Masteron as an Anti-Estrogen
by Anthony Roberts, Author of Anabolic
Steroids - The Ultimate Research Guide
Discussion of pharmaceutical
agents below is presented for information only. Nothing here is meant to
take the place of advice from a licensed health care practitioner. Consult
a physician before taking any medication.
I know it must seem like I sit around all day trying to
find new uses for old drugs, but in this case, nothing could be further
than the truth. Before I get into how and why you can use Masteron as an
Anti-Estrogen, I’ll tell you a bit about where this idea came from, and
why I’m telling you about it. And yes, this works in real life, not just
on paper - I’ve used it and seen it used for this purpose successfully
by several athletes.
A few years ago, I wrote my first piece on Masteron (Drostanolone
Propionate), and discovered what its clinical use actually was: Reduction
of breast cancer tumors, and as hormonal treatment of breast cancer. Well…the
long version of that is that Masteron is an androgenic, anabolic steroid,
used as an agent used to prevent or inhibit the growth of cancerous tumors.
Then, in one of those weird "duh" moments, I realized
that gynocomastia, mastectomy, and Masteron all had that similar word root.
You’d think that having an English degree would have helped me notice this
fact sooner…anyway, I wrote the profile and didn’t think much about it
anymore. I was then contacted by the owner of an underground lab, and asked
why Masteron was always produced with a propionate ester, and whether it
would be ok with a longer ester. This began another long period of research
for me into Masteron. Well, I found out that Masteron would be fine with
a longer ester, but I actually had a chance to test it out with that particular
ester before it hit the market...I was still standing after 3 weeks on
it, so it was produced en masse (as a side note that particular Underground
Lab still produces it and it’s one of their better selling products).
So here I was with all of this research on Masteron and
nothing to do with it. Well, after I took another look at the compound,
a couple of things struck me. The first that struck me is that Masteron
is made for women! Yeah…go back and read that again if you have to. Masteron
is one of the few steroids that were actually created with women in mind,
not men, and it’s the one that most people tell women to avoid! And the
other thing that I noticed right away was that it is used for treatment
of breast cancer. In particular, it’s used for the treatment of estrogen
dependant breast tumors. By now, I’m sure you see where I’m going with
this…Nolvadex is used clinically for this same purpose, as is Arimidex,
Femera, Aromasin (a steroidal Aromatase Inhibitor), and Teslac (a steroid,
technically). That’s some good company to be in, if you’re a steroid. But
interestingly, Teslac is actually a steroid also, and Aromasin is a Steroidal
Aromatase Inhibitor. So why can’t a "real" steroid do the same job at preventing
breast cancer? Well, the answer is that it can!
To understand why Masteron can be used as an anti-estrogen,
first we need to know that it’s derived from DHT. Why is this important?
This is important because DHT directly inhibits estrogenic
activity on tissues. It is possible that it does this, possibly by acting
as a competitive antagonist to the estrogen receptor or by decreasing estrogen
receptor binding. Either way, it has multiple hypothesized mechanisms of
action in some tissues. It has also been hypothesized that DHT actually
suppresses estrogen’s effects not by inhibition of synthesis of estrogen
receptor, but by (get ready…big words coming up) decreasing estrogen-induced
RNA transcription at some point after the actual estrogen receptor binding
has occurred. This means, in much simpler terms, that the estrogen gets
to the receptor, but just doesn’t do its job (1). This means you can take
steroids that convert to estrogen (called aromatizable steroids) and not
worry about that estrogen possibly making you retain water, gain fat, or
watch "Desperate Housewives." Also, this could mean that the antiestrogenic
effect of DHT is mediated by an androgen receptor mediated mechanism. In
fact, DHT has been shown to prevent the estrogen-dependent augmentation
of the progesterone receptor in human breast cancer cells. And, not to
be redundant, but it’s important to remember that virtually all of the
anti-estrogens we use to control gyno and water retention are also used
to treat breast cancer. So, now we know have observed that androgens are
capable of inhibiting both the estrogenic induction and the ongoing stimulation
of PRc synthesis, but have no apparent effect upon basal concentrations
of this receptor. Dihydrotestosterone (DHT) demonstrates a very high degree
of inhibition of estrogen in human breast cancer cells. (2). But it’s not
just DHT that does this; its metabolites have been shown to inhibit aromatization
itself; DHT, androsterone, and 5alpha-androstandione are all potent inhibitors
of the formation of estrone from androstenedione. In fact, it's so potent
at reducing estrogen that transdermal DHT gel applied to the affected area
has been used to treat gynocomastia (3). DHT is such a potent anti-estrogen
that it been even been used to increase height in children with short stature,
and since it’s been determined that this increase is not due to GH-mediated
effects, it was strongly suggested that DHT’s anti-estrogenic effects are
the mechanism by which it can increase height (4) Of course, I suspect
I don’t need to tell you that DHT is structurally incapable or converting
to estrogen…
So all of this tells us that DHT will certainly have beneficial
effects on keeping our estrogen in check, but what about Masteron? Can
it be used as effectively? Well, let’s take a look at what Masteron actually
is, relative to DHT. But before we can do that, I think a quick explanation
of DHT is in order first. Don’t worry; I’ll make it as brief and painless
as possible.
DHT is actually the result of testosterone interacting
with the 5alpha-reductase (5a-R) enzyme. This enzyme is present in the
scalp, prostate, external genitalia, and other places. As far as I can
see, it apparently exists for the sole purpose of converting a steroid
with a double bond between carbon 4 and carbon 5 to one with a single bond
between them, and subsequently adding a hydrogen atom to each carbon. This
process is called (of course) 5alpha-reduction.
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+
5a-Reductase
=
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Testosterone
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Dihydrotestosterone
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So now we know how testosterone becomes Dihydrotestosterone.
And everything would be great if this is the only thing that happened to
our good old friend testosterone, because as you may already know, DHT
is a far more potent androgen than testosterone. But, unfortunately, this
is not the end of the story, because DHT is largely deactivated by the
enzyme 3-alpha Hydroxysteroid Dehydrogenase (3bHSD), which is mainly present
in skeletal muscle.
For our purposes here, we’re only going to be concerned
with one particular action of this enzyme. It can either converts a steroid
with a keto group on position 3 of the steroid to one with a hydroxy group
in that position, thus converting DHT is to androstanediol. This conversion
is part of reason DHT alone has not proven to be a very effective muscle
builder, as androstanediol is not going to be very anabolic at all. If
you look off to the left of the following molecular diagram, and compare
it to the one above for DHT, you’ll notice that the "O" (oxygen) has been
replaced with an "HO" (hydrogen + oxygen) at the third position:
Androstanediol
3bHSD is present all over the body (as is 5a-R, for the
most part), but is found in especially high concentrations in the scalp
and prostate, and it’s even possible that its actions on DHT will exacerbate
male pattern baldness in the former tissue. Also, it’s worth noting that
DHT is the androgen responsible for development of external genitalia.
This is most likely the reason that women experience a temporary clitoral
hypertrophy when they use the often recommended steroids (Primobolan, Anavar,
Winstrol, etc…) in excessive doses. In an interesting aside, I find it
really interesting that the most typical steroids recommended are the most
likely to cause clitoral enlargement and other possible androgenic effects.
But on the bright side, in my experience with female athletes, that first
effect is most welcome...actually, topical DHT can even be used to treat
Microphalia (extremely tiny genitalia) in males (5). This last fact, if
you’ve ever wondered, is the type of information discussed behind closed
doors by of owners and staff of "private/invite-only" anabolic steroid
boards and forums…for obvious reasons…
Ok, so now you know what DHT is, where it comes from,
what it can do, and why it’s not a particularly potent anabolic when used
alone. Here’s what Masteron is, relative to its parent compound, DHT. Masteron
is an injectable steroid that is simply the DHT molecule which has been
altered to be 2alpha-Methyl-DHT…you can see this modification by comparing
the DHT molecule above with the following Masteron one, and paying special
attention to the left hand side again, and the "H3C" modification:
Masteron, aka Drostanolone Propionate
This 2-alpha-methyl alteration makes it much more potent
anabolic, although it’s still only about 60% as anabolic as testosterone
and a quarter as androgenic. I’m going to speculate that these ratings
make it not the most potent anabolic in the world, but its anti estrogenic
effects plus its ability to increase aggression make it a very nice pre-contest
addition. This is also where we get the absurd rumor that Masteron won’t
do anything for you unless you’re already at a very low body-fat percentage.
This is not true at all. No matter what body-fat percentage you’re at going
to get a nice anti-estrogenic effect from Masteron, as well as some nice
aggression and strength in the gym - the former and latter are both known
as "non-genomic" effects, and are a result of the strong Central Nervous
System stimulatory effects of Masteron, which is very common with DHT derived
steroids. Basically, if you’re fat, and you take something that increases
aggression and has anti-estrogenic effects (Halotestin and Arimidex, lets
say), you wouldn’t expect to get huge and ripped. It’s the same thing with
Masteron. Now, what if you add in Arimidex and Halotestin to a pre-contest
cycle, you’ll get harder and look better. That’s exactly what’ll happen
if you add Masteron into a Pre-contest cycle. It’s not that you have to
be at some random body-fat percentage to get results from it, but you’ll
need to be at that lower body-fat percentage to "see" those results. Again,
if you’re fat and take Halo and Arimidex, you aren’t going to look much
better…think of Masteron in similar terms, but it won’t work as well for
aggression as Halotestin, and won’t be as good for combating estrogen as
Arimidex. Gauged against either one of them alone, Masteron will likely
make you look much harder and lift more weight. But if you are looking
to do a low dosage cycle with a minimal amount of compounds in it, a simple
Testosterone (propionate) and Masteron cycle may be exactly what you are
looking for. On a personal note, that is a cycle that I use very frequently,
at about 100mgs of each, shot every other day.
But has Masteron actually lived up to my claims for being
an anti-estrogen? Yes. From 1968 to 1972, a decent sized study was conducted
on Masteron, in a group of premenopausal women with breast cancer. About
a third responded well to Masteron (6). This is because of its anti-estrogenic
effects, clearly- though it doesn’t perform as well as Arimidex, Letrozole,
or Aromasin. If you’re not running huge amounts of aromatizable steroids,
this is a very good choice to add into your cycle. If you’re doing large
amounts of those compounds, then you need to use a traditional anti-estrogen
as your ancillary compound of choice. But if you’re running well under
a gram of aromatizable steroids, Masteron will likely be all the anti-estrogen
you need. This number comes from my person experience, as well as others
I’ve interviewed.
Now, as a bit of an addendum, I’d like to address the
use of Masteron in women. Lets get this straight: Masteron was developed
for women. Okay? Got me? If you’ ve been paying attention up to this point,
you already know that Masteron is intended for females and is derived from
the same root (DHT) as most other steroids commonly used and recommended
for female athletes (Primobolan, Anavar, Winstrol, etc…are all derived
from DHT). And, another shocking fact is that Masteron has a lower androgenic
rating than almost every other commonly recommended steroid used by female
athletes. Anavar has a rating of 24 compared to oral testosterone and Masteron
has a rating of 25 compared to testosterone, expressed as a percent (so
yes that means 24% and 25% respectively).
Basically, Masteron works as a hormonal therapy for breast
cancer and has been shown to be a useful and safe agent for females of
all age groups, even though it may appear to be less effective then other
possible therapies in postmenopausal patients (6). It is, therefore, very
safe for women. Masteron is certainly no less safe than Anavar or Primobolan
for women, as long as it’s used with something resembling a degree of respect
and intelligence.
My recommendations for female use of this compound would
be to start between 10-25mgs every third day, and increase dosages from
there if no side effects are experienced. At those dosages, I suspect no
side effects would be experienced, and I’d be comfortable saying none will
be experienced up through 20mgs, injected every other day.
So there you have it. A totally new way to look at an
old friend - Masteron - it’s useful as an anti-estrogen as well as an anabolic,
and can certainly be safely used by both Men as well as women.
About The Author
Anthony Roberts has been researching anabolic steroids
for over a decade and is the author of the new book, Anabolic
Steroids: Ultimate Research Guide. He began his research at the age
of seventeen while he was a competitive martial artist, ultimately winning
a silver medal in his state martial arts tournament in the black belt division.
His firsthand experience in steroids began after he switched sports and
began playing rugby, in which he ultimately made two consecutive appearances
at the hooker position in the national collegiate all-star games.
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