So as far as I understand, the affinity for binding to androgen receptors is basically how readily a particular androgenic substance activates a receptor in cells. Different compounds have different affinities. Some more than others. Why when multiple steroids are used in a stack does the one with the highest affinity not take up all the "slots" and block out the others.
SERMS work by blocking up the estrogen receptors so actual estrogen can't activate them. Why would the strongest androgen not block out the weaker ones?
Are there different receptors that can be activated only by some androgens and not others? Must be some reason or people would have learned long ago to stick to only single steroid cycles.
Just curious.
SERMS work by blocking up the estrogen receptors so actual estrogen can't activate them. Why would the strongest androgen not block out the weaker ones?
Are there different receptors that can be activated only by some androgens and not others? Must be some reason or people would have learned long ago to stick to only single steroid cycles.
Just curious.
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