godlovesatrier
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Wanted to seperate this from the main thread for tracking as it's getting a bit crowded.
So the 5-ar inhibitors you mentioned @jump44 - which are they in the protocol?
Quote from jump44's comments in original thread:
Also I found this:
https://pubmed.ncbi.nlm.nih.gov/11931850/
cc @joshua.leisk
So the 5-ar inhibitors you mentioned @jump44 - which are they in the protocol?
Quote from jump44's comments in original thread:
jump44 replygodlovesatrier said:
Interesting replies here. All interesting reading too
The covid vaccine is making me grumpy and depressed at the minute. Immune reaction is pretty much on most of the time. So not pleasant. But still have plenty of energy. Feels utterly bizarre to spend most of the time able to just do "loads" of menial jobs and the like. Although mental clarity isn't great as I said due to the covid vax.
What are the issues? Does it induce disease or lower t cell counts? Like Tagamet? Be interested to know.
Although like you based on my experiences so far I'll take this as a treatment until more science emerges.
@xebex you describe the same crash style as me. Sleepy then I rest, then it usually bottoms out or I have 48 hours of PEM and then it usually starts to lift. Although initially when I did the protocol PEM was much worse and seemed to go on for up to a week. This eventually lifted with the higher egcg dose which seemed to be critical to be honest as a protocol supp.
I used to get all the aches and pains you got but since taking Andrographis Paniculata all those pains went. This was a few years ago and I totally dismissed it as irrelevant. But now it makes me wonder when I took andro I had pain in the same places. Had to be viral?
Really pleased your doing well @BrightCandle and thanks for clarifying about him/her Hope the vaccine helps your long covid!
look up post finasteride or accutane syndromes online and you’ll find plenty of horror stories of men taking these 5ar inhibitors and being severely damaged.. now, I -am not- saying that the ones in this protocol do the same thing… however there are a few of them in here being taken at high dosages- and it appears Joshua is saying it’s a main goal of this is to really knock down/block the androgen receptors etc. Tjis isn’t something males should necessarily be taking lightly if they are predisposed to issues(which unfortunately there’s no way to really tell beforehand), so it’s just something I’ve had In the back of my mind.
Also I found this:
https://pubmed.ncbi.nlm.nih.gov/11931850/
The enzyme steroid 5 alpha-reductase (EC 1.3.99.5) catalyzes the NADPH-dependent reduction of the double bond of a variety of 3-oxo-Delta(4) steroids including the conversion of testosterone to 5 alpha-dihydrotestosterone. In humans, 5 alpha-reductase activity is critical for certain aspects of male sexual differentiation, and may be involved in the development of benign prostatic hyperplasia, alopecia, hirsutism, and prostate cancer. Certain natural products contain components that are inhibitors of 5 alpha-reductase, such as the green tea catechin (-)-epigallocatechin gallate (EGCG). EGCG shows potent inhibition in cell-free but not in whole-cell assays of 5 alpha-reductase. Replacement of the gallate ester in EGCG with long-chain fatty acids produced potent 5 alpha-reductase inhibitors that were active in both cell-free and whole-cell assay systems. Other flavonoids that were potent inhibitors of the type 1 5alpha-reductase include myricetin, quercitin, baicalein, and fisetin. Biochanin A, daidzein, genistein, and kaempferol were much better inhibitors of the type 2 than the type 1 isozyme. Several other natural and synthetic polyphenolic compounds were more effective inhibitors of the type 1 than the type 2 isozyme, including alizarin, anthrarobin, gossypol, nordihydroguaiaretic acid, caffeic acid phenethyl ester, and octyl and dodecyl gallates. The presence of a catechol group was characteristic of almost all inhibitors that showed selectivity for the type 1 isozyme of 5 alpha-reductase. Since some of these compounds are consumed as part of the normal diet or in supplements, they have the potential to inhibit 5 alpha-reductase activity, which may be useful for the prevention or treatment of androgen-dependent disorders. However, these compounds also may adversely affect male sexual differentiation.
cc @joshua.leisk