albo tu ciekawe - stala suplemnetacja,osoby odczuwajace itd.:
Carnosine loading and washout in human skeletal muscles.
Carnosine (beta-alanyl-L-histidine) is present in high concentrations in human skeletal muscles. The oral ingestion of beta-alanine, the rate-limiting precursor in carnosine synthesis, has been shown to elevate the muscle carnosine content both in trained and untrained humans. Little human data exist about the dynamics of the muscle carnosine content, its metabolic regulation, and its dependence on muscle fiber type. The present study aimed to investigate in three skeletal muscle types the supplementation-induced amplitude of carnosine synthesis and its subsequent elimination on cessation of supplementation (washout). Fifteen untrained males participated in a placebo-controlled double-blind study. They were supplemented for 5-6 wk with either 4.8 g/day beta-alanine or placebo. Muscle carnosine was quantified in soleus, tibialis anterior, and medial head of the gastrocnemius by proton magnetic resonance spectroscopy (MRS), before and after supplementation and 3 and 9 wk into washout. The beta-alanine supplementation significantly increased the carnosine content in soleus by 39%, in tibialis by 27%, and in gastrocnemius by 23% and declined post-supplementation at a rate of 2-4%/wk. Average muscle carnosine remained increased compared with baseline at 3 wk of washout (only one-third of the supplementation-induced increase had disappeared) and returned to baseline values within 9 wk at group level. Following subdivision into high responders (+55%) and low responders (+15%), washout period was 15 and 6 wk, respectively. In the placebo group, carnosine remained relatively constant with variation coefficients of 9-15% over a 3-mo period. It can be concluded that carnosine is a stable compound in human skeletal muscle, confirming the absence of carnosinase in myocytes. The present study shows that washout periods for crossover designs in supplementation studies for muscle metabolites may sometimes require months rather than weeks.
http://www.ncbi.nlm.nih.gov/pubmed/19131472
suplementacja BA 4,8g/ed przez okres 5-6tyzni spowodowala wzrost poziomu karnozyny o 23-39% (w zaleznosci od miesnia)
co ciekawe jest inaczej niz w przypadku kreaytny
podobnie lecz
dluzej trwa faza wyplukania
po ~9tygodniach poziom karnozyny wrocil do stanu 'normalnosci'
spadek rzedu 2-4% na tydzien!
kolejena ciekawostka-
osoby roznily sie w poziomie karnozyny (nie poprawy wytrzymalosci!, tylko samym poizomie)
jesli chodzi o sam poziom karnozyny w miesniach -> podobnie jak w przypadku monohydrratu)
-osoby zanotowaly wzrost o 55% ! - ktore bardzo odczuwaly dzialanie
-inne tylko +15% - osoby słabo odczuwajace
i tez dla nich okres 'wyplukania' wynosil odpowiednio 15 i 6 tygodni!!!
sumujac - srednio moze byc z biodostepnoscia karnozyny (~20% przyswojone)
lepiej - wedlug bdana - suplementacja BA
it is not known how much carnosine is actually absorbed intact across the intestinal epithelium and how absorption is affected by the type of ingested meat. The paracellular route is not dominant for carnosine absorption. Thus, for intact absorption, carnosine has to cross the brush border membrane of the enterocyte to remain intact within the cell and to cross the basolateral membrane. Carnosine is thought to be transported across the brush border membrane via the peptide transporter PEPT1. Less is known about its outflow through the basolateral membrane. As suggested for small peptides, carnosine may reach the blood stream via a transporter less sensitive to extracellular pH than PEPT1, with lower substrate affinity but similar substrate specificity. Although carnosinase (EC 3.4.13.3) is less abundant than in kidney and liver, its presence has been evidenced in small intestine and part of the absorbed carnosine can be hydrolyzed within the enterocyte.
Dietary carnosine can be absorbed if it is not rapidly and fully hydrolyzed in the intestinal lumen. In our study, we observed in young pigs that, after a meat meal, about one-half of the ingested carnosine flowed to the mid jejunum. Whether the remaining carnosine was absorbed in the first part of the intestine or degraded is not known. In vitro studies suggested that carnosine in cooked meat was not very sensitive to pepsin and pancreatin digestion . Nonetheless, our data showed that even if carnosine was hydrolyzed in the gut lumen, this degradation was not rapid enough to prevent its absorption
Zmieniony przez - solaros w dniu 2011-05-02 17:12:15