I explained this in the past, but here goes.
Some people, women and men, are very sensible to DHT, which is the more potent type
of testosterone.
Even women, part of T will be converted into DHT at scalp level.
Hair that is sensible to it will be destroyed eventually.
If they are susceptible to its effects, they will slowly (or quickly) lose hair.
TS with substantial hair loss prior to HRT have a good chance of still continuing this loss
post HRT but at a much slower speed, post HRT unless they're able to keep as much DHT
away from the hair roots.
To stop all DHT to the root you can do a couple of things:
- Arrest all T production from testes and adrenals.
- While its possible through the pituary feedback loop (with spiro)
or directly (with Lupron) to stop the testes from producing T, its
not possible to stop the adrenals from producing it that way
(the adrenals produce T in women). If you can't stop all T, some
of the adrenal T will be converted to DHT; for those will mild
alopecia prior to HRT, that level of DHT will not be that damageable
to the remaining hair and there will be some regrowth. Still, the remaining
DHT can prevent the smallest miniaturized hair from regrowing even
in those cases.
- So, the DHT converted from T can be blocked at the receptors.
- Spiro has a 60% afinity to T receptors, which is one of the highest
for non T compounds. So, if there is sufficient Spiro in the system,
most T receptors will have a Spiro molecule stuck in it and DHT
will not be able to bind and affect the hair.
- The problem with this is that spiro has a short half life, so
unless your taking big split doses, there will be times in the
day when spiro levels will decrease and less T receptors are
occupied and DHT will be able to bind.
- Even if you take high enough doses of spiro, there's still
the fact that spiro binds to T receptors all over the body while
DHT has a narrower effect. So, there is a bigger chance that
DHT is not bound yet and can still do some damage while
spiro molecules are already bound to T.
- Another issue is that DHT has a 100% affinity to T receptors.
So, if spiro and DHT compete for a receptor, DHT will win.
- The answer to all those issues is simple, reduce the conversion of T to DHT, that's where
finesteride and dutasteride come from.
- By eliminating almost all DHT and T, and binding spiro to T receptors, the amount of DHT reaching hair folicles is almost zero. That allows those with strong alopecia tendencies to at least arrest it and hopefully have the chance to reverse it. Even for all the others will less alopecia, eliminating DHT will allow the smallest miniaturized hair to eventually become viable, the hair will thicken.
- The only problem with eliminating DHT conversiion is free T produced from the adrenals, is slightly boosted +15%. But the adrenals produce a low quantity of T, so your T will still be well within female range.
So, there's not any downside to using finesteride (except money spent), especially since its dirt cheap, a proscar tablet can last 10 days if its split, and has little side effects.