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Among men with hypogonadism included in a urology registry, long-term treatment with testosterone may lead to remission of type 2 diabetes, according to a speaker.

“This registry was not designed to study the effects of testosterone on type 2 diabetes,” Farid Saad, PhD, of Bayer Pharma in Berlin, said during the presentation. “A remission of type 2 diabetes with testosterone has not been described in the literature. It was completely unexpected.”raw Testosterone decanoate powder
Saad and colleagues evaluated data from 400 men included in a urology registry of patients with hypogonadism (testosterone ≤ 12.1 nmol/L) since 2004; 133 (33.3%) of them had been diagnosed with type 2 diabetes and were treated in a diabetes center. All men received injections of testosterone undecanoate 1,000 mg for 12 weeks for hypogonadism. At least twice a year, anthropometric and metabolic measurements were obtained, and fasting insulin was acquired from the diabetes center to calculate homeostasis model assessment for insulin resistance. Participants were followed for a mean of 6.9 years, with a maximum of 11 years. At baseline, mean age of the participants was 60 years.

The researchers found that at the final measurement, 16 men (12%) were in diabetes remission. They observed a reduction in HbA1c from 8.3% at baseline to 5.7%. Also decreased from baseline to last measurement were fasting glucose (from 7.8 mmol/L to 5.4 mmol/L) and fasting insulin (from 24.7 µU/mL to 7.6 µU/mL). HOMA-IR decreased from 8.7 to 1.8, and triglycerides dropped from 3.2 mmol/L to 2.2 mmol/L.

A decrease in body weight from baseline was observed, from 107 kg to 89 kg, and a reduction in waist circumference from 108 cm to 97 cm. At baseline, all participants had been prescribed oral metformin, and five were on a regimen of insulin at an average dose of 21.6 units per day. Patients were observed for an average of 106.3 months. Discontinuation of diabetes medication occurred at an average of 74.8 months. One patient discontinued testosterone after a diagnosis of low-grade prostate cancer and, subsequently, developed new-onset type 2 diabetes. This patient again experience diabetes remission 48 months after resuming testosterone therapy. Because all injections were given in the urology office, medication adherence was 100%.

Saad weighed the potential cardiovascular benefits of diabetes remission, weight loss and decreased lipid levels against assertions that testosterone treatment itself confers CV risk.

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Procaine HCl is a local anesthetic drug of the amino ester group. It is used primarily to reduce the pain of intramuscular injection of penicillin, and it is also used in dentistry. It acts mainly by being a sodium channel blocker.Today it is used therapeutically in some countries due to its sympatholytic, anti-inflammatory, perfusion enhancing, and mood enhancing effects.

Procaine HCl is indicated for the production of local or regional analgesia and anesthesia by local infiltration and peripheral nerve block techniques.

Application of procaine leads to the depression of neuronal activity. The depression causes the nervous system to become hypersensitive producing restlessness and shaking, leading to minor to severe convulsions. Studies on animals have shown the use of procaine led to the increase of dopamine and serotonin levels in the brain.Other issues may occur because of varying individual tolerance to procaine dosage. Nervousness and dizziness can arise from the excitation of the central nervous system, which may lead to respiratory failure if overdosed. Procaine may also induce weakening of the myocardium leading to cardiac arrest.

Procaine can also cause allergic reactions causing the individuals to have problems with breathing, rashes, and swelling. Allergic reactions to procaine are usually not in response to procaine itself, but to its metabolite PABA. About one in 3000 people have an atypical form of pseudocholinesterase,[citation needed] which does not hydrolyze ester anesthetics such as procaine, resulting in a prolonged period of high levels of the anesthetic in the blood and increased toxicity.

Fat loss is the new craze in the world of bodybuilding. There are so many products in the market that claim to help with this and others are still flocking in. The problem is that not all are effective and they may not help you achieve your target. Some may make you lose weight so fast that you are left with sagging skin or no muscles.Methasteron powder

Your ultimate goal should be losing fat by reducing the excess body fat without losing your muscles. When you lose your muscles, you become unshapely, and all your contours disappear.

If you have thought about shedding the extra pounds, then Superdrol should have come to your mind first. Whether you have tried dieting, training or both, you might have discovered that you need something extra. Fortunately, Superdrol helps you reduce weight effectively. It is one of the products that can be trusted.

The advantage with it is that it offers magical results by assisting you to reduce your weight to your ideal level. Since it has the power to preserve your muscles, you will always have an attractive physique since Superdrol aids in burning pure fat and nothing else.
All bodybuilders, young or old, are judged by their muscle symmetry, definition, and size. When one has a superior muscle definition, their fat levels are very low. However, sometimes the muscle definition may be reduced due to water retention.

Some steroids will assist you in gaining huge muscles that are as a result of fluid retention. Honestly, you wouldn’t want to look all puffy because of having too much fluid. You have remained focused with your diet, training and in taking your steroid and then excess fluid builds up just under your hard-earned muscles. The excess fluid should not be the reason why your muscles appear to be blurry.

Such gains will disappear almost immediately once you are done with your dosage. It is just temporary and could go away leaving you as you were before using the steroid.

One unique feature of Superdrol is that it doesn’t cause water retention. That is the reason why the muscles appear to be firmer, and the musculature is impressive. This steroid is worth a buy since it is capable of offering you a perfect definition that will earn you the first position in case you are attending any competition soon.

Masteron Enanthate is the anabolic steroid that is slow acting, but is acts for longer period of time. In fact, Masteron Enanthate comes with an ester, Enanthate attached, and Enanthate is responsible for slower, but longer release of hormone. This house of Masteron Enanthate offers it an edge over the Propionate version of Masteron, which is fast and quick acting anabolic steroid. For its quickly and shot life span, Masteron Propionate is required to be injected time and once more, but it is not identical with Masteron Enanthate, which usually calls for to be injected twice per week. raw Drostanolone powder


Masteron is often an ideal choice for inclusion in a steroid stack, or in some cases for use as the sole injectable for a steroid cycle.
An enanthate ester version having a half-life of probably 5 days has become available. This version of Masteron may be injected as infrequently as twice per week.

The benefits of Masteron Enanthate should be summed up in three words, lean and hard. For the performance enhancers and outside of a breast cancer patient largely it will only be performance enhancers of a bodybuilding nature who supplement with Masteron in the first place as it is an excellent physique transforming steroid but it is not a miracle in a bottle. Even though it has a rather mildly low androgenic rating the story it tells is rather different as it will harden one up quite decently. Further, as is by its nature Masteron Enanthate effects overall metabolic activity by directly stimulating lipolysis; no, it is not the only steroid that presents such benefits nor is it the strongest one but these are largely the traits.raw Drostanolone powder

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Commonly, those in the media or in any popular culture conversation refer to Human Growth Steroid Hormone as an anabolic steroid. However, Human Growth Steroid Hormone is in no shape or form an anabolic steroid. Yes, it does carry strong anabolic properties, but being anabolic does not make something an anabolic steroid. Food is also highly anabolic, but no one would call chicken or ground beef an anabolic steroid.Raw Cardarine powder
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Human Growth Steroid Hormone is not only one of the most beneficial hormones our body produces, but one of the most sought after in exogenous form. In an exogenous form, Human Growth Steroid Hormone is identical to the naturally produced hormone, and represents not only one of the most beneficial exogenous hormones but one of the most well-tolerated among men and women. Its high level of toleration applies not only to medicinal use but performance enhancement as well.
The use of these STH somatotropic hormone compounds offers the athlete three performance-enhancing effects. STH (somatotropic hormone) has a strong anabolic effect and causes an increased protein synthesis which manifests itself in a muscular hypertrophy (enlargement of muscle cells) and in a muscular hyperplasia (increase of muscle cells.) The latter is very interesting since this increase cannot be obtained by the intake of steroids. This is probably also the reason why STH is called the strongest anabolic hormone. The second effect of STH is its pronounced influence on the burning of fat. It turns more body fat into energy leading to a drastic reduction in fat or allowing the athlete to increase his caloric intake. Third, and often overlooked, is the fact that STH strengthens the connective tissue, tendons, and cartilages which could be one of the main reasons for the significant increase in strength experienced by many athletes. Several bodybuilders and powerlifters report that through the simultaneous intake with steroids STH protects the athlete from injuries while inereasing his strength.

The use of Human Growth Steroid Hormone was first successful in 1958. At this time, Human Growth Steroid Hormone was a pituitary extract; it was directly extracted from the pituitary of human cadavers. In 1985, the U.S. FDA would ban its use. Extracted Human Growth Steroid Hormone had been successful in many treatment plans, but it also proved to carry with it strong unsanitary disadvantages. In fact, pituitary Human Growth Steroid Hormone was linked to CJD, a degenerative brain disorder that is fatal. However, very few fell prey to CDJ, approximately 1% of all users, but this was enough for the FDA to impose a ban.

RAD140, from its internal nonsteroidal selective
androgen receptor modulator ("SARM") discovery program, for full preclinical development as a potential therapy for the treatment of age-related muscle loss (sarcopenia) and other musculoskeletal conditions such as osteoporosis. Radius selected RAD140 from a series of promising SARMs after it demonstrated exceptional selectivity for anabolic activity in well-validated in vivo models. Radius expects to complete formal toxicology studies that will allow.Testolone powder
This makes its usage significantly safer and more effective compared to traditional prohormones and anabolic steroids.

According to the Cambridgebased pharmaceuticals company Radius, the potent, orally bioavailable and nonsteroidal RAD 140 SARM is designed to make the hormonal receptors in the tissues of the body act the same way as if they're getting a good dose of testos, setting off the same effects as if you're cycling with prohormones and anabolic steroids minus unwanted side effects.
Moreover, clinical studies also show that RAD 140 SARM also has a few other benefits, which we will discuss more thoroughly in a moment.

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(1) Femara is approved by the United States Food and Drug Administration (FDA) for the treatment of local or metastatic breast cancer that is hormone receptor positive or has an unknown receptor status in postmenopausal women.Raw Letrozole powder
(2) Femara is intended for use only by women who are no longer of childbearing age. Possible candidates must have already ceased to menstruate. It is often used in patients who have already undergone other cancer treatments, such as radiation, chemotherapy, and used other cancer drugs, like tamoxifen. This nonsteroidal aromatase inhibitor may help prevent any remaining cancer cells from spreading.
(3) Femara is a powerful Aromatase Inhibitor that was developed to fight breast cancer. For athletes and bodybuilders, it is a drug used to combat the estrogenic side effects of anabolic steroids water-retention, acne and gynocomastia. It will also raise testosterone levels because of the lowered estrogen in the body. Side effects from include a lowered sex drive and continuous use can lead to lowered lipid function and an impaired immune system.

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Women taking Soltamox (tamoxifen citrate) are no longer advised to take contraception or otherwise avoid pregnancy for nine months after they stop taking it.

Recent postmarketing reports submitted to the FDA and published literature indicate that women who ended their tamoxifen regimen and subsequently became pregnant within two to nine months did not experience any negative drug-associated effects such as birth defects or other maternal or fetal problems.Tamoxifen Citrate powder

This is not the first time that tamoxifen has changed its contraceptive warnings.
The FDA extended its original mandatory two-month contraceptive period after cessation of tamoxifen to nine months in September of 2018.

This revision is not final. Should drug-related adverse effects be reported, the FDA would likely issue a reinstallation of the contraceptive period.

Our results show that there are two important advantages of tamoxifen and raloxifene treatment over steroids, which have limited benefits for patients with MD. First, the SERMs improve both histology and function of all muscles; although steroids improve histology, they improve function to a much lesser extent. Second, SERMs enhance bone density, whereas steroids exacerbate osteoporosis and increase the risk for fractures," explained Qi Long Lu, MD, PhD, director of the McColl-Lockwood Laboratory for Muscular Dystrophy Research, Neuromuscular/ALS Center, Department of Neurology, Atrium Health's (formerly Carolinas HealthCare System's) Carolinas Medical Center, Charlotte (NC).

The mice used in this study have the identical gene defects and show almost the same disease manifestation as patients with MD and are therefore an excellent model for therapeutic evaluation. Investigators administered tamoxifen (2, 10, or 50 mg/kg), raloxifene (50 or 100 mg/kg), or saline to mutant mice with dystroglycanopathy, a form of MD, for up to a year, beginning at three weeks of age.Raloxifene powder

The investigators found several indicators that tamoxifen and raloxifene delay or even halt disease progression. Within one month, treatment with either SERM reduced muscle pathology with significant reduction in the numbers of degenerating fibers. After a year, control mice showed high variation in fiber size with focal inflammatory infiltrations, but these dystrophic changes were much less evident after tamoxifen or raloxifene. A noticeable reduction in collagen accumulation in limb muscles for all treatment groups vs controls was observed. Importantly, treatment with SERMs clearly mitigates muscle damage and enhances functions of both respiratory and cardiac muscles in addition to the limb muscles.

Other benefits were also observed. Control mice showed progressive muscle degeneration and regeneration in the diaphragm, accompanied by increasing fibrosis and infiltration, as well as significant impairment in respiration. Both tamoxifen and raloxifene eliminated focal infiltration and reduced the extent of fibrosis in the diaphragm, increased mass, and improved breathing ability. "Both treatments also improved bone density in the tibia and femur, potentially reducing the risk of fracture, a major threat to patients as MD progresses," added co-author Bo Wu, PhD, a research scientist at the McColl-Lockwood Laboratory for Muscular Dystrophy Research, Neuromuscular/ALS Center, Department of Neurology, Atrium Health's (formerly Carolinas HealthCare System's) Carolinas Medical Center, Charlotte (NC).

These histological changes were accompanied by functional improvements. For example, SERM treatment improved grip strength of both forelimb and hindlimb muscles and enhanced running ability on a treadmill test depending on the dose.

Sex-related differences in the effects of tamoxifen and raloxifene warrant careful consideration if the drugs are to be administered clinically for MD, noted the investigators. This is not surprising since SERMs act on estrogen receptors and interact both as estrogen-receptor agonists and antagonists.

"SERM therapy has great potential to significantly delay or halt MD progression. With the vast amount of safety data available, the selective use of tamoxifen and raloxifene in male and female patients with MD is an attractive and realistic alternative to steroids," noted Dr. Lu. This together with the detailed analyses of potential side effects and benefits in male and female populations provide rationale for early clinical trials. Importantly, the beneficial effects of SERMs are expected to extend to other forms of MD, beyond the specific mouse model investigated here.

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