If you want that, don’t eat for 3 months and you’ll get there without putting anything in your body.
You seem like a guy that’s interested in facts, I like that. I don’t like it either when threads revolve into questions of character.
But what I’m starting to question is the justifying of using steroids if you want a body that’s not only achievable natty but doesn’t even have average gym rat muscle mass. On top of that you have health issues worsening the risk for using roids.
I’d say zac Efron in bay watch isn’t roid territory either, just training, bulking cutting, bulking cutting for like 3-4 years. And that physique has some muscle. Now if you want a The Rock physique, then I’d point you to steroids.
Just be clear in what your goals are.
I know this thread is not intended to discuss your goals. That had to be pointed out though.
Ok enough with that.
I’ll give you something to read here since you seem interested in research and learning like me.
See here:
They demonstrated that podocytes express both androgen and estrogen receptors and that in vitro , testosterone can cause podocyte apoptosis, which is blocked by the addition of flutamide (18)
from:
So the first thing to recognize is from this study is that every AAS is nephrotoxic seemingly dependent on the binding of the AR.
So then we check how strong AR binding affinities for various steroids are:
MT greater than 19-nortestosterone ( NorT ; nandrolone) greater than methenolone (17 beta-hydroxy-1-methyl-5 alpha-androst-1-en-3-one) greater than testosterone (T) greater than 1 alpha-methyl-DHT]. In other cases, AR binding was weak (RBA values less than 0.05): stanozolol (17 alpha-methyl-5 alpha- androstano [3,2-c]pyrazol-17 beta-ol), methanedienone (17 beta-hydroxy-17 alpha-methyl-1,4-androstadien-3-one), and fluoxymesterolone (9 alpha-fluoro-11 beta-hydroxy-17 alpha-methyl-T). Other compounds had RBAs too low to be determined (e.g. oxymetholone (17 beta-hydroxy-2-hydroxymethylene-17 alpha-methyl-5 alpha-androstan-3-one) and ethylestrenol (17 alpha-ethyl-4- estren -17 beta-ol).
from:
That is one variable, AR binding. Now we just need to look at all the others and put them in perspective to come up with a good conclusion. I think this thread has potential, so let’s go on a joint effort to find out which one is the least toxic to the kidneys.
You guys got something to point out or contribute here @unreal24278 @anon18050987 ? I’d appreciate it