RAD140 Testolone vs LGD 4033 Ligandrol vs MK-2866 Ostarine

sarms

Today’s blog post will provide contrasts between RAD-140 or Testolone vs Ligandrol LGD-4033 vs MK-2866 or Ostarine, three of the most well-known SARMs in the athletic and bodybuilding industries for years now.

SARMs are compounds that bind selectively to androgen receptor in cells. Essentially, SARMs are performance enhancers and each one works differently, and were designed to have specific effects on the human body once used.

SARMs are definitely not anabolic steroids; they are not even part of the same chemical family. What SARMs do essentially is they provide the body with ‘instructions’ on how to function, and the body’s tissues acquiesce under the influence of SARMs.

Technically speaking, SARMs are a means to conquer various metabolic diseases, including bone density problems and muscle tissue wasting.

Where To Buy These

If you’re looking for a reputable SARMs dealer, we recommend ProvenPeptides

Disclaimer: We are not recommending any of these products, yet simply reviewing the products based on our research. SARMS are sold for research purposes only & is not approved for human use or consumption! Please do your own research before making any decisions related to these products.

Testolone RAD140

RAD-140 or Testolone is a SARM that was developed in 2010 by Radius Health, Inc.

As one of the ‘youngest’ SARMs, it is touted as one of the more efficient modulators, and it was originally developed as a means to help breast cancer patients.

Animal trials of Testolone showed an increase in both bone and muscle density in the animal subjects.

The unique thing about Testolone (at least in animal trials) is that it helps increase lean muscle mass without triggering a most unsavory side effect, which was also to trigger the increase in mass of the prostate in male rats.

Upon closer investigation, Testolone antagonizes the stimulation of the seminal vesicle in mice. Furthermore, the gains experienced by animal test subjects showed no additional strain on the vital organs, including the liver.

Compared to the more conventional side effects of anabolic steroids that can affect multiple organs at a time, Testolone’s selectivity as a cellular modulator appears to have reduced those risks greatly.

Ligandrol LGD 4033

SARM Ligandrol LGD-4033 is a selective androgen receptor modulator that is capable of evading the vital organs of the body that are often ‘hit’ by growth hormones and anabolic steroids, namely, the brain, heart, liver, and kidneys.

Ligandrol is specifically touted as an effective treatment for older patients who have a more difficult time in building and maintaining lean muscle mass.

Within the context of SARMs like Ligandrol, a clear distinction has to be made between young bodybuilders and older bodybuilders (aged 35 and above) as the physiological function of the body begins to dip at age 35, even with sustained exercise and a good diet.

Ligandrol LGD 4033 has been applied by bodybuilders during the cutting and bulking phases, where the body is supposed to lose fat while building lean muscle mass.

Of particular interest here is the fact that a bodybuilder has to combine Ligandrol with a good macronutrient and micronutrient balance in order to get good results, suggesting that Ligandrol affects not just the uptake and distribution of glucose, but also heightens the dispersal and usage of protein, carbohydrates and other nutrients.

This would also explain how Ligandrol helps older bodybuilders retain their muscle mass even if they are 35 years old or older, by improving the systems involved in using nutrients needed for muscle repair and growth.

Ostarine MK-2866

MK-2866 or Ostarine is a SARM that is primarily associated with bone density increase, muscle growth, lean muscle retention, and joint health.

Unlike other SARMs, Ostarine appears to provide the entire package in terms of helping bodybuilders achieve better results with their regular training programs.

Ostarine is more holistic in its impacts on the body because it not only trains the body to develop denser and stronger bones, but it also helps the patient keep any muscle gains for the long term. Lean muscle retention is different from muscle growth.

Muscle growth can succumb to lean muscle wastage, and Ostarine stands in the way of this, and reduces its impact on the muscles.

Another important aspect of Ostarine is that it is joint-protective, which means the cushion-like tissues between the bones are protected while the patient is working out.

This extra protection leads not only to better performance, but also to less pain, and fewer chances of injury. A patient can get physically stronger if he has healthier joints, mainly because there would no longer be any hindrances to performing sets and movements.

Poor joint health translates to pain during workouts, and this is certainly something that people would avoid, especially when they are cutting and bulking up.

Ostarine, like other SARMs, does not have the side effects that are traditionally associated with anabolic steroids and growth hormones as it acts selectively on specific cellular receptors and tissues.

Best SARMs Cycle Stack For Cutting Fat To Lose Weight 2019

sarms

Let’s take a look at which SARMs are the best for cutting fat aka losing weight. 

As you may know not all of the SARMs are the same, by that I mean each one does something different to the body in terms of the effects.

I won’t go over each of this because this article is strictly about SARMs that would help someone when dieting.

Alright, let’s get into it shall we.

Where To Buy These

If you’re looking for a reputable SARMs dealer, we recommend ProvenPeptides

Disclaimer: We are not recommending any of these products, yet simply reviewing the products based on our research. SARMS are sold for research purposes only & is not approved for human use or consumption! Please do your own research before making any decisions related to these products.

CARDARINE (GW 501516) For Fat Loss

Cardarine or GW-501516 has been mentioned a lot in regards to the endurance benefits it may provide (able to run faster & longer). 

The other major effect is it’s ability for fat loss, more specifically non catabolic fat loss. 

That is where Cardarine starts to become interesting in the fat loss area. Both of these effects could potentially benefit from one another as the subject does more cardio for longer increasing calories burned.

 Cardarine doesn’t cause significant suppression of testosterone, meaning it won’t shut down the natural testosterone production.

SR9009 (Stenabolic) Weight Loss

SR9009 Stenabolic is another popular SARM that is talked about in regards to potential weight loss effects.

One of the main reasons for this could be from it potentially having an effect on lipid and glucose metabolism. 

Ever heard the phrase “I just have a good metabolism” from someone who is skinny but eats everything in site? 

Metabolism is basically the body using the food you eat/stored fat for energy for your body.

S4 (Andarine) Cutting Fat

S4 Andarine has been talked about for it’s effects on fat oxidation, basically breaking down fat to use it as fuel for your body to use.

Fat oxidation promotion would help tell the body to use your fat cells for fuel over muscle or carbs for example.

It has also been mentioned that it may help with aiding in building lean body mass.

Final Thoughts

As I mentioned above in the disclaimer, these SARMs are still only being sold for research purposes only. As SARMs are still relatively new in the medical world, a lot more testing would be required for them to be approved for human consumption, which may happen in the future but currently not at the time of writing this.

Something I didn’t mention is SARMs may help with fatloss indirectly by helping gain lean body mass.

With more muscle, means more calories needed to be used by your body. So this is where there has been a lot of mention of potentially stacking certain SARMs together to get benefits of multiple SARMs, that is IF they ever get approved in such a case as approved for human consumption as a potential fat loss drug. 

Best Reputable SARMs Website Legit Vendor Source 2019

sarms

In todays article I’ll be going over where is the best source to buy SARMs online from & why that is.

With a doubt the best website vendor for buying SARMs is a company called ProvenPeptides.

Here are the SARMs they sell:

Why Buy SARMs From Proven Peptides?

Easy To Purchase Your SARMs

First and foremost. What’s the first thing you think of when you visit their website?

My thoughts were, very professional looking website.

This usually correlates well with how the company as a whole runs (from my experience).

3rd Party Testing

Next & the most import in my book is that they get a 3rd party test results on the purity & identity of their products.

This basically means a 3rd party is vouching to say their products are what they say they are, with documentation proof.

This is a very important factor you should be focusing on when determining on where you want to buy your SARMs from!

I mean think about it, you have zero clue what is actually in the vials you’re buying from vendor who don’t provide documentation like this. Heck, it could be pure water for all we know.

At least, with ProvenPeptides you have documentation that you can see for yourself.

A company that will do this so that it can be transparent with it’s customer about it’s products get a big thumbs up by me.

Shows to me as a customer, that they are not being sneaky or shady about anything. Just trying to provide the best product that they can.

Fast Shipping

You’re looking at a quick turnaround for how fast your product is shipped out. Usually within a day after payment has cleared. 

Can’t ask for more than that in terms of shipping.

Peptide Points

Another great way to show the company cares about it’s customer is that they offer Peptide Points which are basically loyalty points you can use to spend of future purchases.

Here is an easy explanation given on how Peptide Points works from their website.

“By making a purchase, as long as you are logged into your account, you will get Peptide Points.

Each dollar that you spend earns one point, and 10 points can be redeemed for $1.

So, this means that if you purchase an item for $100, you will earn 100 points and be able to get a $10 discount on your next order; this is a 10% discount which can be combined with any of our other discounts.”

Price

With all of this, you would think they would have to charge a lot more for their products right? Nope!

They have are very competitive wit their pricing compared to other vendors in the market.

Testimonials

If you’re not already sold on them then just read their reviews on their website.

Heck even search around and see what others say about them. Across the board positive reviews.

Where To Buy SARMs Online

I’ve listed all of the main reasons here on why I believe ProvenPeptides to be the best SARMs vendor. I always keep my eye out for other compeitors but right now Proven Peptides seems to be setting the gold standard as a SARMS vendor.

I can’t speak for their customer service as I’ve never had to use them. If I do I’ll do my best to remember to come back and update this article on how it went.

There has been a lot of interest in recent years in SARMs or selective androgen receptor modulators.

But what are they exactly? Why are people now interested in reading up about current animal and human trials? What’s there to gain once these substances are finally approved for extensive human use?

Let’s begin with basic mechanics of how SARMs work in the body. From the name itself, SARMs are responsible for interacting with androgen receptors in the human body.

Disclaimer: We are not recommending any of these products, yet simply reviewing the products based on our research. SARMS are sold for research purposes only & is not approved for human use or consumption! Please do your own research before making any decisions related to these products.

The androgen receptor or AR is part of the nuclear receptor subfamily and is a type of nuclear receptor. A nuclear receptor is actually a class of proteins in the body that is responsible for sensing/acknowledging the presence of steroids and other types of hormones in the body.

Nuclear receptors work primarily in regulating the expression and action of genes. Genes are basically blueprints of the body that dictate how cells and proteins grow, develop and function.

Gene expression is affected when a ligand, a type of molecule, is present. Specific ligands or molecules can bind to nuclear receptors and can cause conformational changes in it. So to recap, nuclear receptors are responsible for gene activity, and gene activities require ligand molecules to change track.

So in the grand scheme of things, the body requires different families of nuclear receptors to function properly at the cellular level, because everything about the body needs to be regulated in order to maintain normal function.

What’s truly fascinating about this class of receptors in the body is that they are able to interact with the human DNA in a very direct and essential way, which means the effects are often immediate in the selectively affected tissues.

When did SARMs begin to take over in terms of popularity in the field of hormone replacement therapy? The first wave of serious researches about SARMs came from the University of Tennessee and the independent firm Ligand Pharmaceuticals. In the beginning, compounds were simply cyclic quinolinones that produced an anabolic effect on the muscles and bones.

When we say anabolic effect, we mean that the the growth and/or development of the said tissues are affected. The work of Dalton and Miller on aryl propionamides also paved the way for more researches in the field of SARMs, which were essentially compounds that contained molecules that mimicked the action of steroids and the naturally occurring male hormone, testosterone.

The decade that brought studies from Ligand Pharmaceuticals and the University of Tennessee also brought a wave of other independent studies from competing pharmaceutical companies who saw a massive opportunity to explore these wondrous compounds that not only enhanced the physique of people under treatment, but were also able to avoid the common, serious side effects of steroids.

The side effects of steroids has caused an endless, serious debate on the use of steroids for improving the aerobic capacity, muscle strength, muscle endurance and lean muscle development of athletes and other professionals who engage in regular training.

The same side effects are also problematic for individuals who are already suffering from chronic, degenerative diseases such as breast cancer, type 2 or adult onset diabetes, muscle disease, brittle bone disease, among other conditions that all rely on the regulation of tissue growth and the retention of the same.

From a medical perspective, the rationale for further developing SARM comes from the most natural process known to man: aging. Now we’re not just talking about geriatric healthcare here, where people in their fifties and onward become the foci of attention.

No, we’re actually talking about the steady and nearly unstoppable decline of the human physiology as the years go by. The overall decline of the human body is natural, but with the birth of substances that can re-regulate the body on demand, it appears that science has found the key that will unlock a potential ‘fountain of youth-‘ a way to slow down tissue degeneration, heal chronic conditions and bring vitality to bodies that have been sapped by age and disease.

For decades, medical science has been largely dependent on male hormone supplementation to address low levels of testosterone in the body. This is considered one of the of the ‘final frontiers’ of medical science because of the known adverse effects of synthetic male hormones on the body.

The problem with the administration of testosterone are the adverse, dose-limiting effects. That when higher doses are administered to patients specifically to remodel the musculoskeletal system, a host of undesirable after-effects come to the fore. Some of these after-effects include erythrocytosis, leg edemas or water retention in the lower part of the body and prostate issues, such as the formation of tumors and enlargement of this sensitive part of the male reproductive system.

As the adverse, dose-limiting after-effects of male hormone therapy continue to plague patients, SARMs have become an extremely attractive option because of the tissue selectivity factor that come with their administration – and the administration of SARMs would still fall under ‘anabolic therapy’ as these compounds mimic the male hormone and bind with the androgen receptor.

The main challenge with the development of safe SARMs for human use is examining the signaling in the body that point to the selective action of compounds as they enhance the bone and muscle development.

Now, there are two kinds of SARMs (though classifications tend to get muddled because of the androgenic effect of these substances). The first type is called steroidal SARM because these compounds modify the naturally-occuring male hormone in the patient’s body. The second type is nonsteroidal SARM, which binds to the androgen receptors but do not affect the testosterone molecule.

The most widely known type of SARMs are nonsteroidal SARMs. The first substantial effort to develop and understand how this class of SARMs work came from GTX, Inc., a private pharmaceutical firm. Other firms that have be to be given due credit are BMS, Ligand Pharmaceuticals, Kaken Pharmaceuticals, Inc., Johnson and Johnson and GlaxoSmithKline.

Obviously, there are massive, multinational firms working nonsteroidal SARMs at the moment, and this shows much promise for patients who will greatly benefit from anabolic treatments, minus the adverse side effects brought about by higher doses of testosterone. So what’s happening essentially is that private pharmaceutical companies are trying to find out if alternative compounds can actually take the place of testosterone in a medical setting.

Let’s talk about the various classes of nonsteroidal SARMs and what existing studies have discovered about them.

S1 & S4 – These two compounds have been tested on castrated mice and both have shown the capacity to bind to the androgen receptor and prevent the reduction of prostate mice in the test mice.

Take note that the testicles are the site of natural testosterone production, which means that once the testicles are removed, testosterone levels drop and secondary sexual characteristics of affected male animals will begin to take an adverse hit.

At a dosage of 3 milligrams per day, the test subjects for S1 and S4 have shown better lean muscle development, higher density (as measured from the bone mineral content of examined tissues) and higher bone strength. There has also been marked suppression of proteins associated with muscle wastage and bone mineral reduction.

Findings for these two classes of nonsteroidal SARMs show lots of potential for treating osteoporosis, as those affected with this condition need not just better bone density, but higher bone strength. Brittle bones easily crack under pressure, and the body must thrive with additional physical activity.

Additionally, both S1 and S4 have shown an ability to reduce gonadotropin reduction, which affects spermatogenesis or the production of motile sperm cells, and this means it can be used for male contraception. Paradoxically, these substances can help quell normal spermatogenesis but can help enhance a man’s libido or natural desire of intercourse, which makes it a double win, considering that chemical contraception so far has been linked to a marked reduction of interest in sex.

Hydantoin derivatives – These are SARM compounds that have been developed by the BMS Pharmaceutical Group. Chemically, hydantoin derivatives are structurally similar to bicalutamide.

This class of nonsteroidal SARM has been proven to be highly selective of the tissues, too, and has been shown to have low affinity to prostate tissue. Currently, BMS-564929 is available in oral form, with an effective time of just eight to fourteen hours in the body. After this period, the compound is completely metabolized.

It should be noted that there can sometimes be marked differences between in vivo (inside the body) and in vitro results when testing compounds like hydantoin derivatives.

The reason for this is that these compounds can and will interact with existing pharmacokinetics in the body, and by virtue of other drugs in the body, the effects can either be reduced, enhanced or cancelled out. That’s why it is exceedingly important to only use these compounds in a clinical setting, with a physician knowledgeable enough to administer the proper dosing after necessary tests have been completed.

Tetrahydroquinoline derivatives – These compounds are being primarily researched by Kaken Pharmaceutical Corporation in Japan, and are being developed mainly as an adjunct treatment for bone density reduction and/or bone mineral loss.

Tetrahydroquinoline derivatives have also shown selectivity in its agonist activity, as it primarily works on bone tissue. This type of SARM is administered subcutaneously and high doses have been indicated to produce desired pharmacological effectiveness.

LGD2226 & LGD 2941 – Devised as bicyclic 6-anilino quinolinone derivatives, LGD226 and LGD 2941 are primarily anabolic in nature and have exhibited high affinity for the levator muscle. Benefits of administration of either of these bicyclic 6-anilino quinolinone derivatives include higher bone mineral density, an increase in bone strength and lean muscle development, too.

Fortunately, current tests show that these two compounds have low affinity for prostate tissue, which translates to a better outlook for patients who will undergo therapy using these two ligand compounds. Human trials are not yet underway. Existing literature and data are currently sourced from extensive animal trials, in male reproductive model tests where test subjects are primarily castrated test mice.

The rationale for using castrated test mice in SARM animal trials is quite simple. As we’ve discussed earlier, the testicles of male mammals are the site of testosterone production.

Castrated mammals will suffer from low testosterone levels, to the point that secondary sexual characteristics, as well as physical adaptation associated with having higher testosterone levels will suffer. The introduction of an agonist factor that binds to the androgen receptor will more clearly show the impact of a SARM, as the primary job of SARM compounds is to act as an alternative to testosterone itself, whether in natural or synthetic form.

Theories on SARM tissue selectiveness

We known now that SARM compounds have three basic characteristics. The first one is that these compounds are quite selective in affecting the body. They’re not ‘interested’ in tissues found the lungs, heart, liver, etc. The current line-up of known nonsteroidal SARMs, specifically, show that such compounds are primarily affective of bone tissue and muscle tissue.

These compounds have low affinity for other types of tissues, which make them safer to use than conventional testosterone and other known anabolic derivatives in hormone replacement therapies. The second characteristic is they tend to improve how energy is stored and used in the body. This often translates to higher muscular strength and endurance, and improvement in the way the body ports energy.

That instead of storing fat, the body burns more energy or calories and in the process, also oxidizes fat faster, leading to its direct expenditure as energy. The third characteristic is the relatively safety of the organs themselves upon the administration of SARMs.

Normally, adverse risk factors are present when higher doses of testosterone are given to patients. SARMs tend to eliminate the risk of organ damage, and this is directly linked to their low affinity to tissues that are non-related to the musculoskeletal system.

On the bright side, soft tissues such as joints and cartilages are still technically part of the muscle-bone marriage in the body, and these tissues also improve greatly when SARMs are introduced.

But how do they do it? We already have a lot of information with the after-effects of direct administration of these compounds, but there is no direct explanation as to why these secondary effects exist in the first place.

While direct answers are still being researched, there are some interesting theories from science that may explain why SARMs do wha they do. The first one is called the co-activator theory. Essentially, the natural proteins that bind to the androgen receptor have a different set of tasks when it comes to gene expression.

When any kind of SARM is introduced to the system, the impact of naturally-occurring proteins are reduced, and impact of the SARM is amplified once it binds to the androgen receptor.

Consequently, this theory leads to the thinking that testosterone-bound proteins have a wildly different set of ‘instructions’ for target genes. The second fold of this theory also suggests that SARMs activate other genes, which would explain the detour of target tissue development.

The second theory is the conformational theory. Essentially what this theory states is that when a SARM is administered to the body and binds with the androgen receptor, it has the capacity to change the surface environment or topology of the androgen receptor.

In layman’s terms, SARMs change the ‘face’ or mapping of the androgen receptor. When the new blueprint is conformed by the action of the SARM, the androgen receptor then continues to interact with other proteins and co-regulating variables in the body, leading to a marked change in how the body regenerates tissues and distributes energy.

To simplify this scenario, think of androgen receptors as guides at a crossroad. Oncoming genes approach androgen receptors, waiting for instructions where to go. SARMs are people with a different set of instructions and information, and once these compounds ‘talk’ with the guide (the androgen receptors), the androgen receptors say “well alright, I have a new set of directions and I’ll make sure the genes know about this for the time being.”

When the administered SARM is metabolized, it exits the system and the nuclear receptor goes back to its old set of instructions for gene expression. So in the end, it’s really all about chemical signaling and the activation of certain genes to achieve certain ends.

The third theory of why SARMs work and why they’re selective concerns the actual distributions of such compounds once administered. Researchers also state that tissue selectivity may actually be more related to how specific proteins interact with SARMs and not the other way around.

There are also instances when SARM compounds are converted to other compounds, before they are able to perform the secondary effects desired for the therapy. Whatever the case may be, it is clear that some transformational effects are experienced by this class of compounds in the body, as they are still metabolized.

Data on early trials of SARMs

Admittedly, much of the clinical data available for SARMs are from the private firms that run them and many of them have not been peer-reviewed and published in international journals. However, they do remain valid take-off points for the continued discussion of SARMs as clinical data is clinical data no matter how you brand it.

SARMs have collectively undergone three kinds of clinical tests: animal testing (as is the case of castrated mice), Phase 1 human trials and Phase 2 human trials. A number of SARM compounds have finally reached Phase 1 human trials, but not specifically for enhancing athletic abilities or physical strength.

These compounds are being further researched as possible treatments for cachexia, cancer, brittle bone disease, and other associated conditions where the body experiences weight loss, bone mineral density reduction and lean muscle reduction. Some types of SARMs, as we’ve already discussed, are being explored as possible male contraceptive substances, as is the case with S1 and S4.

The general point of contention in using SARMs as male contraception is this: that if spermatogenesis is inhibited, what would happen in the long term to the sexual health of the male?

Aromatization or the conversion of SARMs to estrogen after it has been metabolized is also a problem. Many SARMs resist aromatization; testosterone (the naturally occurring compound) is naturally aromatized. Until these issues are sorted out, we can expect a fairly tough battle in getting SARMs approved for widespread use. Until such time, these compounds remain available only for scientific studies and not for athletic enhancement and professional bodybuilding.