spinner2

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I'm trying a variation of magnumforce edging right now. My gains have slowed down, so I'm trying to kick everything into high gear before I resort to a deconditioning break. So far I'm taking the following drugs:
4g PABA/day
100mg 5-HTP
1g St. John's Wort
25mg Viagra

I'm taking the St. John's wort and 5-htp to mess with serotonin in order to make ejaculation harder, then I'm edging between 2.5-3.5 hours a night. In the mornings and afternoons I do about 1 hour of light-medium stretching here and there.
I can already tell that this routine is pretty good for girth, but I'm really looking for length right now. My goal is to weaken the collagen cross-linkage to the point that stretching the septum becomes easier. I think all the PGE-1 released during erection should help some, but it's just a stab in the dark. I'm taking the PABA for this goal as well.

What other drugs can people reccommend to help me in my goal of breaking down the septum and making stretching easier. I've considered DMSO as Stagestop posted about before. I'm also thinking about hanging instead of stretching, but I recently had a slight injury so I have to wait a bit longer first.
 
You can try looking into Relaxin... Human Relaxin is pretty difficult to get but Porcine Relaxin is OTC and relatively cheap. I know of a few guys taking this to help augment their Penis Enlargement efforts.

Relaxin is a peptide hormone that was first described in 1926 and is produced by the corpus luteum of the ovary, the breast and, during pregnancy, also by the placenta, chorion, and decidua. In the male, relaxin is produced in the testes.

Structurally, relaxin is a heterodimer of two peptide chains of 24 and 29 amino acids that are linked by disulfide bridges and it appears related to insulin. Relaxin is produced from its prohormone, “pro-relaxin”, by splitting off one additional peptide chain. Different forms of relaxin have been described, relaxin 1,2, and 3.

In women relaxin levels rise after ovulation as a result of its production by the corpus luteum. In the absence of pregnancy its level declines at menstruation. During the first trimester of pregnancy levels rise and additional relaxin is produced by the decidua.

In animals relaxin widens the pubic bone and facilitates labor, it also softens the cervix (cervical ripening), and relaxes the uterine musculature. Thus, for a long time, relaxin was looked at as a pregnancy hormone. However, its significance may reach much further. Relaxin affects collagen metabolism, inhibiting collagen synthesis and enhancing its breakdown by increasing matrix metalloproteinases. It also enhances angiogenesis and is a potent renal vasodilator.

Relaxin interacts with the relaxin receptor LGR7 and 8 which belong to the G-protein-coupled receptor superfamily. They contain a heptahelical transmembrane domain and a large glycosylated ectodomain, distantly related to the receptors for the glycoproteohormones, such as the LH-receptor or FSH-receptor. Relaxin receptors have been found in the heart, smooth muscle, the connective tissue, and central and autonomous nervous system.

Relaxin's role or necessity in human pregnancy remains under investigation, as in humans its peak is reached during the first trimester, not toward the end of pregnancy. Specific disorders related to relaxin have not been described, yet it has been suggested that it could be linked to scleroderma and to fibromyalgia.
 
Yeah, I'm somewhat weary of relaxin as well. If I could make the effect localized it wouldn't bother me. Unfortunately I don't have enough money($80/month) at this point anyways, so it's a moot point. This summer I'll try out the porcilin relaxine from iherb.

I can say that my tunica feels more elastic than usual, though. Hopefully I can squeeze some extra gains out of this.
 
goldmember said:
I'm weary about the efficacy of taking peptide hormones orally.
I agree... virtually all hormone/peptides will be quickly broken down in the digestive tract. I just threw that bit of info as i know of people trying it.

As an alternative... one could possible crush the pills and mix it with DMSO or some other transdermal cocktail and apply it topically. Just a thought...
 
sikdogg said:
I agree... virtually all hormone/peptides will be quickly broken down in the digestive tract. I just threw that bit of info as i know of people trying it.

As an alternative... one could possible crush the pills and mix it with DMSO or some other transdermal cocktail and apply it topically. Just a thought...
Good idea. I'm beginning to question DMSO's worth as a transdermal given its relative polarity. Benzyl alcohol seems like a better option as a trandermal solvent. It has an alcohol on it so it can dissolve slightly polar compounds (such as a peptide) and a non-polar end.
 
goldmember said:
also, make sure you take vitamin D with all that PABA.

The info you provide is always great... Would you please explain why someone would need to take Vitamin D while taking PABA?
 
busyrand said:
The info you provide is always great... Would you please explain why someone would need to take Vitamin D while taking PABA?
Thanks for the compliment. PABA inhibits vitamin D synthesis in the body, and 4 grams is way more PABA than even mega-multivitamins provide.
 
Jason1 said:
What exactly is magnumforce edging?
The idea (modified by a guy named Magnumforce) that extended periods of keeping an erection just shy of ejaculating can produce gains. Not really sure what Magnumforce's stipulations were, but I just gave you the basic idea behind the practice of edging.
 
I'd like to say a few things.

1-It wasn't as easy to block ejaculation as I had hoped. It may have been a little easier than normal, but nothing significant. Keep in mind I left out prozac.

2-If I went 3 hours or longer I got incredible pain in my balls. I never had this with normal edging.
 
Hello Spinner,

The mix that you are using is a bit short on 5 HTP if you want to use Serotonin as the inhibitor.

Serotonin shortage is responsible for a number of conditions and diseases, and in a good number of them, the role of Serotonin is not recognized by mainstream medicine. But it works nevertheless.

An example would be for people with Irritable Bowel Syndrome (IBS). IBS is kind of a catch all diagnosis, and is usually given when there is nothing noticeably wrong, but you still are sick. The symptoms, such as diarrhea/constipation, pain, vomiting, poor sleep, poor mood, are all caused by a shortage of Serotonin. Correcting it for people with the more severe cases usually requires 200mg of 5 HTP.

Cortisol, (the stress hormone) will interfere with the production of 5 HTP in the liver by reducing the availability of the hydroxyl donor used in the hydroxylation of Tryptophan. This causes a drop in Serotonin, and that combination is often the root cause of colitis, and a contributor to the ill effects of Chron's disease.

5 HTP is converted to Serotonin with one enzyme action and that enzyme is "non saturated" which means that there is quite a bit more of it available than is necessary. The regulation of Serotonin production is done at the first enzyme action in the liver. So, when you add 5 HTP, you can put a lot more Serotonin (relatively speaking) in your system than you would otherwise have. Conversion of 5 HTP to Serotonin by supplementation stops when you have exhausted the supply of the enzyme used in that conversion.

Since people that need Serotonin for IBS, and Colitis need around 200 mg, you can see that to get to the point of exhausting the available enzymes will take a lot more than 100 mg.

If you want to max out on 5 HTP I am guessing that it will take around 300 mg a day.

There is a small down side to this that you should be aware of. When you push your Serotonin levels to as high as they can go, you will also cause a "upregulation/downregulation" effect to happen. This is the body's way of dealing with an imbalance, and it will make your receptors less receptive. Then, when you stop all of a sudden, it takes a while to become more responsive. You may feel a bit depressed, have an upset stomach for a week or so, have loose stools, and sleep can be affected for a short time.

One alternative would be to cycle, but I have no idea how long you can cycle without triggering the downregulation that a surplus will trigger.

Good luck with the edging.

Stage
 
Thanks, for the response Stagestop. I've read everything you've posted on here and thundersplace, and I value your input highly. When I give this another go after a decon break I'll give it a shot with 300mg. In the meantime I'm gonna keep my grades up in college so I'll have enough money to visit Dr. Adams in a few years.
 
Hi Spinner,

Thanks for the compliment. I am glad to do what I can.

Do keep those grades up. That is by far and away the best use of your time.

Best of luck!

Stage
 
spinner2 said:
In the meantime I'm gonna keep my grades up in college so I'll have enough money to visit Dr. Adams in a few years.
You and I both.
 
Ok...
Point One, Relaxin, inhibits collagen synthesis and promotes break down.
lets think about that, it's going to stop new collagen(more penis) forming and promote collagen breakdown(less penis).
With collagen manipulation, i'm faily sure collagen link weakening is the way to go not collagen breakdown, Stagestop?
Point Two
5HTP is hypothesized to be metabolized and excreted before reaching the brain. Better off going with a SSRI if you want to stop ejaculating brother.
Just commentary, not solid advise, 5HTP may have benefit and so may Relaxin. Stagestop?
Oh Btw Stage this Rason from �other forum�.
Cheers,
Rason.
 
smileyguy said:
Ok...
Point One, Relaxin, inhibits collagen synthesis and promotes break down.
lets think about that, it's going to stop new collagen(more penis) forming and promote collagen breakdown(less penis).
With collagen manipulation, i'm faily sure collagen link weakening is the way to go not collagen breakdown, Stagestop?
Point Two
5HTP is hypothesized to be metabolized and excreted before reaching the brain. Better off going with a SSRI if you want to stop ejaculating brother.
Just commentary, not solid advise, 5HTP may have benefit and so may Relaxin. Stagestop?
Oh Btw Stage this Rason from �other forum�.
Cheers,
Rason.

Hi Rason,

I think that you may not have the right idea on all of this. So let's go over what the goals are.

The tunica is a collagen sheath that is the strength and support member for the penile tissues. It is kind of analogous to the cords that give support to the a tire.

The collagen in the penis is under constant removal and replacement, as is almost all of our body.

The strength of the tunica is mostly attributable to the weaving of the various fibers together. I use that analogy of a sheet to demonstrate. The individual fibers that make up a sheet do not have much strength at all. If you were to pick one out of the sheet, it would weave back and forth in the wind. However, when woven together, there is directional stability so that even with a strong pull on one side or the other, the combined strength of the sheet resists the force applied.

In the penis, the fact that in an flacid state your penis is free to move easily is because there is no force against the tunica. However, when you are erect, you fill the penis with blood and that puts pressure on the tunica. That it resists that pressure is necessary to allow an erection. If it did not, your penis would swell like a balloon.

The chemical side of Penis Enlargement is most concerned with using whatever chemical means possible to cause the fibers of the penis to relax. Then stretching will put the fibers under mechanical tension, and hopefully, as the force that caused some of the strands of collagen to relax goes away, it will assume the new shape. This is called "tissue remodeling"

To go back to the sheet analogy. Imagine that you start to pull on individual fibers in the middle of the sheet. The more that you do that, the more susceptible that sheet is to being movable in the direction that you have pulled on the fibers. If you do that long enough, your formerly rectangular sheet can now assume different dimensions. That is the reason for trying relaxin. It seems to work rather well in vagina's and that is good as we all went down one once in our life. Hopefully it will do the same with a penis.

As to 5 HTP, I don't know where your got your hypothesis, but it is wrong. If 5 HTP was excreted before reaching the brain, we would all be dead long ago. The process of making 5 HTP into Serotonin is an enzyme reaction called "decarboxylation" (removing a carboxyl from the molecule) This is done with an enzyme (imagine "chemical scissors") The place of the reaction is mostly in the receptor, above the vesicle. And yes, you have them in your brain.

More to the point, and this is a big one for those that use antidepressants, is the comparison of what a SSRI is, and how it compares to taking 5 HTP.

And SSRI is an abbreviation for SELECTIVE SEROTONIN REUPTAKE INHIBITOR. The Selective part means that it works on the 5ht bc receptor, which works with mood in the brain. Serotonin is what the receptor uses as the neurotransmitter. Reuptake is a method of getting rid of Serotonin NOT MAKING IT. Inhibitor is what the function of the drug is.

OK, what I wrote assumes that the reader know a good deal about neurology, so let me see if I can make it easier.

Serotonin is a NEUROTRANSMITTER. We are not "hard wired" like a light bulb in your house is. In the house, you turn on the switch, and the light bulb comes on. In our body, the nerve sends a message to the brain, but it has to go through a receptor first. When the message gets to one side of the SYNAPSE (the space between one side of the receptor and the other) the body needs a NEUROTRANSMITTER, to transmit the signal across the synapse. Imagine that the neurotransmitter is a wheelbarrow, that moves electrons from one side to the other,and then puts them back into a wire (nerve) for transmission to the brain.

The critical thing in this reaction is the AMOUNT of the neurotransmitter AT THE SYNAPSE. If you do not have very many "wheelbarrows" (neurotransmitters and in this case the neurotransmitter is Serotonin) at the synapse, the message that the nerve was carrying is lost and the brain does not receive it.

Alternatively, having too much of the neurotransmitter is a problem as well. The body makes Serotonin continuously, and therefore it has to get rid of Serotonin continuously to have balance at the Synapse.

There are four ways that the body gets rid of Serotonin. They are first. DIFFUSION. What happens in this case is the Serotonin is in the synapse, and simply floats away. This reaction cannot be controlled.

The next way is with GLIAL CELLS. These cells are outside of the synapse and basically eat the Serotonin, thereby converting it into a different, non reactive product.

The next way is with MAO, or Monoamine Oxydase. This is an enzyme that has its own vesicle in the syapse, and when it connects with Serotonin (and any other mono amine) it converts it into another non reactive molecule.

The last way is with REUPTAKE. To understand Reuptake, you have to imagine a bellows that you would use to blow air into your fireplace. As you squeeze that bellows a big stream of air goes into the fireplace to help get a fire going. When you want more air, you open the bellows and air is sucked into the bellows.

In our use, when Serotonin is made, the enzyme reaction takes place above the vesicle (bellows) and is stored in the vesicle. When you need more Serotonin, the vesicle is squeezed, and out comes the Serotonin into the Synaptic cleft (where the wheelbarrows work to move the bits of electricity).

When there is no more messages to move, the vesicle opens causing the Serotonin to be sucked back into the vesicle. THIS IS "REUPTAKE."

When you take a SSRI, you are inhibiting the vesicle in its ability to suck back the Serotonin into the vesicle. This leave (hopefully) more Serotonin in the Synaptic cleft. And if the doctor thinks that you are low in Serotonin, hopefully this will allow you to have more Serotonin where it is needed.

So, what is wrong with this? Easy. NO SSRI MAKES ONE OUNCE OF SEROTONIN. The best that it can do is hopefully keep some Serotonin in the synaptic cleft. So what the doctor is trying to so is to keep more of your wheelbarrows where the work takes place. BUT, HE IS NOT MAKING ONE MORE WHEELBARROW AT ALL. That is the problem. ONLY 5 HTP can make more Serotonin. Nothing else can do it.

This is why SSRI's can do a little bit of good, but they don't do much of all if you have a serious Serotonin shortage.

Further, since SSRI's are SELECTIVE to the 5 ht b6 receptor and none of the other 30 Serotonin receptors, it does nothing for those reactions.

For someone wanting to raise Serotonin levels, they need to know that there are two conversion processes in the conversion of Tryptophan into Serotonin. They are "hydroxylation" (adding a hydroxyl to the molecule) and decarboxylation (removing a carboxyl from the molecule). Hyrdoxylation is the much more difficult reaction, and the one that regulations Serotonin production. Decarboxylation is a "non saturated enzyme reaction" in the Serotonin process. Basically that means that the liver is the regulator of Serotonin production, and that if you supplement with 5 HTP, you WILL increase Serotonin in your body, up to the limits imposed by the availability of the enzyme that causes decarobxylation.

So the bottom line is that the use of Relaxin on the penis is only theoretical as we have no human relaxin to use. The use of porcine relaxin may work, but there are a number of problems that have to be overcome to get it to do what is desired. Certainly if it can be obtained in a topical formulation we would be much happier.

And for those that want to increase their bodies Serotonin levels, 5HTP is the ONLY way that it can be done. SSRI's will only raise the serotonin levels at the synapse on the 5ht b6 receptors, and those work with the mood of the person.

Hope that helps.

Best of luck,

Stage
 
sikdogg said:
I agree... virtually all hormone/peptides will be quickly broken down in the digestive tract. I just threw that bit of info as i know of people trying it.

As an alternative... one could possible crush the pills and mix it with DMSO or some other transdermal cocktail and apply it topically. Just a thought...
After thinking about this one, the only way to take a peptide hormone is by injection. I doubt a molecule this large would be able to work transdermally. Even an oligopeptide would be questionable...
 
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