If you had to use one or the other, which you would rather use for PCT for a cycle.
Yes this the steroid section and there is a PCT section but 97 viewing compared to 4 I hope to get a better response here.
Thanks.
agreed, there are no studies with 6-br that show that this is not a possibility so I would go with atd also6-bromo can convert to an androgen, so its ATD for me
...so you agree, but dont?agreed, there are no studies with 6-br that show that this is not a possibility so I would go with atd also
sorry bad english, lol......so you agree, but dont?
Z my friend , I`m happy to be with you on the forums again bro, I`m always learning when you`re around.I'd doubtfully ever use an OTC AI for PCT but if I did the only one I'd likely choose is 6-OXO. If I HAD to choose between these 2 though it'd be 6-Bromo.
6-Bromo would likely only act as a PH if used at 3-4 times the recommended dose. Just like almost any steroidal AI - formestane, exemestane, all will act like a PH at doses much higher than recommended. But they'll all also act as a good AI at the lower recomended doses. As for ATD I'd never even consider using it. Blocking too much estrogen is just plain bad and ATD does just that.
Plus ATD being an anti-androgen, eliminates males libidos. Also the point of PCT is to restore natural test, by increase luteinizing hormone (LH) and follicle-stimulating hormone (FSH). In clinical tests ATD was shown to decrese testes size and decrease LH - the exact opposite thing you need to happen during PCT.
i forgot about that! my bad brosorry bad english, lol...
what I meant to say is that I don't fell comfortable on taking a compound (on pct)that can act like an androgen in the body , as a anabolic I believe its a good product but as a test booster I still have my doubts and I still haven't seen studies showing me that PA is wrong
Z my friend , I`m happy to be with you on the forums again bro, I`m always learning when you`re around.
I have a question regarding those studies, does lh and fsh decrease since the beginning of the test?
I ask cause if it only decreases in the end I believe it makes sense cause the hypothalamus will fell a major increase in the testosterone values sending signals to decrease lh and fsh, but in the first days I think they probably rise cause test increase a lot.
The big problem with atd is that it binds to ar`s in the brain that manage libido , when atd bind to them dht isn't capable to do the same sending libido to the floor.
I believe that lower atd doses will not bring this problem so with ai`s we always have the same problem , too much is not too good.
By the way I agree with the 6-oxo
it would be really helpful if you could find those tests for me that show the declines
In this study, 1,4,6-androstatriene-3,17-dione (ATD) was demonstrated to cause time-dependent loss of aromatase activity in rat ovarian microsomes in vitro. In vivo, an injection of ATD caused inhibition of ovarian aromatase and reduced estrogen secretion in pregnant mare's serum gonadotropin-primed rats for at least 24 hr after injection. In rats with 7,12-dimethylbenz[a]anthracene-induced, hormone-dependent, mammary tumors, marked regression occurred with ATD treatment. Although estrogen secretion was not reduced below the diestrus level of controls, the rats remained anestrus, indicating that the proestrus surge of estrogen was prevented. LH, FSH and prolactin levels were also basal and LH and FSH did not rise after ovariectomy. ATD had no detectable hormonal activity in bioassay. Consistent with this, the compound did not interact appreciably with either androgen or estrogen receptors, was not uterotrophic, and did not interfere with mammary tumor regression in ovariectomized rats. Thus, the major activities of the compound which cause mammary regression in the rat appear to be inhibition of estrogen synthesis, via aromatase and gonadotropin suppression.
ATD can act as an anitandrogen.....agreed, there are no studies with 6-br that show that this is not a possibility so I would go with atd also
Can you explain exactly how you would taper ATD from 50mg/day down to 25 mg/week...or did you mean 25mg/day???From my experience, a mild, tapered dose of ATD (50mg/day down to 25mg/week) is highly effective at eliminating gyno, while maintaining libido.
correct me if I`m wrong but I think that arimatest combine the 2ATD can act as an anitandrogen.....
6bromo may convert to an active steriod
why not run them together may be beneficial
correct me if I`m wrong but I think that arimatest combine the 2
correct me if I`m wrong but I think that arimatest combine the 2
Reversitol Combinds them along with I3C and trans resveratrol
The trans-resveratrol is combined in Reversitol without absorption aids, which means that its efficacy is compromised.
as a test booster it may work , as a pct for highly suppressive steroids I would not use them on a early phase, either way 6-br needs a little more human research before I use it again...Reversitol Combinds them along with I3C and trans resveratrol
as a test booster it may work , as a pct for highly suppressive steroids I would not use them on a early phase, either way 6-br needs a little more human research before I use it again...
I understand your point of view but believe me using AI`s on a early phase of Pct can be a big mistake IMO, but maybe I`m wrong, lets see what the future brings ...i believe 6 bromo (mixed isomers but favoring the B isomer ) at 60 mg is not enough for suppression along with low dose ATD (highly potent stuff) I3C (hormonal regulater ect, ) the SERM like properties of trans resveratrol will be highly effective with something like Hemotest, and possibly low dose trione, will be more then benificial during PCT may even eliminate the use for a SERM in general.
if more people are willing to try these things rather then put them on a back burner and never touch them people may never know how effective they really are,
especially given issues with BUNK RESEARCH CHEMS which is not unheard of.
may be a while till things like this happen.
and i know how much **** ill get for this.
I understand your point of view but believe me using AI`s on a early phase of Pct can be a big mistake IMO, but maybe I`m wrong, lets see what the future brings ...
I also look forward to see the new pct product from lg, it looks very promising
efficeny is compromised in a lot of products, its easy enough to get a cheap DHB probuct/piperine product.
that's true ,it was a very strong hype and then... a very strong disappointmentiForce are the ones that touted their product as an end all for PCT. It is not and shouldn't be held in any higher regard than Novedex XT or Advanced PCT for post cycle usage.
iForce are the ones that touted their product as an end all for PCT. It is not and shouldn't be held in any higher regard than Novedex XT or Advanced PCT for post cycle usage.
i think in some regaurds it should...... maybe in others no....
but there needs to be more label info on the amount used.
with Novedex XT , its great yes, apct , Its good,
there are a tremendouse amounts that would synergize these supps to no end.
im working on the END ALL PCT. and am right now looking for a company to hear me out with a NDA so it can get things rolling.
iForce are the ones that touted their product as an end all for PCT. It is not and shouldn't be held in any higher regard than Novedex XT or Advanced PCT for post cycle usage.
really?6-bromo gave me nasty gyno.
really?
first time I heard that, you should start a thread explaining what happened
go epi...Epidrol @ 30mg = no more 6-bromo gyno AND got rid of pubertal gyno
Sorry, I almost missed this question.Can you explain exactly how you would taper ATD from 50mg/day down to 25 mg/week...or did you mean 25mg/day???
Sorry, I almost missed this question.
Yeah, I tapered from 2 caps/day down to 1 cap/week. But next time I'll probably try to open the cap and pour half the stuff in my mouth, and use the other half later in the week. That should spread it out better.
Actually, this protocol should even work for gyno. It's almost exactly what I did, and it completely erased my aggressive gyno.I'm not an advocate of running above 2 caps unless it's for gyno treatment so my taper advice would be...
2 caps ED for 2 weeks (one AM, one PM)
1 cap ED for 2 weeks (one PM)
1 cap EOD for 2 weeks (one PM)
REMEMBER! to always take ATD with a fatty meal or EFA supplement such as Flax oil or Olive Oil.
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LOL must of got banned the other day when they made creatine a schedule III substance![]()
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