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Mucuna pruriens, aka velvet beans, is a plant that contains L-dopa. L-dopa can pass the blood-brain barrier, and is metabolized in the brain into dopamine. Dopamine is an excitatory neurotransmitter that, among many other functions, is a good deal responsible for sexual excitement. But not all velvet beans are the same. In India, velvet beans are grown as animal feed, and those cultivars are void of L-dopa as L-dopa would impede weight gain. Tongkatali.org's mucuna pruriens extract is made from wild Thai mucuna pruriens, naturally high in L-dopa. Be careful of cheating products, even on Amazon, which write a high L-dopa content on labels when in fact these products contain almost no L-dopa. If you want to test: the L-dopa of mucuna pruriens would cause nausea at dosages beyond a few grams.



Good sex like crazy


By Serge Kreutz


For sexual enhancement, nothing beats a stack based on mucuna pruriens, the velvet bean.

Mucuna pruriens by itself already has a great reputation for heightening libido. The plant naturally contains L-dopa, which the brain converts into dopamine.

Mucuna pruriens can be used, and is used in the treatment of Parkinson’s disease, a chronic illness characterized by a lack of dopamine in the brain, causing movement impairments.

That is the one side of dopamine. The other side of dopamine is that it plays an important role in human sexual desire.

This is well documented. Extreme sexual motivation, even in men who have had zero sex life for two decades, is a known potential side effect of Parkinson’s medications. If you ever encounter a sex-crazed old man, a man whose sexual agitation warrants psychiatric attention, it's going to be a Parkinson’s patient on L-dopa.

Article continues below printscreens

Parkinson’s sufferers usually are put on synthetic L-dopa, combined with carbidopa to counteract the nausea that can accompany L-dopa. The dosages of synthetic L-dopa for Parkinson’s are up to 5 gram per day.

The effect of consuming 1 gram of synthetic L-dopa or 20 grams of mucuna pruriens containing 5 percent (1 gram) of L-dopa will be somehow different. This is the case because of numerous cofactors in mucuna pruriens.

Cofactors make a difference. Take for example opium. Opium contains about 12 percent morphine. But the effects of opium are much wider than the effects of the isolated morphine. While the physiological impact may be about the same, opium also makes for pleasant dreams.

Correspondingly, the 1 gram of L-dopa in 20 grams of mucuna pruriens has a more pronounced effect on libido than 1 gram of synthetic L-dopa. And more cofactors can be added by stacking other sexual enhancement herbals on top of the mucuna pruriens extract.

First stacking choice would be hormonal enhancers like tongkat ali and butea superba. Another hormonal libido support could be added in the form of fenugreek. And then there are vascular agents like kaempferia parviflora (krachai dam) and boesenbergia rotunda (ton krachai) which translate libido into erections.

A great advantage of stacking regimens is that one can consume a large amount of nutrients that support different parameters of sexual function, and maximise effects while minimizing side effects. Side effects typically are an occurrence of a large dose of just one sexual enhancer, or, for that matter, any medicine.

Users of mucuna pruriens, or those interested in supplementing mucuna beans for brain health and sexual parameters, should be aware of the fact that great differences exist as to the quality of different mucuna pruriens strains and products.

The L-dopa content of mucuna pruriens samples investigated for the treatment of Parkinson’s varied from about 0.5 percent to more than 6 percent. See this study published by the US Institutes of Health:

But that's not yet it. In India, mucuna pruriens is planted as a feedstock, and these dirtcheap mucuna pruriens cultivars are practically void of L-dopa, with contents in the range of 0.1 percent.

What we sell is a Thai mucuna pruriens strain which is a direct descendant from wild mucuna pruriens, and in worldwide comparison, that's the strain with the highest content of L-dopa and libido-supporting catalytic cofactors.

Any mucuna pruriens that you can buy in American or European healthfood stores is most probably worthless for sexual enhancement. That is something anybody can easily test by oneself.

Dopaminergics in higher dosages, including high-dosage mucuna pruriens, have an emetic effect. In plain speak: they can induce nausea and vomiting.

This is so certain an effect that dopaminergics are used as emetics (drugs to induce vomiting) by physicians and vets.

For somebody not accustomed to mucuna pruriens, a large dosage of the genuine stuff will cause nausea. If it doesn't, then a lower dosage won't augment libido either.


Continue to search for the best sex ever: Sexual enhancement with a tongkat ali stack and meaning in life



Better check what you bought - compare to our sample


If you previously bought tongkat ali extract, and it was sold by a scammer pretending it to be 1:200, you can get a free sample of our genuine Indonesian 1:200 tongkat ali extract and compare the two.

Tongkat ali 1:200 extract was developed by us more than 20 years ago. It's not that anybody could go and do a tongkat ali 1:200 extract as easily as boiling a kilo of potatoes. The process to get a batch of tongkat ali 1:200 extract takes a full week of milling, heating, passing through pressure and vacuum chambers, and filtering.

95 percent of all tongkat ali 1:200 extracts on the web, or maybe even 99 percent, are just simply fake. Some dishonest characters, mostly in Singapore, obtain a dubious powder from China, then print 1:200 on the label, and make 50 dollars profit on a price of 60.

We have genuine resellers. They buy for several hundreds of thousands US dollars from us every year. Of course, they get a good price from us. They also sell 100 caps for around 60, but make a much smaller profit than the fakers.

You can see more details on our main website, Tongkatali Org.

It's not that Sumatra Pasak Bumi would be expensive. Indonesian 1:200 extract is expensive because it is expensive to produce. Our Thai products are much cheaper. Thailand is an easier country. So, if you can't afford genuine Indonesian 1:200 extract, Thai relationships enhancement is also good, and less costly. But avoid throwing money to a Singaporean flat and gym operation that calls itself a lab. You either feel nothing, or you feel weird because they add bootleg prescription medicines. Don't be misled by slick web design. With their outrageous profits, they can afford web design.


Tongkatali.org - Engineering happiness


By Serge Kreutz


I have a great interest in the modulation of the human mind and body, with the aim of achieving a higher level of happiness. It’s about engineering happiness through pharmacological means.

We are aware of street drugs used to this end, but they are all inadequate. Cocaine and amphetamines produce happiness through the crude enhancement of dopaminergic brain activity, but they do a lot of long-term damage to the functions they momentarily enhance.

Opiates make happy through sedation, but their effects wear off, and inactivity and dullness accompany the happiness they induce.

Ecstasy surely creates a beautiful sense of harmony, but here, too, the effects wear off, and a desired state of happiness becomes harder to achieve when sober after having relied on ecstasy.

Humans are inadequately predisposed to be happy, simply because a good dose of unhappiness is superior in the Darwinian fight for survival. Natural selection of the fittest sides with those who try harder, and in order to be highly success-oriented, one has to be discontent with one’s status quo.

Until genetic engineering will take care of the current shortcomings of humans in their quest to be universally happy, pharmacological intervention is the only realistic alternative. But, to emphasize it again, the pharmacology of cocaine, opiates, ecstasy, amphetamines and the like is too crude to be a sensible solution.

All humans are equipped by nature with a delicate system to experience happiness: sexuality. Pharmacological mediators of happiness should act to enhance relationships experience. This is the great potential of tongkat ali. By tilting the hormonal balance towards testosterone, tongkat ali creates windows for the best relationships ever, regardless of age. Due to the workings of the hormonal system, the effect of tongkat ali may not be as predictable as that of sildenafil citrate. But tongkat ali can account for the most memorable relationships episodes in a lifetime.

Desexualizing pharmacological agents, such as some antidepressants, do not point into the right direction.



Tongkatali.org's Depressed for a reason


By Serge Kreutz


Optimal relationships experience, followed by a comfortable death, is the only sensible concept in life.

We do not live to please a specific god, or for the sake of our children, and there is no meaning in an, however identified, common good. The only perspective that makes philosophical sense is that we live to please ourselves, and orgasms are the ultimate pleasure.

There are a good number of aspects that play a role in orgasms, and their quality. Orgasms aren’t alike. Men can produce ejaculate as the result of laboring their relationships organs, almost unaccompanied by relationships fantasies or relationships pleasure. They also can ejaculate almost involuntarily, purely as a result of psychological, not physiological stimulation. There is no doubt that the second kind of orgasms provides a much higher level of satisfaction.

In accordance with the materialistic principles of science, psychological aspects have their physiological equivalents. Jealousy, for example, is an emotion, but it also is a biochemical process. Nevertheless, I sort jealousy under psychological aspects because it has a mental expression. The health of my cardiovascular system, a precondition for good erections, does not have a primary mental expression… but nevertheless greatly influences the quality of my orgasms.

I am sure that the solution to the problem of loss of excitement in orgasms will first be pharmacological, then surgical, and finally genetical. It will not be psychological, and even less philosophical. When overcoming the loss of excitement in orgasms will be as easy as stopping by a pharmacy, there will no longer be any need for treatises as the one you are currently reading. Such essays will be as unnecessary as sessions with a psychotherapist for the purpose of overcoming depression. Go and buy yourself some Prozac.

The loss of the orgasm quality is physiological. Our brains and testes no longer produce the right mix of hormones, neurotransmitters, prostaglandins, peptides, and whatever else is of relevance to afford us the ultimate bliss.

Medical science so far does not concern itself much with orgasm quality, but there already are prescription pharmaceuticals, dopaminergics, that somehow improve orgasms. These drugs are used in the treatment of Parkinson’s disease. However, in people not afflicted with Parkinson’s, they tend to cause nausea. Worst in this respect is lisuride.

While the nausea may be bearable for some people more than for others, these Parkinson’s medications are prescription drugs all the same for everyone. Some of them are also extremely expensive.

Butea superba, a Thai herbal, is probably the only pharmacological agent that improves orgasm quality without side effects.

Butea superba has a unique double mode of action by enhancing testosterone synthesis and inhibiting phosphodiesterase at the same time.

Phosphodiesterase inhibition is the route of action of prescription drugs for erectile dysfunction.

But butea superba doesn’t feel like these prescription drugs. Butea superba facilitates erections more naturally because they happen in tandem with heightened libido.

And then, more specifically, butea superba extends the time frame of the pre-orgasmic plateau.

For most men, the pre-orgasmic plateau is just 2 or 3 seconds, and younger men often don’t know how to enjoy it.

The pre-orgasmic plateau is the moment when male ejaculation becomes certain, regardless of whether penetrative thrusting is continued or not. Physiologically, it is the time when sperm and the fluids of the seminal vesicles accumulate at the base of the urethra for expulsion.

This phase of the orgasm is already highly pleasurable, even though younger men are hardly aware of it. Older men more often can enjoy this phase, and they stop penetration, and let it come all by itself.

Butea superba can extend this plateau phase, and give it a duration of 5 to 10 seconds, which feels like an eternity of the most exquisite pleasure.

Because the directors of porn movies usually demand that ejaculation happens in front of the lens, rather than inside the female body, studs often supplement with butea superba. Not only does butea superba help them to stay focused on their assignment of the day in spite of unromantic onlookers; butea superba also allows them more time to withdraw from the woman and position their vital organ before the camera before shooting their loads.



Mucuna pruriens in Parkinson’s disease: a double blind clinical and pharmacological study

R Katzenschlager, A Evans, A Manson, P N Patsalos, N Ratnaraj, H Watt, L Timmermann, R Van der Giessen, A J Lees

Abstract

Background: The seed powder of the leguminous plant, Mucuna pruriens has long been used in traditional Ayurvedic Indian medicine for diseases including parkinsonism. We have assessed the clinical effects and levodopa (L-dopa) pharmacokinetics following two different doses of mucuna preparation and compared them with standard L-dopa/carbidopa (LD/CD).

Methods: Eight Parkinson’s disease patients with a short duration L-dopa response and on period dyskinesias completed a randomised, controlled, double blind crossover trial. Patients were challenged with single doses of 200/50 mg LD/CD, and 15 and 30 g of mucuna preparation in randomised order at weekly intervals. L-Dopa pharmacokinetics were determined, and Unified Parkinson’s Disease Rating Scale and tapping speed were obtained at baseline and repeatedly during the 4 h following drug ingestion. Dyskinesias were assessed using modified AIMS and Goetz scales.

Results: Compared with standard LD/CD, the 30 g mucuna preparation led to a considerably faster onset of effect (34.6 v 68.5 min; p = 0.021), reflected in shorter latencies to peak L-dopa plasma concentrations. Mean on time was 21.9% (37 min) longer with 30 g mucuna than with LD/CD (p = 0.021); peak L-dopa plasma concentrations were 110% higher and the area under the plasma concentration v time curve (area under curve) was 165.3% larger (p = 0.012). No significant differences in dyskinesias or tolerability occurred.

Conclusions: The rapid onset of action and longer on time without concomitant increase in dyskinesias on mucuna seed powder formulation suggest that this natural source of L-dopa might possess advantages over conventional L-dopa preparations in the long term management of PD. Assessment of long term efficacy and tolerability in a randomised, controlled study is warranted.

https://jnnp.bmj.com/content/75/12/1672.short




PT Sumatra Pasak Bumi
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Petisah Tengah, Medan Petisah,
Medan City, North Sumatra 20236,
Indonesia
Tel: +62-813 800 800 20


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