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Question about type-II aas(feedback related)

Italianboy

New member
I know for what I red,that the main difference,to make it short,between the classes are in the binding in A/R.Type-I strongly bind the A/R.Type-II don't bind strongly th A/R and make their anabolic action through others patways.
This should mean that the type-I aas cause a major feedback to hypotalamus and causes a major HPTA shut down than type-II
But for what I know,drugs like anadrol,dbol,winstrol(all type-II)causes a faster shut down than primobolan,oxandrolone,boldenone(the type-II).
The only "right" type-II drugs should be Proviron because it doesn' bind strongly the A/R and it dosn't cause the HPTA shut down.
I ask this just for my knowledge and I don't want to go against anyone.Just a doubt-
 
It also depends on the rate of aromatization. Drugs that aromatize very poorly or not at all are going to have less effect on the hpta.
 
this is messing me up more!
Drugs like halo,anadrol and winstrol don't aromatize but shut down you HPTA faster!!
I think that mrBill roberts have to explain something on this.;)
 
Nimrod25 said:
It also depends on the rate of aromatization. Drugs that aromatize very poorly or not at all are going to have less effect on the hpta.

Huh?? Fina doesn't aromatize.
 
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