| 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. |
| Product Information provided by ALR Industries |

| 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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