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Aminosyror

Skapad av Blodapelsin, 2011-10-06 00:08 i Mat & träning

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Blodapelsin
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Så jag har under de senaste 6 veckorna läst en kurs i biokemi, och då metabolismen har varit en ganska stor del av den kursen så har aminosyror, protein syntes osv, varit något vi gått igenom en hel del. Dock inte alls från ett träningsperspektiv, så av ren nyfikenhet sitter jag här och googlar runt lite och letar studier på aminosyror som kosttillskott... Men är det någon som har lite fakta eller erfarenhet och har lust att skriva det här så uppskattas det!

Det jag undrar mest över är;

Aminosyror vs vanligt vassleprotein tillskott (nackdelar, fördelar, prisvärt?)

Samt vilka aminosyratillskott som är bäst, vad jag förstått så är det; Glutamine, BCAA och EAA som är de vanligaste, så samma sak där, nackdelar, fördelar, prisvärt?

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Joel
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Svar till Blodapelsin [Gå till post]:
Du vill alltså boosta ditt kroppsbyggande genom att se till att det alltid finns tillräckligt med aminosyror för att bygga olika protein (som är relaterade till dina muskler)? Måste du inte då också stimulera cellerna att faktiskt syntetisera dessa proteiner på något sätt? (är helt grön på området, men det verkar intressant!)

Kreatin är väl kanske något som passar in? Såg att den har en en NH2- och en karbonylgrupp med en snabbkoll på wikipedia, men den är nog ingen aminosyra va? (hihi, bristande kunskaper här med, men kul är det ^^). Om jag inte minns fel har man den för att köra slut på vid anaerob ADP->ATP, men det var två år sen jag tittade på det där så jag kan ha heeelt fel...

Kaka

trapz
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Svar till Blodapelsin [Gå till post]:
Bara glutamin är inget att ha bland det sämsta tillskottet som finns. Tydligen ska BCAA vara de mest stimulerande men jag tycker att det är bättre med EAA då det inte finns mycket forskning som jämför dem vad jag har sett.

Sedan finns det studier där man jämför EAA och vassle där tydligen EAA var snäppet vassare, dock sägs det kunna eventuellt ge nervskador men långt ifrån bekräftat. Båda är ungefär lika prismässigt.


Svar till Joel [Gå till post]:
"Måste du inte då också stimulera cellerna att faktiskt syntetisera dessa proteiner på något sätt? (är helt grön på området, men det verkar intressant!)"

Genom träning ;)

Kreatin är en energikälla vid arbete typ som ATP och glykogen och kan inte bygga upp något som aminosyror kan.

Life getting tough? Means god is afraid of your progress!.

viktors
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Svar till Blodapelsin [Gå till post]:
Aminosyror tas upp snabbare eftersom de inte behövs brytas ned som vassle måste.
BCAA är de aminosyror som triggar proteinsyntesen max, detta är bara 4 st aminosyror, och EAA är alla esentiella aminosyror. Mer behöver du inte veta om du läser om proteinsyntesen i skolan.

Blodapelsin
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Svar till Joel [Gå till post]:
Kreatin har inte så mycket med saken att göra just i denna diskussionen. men visst, det är ett bra tillskott. Men det har jag lite bättre koll på hur det fungerar, är mer nyfiken på aminosyra tillskott i allmänhet, om jag kommer prova det är en annan sak :P



Svar till trapz [Gå till post]:
Har du nån länk till någon/några studier? Skulle va intressant att läsa.



Svar till viktors [Gå till post]:
Är inte BCAA bara tre? leucine, isoleucine och valine? eller vilken är den fjärde?
Hur som helst, ser inte logiken i varför BCAA skulle trigga proteinsyntesen mer än EAA, då EAA också innehåller leucine, isoleucine och valine, plus 5 andra. Skulle de fem andra ha en negativ effekt på proteinsyntesen då de kombineras med resten av de essentiella?




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trapz
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Svar till Blodapelsin [Gå till post]:
Om glutamin:

http://www.kolozzeum.com/forum/showpost.php?p=2128061&postcount=11 (ingen studie men en studiehänvisning)

EAA vs vassle (dock äldre människor)

http://www.sciencedirect.com/science/article/pii/S0531556505002548

Life getting tough? Means god is afraid of your progress!.

viktors
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Svar till Blodapelsin [Gå till post]:
Menade 3. BCAA innehåller de aminosyror som stimulerar proteinsyntesen mest. EEA innehåller som sagt alla esentiella aminosyror. Dock har de 5 andra inte en sån stor inverkan på proteinsyntesen. Därför kan man ta bort dem helt och få mer för pengarna.

trapz
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Svar till viktors [Gå till post]:
Har man visat det i någon studie skulle vara intressant att se då man inte vet den exakta kombinationen av aminosyror för optimal proteinsyntes stimulering?

Life getting tough? Means god is afraid of your progress!.

viktors
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Svar till trapz [Gå till post]:
leucine, valine och isoleucine är ju BCAA som triggar proteinsyntesen. De andra har inte ens sån stor inverkan på den.

tryptophan - tryptophan is a precursor for serotonin and melatonin.

lysine - Lysine deficiency can result in a deficiency in niacin (Vitamin B) and this can cause the disease pellagra. It is also beneficial in treating and preventing herpes.

Threonine: Threonine is important for antibody production. It can be converted into glycine and serine. Deficiencies are rare but can result in skin disorders and weakness.

Phenylalanine: Phenylalanine serves in the body as a precursor to the catecholamine family of hormones. These hormones include adrenaline and noradrenaline, which are activating substances in the central and peripheral nervous systems. Deficiencies are rare but can include slowed growth, lethargy, liver damage, weakness, oedema, and skin lesions.

methionine - Methionine supplies sulphur and other compounds required by the body for normal metabolism and growth. It belongs to a group of compounds called lipotropics that help the liver process fats.

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Svar till viktors [Gå till post]:
Önskar att det va så enkelt som du får det att låta, men tyvärr så är det inte riktigt det. De 20 aminosyrorna som finns används till flera tusen olika saker i kroppen, allt från DNA/RNA uppbyggnad, enzymer, hormoner, molekyltransporter, antikroppar osv, listan kan göras grymt lång.

Så jag köper inte riktigt att det går att gör som du gjort i ditt inlägg, dra några exempel av de tio tusentals som finns, och sen köra uteslutningsmetoden att de andra aminosyrorna då måste trigga proteinsyntesen.

Säger inte att det är fel det du säger, det kan mycket väl stämma att BCAA är det viktigaste... men du använder dig inte av ett vettigt argument, då det inte bygger på någon som helst källa vad jag fattar det som?


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viktors
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Svar till Blodapelsin [Gå till post]:
För det första, så handlar detta bara om de esentiella aminosyrorna. Dvs 8 st. Av dessa 8 aminosyror så har det visat sig att ett intag av bcaa triggar proteinsyntesen lika mycket som samma mängd protein fast med alla esentiella aminosyror.
Här är det om bcaa:
Valine: Valine is needed for muscle metabolism, tissue repair, and for the maintenance of proper nitrogen balance in the body. Valine is found in high concentration in the muscle tissue. It is also one of the three branched chain amino acids, which means that it can be used as an energy source by muscle tissue. It may be helpful in treating livere and gallbladder disorders, and it is good for correcting the type of severe amino acid deficiencies that can be caused by drug addiction. Dietary sources of valine include dairy products, grain, meat, mushrooms, peanuts, and soy proteins.
Leucine: Leucine is a branched chain essential amino acid that stimulates muscle protein synthesis and may be the major fuel involved in anabolic (tissue building) reactions During times of starvation, stress, infection, or recovery from trauma, the body mobilizes leucine as a source for gluconeogenesis (the synthesis of blood sugar in the liver) to aid in the healing process. It has recently been suggested that leucine may have beneficial therapeutic effects on the prevention of protein wasting, as it occurs during starvation, semi-starvation, trauma, or recovery after surgery. Insulin deficiency is known to result in poor utilization of leucine; therefore, individuals who suffer from glucose intolerance may require higher levels of leucine intake. Leucine is found in cottage cheese, sesame seeds, peanuts, dry lentils, chicken, and fish.
Isoleucine: Isoleucine is a branched chain amino acid that is important for blood sugar regulation, muscle development and repair, haemoglobin development, and energy regulation. Deficiencies of isoleucine result in possible dizziness, headaches, fatigue, depression, confusion and irritability. Isoleucine is found in eggs, fish, lentils, poultry, beef, seeds, soy, wheat, almonds and dairy.

trapz
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Svar till viktors [Gå till post]:
"Av dessa 8 aminosyror så har det visat sig att ett intag av bcaa triggar proteinsyntesen lika mycket som samma mängd protein fast med alla esentiella aminosyror."

I vilken studie har man visat detta skulle vara intressant att läsa? :)



Life getting tough? Means god is afraid of your progress!.

viktors
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trapz
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Svar till viktors [Gå till post]:
tackar, nu är jag lite seg i huvudet men ingen av de där studierna jämför BCAA mot EAA eller har jag missat något?

Life getting tough? Means god is afraid of your progress!.

viktors
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Svar till trapz [Gå till post]:
Det bevisar ju att det är BCAA som orsakar den största delen av höjningen i proteinsyntesen.

Blodapelsin
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Svar till viktors [Gå till post]:
Det är mycket lättare om du bara länkar källan där allt detta står istället för att kopiera in texten direkt i forumet, och sedan inte ha med en källhänvisning alls...

Men hur som helst, du missar poängen, exempel på vad de olika aminosyrorna gör är ganska meningslöst, alla fyller flera tusen andra funktioner än de som du skrivit också. Så det som är intressant är effekten på proteinsyntesen, och visserligen du har skrivit att leucine stimulerar just detta (men utan källhänvisning är det meningslös fakta).

Dock så har tråden svävat ut lite på andra saker än själva ämnet, dvs, aminosyror som kosttillskot. Så om vi går tillbaka dit och fokuserar på den frågan vi började att diskutera; EAA vs BCAA...

Jag ser fortfarande inte logiken i varför BCAA skulle vara ett bättre tillskott då EAA innehåller BCAA. Enda anledningen som jag kan komma på är att de fem andra aminosyrorna har en negativ effekt tillsammans med BCAA? eller finns det en annan anledningen? att säga att man får i sig mer (gram) av de viktigaste aminosyrorna genom att äta BCAA är ju inget vettigt argument då dosering inte har något med saken att göra egentligen, detta handlar bara om ämnena i sig.


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Svar till Blodapelsin [Gå till post]:
EAA: http://www.springerlink.com/content/4185723k04222034/
BCAA: http://www.ncbi.nlm.nih.gov/pubmed/20300014
I träningssyfte så är man ute efter de anabola aminosyrorna. Och i detta fall är det BCAA, som även finns doserat i EAA.

"Only six amino acids are directly used by muscles during exercise. These amino acids are alanine, glutamine, aspartate, isoleucine, leucine, and valine. Leucine, isoleucine, and valine are known as branch chain amino acids (BCAA) and serve a much more important role in energy and muscle growth than any of the other amino acids.

After participating in resistance exercises such as weight training, muscle protein synthesis increases and the rate of protein degradation rises. The effect of this is a negative protein balance resulting in a catabolic state. The body requires BCAA because of the negative protein balance; therefore, muscle tissues are broken down to provide the needed BCAA. These catabolic conditions lead to the breaking down of amino acids within the muscle tissue. Amino acids have profound effects on muscular growth and when amino acids levels are lowered, growth suffers. External consumption of BCAA allows the need for BCAA during exercise to be met without having to break down amino acids within muscle tissue. The body will remain in a catabolic state with a negative protein balance until amino acids are ingested. Consuming amino acids will result in a positive protein balance enabling the body to be in an anabolic state. Ensuring that the body is in an anabolic state through correct diet and supplementation along with a proper lifting program will lead to muscular hypertrophy. Tipton et al found that “…ingestion of amino acids is an effective method of maximizing the anabolic effect of exercise.”"

Amino Acid Supplementation

By Zach Long (olinerules87)

Most fitness enthusiasts know that an adequate amount of protein is needed whether one wants to gain muscle mass or lose body fat without drastically decreasing lean body weight. Proteins are made of chains of bonded amino acids that help our bodies grow and repair muscles. Amino acids are divided into two categories: essential amino acids (EAA) and nonessential amino acids (NEAA). The difference between EAA and NEAA is that the human body does not produce enough EAA to meet the body’s requirements and consequently, EAA must be consumed in your diet. The body does produce sufficient amounts of NEAA to meet its demands.

Only six amino acids are directly used by muscles during exercise. These amino acids are alanine, glutamine, aspartate, isoleucine, leucine, and valine. Leucine, isoleucine, and valine are known as branch chain amino acids (BCAA) and serve a much more important role in energy and muscle growth than any of the other amino acids.

After participating in resistance exercises such as weight training, muscle protein synthesis increases and the rate of protein degradation rises. The effect of this is a negative protein balance resulting in a catabolic state. The body requires BCAA because of the negative protein balance; therefore, muscle tissues are broken down to provide the needed BCAA. These catabolic conditions lead to the breaking down of amino acids within the muscle tissue. Amino acids have profound effects on muscular growth and when amino acids levels are lowered, growth suffers. External consumption of BCAA allows the need for BCAA during exercise to be met without having to break down amino acids within muscle tissue. The body will remain in a catabolic state with a negative protein balance until amino acids are ingested. Consuming amino acids will result in a positive protein balance enabling the body to be in an anabolic state. Ensuring that the body is in an anabolic state through correct diet and supplementation along with a proper lifting program will lead to muscular hypertrophy. Tipton et al found that “…ingestion of amino acids is an effective method of maximizing the anabolic effect of exercise.”
When being digested, BCAA bypass the liver and are promptly absorbed by the circulatory system, allowing BCAA to be quickly used for protein production. Protein synthesis has been shown to increase 200% when EAA were available following weight lifting. Several studies have reported that amino acid supplementation leads to greater gains of lean muscle mass. Crowe et al found that “upper body power, time to exhaustion and perceived exertion were significantly improved after 6-week dietary leucine supplementation compared to a placebo.”

Many studies have proven that Leucine is the best amino acid. Leucine is directly involved in stimulating protein synthesis and without it protein production is weakened. Leucine levels must be increased for significant increases for protein synthesis to occur. Muscle protein production is increased by as much as 10 times when leucine is added to a protein rich meal. BCAA supplements containing 30-35% leucine have been shown to decrease protein degradation, increase mental and physical performance, and lessen depletion of muscle glycogen levels. Leucine also provides muscles more ATP than the same weight of glucose. While it is important to look for products with relatively large amounts of leucine, supplementation with leucine alone causes BCAA imbalances. Therefore, supplements should contain high levels of leucine as well as isoleucine and valine.
To meet the body’s requirements for amino acids, high amounts of EAA and BCAA are necessary. Faster absorbing proteins are more effective at delivering BCAA to the muscles, therefore, casein, egg proteins, and other slow digesting proteins are not encouraged for meeting BCAA needs. Hydrolyzed whey protein is the fastest digesting protein and is the best for consuming BCAA. Other options for BCAA are the direct supplementation of amino acids through products such as Prolab’s BCAA Plus, NxCare’s Aminovol, and Universal’s BCAA Stack, just to name a few.

Because the purpose of consuming amino acids is to provide muscles with BCAA so that muscle tissues aren’t broken down, amino acids should be consumed before exercise. Consuming BCAA before exercise delivers these nutrients better because the heart pumps 20-25 liters of blood per minute while exercising compared to only 5 when at rest. While exercising, over 80% of blood flow is directed to the muscles while only 15-20% of blood flow goes to the muscles while at rest. This change in blood flow patterns occurs because muscles need more blood while exercising and the body adapts to meet this need. By taking amino acids pre-workout, amino acids are delivered more efficiently to your muscles. This pre-workout shake won’t lessen the value of post workout nutrition, but will instead boost its effectiveness.

Conclusion

Consuming amino acids before you exercise provides your muscles with the nutrients it needs to increase protein synthesis, reach an anabolic state, and increase muscular hypertrophy.

Sources
Crowe, Melissa. "Effects of Dietary Leucine Supplementation on Exercise Performance."
European Journal of Applied Physiology 97(2006): 664-672.
Charlebois, Derek. "BCAA: More Than Just Amino Acids." Strength & Science Weekly
12. 16 Dec 2006 < http://www.strengthandscience.com/october/article8.htm>.
Charlebois, Derek. "Essential Amino Acids." Strength & Science Online 4. 16 Dec 2006
< http://www.strengthandscience.com/august/article9.htm>.
Mero, A. "Leucine Supplementation and Intensive Training." Sports Medicine 27(1999):
347-358.
Norton, Layne. "Leucine: The Anabolic Trigger." Strength & Science Weekly 11. 16
Dec 2006 < http://www.strengthandscience.com/october/article2.htm>.
Tipton, Kevin. "Postexercise Net Protein Synthesis in Human Muscle from Orally
Administered Amino Acids." Endocrinology and Metabolism 276(1999): 628-
634.

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Svar till Blodapelsin [Gå till post]:
Pga ditt tvivel om Leucin kan du läsa detta också.
The Anabolic, Anti-Catabolic/Fat Loss Properties of Leucine

Written by Robbie Durand
Wednesday, 14 January 2009

The Justice League is composed of a bunch of jacked up super heroes each with special powers put together to fight crime and maintain order. Each member of the Justice League plays his role but the league is centered around one superhero, Superman. The Amino Acids are just like the Justice League they are there to build muscle and fight the bad guys (cortisol, myostatin, muscle atrophy, ect). If there is one amino acid that stands out and is more powerful than any other amino, Leucine is the Superman of the Amino Acids. Several studies published this month documents leucine has both the ability to increase muscle growth and lose bodyfat. Obviously, all Amino Acids are required to make proteins, but remarkably a large dose of leucine alone can stimulate human muscle protein synthesis1. In fact, it has been reported that muscle protein synthesis responds linearly to plasma concentration of leucine14. In other words, the more leucine you consume, the greater the muscle protein synthesis rates. In this months Journal of Molecular Reproduction and Development, leucine does a whole lot more than just stimulating protein synthesis, it activates satellite cell activity. When muscles undergo intense exercise, as from a resistance training bout, there is trauma to the muscle fibers. This disruption to fibers activates satellite cells, which are activated to the injury site. In essence, a biological effort to repair or replace damaged muscle fibers begins with the satellite cells fusing together and to the muscles fibers, often leading to increases in muscle fiber hypertrophy. It has previously been documented that resistance exercise stimulates satellite cell activity; it is also well documented that insulin-like growth factor-1 (IGF-1) stimulates satellite cell activity. Leucine has some similarities to IGF-1 as both IGF-1 and leucine increase muscle size by stimulating mTOR signaling in skeletal muscle. Researchers examined the effects of adding either leucine or IGF-1 to muscle satellite cells and found that both IGF-1 and leucine upregulated mTOR signaling in satellite cells8. In addition, there was no difference between IGF-1 and leucine for increasing satellite cell activation. Activation of mTOR signaling is necessary for the protein synthesis in satellite cells stimulated by IGF-1 and leucine. This study was performed with muscle cell in test tubes but it makes you wonder could large dosages of leucine be just as effective as IGF-1 for stimulating muscle growth? Adding a few scoops of leucine powder to your protein/carbohydrate beverage may increase the anabolic drive in muscle. The coingestion of leucine (1 gram per kg of bodyweight) and protein with carbohydrate has been found to increased whole body protein synthesis compared with a combined ingestion of carbohydrate and protein. Interestingly, the combined ingestion of leucine and protein with carbohydrate may enhance IGF-1 levels as the insulin response of leucine, protein, and carbohydrates rose by ~250% compared with the ingestion of only carbohydrate25. Adding some leucine to your post exercise drink may be the missing ingredient to enhance muscle growth.

Leucine: A Fat Loss Agent?
You have heard of myostatin knockouts mice, well get ready for the new genetically altered super leucine mouse. Scientists disrupted the branched chain aminotransferase gene, which is the enzyme which breaks down BCAA in muscle. In essence, the mice have genetically elevated levels of leucine. So is there anything unusual about these super leucine mice? What interesting is that these mice exhibit elevated plasma BCAA’s but also decreased adiposity, despite eating more food, along with increased energy expenditure, remarkable improvements in glucose and insulin tolerance, and protection from diet-induced obesity12. High dosages of leucine may be the able to prevent excess fat gain in the offseason when calories are high. Another article of interest was published in the journal of Diabetes in which they fed rats a high fat diet but also doubled their leucine intake by adding it to their drinking water. Even though the rats ate the exact same calories on the high fat diet increasing leucine intake resulted in up to 32% reduction of weight gain and a 25% decrease in adiposity. The reduction of adiposity resulted from increased resting energy expenditure associated with increased expression of uncoupling protein 3 in brown and white adipose tissues and in skeletal muscle10. Consider being like a rat for a while during the weeks leading up to the competition and adding leucine to your water supply. The final article of interest was published in Journal of Life Sciences which they took rats and put on leucine and phenylalanine and then put them on a calorie restricted diet by 50% for 1 week. The scientists then let the rats eat whatever they wanted for 2 weeks after that. Compared to the group of rats that received nothing, chronic supplementation with leucine and phenylalanine was able to improve the body composition by increasing lean body mass and by reducing, although modestly, the accumulation of body fat11. This means that bodybuilders may be able to prevent putting on excess bodyfat after dieting for a competition by taking leucine. So based on these studies, bodybuilders should be taking leucine especially during the competition phase to reduce bodyfat but also stimulate protein synthesis rates. I even suggest adding it to your drinking water like the lab rats!!!
Leucine can substitute for a complete protein meal
For several years taking branched chain Amino Acids were advocated pre-workout, but taking leucine may be the only amino acid necessary as muscle protein stimulation is responsive to stimulation by leucine, but not the other branched-chain Amino Acids, isoleucine and valine13. Leucine seems to be the most potent of the BCAA with regard to most of these effects and therefore may be the most physiologically relevant. Leucine alone can substitute for a meal in stimulating signal transduction pathways, leading to a stimulation of protein synthesis. Large oral leucine dosages increased muscle protein synthesis within 20 min. similar to meal feeding; the activity of the mTOR-signaling pathway in muscle is augmented following the oral leucine consumption. So when getting ready for a show, consuming extra leucine can enhance protein synthesis.

Leucine Increases Protein Synthesis Independent of Insulin
Leucine has both anabolic effects in skeletal muscle reflecting both stimulated protein synthesis and inhibited protein breakdown. Studies suggest that some of the anabolic effects of leucine are regulated by mechanisms similar to those regulating the effects of insulin20, 21. Leucine is now known to interact with the insulin-signaling pathway with apparent control of protein synthesis, resulting in maintenance of muscle protein during periods of restricted energy intake. Leucine appears to also stimulate protein synthesis independent of insulin17. For example, a dosage of leucine resulted in a stimulation of protein synthesis that was independent of changes of plasma insulin concentrations, whereas a dosage containing carbohydrates (glucose plus sucrose) that raised insulin concentrations over 2.5 times the fasting glucose concentration did not affect protein synthesis3. Overall the results demonstrate that leucine can cause increases in protein synthesis rates that are independent of insulin.
Anti-Catabolic Actions of Leucine
Oral intake of leucine stimulates muscle protein synthesis after exercise or an overnight fast18, 19. These studies support the role of leucine as a key amino acid for reversing catabolic conditions which may be especially important when trying to get ripped for a competition In previous studies, there is evidence that catabolic conditions, muscles tissue becomes resistant to some of the anabolic effects of leucine22, and it is possible that this “leucine resistance” reflects why cortisol breaks down muscle tissue. More recent studies from laboratories provided direct evidence for a role of cortisol in “leucine resistance” in skeletal muscle. For example, Shah et al.6 reported that cortisol opposes the control of protein synthesis by leucine in skeletal muscle. Additionally, Rieu et al. 7 examined the effects of cortisol in young (4–5 wks), adult (10–11 months), and old (21–22 months) rats and made the interesting observation that cortisol induced leucine resistance in adult and old rats, but not in young rats. Considering those findings, the authors speculated that muscle loss during aging may reflect cortisol- induced “leucine resistance.” This may be the reason why you do just about anything in the gym and still grow however with aging the gains are not as apparent. Fasting and calorie restriction also results in an increase in leucine appearance rate in the blood, an index of whole body protein breakdown. The increase in leucine appearance is consistent with a decline in insulin, because insulin normally suppresses protein breakdown. Additionally, fasting increases the hormone glucagon which has a catabolic effect on leucine23. In skeletal muscle, exposure to cortisol is characterized by a reduction in protein synthetic rate coincident with hampered protein synthesis rates; however oral administration of leucine reversed the catabolic effects of with a 1 hour of administration24. It seems that intense training and calorie restriction both increase cortisol however leucine seems to counteract the negative effects of cortisol.

Older Bodybuilders May Need More Leucine than Younger Bodybuilders
Older bodybuilders are becoming more and more common these days. In general, aging is associated with a decrease in protein synthesis which has been termed “anabolic resistance.” This is shown by a decrease sensitivity and responsiveness of protein synthesis in muscle in both rats and humans. The leucine signal is also observed to be less sensitive in older subjects15. In one study, leucine concentrations 1–2 times greater than in young animals were necessary to observe the same changes in older rats. This suggests that the defect in postprandial muscle protein anabolism in old subjects is related to the alterations of the leucine signaling in muscle. However, the molecular mechanism responsible for the blunted signaling pathways for leucine remains unresolved. Interestingly, a recent study reported that when comparing younger (8 months old) and older rats (22-months-old) protein breakdown rates; the rates of protein breakdown were higher in older rats compared to younger rats, but when older rats are fed a diet which is supplemented with 5% Leucine, there is a rejuvenation of muscle and an inhibition of protein breakdown similar to young rats16. Based on the research in old rats and humans, high concentrations of leucine appear capable of stimulating muscle protein synthesis to the same degree as physiological concentrations in younger subjects. Thus, aging seems to be associated with a decrease in leucine-induced stimulation of muscle protein synthesis. The long-term utilization of leucine-rich diets may therefore limit muscle protein wasting during aging.

It seems that taking leucine in large dosages not only increases protein synthesis rates, activates satellite cells, reduced the catabolic actions of cortisol, and reduces bodyfat. The good news is that leucine is among the most tolerated Amino Acids as no adverse effects of increased leucine intake (usually 3x of the daily requirement) were reported in various human studies9. Leucine is clearly the most potent anabolic amino acid on the market today.

Key Points:
• Leucine alone increases protein synthesis independent of insulin
• Leucine had potent fat loss properties
• Leucine has both anabolic and anti-catabolic actions
• Leucine synthesis is decreased with age

1. Rennie MJ. Exercise- and nutrient-controlled mechanisms involved in maintenance of the musculoskeletal mass. Biochem Soc Trans. 2007 Oct;35(Pt 5):1302-5.
2. Buse MG, Reid SS: Leucine: A possible regulator of protein turnover in muscle. J Clin Invest 1975; 56:1250–1261
3. Anthony JC, Anthony TG, Kimball SR, et al: Orally administered leucine stimulates protein synthesis in skeletal muscle of postabsorptive rats in association with increased eIF4F formation. J Nutr 2000; 130:139–145
4. Anthony JC, Yoshizawa F, Anthony TG, et al: Leucine stimulates translation initiation in skeletal muscle of postabsorptive rats via a rapamycin-sensitive pathway. J Nutr 2000; 130:2413–2419
5. Hasselgren PO, James JH, Warner BW, et al: Protein synthesis and degradation in skeletal muscle from septic rats: Response to leucine and _-ketoisocaproic acid. Arch Surg 1988; 123:640–644
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trapz
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Svar till viktors [Gå till post]:
Snälla skriv inte ut allt man orkar ju inte läsa allt ta gärna ut nyckel meningar istället.

Angående leucin:

"We conclude that increasing the proportion of leucine in a mixture of EAA can reverse an attenuated response of muscle protein synthesis in elderly but does not result in further stimulation of muscle protein synthesis in young subjects.

Am J Physiol Endocrinol Metab. 2006 Aug;291(2):E381-7."

Life getting tough? Means god is afraid of your progress!.

viktors
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Svar till trapz [Gå till post]:
Och hur mycket leucin skall det vara då? eftersom man brukar ju använda en 2:1:1 eller 4:1:1 i BCAA och sedan lägga till de aminosyrorna. Är väl antagligen något samband mellan Leucine och Isoleucine.
Har ej hemsidan för dessa studier utan endast hittat dem med källor.


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