Any one got a review on T3

alex994

New Member
Has anyone that tried t3 have a review?

Did it make a difference fat loss wise ?

Did you lose a lot of muscle too if any ?

Does it damage your metabolism ?

Would like to hear from someone who has used it

I am going to use it to speed up my metabolism for this cut , i have a sitting job so i don't move around that much will be taking teest with t3
 
Yes, it makes a difference in fat loss - IF you're already losing.

Yes, it also burns some muscle. AAS will prevent this, or more accurately cause muscle growth in excess of the loss.

It shuts down T3 production in your thyroid when you take it above normal production. 25mcg is "normal" production, or so I've read. Ending T3 intake will let your thyroid restart production. I haven't read of anyone having a problem with this.

Most start with 50mcg, and some like to ramp up from 25mcg. I've read of people taking a lot more than 50mcg. 50mcg gives me a low grade headache 24/7, so I don't go higher.

T3 increases your metabolism AND your body temperature. At 50mcg my temperature stays around 99 deg. I get hot and sweaty easy, and sometimes at night I wake up freezing like I have a fever. When I'm on T3 I take my temperature every day and adjust dose down if it gets too high: 99.4 is too high IMO.
 
I started at 50 mcg. Increased dosage every 3 days up until 125 mcg a day for 4 1/2 weeks. Then tapered down every 3-4 days. No problem. It'll work better if your diet is on point and you're doing cardio. I used it with clen also.

Loss no muscle.
Going to take in again during pct.
Loss fat too.

You won't see results day 1 if that's what your looking for
 
This study was in healthy young men (e.g., bodybuilders). Essentially, for every 2 pounds of fat loss, there is 1 pound of muscle loss. And the length of the study, 9 weeks, is slightly less than a typical AAS cycle leading to more muscle loss.

T3 treatment began following the 3-week run-in period and continued for 63 days (9 weeks). All subjects initially received 75μ g/day T3 (liothyronine sodium, Cytomel, Smith-Kline-Beecham, Philadelphia, PA) in five doses every 4 h during waking hours beginning at 0600 h.

This dose was chosen based on a previously described paradigm suggesting that this dose produced serum levels of approximately 4.6–5.4 nmol/L. The dose was reduced if a subject became symptomatic or if serum T3 levels exceeded 2 SD above the mean for the T3 assay in our laboratory (∼4.6 nmol/L).

All subjects but two received dose reduction to either 62.5 or 50 μg/day T3, in most cases due to higher than desirable levels of serum T3. The timing of dose reduction differed among subjects, with most subjects being reduced to 62.5 μg/day after approximately 2 weeks of treatment.

Lovejoy JC, Smith SR, Bray GA, et al. A Paradigm of Experimentally Induced Mild Hyperthyroidism: Effects on Nitrogen Balance, Body Composition, and Energy Expenditure in Healthy Young Men. J Clin Endocrinol Metab 1997;82(3):765-70. http://jcem.endojournals.org/content/82/3/765.long

Although T3 exerts major regulatory actions in both animals and humans, most clinical studies of T3 administration have been relatively short term. The present study examined the effects of more than 2 months (63 days) of low dose T3 treatment on nitrogen balance, body composition, 24-h energy expenditure (EE), and protein turnover in seven healthy men studied at an in-patient metabolic unit. Subjects were also randomly assigned to either high or low fat diets to determine the effects of diet composition.

T3 treatment produced significant losses in both lean mass (1.5 {+/-} 0.3 kg) and fat mass (2.7 {+/-} 0.4 kg) by 6 weeks, with similar reductions in both at 9 weeks. The high fat diet somewhat attenuated the loss of body fat. Nitrogen balance was significantly negative for the first 3 weeks of T3 treatment, but tended to return to baseline thereafter. There were no significant effects of treatment on protein turnover at 9 weeks, although there was a slight increase in leucine oxidation (P = 0.07). Despite the apparent adaptation in nitrogen balance, total 24-h EE and sleeping EE were significantly increased at 9 weeks.

We conclude that although healthy men are able to adapt to mild hyperthyroidism in terms of nitrogen balance, they exhibit significant and persistent changes in fat and fat-free mass as well as energy balance.
 
What are folks shooting for with T3? My T3 bloods were right in the middle yet my doc called me "hypo" and put me on T3 meds which helped with fatigue and such for a short time, but quit working after a few weeks. What are your reasons for chasing T3?
 
This study was in healthy young men (e.g., bodybuilders). Essentially, for every 2 pounds of fat loss, there is 1 pound of muscle loss. And the length of the study, 9 weeks, is slightly less than a typical AAS cycle leading to more muscle loss.

T3 treatment began following the 3-week run-in period and continued for 63 days (9 weeks). All subjects initially received 75μ g/day T3 (liothyronine sodium, Cytomel, Smith-Kline-Beecham, Philadelphia, PA) in five doses every 4 h during waking hours beginning at 0600 h.

This dose was chosen based on a previously described paradigm suggesting that this dose produced serum levels of approximately 4.6–5.4 nmol/L. The dose was reduced if a subject became symptomatic or if serum T3 levels exceeded 2 SD above the mean for the T3 assay in our laboratory (∼4.6 nmol/L).

All subjects but two received dose reduction to either 62.5 or 50 μg/day T3, in most cases due to higher than desirable levels of serum T3. The timing of dose reduction differed among subjects, with most subjects being reduced to 62.5 μg/day after approximately 2 weeks of treatment.

Lovejoy JC, Smith SR, Bray GA, et al. A Paradigm of Experimentally Induced Mild Hyperthyroidism: Effects on Nitrogen Balance, Body Composition, and Energy Expenditure in Healthy Young Men. J Clin Endocrinol Metab 1997;82(3):765-70. http://jcem.endojournals.org/content/82/3/765.long

Although T3 exerts major regulatory actions in both animals and humans, most clinical studies of T3 administration have been relatively short term. The present study examined the effects of more than 2 months (63 days) of low dose T3 treatment on nitrogen balance, body composition, 24-h energy expenditure (EE), and protein turnover in seven healthy men studied at an in-patient metabolic unit. Subjects were also randomly assigned to either high or low fat diets to determine the effects of diet composition.

T3 treatment produced significant losses in both lean mass (1.5 {+/-} 0.3 kg) and fat mass (2.7 {+/-} 0.4 kg) by 6 weeks, with similar reductions in both at 9 weeks. The high fat diet somewhat attenuated the loss of body fat. Nitrogen balance was significantly negative for the first 3 weeks of T3 treatment, but tended to return to baseline thereafter. There were no significant effects of treatment on protein turnover at 9 weeks, although there was a slight increase in leucine oxidation (P = 0.07). Despite the apparent adaptation in nitrogen balance, total 24-h EE and sleeping EE were significantly increased at 9 weeks.

We conclude that although healthy men are able to adapt to mild hyperthyroidism in terms of nitrogen balance, they exhibit significant and persistent changes in fat and fat-free mass as well as energy balance.

I wonder what the protein turnover rate would have been had they been getting enough protein intake. It says they only received 15% of total kcals from protein. For a relatively lean 200lb person at around 3000cals, that comes out to 112g of protein. Also I don't suppose some ethnics committee would approve of doing the same study on a training population who also were on AAS....wishful thinking on my part.
 
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