House of Mind

"Biology gives you a brain. Life turns it into a mind" - Jeffrey Eugenides

  • 15th May
    2013
  • 15
NIH Details Impact of 2013 Sequester Cuts

After weeks of worrying about how the mandatory across-the-board 2013 budget cuts known as the sequester would play out at the National Institutes of Health (NIH), the biomedical research community now has final figures. The bottom line is as grim as expected: The agency’s overall budget will fall by $1.55 billion compared to 2012, to $29.15 billion, a cut of about 5%, according to an NIH notice today. That is essentially what NIH predicted as part of the 5.1% sequestration.

As a result, NIH expects to fund 8283 new and competing research grants this year, a drop of 703, according to this table. That number firms up the “hundreds fewer” awards that NIH officials warned of earlier this year. Including ongoing (already awarded) grants that are ending, the total number of research grants will drop by 1357 to 34,902 awards. The decline “reflects the fact that NIH’s budget is being shrunk due to the new budget and political reality, which is bad news for researchers and the patients they are trying to help,” says Tony Mazzaschi of the Association of American Medical Colleges in Washington, D.C.

NIH will try to keep the size of the average award consistent with 2012; it will not award inflationary increases for future years. The agency also expects to trim continuing grants. Grants that were cut up to 10% earlier this year because of budget uncertainty “may be partially restored,” but probably not to the original commitment level, NIH’s notice says.

To be honest, when I read this article my heart dropped a little because it highlights one of the harsh realities that people in science would rather not think/talk about. I’ve always felt it was a privilege to be able to do science with federal funds but this is still disappointing. I can’t help but think how much harder getting a PhD and a postdoc is going to be :( However, I understand that sometimes you just gotta do what you gotta do and cut corners when and where you have to.

Science is not for the faint of heart. You’ve been warned. 

  • 5th May
    2013
  • 05

Terminal Lucidity

I was introduced to this concept last week while I was attending the funeral of someone who was thought to have experienced this during his last day alive. I visited the home where he passed away and was told that the nurses and family members were in awe of his passing because he had become “another person” during his last days of life. Some aspects of his memory seemed to have come back and he was more lively that he had been in awhile. I had never heard of such phenomena and decided to look into it. Below are some of the things I found. 

Terminal lucidity refers to the unexpected return of mental clarity and memory shortly before death in patients suffering from severe psychiatric and neurological disorders. This return of mental clarity usually occurs in the last minutes, hours of days before the patient’s death. Examples include case reports of patients suffering from tumors, strokes, meningitis, dementia or Alzeheimer’s disease, schizophrenia, and affective disorders. This is particularly striking considering that many of these disorders are caused by degeneration and degradation of the cerebral cortex, hippocampus, and other brain areas that are involved in memory and cognition processes. 

Several accounts suggest that during terminal lucidity, memory and cognitive abilities may function by neurologic processes that differ from those of the normal brain. So far the assumption is that the improvement of brain disorders or dysfunctions is caused by the altered brain physiology of the dying. There are two ways in which terminal lucidity is thought to exist: the severity of mental disturbance can improve slowly in conjuction with the decline of body vitality (typically schizophrenia cases) or full mental clarity may appear abruptly and unexpectedly shortly before death (more common in dementia cases). Although terminal lucidity has not been attributed to a specific medical cause, some authors have suggested that a high fever prior to dying might induce terminal lucidity.

Although terminal lucidity has been reported for around 250 years, it has received little medical attention because of its complexity and transience. Not to mention the ethical guidelines for the responsible conduct of research and the fact that these patients are  already mentally ill, making it even more difficult to include them in empirical studies. Academic interest in terminal lucidity declined after the mid-19th century. However, in 1975, Turetskaia and Romanenko published a detailed article concerning 3 cases of schizophrenic patients in a medical journal. According to Nahm and Greyson, this article is the only publication on terminal lucidity and mental disorders in medical journals throughout the 20th century. However, within the last few years interest in terminal lucidity in mental disorders has increased again due to recent case reports published by Brayne et. al (2008) and Grosso (2004) (see reviews below). 

The authors’ goal is to stimulate research on the pathophysiology of terminal states. For example, research on terminal lucidity could help elucidate the factors influencing the relationship between the mind and the brain, particularly as the brain deteriorates. Moreover, it could further understanding of memory and cognition processes and facilitate the development of new therapies aimed towards reversing the loss of memory and cognitive function in these patients. 

Sources: 

Nahm, M., Greyson, B., Kelly, EW., & Haraldsson, E.  (2012). Terminal Lucidity: A review and case collection. Archives of Gerontology and Geriatrics, 55:138–142.

Nahm, M., and Greyson, B. (2009). Terminal Lucidity in Patients With Chronic Schizophrenia and Dementia: A survey of the literature. Journal of Nervous and Mental Disease, 197 (12): 942-4. 

  • 13th March
    2013
  • 13

Inside the NYU Community Brain Fair

Hi guys! 

Just wanted to give you an update regarding the NYU Community Brain Fair and NYC Brain Awareness Week… In regards to the Brain Fair, we’re still here! So feel free to drop by and visit one of our many exhibits. Topics covered include : History of Neuroscience, Top 10 Brain Myths, Famous Brains (think H.M., Oliver Sacks, and Chuck Close), Chemical Senses, Alzheimer’s Disease, Parkinson’s Disease, Addiction Pathways, Caloric Sensing in Flies, Neuroeconomics and Neuropsychology. The Neuroanatomy table even has real human brains on display for the oddly curious :) 

Other hands-on exhibits include risk discounting games, optical illusions the jelly bean flavor experiment, observing C. elegans mutants under the microscope, and playing a reward related game that resembles beer pong! 

Also, we tried to have something for everyone and we even have a Kids table with (anatomically correct) brain hats, arts and crafts, brain mazes, etc… 

If you can’t make it, that’s ok! Click here  for other braiNY events you can make it to. 

Pictures coming later! 

  • 8th March
    2013
  • 08
Brain Awareness Week in NYC (March 9-17, 2013)
Starts tomorrow at the AMNH with the Food and the Brain exhibit :) Throughout next week, multiple institutions and research groups have joined forces in promoting outreach efforts and making our field more accessible (and fun) to the general public. Chances are, whatever your interest may be, somebody will be able to talk to you about it. So get out there and start learning! In addition, think of it as a networking opportunity; especially if you are interested in applying to grad school. 
Also, NYU’s Neuroscience department will be hosting a special brain fair in which all are welcome. Stop by and you might even meet me in person. I’ll be at the Chemical Senses table :) 

Brain Awareness Week in NYC (March 9-17, 2013)

Starts tomorrow at the AMNH with the Food and the Brain exhibit :) Throughout next week, multiple institutions and research groups have joined forces in promoting outreach efforts and making our field more accessible (and fun) to the general public. Chances are, whatever your interest may be, somebody will be able to talk to you about it. So get out there and start learning! In addition, think of it as a networking opportunity; especially if you are interested in applying to grad school. 

Also, NYU’s Neuroscience department will be hosting a special brain fair in which all are welcome. Stop by and you might even meet me in person. I’ll be at the Chemical Senses table :) 

  • 21st November
    2012
  • 21
ohyeahdevelopmentalbiology:

fuckyeahneuroscience:

Scientists Identify Gene Required for Nerve Regeneration | Sci-News.com
A gene that is associated with regeneration of injured nerve cells has been identified by a team of researchers led by Prof Melissa Rolls of Penn State University.
The team has found that a mutation in a single gene can entirely shut down the process by which axons – the parts of the nerve cell that are responsible for sending signals to other cells – regrow themselves after being cut or damaged.
“We are hopeful that this discovery will open the door to new research related to spinal-cord and other neurological disorders in humans,” said Prof Rolls, who co-authored a paper published online in the journal Cell Reports.
“Axons, which form long bundles extending out from nerve cells, ideally survive throughout an animal’s lifetime. To be able to survive, nerve cells need to be resilient and, in the event of injury or simple wear and tear, some can repair damage by growing new axons,” Prof Rolls explained.
Previous studies suggested that microtubules – the intracellular ‘highways’ along which basic building blocks are transported – might need to be rebuilt as an important step in this type of repair.
“In many ways this idea makes sense: in order to grow a new part of a nerve, raw materials will be needed, and the microtubule highways will need to be organized to take the new materials to the site of growth,” Prof Rolls said.
The team therefore started to investigate the role of microtubule-remodeling proteins in axon regrowth after injury. In particular, they focused on a set of proteins that sever microtubules into small pieces. Out of this set, a protein named spastin emerged as a key player in axon regeneration.
Above: In fruit flies with two normal copies of the spastin gene, a team of scientists led by Prof Melissa Rolls of Penn State University found that severed axons were able to regenerate. However, in fruit flies with two or even only one abnormal spastin gene, the severed axons were not able to regenerate (Melissa Rolls / Penn State University)

Original paper here. 

ohyeahdevelopmentalbiology:

fuckyeahneuroscience:

Scientists Identify Gene Required for Nerve Regeneration | Sci-News.com

A gene that is associated with regeneration of injured nerve cells has been identified by a team of researchers led by Prof Melissa Rolls of Penn State University.

The team has found that a mutation in a single gene can entirely shut down the process by which axons – the parts of the nerve cell that are responsible for sending signals to other cells – regrow themselves after being cut or damaged.

“We are hopeful that this discovery will open the door to new research related to spinal-cord and other neurological disorders in humans,” said Prof Rolls, who co-authored a paper published online in the journal Cell Reports.

“Axons, which form long bundles extending out from nerve cells, ideally survive throughout an animal’s lifetime. To be able to survive, nerve cells need to be resilient and, in the event of injury or simple wear and tear, some can repair damage by growing new axons,” Prof Rolls explained.

Previous studies suggested that microtubules – the intracellular ‘highways’ along which basic building blocks are transported – might need to be rebuilt as an important step in this type of repair.

“In many ways this idea makes sense: in order to grow a new part of a nerve, raw materials will be needed, and the microtubule highways will need to be organized to take the new materials to the site of growth,” Prof Rolls said.

The team therefore started to investigate the role of microtubule-remodeling proteins in axon regrowth after injury. In particular, they focused on a set of proteins that sever microtubules into small pieces. Out of this set, a protein named spastin emerged as a key player in axon regeneration.

Above: In fruit flies with two normal copies of the spastin gene, a team of scientists led by Prof Melissa Rolls of Penn State University found that severed axons were able to regenerate. However, in fruit flies with two or even only one abnormal spastin gene, the severed axons were not able to regenerate (Melissa Rolls / Penn State University)

Original paper here

  • 20th November
    2012
  • 20
Is Medical Science Built on Shaky Foundations?

Replication of empirical findings is the cornerstone of science. To me, reproducibility of the data is actually a qualifier for an experiment/project to be considered “science”. However, multiple groups are finding something that makes me and many other members of the scientific community REALLY uncomfortable- failure to replicate experimental results published in top tier journals such as Nature

The whistle blowing has primarily been done by pharmaceutical companies like Bayer or Amgen that scour published literature for promising leads. These companies search the literature for novel models, mechanisms, and tools published by top labs (usually because of scientific reputation) and try to build on their work. In many cases, this results in a dead end, as an alarmingly high number of publications are not reproducible and result in the loss of thousands or even millions of dollars. And to think that the money could be spent on making real progress towards drug development…

The article above mentions some of the possible factors contributing to this situation. First, experimental methods rarely control for all possible variables. Limited funding also  puts pressure on the PIs push out “good” results for publication before conducting replication experiments and many times reviewers don’t ask for replication experiments. There is also the possibility that some groups provide the minimum amount of information necessary for publication because they are competing with other labs and are trying to safeguard their experimental procedures. Then we have experimenter bias: they see what they want to see and make a case for it. Finally, failed replications are seldom published, which means that if a group can’t replicate the results they will probably keep it to themselves instead of publishing discrepant results. 

Clearly, “failure to replicate” is a time-consuming, frustrating and costly process. Elizabeth Iorns, co-founder/CEO of the Science Exchange and the author of the linked article, has partnered up to create the Reproducibility Initiative-a new program to identify and reward high quality reproducible research. Here,  results can be submitted for independent validation to more than 1000 expert experimental providers. Validations are conducted blind, on a fee-for-service basis. This is an interesting approach, but will it really solve anything? For example, the initiative is on a voluntary basis (researchers submit work they want to see replicated) and scientists would have to pay to have their results replicated, which seems like an additional cost that not many scientists would be willing to add to their expenses. Moreover, who will these “replication experimenters” be? I can think of more than one situation in which it may result in a conflict of interest. Will they be made publicly known, do you get assigned a group or do can you pick who gets to replicate your work? Last but not least, what if the results are not reproducible? Will there be a way of making this publicly known or will it just be swept under the rug like nowadays?