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  #1  
Old 23-12-2008, 07:54
shatteredparadigm shatteredparadigm is offline
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Best Choline Source?

It seems nootropics should be stacked with Choline. Just wondering on the opinions out there as to which type is best. Is Alpha GPC worth the cash?
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Old 23-12-2008, 08:39
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Re: Best Choline Source?

Alpha-GPC is indeed worth the cash. Especially if you buy it as a bulk powder and cap it yourself, as it is significantly cheaper that way.

Choline-citrate is almost as effective, and much less expensive if finances are tight. It must be taken in higher doses, but its bioavailability is still much greater than lecithin or other more common choline sources.
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Old 07-01-2009, 02:06
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Re: Best Choline Source?

Quote:
Originally Posted by Shampoo View Post
Alpha-GPC is indeed worth the cash. Especially if you buy it as a bulk powder and cap it yourself, as it is significantly cheaper that way.

Choline-citrate is almost as effective, and much less expensive if finances are tight. It must be taken in higher doses, but its bioavailability is still much greater than lecithin or other more common choline sources.
I read that Lecithin is a much better source of choline than the choline salts (bitartrate, citrate, chloride) & makes choline more bioavailable than compared with the salts (265% w/ lecithin)

Source: Sports Nutrition: vitamins & trace elements by Judy Anne driskell ...http://books.google.com/books?id=iv8...um=4&ct=result

Through what source did you determine choline-citrate as having a greater bioavailability than choline found in lecithin?

Last edited by Herbal Healer 019; 07-01-2009 at 03:26.
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Old 15-01-2009, 02:57
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Re: Best Choline Source?

I buy lecithin from a reliable vitamin company here in Canada, and it is inexpensive. I see no need to pay alot of money for choline or lecithin.

derek30 added 20 Minutes and 54 Seconds later...

Quote:
Originally Posted by shatteredparadigm View Post
It seems nootropics should be stacked with Choline. Just wondering on the opinions out there as to which type is best. Is Alpha GPC worth the cash?
Try all of them and see what works for you. Everyone is different, and if one source of choline works for someone, it might not work the same for you.

Last edited by derek30; 15-01-2009 at 02:57. Reason: Automerged Doublepost
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Old 24-12-2008, 12:50
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Re: Best Choline Source?

one should avoid DMAE though
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Old 25-12-2008, 22:35
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Re: Best Choline Source?

Quote:
Originally Posted by outriderx View Post
one should avoid DMAE though
There have been some studies that show that DMAE shortens life spans in certain animals such as Quails - http://www.ncbi.nlm.nih.gov/sites/en...t=AbstractPlus

Quote:
Effects of dimethylaminoethanol upon life-span and behavior of aged Japanese quail.

The lysosome hypothesis of aging predicts that membrane stabilizers will extend life-span. Stabilizers containing the dimethylaminoethanol moiety (DMAE) have been reported to extend the life-span of drosophila and mice. We tested the prediction in Japanese quail (N = 15) by administering DMAE bitartrate (18.4 mg/kg/day) in the drinking water for 69 weeks, starting at 195 weeks of age. A matched control group (N = 14) received tartaric acid (4.0 mg/kg/day) in the water. Contrary to the prediction, the DMAE-treated group has a shorter life-span after start of treatment (49 weeks) than the controls (69 weeks). No significant differences between the groups were observed in body weight or daily fluid intake. Three behavioral studies were carried out on survivors at 243-249 weeks of age, namely; activity response to light-flash; sexual mounting response to a female quail; and classical conditioning of the heart rate. Aged quail differed from young-adults in changes in motor activity in response to light flashes. Aged quail appeared less responsive initially to reinforced conditioning trials and demonstrated extinction when light flash was not followed by electric shock. There were no detectable differences in latency to mount or in basal heart rate, either as a function of age or as a function of DMAE treatment.
-----------------------------------------------------------------------

DMAE ineffective for increasing levels of acetylcholine in the brain

Quote:
Dimethylaminoethanol (deanol) metabolism in rat brain and its effect on acetylcholine synthesis.
Quote:

Specific methods utilizing combined gas chromatography mass spectrometry were used to measure the metabolism of [2H6] deanol and its effects on acetylcholine concentration in vitro and in vivo. In vitro [2H6]deanol was rapidly taken up by rat brain synaptosomes, but was neither methylated nor acetylated. [2H6]Deanol was a weak competitive inhibitor of the high affinity transport of [2H4]choline, thus reducing the synthesis of [2H4]acetylcholine. In vivo [2H6]deanol was present in the brain after i.p. or p.o. administration, but was not methylated or acetylated. Treatment of rats with [2H6]deanol significantly increased the concentration of choline in the plasma and brain but did not alter the concentration of acetylcholine in the brain. Treatment of rats with atropine (to stimulate acetylcholine turnover) or with hemicholinium-3 (to inhibit the high affinity transport of choline) did not reveal any effect of [2H6]deanol on acetylcholine synthesis in vivo. However, since [2H6]deanol did increase brain choline, it may prove therapeutically useful when the production of choline is reduced or when the utilization of choline for the synthesis of acetylcholine is impaired.
http://www.ncbi.nlm.nih.gov/sites/en...t=AbstractPlus

Quote:
Is 2-dimethylaminoethanol (deanol) indeed a precursor of brain acetylcholine? A gas chromatographic evaluation.

Acute administration of deanol-p-acetamidobenzoate (Deaner; deanol) has been reported to elevate brain choline (CH) and acetylcholine (ACh) levels. We have developed a specific and sensitive gas chromatographic assay to measure deanol levels in tissue and have applied this assay to our studies of the effect of acute deanol administration on deanol, ACh and Ch levels in rodent brains. Details of the method are described in this text. This procedure is quantitative and yields reproducible results over a wide range of deanol concentrations (0.30-200 nmol). Seven endogenous and pharmacological parameters have been studied using this procedure. In control rodent brain, liver, heart, lung and plasma, we detected no free endogenous deanol (less than 1 nmol/g). After deanol administration, we were able to detect deanol in tissue and have attempted to determine a relationship between these levels and values of ACh in the same tissue. Regardless of deanol pretreatment time (1-30 minutes) or doses (33.3-3000 mg/kg i.p.) used, we detected no increase in mouse whole brain ACh levels. Likewise, there was no detectable elevation in ACh levels in rat whole brain, cortex, striatum or hippocampus after a 15-minute pretreatment with 550 mg/kg of deanol (i.p.). The only elevation in ACh levels which we detected occurred selectively in the striatum of mice pretreated with a massive dose (900 mg/kg i.p.) of deanol for 30 minutes. This selective increase in striatal ACh levels oculd not, however, be related to levels of deanol in the striatum because there was no greater accumulation of deanol in the striatum than in other brain areas tested or in whole brain. These data do not confirm the results of other investigators who reported elevations in whole brain or striatal ACh levels after acute administration of lower doses of deanol. The data emphasize the need for further investigation into the mode of action of deanol and question its suggested role as an immediate precursor of ACh synthesis in the central nervous system.
http://www.ncbi.nlm.nih.gov/sites/en...RVAbstractPlus
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Some users have reported that DMAE has positive effects for short term use(around a week) and after that negative effects are much more apparent.

Since I am assuming you are talking about Nootropic use, you want the choline to become acetylcholine.

Quote:
Choline supplements are often taken as a form of 'smart drug' or nootropic, due to the role that the neurotransmitter acetylcholine plays in various cognition systems within the brain. Choline is a chemical precursor or "building block" needed to produce the neurotransmitter acetylcholine, and research suggests that memory, intelligence and mood are mediated at least in part by acetylcholine metabolism in the brain.
http://en.wikipedia.org/wiki/Choline

-------------------------------------------------------------------------

I found a really good post on Centrophenoxine on another board, so I will just be quoting that post.


Quote:
Quote:
is citicholine or centro preferable for some reason, since they both seem to work the same, for me?
There is a huge advantage to take centrophenoxine a.k.a. meclofenoxate over CDP-choline a.k.a. citicoline!

What is this advantage you may ask? Well, the absolutely fabulous drug centrophenoxine is an anti-lipofusin drug. You see, as your brain ages, your brain cells acquire dark, age-related deposits (junk) called lipofuscin. To keep your brain young, you want to keep your lipofuscin level low.




http://www.ncbi.nlm.nih.gov/pubmed/8979484...Pubmed_RVDocSum
Quote:
Age-related decline in multiple unit action potentials of cerebral cortex correlates with the number of lipofuscin-containing neurons.
Sharma D, Singh R.

Neurobiology Laboratory, School of Life Sciences, Jawaharlal Nehru University, New Delhi, India.

The present study examined whether there is any obvious correlation between the density of lipofuscin-containing neurons and the spontaneous neuronal action potentials (Multiple Unit Activity, MUA) in the parietal cortex of the aging rat brain. The results showed that MUA counts were decreased with age while the number of lipofuscin-containing neurons was increased. The cortex with the highest percentage of lipofuscin-containing neurons had the lowest MUA counts while the cortex with the lowest percentage of lipofuscin-containing neurons had the highest MUA counts. The inverse correlation between MUA and lipofuscin-containing neuron number was also evident when the population of the lipofuscin-containing neurons was pharmacologically altered in vivo by the administration of anti-lipofuscin drug centrophenoxine. The inverse relationship between MUA and the lipofuscin-containing neuron numbers is consistent with: (i) the correlations of MUA with age-related changes in lipid peroxidation and biochemically measured lipofuscin concentration, and (ii) the oxidative stress-induced impairments of neuronal electrophysiology.

PMID: 8979484 [PubMed - indexed for MEDLINE]
http://www.ncbi.nlm.nih.gov/pubmed/8821338...Pubmed_RVDocSum
Quote:
Brain lipofuscinolysis and ceroidolysis--to be or not to be.
Riga D, Riga S.

Institute of Neurology and Psychiatry, Bucharest, Romania.

Lipofuscin pigment (LP) accumulations and ceroid pigment (CP) storages were demonstrated by multiple consensus studies. On the contrary, fewer researches, sometimes with opposite conclusions were made on brain LP and CP decrease, dissolution and elimination. Neuroactive agents (such as Meclofenoxate, Orotic acid, Antagonic-Stress, Piracetam, L-Deprenyl, Geriforte) generate LP and CP decrease and dissolution by cytoplasm rehydration, optimization of the brain cellular recycling system activities, by neuronal, glial and capillary LP lysis and CP lysis, by neurono-glio-endothelial transfer of highly processed LP and CP, with final capillary elimination. Therefore, these nootropic drugs may become therapeutical solutions in brain aging deceleration, in CP inductive circumstances and in age-associated diseases.

PMID: 8821338 [PubMed - indexed for MEDLINE]
This doesn't just remove nasty lipofuscin from your brain, but it removes lipofuscin from your entire body. As you age, your whole body acquires these horrid cellular waste deposits!
http://www.ncbi.nlm.nih.gov/pubmed/1512044...Pubmed_RVDocSum
Quote:
Lipofuscin accumulation in ageing myocardium & its removal by meclophenoxate.
Patro N, Sharma SP, Patro IK.

Department of Zoology, Kurukshetra University.

A study was undertaken on the age-associated histochemical changes in the ventricular myocardium and the influence of meclophenoxate hydrochloride (MPH) on the age pigment lipofuscin. Sixty Wistar albino rats in three age-groups (3, 15 and 30 months old) were treated with meclophenoxate hydrochloride (100 mg/kg body wt/day, ip) for a period of 2-8 wk. Five animals each from the three age-groups served as controls. Various histochemical and micromorphometric studies were carried out on the myocardial tissue. A linear increase in the myocardial volume occupied by the pigment was observed with advancing age. As a result of meclophenoxate treatment, a gradual decrease in the myocardial volume occupied by the pigment was noted. After 4-6 wk treatment, the pigment bodies were found lodged into the capillary endothelium and the lumen, facilitating the removal of the pigment via blood stream. Histochemical and micromorphometric analyses of ventricular myocardium of albino rats have shown thus that deposition of the age-pigment, lipofuscin, can be accepted as an index of cellular ageing.

PMID: 1512044 [PubMed - indexed for MEDLINE]
I can't believe I've thus failed to mention that centrophenoxine enhances your brain anti-oxidant systems within your brain! How could I have?
http://www.ncbi.nlm.nih.gov/pubmed/6416880...Pubmed_RVDocSum
Quote:
Effect of centrophenoxine on the antioxidative enzymes in various regions of the aging rat brain.
Roy D, Pathak DN, Singh R.

This study investigated the effect (in vivo) of centrophenoxine (Helfergin) on the activity of antioxidant enzymes (glutathione peroxidase GSH-PER, glutathione reductase GSSG-RED, superoxide dismutase SOD and catalase) in subcellular fractions from the regions of the brain (cerebrum, cerebellum and brain stem) of rats aged 6, 9 and 12 months. In all age groups, normal (control) activity of GSH-PER, GSSG-RED and SOD in the three brain regions was higher in the soluble fractions than in the particulate fractions. The three regions of the brain showed different levels of the enzyme activities. Enzymes in soluble fractions (except GSSG-RED in cerebrum of rats aged 12 months) did not change with age. In particulate fractions, however, the enzymes showed age-related changes: GSH-PER decreased with age in cerebellum and brain stem, but showed an age-related increase in cerebrum, GSSG-RED and SOD increased with age in all the three brain regions. Catalase activity in all the three brain regions remained unchanged in all age groups. Six week administration of centrophenoxine (once a day in doses of 80 mg/Kg and 120 mg/Kg) to the experimental animals produced increases in the activity of SOD, GSH-PER and GSSG-RED in particulate fractions from all the three brain regions. In the soluble fractions, however, only SOD and GSH-PER activity was increased. In vitro also centrophenoxine stimulated the activity of GSH-PER. A dosage of 80 mg/Kg produced greater changes than a 120 mg/Kg dosage. The drug had no effect on the activity of catalase. Centrophenoxine also reduced lipofuscin deposits (studied both biochemically and histochemically) thus indicating that the drug inhibited lipofuscin accumulation by elevating the activity of the antioxidant enzymes. The data suggest that alleviation of senescence by centrophenoxine may, at least, partly be due to activation by it of antioxidant enzymes.

PMID: 6416880 [PubMed - indexed for MEDLINE]
There are many many many more studies on pubmed. I suggest you search for more.

You will also notice that there are no, I repeat no negative studies on centrophenoxine out there! Do your brain and body a favor and get on some centro today!


Reputation Comments on this post:
  
  Excellent post. Thanks for citing and giving sources of information
  
  significant post!
  
  Good info on DMAE and Centrophenoxine. Gave me some damn good leads to follow.
  
  Useful provision of abstracts
  
  a lot of interesting info there
  
  Very well laid out examples of older and current reserach on DMAE. It does wonders for the quality of my sleep though so...

Last edited by Milk man; 25-12-2008 at 22:44.
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Old 24-12-2008, 13:00
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Re: Best Choline Source?

Why avoid dmae?

SWIM takes ~ 1g choline, 350 mg alpha gpc, 300 mg centrophenoxine and about 100 mg DMAE daily with piracetam. Seems to work though the choline does taste awful if not capped and cause some transient nausea after ingestion.
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Old 25-12-2008, 23:35
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Re: Best Choline Source?

SWIM's been using centrophenxine for 6 years now and thinks it is well worth the hassle and expense of getting. Thanks for the DMAE info - SWIM has some bulk that swim was slowly using up as part of SWIM's stack, but now maybe SWIM will eliminate it. SWIM was mainly using it as a choline donor...
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Old 27-12-2008, 03:56
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Re: Best Choline Source?

yea.. swim also read some more nasty stuff about dmae, at least compared to the other choline sources
however, he also reads of centro... being "split"/metabolized into dmae in the body. is that not correct?
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Old 27-12-2008, 09:28
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Re: Best Choline Source?

Yes, which leaves SWIM unsure about the true benefit or not of DMAE.
What is the consensus on daily dosage and frequency of centrophenoxine on those who use it ?
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Old 22-03-2009, 14:57
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Smile Re: Best Choline Source?

Quote:
Originally Posted by snapper View Post
Yes, which leaves SWIM unsure about the true benefit or not of DMAE.
Yes, it was interesting information. SWIM has used DMAE on and off for the last three years, this last year in conjunction with piracetam. No headaches even without choline supplementation, but SWIM haven't noticed any synergy between DMAE and piracetam.

One thing that makes SWIM continue using DMAE is the fact that when consuming 300-700 mg of DMAE before going to bed, sleep quality is improved and it seems the body doesn't demand as much sleep as before. Generally SWIM wakes up early which is useful since SWIM is a sucker for sleeping over important things.

SWIM has Centrophenoxine at home to, perhaps a switch to see differences is in order to evaluate. This thread is a good one.
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Old 27-12-2008, 22:08
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Re: Best Choline Source?

for swim the consensus right now would be alpha-gpc. however.. interested in cento.. as well
Quote:
Centrophenoxine (also called Meclofenoxate, and formerly sold under the brand name Lucidril) is a drug used to treat the symptoms of senile dementia and Alzheimer's Disease. It is a compound of two biochemicals: dimethylaminoethanol (DMAE) and parachlorophenoxyacetate (pCPA). DMAE is a natural substance, found especially in fish, and also produced in the human brain. pCPA is a synthetic compound that resembles a variety of plant hormones called auxins.
Like DMAE, it is a precursor to the neurotransmitter acetylcholine and may increase levels of this chemical in the CNS. It also increases cellular membrane phospholipids which is considered by some to be an important antiaging effect. It is clinically shown to improve memory, have a mentally stimulating effect, and improve general cognition.
It is also used off-label as a nootropic, often combined with a racetam drug such as piracetam. A typical nootropic dose is 250-3,000 mg taken in 1 or more doses.
Well, for SWIM DMAE just sounds too bad. He read some other threads in this forum and others and on the web generally, it is just not the best source, alpha-gpc may be cheaper, but safer and easier to dose. Especially on the long-run DMAE showed some undwanted side-effects. Centro.. sounds good, yet its strange that its this closely related to DMAE.
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Old 02-01-2009, 09:13
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Re: Best Choline Source?

Thanks for the feedback!!! This was so helpful and intellectually stimulating (no pun intended)!
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Old 04-01-2009, 07:19
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Re: Best Choline Source?

Quote:
Originally Posted by outriderx View Post
Centro.. sounds good, yet its strange that its this closely related to DMAE.
Swim has a bottle of Centro, it says it is "Neuro-enhanced DMAE"
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Old 04-01-2009, 19:24
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Re: Best Choline Source?

yeah exactly! So it seems a little strange that DMAE on the one side is actually worse than thought at first glance, on the other Centro.. is said to be pretty good.. so whats going on with that? Or does one also have to take the effects of DMAE into account when talking about Centro? Probably..
The most interesting thing is this lipofuscin-removal (or whatever these grey-brain spots are called), other than that alpha-gpc sounds better
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Old 16-03-2009, 10:27
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Re: Best Choline Source?

*Subscribed*
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Old 17-03-2009, 10:38
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Re: Best Choline Source?

So would this be nice combination to take?

Piracetam
Alpha-GPC
Choline
Modafinil
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Old 17-03-2009, 13:17
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Re: Best Choline Source?

Quote:
Originally Posted by Faktum View Post
So would this be nice combination to take?

Piracetam
Alpha-GPC
Choline
Modafinil
Alpha-GPC and Choline are both Choline sources, and thus taking them both is redundant. Cut out the choline, keep the alpha-GPC, and that is a fine stack, though taking them all at once is probably not the most effective way to go about that.
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Old 17-03-2009, 15:32
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Re: Best Choline Source?

alpha GPC is expensive and choline is cheap. SWIM combines the two to cut down on the amount of alpha GPC used. They are also different sources hence have different bioavailabilities so a combination may represent a more beneficial supplementation. SWIM combines them due to cost, however.
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Old 17-03-2009, 21:17
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Re: Best Choline Source?

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Originally Posted by snapper View Post
They are also different sources hence have different bioavailabilities so a combination may represent a more beneficial supplementation.
The first part of this statement is certainly true, Choline and Alpha-GPC do have different bioavailabilities. However, Im not sure how this would "represent a more beneficial supplementation." Could you please expand on what you mean by this? I dont mean to challenge, just to clarify.

Is there any evidence to support the concept that using multiple sources of a neurotransmitter precursor may have greater efficacy in increasing the production of that neurotransmitter than a single source? By this logic, would taking 5-HTP with a hefty dose of cheese, poultry, or Griffonia simplicifolia seeds have a greater effect on serotonin production than taking any of those elements on their own?
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Old 18-03-2009, 16:36
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Re: Best Choline Source?

I'm trying to order piracetam now, but which one should I choose?

Nootropil (Nootropyl, Generic Piracetam) or Normabrain (Cerecetam, Nootropyl, Generic Piracetam?

Also, which of the Modafinil products are the best one?

Modalert (Provigil, Modapro, Generic Modafinil) or Modapro (Modalert, Provigil, Generic Modafinil)
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Old 22-03-2009, 19:57
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Re: Best Choline Source?

Quote:
Originally Posted by Faktum View Post
I'm trying to order piracetam now, but which one should I choose?

Nootropil (Nootropyl, Generic Piracetam) or Normabrain (Cerecetam, Nootropyl, Generic Piracetam?

Also, which of the Modafinil products are the best one?

Modalert (Provigil, Modapro, Generic Modafinil) or Modapro (Modalert, Provigil, Generic Modafinil)
If you are merely listing different brand names of the same thing, there will be very little difference between them (with equivalent doses).
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Old 18-03-2009, 23:13
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Re: Best Choline Source?

Different bioavailabilities means just that- each formulation, be it a salt, natural product containing said supplement, conjugated molecules, etc. is absorbed, metabolized, broken down at a different rate, and potentially even has different receptor binding characteristics. There is not a lot of definitive information about what type of choline is best, much less best for SWIM's individual metabolism. SWIM also has a really hard time quantifying the level of cognitive enhancement that choline supplementation with each type really has, much less in combination with other nootropics. Taking different forms of choline compensates for the failings of each individual form. Taking too much choline (within reason) is not going to be a problem for most people unless doses are really high (excess of 10g/day).
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  #24  
Old 02-04-2009, 16:27
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Re: Best Choline Source?

Whats the dosage for Alpha-GPC?

SWIM planes on doing a stack with:

Alpha-GPC - ?
picamilon - 100mg
Oxiracetam 500mg
Sulbutiamine 200mg
L-Tyrosine 500mg + P-5-P 50mg

Would this make a good nootropic/wellbeing stack? Thanks.

Ps: BN used to stalk all these supplements but they only have Alpha-GPC and L-Tyrosine, I have P-5-P. Is there any other bulk nootropic stores?

Last edited by oggy; 06-04-2009 at 11:01. Reason: self incrimination!! whoops!:O
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  #25  
Old 02-04-2009, 22:47
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Re: Best Choline Source?

Quote:
Originally Posted by oggy View Post
Whats the dosage for Alpha-GPC?

I plane on doing a stack with:

Alpha-GPC - ?
picamilon - 100mg
Oxiracetam 500mg
Sulbutiamine 200mg
L-Tyrosine 500mg + P-5-P 50mg

Would this make a good nootropic/wellbeing stack? Thanks.

Ps: BN used to stalk all these supplements but they only have Alpha-GPC and L-Tyrosine, I have P-5-P. Is there any other bulk nootropic stores?
Looks pretty good. Oxiracetam could be expensive so SWIM might want to try Piracetam at times too Never heard about Sulbutiamine, but Tyrosine is some good stuff + it makes SWIM more tan. If SWIM would add anything it would be ALCAR and Selegiline.
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