Monthly Archives: October 2012

Mind Hack XV: Cool Techniques And Rules Of Thumb Tips To Increase Your Cognitive Ability And Memory From Joshua Foer

Me: For Mind Hack XV, I found this amazing interview a past memory champion Joshua Foer did on his journey and process to learn the ways and techniques to make one’s mind better at memorization and thinking. I highly recommend the interview since it is very insightful. If you don’t have the time to watch the video, I will outline the major points they bring up in the video.

You can train yourself to do unbelievable feats.The memory champions in memory competition are using their brains differently so you can learn what they are doing..

In Ancient times like in Greece, there were many well known memory techniques and tools for the scholar. We have totally forgotten about these techniques.

Major Technique #1: Creating a memory palace – Most people have terrific spatial memory. If we can use that spatial memory to remember stuff that we actually want to remember, it gives you an extraordinary advantage. The memory palace is an imaginary building in your mind’s eye that you are intimately familiar with. You walk through it in your imagination creating images of the stuff that you wish to remember.

By putting imagery in a specific location in the memory palace, you are attaching it in an order, in a spatial arrangement,

Idea: If you can create images that are so weird, so bizzarre, so strange, gory, raunchy, etc. something that is so emotionally resonant, where you use all of your senses to embrace the image, that will be a memory you will not be able to shake away from your memory.

  • Interesting fact #1: The term “In the first place” actually is referring to the “First Place” in your memory palace.
  • Interesting fact #2: The word “Topic” comes from the Greek word “Topos” which means “place”.

Idea: The things that we remember are the things that are …

  • 1. NEW,
  • 2. STRANGE,
  • 3. UNUSUAL,
  • 4. THINGS THAT MAKE AN IMPRESSION ON US,
  • 5. THINGS THAT GRAB OUR ATTENTION

We can will our brains to remember.

Idea: We can change our brain through memory. Remembering a lot like cab drivers enlarges the hippocampus which is what controls spatial memory.

Our working memory capacity has a clear limit. We can only hold roughly 7 things in our head at one time. The idea and key is then to see how we can package and put as much stuff in those 7 parts as possible.

Chunking – The process of packaging large sets of data and information into smaller parts to make it easier to recall.

Baker-Baker Paradox (from psychology): A person who is asked to remember a guy’s name is Baker is less likely to remember than a guy who is asked to remember that a guy’s profession is a baker. 

The name “Baker” does not mean anything. It is not associated or attached to anything in our memory as a hook. The word Baker however does have something we can associate with. There is a whole network of meaning that the word “baker” is attached with it.

The entire trick to remembering other people’s names is to take their names, turn it into something that they can associate with, in a visual way that would give it more meaning.

Most of the memory techniques uses a concept from psychology called elaborative encoding – You take information and make it memorable by embedding it in other information we already know.

William James – “We structure our experience of time around chronological landmarks” – Exciting things that happen in our life helps shape the passage of time. As we grow older, our lives get less interesting. We are doing less new stuff everyday. Things start to become routine. They become rote….And as a result, time starts to feel like it is flying by….So, literally our life is becoming less memorable.”

Solution: To live a life that is memorable. To do things that are new, different, exotic.

Case with EP (patient): Struck with viral disease that ate away a significant part of his brain, the hippocampus. Lead to him being fully functional except not remembering short term memory and long term memory up to a certain point. Does not even realize that he even has a memory problem. Is content and happy because he can’t remember the past and does not worry about the future.

Memory is very costly due to energy consumption: Brain uses up to around 20% of all the Oxygen and 25% of the glucose that is available in the body. We need memory to shape our perceptions of the present, our ability to make sense of the present, to plan for the future.

Our identity can be defined as our memories. EP could be considered to be an empty vessel and incapable of telling you anything about time.

Thinking is not so much about remembering, but actually about forgetting – processing what things do they not need to remember.

Even at elite memorizing level, everyone has a weakness. Conversely, almost everyone has a great memory for something. Thus, the things that we are fascinated with and become experts in, we develop an extraordinary memory for the details of that field of study.

With great expertise comes memory. People are structuring memory differently. Theya re seeing the world differently. and as a result are remembering better.

True knewledge is having an understanding of the world, make sense of it, find meaning in its structure.

We are probably all better off not having to remember numbers and facts which we can find easily through books and google.

The Latin word inventio is the source or root word for two modern words, invention and inventory.

We should be teaching kids better how their memories work. If you teach kids how to think about thinking, they think better. The principles behind the memory devices and techniques like the memry palace are crucial in helping us do well in the world.

The best way to learn something is to space out the information over time. When we start learning, we will start forgetting.

The single best piece of advice for a person who just wants to improve their memory: The art of remembering is the art of paying attention. To be mindful..

The difference between natural memory and artificial memory – natural memory is what we are born with in terms of raw talent, artificial memory is what we can develop through learning and using structuring for information processing.

Grit and tenaciousness is very good at creating success

The YouTube link where the source is found is HERE


Mind Hack XIV: Top 10 Mistakes To Avoid In Your 20s, For Men – Tim The Right Hand Man – 21 Convention 2010

Me: This is one of those posts which I felt was extremely insightful in its wisdom on how the modern male in Western developed countries should be living his life. As always, this type of advice should never be used as gospel and not questioned but to be critically reviewed for its practically, usefulness, and value.

The reason why I felt this video is so powerful is because it tells us young men still in our 20s how to avoid some of the biggest traps which can sap away our resources. In our 20s, whether we have been to college or graduate school, most men are very busy at trying to achieve, win, and climb the corporate ladder in making a name for themselves in the world. We have the energy, ambition, and motivation to try to, as Steve Jobs put it, “put a dent in the universe”. Whether we ultimate succeed in whatever endeavor we have set for ourselves, that is still need to be proven. However there are some clear decisions we make which will make us far less likely to succeed.

On a side note, I would like to state that in many polls done on people in their 40s, they would say that the #1 decision which will determine the quality of their later years, whether it is in the area of health, finances, or relationships is the person they choose to marry, is they ever do get married ever at all. One’s decision on who will be one’s life partner is far greater in determining one’s happiness and success in life than almost anything else. We find from many reports that divorce is not just an emotional and mental negative event, but also for one’s finances too. So besides the tips that Tim will tell you, I wanted to give 4 tipes of my own.

  • Tip #1: Be extremely careful on who you choose to spend your life with. Your emotional health and financial health will depend on it later on.
  • Tip #2: It is important to realize that the two most common causes for personal bankruptcy is a major health issue racking up healthcare costs or divorce.
  • Tip #3: Having a child is extremely expensive, and be wise about having children.
  • Tip #4: Things become harder to do as one gets older so go ahead in your younger years, go crazy and have fun, and try to reach for one’s dreams. If you want to do something, do it now. You will definitely regret on doing trying it out later in life if you don’t try and go for what you want.

This video is taken from Youtube link HERE


Mind Hack XII: The Power Of Galantamine To Increase Intelligence, Memory, And Just About Every Other Type Of Cognitive Ability

Me: I have recently found out from the website and publication Life-Enhancement about this really powerful supplement product called Galantamine and the articles and information about it is enormous. In my most recent post in Mind Hack XI I showed that IGF-2 dosage can increase memory ability but it seems that the pathway of IGF-2 is actually controlled by Galantamine. I had posted an article from the Nov. 2012 edition of LIfe-Enhancement. If you actually go through the entire LIfe-Enhancement website you will find that there are a lot of articles written about the power of Galantamine. 

Seriously, the entire Life-Enhancement website is FILLED with Galantamine articles and how it improves some form of mental/cognitive ability. From the research on the internet on the effectiveness and ability of galantine supplements, it seems that one of the effects of Galantamine is that gives you more vivid and even lucid dreams. It seems that quite a few studies have been tested on the ability of Galantamine to treat and reduce the effects of Alzheimer’s Disease.

Mind Hack XI: Improve Your Memory Using IGF-2 Injections And Galantamine

Me: I had stated before in a previous Mind Hack post that we can use creatine to improve intelligence by upwards of even 15 IQ points. Now from my research on IGF-2 I have found a few articles an studies down in 2011 that showed that mice which had IGF-2 injected into their hippocampus had increased levels of memory.

Further Analysis: It is really amazing since IGF-2 is one of the few molecules that can actually cross the blood brain barrier. It is suggested that a clinical way of getting humans to take it is through intra-nosal approach. To get the IGF-2 to actually work, it must “coincides with a stage in the learning process called “memory consolidation.” That’s a poorly understood transition period when a memory is still malleable but becoming more established and robust.” It is

From Live Science, Nature, ISSNAF, Science Illustrated, Science Mag, Life-Enhancement

The article post below is from the LIfe-Enhancement link…

Better for your neurons in 3 ways …Galantamine protects, stimulates,and improves memory… through elevation of insulin-like growth factor 2 By Will Block

Intelligence is the wife, imagination is the mistress, memory is the servant.— Victor Hugo, Post-scriptum de ma vie (1901)

Insulin-like growth factor 2 (IGF2) significantly enhances memory retention and prevents forgetting. That’s what researchers reporting in Nature found last year.1IGF2 is known to be important in body growth and development, but its role in the adult brain has not been established. While highly expressed in the hippocampus, Alberini and colleagues (the authors of the Nature paper) showed that in this region IGF2 has a crucial role in memory consolidation and can make memories last longer.

Using what is known as inhibitory avoidance learning training—a hippocampus-depend­ent learning task that measures fear memory—the researchers placed rats in an environment where upon entering dark areas the rats received a shock to the feet. Their fear memory was enhanced as they learned to avoid the dark areas (into which they are naturally inclined to enter), and this in turn led to an increase in the hippocampal expression of IGF2.

The creation of this IGF2 requires the transcription factor CCAAT enhancer binding protein β,* which is also essential for memory consolidation. Furthermore, injections of recombinant IGF2 into the hippocampus, after either training or memory retrieval, significantly enhanced memory retention and prevented forgetting.


* CCAAT-enhancer-binding proteins are a family of transcription factors, composed of six members that promote the expression of certain genes through interaction with their promoter. Once bound to DNA, these transcription facts can recruit so-called co-activators that, in turn, can open up chromatin structure or recruit basal transcription factors. They are involved in different cellular responses, such as in the control of cellular proliferation, growth, and differentiation, metabolism, immunity, and memory enhancement.


The time factor for efficacy

To be effective, IGF2 needs to be administered within a sensitive period for memory consolidation. IGF2-dependent memory enhancement requires IGF2 receptors, new protein synthesis, the function of activity-regulated cytoskeletal-associated protein, andglycogen-synthase kinase 3 (GSK3). This is intriguing because GSK3 is a regulatory kinase that is implicated in a number of diseases, including type 2 diabetes, Alzheimer’s disease, inflammation, cancer, and bipolar disorder. In hippocampal slices, IGF2 promotes IGF2 receptor-dependent, persistent long-term potentiation after weak synaptic stimulation. Thus, IGF2 may represent a novel target for cognitive enhancement therapies.

Galantamine significantly increases IGF2

In a new study conducted in Japan, researchers examined the effects of acutegalantamine treatment on the mRNA levels of neurotrophic growth factors in the mouse hippocampus and prefrontal cortex.2

The systemic administration of galantamine at doses of 0.3–3 mg/kg (for 3/mg/kg, the human equivalent is 21 mg for a 187 lb person) caused a significant increase in IGF2 mRNA levels in the hippocampus, but not in the prefrontal cortex. The effect of galantamine was also observed at the protein level. IGF2 promotes cell growth, survival, migration, and differentiation and plays an important role in normal fetal development.


IGF2 significantly enhances memory retention and prevents forgetting.

IGF2 increases memory consolidation in rats

In the study cited above,1 it was shown that inhibitory avoidance learning led to an increase in hippocampal expression of IGF2, closely linking to memory consolidation in rats. The researchers showed that injection of recombinant IGF2 into the hippocampus after either training or memory retrieval enhanced memory retention and prevented forgetting. They also showed that IGF2 promoted IGF2 receptor-dependent persistent long-term potentiation after weak synaptic stimulation in the rat hippocampal slices.

Three-way neuronal help

Thus, IGF2 has been implicated in cognitive function associated with the hippocampus. In addition, another study recently demonstrated that IGF2 is an important regulator of adult hippocampal neurogenesis.3 As the authors of the Japanese galantamine/IGF2 study2 observed in a separate experiment, acute galantamine treatment (3 mg/kg) increased newly divided cell proliferation in the hippocampal dentate gyrus of mice 24 hours after the injection (unpublished).


IGF2 has a crucial role in memory consolidation and can make memories last longer.

When taken together, the present finding implies that galantamine: 1) protects neurons, 2) stimulates neurogenesis, and 3) improves cognitive dysfunction in Alzheimer’s disease via its action on IGF2 expression.

The researchers also observed that the higher dose of galantamine (3 mg/kg) caused a transient increase in fibroblast growth factor 2 (FGF2) mRNA level and a decrease inbrain-derived neurotrophic factor (BDNF) mRNA level in the hippocampus of mice. The exact reason for these effects is not known, but previous studies show that nicotine ornicotine acetylcholine receptor (nAChR) agonists increase the expression of FGF2 and decrease the expression of BDNF in the hippocampus.

What is suggested, however, is that the galantamine-induced changes in FGF2 and BDNF mRNA levels may be due to its action on nAChR, although galantamine even at low doses binds allosterically to nAChR and potentiates its function which is to make acetylcholine perform better.With regard to the effect of galantamine on BDNF levels, the Japanese researchers reported that galantamine increases phosphorylation of BDNF’s trkB receptor and transcription factor CREB in the mouse hippocampus. Thus, it is thought unlikely that galantamine-induced reduction in the BDNF mRNA levels per se is involved in the facilitation of hippocampal neurotrophin signaling.


† CREB (cAMP response element-binding protein) is a cellular transcription factor. It binds to certain DNA sequences called cAMP response elements (CRE), thereby increasing or decreasing the transcription of the downstream genes. cAMP (cyclic adenosine monophosphate) is a second messenger important in many biological processes.


Other signals that are not involved

Among the neurotrophic/growth factors examined in the study, galantamine did not affect NGF, VEGF, or IGF1 mRNA levels in the hippocampus and prefrontal cortex. Thus, these factors may not act as the downstream signals of galantamine in either brain region.


Galantamine 1) protects neurons, 2) stimulates neurogenesis, and 3) improves cognitive dysfunction in Alzheimer’s disease via its action on IGF2 expression.


Previous in vitro studies have shown that galantamine is an allosterically potentiating ligand of nAChR. In fact, the nAChR-modulating properties play a key role in the effects of galantamine, while muscarinic acetylcholine receptor (mAChR) activation contributes at least partly to the antipsychotic effect and improvement of cognitive dysfunction by galantamine in rodents.

Antagonists and agonists

The present study2 found that both a nonselective nAChR antagonist and a selective α7 nAChR antagonist block the galantamine-induced increase in hippocampal IGF2 mRNA levels. But, it is not blocked by a preferential M1 mAChR antagonist.


These findings suggest that α7 nAChR is involved in the increasing effect of galantamine on IGF2 expression.


Moreover, the injection of a selective α7 nAChR agonist, at doses of 0.3 and 1 mg/kg increased IGF2 mRNA levels in the hippocampus. These findings suggest that α7 nAChR is involved in the increasing effect of galantamine on IGF2 expression.


In contrast to galantamine, donepezil did not affect IGF2 mRNA levels in the hippocampus.

Getting the dose right

Concerning the effect of the selective α7 nAChR agonist, others have reported that its injection at doses of 1 mg/kg, but not 0.3 mg/kg, improved the performance of rats in the novel object recognition test and much higher doses (0.3 and 1 mg/kg, intravenously) reversed amphetamine-induced auditory gating deficits in rats. The apparent difference in the effect of this agonist at 0.3 mg/kg between the behavioral and biochemical studies may be due to the difference in pharmacokinetics of the drug between rats and mice. Rats have twice the surface area of mice, and this difference determines the right dose.

Donepezil, another inhibitor of acetylcholinesterase, fails

In another study,4 the effect of donepezil was also examined to study the role of galantamine as an allosterically potentiating ligand of nAChR. Donepezil, an inhibitor of acetylcholinesterase, increases extracellular levels of acetylcholine (ACh), which interacts with the α7 nAChR as well, but is not an allosterically potentiating ligand of nAChR.


Galantamine increases hippocampal IGF2 mRNA levels in a dose-dependent manner.

In contrast to galantamine, donepezil did not affect IGF2 mRNA levels in the hippocampus. This difference may be explained by the evidence that ACh has a lower affinity for the α7 nAChR compared to the α7 nAChR agonist references above, and that galantamine is an allosterically potentiating ligand of nAChR.


The present finding suggests that the effect of galantamine on hippocampal IGF2 levels may contribute to the mechanism for its neuroprotective and neurogenesis effects.

Recalling the music of memory

In conclusion, the Japanese researchers found that acute administration of galantamine increases hippocampal IGF2 mRNA levels in a dose-dependent manner. Their study suggests that the galantamine-induced increase in the hippocampal IGF2 mRNA and protein levels is mediated by the α7 nAChR. Recall that IGF2 has been implicated in cell growth and survival, and hippocampus-associated function. Consequently, the present finding suggests that the effect of galantamine on hippocampal IGF2 levels may contribute to the mechanism for its neuro­rotection or neurogenesis. This may be why people taking galantamine like they way that they feel, and that one musician who was forgetting certain music chords that he had known by heart for years, brought back those chords, instrumental to his music, with galantamine.

References

  1. Chen DY, Stern SA, Garcia-Osta A, Saunier-Rebori B, Pollonini G, Bambah-Mukku D, Blitzer RD, Alberini CM. A critical role for IGF-II in memory consolidation and enhancement. Nature 2011 Jan 27;469(7331):491-7.
  2. Kita Y, Ago Y, Takano E, Fukada A, Takuma K, Matsuda T. Galantamine increases hippocampal insulin-like growth factor 2 expression via α7 nicotinic acetylcholine receptors in mice. Psychopharmacology (Berl). 2012 Aug 30. [Epub ahead of print]
  3. Bracko O, Singer T, Aigner S, Knobloch M, Winner B, Ray J, Clemenson GD Jr, Suh H, Couillard-Despres S, Aigner L, Gage FH, Jessberger S. Gene expression profiling of neural stem cells and their neuronal progeny reveals IGF2 as a regulator of adult hippocampal neurogenesis. J Neurosci 2012 Mar 7;32(10):3376-87.
  4. Koda K, Ago Y, Kawasaki T, Hashimoto H, Baba A, Matsuda T. Galantamine and donepezil differently affect isolation rearing-induced deficits of prepulse inhibition in mice. Psychopharmacology (Berl) 2008;196:293–301.

Will Block is the publisher and editorial director of Life Enhancement magazine.

The interview below is taken from the ISSNAF link.

CRISTINA ALBERINI AWARDED THE DEAN’S AWARD FOR EXCELLENCE IN BASIC SCIENCE RESEARCH
May 2011 – Cristina Alberini, Professor in Neuroscience, Psychiatry and Structural and Chemical Biology at Mount Sinai School of Medicine in New York was awarded the Dean’s Award for Excellence in Basic Science Research. Earlier this year, the discovery of the IGF-II protein in the hippocampus earned her the cover on “Nature”. For Dr Alberini’s interviewCristina Alberini Awarded the Dean’s Award for Excellence in Basic Science Research

Cristina Alberini is a graduate in Biological Sciences at the University of Pavia and received her doctorate in Immunology at the University of Genoa. After holding positions at the Dana Farber Cancer Institute, Harvard Medical School in Boston, Columbia University in New York, the University of Brescia, and Brown University in Providence, Alberini has been Faculty at Mount Sinai School of Medicine  since 2001, where she currently is Professor in Neuroscience, Psychiatry and Structural and Chemical Biology. Among many other acknowledgments, Alberini received the Golgi prize in 2009. This year, she received a 300,000$ grant from the McKnight Endowment Fund for Neuroscience for a three year study on the Role of Astrocytes in Memory and Cognitive Disorders and the discovery of the IGF-II protein in the hippocampus earned her the cover on “Nature”.

Dr Alberini, what is the focus of your research?

I have now focused my interest on how the brain changes in response to external and internal stimuli.  In particular, I am intrigued by how memories are formed, stored and elaborated.  Memory is a fundamental biological function and a critical component of our identity. As such, it involves our brain, mind and psyche. I am interested in exploring the biological mechanisms underlying memory formation.  I am also interested in applying this knowledge to understand how memory becomes an integral part of pathologies such as addiction and trauma and how we can combat memory decay and memory loss.

 

Is IGF2 a growth promoting hormone during gestation? How did you realize that this hormone could be related with memory?

IGF2 is a growth factor that promotes growth during gestation; targeted deletion of IGF2 inhibits growth whereas over-expression of IGF2 promotes growth.

We have been studying the biological changes after learning and required for long-term memory formation in a brain region called the hippocampus. This region is important for the formation of long-term memory. We found that IGF2 levels are regulated by learning in the hippocampus. IGF-II is regulated as a target protein of a pathway that we know to be essential for memory formation. This pathway is the cAMP-response element binding protein – CCAAT enhancer binding protein (CREB-C/EBP), which are proteins that are necessary for the production of other new proteins, like IGF2.  Therefore, we identified a new function for IGF-II in the adult brain.
How did you inject IGF-II in the hippocampus? Are you going to try others methods in clinical tests?

We use a rat model in our lab. To deliver IGF2 into the hippocampus, we implant bilateral cannulae, which allow us to directly inject IGF2 acutely into a targeted brain region.

We are planning to try systemic injections as well as intra-nasal administrations of IGF2. As IGF-2 is one of the factors that readily cross the blood brain barrier, systemic (e.g.subcutaneous) administration of IGF2 would deliver IGF2 to the brain. Intranasal administration will also readily bypass the blood brain barrier, which is the structural barrier of that protects our brain from foreign substances in the blood.
Could you explain how memory consolidation works and how IGF-II is important to enhances memory?

Memory consolidation is the process through which newly learned information becomes long-term. If new  information we encounter is important it will become a long-term memory.  The new memory remains fragile and sensitive to disruption for some time, but over a day or two it becomes stronger and resilient to disruption. This process is the process of consolidation, that is the process that stabilizes a long-term memory. This process depends on the synthesis of new proteins. In our lab we are interested in identifying these newly synthesized proteins that are essential for long-term memory formation. We found IGF2 to be one of these newly synthesized proteins. First we found that the levels of IGF2 increase in the hippocampus after learning, and disrupting the new synthesis of IGF2 impairs the formation of long-term memory. Furthermore, we found that if we give IGF2 after learning, memory is significantly enhanced.  The enhancing effect is only seen if we administer IGF-II during the “active” period of memory: right after learning or after memory is retrieved. Retrieval (or recall) in fact reactivates the memory.  The active phase after memory retrieval is the reconsolidation phase, during which the memory is again labile for some time and restabilizes over time.
In your opinion, why IGF2 could represent a novel target for cognitive enhancement?

IGF2 is a physiological factor that’s produced is our body, so we don’t predict too serious problems with rejecting exogenously administered IGF2 or toxicity. However, careful studies need to be done to exclude that there are unwanted effects and to prove that the treatment is safe.  Since we found that even under an acute administration (single injection of IGF-2) after learning or memory retrieval, memory is robustly and persistently enhanced and forgetting prevented, it represents a simpler and easy to follow clinical regiment (it does not require multiple or chronic treatments) and would presumably also minimize side effects. Lastly, as I mentioned earlier, IGF2 readily crosses the blood brain barrier, so the route of administration won’t hinder its clinical applicability.

Increase Height And Grow Taller Through IGF-2 Localized Injections. (BREAKTHROUGH?)

Me: This is the first article I have posted that showed that using IGF-2 will also lead to longitudinal growth. The authors Zhang and Yokota are the same guys who have been doing the mice hind limb loading tests. This study showed that if you make a localized injection of IGF-2 in the distal epiphysis femur region you would get about an increase of 1.6-1.7% in length. The dosage of IGF-2 was 100 μg/kg/day for 5 consecutive days. Bone samples were taken after 14 days for analysis. The cause is the upregulated phosphorylation of an extracellular signal-regulated kinase in the treated femur.

Further Analysis: It is important to note that the purpose of the study was to see whether there was a way to correct for limb length discrepancies. Two things to note is the life expectancy and age at which mice will stop growing. Mice usually live 1-3 years, but the records have them at 5 years. Assume that mice live usually 2-3 years. The time they stop growing I’ve researched and the numbers seem to suggest that they can stop growing around 4-5 months or as early as 2-3 months. I would assume that the mice tested in the study at 8 weeks still had some growing to do. What is interesting is that the hormone was injected into the bone, specifically the epiphysis, but NOT the growth plate. I would guess that an IGF-2 Injection into the epiphysis while a patient goes through limb lengthening surgery will lead to a faster distraction rate. What I really wonder is whether the mice’s limb grew by themselves or was the lengthening a part of the greater speed of the growth plates which would still be there.

Overall the IGf-2 has been shown to be a really good supplement for muscle mass building, increased energy, and sexual enhancement and drive.

Places to get IGF-2: Bodybuilding.Com, MassNutrition.com, NutraPlanet.com, PredatorNutrition.com, StrongNutrition.com.  These places are only for the oral intake supplement variety of IGF-2 which would not work if you are already physically mature. The cost ranges from usually $40-$60 . However I don’t see any issues with grinding up the pill, mixing it with a saline compound and injecting it into the localized epiphysis area. I personally would try to get some mice from my local pet store, grow them to 1 years age, and repeat this experiment to see what would happen to their limbs with the IGF-2 injections. I know of many bodybuilders who inject themselves intravenously or Intramuscular with liquid IGF-2 and I would wonder where they got the liquid version. For our purposes we would have to get into the very bone to the center.

From PubMed study link HERE

J Chin Med Assoc. 2012 Oct;75(10):494-500. doi: 10.1016/j.jcma.2012.07.009. Epub 2012 Sep 28.

Lengthening of mouse hind limbs with local administration of insulin-like growth factor 2.

Zhang P, Jiang C, Yokota H.

Source

Biomedical Engineering, Indiana University Purdue University, Indianapolis, Indiana, USA; School of Basic Medical Sciences, Tianjin Medical University, Tianjin, China; Anatomy and Cell Biology, Indiana University School of Medicine, Indianapolis, Indiana, USA. Electronic address: pizhang@iupui.edu.

Abstract

BACKGROUND:

For devising potential clinical approaches for limb length discrepancies, we examined local administration of insulin-like growth factor 2 (IGF2).

METHODS:

C57/BL/6 mice (∼ 8 weeks old) were used in this study, and the mice were separated into two groups: an IGF2-treated group and a placebo group. In the IGF2-treated group, IGF2 was locally administered into the distal epiphysis of the left femur, and the right femur was used as a contralateral control. In the placebo group, saline was administered to the left femur as a vehicle control. The left and right tibiae, without any direct intervention, were employed as negative controls. The dosage of IGF2 was 100 μg/kg/day for 5 consecutive days, and bone samples were harvested on Day 14. Microcomputed tomography images did not show any anomaly at the IGF2 or saline injection sites.

RESULTS:

In comparison with the vehicle control as well as the contralateral control, the results revealed that IGF2 significantly lengthened the treated femur, with an elevation of bone mineral density (BMD) as well as bone mineral content (BMC). The increase in the femoral length of the IGF2-treated left limb was 1.6% (p < 0.05) to the vehicle control, and 1.7% (p < 0.05) to the contralateral control. However, the length, BMD, and BMC of the tibiae were not affected by administration of IGF2 or saline. Western blotting analysis demonstrated that this administration of IGF2 upregulated phosphorylation of an extracellular signal-regulated kinase in the treated femur.

CONCLUSION:

The current study supports for the first time the potential effectiveness of administration of IGF2 in adjusting limb length discrepancy.

Copyright © 2012. Published by Elsevier B.V.

PMID: 23089400    [PubMed – in process]