sespress
Well-known member
- Awards
- 0
OK so I've been looking about and I've been wondering - I'm taking a product right now with 10/10/10 DMZ/MSten/Alpha1 - but people tend to look down on these pre-built prohormone stacks.
I guess I'm wondering:
With other drugs receptor sites can be fought over by drugs with roughly the same binding affinity, or totally displaced by another one with a higher affinity. Does this happen to a lesser or greater effect with gear? For instance, why not take the SDMZ, and other low doses of like anavar, and maybe a TD 1-Andro. Obviously this is too much. But why?
Is it too many things for the liver (in combination?), with the PH I can see this being the case.
Is it receptor site issues - too many cooks in the kitchen?
Is it simply that effective "Threshold" doses exist and to increase the qty of substances and still get an effect one would have to take too many of them to process?
I guess I'm wondering:
With other drugs receptor sites can be fought over by drugs with roughly the same binding affinity, or totally displaced by another one with a higher affinity. Does this happen to a lesser or greater effect with gear? For instance, why not take the SDMZ, and other low doses of like anavar, and maybe a TD 1-Andro. Obviously this is too much. But why?
Is it too many things for the liver (in combination?), with the PH I can see this being the case.
Is it receptor site issues - too many cooks in the kitchen?
Is it simply that effective "Threshold" doses exist and to increase the qty of substances and still get an effect one would have to take too many of them to process?