Anabolic steroids, bodybuilding discussion forums. - SteroidologyGoing into my steroid cream for hand dermatitis week of anavar only, 50mg ED for 6 weeks and I'm starting to wonder if 50mg ED is enough to see good results. I'm working out 5 days a week, really clean low carb diet and I've seen results, but I'm questioning if I'd be seeing the 75 mg of anavar a day results if I wasn't taken 50mg of Anavar per day. I just wanna get my money's worth Read more or register here to join the discussion below Please complete this form and click the button below to gain instant access.
Anavar. 75mg per day for 50 days, or 50mg per day for 75 days? - World Class Bodybuilding Forum
Results 1 to 7 of 7. Add Thread to del. Anavar Cycles Here is an article I had sitting on my computer wanted to share it Going to ask about Anavar alone? First, I'd like to get a few things straight about Var. Anavar , used in adequate dosages, will shut you down. To what degree you experience side effects of suppression loss of libido, lethargy is entirely dependent upon the individual and the dosages used.
Myth 2 - Var is a weak anabolic , and is not effective unless stacked with a more androgenic compound. This could not be further from the truth. At dosages of 50mg a day and higher, Anavar is incredibly effective at adding water free LBM. At around day , increased vascularity should become apparent assuming your Oxandrolone is legitimate in its dosing , and strength gains should start appearing around day If used during a clean bulk, gains of pounds are possible. You will keep all of your gains with proper PCT.
Myth 3 - Anavar will not require any type of PCT. This is one ive never understood. It's a pretty commonly known fact now that var is a suppressive compound. There are three options to counteract this. Some of the more popular uses for which the herb is used are: But 25mg ED proviron, starting after week 2, will keep you rock hard. And it will help to harden up your muscles too.
At a dosage of around mg, split bi weekly, everything should keep running smoothly. Also, this will contribute to your gains much moreso than than options 1 or 2. I would keep nolva onhand on the off chance that you are severely gyno prone. Bloating should not be an issue at this dosage. Look out for brand new bulging forearms veins by around day 6.
If you are following a cutting regimen, expect new spider webs in your chest, shoulders and quads by around day Do some unweighted calf raises.
After about three minutes, your calves will be ready to pop. Youll be doing something like drinking a cup of water, and after a minute of holding it, your bi will be completely full and pumped. You may have to cut some sets short in the gym due to the painful pumpage.
And if youve used the drug, you can attest to this Dosages upwards of mg have been shown to exhibit diminishing returns. Also, I cant imagine the intensity of the pumps at that kind of dosage. It has been shown to be less toxic than other orals, and is even used as liver treatment for recovering alcoholics.
Still, i would limit my time using it to 8 weeks, 10 at the most. It would be beneficial to you liver to use several different OTC supplements during, and perhaps after your cycle. A few preventive measures never hurt anyone.
UDCA is prescribed for the treatment of cholestatic liver disease. Do not use for more than days, as liver toxicity can be an issue when using those dosages of niacin for long periods of time. Omega Red Kill Fish Oil: The antioxidants in Mega Red Krill Oil also help neutralize free radicals. I hope that people read this, and that it helps those doing their research to make the correct decision. If anyone sees any glaring errors, or has something important to add, hit me with a PM and I'll do some editing.
Just giving you all the options I can. Hope you enjoy all of this. After all of this if you are still dead set on running Var alone cause you dont like needless. I would get Test or DHT cream at the minimum and then read this thread to support steady blood lvl's after being shutdown. Subsequent Studies Oxandrolone and fat burning Oral anabolic steroid treatment, but not parenteral androgen treatment, decreases abdominal fat in obese, older men.
To compare the effects of Testosterone Enanthate TE , anabolic steroid AS or placebo PL on regional fat distribution and health risk factors in obese middle-aged men undergoing weight loss by dietary means.
Randomized, double-blind, placebo-controlled clinical trial, carried out for 9 months with primary assessments at 3 month intervals. Abdominal fat distribution and thigh muscle volume by CT scan, body composition by dual energy X-ray absorptiometry DEXA , insulin sensitivity by the Minimal Model method, blood lipids, blood chemistry, blood pressure, thyroid hormones and urological parameters.
After 3 months, there was a significantly greater decrease in subcutaneous SQ abdominal fat in the ASOX group compared to the TE and PL groups although body weight changes did not differ by treatment group. There was also a tendency for the ASOX group to exhibit greater losses in visceral fat, and the absolute level of visceral fat in this group was significantly lower at 3 months than in the TE and PL groups. There were significant main effects of treatment at 3 months on serum T and free T increased in the TE group and decreased in the ASOX group and on thyroid hormone parameters T4 and T3 resin uptake significantly decreased in the ASOX group compared with the other two groups.
The previously reported effect of T to decrease visceral fat was not observed, in fact, visceral fat in the TE group increased slightly from 3 to 9 months, although SQ fat continued to decrease.
Neither TE nor AS treatment resulted in any change in urologic parameters. Oral Oxandrolone decreased SQ abdominal fat more than TE or weight loss alone and also tended to produce favorable changes in visceral fat.
TE and ASND injections given every 2 weeks had similar effects to weight loss alone on regional body fat. Most of the beneficial effects observed on metabolic and cardiovascular risk factors were due to weight loss per se. These results suggest that SQ and visceral abdominal fat can be independently modulated by androgens and that at least some anabolic steroids are capable of influencing abdominal fat. It has been postulated that Oxandrolone is especially good at reducing visceral fat due to its high AR binding affinity.
It appears to be better at binding to the AR at even amounts then Test or Deca. It would make sense if it is working through the AR if it also increases AR expression in adipose tissue as well upregulating the AR in adipose tissue adding to lipolytic effects , which the following study seems to show: Short-term Oxandrolone administration stimulates net muscle protein synthesis in young men. We investigated whether Oxandrolone [Oxandrin OX ], a synthetic analog of Testosterone , would improve net muscle protein synthesis and transport of amino acids across the leg.
Muscle protein synthesis and breakdown were determined by a three-compartment model using stable isotopic data obtained from femoral arterio-venous sampling and muscle biopsy. The precursor-product method was used to determine muscle protein fractional synthetic rates.
Fractional breakdown rates were also directly calculated. Model-derived muscle protein synthesis increased from We conclude that short term OX administration stimulated an increase in skeletal muscle protein synthesis and improved intracellular reutilization of amino acids. The mechanism for this stimulation may be related to an OX-induced increase in AR expression in skeletal muscle. Anavar 's anabolic Effects and Liver Safety The anabolic androgenic steroid Oxandrolone in the treatment of wasting and catabolic disorders: Orr R, Fiatarone Singh M.
One such agent is the anabolic androgenic steroid AAS Oxandrolone , which has been used in such clinical situations as HIV-related muscle wasting, severe burn injury, trauma following major surgery, neuromuscular disorders and alcoholic hepatitis for over 30 years.
Our review of the use of Oxandrolone in the treatment of catabolic disorders, HIV and AIDS-related wasting, neuromuscular and other disorders provides strong evidence of its clinical efficacy. Improvements in body composition, muscle strength and function, status of underlying disease or recovery from acute catabolic injury and nutritional status are significant in the vast majority of well designed trials.
However, Oxandrolone has not yet been studied in sarcopenia. Unlike other orally administered C17alpha-alkylated AASs, the novel chemical configuration of Oxandrolone confers a resistance to liver metabolism as well as marked anabolic activity. In addition, Oxandrolone appears not to exhibit the serious hepatotoxic effects jaundice, cholestatic hepatitis, peliosis hepatis, hyperplasias and neoplasms attributed to the C17alpha-alkylated AASs.
Oxandrolone is reported to be generally well tolerated and the most commonly documented adverse effects are transient elevations in transaminase levels and reductions in high density lipoprotein cholesterol level. Oxandrolone and Keeping Gains Oxandrolone induced lean mass gain during recovery from severe burns is maintained after discontinuation of the anabolic steroid.
Weight loss and lean mass loss from burn induced catabolism can be more rapidly restored when the anabolic steroid Oxandrolone is added to optimum nutrition compared to nutrition alone. Our purpose in this study was to determine whether the regained lean body mass LBM is retained 6 months after stopping Oxandrolone.
Forty-five severe burn patients, entering the recovery phase were randomized into a nutrition group alone or with the addition of Oxandrolone , 20mg per day upon admission to the acute burn rehabilitation RH unit. Body composition was measured using bioelectric impedence analysis BIA.
We found that patients receiving Oxandrolone , in the rehabilitation unit, regained weight and lean mass two to three times faster than with nutrition alone. All patients were discharged from RH on a nutrition and exercise program and monitored in the outpatient burn center.
After 6 months, body weight and body composition were again measured. We found that the body weight and lean mass which was restored during RH, was maintained 6 months after discontinuation of Oxandrolone. Lost lean mass was not yet restored in the nutrition alone group.
We can conclude that body weight and lean mass which is lost, due to burn induced catabolism, can be effectively restored in the post-burn recovery period with Oxandrolone. The body weight and lost lean mass which is regained, is maintained 6 months after stopping the drug. Anavar is indeed suppressive Prospective double-blind placebo-controlled trial. Sixteen boys with constitutional delay of growth and puberty CDGP with testicular volumes ml were randomized to 3 months treatment: LH and GH profiles minute samples were analysed by peak detection Pulsar , Fourier transformation and autocorrelation.
Statistical analysis was by multivariate analysis of variance for repeated measures. In Group 2, however, LH and Testosterone parameters decreased at 3 months followed by a rebound increase at 6 and 12 months. IGF-I levels were increased at both 3 and 12 months.