You wont BELIEVE what happens on page 328. Click here to find out!This thread has become a freaking click bait... A million views.. f*****g tens of thousands of replies..
Still little news, lots of anxiety..
There are people here far more knowledgeable on this than I am, but based on the little that I know I wouldn't be surprised if it results similar to the Big 3 aren't out of the question IMO. Long term maintenance depends on how efficient Equol is at inhibiting DHT I guess, while PGE1 acts on similar pathways to minoxidil. Not sure though how effective it is compared to minoxidil, or to PGE2 or castor oil which some have used. Carnitine is interesting as it could attenuate oxidative stress, which is known to be high in balding hair follicles. Ultimately though, we'll have to wait for the trial results to find out how well it works.
There are many studies on the Internet about the capacities of Equol, many of them tried a lot of % in vitro tests. Equol and finasteride, as you know, act different ways. I don't wanna repeat the already 100 times discussed point, but I don't care about the power of it, while I can introduce Finasteride in my regimen. DHT would be reduced sistemically by fina, and topically could be totally detroyed by equol. Fun fact is that we do not know S-Equol's half-life, but with a therapy comprehensive of both, we should be ok, even against aggressive forms. Or maybe an upgrade to Dutasteride to systemically destroy almost every % of DHT, even if the risk of sides would be higher.
I know it's inevitable to compare Brotzu Lotion to the big 3, but right now it is the most senseless thing to think at (no offense on you though), it's better to think what products can support it when available. Finasteride for sure, I would put out Minoxidil because the action of DGLA is similar on the theorical side, but it's very different on the practical side. Stimulating the microcirculation means stimulating ALSO the perycite (minoxidil's effect) but causing no initial shedding nor the sides of minoxidil, because we are not going to superficially "drug" it, but we are going to repair it and the smaller and deeper cells, so it's not resulting in an "overpumping blood" effect only on the last parts of the blood's trip to the hair bulb. As Brotzu said when spoke at Genova's Gaslini, the Minoxidil can't go deeper than the perycite, because he can not reach the endothelial cells, but DGLA can if carried into cathionic liposomes (reaching the endothelial cells).
View attachment 46711
4 Days? I'm using it for 3 months now, with a ton of regrowth, so every couple of days Nizoral shampoo 2%, going well so far.
I lost a sh*t ton of thin hairs in the first 3 weeks and now I'm losing almost nothing
Minoxidil did nothing in terms of regrowth. Haven't had any side effects as well. Same story with keto.
i like minoxidil...i put it off for a long time...i had no reaction for 2 weeks..then 2 weeks heavy shedding..then by 5th week in magnifying mirror i saw regrowth...still seeing regrowth--i also stopped shedding small hairs and hair is 'rooted' compared to before minoxidil...i use topical spironolactone also.
Four days...
I shed for months and after about six or seven months I have lots of regrowth and new regrowth still.
If you don't lose these hairs now, you will lose them some hours later or when you shower. Hold on boy, just continue and stay strong
This is my problem. If i use Minoxidil, I will lose tons of hair just applying the stuff. So if it doesnt work then my hair will look worse than when i started
I'm curious about dermarolling's potential role in tandem with the lotion. I can't say I understand the exact science behind it, but it clearly is effective at helping minoxidil reach its desired location. I wonder what the adherence rate of the liposomes to the target cells are for the lotion and if it can be improved. Maybe dermarolling can bump the rate of the lotion's ingredients properly activating even higher.
If this is in fact the real deal, I wonder what type of effect if could be in combination as the big 4? Could minoxidil and finasteride, have complimentary effects to the point where full regrowth could be achieved? Every component has positive results due to different mechanisms.
I cant wait to find out, but if minoxidil stimulates growth, I dont see why brotzu wont help you keep the additional growth even after dropping minoxidil (assuming it works).
@Barbe a papa Dermarolling does not help Minoxidil to reach internal parts (endothelial cells in my previous explanation) but it helps to penetrate the skin: for example, all of the molecules contained in the Brotzu Lotion can't penetrate the skin by themselves (minoxidil can do in a moderate way). The strategy is to carry the DGLA with liposomes. But, you may say, there already are marketed liposomed Minoxidils like Nanoxidil and even in a better method: the "nanosomes", and, even if we have slightly better results, they are not enough to even be famous or to substitute the regular minoxidil. We have to remember, in this, the peculiarities of the DGLA common to all the other members of the evolutionary-chain which leads to the final member, the PGE1. That's the key and the difference. Also, we do not need in theory to get the PGE1 because DGLA already has most of its properties. Brotzu's innovation, aside from the synergies between the components, is the "CATHIONIC" liposomes; being positively charged, these liposomes can fully attach to the skin, using the "negative charges attract positive charges" used also in the doctor's example in the example of the "unwrapping of the candy", when he says that we often struggle when getting rid of the wrapper, attached to our hands and fingers by that system.
@worm I tried to explain it 100 times before, the Nizoral if I remember well fights the excess of sebum and has a minimal impact on 5-alfa-reductase in one of the versions marketed; it would be useful.
Finasteride and Dutasteride, I explained it well many pages ago: in synthesis, Fina inhibites the enzyme 5-alfa-reductase type 2, Duta inhibites also the type 1; they work by physically destroy the possibility to synthetize DHT from T, lowering DHT levels systemically (so causing on some people side effects), while S-Equol has the property to competitively bind to the DHT itself, making impossible for it to attach to the receptor and damage the hair bulb (because the complex S-Equol+DHT creates in fact a new molecule which can no more interact with the receptor, making impossible to cause damage to the follicle). My strongest opinion is that if we can systemically destroy the majority of DHT with fina or duta, and also use Equol to make the leftovers uneffective, we SHOULD be able to "freeze" the Androgenetic Alopecia. But inhibiting high % of DHT means theorically making more dangerous the side effects. In this, my questions are:
- What % of DHT is made unoffensive by using the prescribed dose of Brotzu Lotion?
- Is the lotion alone able to contrast the DHT or do we need the action of Fina or Duta?
- Since the theories and experimentations of the doctor seem to answer "No, fina and duta are not needed" to my last question, what results can we achieve by introducing fina or duta in a regime with the lotion only?
- If the results are better for real, how good is the (Effects)÷(Sides) evaluation, since the anti-DHT are not sides-free?
- In that evaluation, do we have the possibility that Equol goes systemic on those percentages? What happens if it goes? (I don't fully believe some of the users of the Spatolotion / fake lotion who reported the same sides of finasteride).
I personally think that everything that attacks Androgenetic Alopecia on a different side is useful. That's why on the last page I explained the theory of the uselessness of Minoxidil in a regime comprehending Brotzu lotion, go read again it @worm because from your post you didn't understand the doctor's theories about the microcirculation.
Also, even if the Minoxidil was partially understood before (we have some explanations of it in the SITRI archives, which say it helps the circulation), the majority of doctors just prescribes it because is FDA-approved and not because its mechanisms are well-known. Brotzu at ASAA conference made it so clear that many correctly said that he "discovered" the real Minoxidil effects, because, for him: it's a vasodilator, and can act ONLY on the perycite, not deeper (he repeated this so many times). DGLA in Brotzu formula acts, like PGE1, deeper, on the endothelial cells.
By myself I create an example for you: imagine you have a tube, but it's partially clogged, and you want to water your plants; this tube is made of two elastic parts; a deeper circumference made of rubber (endothelial cells) and a more superficial circumference (perycite) attached firmly to the deeper one, but they can't enlarge themselves alone, only if stimulated. The fact is: it is better to stimulate the deeper ones (DGLA or PGE1 carried by cathionic liposomes when stimulating endothelial cells) to enlarge, because you are going to expand also the superficial (perycite), and you are affecting both of them. Minoxidil stimulates only the perycite, so you are going to enlarge the external circumference, but you are making fatigue due to the fact you're not making to enlarge the deeper one by itself, you are forcing it to do so, like carrying it away.
I would ask also some other experienced user like @That Guy to help me understand better the mechanisms if I went wrong or if I seem logic. I post another time Brotzu's graphics:
View attachment 46727
I must repeat another time, even Brotzu himself in the patent experimented 5 different formulations; he also asked himself if only DGLA was effective, then tried with only it, and he didn't even achieve the stop of hairs' fall. By introducing Equol and DGLA and Carnitine on the current percentages, the initial effectiveness quantified in a 1 scale, rose to 10. In the patent is written clearly by Brotzu himself that the extraordinary effects were not due to the singular properties of the molecules (DGLA, Equol, Carnitine), but the SYNERGISTIC EFFECT of all of them at the right percentages.
And maybe that's what can interfere with the introduction of another member in a regime (fina, duta, dermaroller, RCH-01, Kelopesia... ), because we may lose the synergies that the lotion requires. Don't worry: I'll probably be the one to experiment for you Finasteride + Lotion if next week I'll be finally diagnosed with Androgenetic Alopecia and if I get a prescription for fina.
@Barbe a papa Dermarolling does not help Minoxidil to reach internal parts (endothelial cells in my previous explanation) but it helps to penetrate the skin: for example, all of the molecules contained in the Brotzu Lotion can't penetrate the skin by themselves (minoxidil can do in a moderate way). The strategy is to carry the DGLA with liposomes. But, you may say, there already are marketed liposomed Minoxidils like Nanoxidil and even in a better method: the "nanosomes", and, even if we have slightly better results, they are not enough to even be famous or to substitute the regular minoxidil. We have to remember, in this, the peculiarities of the DGLA common to all the other members of the evolutionary-chain which leads to the final member, the PGE1. That's the key and the difference. Also, we do not need in theory to get the PGE1 because DGLA already has most of its properties. Brotzu's innovation, aside from the synergies between the components, is the "CATHIONIC" liposomes; being positively charged, these liposomes can fully attach to the skin, using the "negative charges attract positive charges" used also in the doctor's example in the example of the "unwrapping of the candy", when he says that we often struggle when getting rid of the wrapper, attached to our hands and fingers by that system.
@worm I tried to explain it 100 times before, the Nizoral if I remember well fights the excess of sebum and has a minimal impact on 5-alfa-reductase in one of the versions marketed; it would be useful.
Finasteride and Dutasteride, I explained it well many pages ago: in synthesis, Fina inhibites the enzyme 5-alfa-reductase type 2, Duta inhibites also the type 1; they work by physically destroy the possibility to synthetize DHT from T, lowering DHT levels systemically (so causing on some people side effects), while S-Equol has the property to competitively bind to the DHT itself, making impossible for it to attach to the receptor and damage the hair bulb (because the complex S-Equol+DHT creates in fact a new molecule which can no more interact with the receptor, making impossible to cause damage to the follicle). My strongest opinion is that if we can systemically destroy the majority of DHT with fina or duta, and also use Equol to make the leftovers uneffective, we SHOULD be able to "freeze" the Androgenetic Alopecia. But inhibiting high % of DHT means theorically making more dangerous the side effects. In this, my questions are:
- What % of DHT is made unoffensive by using the prescribed dose of Brotzu Lotion?
- Is the lotion alone able to contrast the DHT or do we need the action of Fina or Duta?
- Since the theories and experimentations of the doctor seem to answer "No, fina and duta are not needed" to my last question, what results can we achieve by introducing fina or duta in a regime with the lotion only?
- If the results are better for real, how good is the (Effects)÷(Sides) evaluation, since the anti-DHT are not sides-free?
- In that evaluation, do we have the possibility that Equol goes systemic on those percentages? What happens if it goes? (I don't fully believe some of the users of the Spatolotion / fake lotion who reported the same sides of finasteride).
I personally think that everything that attacks Androgenetic Alopecia on a different side is useful. That's why on the last page I explained the theory of the uselessness of Minoxidil in a regime comprehending Brotzu lotion, go read again it @worm because from your post you didn't understand the doctor's theories about the microcirculation.
Also, even if the Minoxidil was partially understood before (we have some explanations of it in the SITRI archives, which say it helps the circulation), the majority of doctors just prescribes it because is FDA-approved and not because its mechanisms are well-known. Brotzu at ASAA conference made it so clear that many correctly said that he "discovered" the real Minoxidil effects, because, for him: it's a vasodilator, and can act ONLY on the perycite, not deeper (he repeated this so many times). DGLA in Brotzu formula acts, like PGE1, deeper, on the endothelial cells.
By myself I create an example for you: imagine you have a tube, but it's partially clogged, and you want to water your plants; this tube is made of two elastic parts; a deeper circumference made of rubber (endothelial cells) and a more superficial circumference (perycite) attached firmly to the deeper one, but they can't enlarge themselves alone, only if stimulated. The fact is: it is better to stimulate the deeper ones (DGLA or PGE1 carried by cathionic liposomes when stimulating endothelial cells) to enlarge, because you are going to expand also the superficial (perycite), and you are affecting both of them. Minoxidil stimulates only the perycite, so you are going to enlarge the external circumference, but you are making fatigue due to the fact you're not making to enlarge the deeper one by itself, you are forcing it to do so, like carrying it away.
I would ask also some other experienced user like @That Guy to help me understand better the mechanisms if I went wrong or if I seem logic. I post another time Brotzu's graphics:
View attachment 46727
I must repeat another time, even Brotzu himself in the patent experimented 5 different formulations; he also asked himself if only DGLA was effective, then tried with only it, and he didn't even achieve the stop of hairs' fall. By introducing Equol and DGLA and Carnitine on the current percentages, the initial effectiveness quantified in a 1 scale, rose to 10. In the patent is written clearly by Brotzu himself that the extraordinary effects were not due to the singular properties of the molecules (DGLA, Equol, Carnitine), but the SYNERGISTIC EFFECT of all of them at the right percentages.
And maybe that's what can interfere with the introduction of another member in a regime (fina, duta, dermaroller, RCH-01, Kelopesia... ), because we may lose the synergies that the lotion requires. Don't worry: I'll probably be the one to experiment for you Finasteride + Lotion if next week I'll be finally diagnosed with Androgenetic Alopecia and if I get a prescription for fina.
I resonate a lot with the 'rooted' part. I feel like I can pick all the hairs off my head because theyre not rooted. I cant comb it without the comb filling up with hair. What does spironolactone do and does it have any side effects? Do you think its the Minoxidil causing the regrowth or the Spir?
Also, how are you finding the application of it? In the short time I used it, it was such an effort to get up to apply it. You've been using it for a while now, how are you finding the overall experience?
I don't think dermarolling is to help penetration.
It helps for wouding.
@Barbe a papa Dermarolling does not help Minoxidil to reach internal parts (endothelial cells in my previous explanation) but it helps to penetrate the skin: for example, all of the molecules contained in the Brotzu Lotion can't penetrate the skin by themselves (minoxidil can do in a moderate way). The strategy is to carry the DGLA with liposomes. But, you may say, there already are marketed liposomed Minoxidils like Nanoxidil and even in a better method: the "nanosomes", and, even if we have slightly better results, they are not enough to even be famous or to substitute the regular minoxidil. We have to remember, in this, the peculiarities of the DGLA common to all the other members of the evolutionary-chain which leads to the final member, the PGE1. That's the key and the difference. Also, we do not need in theory to get the PGE1 because DGLA already has most of its properties. Brotzu's innovation, aside from the synergies between the components, is the "CATHIONIC" liposomes; being positively charged, these liposomes can fully attach to the skin, using the "negative charges attract positive charges" used also in the doctor's example in the example of the "unwrapping of the candy", when he says that we often struggle when getting rid of the wrapper, attached to our hands and fingers by that system.
@worm I tried to explain it 100 times before, the Nizoral if I remember well fights the excess of sebum and has a minimal impact on 5-alfa-reductase in one of the versions marketed; it would be useful.
Finasteride and Dutasteride, I explained it well many pages ago: in synthesis, Fina inhibites the enzyme 5-alfa-reductase type 2, Duta inhibites also the type 1; they work by physically destroy the possibility to synthetize DHT from T, lowering DHT levels systemically (so causing on some people side effects), while S-Equol has the property to competitively bind to the DHT itself, making impossible for it to attach to the receptor and damage the hair bulb (because the complex S-Equol+DHT creates in fact a new molecule which can no more interact with the receptor, making impossible to cause damage to the follicle). My strongest opinion is that if we can systemically destroy the majority of DHT with fina or duta, and also use Equol to make the leftovers uneffective, we SHOULD be able to "freeze" the Androgenetic Alopecia. But inhibiting high % of DHT means theorically making more dangerous the side effects. In this, my questions are:
- What % of DHT is made unoffensive by using the prescribed dose of Brotzu Lotion?
- Is the lotion alone able to contrast the DHT or do we need the action of Fina or Duta?
- Since the theories and experimentations of the doctor seem to answer "No, fina and duta are not needed" to my last question, what results can we achieve by introducing fina or duta in a regime with the lotion only?
- If the results are better for real, how good is the (Effects)÷(Sides) evaluation, since the anti-DHT are not sides-free?
- In that evaluation, do we have the possibility that Equol goes systemic on those percentages? What happens if it goes? (I don't fully believe some of the users of the Spatolotion / fake lotion who reported the same sides of finasteride).
I personally think that everything that attacks Androgenetic Alopecia on a different side is useful. That's why on the last page I explained the theory of the uselessness of Minoxidil in a regime comprehending Brotzu lotion, go read again it @worm because from your post you didn't understand the doctor's theories about the microcirculation.
Also, even if the Minoxidil was partially understood before (we have some explanations of it in the SITRI archives, which say it helps the circulation), the majority of doctors just prescribes it because is FDA-approved and not because its mechanisms are well-known. Brotzu at ASAA conference made it so clear that many correctly said that he "discovered" the real Minoxidil effects, because, for him: it's a vasodilator, and can act ONLY on the perycite, not deeper (he repeated this so many times). DGLA in Brotzu formula acts, like PGE1, deeper, on the endothelial cells.
By myself I create an example for you: imagine you have a tube, but it's partially clogged, and you want to water your plants; this tube is made of two elastic parts; a deeper circumference made of rubber (endothelial cells) and a more superficial circumference (perycite) attached firmly to the deeper one, but they can't enlarge themselves alone, only if stimulated. The fact is: it is better to stimulate the deeper ones (DGLA or PGE1 carried by cathionic liposomes when stimulating endothelial cells) to enlarge, because you are going to expand also the superficial (perycite), and you are affecting both of them. Minoxidil stimulates only the perycite, so you are going to enlarge the external circumference, but you are making fatigue due to the fact you're not making to enlarge the deeper one by itself, you are forcing it to do so, like carrying it away.
I would ask also some other experienced user like @That Guy to help me understand better the mechanisms if I went wrong or if I seem logic. I post another time Brotzu's graphics:
View attachment 46727
I must repeat another time, even Brotzu himself in the patent experimented 5 different formulations; he also asked himself if only DGLA was effective, then tried with only it, and he didn't even achieve the stop of hairs' fall. By introducing Equol and DGLA and Carnitine on the current percentages, the initial effectiveness quantified in a 1 scale, rose to 10. In the patent is written clearly by Brotzu himself that the extraordinary effects were not due to the singular properties of the molecules (DGLA, Equol, Carnitine), but the SYNERGISTIC EFFECT of all of them at the right percentages.
And maybe that's what can interfere with the introduction of another member in a regime (fina, duta, dermaroller, RCH-01, Kelopesia... ), because we may lose the synergies that the lotion requires. Don't worry: I'll probably be the one to experiment for you Finasteride + Lotion if next week I'll be finally diagnosed with Androgenetic Alopecia and if I get a prescription for fina.
Don't know if he directly said it works as well as finasteride, but these quotes from the patent seems to imply that it's even more effective.Did Brotzu ever actually 'write' that it works as well as finasteride/Propecia ?
andThere are many methods described for treatment and prevention of baldness through aids acting on the hair shaft, trying to make it stronger, or on the bulb, attempting to identify the reasons why it becomes atrophied to find a solution. Some positive attempts were made by employing actual drugs, such as the well known Minoxidil and Finasteride.
Clinical trials that were carried out further demonstrated a surprisingly higher efficacy of the products described herein in comparison with what is known, so as to make their use possible at concentrations markedly lower than those of already known products.
i remember he said that.Did Brotzu ever actually 'write' that it works as well as finasteride/Propecia ?