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Your Guide to Revolutionary Cognitive Enhancement

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Intranasal Insulin: A Revolutionary New Treatment for Alzheimer’s

Home UncategorizedIntranasal Insulin: A Revolutionary New Treatment for Alzheimer’s

Intranasal Insulin: A Revolutionary New Treatment for Alzheimer’s

June 22, 2016 Posted by lostfalco@gmail.com 4 Comments

Quick Summary

Intranasal insulin halts the progression of Alzhiemer’s disease and enhances cognition in humans.

How to Buy: Go to a Walmart pharmacy and ask for Novolin R. It’s perfectly legal to buy over the counter without a prescription for $25.

Pour it into a nasal spray bottle and you’re good to go.
Nasal Spray Bottle
Nasal Spray Bottle (Swiveling Head)

Take 10IU after breakfast and 10IU after dinner.

Study Results

Intranasal insulin improved memory, caregiver-rated functional ability, and general cognition in Alzheimer’s Disease patients (see full study abstracts below for more info).

“Treatment with 20 IU of insulin improved delayed memory (P < .05), and both doses of insulin (20 and 40 IU) preserved caregiver-rated functional ability (P < .01)."

“Both insulin doses also preserved general cognition as assessed by the ADAS-cog score for younger participants and functional abilities as assessed by the ADCS-ADL scale for adults with AD (P < .05)."

How Does It Work?

Intranasal insulin bypasses the blood brain barrier and absorbs into the brain where it activates insulin receptors which are particularly prevalent in the hippocampus, hypothalamus, and cortex.

This picture explains it nicely!

What Type of Insulin?

“…insulin (Novolin R; Novo Nordisk, Princeton, New Jersey) was administered…”

Here’s what Novolin R looks like.

How Much Insulin?

“…36 participants received 10 IU of insulin twice a day…”

“…38 participants received 20 IU of insulin twice a day…”

Therefore, either take 10IU after breakfast and 10IU after dinner OR 20IU after breakfast and 20IU after dinner.

I would start with the lower dose (10IU).

I’ve done really well with 10IU twice a day in my own self-experiments for cognitive enhancement (although I don’t have Alzheimer’s).

How Was Insulin Administered?

“Saline or insulin (Novolin R; Novo Nordisk, Princeton, New Jersey) was administered after breakfast and dinner with a ViaNase nasal drug delivery device…”

Here’s the ViaNase.

While something like the ViaNase might be nice other human studies on intranasal insulin have used spray bottles or droppers with very good results.

I use this and it works great. Nasal Spray Bottles

Each spray should be about 10IU.

How Long Did They Take It?

“Participants received placebo (n = 30), 20 IU of insulin (n = 36), or 40 IU of insulin (n = 38) for 4 months…”

The subjects dosed for four months and the best part was, “No treatment-related severe adverse events occurred.”

Four months is the longest that I’ve seen intranasal insulin dosed in humans and I would currently consider it an upper limit until the results of the multi-year SNIFF trial are published (see link below to SNIFF study on intranasal insulin for Alzheimer’s).

How Do I Make My Own?

Simply purchase Novolin R, pour it into a nasal spray bottle, and store it in the fridge.

No need to dilute it or mix it with anything else.

It really is that easy!

I’ve discussed this in much greater detail here.

Where To Buy

Purchase Novolin R at a Walmart pharmacy legally over the counter without a prescription for $25.

Get nasal spray bottles here: Nasal Spray Bottles

The Science

https://www.ncbi.nlm.nih.gov/pubmed/21911655

Arch Neurol. 2012 Jan;69(1):29-38. doi: 10.1001/archneurol.2011.233. Epub 2011 Sep 12.

Intranasal insulin therapy for Alzheimer disease and amnestic mild cognitive impairment: a pilot clinical trial.


Craft S1, Baker LD, Montine TJ, Minoshima S, Watson GS, Claxton A, Arbuckle M, Callaghan M, Tsai E, Plymate SR, Green PS, Leverenz J, Cross D, Gerton B.
Author information

Abstract


OBJECTIVE:
To examine the effects of intranasal insulin administration on cognition, function, cerebral glucose metabolism, and cerebrospinal fluid biomarkers in adults with amnestic mild cognitive impairment or Alzheimer disease (AD).
DESIGN:
Randomized, double-blind, placebo-controlled trial.
SETTING:
Clinical research unit of a Veterans Affairs medical center.
PARTICIPANTS:
The intent-to-treat sample consisted of 104 adults with amnestic mild cognitive impairment (n = 64) or mild to moderate AD (n = 40). Intervention Participants received placebo (n = 30), 20 IU of insulin (n = 36), or 40 IU of insulin (n = 38) for 4 months, administered with a nasal drug delivery device (Kurve Technology, Bothell, Washington).
MAIN OUTCOME MEASURES:
Primary measures consisted of delayed story recall score and the Dementia Severity Rating Scale score, and secondary measures included the Alzheimer Disease’s Assessment Scale-cognitive subscale (ADAS-cog) score and the Alzheimer’s Disease Cooperative Study-activities of daily living (ADCS-ADL) scale. A subset of participants underwent lumbar puncture (n = 23) and positron emission tomography with fludeoxyglucose F 18 (n = 40) before and after treatment.
RESULTS:
Outcome measures were analyzed using repeated-measures analysis of covariance. Treatment with 20 IU of insulin improved delayed memory (P < .05), and both doses of insulin (20 and 40 IU) preserved caregiver-rated functional ability (P < .01). Both insulin doses also preserved general cognition as assessed by the ADAS-cog score for younger participants and functional abilities as assessed by the ADCS-ADL scale for adults with AD (P < .05). Cerebrospinal fluid biomarkers did not change for insulin-treated participants as a group, but, in exploratory analyses, changes in memory and function were associated with changes in the Aβ42 level and in the tau protein-to-Aβ42 ratio in cerebrospinal fluid. Placebo-assigned participants showed decreased fludeoxyglucose F 18 uptake in the parietotemporal, frontal, precuneus, and cuneus regions and insulin-minimized progression. No treatment-related severe adverse events occurred. CONCLUSIONS: These results support longer trials of intranasal insulin therapy for patients with amnestic mild cognitive impairment and patients with AD. Trial Registration clinicaltrials.gov Identifier: NCT00438568.

http://www.ncbi.nlm.nih.gov/pubmed/17942819/

Neurology. 2008 Feb 5;70(6):440-8. Epub 2007 Oct 17.

Intranasal insulin improves cognition and modulates beta-amyloid in early AD.


Reger MA1, Watson GS, Green PS, Wilkinson CW, Baker LD, Cholerton B, Fishel MA, Plymate SR, Breitner JC, DeGroodt W, Mehta P, Craft S.
Author information
Erratum in
Neurology. 2008 Sep 9;71(11):866.

Abstract


BACKGROUND:
Reduced brain insulin signaling and low CSF-to-plasma insulin ratios have been observed in patients with Alzheimer disease (AD). Furthermore, intracerebroventricular or IV insulin administration improve memory, alter evoked potentials, and modulate neurotransmitters, possibly by augmenting low brain levels. After intranasal administration, insulin-like peptides follow extracellular pathways to the brain within 15 minutes.
OBJECTIVE:
We tested the hypothesis that daily intranasal insulin treatment would facilitate cognition in patients with early AD or its prodrome, amnestic mild cognitive impairment (MCI). The proportion of verbal information retained after a delay period was the planned primary outcome measure. Secondary outcome measures included attention, caregiver rating of functional status, and plasma levels of insulin, glucose, beta-amyloid, and cortisol.
METHODS:
Twenty-five participants were randomly assigned to receive either placebo (n = 12) or 20 IU BID intranasal insulin treatment (n = 13) using an electronic atomizer, and 24 participants completed the study. Participants, caregivers, and all clinical evaluators were blinded to treatment assignment. Cognitive measures and blood were obtained at baseline and after 21 days of treatment.
RESULTS:
Fasting plasma glucose and insulin were unchanged with treatment. The insulin-treated group retained more verbal information after a delay compared with the placebo-assigned group (p = 0.0374). Insulin-treated subjects also showed improved attention (p = 0.0108) and functional status (p = 0.0410). Insulin treatment raised fasting plasma concentrations of the short form of the beta-amyloid peptide (A beta 40; p = 0.0471) without affecting the longer isoform (A beta 42), resulting in an increased A beta 40/42 ratio (p = 0.0207).
CONCLUSIONS:
The results of this pilot study support further investigation of the benefits of intranasal insulin for patients with Alzheimer disease, and suggest that intranasal peptide administration may be a novel approach to the treatment of neurodegenerative disorders.

https://www.nia.nih.gov/alzheimers/clinical-trials/study-nasal-insulin-fight-forgetfulness-sniff

Study of Nasal Insulin to Fight Forgetfulness (SNIFF)

Overall Status:
Recruiting

Brief Description:
This Phase II/III clinical trial will examine whether a type of insulin, when administered as a nasal spray, improves memory in adults with a mild cognitive impairment or Alzheimer’s disease. The study will also provide evidence about how intranasal insulin works in the body.

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Over the past decade I've taken 500+ substances and performed thousands of self-experiments to improve my brain and my life. And now, I'm here to share with you the best of the best so that you can achieve life-changing results in a fraction of the time at fraction of the price. You won't find information like this anywhere else in the world! So, read on to discover how to attain the mind, and the life, you've always wanted.

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4 Comments

Leave your reply.
  • Chris
    · Reply

    December 29, 2017 at 7:19 PM

    I just took my first dose of Novolin R and had a minor allergic reaction (nasal congestion/slight wheezing). It lasted about 30 minutes. From what I’ve read it’s probably a reaction to an additive, but some people can be allergic to the insulin itself. Is this a deal breaker for me? Might this reaction lessen over time? Are there other insulin types/brands I can try?

    Thanks!

  • Algerd Monstavicius M.D
    · Reply

    June 3, 2017 at 7:25 PM

    HI, I have had my spouse on Intr-nasal insulin now for 8 months withou adverse effects. Initially I used a Mabis nebulizer and administerd 50 units of Levemir insulin BID. Using a nuebulizer is not as effeicient as a significant portion is lost as one exhales etc.. I found this site an ordered the spray bottles and started using those. Much easier and faster but after a while I started to use the nebulizer again because I felt that the mist is inhaled through the nose penetrates deeper into the olfactory region were te absorptin takes place. I noted also that her response to the nebulizer appeared to be better but this was very subjective as the symptoms of the disease wax and wane.. At the present time I am using the nebuluzer in the AM and the spray bottles for the PM administration. During this 8 month period my spouse appears to have stabiized. So- I am optimistic in respect to this treatment.
    About one month ago we modified the treatment plan agiain by continuing the insulin as described above but in addition adding chroolyn to the treatment. After the AM insulin administration, one via of chromolyn is added to the neublizer and administered. It appears that chrmolyn inhibits mast cell degranulation and release of inflammatory mediators- which appear to be a big part of the problem. Initially most of the chromolyn was inhaled via a face mask but then I also started to administerd it vial the nasal attachment. At first only 5 inhalation were done via the nasal attachment and gradually increased. At the oreenttime she takes the entire vial of chromolyn via the nasal attachement and has show no bad effects. I understand why chromolyn may help in that it may supress the inflammation but at the present tim after using this agent for almost one month I see no striking obvious benefit but plan to contiue it for a longer period of time. i ma of the opinion that the Levemir insulin has been effetive in stabilzing her symptoms and has stopped the decline but still may be too early ti be sure.

  • a
    · Reply

    March 7, 2017 at 5:49 AM

    Hi there – I’ve read all your posts about intranasal insulin and have a question. Do you have any info about tolerance or insulin resistance from this dosing? Would there be bad side effects from stopping for a while? As a CFS patient I am interested in trying, but I don’t want to cause insulin resistance of the brain as this is associated with Alz. Thanks.

    • lostfalco@gmail.com
      · Reply

      Author
      March 19, 2017 at 2:45 PM

      Hey, thanks for checking out my posts. =)

      Long term tolerance/resistance is currently an issue being pursued in the scientific studies of intranasal insulin. So, it’s somewhat of an open question at this point.

      In the short term, it doesn’t seem to develop tolerance or accelerate insulin resistance. Healthy subjects have been tested at the very high dose of 160IU per day for 8 weeks without issue. Alzheimer’s patients have taken 20 to 40IU per day for 4 months and actually showed continued positive benefits when tested two months after cessation.

      That’s pretty much where the data stands right now.

      I do a few things to lower my risk for tolerance/resistance: 1) find the absolute lowest dose where I still have effects, 2) take periodic breaks (cycle it), and 3) occasionally take very long breaks.

      For example, in 2016 after experimenting varying doses of i-insulin for a few months starting in January, I ran an 8 week cycle of i-insulin at 40IU per day (breakfast, lunch, dinner, bedtime) took a break and then ran a 4 month cycle of i-insulin at 20IU per day (upon waking, at bedtime). I pretty much tested it the entire year (with the aforementioned breaks, of course). I stopped at the end of 2016 and haven’t taken i-insulin at all in 2017 so far. This is just an anecdote, but I’ve suffered no noticeable ill effects.

      Anyway, I hope that gives you an idea of my approach and answers your question a little. =)

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