Natural Test Shut Down

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HootSnik

New Member
Howdy,

Basic question--I tried the search feature but could not find definitive information on the following.

The specific question: Is there a dosing of Testosterone Enanthate (in mg per week) below which you can expect to preserve what is left of natural testosterone production? Does the introduction of ANY exogenous testosterone completely shut that production down--or is the shut down proportionate to the dosing.??

If you are aware of any research on this subject please direct me.

Cheers,
1DB
 
Defy Medical TRT clinic doctor
search for the thread "infrequent dosing to avoid shutdown". Short answer is 1) use the term suppression , not shutdown 2) some oral protocols in combination with a SERM appear to minimize suppression 3) Test E is is likely not a good choice for this purpose 4) use of a SERM like clomid or enclomiphene may reduce suppression, but in general this topic requires individual experimentation and there is not yet a large pool of data to draw on.
 
Howdy,

Basic question--I tried the search feature but could not find definitive information on the following.

The specific question: Is there a dosing of Testosterone Enanthate (in mg per week) below which you can expect to preserve what is left of natural testosterone production? Does the introduction of ANY exogenous testosterone completely shut that production down--or is the shut down proportionate to the dosing.??

If you are aware of any research on this subject please direct me.

Cheers,
1DB

Other than nasal T gel (Natesto) any form of exogenous whether T pellets, oral esterified T (Jatenzo), transdermal gels/creams, injectable esterified T when used in therapeutic doses to treat low testosterone will have a strong impact on suppression on the hpta.

Formulation/PKs, dosing protocol/minimum effective doses needed to raise T levels in order to achieve a healthy FT level in order to provide relief/improvement of symptoms will results in suppression of the hpta.

Long and medium-acting injectable esterified TU/TC/TE/mixed will have the strongest impact.

Even short-acting injectable esterified TP can still have a strong suppressive effect on the hpta

Next would be oral TU (Jatenzo) and transdermals.

Nasal T gel would be the least suppressive due to the PK/dosing protocol.






FIGURE 1 | Percent change in mean gonadotropin levels (LH & FSH), from baseline through 6 months of testosterone treatment. Nasal testosterone (blue), dosed t.i.d., adapted from (15), n = 33. Topical testosterone (orange), dosed daily, adapted from (9), n = 123. IM injectable - 100 mg testosterone enanthate, (red), adapted from (10), n = 10. All changes from baseline were statistically significant. Nasal testosterone—FSH p = 0.03, all others p < 0.001. Standard error calculated using the delta method
1719361888466.png








Figure 6: Effects of different types of T preparations on FSH (dark grey) and LH (light grey). Data from [22] [14]
1719361771923.png






 
Beyond Testosterone Book by Nelson Vergel
Thanks for the info guys. After reading through the information provided by Madman and Voices, it appears that my hope to preserve my natural production (TT currently 586), drive down SHBG (currently 58), and bring my FT up (currently 5.3 on 6.6 to 18 scale) to a healthy level by injecting small doses of T. Enan (20-30mg/wk) is not a viable protocol. I will, however, continue this process for 8 wks and get some labs to see where I am.
Cheers,
1db
 
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