Alzheimer's is a neurodegenerative disease which is characterized by cognitive decline and the loss of ability to form short-term memories. The disease gradually progresses to affect all facets of life and is incredibly sad to watch helplessly as a loved one goes through the progression. This disease has struck my own family and I can imagine that many of you have seen what I have.
Biochemically, Alzheimer's is thought to occur at least party due to the accumulation of thick waxy plaques in the brain comprised of a protein called amyloid beta (Abeta). There have been (and are still) numerous research projects looking into better understanding the accumulation of this protein plaque and to develop drugs which would work to either prevent it from accumulating more or break up what has formed.
Today let us briefly discuss some work published in the journal Nature: Scientific Reports titled "Chronic treatment with a smart antioxidative nanoparticle for inhibition of amyloid plaque propagation in Tg2576 mouse model of Alzheimer’s disease". The first person to reply to this post stating "Monkey Monkey, Tree, Look At Me, I'm talking Nonsense!" Will be sent 2 SBD. In this work the authors were studying a new nanoparticulate compound with reducing properties that could potentially allow it to break down these Abeta plaques.
Briefly Tell Me About This Nanoparticle
The nanoparticle which they abbreviate (RNPN) is actually a long polymer comprised of the compound (poly(ethylene glycol)-b-poly[4-(2,2,6,6-tetramethylpiperidine-1-oxyl)aminomethylstyrene]), this compound has a water loving part (poly(ethylene glycol) and a water hating part (the rest of it). This results in the polymer forming what is known as a mycelle which basically is a ball like structure where a bunch of the water hating tail groups point inward together, leaving the water loving part to be in contact with water on the outside of the ball. The compound breaks apart under acidic conditions (like the stomach) which allows it to be absorbed by the body, where it can again reform (our blood is non acidic). [2]
This compound has reductive properties (it can gobble up radical oxygen species, and acts as an antioxidant), and has previously been shown to have antioxidant activities in the brains of some mice! [3] Knowing this, the authors here wanted to test whether it might be useful against Abeta plaques.
What Did They Find?
The researchers were using a transgenic mouse which had the Alzheimer's causing Abeta protein overexpressed (meaning they artificially induced the protein to be in these mouse's brains in high concentrations). These mice have cognitive difficulties just like humans with Alzheimer's. Next they confirmed that their nano-particle could get into the brains of these mice as had been previously shown for a different variety of mouse, and saw that yes it could. Okay step one, check, compound gets to the mouse brain...but does it do any good?
In this first test, mice were acclimated to a box containing an object in a particular position (in one corner). The mouse was removed, the object was moved, and the mouse was placed back in. Now mice are pretty smart, and they notice when something has changed in the environment and will go explore what has changed. Well unless they have alzheimers, then they can't remember and no longer spend time exploring. This test reports the difference in time that the mice spent exploring the change in object location allowing us to see what effect the compound had.
The important part to compare is first the wild type (non Alzheimers mice) vs the AD + Water group (alzheimers mice given water to drink). We see that the wild type mice spent much more time exploring the objects new location then the alzheimers mice (which spent no time... I guess they forgot). Next look to the bar showing AD + RNPN this is the alzheimers mouse treated by their nano-particle. You can see that the nanoparticle greatly improved the mice's curiocity for the objects new location vs the AD + water group!
Other Article Observations (The "Brief" Rundown!)
- RNPN improved the alzheimers mice's abilities to navigate their way to an invisible platform in a pool of water in the "Morris Water Maze test."
- Expression of proteins indicative of oxidative stress (known to be high in the alzheimers mouse) were significantly reduced upon treatment with the RNPN nanoparticle.
- Decreased levels of both forms of Abeta (1-40) and (1-42) were observed in the brains of the alzheimers mice given RNPN treatment. (1-42 is the form of the protein that typically forms the aggregate, seeing a reduction in the amount present in the mouse brains is very promising).
Conclusions
The authors report that their nanoparticle (RNPN) which has the ability to break down in the stomach, easily get absorbed, re-assemble and get to the brain. Also has antioxidative properties, reduced the amount of amyloid beta in a mouse model, as well as helped those mice regain some cognitive functioning. A very interesting and promising piece of work!
Sources
- https://www.nature.com/articles/s41598-017-03411-7
- http://pubs.acs.org/doi/abs/10.1021/bc900214f
- http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0126013
All Non Cited Images Are From Pixabay.com or Flickr.com And Are Available Under Creative Commons Licenses
Any Gifs Are From Giphy.com and Are Also Available for Use Under Creative Commons Licences
If you like this work, please consider giving me a follow: @justtryme90. I am here to help spread scientific knowledge and break down primary publications in such a way so as to cut through the jargon and provide you the main conclusions in short (well compared to the original articles at least!) and easy to read posts.
Monkey Monkey, Tree, Look At Me, I'm talking Nonsense!
Is that still up for grabs? lol :)
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Hey someone ACTUALLY read it!
Edit: Sent 2 SBD.
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Yep :) . By the way i'm half way through it. Its pretty good so far.
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Well thank you :)
For these shorter posts it's tough to balance any sort of brevity while maintaining some detail. Still working on how to best accomplish this.
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Yes, I know, but you're getting pretty good responses, which must feel satisfying.
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I have had a few posts that have generated some really great and interesting discussion. That is honestly the best part. I feel like a big part of the struggle to inspire this is my own limitations in writing. So yeah, it's wonderful when I get awesome responses! That is super encouraging that I am on the right track as I keep learning how to blog. Science I can handle, effective communication, that has a steep learning curve :)
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https://steemit.com/diabetes/@healthiswealth/doctors-corner-type-3-diabetes-also-known-as-diabetes-of-the-brain
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Thx I have two cases of Alzheimer's in my family
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Ugh, I am sorry to hear this.
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Are dimentia and alzheimers the same thing or caused my similar thing? I have heard both terms am not sure of the difference
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Dementia is any disease of the brain which reduces ones ability to think. It can be caused by a variety of factors, even things like arterial hardening and reduced oxygen flow in the brain.
Alzheimer's disease is one such cause of dementia (and a very prominent one) with very specific causes (some of which I mentioned above in the post!). So in short, all Alzheimer's is dementia, but not all dementia is Alzheimer's.
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WRONG!
Suzanne de la Monte, a neuropathologist at Brown University, has been working on these phenomena in humans and rats. When she blocked the path of insulin to rats’ brains, their neurons deteriorated, they became physically disoriented and their brains showed all the signs of Alzheimer’s. The fact that Alzheimer’s can be associated with low levels of insulin in the brain is the reason why increasing numbers of researchers have taken to calling it Type 3 diabetes, or diabetes of the brain.
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Alzheimer's Disease is Type 3 Diabetes: Evidence from Human Studies
This hypothesis was directly investigated by first examining postmortem cases of advanced AD and determining if the neurodegeneration was associated with significant abnormalities in the expression of genes encoding insulin, IGF-1, and IGF-2 peptides, their receptors, and downstream signaling mechanisms.5 In that study, we demonstrated advanced AD to be associated with strikingly reduced levels of insulin and IGF-1 polypeptide and receptor genes in the brain (Figure 1). In addition, all the signaling pathways that mediate insulin and IGF-1-stimulated neuronal survival, tau expression, energy metabolism, and mitochondrial function were perturbed in AD. This study carries additional significance because it established that, like all other pancreatic and intestinal polypeptide genes, the insulin gene was also expressed in the adult human brain. Moreover, the results taught us that endogenous brain deficiencies in insulin, IGF-1, IGF-2, and their corresponding receptors, in the absence of T2DM or obesity, could be linked to the most common form of dementia-associated neurodegeneration in the Western hemisphere. Since the abnormalities identified in the brain were quite similar to the effects of T1DM or T2DM (though none of the patients had either of these diseases), including abnormalities in IGFs,81–83 which are important for islet cell function,84,85 we proposed the concept that AD may represent a brain-specific form of diabetes mellitus and coined the term “type 3 diabetes.”
Source: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2769828/
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So? I don't agree with the assessment to call it diabetes. Diabetes is a systemic terminology, effecting many systems. In fact usage of the term diabetes for both type 1 and type 2 is a poor idea, as they are two largely dissimilar diseases. Calling Alzheimer's type 3 diabetes is disingenuous at best, regardless of whether or not brain insulin sensitivity can induce Alzheimer's like symptoms in mice.
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Read the human studies.
I have taught many ND's and MD's in my career.
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Of course, I will take a closer look at the article you presented here for my train commute reading.
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Enjoy the read.
Have a good weekend.
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Will do, you as well.
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@maszblogs,
Great question.. you were correct!
I am upvoted and following you
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Great idea to try and make this easier to access. My Mum has vascular dementia (not quite the same but the prognosis is similar) but I do spend quite a bit of time online sussing out the latest research on her condition as her daughter and carer. Thank you and keep up the good work.
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Yep, vascular dementia is indeed a bit different (brain oxygen/blood flow restriction). Sorry to hear about your mom, she is in good hands if you are putting in the extra effort to better understand the condition. Thanks for giving this a read, glad you were able to get something out of it.
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Yep, online when I'm searching for medical info my motto is 'if it isn't peer reviewed move on'... the problem with that is its usually very difficult to read. Thanks for your kind words.
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That's a good motto. There are also good breakdowns of primary literature. Scientific American does nicely. There are many others, as well, trying to cut through the jargon of science writing, and also get passed the dryness and distill out the important factual tidbits. So hopefully your researching doesn't have to happen entirely on pubmed.
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I hear ya! Pubmed has become a bit of go-to I've need to do extensive research so I'm getting quite a bit of practice and it has been very helpful to have knowledge on board when making treatment decisions. So I'll be back...
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This post received a 4.3% upvote from @randowhale thanks to @justtryme90! For more information, click here!
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Great Post...Thanks for sharing this research paper. I can see the beauty of this posts Being the Medicine guy...Alzheimer right now is the common disorder of developed countries occuring in the later years of life. A lot of research is being done about the causes and how to treat Alzheimer's. Still much is needed to be done in this field. Thanks Again for the Informative Post. A doctors' upvote.
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Thanks for reading! Yeah there is still so much that isn't well understood about the biology of this disease. For instance is Abeta really the best target? Just how relevant is the Tau protein? There are a variety of conflicts in the literature which I hope will gel into a more concrete story in the near future.
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https://steemit.com/diabetes/@healthiswealth/doctors-corner-type-3-diabetes-also-known-as-diabetes-of-the-brain
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true ,as it happened in algeria a cure of diabeties was found by a biologist called D ziibet last year ;he was attacked by media and almost been killed now he has sold the medecin to a turkish company
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https://steemit.com/diabetes/@healthiswealth/doctors-corner-type-3-diabetes-also-known-as-diabetes-of-the-brain
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Yeah, right. Uh huh.
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if you dont believe me you can google it
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As usual the pharmaceutical companies will buy the patent and never use it because curing diseases does not bring anything
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https://steemit.com/diabetes/@healthiswealth/doctors-corner-type-3-diabetes-also-known-as-diabetes-of-the-brain
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Not at all true (at least not for all pharma, perhaps it is more true for the larger pharmaceuticals, but there are plenty of smaller ones that work on cures... like mine). This treatment would be pharma's dream anyway. The nanoparticle would need to be continuously taken to prevent the amyloid beta from re-aggregating. That has all the signs of making profits.
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Very interetsing !!!
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Thank you for reading ;)
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Dam someone beat me to "Monkey Monkey, Tree, Look At Me, I'm talking Nonsense!". Oh well, I wonder how long before human trials, it can't come soon enough!
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At minimum at least 5-7 years probably. If pharma picks it up they have to go through a boatload of toxicology studies before a human clinical trial can be initiated and those take forever...
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That would be my guess, pity though, it will be too late for a lot of people.
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Hey - very interesting article. I am also interested in nanotechnology. Lateley I read an article in which they described how to destroy cancer cells using nanoparticles and MRI fields. Very interesting stuff going on.
If you are interested in groundbreaking science stuff: Check out CRISPR Cas 9
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I've worked with Cas 9 :)
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Cool stuff - what do you think, will there be use of it in treating deseases within a reasonable timeframe? (Let's say within the next 5-10 years)? I know that China already started human trials and the USA is about to do so as well in 2017
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Human clinical trials on this compound?
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Yep - in China they already treated people with lounge desease - maybe I will make an article about that ;)
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To use it for a radical oxygen sponge, in chemo therapy correct? Not for potential alzheimers treatment.
Don't know about Lounge disease, yeah you should definitely make a post :D
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Never knew much on the cure of the Alzheimers Disease. Great to see that there are some positive results!
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https://steemit.com/diabetes/@healthiswealth/doctors-corner-type-3-diabetes-also-known-as-diabetes-of-the-brain
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Yeah it's nice. Thanks for taking a look :)
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You're welcome :)
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This is great news! I hope this research gets more funding. It could open a lot of doors and save many lives. I'm sorry you have to see Alzheimers up close. Hopefully, this study is the beginning of something great. I do hope if this ends up being IT, pharmaceutical companies don't attempt to burn through people's pockets.
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https://steemit.com/diabetes/@healthiswealth/doctors-corner-type-3-diabetes-also-known-as-diabetes-of-the-brain
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Thanks. Yeah unfortunately pharma is a for profit business, it's just the nature of capitalism to maximize those profits. Would be nice if we could not do that, but rather just charge a reasonable amount to recoup investment and research costs and turn a small profit. However greed does seem to drive the world...
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Sad but true. Sometimes I wonder if it's the reason why cancer treatment research only start at "promising" for years on end and never progress to anything more. Curing cancer or any expensive disorder is like saying bye bye to big cash.
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Usually not. A lot of promising work doesn't carry over to humans. The reason for this is the vastly differing metabolic enzymes found in us versus other test model animals. So say you have this treatment that looks super promising in a mouse model like this one. For it to be effective you need to establish a working dose concentration of the compound you are using which achieves the desirable effect while minimizes off target effects. Okay having established this in your model you go to try to use it in humans.
A clinical trial begins. You dose people with your drug and... Nothing happens. So you try to titrate the dose up. Nothing happens nothing happens you in crease further... Uh oh, weird side effects happen.
They aren't a problem though, and the desired effect is starting to happen (say a tumor has slowed it's growth for a cancer drug). But it's not enough, for a drug it needs to be superior to current treatments or nobody will use it. So you keep going with trials, upping dosing trying to see what you saw in the model system.
But many times it doesn't happen, side effects get to be too bad, or someone dies in a trial FROM the drug, all because human metabolism is just different. Our livers break drugs down, or modify them in ways which change how they work.
I used to think pharma was withholding drugs (and maybe some do) until I started working for one doing drug discovery. Now I've found that... It's just really hard.
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Thanks for answering that especially in a detailed manner. I'm now utterly curious about your work. I hope breakthroughs in a lot of disorders would happen soon but I suppose it's asking for too much. In any case, I'm still hoping for the best. Thank you for sharing your knowledge.
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Sure, you're welcome. :)
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I am hoping that they will find some sort of good treatment before too long. Don't want to see my dad go through what my grandfather went through.
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Watched my grandmother suffer with this disease. I honestly believe it was harder on all of us then her toward the end, as I don't think she even realized what was going on. Still what she went through early on was awful to watch, she knew her mind was failing her and we were all powerless to help.
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https://steemit.com/diabetes/@healthiswealth/doctors-corner-type-3-diabetes-also-known-as-diabetes-of-the-brain
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Great written article. Would be so good if we can get to a cure for Alzheimer. It'll help a lot of people in a very good way!
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Thanks, yeah I hope that things can progress forward on any of the projects that are on going. So many people and so many families struggle through this disease. It is truly one that effects everyone in a family. Not just the person directly diagnosed with it.
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Absolutely! Maybe even worse for those around the person who have this illness. It is dramatically impacting the lives and can get to your emotions in a bad way as well.
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Nice article, nice paper, nice approach and nice hidden gem. Classic @justtryme90.
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Thanks man ;)
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https://steemit.com/diabetes/@healthiswealth/doctors-corner-type-3-diabetes-also-known-as-diabetes-of-the-brain
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Hello brother, great information. follower
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Thanks!
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I like it.
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Thanks man :)
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I think this is not the first time you write about Alzheimer. Every time I read, I have the impression we may get closer and closer to a breakthrough. Hopefully thus will happen soon enough!
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How many mice were involved in this research? My fiance' has personally done research in this area during her Masters...
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In their materials and methods they state 50 mice. 40 Alzheimers model mice, and 10 Wild type.
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Alzheimer's is stage 3 Diabetes
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No, it's not.
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You have a lot to learn junior. :)
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Suzanne de la Monte, a neuropathologist at Brown University, has been working on these phenomena in humans and rats. When she blocked the path of insulin to rats’ brains, their neurons deteriorated, they became physically disoriented and their brains showed all the signs of Alzheimer’s. The fact that Alzheimer’s can be associated with low levels of insulin in the brain is the reason why increasing numbers of researchers have taken to calling it Type 3 diabetes, or diabetes of the brain.
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Alzheimer's Disease is Type 3 Diabetes: Evidence from Human Studies
This hypothesis was directly investigated by first examining postmortem cases of advanced AD and determining if the neurodegeneration was associated with significant abnormalities in the expression of genes encoding insulin, IGF-1, and IGF-2 peptides, their receptors, and downstream signaling mechanisms.5 In that study, we demonstrated advanced AD to be associated with strikingly reduced levels of insulin and IGF-1 polypeptide and receptor genes in the brain (Figure 1). In addition, all the signaling pathways that mediate insulin and IGF-1-stimulated neuronal survival, tau expression, energy metabolism, and mitochondrial function were perturbed in AD. This study carries additional significance because it established that, like all other pancreatic and intestinal polypeptide genes, the insulin gene was also expressed in the adult human brain. Moreover, the results taught us that endogenous brain deficiencies in insulin, IGF-1, IGF-2, and their corresponding receptors, in the absence of T2DM or obesity, could be linked to the most common form of dementia-associated neurodegeneration in the Western hemisphere. Since the abnormalities identified in the brain were quite similar to the effects of T1DM or T2DM (though none of the patients had either of these diseases), including abnormalities in IGFs,81–83 which are important for islet cell function,84,85 we proposed the concept that AD may represent a brain-specific form of diabetes mellitus and coined the term “type 3 diabetes.”
Source: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2769828/
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Lol, not from you. :)
I learn from intelligent, knowledgeable people. Not people spreading disinformation on the internet. Go spend your time with more gullible people.
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Excuse me?
you don't need to be rude???
I was trying to help you and your followers????
nothing like showing your true colors, I will not be following you.
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Well now you make me feel bad. You were acting like an internet troll, so I treated you like one. Had you actually lead with a rational scientific discussion then I would have treated you becoming of that as well.
On the internet it's difficult to tell, when the poster provides no reasoning, evidence, citations, or general educational demeanor. Perhaps lead with data next time :)
You don't want to follow me? Okay. Thats up to you, I don't ask for followers. I will keep doing my thing either way, as well as I can (which may or may not be good at all, but it's my best.)
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I have been following you for a bit.
I spoke out because I felt your post was a bit inaccurate.
My appologies for coming across as a internet troll.
Keep on STEEMING friend!
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My apologies for being overly defensive as well. I should not have jumped to conclusions.
I'm just trying to summarize articles to the best of my ability. Provide constructive additions and I will do everything I can to help them get exposure on the post. I am by no means a subject expert in all of the papers I discuss (enzymology yes, every disease ever... Nope) so I assume I will not be perfectly accurate by nature. Hopefully I can do better then say... CNN.
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