ALR Industries BAM® 60 capsules

When you want...Superior Mass! When you need...Superior Strength!

BAM® is designed to support serious mass gain through the most effective pro-anabolic pathways.

1. Stimulate muscle AR’s for enhanced protein synthesis and tissue repair.
2. Bind SHBG to increase levels of free testosterone.
3. Increase LH/FSH to maximize output of natural testosterone.
4. Increase glycogen retention and optimize internal hydration levels.
5. Support superior protein synthesis through modulation of transcription factors.
6. Inhibits excessive cortisol levels for an anti-catabolic effect.
7. Promote recovery of the neuromuscular matrix.
8. Provide superior results either in a synergistic stack or as a standalone supplement.
   

Okay, So I Was Wrong…

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Do You Have Serious Bad Ass Mass?

BAM® from ALR Industries

The unique sapogenins matrix in BAM® is specifically structured to optimize a healthy pro-anabolic environment without producing any unwanted side effects. Notably, we have included sapogenins from a variety of sources that encompasses the broadest range of desirable effects on supporting pro-anabolism in the body with the greatest potency possible. Although there are a few other good sapogenins products available, this is not like any other product out at this time. (Hey, try it and get back to us)

We have extracted and structured four active (thought I would never say this) sapogenins for the following purposes that synergistically work together to create an optimized effect for muscle repair and recovery.

A Complete unique sapogenin matrix supports a mass building pro-anabolic environment through synergistic mechanisms:

1. Stimulate muscle AR’s for enhanced protein synthesis and tissue repair.
2. Bind SHBG (you know, those proteins that keep testosterone in bondage) to increase levels of free testosterone.
3. Increase LH/FSH (testes stimulating hormones) to maximize output of natural testosterone.
4. Increase glycogen retention and optimize internal hydration levels.
5. Support superior protein synthesis through modulation of transcription factors.
6. Inhibits excessive cortisol levels for an anti-catabolic effect.
7. Promote recovery of the neuromuscular matrix .
8. Provide superior results either in a synergistic stack or as a standalone supplement

Notably this is all achieved without any exogenous hormones whatsoever, and importantly (in the case of creating optimal environment for increasing lean body mass and weight) not utilizing anti-estrogenic compounds. What, no AI’s? (Aromatase inhibitors)

The use of AI’s has pretty much become the supplement industry standard for testosterone boosting. And it works pretty well. Jungle Warfare™ and Restore™ are serious products for this reason….and others.

The way AI’s work is by controlling the aromatase enzyme that converts susceptible androgens (like testosterone, androstenediol and others your body makes) into estrogens. When there is too much estrogen in the body it shuts down the HPTA and the “boys” stop kicking out the testosterone. Well, AI’s shut down the excess estrogen production and the “boys” get to run wild for awhile. Big problem with most AI’s is the possible false positive test results for athletes.

This is important for superior mass gains:

Usually the very low circulating estrogen levels required for anti-estrogens to positively affect natural testosterone levels will suppress or decrease proper intracellular fluid retention in muscle. This in return prohibits the muscle from achieving maximal glycogen, nutrient and water up-take that promote muscle fullness and optimized anabolism. In short, less cell food means less cell size and growth.

While being very dry is important for shows, and there is a period in every protocol that estrogen suppression is significantly beneficial. In fact, lately there is a much needed and much over looked mass gaining synergy that results from having the “right amount” of circulating estrogen at the right period to assure maximum growth and recovery.

Even more so when you really need to pack on the mass. Of course this makes BAM® a Bad Ass stacker too.

Note that illegal true mass building steroid cycles always included the ability to have an optimal effect of this nature, without falling over into excess.

(25R) – 4-Spirosten-3b,6b-diol: The plant 4-Spirosten analogs appear to have the potential for mild aromatization thus aiding synergistically in mass gain oriented product designs. In the original testing (and according to the Russians) the structure overall was a good standalone compound for weight and strength gain support but in our opinion was best when we augmented BAM® with synergists like any stack. Does it work? Well, we have a patent pending on it at the moment so we obviously think so.

(25R) -5- Alpha-Spirostan-6-one-3b-ol: Here is an interesting non-aromatizing compound that the Russians bragged a bit about as being superior for strength and hardness. Personally (and I do not blame other sharp researchers for continuing to doubt its value) I noted an increase in hardness, strength and libido after about the first week of use.

Since we were getting good results with these two unlikely compounds we finished the design with two extracts we have had good results from.

Ptychopetalum Olaoides Extract: Okay, so this is also another odd one but so was creatine monohydrate when it first hit the general market. (Athletes had been using it for years before then). A simple name for this herbal is Muira Puama which is an extract from a plant in the Amazon region of South America. It has been widely used as a powerful aphrodisiac, nerve stimulant, tonic and cure for rheumatism and muscle paralysis. We used it as an overall adaptagen. Over a period of about 2 weeks we have seen (and felt) a significant increase in training intensity as a result of use. Finding the right extraction method for potency and affect was the hard part. (Lots of Third Party Reference reading at the end for those interested)

Basella Rubra: No doubt many are going nuts on PubMed and elsewhere trying to figure this one out. Simple, it has some interesting carriers in it, and some other aspects I will explain in the up-coming FAQ.

With the addition of BAM® we have created this optimized environment that is so important in fostering the ultimate conditions for maximum accrual of lean body mass. Yes, and this facet seems to be all too often neglected. As such BAM® is, as the name says, the newest tool to slap layers of Bad Ass Mass on your frame.

Of course each of the ALR Industries Size and Strength Series products will provide excellent results. However many muscle and performance enthusiasts are looking for the ultimate edge in total Lean Mass accruement and how can they get it the fastest. For them we offer the Size and Strength Evolution Stack.

Third-Party Published Research

1. Experimental study of the anabolic activity of 6-ketoderivatives of certain natural sapogenins (In Russian) 1976 Sep-Oct;39(5):631-5
2. Rowland, D. L., et al. “A review of plant-derived and herbal approaches to the treatment of sexual dysfunctions.” J. Sex. Marital Ther. 2003 May-Jun; 29(3): 185-205.
3. Waynberg, J., et al. ”Effects of Herbal vX on libido and sexual activity in premenopausal and postmenopausal women.” Adv. Ther. 2000 Sep-Oct; 17(5): 255-62.
4. Waynberg, J. “Male sexual asthenia—interest in a traditional plant-derived medication.” Ethnopharmacology; 1995.
5. Waynberg, J. “Contributions to the clinical validation of the traditional use of Ptychopetalum guyanna.” Presented at the First International Congress on Ethnopharmacology, Strasbourg, France, June 5-9, 1990.
6. Gaebler, H. “Revival of the drug Muira puama.” Deut. Apoth. 1979; 22(3): 94–6.
7. da Silva, A. L., et al. “Anxiogenic properties of Ptychopetalum olacoides Benth. (Marapuama).” Phytother. Res. 2002; 16(3): 223-6.
8. Siqueira, I. R., et al. “Psychopharamcological properties of Ptychopetalum olachoides Bentham (Olacaceae).” Pharmaceutical Biol. 1998; 36(5): 327–34.
9. Raymond-Hamet, A. “Physiological action of the extract of muira puama.” Comp. Rend. Soc. Biol. 1932; 109: 1064-7
10. Olofsson, Eric. “Action of extract of Liriosma ovata on the blood pressure, vessels and respiration of the rabbit.” Compt. Rend. Soc. Biol. 1927; 97: 1639-40.
11. Bucci, L. R., et al. ”Selected herbals and human exercise performance.” Am. J. Clin. Nutr. 2000 Aug; 72(2 Suppl): 624S-36S.
12. Paiva, L., et al. “Effects of Ptychocepalum olacoides extract on mouse behaviour in forced swimming and open field tests.” Phytother. Res. 1998; 12(4): 294–96.
13. Waynberg, J. “Male sexual asthenia—interest in a traditional plant-derived medication.” Ethnopharmacology; 1995.
14. Hanawa, M., et al. “Composition containing an extract from muira puama root and plant worm extract.” Taisho Pharmacuetical Co., Ltd., Tokyo, United States Patent No. 6024984, 2000.
15. Siqueira, I. R., et al. “Psychopharamcological properties of Ptychopetalum olachoides Bentham(Olacaceae).” Pharmaceutical Biol. 1998; 36(5): 327–34.
16. da Silva, A. L., et al. “Memory retrieval improvement by Ptychopetalum olacoides in young and aging mice.” J. Ethnopharmacol. 2004 Dec; 95(2-3): 199-203.
17. Siqueira, I. R., et al. “Neuroprotective effects of Ptychopetalum olacoides Bentham(Olacaceae) on oxygen and glucose deprivation induced damage in rat hippocampal slices.” Life Sci. 2004 Aug; 75(15): 1897-906.
18. Siqueira, I. R., et al. “Ptychopetalum olacoides, a traditional Amazonian "nerve tonic," possesses anticholinesterase activity.” Pharmacol. Biochem. Behav. 2003 Jun; 75(3): 645-50.
19. Siqueira, I. R., et al. “Psychopharamcological properties of Ptychopetalum olachoides Bentham(Olacaceae).” Pharmaceutical Biol. 1998; 36(5): 327–34.
20. Forgacs, P., et al. “Phytochemical and biological activity studies on 18 plants from French Guyana.” Plant Med. Phytother. 1983; 17(1): 22–32.
21. Dias Da Silva, Rodolpho. “Medicinal plants of Brazil. Botanical and pharmacognostic studies. Muira puama.” Rev. Bras. Med. Pharm. 1925; 1(1): 37–41.
22. Jayasuriya, H., et al. “Diterpenoid, steroid, and triterpenoid agonists of liver X receptors from diversified terrestrial plants and marine sources.” J. Nat. Prod. 2005; 68(8): 1247-52.