Tuesday, February 16, 2021

Oxygen Deficit Makes Nerve Cells Grow

Summary: Mentally and physically demanding tasks trigger functional hypoxia across the brain. This oxygen shortage activates Epo, which stimulates the growth of new neurons and synapses.

Source: Max Planck Institute

Oxygen deficit, also called hypoxia, in the brain is actually an absolute state of emergency and can permanently damage nerve cells. Nevertheless, there is growing evidence that to a certain extent, hypoxia can also be an important signal for growth.

Together with scientists from the University Hospitals of Copenhagen and Hamburg-Eppendorf, researchers from the Max Planck Institute for Experimental Medicine in Göttingen have shown in mice that mentally and physically demanding activity triggers not only a local but also a brain-wide ‘functional hypoxia’. Although in an attenuated form, the effects are similar to oxygen deprivation.

The shortage of oxygen activates, among other things, the growth factor erythropoietin (Epo), which stimulates the formation of new synapses and nerve cells. This mechanism could explain why physical and mental training have a positive effect on mental performance into old age.

Last year, researchers at the Max Planck Institute in Göttingen found out in experiments in animal studies with mice that mentally and physically demanding activities trigger a slight oxygen deficit in certain brain regions. This ultimately leads to the formation of new nerve cells. They observed that hypoxia activates the growth factor erythropoietin (Epo) in the brain. Although it is known primarily for its stimulating effect on red blood cells, Epo also promotes the formation of nerve cells and their networking in the brain.

In a new study, the research group examined in detail which brain regions and cell types are affected by the shortage of oxygen. To do this, they used genetically modified mice that produce a molecule throughout the brain that leads to the formation of a fluorescent dye when there is an oxygen deficit. In order to challenge the mice both mentally and physically, the researchers let them run on specially prepared running wheels for several days.

The mice had to concentrate while running on these wheels to avoid stumbling in addition to being physically exerted. Mice that had no access to a running wheel and mice exposed to oxygen-depleted air served as comparator groups. The researchers also examined the activation of genes in different brain regions and cell populations in order to find out how the brain reacts to activity-induced hypoxia.

Change in gene activity

In fact, running wheel training had effects similar to reducing the oxygen content in the air we breathe. In both cases, the change in the activity of many genes was similar, and a mild oxygen deficit occurred throughout the brain.

However, there were major differences between different cell types: nerve cells were particularly affected, whereas the glial cells (auxiliary cells of the neurons) were only slightly affected. In addition, the Epo gene in the brain, together with a number of other genes, is particularly stimulated during both mental and physical activity.

“We still don’t know whether mild hypoxia as a result of activity also leads to stronger networking of nerve cells – and even to their formation – in humans. We therefore want to carry out similar studies on humans – for example on test subjects who are active on exercise bikes”, says Hannelore Ehrenreich, head of the study. The findings could ultimately benefit patients with neurodegenerative diseases in which nerve cells die or lose synapses.

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Monday, June 24, 2019

New method found to inhibit Parkinson’s disease

Contrary to earlier discovery that a chemical found in a synthetic opioid, MPTP, induced a form of Parkinson's disease, a new study has found that it is an enzyme in the body that can metabolise compounds formed in the brain from alkaloids causing a neurodegenerative condition in mice.

The study  suggested that the enzyme, mitochondrial CYP2D6, presents a potentially powerful new target for Parkinson's treatment. "Over the past two or three decades, researchers have tried inhibiting the process by they believed MPTP was metabolised, with mixed success," he said.

"We believe that mitochondrial CYP2D6 is the more direct drug target, which might prove better in treating idiopathic Parkinson's disease," added one of the researchers. The study investigated the mechanism of Parkinson's disease when a specific cause cannot be pinpointed.

Previous studies have shown that MPTP and similar toxic compounds induce Parkinson's disease in rodents and primates. The mechanism of action, as scientists understood it, involved the compounds being oxidised to form MPP+, a toxic metabolite.

The enzyme that was believed to be responsible is called monoamine oxidase B (MAO-B), present in the nervous system's glial cells. In that conception of the mechanism, MPP+ was thought to then be transferred to dopamine neurons by dopamine transporter proteins, and, indeed, Parkinson's is characterised by unusually low dopamine levels in the brain.

Researchers have tried to stem the effects of Parkinson's by targeting two players in this presumed pathway, both MAO-B and the dopamine transporter protein, with only mixed success. In earlier work, Avadhani and colleagues had shown that the enzyme CYP2D6, localised to the body's energy factories, the mitochondria, could play a role in metabolising MPTP to MPP+.

In the new investigation, they took a closer look at beta-carbolines and isoquinolines, toxins that resemble MPTP which the body produces from substances found in tobacco smoke, alcohol, and some foods.

They found that, instead of MAO-B, it was mitochondrial CYP2D6 that activate the beta-carbolines and isoquinolines inside the dopamine-producing neurons, rather than the glial cells. This route of activation, in a mouse model, results in neuronal damage and oxidative stress, symptoms akin to Parkinson's. "CYP2D6 is known to play a role in influencing the activity of a number of drugs," said a researcher.

In an attempt to target this pathway, the researchers showed that mice lacking CYP2D6 did not exhibit severe symptoms than mice with the protein did. In addition, an inhibitor of CYP2D6 prevented neuronal damage in the mice.

"The CYP2D6 inhibitor ajmalicine is a member of the reserpine family of alkaloids, found in the plant Rauwolfia serpentine and was long used in India for treating mental illness, such as paranoia and schizophrenia," he said. "Mitochondrial targeting of such compounds is likely to be effective in treating Parkinson's patients, and pursuing that is our future strategy," said the researcher.

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Saturday, March 02, 2019

Cause behind behavioural difference in males and females found

Researchers have discovered a mechanism for how androgens -- male sex steroids -- sculpt brain development, which could ultimately help understand development of social behavioural differences  between males and females.

The team,  discovered a mechanism for how androgens sculpt the brains of male rats to produce behavioural differences, such as more aggression and rougher play behaviour. 

“We already knew that the brains of males and females are different and that testosterone produced during the second trimester in humans and late gestation in rodents contributes to the differences but we did not know how testosterone has these effects,” said one of the researcher.

The study, revealed that the number of newborn cells in the part of the brain called the amygdala, which controls emotions and social behaviours acts as a key contributor to the differences in behaviour between males and females. 

Males have fewer of these newborn cells, because they are actively eliminated by immune cells by endocannabinoids which plays a role in reproductive functions and response to stress.

Female rats were, however, found to be unaffected. Moreover, in females, the newborn cells differentiated into a type of glial cell, the most abundant type of cell in the central nervous system.
“These discoveries into brain development are critical as we work to tackle brain disorders as early in life as possible, even in pregnancy,” said a Prof. of Medicine.

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Tuesday, February 12, 2019

New Drug Combo Could Repair the Brains of Alzheimer’s Patients

Neurons receive, process, and transmit all the impulses in our brains. Essentially, they’re the building blocks of the human nervous system, and once they’re damaged by Alzheimer’s disease or some other brain injury, they’re done for — they have no regenerative abilities.

In contrast, the glial cells that support and insulate neurons do have regenerative abilities, and now, researchers think they've found an efficient way to actually transform glial cells into neurons — a discovery that could lead to a pill to repair brain damage.

Molecular Report

Based on a previous study, the team knew it was possible to convert human glial cells into neurons using a sequence of nine tiny molecules. However, the large number of molecules and specific sequence made transitioning the research from the lab to something that could work in a clinical environment difficult.

In a study published on Thursday, the  team describes how it found a way to streamline the process of creating neurons out of a type of glial cells called astrocytes with remarkable success.

“We identified the most efficient chemical formula among the hundreds of drug combinations that we tested,” a researcher said in a press release. “By using four molecules that modulate four critical signaling pathways in human astrocytes, we can efficiently turn human astrocytes — as many as 70 percent — into functional neurons.”

Dream Delivery

 The team acknowledged in the press release that it still has a long road ahead before its latest research will be able to help people with brain damage, but it’s extremely optimistic about the future.
“The most significant advantage of the new approach is that a pill containing small molecules could be distributed widely in the world, even reaching rural areas without advanced hospital systems,” research leader said.

“My ultimate dream is to develop a simple drug delivery system, like a pill, that can help stroke and Alzheimer's patients around the world to regenerate new neurons and restore their lost learning and memory capabilities,” he continued. “Our years of effort in discovering this simplified drug formula take us one step closer to reaching our dream.”
 
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Saturday, February 09, 2019

Drug Combination Generates New Neurons from Neighboring Cells

In a study published in Stem Cell Reports, scientists at Penn State University have developed a drug cocktail that converts neighboring cells—often known as glial cells-- of damaged neurons into functional new neurons. The study could open doors to treating stroke, Alzheimer's disease, and brain injuries. Glial cells normally provide support and insulation for neurons.

" The biggest problem for brain repair is that neurons don't regenerate after brain damage, because they don't divide," explain researchers. "In contrast, glial cells, which gather around damaged brain tissue, can proliferate after brain injury. I believe turning glial cells that are the neighbors of dead neurons into new neurons is the best way to restore lost neuronal functions."

The current research study tested various numbers and combinations of molecules that will identify a streamlined approach to the reprogramming of astrocytes, a type of glial cells, into neurons. The result was chemically converted neurons that can survive for a while in a culture dish. These neurons form robust neural networks that send electrical and chemical signals for communication—just as normal neurons do.

"We identified the most efficient chemical formula among the hundreds of drug combinations that we tested," says a researcher. "By using four molecules that modulate four critical signaling pathways in human astrocytes, we can efficiently turn human astrocytes -- as many as 70 percent -- into functional neurons."

"The most significant advantage of the new approach is that a pill containing small molecules could be distributed widely in the world, even reaching rural areas without advanced hospital systems," he said. "My ultimate dream is to develop a simple drug delivery system, like a pill, that can help stroke and Alzheimer's patients around the world to regenerate new neurons and restore their lost learning and memory capabilities."

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Tuesday, January 01, 2019

Neural Stem Cells Grown From Blood Could Revolutionize Medicine

The scientists hope that their findings will improve regenerative medicine, a kind of treatment in which new cells help rejuvenate the body. Specifically, the neural stem cells could grow into either the neurons found in the central nervous system or the glial cells that support and protect those neurons. Both could help treat people who have survived strokes or been diagnosed with neurological diseases.

Previous research that reprogrammed cells into stem cells was never as useful in a medical context because those cells couldn’t continue to multiply, and sometimes grew tumours called teratomas , according to the research.

While this new type of stem cell shows promise for future regenerative medicine, there’s still a ways to go.

Additionally, it’s important to note that the team’s findings show only a new method of programming stem cells, rather than any actual medical applications. But given recent years' progress in stem cell research and utility, it’s safe to assume doctors will want to find a way to use these new cells soon.


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