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- Jan 10, 2010
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Great info in this thread, I am going to be giving it a shot in the next few weeks. I will post my feedback.
Starting tonight I will be taking MK every night with 1 mg of dac EOD, along with gw starting tomorrow. Hex will be 200mcg 2x day and Ipam at 500mcg once a day. My goal is to lose body fat and improve my cardio
That looks like a very good protocol.
What is hex and IPam? I have not herd of these compounds yet.Starting tonight I will be taking MK every night with 1 mg of dac EOD, along with gw starting tomorrow. Hex will be 200mcg 2x day and Ipam at 500mcg once a day. My goal is to lose body fat and improve my cardio
What is hex and IPam? I have not herd of these compounds yet.
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Thank you hitman911
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If you dont mind me asking. What brand do you use?no prob!
On another note, I took 5mg today of GW, and I had to make myself stop working out, and I was covered in sweat.
I did my weight workout, and then:
20 mins on the bike
5 mins on the rower
then 100 Leg kicks with each leg at full speed and I could have kept going. Not sure if it was a placebo effect or what, but it was crazy!!
I took it at 430 so i hope I can sleep, but Im sure my 1mg of dac and 10mg of mk should help
Sounds good to me either way.
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If you dont mind me asking. What brand do you use?
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Ok so if u have been away from cardio for yrs and lifting due to injuries foa about 1 yr or so, would gw be like an automatic i see improvement type thing? Or do u already have to be in some sort of cardio shape?
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maybe the vets can chime in on this because Im pretty new to peptides and RC, but, I always tell people to get a solid 4-6 months of consistent lifting in before you start messing with ANY type of supplement other than protein powder or creatine.
Just my .02 cents
Do the fat burning effects just come from training more due to the energy or does GW actually burn fat by itself?
Also how does the endurance increase compare to syntheselen or myosine.
Perfect answer. Needed this info.The fat burning effects come from the drug itself(GW-501516)
Activation of peroxisome proliferator-activated receptor delta induces fatty acid beta-oxidation in skeletal muscle and attenuates metabolic syndrome.
Tanaka T, et al. Proc Natl Acad Sci U S A. 2003.
Abstract
In this study, we defined the role of peroxisome proliferator-activated receptor beta/delta (PPARdelta) in metabolic homeostasis by using subtype selective agonists. Analysis of rat L6 myotubes treated with the PPARdelta subtype-selective agonist, GW501516, by the Affymetrix oligonucleotide microarrays revealed that PPARdelta controls fatty acid oxidation by regulating genes involved in fatty acid transport, beta-oxidation, and mitochondrial respiration. Similar PPARdelta-mediated gene activation was observed in the skeletal muscle of GW501516-treated mice. Accordingly, GW501516 treatment induced fatty acid beta-oxidation in L6 myotubes as well as in mouse skeletal muscles. Administration of GW501516 to mice fed a high-fat diet ameliorated diet-induced obesity and insulin resistance, an effect accompanied by enhanced metabolic rate and fatty acid beta-oxidation, proliferation of mitochondria, and a marked reduction of lipid droplets in skeletal muscles. Despite a modest body weight change relative to vehicle-treated mice, GW501516 treatment also markedly improved diabetes as revealed by the decrease in plasma glucose and blood insulin levels in genetically obese ob/ob mice. These data suggest that PPARdelta is pivotal to control the program for fatty acid oxidation in the skeletal muscle, thereby ameliorating obesity and insulin resistance through its activation in obese animals.