Showing posts with label oxidative stress. Show all posts
Showing posts with label oxidative stress. Show all posts

Sunday, October 23, 2011

Glutathione

Oxidative stress impairs the body's ability to readily detoxify offending substances such as free radicals or to easily repair the resulting damage. It is oxidative stress that is linked to atherosclerosis, cell aging and neurologic disorders in Down syndrome.

On the other hand, glutathione is an powerful antioxidant. It helps remove free radicals and deal with oxidative stress. Studies show that levels of all forms of glutathione is low in children with Down syndrome. (And would make sense that it's low in adults as well.) This is caused by the overexpression of the SOD-1 gene.

Studies show that supplementing with B12 and folic acid can help, but you may want to look into a more direct source of glutathione.

Qadoshyah Fish has more information on glutathione and studies related to DS at her blog post: http://www.gotdownsyndrome.net/glutathione&acetaminophen.html

Glutathione - Your Brain's Master Antioxidant Defense

Apr-16-2004

Copyright 2004 Priya Shah

_____________________________________________

This article was first published in the May 2004 issue of The Glutathione Report, a newsletter featuring regular updates on the health benefits of glutathione.

Free radicals and oxyradicals play an important role in the development and progression of many brain disorders such as brain injury, neurodegenerative disease, schizophrenia and Down syndrome.

Glutathione is the brain's master antioxidant and plays an important protective role in the brain.

According to Dr. Jimmy Gutman, "The brain is particularly susceptible to free radical attack because it generates more oxidative by-products per gram of tissue than any other organ."

Many neurological and psychiatric disease processes are characterized by... abnormalities in glutathione metabolism and antioxidant defenses."

Generation of reactive oxygen species (free radicals) and oxidative damage are an important cause of neuron (brain cell) death from brain injury.

Chemicals that cause toxicity to certain brain cells are known to decrease cerebral glutathione (GSH), making the cells more vulnerable to reactive oxygen species (ROS). (1)

On the other hand, over-expression of the glutathione peroxidase (GPX) enzyme potently decreases cell death from brain injury. (2)

Brain Injury and Glutathione - The Gender Difference

Researchers at Children's Hospital of Pittsburgh have found that males and females respond differently to brain injury. (3)

In animal models, levels of glutathione remain constant in females who have suffered a brain injury, but drop by as much as 80 percent in males with the same injury.

When glutathione levels drop, brain cells die much more quickly. This suggests that boys with brain injuries may require different life-saving treatments than girls.

N-acetyl-cysteine (NAC), a precursor of glutathione, already approved for use by the U.S. Food and Drug Administration to treat people who have overdosed on acetaminophen, may be an effective treatment for brain injury in boys whose brains are deprived of oxygen.


Brain Disorders and Glutathione - A Genetic Cause?

Genetics researchers have found that the glutathione S-transferase gene controls the onset of Alzheimer's, Parkinson's disease and determines, not if we get these diseases, but when. (4)

The glutathione S-transferase gene has previously been linked to the risk for Parkinson's disease among people who used pesticides.

Alzheimer's Disease and Glutathione

Free radicals and oxidative damage in neurons is known to be a primary cause of degenerative diseases like Alzheimer's disease.

Amyloid- peptide (A) accumulation in senile plaques, a pathological hallmark of Alzheimer's disease (AD), has been implicated in neuronal degeneration.

Amyloid plaques encroaching on the brain increase the production of free radicals, or oxidative stress. Antioxidants, such as vitamin C and E "mop up" the damaging free radicals.

Glutathione (GSH) precursors can prevent death of brain cells induced by amyloid plaques in Alzhiemer's disease, while substances that deplete GSH increase cell death. (5)

Evidence has been piling up over the link between the amount of an amino acid called homocysteine in the blood and the chance of developing Alzheimer's.

For people not genetically predisposed to developing Alzheimer's, cholesterol and homocysteine, largely caused by an unhealthy lifestyle, are the core causal factors.

Welsh GP, Andrew McCaddon, showed that the more homocysteine that patients with Alzheimer's had, the worse their mental performance, and the worse their "cognitive impairment," the less they had of the antioxidant glutathione. (6)

Glutathione and Mood Disorders

Studies have found that the mood stabilizing drug, valproate, used to treat epilepsy and bi-polar disorder, regulates expression of the genes that make glutathione-S-transferase (GST).

In addition, chronic treatment with lithium, another commonly prescribed mood stabilizer used in treating manic-depression, also increased levels of GST.

These findings led researchers to conclude that glutathione S-transferase may be a novel target for mood stabilizing drugs. (7)

Alcohol Consumption and Glutathione

Alcohol abuse is known to impair memory and other brain functions and increase brain cell death. A new study in rats has shown that alchol consumption causes fewer new brain cells to form and results in greater cell death. (8)

But rats that were fed alcohol along with Ebselen - a glutathione peroxidase mimic that acts as a free radical scavenger - showed no similar reduction in brain-cell formation and no increase in cell death.

Substances that Boost Glutathione Levels and Protect Brain Cells

Taking glutathione itself as a supplement does not boost cellular glutathione levels, since it breaks down in the digestive tract before it reaches the cells. (Unless you take the reduced l-glutathione form, sublingually, or under the tongue. Good brands include Douglas Laboratory [the kind without NAC] or Klaire Lab. Liquid is supposed to be bioavailable as well, such as www.gshnow.com . The dosage is 75 mg/day for a child. -Andi)

However, intravenous glutathione therapy and glutathione precursors or dietary supplements are effective in boosting intracellular levels of glutathione.

Intravenous Glutathione Injections: Intravenous glutathione injections have been shown to produce amazing and rapid results, in patients with Parkinson's disease. Following even a single dosage of intravenous glutathione, many of the symptoms of Parkinson's disease rapidly improve, often in as little as 15 minutes.

Glutathione Precursors: In the Alzheimer's study conducted by Welsh GP, Andrew McCaddon, adding the glutathione precursor, N-acetyl-cysteine (NAC) to a protocol that lowered homocysteine levels by simple supplementation with B12 and folate, resulted in prompt, striking, and sustained clinical improvement in nearly all the patients. (9)  (N-acetyl-cysteine may cause leaky gut syndrome after extended use and has been seen to increase oxidative stress in those with DS, so weigh your options carefully.-Andi)

Excerpt from Treatment Options for Mercury/Metal Toxicity in Autism and Related Developmental Disabilities:  Consensus Position Paper by Autism Research Institute
  ...a study by James et al.7 found that 800 mcg of folinic acid and 1000 mg of TMG
partially raised levels of glutathione in children with autism, and the addition of
subcutaneous injections of methyl-B12 (75 mcg/kg, 2x/week) normalized glutathione
levels.  Note that the dosage of methyl-B12 was suggested by Dr. J. Neubrander, based
on injecting it into the adipose tissue of the buttocks. (Note that Dr. Neubrander now
recommends a dosage of 64.5 mcg/kg every three days)8  The addition of vitamin B6 (a
necessary co-factor) is likely to raise levels further.  The addition of methionine may be
helpful, but it should be done with extreme caution after methyl-B12 has been given to
prevent negative reactions.8  
Vitamin C:  a study by C. Johnston9 of college students found that the addition of 500
mg/day of vitamin C raised glutathione levels 50%.  Raising the vitamin C to 1000 mg
had no additional benefit.

Cucurmin (turmeric): Studies have shown that the Indian curry spice, cucurmin, has neuroprotective effects because of its ability to induce the enzyme, hemeoxygenase-1 (HO-1), which protects neurons exposed to oxidant stress. Treatment of brain cells called astrocytes, with curcumin, increases expression of HO-1 protein as well as glutathione S-transferase. (10) (The most bioavailable brand is Longvida Curcumin.)

Ebselen: Ebselen is a glutathione peroxidase mimic and potent synthetic antioxidant that acts as a neuroprotective agent and an inhibitor of free-radical induced apoptosis (cell death). It can protect brain cells from the neuro-toxic effects of alcohol consumption. (8)

Undenatured Whey Protein: Undenatured whey protein provides glutathione precursors, has been shown to raise intracellular glutathione levels in clinical trials, and has anecdotally been reported to improve the symptoms of Parkinson's disease.

References

1. Journal of Neurochemistry, Vol. 88, No. 3, 2004 513-531

2. Journal of Neurochemistry, Vol. 87, No. 6, 2003 1527-1534

3. Researchers Find Brain Cells Die Differently in Males and Females; Pediatric Academic Societies Press release; 21-Apr-2004

4. Human Molecular Genetics, 2003, Vol. 12, No. 24 3259-3267

5. The Journal of Cell Biology, Volume 164, Number 1, 123-131; 5 January 2004

6. Biol Psychiatry. 2003 Feb;53(3):254-60

7. Journal of Neurochemistry, Vol. 88, No. 6, 2004 1477-1484

8. Proc Natl Acad Sci U S A. 2003 Jun 24;100(13):7919-24. Epub 2003 Jun 05.

9. Am J Geriatr Psychiatry. 2003 Mar-Apr;11(2):246-9

10. Can Curry Protect Against Alzheimer's?; American Physiological Society (APS) Press Release;

Glutathione in Brown Rice

Whole article here: http://www.whole-body-detox-diet.com/brown-rice.html

Rice bran (tocotrienols) has glutathione peroxidase. It is also available in brown rice / whole grain rice, but not in white.

“Brown rice is high in dietary fiber, vitamins, minerals, essential oils and protective antioxidants. Rice bran lowers high blood sugar and has been found to be one of the most nutrient dense substances ever studied. It contains over 70 antioxidants, protects against cellular damage, and preserves youthfulness.

Rare forms of vitamin E that lower excess of fat and cholesterol have also been discovered in rice bran. It is also calming to the nervous system due to an abundance of B vitamins and trace minerals.

Gamma-oryzanol is a rare and powerful antioxidant found only in rice bran. It strengthens muscles and converts fat into lean body mass. The antioxidant Alpha Lipoic Acid in brown rice promotes liver restoration, slows the aging process and converts glucose to energy.

Glutathione peroxidase (GPx) is an enzyme antioxidant in rice that reduces mucous excesses, boosts respiratory function and helps detoxify the body. The CoQ10 it contains burns fat into energy helping you lose weight and protecting your heart. Unrefined rice also contains proanthocyanidins that are additionally protective against poisons and toxins in the blood, lymph and organ systems.

Related Posts

Wednesday, October 19, 2011

Piracetam

Piracetam used to the be "in" drug for children with T21. And today, a lot of parents give their child Piracetam and believe that it helps him or her. Although I know some who saw no difference. Here is a brief overview on its purported benefits and then an article that talks about its use in the DS community as not properly supported through research. (I'm not one to wait for double blind studies on the actual DS population, but it would be nice to have.)  I've also included my notes as Jett has been taking it for a month and has shown huge improvement! Not knowing that I'd see such a huge improvement, I started Jett on Neuroprotek at around the same time, so I'm sorting through which benefits to attribute to P & which to attribute to NP.

Benefits

Piracetam is said to promote the flow of information (or messages) between the right and left hemisphere of the brain. Dean and Morgenthaler claim that it can enhance memory, language and learning abilities. It may also prevent memory loss and learning difficulties caused by trauma. By its action on the brain membranes it is also thought to prevent seizures. Finally it may be used for the treatment of myoclonus (uncontrolled muscle twitching or jerking) and for the treatment of Dyslexia.

Piracetam, a derivative of the neurotransmitter GABA, is a racetam a category of cognitive enhancers that includes aniracetam, pramiracetam, oxiracetam, and others. Cognitive enhancers are also called noötropics. Piracetams effects on both nerve cells and on blood may be explained by the fact that it alters the fluidity of membranes of cells. Such a change in fluidity would affect the function of various proteins that float in these membranes proteins such as ion channels in nerve cell membranes, and metabolic enzymes in mitochondrial membranes. Cell membrane fluidity would also affect the ability of blood cells to pass through small veins and capillaries.

For more information, please go to http://www.riverbendds.org/index.htm, click the Medical Series folder on the left hand side, then Supplements & Drugs, and then Piracetam.

Research:
- Epilepsy: Koskiniemi M, Van Vleymen B, Hakamies L, Lamusuo S, Taalas J. Piracetam relieves symptoms in progressive myoclonus epilepsy: a multicentre, randomised, double blind, crossover study comparing the efficacy and safety of three dosages of oral piracetam with placebo. J Neurol Neurosurg Psychiatry 1998 Mar;64(3):344-348.

- Aphasia: Kessler J, Thiel A, Karbe H, Heiss WD. Piracetam improves activated blood flow and facilitates rehabilitation of poststroke aphasic patients. Stroke 2000 Sep;31(9):2112-2116

- Dyslexia: - Wilsher CR, Bennett D, Chase CH et al. Piracetam and dyslexia: effects on reading tests. J Clin Psychopharmacol 1987 Aug;7(4):230-237. "Piracetam-treated children showed significant improvements in reading ability (Gray Oral Reading Test) and reading comprehension (Gilmore Oral Reading Test)."

Source
http://www.henryspink.org/smart_drugs.htm

Piracetam improves mitochondrial dysfunction following oxidative stress. 
British Journal of Pharmacology.
147(2):199-208, ... 2006. Peer-Reviewed Professional Journals
· Keil, U., et al.
Department of Pharmacology, University of Frankfurt, Frankfurt, Germany.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1615864/
Mitochondrial dysfunction including decrease of mitochondrial membrane potential and reduced ATP production represents a common final pathway of many conditions associated with oxidative stress, for example, hypoxia, hypoglycemia, and aging. Since the cognition-improving effects of the standard nootropic piracetam are usually more pronounced under such pathological conditions and young healthy animals usually benefit little by piracetam, the effect of piracetam on mitochondrial dysfunction following oxidative stress was investigated using PC12 cellsand dissociated brain cells of animals treated with piracetam.

Piracetam treatment at concentrations between 100 and 1000 muM improved mitochondrial membrane potential and ATP production of PC12 cells following oxidative stress induced by sodium nitroprusside (SNP) and serum deprivation. Under conditions of mild serum deprivation, piracetam (500 muM) induced a nearly complete recovery of mitochondrial membrane potential and ATP levels. Piracetam also reduced caspase 9 activity after SNP treatment. Piracetam treatment (100-500 mg kg(-1) daily) of mice was also associated with improved mitochondrial function in dissociated brain cells. Significant improvement was mainly seen in aged animals and only less in young animals. Moreover, the same treatment reduced antioxidant enzyme activities (superoxide dismutase, glutathione peroxidase, and glutathione reductase) in aged mouse brain only, which are elevated as an adaptive response to the increased oxidative stress with aging. In conclusion, therapeutically relevant in vitro and in vivo concentrations of piracetam are able to improve mitochondrial dysfunction associated with oxidative stress and/or aging. Mitochondrial stabilization and protection might be an important mechanism to explain many of piracetam's beneficial effects in elderly patients.
 

Some History of Piracetam and Down syndrome

Excerpt from a summary by Len Leshin, MD, FAAP
Full text:  http://www.ds-health.com/piracet.htm

Note: I'm not sure why, when Piracetam was tested, it didn't show impressive results. I do know that the parents in the study continued giving their child P. Why would they continue to pay for it and give it if they didn't see results? -Andi

Piracetam became a controversial topic in the mid-1990s when a parent group began advocating its use for Down syndrome. There was notable publicity due to two ABC news shows about it and internet advocacy on the part of the parent group. However, the company licensing it, UCB Pharma in Belgium, has discouraged its use in children with Down syndrome. In July 1998, UCB Pharma specifically denied all rumors that it will fund or has plans to fund any study with children with Down syndrome in the United States or elsewhere. Many advocates of its use in Down syndrome claim that UCB Pharma's reluctance stems more from economic motives than scientific; however, UCB Pharma has obtained "orphan drug" status for piracetam in the US, and is currently planning a controlled trial of piracetam and myoclonus in the US. If given approval by the FDA for myoclonus, UCB Pharma would have several years of exclusivity of the drug in the US.

I have listed below the studies that involve children with Down syndrome. I have a separate page for other research on piracetam.

Lobaugh NJ et al. Piracetam does not enhance cognitive abilities in moderate to high-functioning 7 to 13 year-old children with Down syndrome. Presented at the PAS/SPR meeting in San Francisco May 3, 1999; published in Archives of Ped and Adol Med, April 2001, 155(4):442-448.

"Piracetam, a drug reported to enhance cognitive performance in many neurobehavioural conditions, has become popular in the treatment of children with Down Syndrome (DS). However, reports of its efficacy in DS have been anecdotal, not from evidence-based studies. Some caregivers have noted no effect of piracetam, while others claim substantial improvement in cognitive functioning. To address the need for objective analysis, we conducted a double-blind placebo-controlled crossover study assessing the cognitive and behavioral effects of piracetam in children with DS. Patients and Study Design. Children with DS (n = 25, 13 males, 6.5 - 13 yrs) and their parents participated. The first phase of the study was a baseline cognitive assessment. Children were then randomly assigned to one of two four-month treatment arms: Piracetam. Placebo or Placebo. Piracetam. Children were retested at the end of the two treatment phases. Children received 80-100 mg/kg piracetam per day in capsules. Placebo was administered in the same manner. Test Battery. The test battery included 16 tasks assessing attention, learning, memory, verbal fluency, perceptual and spatial abilities, processing speed, fine motor skills, and executive function. Both standardized and experimental tasks were included. Secondary outcome measures were questionnaires completed by parents and teachers at each of the three phases. Results. Eighteen children (7 - 13 yrs) completed the study, 5 withdrew, and 2 could not complete the battery at baseline testing. The mean mental age for the final sample was 4.2 ± .7 years (Stanford Binet). The 16 tasks yielded 75 measures and the parent and teacher questionnaires had 80 and 24 items, respectively. Piracetam did not show significant effects over placebo on any outcome measure. All significant interactions (p's < 0.05) with drug order or the covariate were examined further to ensure drug effects were not being masked. That analysis did not alter the results. Piracetam administration was associated with CNS stimulatory effects: aggressiveness (n=4), agitation (n =3), sexual arousal, (including masturbation in public, n=2), irritability (n=1), and poor sleep (n=1). Conclusion. Piracetam has received a great deal of attention in the popular press purporting its efficacy in improving cognitive function in children with Down Syndrome. In this study, we were unable to substantiate these claims, even at doses associated with adverse effects. Neither cognitive nor behavioural measures demonstrated improvement under piracetam. Due to the serious adverse effects, it is unlikely that larger doses can be tolerated."
©1999 Pediatric Academic Societies

Fialho J Dromia and Piracetam: a useful association in the treatment of Down syndrome. Tempo Medico 30:944, 1977. (The original was published in Spanish; an English version was reprinted in a book whose specifics are unknown to me.) 26 children with DS between 3 months and 12 years were given Dromia (mixture of pyriglutine and 5-hydroxytryptophan) alone, and then a combination of Dromia and Piracetam. The children were then evaluated based on their muscle tone, motor development, mental development, speech, affective-social development, scholastic achievement and EEG trace. The author concludes that the combination of the two drugs caused an improvement in all aspects, but especially speech. There were no side effects noted. (Unfortunately, this is a terrible study. There were no controlled subjects, the investigator does not tell how he evaluated the above categories and does not say if the subjects, parents, or investigators were "blinded" as to which children were getting one or both drugs.)

An unpublished feasibility study was conducted in 1999 at the Kennedy Kriger Institute in Baltimore under the guidance of Dr. George Capone. Five school-aged children with DS were given piracetam and compared to five children with DS not on piracetam. The piracetam was given at 100 mg/kg body weight per day. After six months, the children were assessed for auditory verbal memory, auditory non-verbal memory, visual memory, and spatial working memory. There were no statistically significant differences in the two groups. It should be noted that this was a study that was set up more to prove to the NIH that the study was doable and deserving to be funded on a large-scale basis rather than to prove whether to not piracetam had any measurable effects. A lack of funds kept this study from being carried out to a point where the research could be published.

In 2002, Dr. Capone and his associates published their trial of piracetam on trisomy mice: The effects of piracetam on cognitive performance in a mouse model of Down's syndrome Physiology & Behavior 77: 403-409, 2002.

"Piracetam is a nootropic agent that has been shown to improve cognitive performance in a number of animal model systems. Piracetam is reported to be used widely as a means of improving cognitive function in children with Down's syndrome (DS). In order to provide a preclinical assessment of the potential efficacy of piracetam, we examined the effects of a dose range of piracetam in the Ts65Dn mouse model of DS. Ts65Dn mice are trisomic for a region of mouse chromosome 16 with homology to human chromosome 21. Daily piracetam treatment at doses of 0, 75, 150, and 300 mg/kg ip was initiated in 6-week-old male Ts65Dn and euploid control mice. Following 4 weeks of treatment, mice were tested in the visible and hidden-platform components of the Morris water maze and were placed overnight in computerized activity chambers to assess effects on overall activity. Piracetam treatment was continued through the 4 weeks of testing. In control mice, 75 and 150 mg/kg/day piracetam improved performance in both the visible- and hidden-platform tasks. Although low doses of piracetam reduced search time in the visible-platform component in Ts65Dn mice, all piracetam doses prevented trial-related improvements in performance in Ts65Dn mice. The 300-mg/kg/day-piracetam dose was associated with a reversal of the nocturnal spontaneous hyperactivity in Ts65Dn. These data do not provide support for piracetam treatment for individuals with DS."

Advocates of piracetam have argued that choline must also be supplemented with piracetam to get any effect, thus explaining the results of the Toronto and Johns Hopkins studies. The main basis for this belief are the following studies:

Bartus RT et al. Profound effects of combining choline and piracetam on memory enhancement and cholinergic function in aged rats. Neurobiol Aging Summer;2(2):105-11, 1981. Rats given both choline and piracetam did better on a memory test than on choline or piracetam alone.
Platel A et al. Habituation of exploratory activity in mice: effects of combinations of piracetam and choline on memory processes. Pharmacol Biochem Behav 21(2):209-12, 1984. Mice did better on memory of their environment with the combination of choline and piracetam than on either separately.
Mosharrof AH & Petkov VD. Effects of citicholine and of the combination citicholine + piracetam on the memory. Acta Physiol Pharmacol Bulg 16(1):25-31, 1990. Mice did better with memory retention with the combination of citicholine and piracetam than the compounds separately.
Friedman E et al. Clincal Response to choline plus piracetam in senile dementia: relation to red-cell choline levels. New Eng J Med 1981 Jun 11; 304(24): 1490-1. This is actually a "letter" rather than a full paper, and consisted giving 10 patients with presenile dementia piracetam and choline for 7 days in a non-controlled study. 3 of the 10 had "marked improvement" cognitively, but no description of the cognitive tests or whether the testing was blinded is mentioned. The 3 who responded had higher choline red blood cell levels than the 7 who didn't respond.

However, other studies show a lack of usefulness of the combination:

Ennaceur A & Delacour J. Effect of combined or separate administration of piracetam and choline on learning and memory in the rat. Psychopharmacology 92(1):58-67, 1987. Rats given choline alone did better than rats given piracetam alone on memory test, and rats given piracetam and choline together did worse than the other groups.
Growdon JH et al. Piracetam combined with lecithin in the treatment of Alzheimer's disease. Neurobiol of Aging 7:269-276, 1986. Piracetam was administered alone or with lecithin (phosphatidylcholine) in a double-blinded test. No effect was seen, with or without lecithin, on cognition or memory test scores.
Corona GL et al. Clinical and biochemical responses to therapy in Alzheimer's disease and multi-infarct dementia. Eur. Arch. Psychiatr. Neurol. Sci. 239:79-86, 1989. Patients with either AD or multi-infarct dementia were given either piracetam or piracetam with choline. This was not paired with placebos. Despite biochemical changes, there was no change in memory performance.

It should be noted that the maker of piracetam, UCB Pharma, has never incorporated choline as part of any of its research on humans with Alzheimer's disease or myoclonus.

Products

NooRacetam (Piracetam) 800mg $17.95 plus $6 shipping


Dosage

75 mg per kilo per day is the recommended dosage.  Is recommended to take with choline. (Body Bio PC is the brand of choice.) May cause hyperactivity so you may need to avoid at night. Piracetam tastes bitter so if you have to break open the capsules, you'll need to be a little creative when giving it. Jett takes it fine with a chunk of banana and a little bit of honey. If I add fermented ketchup to a mashed vegetable such as acorn squash or avocado, it works as well.

My notes on Jett's experience with Piracetam

Day one
Age: 20 months  
Dosage: Jett weighs 19.8 lbs which is 8.98 kilos. So he'd get 673 mg per day. One capsule is 800 mg. So I will give him 1/2 a capsule (400) in the morning and 6 hours later, give him a third of a capsule (266) and see how it goes. But for day one, I'm giving him 1/3 of a capsule in the am and 1/3 in the afternoon.
He's not on Prozac at the moment and we ran out of LC and EGCG and have a full bottle of Piracetam that I haven't tried so... I'll let you know what I see...
I take 840 mg of choline a day and Jett still breastfeeds, so I am assuming that he is getting some choline 3 times a day. (I did look this up and a study supports the fact that breastfeeding woman who supplement with choline have higher choline content in their breast milk.)
Cognition test: I wrote 6 words on the magnadoodle, one at a time and showed him what they were in the room:  bean bag, chair, cow (a picture), shoe laces, stool and umbrella. (Bean bag, shoe laces and umbrella are brand new words. The others he has seen this week.) Sometimes he wanted to write them as well after I wrote them (I mean that he made me hold his hand and he wrote them with me). Then I immediately wrote each one again and asked him where they were. He got them all right. I called my husband and stepdaughter into the room and although he was distracted and "talking" to them, he got them all right again. He's taking a nap now, but I'll try again when he wakes up to see if he remembers.
He did remember when he woke up and remembered all but one (bean bag) the next night. This test only proves that Piracetam doesn't seem to hurt his cognition. I can't say he did this because of it.
I'm excited because he's not on Prozac, LC or EGCG. Just ginkgo and vitamins (and Piracetam). Hopefully we can afford LC and EGCG again soon. He's not been hyper at all and he actually crawled around the house and played a lot on his own (w/out being irritable--being happily independent). I did read a lot of books to him and did some Little Reader and magnadoodle, as I mentioned. When I do a lot of that, he seems to feel happier and more independent. If I don't spend a lot of time with "lessons" he gets really irritable and whines for me to read to him.
Obviously, it's caused no sleep issues so far because he's taking a nap now.

Day two
I noticed by day two on Piracetam that it doesn't support the eyes as well as: LC, Prozac & EGCG since his eyes are crossing very badly. (Shows that the communication between the brain and eyes are not doing well.) We've ordered LC (yeah!!!) and should expect it in 3-5 days. But, his language is coming along nicely. Usually, off LC, he either stops talking or really regresses language wise, but yesterday he said a bunch of words, actually repeated after me. (Unfortunately one was "shut up" (I did say PLEASE, first...) which of course he repeated like twenty times with enthusiasm. And then it was the first thing he said this morning. I said, "Good morning, Jett." and he smiled and said, "Shut up!" Hopefully people will think it's cute... like Ann Hathaway in Princess Diaries...
I did also add Neuroprotek which he took before w/no side effects.
I showed Jett colors, but he didn't get them all right. I'll try again another day. Maybe the concept is more difficult than words?

Day three
I'm upping the dose to 1/2 in morning and 1/3 in the afternoon. Ooops... Jett was fed the last dose of Piracetam at 7pm! So, he didn't sleep very well at all. He didn't fall asleep until 2 am. Once he fell asleep, he was fine though. So, it looks like it takes about 7 hours to get out of his system... We won't make that mistake again!

Day four and five
He turned 21 months old on Nov. 25, 2011. These past two days he has been playing independently for very long periods of time! And instead of sitting and going "ehhhhhh" when he wants me to read a book, he takes the book, crawls over to me and hands it to me to read. He also has been more interested in his bath time and has been taking an hour long bath and not wanting to get out. For the first time. (He's always enjoyed bath time, he's just more engaged and for a longer period of time.) So, it appears to me that he's more focused with a longer attention span on the Piracetam and NeuroProtek (NP has a lot of the same things as ginkgo, EGCG and curcumin, so I think it's more the Piracetam). Any one else notice that on Piracetam?

Day six
Saturday, Nov. 26, 2011 I had to work (2-4 a month) and there was a "miscommunication" so Jett got 1/2 a capsule of Piracetam at 10am and then another 1/2 at 1pm. (I fixed the small bowls of supps, but my husband got the times wrong--I didn't write it down for him this time.) He seemed fine though and Kenny said that he didn't "give him any trouble" which means that Jett did a lot of independent play, was in a good mood, ate well and took almost a 2-hour nap. :D

Day seven
Sunday, Nov. 27, 2011 My mother came over and had Jett outside for his 30 minutes of sun. While outside, Jett stood up and walked behind a rolling toy car! She said that he took three steps! I took him outside an hour later and he took five steps! So I got my husband and stepson to see and take a video. I'll get my husband to upload it soon and will provide a link here. I'm excited!! I would love for him to walk soon! (As part of the ND program, I haven't initiated much walking because crawling is so important for brain development. I don't know if my mother "put him up to this" or if he thought of trying to walk behind the toy on his own... I do wonder how long he's been able to do this. I don't really think I'm supposed to encourage him to walk like this...) He has taken a couple of steps forward on his own just in this week, so maybe it was his idea? The average age of a child w/DS who can walk 10 feet with a push toy is 22 months and 11 months for a typical child. Jett did walk about 5 feet today. I'm not sure how much Kenny recorded. I don't think it would hurt for me to try this again tomorrow.

Day eight
I played Little Math for the first time and he LOVED. He shouted with protest when it was over. They counted to five really fast and he shouted out "six"! So funny because no one taught him any of that! (There is a Readeez song that counts to 12 very fast so he probably learned it that way.) He did it twice more when my husband played it later on in the day, so it wasn't my imagination.

Day 11/Dec. 1:
Jett's finally back on curcumin. Yeah! He said five recognizable words in front of the speech therapist today. I figure that's pretty good for an hour, right? (Horse was one.)  His walking is progressing as well. And he learned to read the names of some of his instruments: drum, tambourine, morocco and xylophone as well as shake and beat. He was very excited to learn these & would play each one when I wrote the name. He also loves to dance, bounce and shake. He wouldn't vocalize for "sing" but he did sway his arms from side to side and looked toward the computer where I play pandora.com (music).
When I wrote "together" he laced his hands together. I only showed him that word once a couple of days ago. But it's one of his favorite words, so it makes sense that he learned it immediately. When I wrote "chair" he pointed to the chair closest to him then he also pointed to the chair that was on the other side of him. These chairs look very different so he does understand what a chair is and not just the chair I showed him first. He remembered all the old words except bean bag--again! It's not a word we use a lot so maybe that's why? We worked on shapes yesterday and colors the day before but he didn't seem to either get them or be too interested so I didn't check today to see if he magically got them. I know that he knows star, though because he's said it a couple of times and will point to one.
Some meaningful words he said today were: Jett, yes, eyes, "S", "Ah" (for A-apple), "kuh" for book (upon request), "zzz" for buzz, shapes... that's all I can think of off the top of my head. He jibber jabbers constantly so I forget to remember all the stuff he says. His favorite book today is Mr. Brown Can Moo, Can You? He was having fun tonight pretending to read it out loud. He made a lot of noises but they didn't exactly match the word. I'll have to teach him those words tomorrow--he'll love that!
Oh, we did Little Reader in Chinese and he freaked out. He hated it! He rolled off my lap onto the floor he was so disturbed by it. I think it's because it was all too foreign to him and he LOVES reading English so much that it was not a pleasant experience. I'll have to try again later--once he's got a good grasp of the English language. (Learning another language is really good for the brain.)
I gave him the Piracetam a little after 5 so he fell asleep about an hour late (midnight). I have to remember that he won't fall asleep until 7 hours after the last dose -- so no later than 4pm.

Dec. 4
Discovered for sure that he knows and will verbally say ten letters of the alphabet. He says the sound, not the letter name. When I read the alphabet to him, I say "wuh" instead of "double-u", etc. He knows A, C, E, O, P, S, T, W, X and Z. (I found out the next day that he knew M as well.)
Yesterday, he spontaneously gave me a hug for the first time and my mother said he hugged her too. This afternoon, when he was supposed to be napping, he spontaneously gave me like 5 kisses on my nose. He never initiated kisses and hugs before. But he recently started to give me kisses from afar by making the smack sound.
Yesterday I also noticed that he put a lid on a container which I don't think he's done before.

Dec. 11
Okay, so now Jett can put in a puzzle piece for the first time. (It was the Melissa & Doug farm sound puzzle of the sheep.) And he wanted to put the shapes into the shape sorter, but was having difficulty so he had me come over. I set it up so he could succeed better (less choice of shapes, at the right side where the correct shape hole is, etc.) and he was able to do it better and better! He put them in himself! (He's not great at it yet, but he understood the concept and was interested and tried and did it!)
Yesterday, he spontaneously said, "A B C" while playing in the bathtub and my husband parroted him and then Jett said, "D!" He's started singing (ba, ba, ba) and has been singing with the Readeez version of the alphabet song. (I mean that he tries to, he can't actually sing the alphabet song.) I can tell that his brain is more organized... He went around and gathered all the parts of his floatable xylophone where each musical bar is on its own colored puzzle piece. So, he's picking through his toys and brings me a pile of his xylophone and says "together" (his version of the word) so that I will put it together for him! (Then he immediately ripped them apart so I'd do it again.)
He did something similar last night, he sorted out the red puzzle pieces from only one puzzle and just brought those to me.
I was unhanging socks that were dry and I dropped each one on his head as if it were raining socks and then I rolled the matching ones together into "sock balls." So he gathered the sock balls and we played catch for a while and then he gathered them and carried them all through his crawl tube and went back and got the ones he dropped, etc. And played with them for a good while, very creatively!
All this type of play is NEW NEW NEW! I don't know if it's the Piracetam or the NAET or what, but I'm loving this burst of amazing cognitive progress!
And his mood... he is smiling much more and seems to be an all around happier kid! His eyes are doing great as well. Very little crossing. Yes, we are still doing the neurodevelopmental exercises for his eyes. I'll have to ask around and see what other moms have seen in their child on Piracetam.
He also has been reading--out loud--words that I haven't specifically taught him, from his books. Like in the Hide and Squeak book, he read: Pup and the Mr. Brown book, he read: Hoo, Buzz, Pop, Klopp, Boom, and Grum... In a pig book, he read splash and like three other words. And in other books, I see him react to the words before I say them. Like a Barney books says pat your head and he's already doing it before I read it out loud.

Dec. 17
We have contact! Eye contact, that is! I didn't realize what little eye contact Jett had before, but today, he really held my gaze. Because of this, he parrots more--both verbally and "gesticularly." I'm rather animated with my hand movements when I talk and I see him copying me. Too funny. I always thought he was engaged, but the change has been amazing.
Also new--I had noticed that when I pointed, Jett looked at my finger or the end of my finger and not at the object to which I was pointing. This is significant because studies show that children who can follow where you point learn better. Jett just started looking at the object! I try this everyday so I can tell you that this is the first time he's done it!

Dec. 18
I've readded TriEnza enzymes to help w/Jett's bowel movements. Because of the uncomfortable nature of getting his stomach in order, he was very clingy and irritable all day and night. He had 2 BMs in one day--1 BM a week is "normal" for him, so this will take some time for him to adjust.
As I learn more about Neuroprotek, I'm thinking that I need to attribute all the elimination of Jett's borderline Autistic tendencies on it rather than the Piracetam. I don't know how much of the P to attribute the speech and cognitive advances, but I am quite pleased so far!

March 24
Jett's been off P and only on NP for months and he's still doing great! I'm going to reintroduce P along with BodyBio PC soon and see if I observe a difference. He's 24 months and has been putting together the Melissa and Doug stacking puzzle, the M & D wooden puzzles with the little red knobs, reading words out loud like "helicopter, enterprise, happiness" and has been repeating two-three words at a time instead of just one. He's also been playing appropriately with cars and has been showing me things (new behavior). He recently starting following my point to far away objects instead of just looking at the end of my finger. And now he points himself. Last week he pointed excitedly to a flock of birds flying overhead and said, "Birds! Birds!" He didn't point to anything except for things up close until about 3 weeks ago. (This is another autistic tendency that is going away.) And just today, he called out to a boy on a bicycle as he rode by. So, he's wanting to be more social. And the past two weeks he's been memorizing songs including "Itsy Bitsy Spider" and the ABC song. He hasn't gotten it perfect yet, but he's having fun with it. And he's been playing with stuffed animals and dolls--brand new behavior as well!

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