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A team of Stanford researchers led by Professor Wyss-Coray set out to find out which genes were linked to age-related cognitive decline. Not only did the researchers find the culprit, they were able to reverse cognitive decline and rejuvenate aged mouse brains.

Searching for the cause of cognitive decline

Microglia are immune cells that reside in the brain and spinal cord. These cells mediate immune responses in the central nervous system and act like other macrophages, clearing cellular debris and dead neurons from nervous tissue through the process of phagocytosis (cell eating).


A permanent neural implant that reads brain activity and churns out text could prove to be a valuable medical tool, but it also could provide doctors with an unprecedented 24/7 stream of neural data.

Oxley recognizes that an endless feed of brain activity could be invaluable to medical researchers, but he doesn’t have plans to tap into that yet.

“[The Stentrode is] going to show us information that we hadn’t had before. Whether that helps us understand other things is not what we’re trying to do here,” he said, clarifying that Synchron’s primary goal is to get the new brain-computer interface working so that it can help paralyzed patients. “This is a novel data set, but this raises questions around privacy and security. That’s the patient’s data, and we can’t be mining that.”

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The memory of older people has been returned to the state of someone in their 20s for the first time by applying electrical stimulation to the brain to reconnect faulty circuits.

Scientists at Boston University in the US have proven it is possible to restore working memory by ‘recoupling’ areas of the brain which have become out-of-sync as people grow older.

Short-term working memory is crucial for everyday life, storing information for around 10 — 15 seconds to allow problem solving, reasoning, planning and decision making, allowing someone, for example, to keep a telephone number in mind while writing it down.

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“Why are we impatient? It’s a heritage from our evolution,” says Marc Wittmann, a psychologist at the Institute for Frontier Areas of Psychology and Mental Health in Freiburg, Germany. Impatience made sure we didn’t die from spending too long on a single unrewarding activity. It gave us the impulse to act.


Not long ago I diagnosed myself with the recently identified condition of sidewalk rage. It’s most pronounced when it comes to a certain friend who is a slow walker. Last month, as we sashayed our way to dinner, I found myself biting my tongue, thinking, I have to stop going places with her if I ever want to … get there!

You too can measure yourself on the “Pedestrian Aggressiveness Syndrome Scale,” a tool developed by University of Hawaii psychologist Leon James. While walking in a crowd, do you find yourself “acting in a hostile manner (staring, presenting a mean face, moving closer or faster than expected)” and “enjoying thoughts of violence?”

Slowness rage is not confined to the sidewalk, of course. Slow drivers, slow Internet, slow grocery lines—they all drive us crazy. Even the opening of this article may be going on a little too long for you. So I’ll get to the point. Slow things drive us crazy because the fast pace of society has warped our sense of timing. Things that our great-great-grandparents would have found miraculously efficient now drive us around the bend. Patience is a virtue that’s been vanquished in the Twitter age.

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A revolutionary 60-minute therapy for high blood pressure could allow patients to throw their tablets away for good.

The unlikely remedy involves blasting nerves in the kidneys with sound waves to stop them sending signals to the brain that drive up blood pressure.

It could slash the risk of heart attacks and strokes, two of Britain’s biggest killers.

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Scientists at Stanford University say they’ve devised antibodies that block a specific gene related to brain aging — and that it’s giving old mice the cognitive prowess of younger ones.

“The mice became smarter,” senior author Tony Wyss-Coray said in a statement. “Blocking [the gene] CD22 on their microglia restored their cognitive function to the level of younger mice. CD22 is a new target we think can be exploited for treatment of neurodegenerative diseases.”

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The humble honeybee can use symbols to perform basic maths including addition and subtraction, shows new research published today in the journal Science Advances.

Despite having a brain containing less than one million neurons, the honeybee has recently shown it can manage complex problems – like understanding the concept of zero.

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Through a new approach dubbed AMBAR, the biotechnology company Grifols has attempted to reduce the amount of harmful, Alzheimer’s disease-causing amyloid beta in the brain by collecting it with a blood protein called albumin and draining it out of the bloodstream. This approach differs from the previous antibody and catabody approaches and offers new hope for sufferers of this neurodegenerative disease.

What is Alzheimer’s disease?

Alzheimer’s disease, named after its discoverer, is a slow and progressive disease that causes the degradation of the brains of its sufferers. This leads to memory loss, a decrease in problem-solving abilities, changes in personality, and other symptoms. It is associated with the accumulation of tau and amyloid beta in the brain.

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According to a report in the official magazine of its Defense Ministry, Russian “supersoldiers” are able to use “parapsychology” techniques to crash enemy computers, access the minds of foreign soldiers, and read documents inside locked safes — abilities they gained, according to the article, from telepathic dolphins they can now communicate with.

The report is almost certainly nonsense. But it does raise questions about the ambitions — and perhaps dysfunctions — of Russia’s military.

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