Risingfire
Member
- Joined
- May 10, 2016
- Messages
- 1,063
How long have you been using the scrotal base?I had 350 with 22 years. Pulled the trigger on scrotal T base after this result.
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How long have you been using the scrotal base?I had 350 with 22 years. Pulled the trigger on scrotal T base after this result.
Please keep us updated over the next few weeks. After three weeks, I didn't like the results. It was a huge boost in the beginning but soon changed around week 3About 2 weeks. Dissolved in DMSO btw, a la @TheBeard
Please keep us updated over the next few weeks. After three weeks, I didn't like the results. It was a huge boost in the beginning but soon changed around week 3
Water restriction could induce the upregulation of the CYP3A4 enzyme in the liver.
This enzyme seems to be able to convert cholesterols into oxysterols (25-hydroxycholesterol and 4β-hydroxycholesterol).
Moreover, these oxysterols are known to be ligands for the Liver X Receptor (LXR). What is interesting is that the LXR seems to be involved in testosterone synthesis in testis:
Liver X Receptor: A Cardinal Target for Atherosclerosis and Beyond
"Initially, this receptor was identified in tissue obtained from a rat liver, with no known endogenous ligands, and was named LXR. Later, LXR was termed an ‘adopted’ nuclear receptor with the discovery of oxysterols as endogenous ligands for this receptor."Another hypothetical reasoning:
"The cardinal functions of the testis are testosterone production and spermatogenesis. Leydig and Sertoli cells are testicular cells. Leydig cells secrete testosterone, while Sertoli cells provide structural and nutritional support for developing germ cells.
Furthermore, Leydig cells express LXRα, while Sertoli cells LXRβ, whereas germ cells express both LXRs. LXRα regulates basal testosterone synthesis and is involved in the control of germ cell apoptosis. In contrast, LXRβ controls lipid metabolism in Sertoli cells by regulating cholesterol export, as well as germ cell proliferation. Moreover, both LXRs together regulate ligand-induced steroidogenesis, fatty acid metabolism and, surprisingly, the retinoic acid signaling pathway in the testis."
"Moreover, both LXRs together regulate ligand-induced steroidogenesis, fatty acid metabolism and, surprisingly, the retinoic acid signaling pathway in the testis."
- the enzyme CYP11A1, also called CYP450scc, is in charge of converting cholesterol: "P450scc is a mitochondrial enzyme that catalyzes conversion of cholesterol to pregnenolone. This is the first reaction in the process of steroidogenesis in all mammalian tissues that specialize in the production of various steroid hormones. " (wikipedia)
- It seems like the transcription factor NFAT5 could have a link with this enzyme, RNA-Seq analysis of high NaCl-induced gene expression:
- "Categories of NFAT5 Target Genes Upregulated after Adaptation to High NaCl, but Not after as Little as 24 h of High NaCl.
- Steroid hormones. Cyp11a1 protein localizes to the mitochondrial inner membrane and catalyzes the conversion of cholesterol to pregnenolone, the first and rate-limiting step in the synthesis of the steroid hormones."
- NFAT5 is upregulated during water restriction.
maybe add progesteron to test ?Exogenous testosterone caused way more problems than it fixed for me long term, and I tried everything -- cream, cyp, prop, enanthate, sustanon, testosterone monothearpy, testosterone + hcg, testosterone + ai, weekly injections, daily injections, keeping levels in the middle, at the top and above the range, etc. I spent three years on trt from the ages of 19 -> 22, and things just got worse the longer I was on it.
The problem with exogenous test is that it does nothing to address the underlying pathology which caused it to become low in the first place. I spent three years in the trt community, and as a whole, I've never seen a sicker group of people anywhere else online. The majority of people there still have fatigue, zero sex drive, erection issues, brain fog, estrogen dominance, etc.
Shutting down the upstream production of hormones like preg, prog and dhea whilst ramping up estrogen production just adds to the underlying problem imo. The heavy adrenal suppression from the long term use of potent androgens also becomes problematic, with many having to resort to the use of Prozac or other ssri's as a work around to stop their cortisol from dropping into truly deficient territory from chronic ACTH suppression.
The long term risk of HPTA-suppressive doses of testosterone just isn't worth it. I personally feel much better with 500 ng/dL and a working hpta vs the 800 - 1400 ng/dL I had during my time on injections and cream. Just my 2c.
Exogenous testosterone caused way more problems than it fixed for me long term, and I tried everything -- cream, cyp, prop, enanthate, sustanon, testosterone monothearpy, testosterone + hcg, testosterone + ai, weekly injections, daily injections, keeping levels in the middle, at the top and above the range, etc. I spent three years on trt from the ages of 19 -> 22, and things just got worse the longer I was on it.
The problem with exogenous test is that it does nothing to address the underlying pathology which caused it to become low in the first place. I spent three years in the trt community, and as a whole, I've never seen a sicker group of people anywhere else online. The majority of people there still have fatigue, zero sex drive, erection issues, brain fog, estrogen dominance, etc.
Shutting down the upstream production of hormones like preg, prog and dhea whilst ramping up estrogen production just adds to the underlying problem imo. The heavy adrenal suppression from the long term use of potent androgens also becomes problematic, with many having to resort to the use of Prozac or other ssri's as a work around to stop their cortisol from dropping into truly deficient territory from chronic ACTH suppression.
The long term risk of HPTA-suppressive doses of testosterone just isn't worth it. I personally feel much better with 500 ng/dL and a working hpta vs the 800 - 1400 ng/dL I had during my time on injections and cream. Just my 2c.
Sounds good. I felt incredible the first few days on it. Lots of energy and virility. Between the second and third week my pulse had increased and I didn't feel too hot. I shortly after stopped the scrotal test base administration. It's possible I started becoming suppressed and my body was going through that changeWill do. Might start a thread on my experience with it. Also interested in a more detailed account of your experience. Cheers!
Truest words spokenI just got tired of being in shi-tty health and making no progress at all fixing it tbh. I want to live in my twenties instead of just hibernating.
some guys try nettle on **** directly, it is know way to improve your erection or even increase size-it's not a joke. nettle decrease aromatization so lower estradiol, and decrease 5alpha reductase so decrease dht and at the same time lower shbg- so it' is increasing free testosterone.Anyone tried topical thyroid on the testes / penis?
Exogenous testosterone caused way more problems than it fixed for me long term, and I tried everything -- cream, cyp, prop, enanthate, sustanon, testosterone monothearpy, testosterone + hcg, testosterone + ai, weekly injections, daily injections, keeping levels in the middle, at the top and above the range, etc. I spent three years on trt from the ages of 19 -> 22, and things just got worse the longer I was on it.
The problem with exogenous test is that it does nothing to address the underlying pathology which caused it to become low in the first place. I spent three years in the trt community, and as a whole, I've never seen a sicker group of people anywhere else online. The majority of people there still have fatigue, zero sex drive, erection issues, brain fog, estrogen dominance, etc.
Shutting down the upstream production of hormones like preg, prog and dhea whilst ramping up estrogen production just adds to the underlying problem imo. The heavy adrenal suppression from the long term use of potent androgens also becomes problematic, with many having to resort to the use of Prozac or other ssri's as a work around to stop their cortisol from dropping into truly deficient territory from chronic ACTH suppression.
The long term risk of HPTA-suppressive doses of testosterone just isn't worth it. I personally feel much better with 500 ng/dL and a working hpta vs the 800 - 1400 ng/dL I had during my time on injections and cream. Just my 2c.
I have seen the opposite. Groups filed with thousands of men stating trt was the single greatest thing they have done to improve their health.
I personally have mixed experiences with trt, i had better luck with thyroid and adrenals
@Broco6679 what is your daily supplement diet like these days. Also what do you think of this?Deca Nandrolone As A Bio Identical Form Of Trt