IGF-1LR3 sub q??
- Thread starter gymrat827
- Start date
956Vette
Member
Yes, although Needto's endorsement means little
No issues if you dont want to go IM w/ LR3. Claims of better and fatloss help is silly/marketing imho
956Vette
Member
Nope, n/a imho
gaijininjapan
Active member
From all my limited research over the past few weeks, this is what I've gathered.
IGF attaches to receptor sites that make cells grow. I don't know what cells have receptors, but seems like all cells have receptror, which is why too much will give you GH gut, and also why IGF is commonly pinned bilaterally in the trained muscles. The injected stuff will atach to local receptors, and the rest will circulate. LR3 makes it not break down immediately when it hits the bloodstream, alowing it to travel and attach to other receptors when/if it gets into the bloodstream.
Fat cells are still cells, and I hope they don't have IGF receptors... get what I'm saying?
It's easy to pin IM with IGF. a slin pin in your quads, biceps, delts, tris, lats, etc... so why subQ?
IGF attaches to receptor sites that make cells grow. I don't know what cells have receptors, but seems like all cells have receptror, which is why too much will give you GH gut, and also why IGF is commonly pinned bilaterally in the trained muscles. The injected stuff will atach to local receptors, and the rest will circulate. LR3 makes it not break down immediately when it hits the bloodstream, alowing it to travel and attach to other receptors when/if it gets into the bloodstream.
Fat cells are still cells, and I hope they don't have IGF receptors... get what I'm saying?
It's easy to pin IM with IGF. a slin pin in your quads, biceps, delts, tris, lats, etc... so why subQ?
MattPorter
Banned
Like most, we have all been "taught" and heard things about numerous "facts" and protocols regarding IgF1
Arguments such as pinning in the abdomen subQ will attach to igf1 receptors in the intestines FIRST, before circulating to skeletal muscle. So out of fear, one would pin IM bilaterally....right????
But, if you pin too much the circulating igf1 in the blood stream is active and will eventually attach to some cells in the body, so how much igf1 dosage is "too much"
These are all questions NO ONE has any definitive answer for,,,,,
When you think about this simple logic it makes sense and would leave one to believe IM is the bets route to go...
Arguments such as pinning in the abdomen subQ will attach to igf1 receptors in the intestines FIRST, before circulating to skeletal muscle. So out of fear, one would pin IM bilaterally....right????
But, if you pin too much the circulating igf1 in the blood stream is active and will eventually attach to some cells in the body, so how much igf1 dosage is "too much"
These are all questions NO ONE has any definitive answer for,,,,,
When you think about this simple logic it makes sense and would leave one to believe IM is the bets route to go...
gaijininjapan
Active member
And going off of that, if you're pinning site specific, might as well use a lower dose. you can't really have "too low" a dose I think. Personally, I think I'll be doing 20mcg per side when I start, so a total of 40mcg post-WO. I still got months to plan it though, since I'll be doing this in PCT.
now for more PEG-MGF research...
MattPorter
Banned
Thats a practical approach. If you read up on Datbtrues ideology on igf/mgf he likes to emphasize proliferation -- differentiation. rotating back and forth between both compounds.
Has there EVER been anyone who truthfully ran igf-1 / mgf all on its own and kept all variables in check that recorded progress pictures/measurements?
I would love to see it.