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Hey Smart Guys...Why is Anavar suppressive?

THANK YOU THANK YOU I have said this all along with no avail. i've been called crazy many times over for stressing this but oh well thanks again.good post
 
There is a estrogen feedback loop as well as androgen feedback loop. That simple. In a normal male, if estrogen production is inhibited, testosterone levels will increase. But they will only increase so much before androgen suppression kicks in.
 
atutt2 said:
http://jcem.endojournals.org/cgi/co...jkey=17cfa0e6eacf0320a6cb1c47233c6e08a627fd3d
I'm sure most of you have seen this study which shows that daily admin of 15mg of anavar will cut your natural Total Test production in half in just 5 days. Does anyone know the exact reason/cause?
If we assume that it is a non-aromatizing AAS, and estrogen loop feedback is what causes typical HPTA shutdown, why is var doing this????
Fonz? Dr JMW? Anyone know???
There's 3 negative feedback loops that effect the HPTA- androgens,estrogens and progestogens.

I've read that oxandrolone has an affinity for the androgen receptor.
Also your study demonstrates that ox induced an increase in AR expression.

Binding to the AR by ox has been shown to be stronger then testosterone and nandrolone.

Therefore negative feedback via the androgen system will be the culprit in HPTA supression.

B32
 
b1ewsw32 said:
There's 3 negative feedback loops that effect the HPTA- androgens,estrogens and progestogens.

I've read that oxandrolone has an affinity for the androgen receptor.
Also your study demonstrates that ox induced an increase in AR expression.

Binding to the AR by ox has been shown to be stronger then testosterone and nandrolone.

Therefore negative feedback via the androgen system will be the culprit in HPTA supression.

B32

Agreed.
 
b1ewsw32 said:
There's 3 negative feedback loops that effect the HPTA- androgens,estrogens and progestogens.

I've read that oxandrolone has an affinity for the androgen receptor.
Also your study demonstrates that ox induced an increase in AR expression.

Binding to the AR by ox has been shown to be stronger then testosterone and nandrolone.

Therefore negative feedback via the androgen system will be the culprit in HPTA supression.

B32

But isn't estrogen the number one mechanism over HPTA vs all others?
Could the drop in test levels be due to increased neuro-net activity?
Some type of neuro-net overload and effect of DHT?
 
this isnt some'n new..

ANY steroid will slow down naturaly test levels.
 
Are we still looking for the best bridge here or what? This has been going on for as long as I can remember. I have never tried var, but d-bol in the am is a viable option. Sure, there is definitely suppression but that's the decision you make with a bridge or with taking any AAS whatsoever really. That's the trade off. Nothing is free.
 
Nathan said:
Are we still looking for the best bridge here or what? This has been going on for as long as I can remember. I have never tried var, but d-bol in the am is a viable option. Sure, there is definitely suppression but that's the decision you make with a bridge or with taking any AAS whatsoever really. That's the trade off. Nothing is free.

cooking oil will not shut you down
 
Nathan said:
Are we still looking for the best bridge here or what?

Actually, no we're not. Please stick to the topic on this thread. If you want to start your own, "is var good for bridging thread" then feel free.

Anyways, back to the point....anyone know the actual mechanisms, processes, physiology, etc that goes on with administration of oxandrolone?
It must not have much of a signal, if once administration is ceased a quick return to full HPTA ensues without any type of pc therapy.
 
b1ewsw32 said:
There's 3 negative feedback loops that effect the HPTA- androgens,estrogens and progestogens.

I've read that oxandrolone has an affinity for the androgen receptor.
Also your study demonstrates that ox induced an increase in AR expression.

Binding to the AR by ox has been shown to be stronger then testosterone and nandrolone.

Therefore negative feedback via the androgen system will be the culprit in HPTA supression.

B32

Good explanation. It's through binding to the AR that thr HPTA gets supressed. HOWVER. This is very individualized. At 15-20mg/day, my test levels hover at around 600, while somebody else hover at around 100. This is wht it is crucial to get blood work done.

Also, I run 25-50mg Proviron about 4 weeks before my bridge(to saturate) the bloodstream of mesterolone, and increase the levels of endo LH as high as they can possibly go. This will also elevate your endo test by a small degree...100 or so points.
 
Well,
Let's just say a guy who really knows his shit...had this to say. Anyone here agree or disagree w/him and a reason why?

"Nope. It is the constant binding to the sytemic neuronet itself through these receptors that the LH levels decrease. Not the Hypothalamus, Pitutary or testes. Therefore not an HPTA issue."
 
Last edited:
atutt2 said:
Actually, no we're not. Please stick to the topic on this thread. If you want to start your own, "is var good for bridging thread" then feel free.

Anyways, back to the point....anyone know the actual mechanisms, processes, physiology, etc that goes on with administration of oxandrolone?
It must not have much of a signal, if once administration is ceased a quick return to full HPTA ensues without any type of pc therapy.

I was simply asking. Don't be rude princess.
 
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