Human growth is a complex process that involves the development and maturation of various body tissues and organs. Anabolic steroids, synthetic substances similar to the male sex hormone testosterone, can have significant effects on human growth.
When used improperly, anabolic steroids can interfere with the normal hormonal balance in the body. These substances can lead to an increase in muscle mass and strength, which is why they are sometimes misused by athletes and bodybuilders. However, it's important to note that the use of anabolic steroids for non-medical purposes is illegal and can have serious health consequences.
While anabolic steroids can promote muscle growth and enhance athletic performance, they can also cause harmful side effects. These may include liver damage, cardiovascular problems, hormonal imbalances, mood swings, and stunted growth in adolescents.
In summary, anabolic steroids can impact human growth by promoting muscle development, but their misuse can lead to detrimental effects on overall health. It is essential to prioritize proper nutrition, exercise, and a healthy lifestyle to support natural and sustainable growth.
Methenolone enanthate, also known as Primobolan Depot, is an anabolic androgenic steroid (AAS) that is derived from dihydrotestosterone (DHT). It is classified as a mild steroid due to its low androgenic properties, making it popular among athletes and bodybuilders who seek lean muscle gains with minimal side effects.
Methenolone enanthate is available in injectable form, with the enanthate ester attached to the hormone, which allows for a slow and steady release in the body. This esterification process extends the half-life of the steroid, resulting in a longer duration of action.
When it comes to its anabolic effects, methenolone enanthate promotes protein synthesis and nitrogen retention, leading to muscle growth and improved recovery. It is often used during cutting cycles to preserve lean muscle mass while reducing body fat. Due to its mild nature, it is less likely to cause water retention or estrogenic side effects such as gynecomastia.
One of the key benefits of methenolone enanthate is its ability to increase strength without adding excessive muscle mass. This makes it an ideal choice for athletes who compete in weight-class sports or those who want to enhance their performance without gaining significant bulk.
Another advantage of methenolone enanthate is its low potential for androgenic side effects. This means that users are less likely to experience acne, oily skin, hair loss, or aggression often associated with more potent androgenic steroids.
However, it is important to note that methenolone enanthate is a relatively weak steroid compared to some others on the market. Consequently, significant muscle gains may require higher dosages, which can increase the risk of adverse effects.
Like any steroid, methenolone enanthate carries potential side effects, although they tend to be milder compared to stronger AAS. These can include suppression of natural testosterone production, cholesterol imbalances, liver toxicity (when used orally), and cardiovascular strain. Post-cycle therapy (PCT) is recommended to help restore hormonal balance and minimize the risk of side effects.
It is crucial to mention that the use of methenolone enanthate, like any other AAS, should be done under the supervision of a qualified healthcare professional. They can provide guidance on dosages, cycle length, and any necessary support to ensure safety and maximize benefits.
In conclusion, methenolone enanthate is a mild AAS that offers lean muscle gains, increased strength, and improved recovery. It is a popular choice for athletes and bodybuilders seeking moderate effects with a lower risk of androgenic side effects. However, it is essential to approach its use with caution, follow proper dosage guidelines, and prioritize overall health and well-being.
The recent boom in biotechnology has opened the door for studying new biologically-active compounds, including “cognitive enhancers” or “nootropics.”
One such compound is Selank — previously known as “TP-7” — which belongs to a class of molecules called synthetic peptides, or small artificially-designed proteins.
Selank has been touted as an “anti-anxiety” compound, and has also been claimed to improve learning and increase energy — supposedly without side-effects or the risk of addiction.
Selank is small and only a fraction of the size of most naturally-occurring proteins. It was developed at the Institute of Molecular Genetics (Russian Academy of Sciences) in cooperation with the V.V. Zakusov Research Institute of Pharmacology (Russian Academy of Medical Sciences), along with its “cousin” drug, Semax.
Selank was derived by combining the sequence of a peptide called tuftsin with another sequence that improves its molecular stability. Tuftsin is naturally-occurring, and makes up one part of the natural antibody IgG.
Both tuftsin and Selank have been reported to reduce anxiety and increased serotonin levels in rats, with Selank being slightly more effective.
Selank has been approved in Russia for the treatment of generalized anxiety disorder (GAD) and for its use as a nootropic. However, the FDA has not approved its use for any conditions. Nonetheless, Selank continues to be available in several countries, where it is often sold as a “nutritional supplement.”
Selank Mechanism of Action
Although the mechanisms behind Selank are not yet fully known for certain, Selank is believed to act in part by stabilizing enkephalins in the blood. Enkephalins are natural peptides in the body that are believed to counteract the stress response.
However, one animal study in mice did not demonstrate the stabilization of enkephalins following dosing with Selank, and the treated mice also did not appear to benefit from any significant “anti-anxiety” effects.
According to some cell studies, Selank may bind to GABA receptors. By extensions, most compounds that bind to GABA receptors generally cause “sedative” effects. In one study of mice treated with Selank, researchers reported increased activity in inhibitory neurons, which rely on GABA. This resulted in less overall brain activity, which is generally consistent with a sedative effect.
In addition, some researchers have reported an increase in BDNF, an important brain-growth compound (neurotropic factor) which has been implicated in learning and memory. Some researchers have suggested that this mechanism may be responsible for some of Selank’s claimed cognitive effects.
Selank has also been reported to influence the levels of the neurotransmitters norepinephrine, dopamine, and serotonin in mice. These neurotransmitters are widely believed to be involved in motivation, focus, and pleasure.
However, according to one animal study in mice, Selank was reported to increase norepinephrine, but reportedly decreased dopamine and serotonin levels. In contrast, in some other treated mice, Selank was reported to increase norepinephrine and dopamine levels, and did not change serotonin. Therefore, its exact effects and mechanisms remain unclear.
Possibly Effective for:
Anxiety
According to one preliminary clinical trial on 62 people, those given Selank reported fewer anxiety symptoms, with a greater decrease being observed in those suffering from pre-existing anxiety disorders.
In another trial, similar benefits were reported in 60 patients suffering from anxiety and phobias, with these effects lasting up to a week after the final dose.
Additionally, in one study of 70 anxiety patients, Selank was reported to increase the effects of phenazepam (an anti-anxiety drug banned in some U.S. states for its recreational use), while also reportedly reducing its rates of negative side-effects (such as drowsiness and memory loss).
In one animal study, Selank was reported to reduce anxiety in mice. The more anxious the mice were to begin with, the more significant the observed changes in their behavior after treatment.
Additionally, Selank was reported to show “anti-anxiety” effects in one study of rats who received 4 weeks of daily treatment.
Although limited, some of the above evidence suggests that Selank may potentially help curb anxiety, although much more research will still be needed to confirm its effectiveness and safety in human users. If you suffer from anxiety, you could have a discussion with your doctor about whether taking Selank might help you — however, always remember that you should never take this supplement in place of what your doctor recommends or prescribes.
Memory
Selank was reported to stabilize memory traces (i.e. potentially improve memory storage) in rats during one 30-day trial. However, it is unclear how these measurements were performed, as memory traces are not detectable as discrete locations in the brain.
One other animal study has reported that Selank may also preserve memory in monkeys.
However, appropriate human studies are lacking, and remains unknown what effects — if any — Selank might have in healthy human users. It is also unclear whether or not this compound would be safe for such users to take (either in the short- or long-term), and so caution would be advised until much more additional research is performed.
Brain Damage Recovery
In one study, researchers gave Selank supplements to rats with toxin-induced brain damage. This drug reportedly restored their brain activity to normal levels.
Depression
Selank has been reported to decrease depression symptoms (immobility during a forced swimming test) in mice. Curiously, it was reported to be more effective at relatively lower rather than higher doses.
Antioxidant Activity in the Liver
In one preliminary animal study, injection of Selank was reported to increase the levels of antioxidants in the livers of stressed mice.
Blood Flow
In one animal study of sedated cats, Selank was reported to decrease blood pressure by about 30% for up to 3 minutes.
It also increased blood flow to the cats’ brain by about 24% for up to 10 minutes [30].
While these preliminary findings are interesting in that they suggest that Selank may have some short-term cardiovascular effects on blood flow, the relatively short durations of these effects is hard to interpret, and may suggest that these effects are not strong or medically significant.
Additionally, these were only observed in animals, and so whether these effects would be similar in healthy human users remains unclear.
Alcohol Withdrawal
Anxiety is one of the more common symptoms involved in alcohol withdrawal. To mimic high alcohol intake, rats were given a 10% solution of ethanol (alcohol) as their sole drinking source for 24 weeks. Selank reportedly decreased the anxiety of these rats after a 48-hour alcohol withdrawal period.
Preventing Weight Gain and Reducing Cholesterol
According to one animal study, rats who were fed a high-fat diet reportedly showed 35% less weight gain when treated with Selank. Additionally, total cholesterol levels for these rats were reportedly reduced by over 58%, and blood glucose levels were reduced by 23.5%.
Cancer
In one animal study, mice with breast cancer were treated with daily doses of Selank and had slower tumor growth. Also, these mice reportedly lived longer than their untreated counterparts.
However, this preliminary finding doesn’t mean that Selank has any value in anticancer therapy. Much more research would be needed to verify and extend these early findings into legitimate medical treatments for cancer. Do not under any circumstances attempt to replace conventional cancer therapies with Selank (or any other supplements)!
Inflammation in the Spleen
After treatment with Selank, the spleens of mice were reported to show increased levels of several inflammatory response genes, which may suggest some degree of protection against the harmful effects of inflammation.
Ulcers
Selank has been reported to reduce the size (area) of stomach ulcers in animal models.
Some researchers have speculated that this may be because this drug increases the flow of lymph — an important component of the immune system — to the stomach.
Nonetheless, much more research in humans would be needed to confirm this effect, as well as its potential mechanisms.
Immune Function
Selank reportedly increased IL-6 in blood cells collected from patients suffering from depression. IL-6 is an inflammatory protein that is believed to help fight off infections.
Additionally, according to one cell-based study, Selank was reported to stimulate the release of interferons, which are anti-viral molecules.
Selank has also been proposed to potentially protect cells against some viral infections. However, one animal study in mice infected with a virus did not report any anti-viral benefits from Selank treatment, which casts doubt on this potential use.
BPC 157, also known as Body Protective Compound 157, is a peptide that has gained attention for its potential therapeutic benefits. It is a synthetic peptide derived from a protein called Body Protection Compound, which occurs naturally in the human body.
BPC 157 is made up of 15 amino acids and has a molecular weight of 1419. It is primarily used for its regenerative properties and is believed to promote healing and repair in various tissues and organs. While more research is needed to fully understand its mechanisms of action, preliminary studies suggest that it may have several beneficial effects.
One of the prominent effects of BPC 157 is its ability to accelerate the healing process. It has been shown to enhance the formation of new blood vessels (angiogenesis), which improves blood flow to injured areas and aids in tissue repair. This is particularly beneficial for individuals with musculoskeletal injuries, as BPC 157 may help to speed up the recovery of tendons, ligaments, and muscles.
In addition to its regenerative properties, BPC 157 has also shown potential anti-inflammatory effects. It can reduce inflammation by modulating the immune response, which may be beneficial in conditions such as arthritis or inflammatory bowel disease.
Moreover, BPC 157 has demonstrated protective effects on the gastrointestinal system. It has been studied for its ability to heal and protect the stomach lining from damage caused by non-steroidal anti-inflammatory drugs (NSAIDs) and other irritants. This makes it a promising option for individuals dealing with gastric ulcers or other digestive issues.
BPC 157 is typically administered via injection, either subcutaneously or intramuscularly. The recommended dosage varies depending on the specific condition being treated, but it is generally available in 5mg vials. It is important to note that BPC 157 is still under investigation, and its use should be supervised by a healthcare professional.
While BPC 157 has shown promising results in preclinical and early clinical studies, more research is needed to fully understand its safety profile and efficacy in humans. It is always advisable to consult with a healthcare professional before starting any new treatment or using peptide-based substances like BPC 157.
Stenabolic (SR 9009) is a PPAR alpha modifier drug that is still in development as of 2015. Its creator is professor Thomas Burris of the Scripps research institute. Interestingly, it is sold as a SARM and research chemical, and it can be compared to Cardarine (GW-501516), as it is also an agonist of Rev-ErbA. According to an article by “National Medicine,” it enhances exercise capacity in mice by increasing mitochondria in skeletal muscle. This is why it has been marketed and hyped around the internet as “exercise in a bottle.”
As mentioned above, Stenabolic has the ability to alter the activity of the skeletal muscle mitochondria, or in simple terms – it boosts your metabolic activity. This makes it similar to what DNP does, being SR 9009 much safer and not counterproductive to your endurance goals. What’s more, unlike DNP, SR 9009 has the ability to mimic actual aerobic exercise without actually putting in the conditioning. Therefore, it will boost your endurance instead of hurting it.
(SR 9009) binds to a protein called Rev-erbA. This is important, as this protein influences fat and sugar burning in the liver, the production of fat cells, and the body’s inflammatory responses. As a result, this interaction between SR 9009 and Rev-erbA allows you to make your current exercise regiment much more effective. In fact, even sitting on your butt all day will not hinder your objectives. All in all, the ultimate goal is to burn off energy from what you eat, instead of getting it stored as fat, which SR does great. Furthermore, it will attack the existing fat and burn it off.
Results
Stenabolic (SR 9009) will help a person become leaner, and it will help them do more distance with cardio without getting winded as fast. Overall, it will increase your VO2 max, allowing you to improve your endurance.
Additionally, SR 9009 can benefit nonathletes as well, since it can reverse obesity, metabolic syndrome, and type 2 diabetes.
Mice studies
Developers took mice with low amounts of muscle, low metabolic rate, and poor running capacity. Hence, the mice were basically human versions of out-of-shape couch potatoes. Once given Stenabolic, muscle and metabolic rate increased, even without being allowed to exercise. Then, once these mice were allowed to exercise, they were able to run 50% further without getting winded.
Side effects
SR 9009 does not act like a fat burner, thyroid accelerator, or appetite suppressant (such as clenbuterol, T3, or certain stimulants). Therefore, you won’t experience a crash or feel tired on it. However, due to the fact that Stenabolic is so new and hasn’t been used very much by human athletes, we are still waiting for more information on what kind of undesired effects it can possibly have.
Dosages
Stenabolic should be dosed at 20-30 milligrams (mg) per day and adjusted up or down by 10 mg depending on user preference. Regarding the cycle duration, the typical cycle length is 6-8 weeks, and it would be wise to stack SR 9009 with Cardarine (GW-501516) for a double dose of endurance power.
There is a big inconvenience with Stenabolic when compared to Cardarine, SR 9009 does not have a long half-life, so it must be dosed 3-4 times per day. However, some forum members have had good success doing it 2-3 times per day.
Oxandrolone, also known by its brand name Anavar, is an anabolic steroid that belongs to the class of drugs called androgens. It was first introduced in the 1960s and has gained popularity among athletes and bodybuilders due to its relatively mild nature and beneficial effects on muscle growth and strength.
Oxandrolone is derived from dihydrotestosterone (DHT), which is a naturally occurring hormone in the body. It has been modified to enhance its anabolic properties while minimizing its androgenic effects. As a result, Oxandrolone is considered a mild steroid with lower androgenic activity compared to other anabolic steroids.
One of the main uses of Oxandrolone is to promote weight gain and muscle growth in individuals who have experienced weight loss due to certain medical conditions, such as severe burns, chronic infections, or surgery. It can also be used to counteract the catabolic effects of long-term corticosteroid therapy.
Oxandrolone works by increasing protein synthesis, which helps in the building and repair of muscle tissues. It also enhances nitrogen retention, leading to a positive nitrogen balance in the body. This anabolic effect contributes to increased muscle mass and improved muscle strength.
In addition to its muscle-building properties, Oxandrolone has been found to have other beneficial effects. It can help increase bone density, which is particularly important for individuals at risk of osteoporosis. It has also been shown to improve wound healing and enhance the production of red blood cells, which can be beneficial for individuals with certain medical conditions.
When used under medical supervision and at prescribed dosages, Oxandrolone is generally well-tolerated with minimal side effects. However, like any other anabolic steroid, it does carry potential risks and side effects. These may include liver toxicity, cardiovascular complications, hormonal imbalances, and virilization in females (development of male characteristics).
Due to its potential for abuse and misuse, Oxandrolone is classified as a controlled substance in many countries. Its use without a prescription is illegal and can lead to serious health consequences.
It is important to note that the use of Oxandrolone should always be done under the guidance of a healthcare professional. They can provide proper dosing instructions, monitor potential side effects, and ensure the individual's safety and well-being.
In conclusion, Oxandrolone is an anabolic steroid commonly used to promote weight gain and muscle growth in individuals with certain medical conditions. It has mild androgenic properties and offers benefits such as increased muscle mass, improved strength, enhanced bone density, and accelerated wound healing. However, its use should be approached with caution and only under medical supervision to minimize the risk of potential side effects.
Ultima-Deca 250 is a popular anabolic steroid that is widely used in the bodybuilding and fitness communities. It is a brand name for the active ingredient nandrolone decanoate, which belongs to the class of drugs known as anabolic-androgenic steroids (AAS).
Nandrolone decanoate is derived from testosterone, the primary male sex hormone. However, it has been modified to have a longer ester chain, which slows down its release into the bloodstream. This results in a longer half-life, allowing for a sustained and gradual release of the hormone over a period of time. As a result, Ultima-Deca 250 has a longer duration of action compared to other forms of nandrolone.
Ultima-Deca 250 is known for its powerful anabolic properties, meaning it promotes muscle growth and enhances protein synthesis in the body. This leads to increased muscle mass and strength gains. It also has mild androgenic properties, which contribute to its ability to enhance athletic performance and improve recovery.
One of the key benefits of Ultima-Deca 250 is its ability to increase nitrogen retention in the muscle tissue. This is crucial for promoting an anabolic environment that supports muscle growth and repair. It also helps to reduce muscle catabolism, which is the breakdown of muscle tissue. This means that users can experience improved recovery and reduced muscle soreness after intense workouts.
In addition to its muscle-building properties, Ultima-Deca 250 is also known to improve joint health and alleviate joint pain. This is particularly beneficial for athletes and bodybuilders who engage in heavy weightlifting or high-impact activities that can strain the joints. Nandrolone decanoate has been shown to promote collagen synthesis and increase bone mineral density, which can help protect the joints and reduce the risk of injuries.
However, it is important to note that Ultima-Deca 250, like all AAS, does come with potential side effects. These can include androgenic effects such as oily skin, acne, and increased body hair growth. It can also suppress natural testosterone production, which may result in hormonal imbalances and potential fertility issues. Other side effects can include cardiovascular strain, liver toxicity, and mood swings.
It is crucial to use Ultima-Deca 250 responsibly and under the guidance of a healthcare professional. Proper dosing, cycle duration, and post-cycle therapy are important considerations to minimize the risk of side effects and maximize the benefits. Additionally, it is essential to adhere to legal and regulatory guidelines regarding the use of steroids in your region.
In conclusion, Ultima-Deca 250 is a powerful anabolic steroid that is primarily used for muscle growth, strength gains, and joint health. It can provide significant benefits to athletes and bodybuilders when used responsibly, but it is important to be aware of the potential side effects and to use it under professional supervision.
CHARACTERISTICS
ACTIVE HALF-LIFE
1 DAY
CLASSIFICATION
THYROID HORMONE
DOSAGE
25-75 MCG/DAY
ACNE
NO
WATER RETENTION
NO
HBR
YES
HEPATOTOXICITY
NO
AROMATIZATION
NO
ACTIVE SUBSTANCE
LIOTHYRONINE SODIUM
FORM
50 PILLS X 50 MCG
MANUFACTURER
Rx Pharmaceuticals
DESCRIPTION
Chemical name: (2S)-2-amino-3-[4-(4-hydroxy-3-iodophenoxy)-3,5-diiodophenyl]propanoic acid
Formula: C15H12I3NO4
Anabolic activity index: not a steroid
Androgenic activity index: not a steroid
T3 50mcg
T3 is originally a medicinal hormone drug (a drug of the thyroid hormone group), also widely used as a sport dope. In sports practice, it is effectively taken by all genders (male and female), ages (over 18 years), physical fitness levels and experiences with sports pharmacology (from beginners to professional athletes). The goal of purchasing this product is usually weight loss, so it is used primarily for cutting cycles.
The active substance in the composition of this drug is Liothyronine - a synthetic analogue of the natural hormone triiodothyronine (T3), the active form of thyroid hormones, which has the main biological effect. Liothyronine was approved for human prescribing, as: when the recommendations are followed, it differs predominantly over the side effect; It is not a steroid, and do not possesses androgenic properties, especially a narcotic, addictive, component.
T3 effects:
Accelerates metabolism;
Enhances heat production;
Burns fat;
Increases the hardness and texture of muscles;
Stimulates the central nervous system;
Reduces the need for sleep;
Increases physical performance.
T3 reviews are only positive, because the product effectively cope with its tasks, on the impact of bypassing the majority of analogs, including specially designed for sports pharmacological fat burners.
It is important that T3 (Liothyronine) acts naturally (as a natural thyroid hormone triiodothyronine - T3) without provoking reactions foreign to the body. But there are potential side effects, so it is extremely important to follow the recommendations established by experienced athletes and doctors. Otherwise, uncontrolled administration of this drug leads to the development of complications from increased sweating to osteoporosis of bones.
T3 Dosage and Administration
Effective T3 doses are only individually selected: usage, typically starts with the minimum amount of drug (from 5-25 to 50 mcg per day), and then gradually increase the amount (by 5-25 to 50 mcg per day) up to determine the optimal dosage. Such a scheme of reception allows to avoid the risk of insufficiency or, on the contrary, excessive product, which in both cases is fraught with consequences.
The duration of taking T3 is also an individual matter, hanging from the need and tolerance of the substance by the body. On average, the course continues to 4-8 (6) weeks, which is enough for most athletes to form pronounced results without provoking critical complications.
T3's solo cycle is a rare practice. For maximum progress in sports, athletes combine this drug with Yohimbine, Clenbuterol, even anabolic and androgenic steroids. Such cycles allow achieving a powerful synergetic effect, but accordingly increase the risks of side effects, as a consequence, are recommended mainly to experienced athletes.
Solo or combined T3 reception is passed without any problems, advanced users recommend to be surveyed and consult with a specialist, for eliminating the possibility of contra-indications: hypersensitivity to the components in the composition of this drug, untreated hyperthyroidism, angina pectoris, myocardial infarction, myocarditis, cachexia, as well as untreated adrenal insufficiency - for both sexes.
Warnings: Keep out of reach of children. For adults only.
Cialis, also known by its generic name Tadalafil, is a medication primarily used to treat erectile dysfunction (ED) in men. It is a prescription-only drug and comes in various strengths, including 25mg tablets.
Tadalafil belongs to a class of drugs called phosphodiesterase type 5 (PDE5) inhibitors. It works by increasing blood flow to the penis during sexual stimulation, which helps a man achieve and maintain an erection. Unlike other erectile dysfunction medications, Cialis has a longer duration of action, allowing for up to 36 hours of effectiveness.
The 25mg strength of Cialis is considered a lower dose and is typically prescribed for individuals who may have certain health conditions or who are more sensitive to the effects of the drug. It is important to note that the dosage may vary depending on the individual's response to the medication, overall health, and other medications they may be taking. It is always best to consult with a healthcare professional to determine the appropriate dosage for your specific situation.
Cialis 25mg tablets should be taken orally, with or without food, at least 30 minutes before sexual activity. The medication should not be taken more than once a day. It is important to follow the prescribed dosage and not exceed the recommended amount.
As with any medication, Cialis may have potential side effects. Common side effects include headache, indigestion, back pain, muscle aches, flushing, nasal congestion, and dizziness. These side effects are usually mild and temporary, but if they persist or become bothersome, it is recommended to consult a healthcare professional.
It is crucial to inform your doctor about any existing medical conditions, such as heart problems, liver or kidney disease, high or low blood pressure, history of stroke or heart attack, or any other health issues, as well as any medications you are currently taking, including over-the-counter drugs, supplements, or herbal products. This will help ensure that Cialis is safe and appropriate for you to use.
It is essential to remember that Cialis is not a contraceptive and does not protect against sexually transmitted infections. It is also not recommended for use by women or individuals under the age of 18.
In conclusion, Cialis (Tadalafil) 25mg tablets are a prescription medication used to treat erectile dysfunction in men. It works by increasing blood flow to the penis, allowing for improved sexual performance. It is important to follow the prescribed dosage and consult with a healthcare professional for personalized guidance and to ensure the safe and effective use of this medication.
