I've run 25mcg on tren a couple times. No need to go high on the dose. It would be a good addition to a recomp
i gotta give u a rep bro, because no never replies to the advice i try to get haha. Well then I'll run the .40mg just till week 5 and then taper down to 25mcg.
Hey bro I have another question, im not shedding hair now, but i had dutast, have you ever used it or any product similar to it>?
And hows your cycle going
Thanks bro, 25mcg is good on tren because tren is slightly suppressive to the thyroid. 25mcg is pretty much a replacement dose and I wouldn't worry about catabolism at this dose while on tren. Never run dutast, I've heard shitty things about sides but never used it. I just shave my head. I accept that I'll be bald lol. My cycles good so far...I'm about two weeks into the tren/mast and just added in Anavar (var) a couple days ago at 80mg a day. Let the good times roll![]()
T3 is highly catabolic no matter what people say. Of course dosage dependent! Some say that 25mcg is just too low for a ED dosage since that's what aprox what your own body produces per day.
The man speaks the truth! Why suppress your thyroid for a replacement dose? Go with t4 it's better, especially with GH![]()
im just gonna run 40mcg and i dont have any t4 and dont plan on getting anymore shit ahaha
The man speaks the truth! Why suppress your thyroid for a replacement dose? Go with t4 it's better, especially with GH![]()
does t3 make you more hungry by any chance>>> ?
I hear this too often and yeah it can be catabolic at high ass doses that people take but 25mcg on cycle is not going to be a catabolic. It will increase protein turnover rate allowing your body to process more of it. Tren is slightly suppressive to the thyroid so t3 is an excellent addition to a tren cycle. Yes, 25mcg is what is considered a replacement dose but that's assuming your thyroid is functioning at 100 percent which probably isn't the case, especially on tren.
T3The effect of tri-iodothyronine (T3) on protein turnover and metabolic rate.
The effect of tri-iodothyronine (T3) on protein t... [Int J Obes. 1985] - PubMed - NCBI
Wolman SI, Sheppard H, Fern M, Waterlow JC.
Abstract
Obese patients who had an unusually slow weight loss on a restricted energy intake (2 MJ/d) were treated for approximately two weeks with small doses of T3 (20 micrograms three times daily). At the beginning and end of treatment whole body protein turnover was measured with a single dose of 15N-glycine and both ammonia and urea as end-products. T3 increased the rate of weight loss, with a significant increase in urinary nitrogen excretion. There were small increases in basal metabolic rate and protein turnover, which were not significant. It is concluded that the extra weight loss produced by T3 was at the expense of lean body mass and not of fat.
T4The effects of triiodothyronine on energy expenditure, nitrogen balance and rates of weight and fat loss in obese patients during prolonged caloric restriction.
The effects of triiodothyronine on energy expendi... [Int J Obes. 1985] - PubMed - NCBI
Abraham RR, Densem JW, Davies P, Davie MW, Wynn V.
Abstract
We studied ten obese patients on prolonged caloric restriction by metabolic balance techniques two weeks before and two weeks after the start of treatment with triiodothyronine (T3) (0.36-1.01 micrograms/kg/d)[36-100mcg for a 100kg man]. The rate of weight, nitrogen and fat loss calculated from metabolic balance increased during T3 therapy and these effects were maximal in the second week of treatment. In seven patients studied continuously for four weeks on T3 therapy, the rates of weight and fat loss during the fourth week of treatment were not significantly different from pretreatment values while nitrogen loss was still significantly greater. The increase in nitrogen loss, studied after the period of adaptation to caloric restriction, implies that prolonged treatment with T3 can result in significant losses of lean tissue in addition to that resulting from caloric restriction alone. Mean weight loss increased by 92 g/d during T3 therapy. T3 significantly increased the metabolic rate as measured by two other independent measures: the resting energy expenditure (REE), measured by indirect calorimetry (fourteen patients), and the sleeping heart rate (six patients).
T4vsT3Effects of thyroxine on protein turnover in rat skeletal muscle
Effects of thyroxine on protein turnover in rat skeletal muscle
KE Flaim, JB Li, and LS Jefferson
Abstract
The effects of thyroxine (T4) on protein turnover in skeletal muscle were studied using normal, thyroidectomized (thyrex), and hypophysectomized (hypox) rats. Thyrex rats had a depressed growth rate that was accompanied by 50% reductions in the level of RNA and the rate of protein synthesis in gastrocnemius muscle, as determined in the perfused hemicorpus. Protein synthetic efficiency (protein synthesis per unit RNA) was decreased by 18%. Daily treatment of thyrex rats with T4 at different dose levels for up to 16 days led to improved growth rates, elevated RNA concentrations, and increased protein synthesis rates. The primary effect of T4 was to increase the protein synthetic capacity of muscle. Protein degradation, determined in the perfused hemicorpus, and activity of a lysosomal protease, determined in unperfused muscle, were reduced in the thyrex condition. Treatment of thyrex rats with T4 increased protein degradative rates, but not protease activity. Hypox rats, which also exhibited depressed skeletal muscle protein synthesis, responded to T4 and combined T4 and growth hormone with marked improvements in protein synthesis.
Comparison of the Effects of Thyroxine and Triiodothyronine on Protein Turnover and Apoptosis in Primary Chick Muscle Cell Cultures
ScienceDirect.com - Biochemical and Biophysical Research Communications - Comparison of the Effects of Thyroxine and Triiodothyronine on Protein Turnover and Apoptosis in Primary Chick Muscle Cell Cultures
Abstract
Primary chick muscle cells were treated with physiological level of thyroxine (T4) or triiodothyronine (T3) to examine the effects of the hormones on growth, protein turnover, and apoptosis of the cells. Creatine kinase activity, as an index of differentiation, was increased by both T4and T3.Even when the conversion from T4to T3was blocked by iopanoic acid, T4increased creatine kinase activity. The rate of protein degradation estimated from [3H] tyrosine release was increased by T3but not by T4. DNA cleavage and fragmentation, as indices of apoptosis, were induced by T3but not by T4. These results show that T4stimulates cell differentiation but not protein degradation and apoptosis in primary chick muscle cells, while all events are stimulated by T3.
Pretty much all drugs will exhibit effects in dose dependent manner, cycling is all about personal preference. Go ahead and try it! Some like t3, some do not. In the end, you have to find what works for you. If you don't notice much from t3, try t4 next go!