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Apr-30-2011

TestoBoost version IV

 

Natural Testosterone and Sex Drive Booster

 

 

Anabolic effects of TestoBoostA safe and effective way to dramatically increase your own natural testosterone production.

 

TestoBoost is by far the most powerful natural testosterone booster, and libido and sex drive enhancer on the market today. Version 4 is the third reformulation of the original TestoBoost, which came out in February of 2000. Each version has been improved by taking into account new research, my own clinical work, and feedback from those who used it.

 

http://www.mdplusstore.com

 

The original formula laid down the base for what I wanted to achieve for TestoBoost and that was to naturally increase testosterone levels and sex drive in both men and women. The pathways that I targeted included stimulating all the relevant areas of the hypothalamic-pituitary-testicular axis (HPTA) through several independent mechanisms, and to decrease any potential side effects from increases in estrogen and dihydrotestosterone. Subsequent versions of TestoBoost, while keeping the base intact, added several ingredients that I felt would further increase testosterone levels and sex drive, and further decrease any potential side effects.

 

The basis of the formula in TestoBoost, and in all the MD+ formulations, is to involve all possible pathways that lead to the desired effects, and to use multiple ingredients that work together to produce superior results. In the case of TestoBoost the desired effect was an increase in basal and elevated testosterone levels in the body, a decrease in counter productive elevations in cortisol, and a salutary effect on overall health, libido and sex drive.

 

All of this can be accomplished by using ingredients that are known or suspected to boost testicular steroidogenesis, increase sexual desire and performance.

 

For example, using a variety of ingredients to effectively act as a testosterone sink by trapping testosterone production is the most effective way to increase endogenous androgen production.

 

In order to do this you have to consider all the possible pathways that are involved in maximizing testosterone production, including:

 

 

As well, other compounds that have been shown to have effects on sexual desire and performance can be used in the mix. On top of this TestoBoost contains bioperine, which significantly enhances the bioavailability of supplemented nutrients through increased absorption.

 

The list of ingredients that could prove useful for increasing testosterone levels is long and includes various vitamins such as vitamin A, B6 and E, minerals such as zinc, magnesium, manganese, and other ingredients such as arginine, beta ecdysone boron, calcium-d-glucarate, catuaba bark, chasteberry (vitex agnus-castus), chrysin, co-enzyme q10 (ubiquinone), forskohlin, damiana, 5-methyl methoxy isoflavone, deer antler extract, eurycoma longifolia, genistein, GLA, glutathione, prickly pear extract, indole-3-carbinol, ipriflavone, maca root, muira puama, quercetin dihydrate, saw palmetto, schisandra chinensis, stinging nettle extract and tribulus terrestris.

 

Why TestoBoost is Better than the Prohormones or Replacement therapy with Testosterone or Anabolic Steroids

 

Prohormones

 

In the past decade the big push for those who want “anabolic steroid-like” effects was the prohormones. And even though some have been taken off the over the counter market, they are still available in one form or another either in North America or internationally over the Internet. They range from DHEA to androstenedione, to the more sophisticated ones that are supposed to be precursors to other anabolic steroids including nandrolone (Deca), boldenone, and even 1-testosterone compounds. The even include steroid like compounds that have various effects on either or both estrogen and testosterone.

 

DHEA, while it may be useful for women, and for other purposes, is useless for increasing endogenous testosterone levels in men. Ditto for androstenedione and androstenediol. Norandrostenediol, norandrostenedione, the boldenone and 1-testosterone precursors, and in fact any precursor prohormones are also relatively useless at providing real androgenic-anabolic effects.

 

The trend in the prohormones, as the manufactures get bolder and bolder, is to actually have weak versions of anabolic steroids on the supplement market. This is the case with 1-testosterone and the 17-alpha methylated 1-testosterone, which in fact are weak anabolic steroids, with lower androgenic and anabolic effects than the more potent anabolic steroids that have been marketed over the years. Basically the ones being produced now and passed off as over the counter prohormones/steroids are the cast offs of the steroid producing drug industry.

 

The problem with all of these compounds on the market today is that while they have minimal androgenic and anabolic effects, they have significant side effects, both known and unknown. The prohormones that are being developed today as over the counter nutritional supplements (read that as drugs) haven’t been investigated or studied for their potential short term or long term side effects.

 

This is where the real problem with these compounds lies. We don’t know what effects they have on various parts of the body including the liver, cardiovascular system, prostate, kidney, and especially on the hypothalamic-pituitary-testicular axis (HPTA). These products would never be allowed as prescription drugs because of the lack of proper animal and more importantly human trials. However, they’re blatantly dumped on the market as nutritional supplements, when in fact they’re drugs, or more correctly low level, and usually ineffective, anabolic steroids – with less efficacy than the commercial anabolic steroids, but with unknown, and potentially very harmful side effects.

 

While most of the prohormones and hormones that are available as nutritional supplements are of no use or marginally useful for body composition purposes, they can have significant side effects. One of the side effects that is most troubling is the effect they have on the hypothalamic-pituitary-testicular axis (HPTA), the pathway that’s involved in endogenous testosterone production and control.

 

The worst-case scenario, and one that is common with the use of most of the prohormones, is that there is very little anabolic effect from the compounds themselves, but significant side effects, especially with a dampening effect on the HPTA, which in turn shuts off the production of endogenous testosterone. This HPTA shutdown also occurs with the use of exogenous testosterone and anabolic steroids, and can result in permanent dysfunction of the normal HPTA, to the point where when these compounds are discontinued (as they invariably are) endogenous testosterone levels remain in the basement, and replacement therapy is sometimes the only solution to achieving normal systemic testosterone levels. In other words they become either temporarily, or sometimes permanently eunuchoid. 

 

Thus, the overall effect is a negative one in that the level of effective anabolic androgens in the body is decreased and the person thus has less anabolic hormones in their body. On top of that there are several possible side effects including a refractory HPTA, estrogen side effects, hepatoxicity, and adverse effects on cholesterol and the cardiovascular and immune system.

 

And if you’re a drug-tested athlete, there is the very real possibility that you will test positive for the prohormones, especially with the norsteroid and boldenone precursor prohormones. A positive test, because of the difficulty of distinguishing the metabolites of the prohormones from the metabolites of the real anabolic steroids, leads to the same severe penalties, often a two to four year ban, as a positive for anabolic steroids.

 

Replacement Therapy with Testosterone and Anabolic Steroids

 

Using testosterone and/or anabolic steroids to increase your levels of androgens in your body is also the wrong way to approach the problem of low systemic testosterone levels. For example, use of exogenous testosterone shuts down the hypothalamic-pituitary-testicular axis (HPTA) that controls testosterone production on the body.

 

Instead of helping stimulate testosterone production, the use of testosterone and anabolic steroids decreases the natural production of testosterone and basically shuts down your internal machinery for making testosterone. Once you go off the replacement therapy, your testosterone levels often end up lower than before you started taking the exogenous androgens. In some cases testosterone levels never even come close to recovering the pre androgen use levels, and the only alternative, if the system can’t be “kick started” to produce testosterone, is to go back on replacement therapy with testosterone or anabolic steroids.

 

On the other hand, endogenous (developed within the body) hormone production avoids many of the problems associated with exogenous hormone use. By promoting the natural production of the hormone within the body, the regular feedback mechanisms are not by-passed and do not lead to many of the side effects associated with exogenous hormone use.

 

In fact the use of TestoBoost and other methods to increase endogenous testosterone production ramps up your natural testosterone producing machinery so that even if you stop taking it, your natural levels will be at least as high as before you started, and sometime higher as the body recognizes the higher level as normal and maintains that level naturally.

 

The bottom line is that whatever your reasons for wanting physiologically increased levels of testosterone, TestoBoost is the best way to go. Besides being more effective in increasing testosterone levels and providing an anabolic drive, the use of TestoBoost won’t result in a positive drug test, as is the case with the prohormones, especially the norsteroid ones, exogenous testosterone and anabolic steroids.

 


New Version of TestoBoost

 

Research in nutrient metabolism and its effects on the body’s hormonal and other systems is accumulating on a daily basis. The advancements made in the scientific and medical fields far outstrips the advancements made in computer chip technologies. However, although Intel puts out a new improved chip on a regular basis, most nutritional supplement products are rarely updated.

 

In the nutritional supplement field, changes made to formulations are usually to remove a substance that has been either banned or found harmful. Thus the new formulations aren’t done for the sake of improving the formula but simply to stay compliant and thus to avoid any legal problems. Examples of this are the new formulations of weight loss products that have removed ephedra and tried to fill the gap by introducing one or two other substances to make it look like they’ve actually improved the product rather than lessened it. These reworked products are a far cry from products, such as MD+ LipoFlush that are built from the ground up without even giving a thought to the use of ephedra.

 

My reasons for reformulating include:

 

  1. The use of new scientific information.
  2. The use of information from athletes who found certain ingredients useful.
  3. The use of information from personal clinical studies on the effectiveness of adding certain ingredients to the present formulation.
  4. Feedback from colleagues and others who have used the product, including their subjective results and blood work.

 

TestoBoost V4.0 contains a unique formulation that will:

 

 

TestoBoost is useful for anyone who wants to naturally increase their testosterone levels in order to increase muscle mass and strength and boost sex drive. It’s also useful for those who have lower than normal endogenous testosterone levels whether due to age, overtraining, stress, sickness, or even while on or after the use of anabolic steroids and prohormones.

 


Changes in TestoBoost v4.0

 

A number of ingredients have been added to the TestoBoost formula. TestoBoost was already a very popular and effective supplement and very few of the original ingredients have been altered except to vary the concentrations of some of them.

 

As well new ingredients have been added.

 

New ingreients include:

 

Vitamin D – 400 IU

Coenzyme Q10 – 20 mg

Piridoxyl form of B6 was combined with

 

The following ingredients were increased:

 

Vitamin C

Vitamin E

Vitamin B12

Magnesium

Zinc

Tribulus

Acetyl-L-Carnitine

Alpha Lipoic Acid

 

The Proprietary Complex ingredient amounts were rearranged with the major change being the significant increase in D-aspartate, which now is now the most abundant ingredient in the complex.

 

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Vitamin B12 (as methylcobalamin) was increased from 100mcg to 200 mcg. Methylcobalamin is the biologically active form of B12, whereas cyanacobalamin, the form used in most supplements, is the synthetic form. The body has to change the cyanacobalamin into methylcobalamin. This process may be compromised in some people so using the metabolically active form is more efficient and improves bioavailability and function. B12 helps to optimize macronutrient metabolism, maximize muscle mass and decrease body fat. As well, it helps to decrease serum levels of homocysteine, cholesterol and C-Reactive proteins, markers of heart disease and inflammation in the body. Decreasing inflammation helps to decrease cortisol levels and thus increase the anabolic effects of TestoBoost.

 

Magnesium

 

A combination of magnesium salts (aspartate, oxide and octadecanoate) were incorporated to take the place of the magnesium oxide. While most of the magnesium is in the form of the aspartate (the form that has been shown influence testosterone levels and is the ingredient that is ZMA, along with zinc monomethione and B6, which are also in TestoBoost). Magnesium in the form of oxide and octadecanoate are also included as both sources of magnesium and to make the tablets more cohesive and less susceptible to breaking in transport.

 

Arginine alpha-ketoglutarate

 

Arginine alpha-ketoglutarate has both its pluses and its minuses. This compound has several important effects. There is evidence that alpha-ketoglutarate preserves muscle mass and acts as an efficient anticatabolic compound.[i],[ii] Addition of alpha-ketoglutarate to postoperative total parenteral nutrition prevented the decrease in muscle protein synthesis and free glutamine that usually occurs after surgery.[iii] One study has found that an alpha-ketoglutarate-pyridoxine complex may have some beneficial effects on human maximal aerobic and anaerobic performance.[iv]

 

Thus, by ingesting AKG in sufficient quantities, the demand for muscle glutamine might ultimately be spared to some degree, thereby allowing muscle protein synthesis to proceed unhindered (e.g. such as during the muscle hypertrophic response which follows a resistance training workout), and reducing the catabolism of muscle tissue.

 

Studies have shown that:

 

1.AKG reduces the decline in muscle free glutamine that is associated with reductions in protein synthesis.[v]

 

2. The use of AKG, instead of glutamine, prevents the decline in protein anabolism observed following surgery.[vi]

 

AKG seems to exert anti-catabolic effects by preserving muscle glutamine.[vii]

These results are not surprising in that the carbon skeleton of BCAAs can be used to synthesize glutamine after the transamination reaction of BCAAs, and ketoglutarate is the immediate carbon donor for glutamine synthesis. The utilization of arginine and ornithine as a carbon source for glutamine synthesis is also a possibility.

 

A recent study looked at the effects of L-arginine alpha-ketogluterate (AAKG) on measures of body composition and performance.[viii] Two separate studies were conducted to assess the pharmacokinetic profile of ingesting two forms of AAKG, timed released and non timed release, in the blood (study 1) and the effects of dietary supplementation of AAKG on training adaptations in resistance-trained men (study 2).

 

The study found that the 2 formulations have different pharmacokinetic patterns that may affect arginine release, uptake, and/or physiologic effect over time. As well, the L-arginine alpha-ketogluterate (AAKG) in both formulations positively influenced strength (as measured by one rep maximum bench press) and Wingate peak power performance.

 

 

Arginine also has several beneficial effects.[ix] First of all it moderately increases nitric oxide (NO), which in turn facilitates vasodilation, improves sexual functioning, increases growth hormone secretion, and helps keep you cool during exercise thereby increasing your ability to exercise longer.[x]

 

However, the ability of arginine in higher doses to increase nitric oxide is one of the reasons that TestoBoost contains only 100 mg of arginine exerts The beneficial effects of arginine in increasing nitric oxide

 

Info on arginine not affecting NO – nitrite and nitrate different.

 

 

 

 

D-Aspartate

 

D-aspartate (D-Asp) was increased to 1.2 grams per dose for two reasons. First of all aspartate has been shown to increase testosterone production in murine models.[xi] A study set up to see if a relationship exists between the presence of D-Asp and the hormonal activity[xii] had the following results:

 

1) Both D-Asp and testosterone are synthesized in rat testes in two periods of the animal's life: before birth, about the 17th day after fertilization and, after birth, at sexual maturity.

2) Immunocytochemical studies have demonstrated that this enantiomer is localized in Leydig and Sertoli cells.

3) In vivo experiments, consisting of i.p. injection of D-Asp to adult male rats, demonstrated that this amino acid accumulates in pituitary and testis (after 5 h, the accumulation was of 12 and 4-fold over basal values, respectively); simultaneously, luteinizing hormone, testosterone and progesterone significantly increased in the blood.

4) Finally, in vitro experiments, consisting of the incubation of D-Asp with isolated testes also demonstrated that this amino acid induces the synthesis of testosterone.

 

Recent studies have shown that D-Asp has similar effects in man in that it has a role in the regulation and physiological levels of luteinizing hormone and testosterone.[xiii] For the full PDF version of this study go to http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2774316/pdf/1477-7827-7-120.pdf.

 

Also this compound has significant metabolic effects, including AMP production, improving the salvage of ATP from in muscle cells, and also acts as an anaplerotic precursor and thus increases TCA flux and ATP formation. This aids in the synthesis of hormones, including testosterone and growth hormone.[xiv]

 

 

 


Reprod Biol Endocrinol. 2009 Oct 27;7:120.

The role and molecular mechanism of D-aspartic acid in the release and synthesis of LH and testosterone in humans and rats.

Topo E, Soricelli A, D'Aniello A, Ronsini S, D'Aniello G.

Source

1Stazione Zoologica Anton Dohrn, 80121, Villa Comunale, 80121, Napoli, Italy. enza.topo@szn.it

Abstract

BACKGROUND:

D-aspartic acid is an amino acid present in neuroendocrine tissues of invertebrates and vertebrates, including rats and humans. Here we investigated the effect of this amino acid on the release of LH and testosterone in the serum of humans and rats. Furthermore, we investigated the role of D-aspartate in the synthesis of LH and testosterone in the pituitary and testes of rats, and the molecular mechanisms by which this amino acid triggers its action.

METHODS:

For humans: A group of 23 men were given a daily dose of D-aspartate (DADAVIT) for 12 days, whereas another group of 20 men were given a placebo. For rats: A group of 10 rats drank a solution of either 20 mM D-aspartate or a placebo for 12 days. Then LH and testosterone accumulation was determined in the serum and D-aspartate accumulation in tissues. The effects of D-aspartate on the synthesis of LH and testosterone were gauged on isolated rat pituitary and Leydig cells. Tissues were incubated with D-aspartate, and then the concentration (synthesis) of LH and cGMP in the pituitary and of testosterone and cAMP in the Leydig cells was determined.

RESULTS:

In humans and rats, sodium D-aspartate induces an enhancement of LH and testosterone release. In the rat pituitary, sodium D-aspartate increases the release and synthesis of LH through the involvement of cGMP as a second messenger, whereas in rat testis Leydig cells, it increases the synthesis and release of testosterone and cAMP is implicated as second messenger. In the pituitary and in testes D-Asp is synthesized by a D-aspartate racemase which convert L-Asp into D-Asp. The pituitary and testes possesses a high capacity to trapping circulating D-Asp from hexogen or endogen sources.

CONCLUSION:

D-aspartic acid is a physiological amino acid occurring principally in the pituitary gland and testes and has a role in the regulation of the release and synthesis of LH and testosterone in humans and rats.

 

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Brain Res Rev. 2007 Feb;53(2):215-34. Epub 2006 Nov 21.

D-Aspartic acid: an endogenous amino acid with an important neuroendocrine role.

D'Aniello A.

Source

Laboratory of Neurobiology, Stazione Zoologica A Dohrn, Villa Comunale 1, 80121 Napoli, Italy. daniello@szn.it

Abstract

D-Aspartic acid (d-Asp), an endogenous amino acid present in vertebrates and invertebrates, plays an important role in the neuroendocrine system, as well as in the development of the nervous system. During the embryonic stage of birds and the early postnatal life of mammals, a transient high concentration of d-Asp takes place in the brain and in the retina. d-Asp also acts as a neurotransmitter/neuromodulator. Indeed, this amino acid has been detected in synaptosomes and in synaptic vesicles, where it is released after chemical (K(+) ion, ionomycin) or electric stimuli. Furthermore, d-Asp increases cAMP in neuronal cells and is transported from the synaptic clefts to presynaptic nerve cells through a specific transporter. In the endocrine system, instead, d-Asp is involved in the regulation of hormone synthesis and release. For example, in the rat hypothalamus, it enhances gonadotropin-releasing hormone (GnRH) release and induces oxytocin and vasopressin mRNA synthesis. In the pituitary gland, it stimulates the secretion of the following hormones: prolactin (PRL), luteinizing hormone (LH), and growth hormone (GH) In the testes, it is present in Leydig cells and is involved in testosterone and progesterone release. Thus, a hypothalamus-pituitary-gonads pathway, in which d-Asp is involved, has been formulated. In conclusion, the present work is a summary of previous and current research done on the role of d-Asp in the nervous and endocrine systems of invertebrates and vertebrates, including mammals.

 

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Life Sci. 1996;59(2):97-104.

Involvement of D-aspartic acid in the synthesis of testosterone in rat testes.

D'Aniello A, Di Cosmo A, Di Cristo C, Annunziato L, Petrucelli L, Fisher G.

Source

Department of Biochemistry, Zoological Station of Naples, Italy.

Abstract

D-Aspartic acid (D-Asp) is an endogenous amino acid which occurs in many marine and terrestrial animals. In fetal and young rats, this amino acid occurs prevalently in nervous tissue, whereas at sexual maturity it occurs in endocrine glands and above all in pituitary and testes. Here, we have studied if a relationship exists between the presence of D-Asp and the hormonal activity. The following results were obtained: 1) Both D-Asp and testosterone are synthesized in rat testes in two periods of the animal's life: before birth, about the 17th day after fertilization and, after birth, at sexual maturity. 2) Immunocytochemical studies have demonstrated that this enantiomer is localized in Leydig and Sertoli cells. 3) In vivo experiments, consisting of i.p. injection of D-Asp to adult male rats, demonstrated that this amino acid accumulates in pituitary and testis (after 5 h, the accumulation was of 12 and 4-fold over basal values, respectively); simultaneously, luteinizing hormone, testosterone and progesterone significantly increased in the blood (1.6-fold, p < 0.05; 3.0-fold, p < 0.01 and 2.9-fold, p < 0.01, respectively). 4) Finally, in vitro experiments, consisting of the incubation of D-Asp with isolated testes also demonstrated that this amino acid induces the synthesis of testosterone. These results suggest that free D-Asp is involved in the steroidogenesis.

 

 

 


5-Methyl Methoxy Isoflavone

 

Methoxy Isoflavone has been shown to increase protein synthesis in animal models, including livestock, with no significant side effects. Anecdotal evidence over the past year has shown that it may exhibit some mild anabolic and anti cortisol effects. Similarly ecdysone, also known as beta ecdysterone and 20 beta hydroxyecdysterone, has shown to have some anabolic effects.

 

Ecdysone (beta ecdysterone, ecditen, 20 beta hydroxyecdysterone)

 

Ecdysone was popular with Olympic lifters and other athletes in the East and several quasi scientific studies, 2 which were never published, showed that it might have significant anabolic effects.[xv] Real world use has not shown dramatic effects and most of the information is available through nutritional companies that vastly overstate the anabolic properties of ecdysone. Nevertheless it makes a useful synergistic ingredient for TestoBoost even though on its own its effects are minimal.

 

Deer Antler Extract

 

Velvet deer antler extract has been used in the Orient as an aphrodisiac and a treatment for male impotence, and in Russia as an anabolic agent for athletes. Anecdotal evidence again shows that it may have some effect on increasing serum luteinizing hormone and testosterone levels and increasing sexual drive, with no significant side effects. As such, it works synergistically with other ingredients in TestoBoost that work in similar ways, especially tribulus terrestris,

 

Eurycoma Longifolia (Longjack)

 

Longjack has been used in the Orient to increase libido and male performance. While formal studies have not been done in humans, recent informal ones on murine models have shown that Longjack may increase free serum testosterone levels and sexual drive and performance.[xvi][xvii] As such, it works synergistically with other ingredients in TestoBoost that work in similar ways, including acetyl-L-carnitine, catuaba bark, maca root, coleus forskohlii (forskolin), muira puama, chasteberry (vitex agnus-castus - ecdysteroids), suma root (beta ecdysone – also known as beta ecdysterone and 20 beta hydroxyecdysterone), schisandra chinensis, and avena sativa.

 

For example, a recent study found that carnitines including acetyl-L-carnitine (ALCAR) worked as well as replacement testosterone therapy in improving sexual dysfunction, depressed mood, and fatigue in aging men.[xviii]

 

As well, ALCAR seems to have an effect on the hypothalamic-pituitary-testicular axis. Studies have shown that ALC prevented the decrease in plasma testosterone levels after chronic swimming[xix], and that ALC stimulates testosterone production[xx].

 

Genistein

 

Genistein (4',5,7-trihydroxyisoflavone), a major isoflavone in soybeans and a specific inhibitor of protein tyrosine kinase, acts to decrease estrogen in the body. A recent study has shown that there is a synergistic anti-estrogenic effect of indole-3-carbinol and genistein.[xxi] As well as these two ingredients, TestoBoost also contains other anti-estrogenic compounds including calcium-d-glucarate,[xxii] chrysin and ipriflavone.[xxiii][xxiv] The addition of bioperine increases the absorption of these and other ingredients  increasing the biological synergistic effects of the combination of ingredients on lowering estrogen effects.

 

Prickly Pear Extract *

 

This extract is felt to have neuroprotective and antioxidant effects. Also has insulin like effects and has been shown to have a favorable effect on cholesterol in the body. There is some anecdotal evidence that the use of prickly pear acts as an adaptogen, boosting recovery via an anti-cortisol action. As such it works with other ingredients in TestoBoost to boost recovery and decrease counter productive cortisol levels.

 

Schisandra Chinensis

 

Schizandra is a woody vine with clusters of red berries that is found in northern and northeastern China and adjacent regions in Russia and Korea. It is used to treat a variety of medical conditions and is widely known as a longevity herb and aphrodisiac. Athletes have used schisandra in the belief that it will increase endurance and combat fatigue under physical stress.[xxv] It is also felt to have liver protective effects.

 

 

Health Benefits and Protective Effects of TestoBoost

 

Although TestoBoost is formulated to increase testosterone levels and enhance anabolism, it’s also formulated to provide substantial health benefits. For example it has several ingredients, including saw palmetto (serenoa repens), zinc, quercetin, GLA (in borage oil) and stinging nettle that enhance prostate health in males, and provide anti-inflammatory effects in both males and females.

 

Some of these ingredients also decrease the formation of dihydrotestosterone from testosterone,[xxvi] thus maximizing testosterone levels while at the same time decreasing the adverse effects of higher systemic and tissue levels of dihydrotestosterone, which includes adverse effects on the prostate and hair loss.[xxvii]

 

TestoBoost also contains several potent antioxidants, such as alpha lipoic acid, beta carotene, vitamin C, vitamin E, Coenzyme Q10, and turmeric, which act to improve pituitary and testicular/ovarian function, and decrease the adverse effects of free radicals on the hypothalamic-pituitary-testicular/ovarian axis, and the associated pathways that are responsible for maximizing endogenous testosterone production.

 

For example, a recent study has found that vitamin E and vitamin C protect the testes from damage secondary to oxidant damage.[xxviii] Alpha lipoic acid (ALA), because it is a sulphur compound, can bind and help eliminate heavy metals such as copper, iron, mercury and cadmium, all of which can cause oxidant damage to the gonads (testes and ovaries).

 

Alpha lipoic acid (ALA) has a double antioxidant effect as it has significant antioxidant properties on its own, but also regenerates glutathione, the most important endogenous antioxidant. ALA and glutathione have been shown to have significant effects in decreasing mercury toxicity in the body.[xxix]

 

The combination of forskohlin and antioxidants in TestoBoost may also impact on Leydig cell function (these are the testicular cells that make testosterone) and result in combating the normal decrease in testosterone seen with aging and stress.[xxx]

 

TestoBoost also contains several other vitamins, minerals and nutrients that are important for optimizing testosterone levels. These include vitamin A, vitamin B6, vitamin B12, niacin, calcium, magnesium, manganese, boron, zinc, ginger and Coenzyme Q10.

 

 

The bottom line is that TestoBoost v3.0 is the most effective testosterone booster on the market today. And although it doesn’t contain any prohormones, which can have significant side effects, it surpasses any prohormone formulation in increasing testosterone levels and in providing potent anticatabolic and fat burning effects.

 

 

If increasing your anabolic drive, and maximizing muscle mass while minimizing body fat is important to you, check out NitAbol, the nighttime anabolic, fat burning combo that combines TestoBoost with GHboost and Myosin Protein.

 

NitAbol is also perfect for those who want to lose weight, but would prefer to maintain the muscle they have and strictly lose body fat. In this case I’d also recommend that you use LipoFlush as the ultimate fat loss supplement.

 

TestoBoost version III Nutrition Panel

 

 


References

 



[i]
Hammarqvist F, Wernerman J, von der Decken A, Vinnars E. Alpha-ketoglutarate preserves protein synthesis and free glutamine in skeletal muscle after surgery. Surgery 1991; 109(1):28-36.

[ii] Roth E, Karner J, Roth-Merten A, Winkler S; Valentini L; Schaupp K. Effect of alpha-ketoglutarate infusions on organ balances of glutamine and glutamate in anaesthetized dogs in the catabolic state. Clin Sci 1991; 80(6):625-631.

[iii] Wernerman J, Hammarqvist F, Vinnars E. Alpha-ketoglutarate and postoperative muscle catabolism. Lancet 1990; 335(8691):701-703.

[iv] Marconi C, Sassi G, Cerretelli P. The effect of an alpha-ketoglutarate-pyridoxine complex on human maximal aerobic and anaerobic performance. Eur J Appl Physiol 1982; 49(3):307-17.

[v] Hammarqvist F, Wernerman J. Ali R. Vinnars E. Effect of an amino acid solution enriched with branched chain amino acid or ornithine-ketoglutarate on the post-operative intracellular amino acid concentration of muscle. British Journal of Surgery 1990; 77(2):214-218.

[vi] Wernerman, J Hammarqvist-F; Vinnars-E. Alpha-ketoglutarate and postoperative muscle catabolism. Lancet 1980; 335:701.

[vii] Blomqvist BI, Hammarqvist F, von der Decken A, et al. Glutamine and alpha-ketoglutarate prevent the decrease in muscle free glutamine concentration and influence protein synthesis after total hip replacement. Metabolism 1995; 44:1215-1222.

[viii] Campbell B, Roberts M, Kerksick C, Wilborn C, Marcello B, Taylor L, Nassar E, Leutholtz B, Bowden R, Rasmussen C, Greenwood M, Kreider R. Pharmacokinetics, safety, and effects on exercise performance of l-arginine alpha-ketoglutarate in trained adult men. Nutrition. 2006 Sep;22(9):872-81.

[ix] Huynh NN, Chin-Dusting J. Amino acids, arginase and nitric oxide in vascular health. Clin Exp Pharmacol Physiol. 2006 Jan-Feb;33(1-2):1-8.

[x] Lacerda AC, Marubayashi U, Coimbra CC.  Nitric oxide pathway is an important modulator of heat loss in rats during exercise. Brain Res Bull. 2005 Sep 30;67(1-2):110-6.

[xi] Nagata Y, Homma H, Lee JA, Imai K. D-Aspartate stimulation of testosterone synthesis in rat Leydig cells. FEBS Lett. 1999 Feb 12;444(2-3):160-4.

[xii] D'Aniello A, Di Cosmo A, Di Cristo C, Annunziato L, Petrucelli L, Fisher G, Involvement of D-aspartic acid in the synthesis of testosterone in rat testes. Life Sciences 1996; 59(2):97-104.

[xiii] Topo E, Soricelli A, D'Aniello A, Ronsini S, D'Aniello G. The role and molecular mechanism of D-aspartic acid in the release and synthesis of LH and testosterone in humans and rats. Reprod Biol Endocrinol. 2009 Oct 27;7:120.

[xiv] D'Aniello A. D-Aspartic acid: an endogenous amino acid with an important neuroendocrine role. Brain Res Rev. 2007 Feb;53(2):215-34.

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