Bill, I've seen other posts saying that EQ is directly comparable to testosterone in side effects and the mechanism of those side effects. Whats the real story? What sides can one get from EQ, and by what mechanism do these sides occur?BOldenone is not 5-alpha reduced in the human body to any appreciable degree at all. Propecia is of no relevance.
Silent Method said:Bill, I've seen other posts saying that EQ is directly comparable to testosterone in side effects and the mechanism of those side effects. Whats the real story? What sides can one get from EQ, and by what mechanism do these sides occur?
What is the difference between "a 5-alpha reduced version of boldenone" and boldenone? Or have I misread this point? Does EQ target a particular mechanism(s) of hair loss and acne, and to what degree? If so, what, if any, androgen receptor inhibitor (or other drugs) would be effective against boldenone side effects?All androgenic side effects occur via androgen receptor stimulation. All AAS activate this receptor, and all potentially cause such side effects. T is a more potent androgen than most agents of course because it is reduced via 5-alpha reductase to DHT (a more potent steroid) in many androgen target tissues. Although a 5-alpha reduced version of boldenone (1-testosterone actually) is a more potent activator of the AR than boldenone, boldenone also has an extremely LOW affinity for 5-AR. 99.8% of the dihydro metabolites are relatively inactive 5-beta's. There are virtually no 5-alpha metabolites of boldenone found in humans. This is why Propecia, which inhibits 5AR, can lower the androgenic nature of T but not of boldenone.
w_llewellyn said:
All androgenic side effects occur via androgen receptor stimulation. All AAS activate this receptor, and all potentially cause such side effects. T is a more potent androgen than most agents of course because it is reduced via 5-alpha reductase to DHT (a more potent steroid) in many androgen target tissues. Although a 5-alpha reduced version of boldenone (1-testosterone actually) is a more potent activator of the AR than boldenone, boldenone also has an extremely LOW affinity for 5-AR. 99.8% of the dihydro metabolites are relatively inactive 5-beta's. There are virtually no 5-alpha metabolites of boldenone found in humans. This is why Propecia, which inhibits 5AR, can lower the androgenic nature of T but not of boldenone.
- Bill Llewellyn
Silent Method said:
What is the difference between "a 5-alpha reduced version of boldenone" and boldenone? Or have I misread this point? Does EQ target a particular mechanism(s) of hair loss and acne, and to what degree? If so, what, if any, androgen receptor inhibitor (or other drugs) would be effective against boldenone side effects?
pa1ad said:
Have fun Bill!!![]()

Thanks guys - you make me feel good about me!quote:
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Originally posted by pa1ad
Have fun Bill!!
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Thanks Pat!
I’ll try a more succinct explanation in a couple of minutes… as soon as the dizziness subsides from repeatedly hitting my head against the desk.
- Bill
Silent Method said:
Thanks guys - you make me feel good about me!
I reread your explination and it made more sense to me. (No really, it did.)
I'll pose a more succinct question - Will boldenone fuck with your hair in other ways? If so, is their an anti-androgenetic drug that can help?
ErgoGal said:
My answer to this is that all androgenic/anabolic steroids have the potential to cause male pattern baldness. However, since boldenone and its metabolites are not strongly androgenic, or related to DHT in any way, it probably is one of the milder steroids out there in regards to hairline.
BTW, we still don't really know if steroid's attacking of the hairline is just do to an androgen receptor mediated mechanism or if there is something unique about DHT that enables it to initiate some unique mechanism that is yet to be identified.
So we've determined that 5AR doesn’t touch EQ. Either boldenone flat out doesn’t touch your hair, or adverse effects regarding steroids and hair are at least partially androgen receptor mediated. I vote for the later. As Bill said, "all androgenic side effects occur via androgen receptor stimulation."BTW, we still don't really know if steroid's attacking of the hairline is just do to an androgen receptor mediated mechanism or if there is something unique about DHT that enables it to initiate some unique mechanism that is yet to be identified.
Silent Method said:
So we've determined that 5AR doesn’t touch EQ. Either boldenone flat out doesn’t touch your hair, or adverse effects regarding steroids and hair are at least partially androgen receptor mediated. I vote for the later. As Bill said, "all androgenic side effects occur via androgen receptor stimulation."
So whats the deal? Does boldenone fuck with your hair or not? From what I've gathered it does to some extent, so would a drug that inhibits androgen reception in the scalp (which we have determined finastride does not do) help?
Bill, you think up that concise answer yet?
pa1ad said:
Bill's statement is too absolute. We don't know for sure at this point if there are non androgen receptor mediated mechanisms involved in steroid side effects. Or steroid anabolic effects for that matter.
Great points pa1ad.Bill's statement is too absolute. We don't know for sure at this point if there are non androgen receptor mediated mechanisms involved in steroid side effects. Or steroid anabolic effects for that matter.
ONe more thing. In women at least, stanozolol ( a DHT derivative) seems to promote alot more hair loss then would be predicted by its androgenic potency. This suggests the possibility of non-androgenic mediated promotion of MPB by DHT and some of its derivatives
pa1ad said:Bill's statement is too absolute. We don't know for sure at this point if there are non androgen receptor mediated mechanisms involved in steroid side effects. Or steroid anabolic effects for that matter.
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