Suggested Use: as a dietary supplement, take one capsule three
times daily with meals.  After 8 weeks of continuous use,
discontinue for 4 weeks.  Do not exceed 8 weeks of continuous
use.

PLEASE NOTE: WARNING: NOT FOR USE BY INDIVIDUALS UNDER
THE AGE OF 21 YEARS. DO NOT USE IF PREGNANT OR NURSING.
KEEP OUT OF REACH OF CHILDREN. Do NOT consume this product
if you have a medical condition and/or taking any prescription
medication. Do not exceed recommended serving. Discontinue
use and call a physician or licensed qualified health care
professional immediately if you experience rapid heartbeat,
dizziness, severe headache, or other similar symptoms.

These statements have not been evaluated by the FDA. This
product is not intended to diagnose, treat, or prevent any disease.

More information is available at www.alrindustries.com
Product Information provided by ALR Industries
ALRI Restore / 90 capsules  [Expiration JUNE 2009]
Time to Restore™

ALR Industries Restore™ is not just
another testosterone booster. Though
an increase in testosterone
production alone is pretty cool, and
one of the reported major benefits of
Restore™, it would be only part
of the Restore™ optimized male
matrix.  Instead we have opted to see
how many arguments we can start
(and knock-offs we can inspire) this
time by raising the bar for product
expectations beyond what any one
product can currently offer
performance oriented males…by
doing the whole job. Its okay, we are
men, we like competition!

In today’s “soy-everything/estrogen is
good/testosterone is evil” world, men
have to deal with countless phyto and
xeno-estrogens in our foods and
environment.  Naturally it only gets
worse when we realize that these
feminizing phyto and xeno-estrogens
are ADDED to our own natural
estrogen production in our bodies.
Not bad enough? Okay, then some of
us also add products that aromatize
to estrogens.

Each of these feminizing factors
cause a net and additive negative
affect upon our lean mass and other
things male…and they add up. The
results are 3 fold:

Additional fat that produces additional
aromatase enzyme resulting in even
more of our manly testosterone being
converted into un-manly estrogens.
As most are now aware, aromatase
enzyme converts testosterone and
other androgens into estrogens.

The increase in estrogens
suppresses our male testosterone
production system via inhibition of the
the HPTA.

Excess estrogen production causes
another feminizing hormone to kick
in…

more info below...
1 bottle
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Testosterone booster +
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90 capsules
1 capsule 3X daily
Free on all orders
(7-9 days to the UK)
Pro-Anabol
Continued from above...

Estrogen Control

6-Bromodione: There are two types of estrogen aromatase inhibitors and application of only one leaves the other pathway open for feminizing potential.

6 alpha-Bromodione is a competitive inhibitor of aromatase enzymes. Basically this means it works by way of binding to the active binding site of the
aromatase enzyme resulting in prevention of interaction with other steroids that aromatize like testosterone and the rest of our favorite male androgens.
This is great for rapid binding and short term aromatase control, but unfortunately a competitive inhibitor will eventually let go of the enzyme and allow
it to do feminizing things to manly hormones. So, only half of the job is done, but it has its important role as well.

6 beta-Bromodione is a mechanism-based irreversible inhibitor of the aromatase enzyme. An irreversible aromatase inhibitor is also referred to as a
suicide inhibitor. It’s pretty cool in that it acts similar to a competitive inhibitor in the way it binds, but like a pissed-off ex-girlfriend, it is both highly
selective and it will not let go until death do they part.

Together the two analogs in 6-Bromodione make sure that estrogen is under control, and many would assume that less estrogen means the prolactin
would be under control as well. Often, once prolactin increases are stimulated, shutting it back down takes some extra effort and a protracted period of
time. How long are you willing to wait to be an optimized male?

Prolactin Inhibition

Many have heard of or used drugs like bromocriptine that inhibit prolactin production for medical needs. Of course one of the benefits is an often
reported increase in libido, and “related factors”, but the side-effects such as nausea and dry mouth can certainly negate the positive.

Prolact-X™ (Chasteberry Diterpine Matrix Extract)
There has been a long history of supplemental use of Chasteberry for treatment of PMS in women. Most researches believe that PMS is commonly the
result of high prolactin levels so no surprise that we took an interest in this herb.

The amino acid dopamine is the body’s natural controller of prolactin release. Of course many dopaminergic compounds have been noted as effective
treatments for increasing GH secretion as well, which correlates rather well with optimization in male performance due to the fact that elevated prolactin
results in decreased GH and IGF-1 production.

The search for the prolactin-suppressive principles in Chasteberry provided a number of compounds with dopaminergic properties. In short, research
showed that they bound to recombinant dopamine DA2-receptors and suppressed prolactin release from cultivated lactotrophs as well as in animal
experiments. The search for the chemical identity of the dopaminergic compounds resulted in isolation of a number of diterpenes of which some
clerodadienols were most important for the prolactin-suppressive effects. They were almost more effective in their prolactin-suppressive properties than
dopamine itself.

Naturally just crushing up a bunch of Chasteberry is not likely to do the job, but proper preparation of the de-feminizing herb has finally
given us an effective synergist to support male optimization.

So, cool, now that we have dealt with the HPTA suppression and feminizing issues. By doing so the obvious result is a notable and welcomed increase
in testosterone production. But hey, why not push all the way and reach for optimization?

Increased Free Testosterone

Free-T™ (Proprietary Pure Avenacosides Matrix)
Seems most males who use supplements for either lean mass gains, libido augmentation or both have heard of Avena Sativa. Yeah, I know, lots of
products already have some form avena sativa or its extracts in it, so what makes this one special? Of course we used an extraction process for maximum
active compound content (greatest possible amount of active milligrams per capsule), but in truth Restore™ as a product is special, our Free-T™
(Proprietary Pure Avenacosides Matrix) from avena sativa just works well in the whole matrix to provide maximum results.

In the body testosterone travels around in two forms: Bound or inactive…meaning it is bound to a protein called SHBGB, and Unbound or free…meaning
it is free to do manly things like build muscle and increase your capacity to perform sexually.

Basically there are phytochemicals in avena sativa called avenacosides A and B. Some studies indicate avenacosides increase actual active or free
testosterone in the body by freeing up the bound testosterone from SHBG so there is more active testosterone. What good is it to have all kinds of extra
testosterone if it is playing S & M games with SHBG?

Cortisol Inhibition

MbAET
Unless you went coma bound in the early 90’s you have been aware of the on going benefits reaped and progress made with DHEA and its even better
metabolites. As an example are the patented and effective products 7-OXO-DHEA and of course 7-Hydroxy-DHEA analogs. Since these analogs prevent
conversion into androgenic metabolites they have been touted by many as the best thing since pizza. Considering the lack of androgenic side effects
possible while promoting fat loss, lean mass retention and even maximizing thyroid gland activity, not a real surprise they have become very popular. Of
course oral bioavalability is pretty poor with most of these analogs thus requiring higher dosages.

Likely the most powerful and effective DHEA analog is b-AET (beta-androstenetriol). It has been shown in studies to be between 100 and 100,000 times
more active than its DHEA precursor metabolites. However, like most DHEA analogs there is the issue of poor oral bioavailability. By supporting the
delivery value through simple alkylation, MbAET is nearly 100% orally bioavailable and only takes a few milligrams to do its job.
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