity of this “exercise factor” was revealed when the connection between muscle and the immune system was discovered.
Hard training activates the immune system, which is intimately involved in the muscle growth and repair process.
The connection between muscle and the immune system remained a mystery for many years, until it was discovered that exercise changes the distribution and concentration of different types of immune cells. Scientists knew at the time that hormones called cytokines regulated immune activity, so early work focused on cytokines as a possible link between muscle contractions and changes to the immune system.
This work led to the discovery that exercise causes an increase in the number of cytokines in the blood stream, particularly IL-6. Because IL-6 is one of the “classical” inflammatory cytokines of the immune system, scientists initially reasoned that IL-6 was released by immune cells in response to muscle damage, possibly as part of an early inflammatory response. After all, IL-6 is produced by muscle fibres and accumulates during exercise. It turned out that negative contractions, which are the most damaging type of contraction, didn’t increase IL-6 any more than non-damaging positive contractions. This ruled out the idea that muscle damage was the trigger for increased blood levels of IL-6 during exercise. In 2000 scientists discovered that intensely contracting skeletal muscle actually produces massive amounts of the cytokine IL-6, which is also released into the circulation. Finally, the mystery “exercise factor” was discovered, and the term “myokine” was born.
THE SPLIT PERSONALITY OF IL-6
As the most potent myokine known to date you might think it is slightly strange that the full potential of IL-6 has only recently come to light. The major reason for this is due to the fact that IL-6 has a dark side. This led to some initial disagreement over whether it is helpful, harmful or something in-between.
IL-6 activity is a bit of a paradox: On one hand, high IL-6 levels are associated with metabolic disease, insulin resistance and obesity. Independent of these disease-states, IL-6 is linked to low levels of physical activity. So, in that sense, it could also be considered the “out-of- shape” hormone. Because of this IL-6 was previously thought to be an actual cause of insulin resistance. This belief was challenged by the discovery that IL-6 is a myokine, produced and released from skeletal muscle in response to hard work.
We know that intense training increases insulin sensitivity and that insulin action is enhanced in the post-workout period. Why then would muscle shoot itself in the foot by producing massive amounts of something that decreases insulin sensitivity? It turns out that IL-6 has a split personality. Chronically high IL-6 levels are associated with low levels of physical activity, insulin resistance and obesity, in spite of the fact that IL-6 levels increase in the post-exercise period, where it enhances insulin action and fat-burning.
So IL-6 has both negative and positive effects… but how does this work, you may ask? It turns out that there is a big difference between acute and chronic IL-6 production. Acute levels of IL-6 are good, chronic levels of 11-6 are bad. When you are at rest you want IL-6 to be as low as possible. Acute levels of IL-6, released in response to intense training, enhances glucose uptake and fatty acid oxidation in skeletal muscle. Chronically elevated IL-6 causes IL-6 resistance, which is a driver of insulin resistance in those who are overweight, obese and/or generally out of shape.
Likewise, there is a lot of evidence that IL-6 sensitivity improves with physical activity, causing baseline IL-6 levels to decrease. Cardio work in elderly adults has been shown to decrease resting IL-6 levels and the combination of a low calorie diet and regular exercise also reduces resting plasma IL-6 in the severely obese. While resting IL-6 levels are reduced by training, expression of muscle IL-6 receptors actually increases up to 100% in response to regular exercise. The more IL-6 receptors you have, the more sensitive you will be to its effects. This is why resting IL-6 levels actually decrease when you are in good condition. The better shape you are in, the lower your IL-6 levels will be at rest.
Acute (good) and chronic (bad) IL-6 levels may also come from completely different sources.
“Bad” IL-6, which drives insulin resistance, is released from adipose tissue and contributes more to chronically increased IL-6 levels at rest.
“Good” IL-6 is released from muscle tissue in response to hard training, where it increases insulin sensitivity and fat-burning.
HOW DOES IL-6 WORK. AND WHAT DOES IT DO?
IL-6 activates pathways that burn fat, increase insulin sensitivity and decrease inflammation.
It also acts as a fuel gauge for muscle tissue, where it is released when muscle glucose levels are low. This causes an increase in glucose production in the liver while also increasing lipolysis during exercise.
IL-6 is also responsible for much of the direct fat-burning effects from intense training, amplifying fat oxidation in intramuscular and whole-body fat stores. IL-6 also enhances insulin signaling by at least three different mechanisms. First, IL-6 plays a role in insulin- independent glucose uptake, which is activated by muscle contraction during exercise. When hard contracting muscle releases IL-6, this action increases the amount of GLUT4 translocation to the muscle cell membrane, leading to increased glucose uptake. Secondly, IL-6 also enhances insulin-dependent glucose uptake by increasing insulin sensitivity and insulin release. This increases insulin-stimulated glucose uptake during and after exercise, leading to increased glucose disposal, protein synthesis and much fuller muscles. Finally, IL-6 increases insulin sensitivity by suppressing chronic inflammation.
The role of IL-6 in insulin signaling can’t be understated. This has huge implications for hard training athletes as enhanced insulin action in the post-workout period doesn’t stop at better glucose disposal. You are more anabolic as protein synthesis increases and protein degradation is suppressed. IL- 6 also prevents the fat burning machinery from being turned off during the insulin response. Under normal circumstances, elevated insulin levels flip a biochemical switch that turns off fat oxidation and lipolysis. With IL-6 in the picture, post-exercise insulin signaling is enhanced but fat burning actually increases, instead of being shut down. In doing this, IL-6 performs nothing short of metabolic magic – it hacks your metabolism to prevent the fat burning machinery from being shut down during the insulin response.
IL-6 AND INFLAMMATION
While chronic, low-level inflammation doesn’t put your health in immediate danger, it can wreak havoc over time. Low grade inflammation is a big cause of ageing and is also part of the cause and effect of obesity, insulin resistance and diabetes. Chronic, low- grade inflammation causes a two to three fold increase in the inflammatory cytokines TNFa, IL-1, CRP and others. TNFa induces insulin resistance by several different pathways and it is a direct molecular link between low-grade systemic inflammation and insulin resistance. While acute TNFa is vital to the muscle repair process, we generally want to do whatever we can to keep TNF levels as low as possible at other times. This is where IL-6 comes in. Exercise is an inhibitor of chronic inflammation and this happens by way of increased systemic levels of a number of anti-inflammatory cytokines, including IL-6. As the first cytokine present in the circulation during exercise, IL-6 is a driver of the anti-inflammatory effects of training, which protects against chronic, low grade inflammation. By suppressing chronic inflammation, exercise-induced IL-6 also increases insulin sensitivity.
THE “LEPTIN” OF MUSCLE TISSUE
The IL-6 signaling pathway has many similarities to leptin signaling.
The major one is that both leptin and IL-6 function as a type of metabolic “fuel gauge”, but in different tissues. Leptin monitors whole-body energy levels to coordinate energy expenditure, fat oxidation and overall metabolism. IL-6 is also the “fuel gauge” of muscle tissue, cranking up glucose disposal and increasing fat oxidation when muscle glycogen levels are low.
IL-6 and leptin also operate through similar signaling pathways. In their role as metabolic “fuel gauges”, leptin and IL-6 both activate AMPK, a cellular energy sensor. AMPK activation is responsible for much of the fat burning effects of leptin and IL-6. Finally, as with leptin resistance, IL-6 resistance is associated with paradoxically high IL-6 levels, insulin resistance, inflammation and obesity.
THREE TIPS TO HARNESS THE POWER OF IL-6
1: TRAIN HARD AND TRAIN CONSISTENTLY
Obviously hard, consistent training is a prerequisite to get anywhere. However, it also turns out that IL-6 mediates many of the beneficial effects associated with this type of training. Type, intensity and duration of exercise determine the amount of IL-6 release. The harder you train, the more IL-6 is released and working larger muscle groups releases more IL-6 than smaller muscle groups. Hard, consistent training also increases IL- 6 sensitivity, which decreases resting IL-6 levels (i.e. “bad” IL- 6).
Because of the relationship between IL-6 and exercise duration and intensity, higher volume training protocols such as Mountain Dog training may have a distinct advantage over lower-volume approaches when it comes to IL-6 release.
Calcium drives muscle contraction and mechanical load is a big factor in muscle calcium signaling. The IL-6 gene promoter is also calcium-responsive, so heavy loads with sufficient time under tension will tend to promote greater IL-6 release.
2: AVOID SUPPLEMENTAL ANTIOXIDANTS
Research has demonstrated that IL-6 release in working muscles is blocked by antioxidants. Oral supplementation with vitamin C and E for four weeks almost completely prevented IL-6 release in working muscles. Try to get your antioxidants mostly from whole-food sources. If you are still convinced you need to take antioxidant supplements, avoid taking them around the times that you train.
3: TRAIN LOW
There are many good reasons to have plenty of carbs around the peri-workout period. However, IL-6 release from muscle tissue is maximised when muscle glycogen levels are low. This triggers the stress-response protein P38 MAPK, which turns on the IL-6 gene, resulting in increased IL-6 production. It has also been demonstrated in a number of studies that glucose ingestion during training weakens exercise-induced IL-6 release. Glucose ingestion during exercise does not, however, stop IL-6 from being produced in muscle, only from being released into the blood stream. While carbs during training may negate some of the overall fat-burning effects of IL-6, the positive effects of IL-6 in muscle tissue (increased glucose disposal and insulin sensitivity) are not affected. Therefore, it is best to keep the carbs in the peri- workout period when you are in mass-gaining phases of your training. For maximal fat loss phases you can best take advantage of the fat-burning effects of IL-6 by training “low”. Fat-burning effects of IL-6 are maximised if you keep carbs on the low side before and during training.
IL-6 coordinates the insulin-potentiating and fat-burning effects of exercise. Very leptin-like in character, IL-6 functions as a sort of muscle “fuel gauge” and also increases insulin sensitivity, lipolysis and fat oxidation. In the fitness industry, truly “academic” knowledge is of little use without a practical application, which is why a few tips on getting the most out of IL-6 have been listed in this article. It is important to stress however, that our knowledge of IL-6 and other myokines is still evolving. IL-6 is a big part of the picture, but it is definitely not the whole picture. With that said, the tips listed above are effective, practical and based on the latest scientific research. Use them to take your training to the next level.