November 9, 2011

Wednesday, November 09, 2011
Research reveals that people that experience recurring episodes of depression or those that are exposed to chronic stress have shorter telomeres in their white blood cells.

“A telomere is a region of repetitive DNA sequences at the end of a chromosome, which protects the end of the chromosome from deterioration or from fusion with neighboring chromosomes.” Consequently, as we age, telomeres, the outermost part of the chromosome, shorten.

Moreover, research suggests that oxidative stress and inflammation can accelerate this process. The lengths of telomeres are suggestive of our biological age and have been associated with age-related diseases, unhealthy lifestyle, and longevity. Additionally, new studies now show that the shortening of telomeres is also linked to recurrent depression and exposure to chronic stress.

To demonstrate, researchers studied 91 patients with recurrent depression and 451 healthy patients by measuring the telomere length in their white blood cells.

Results showed that telomeres were shorter among the patients with recurrent depression. Also, by examining the participants' stress regulation using a dexamethasone suppression test, researchers again revealed that cortisol levels, indicative of chronic stress, were also associated with shorter telomeres in both depressed participants and healthy ones.

“The fact that depressed patients as a group have shorter telomere lengths compared to healthy individuals can be largely explained by the fact that more depressed people than healthy people have disturbed cortisol regulation, which underscores that cortisol regulation and stress play a major role in depressive disorders” says Mikael Wikgren, a doctoral candidate in the research group.

Accordingly, people could experience age-related complications much earlier in life; therefore properly treating and managing stress and/or depression may significantly impact the quality of life throughout the lifetime.

Depression and Chronic Stress Accelerates Aging
Telomere

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September 11, 2011

Sunday, September 11, 2011
Remembering9-11


Although most of us remember 9/11 through media coverage, a vast amount of victims and heroes now remain permanently scarred from witnessing the tragedy first-hand. Many are still physically suffering from their exposure to a mix of fibers, metals, concrete, noxious chemicals and gases. Yet many others are suffering mentally from their experiences on that day and the days following.
“Officially, as many as 10,000 firefighters, police officers and civilians who were at the disaster site here have been diagnosed with post traumatic stress disorder (PTSD). Other figures suggest more than 60,000 of the 409,000 who were at Ground Zero have shown elements of PTSD.”
In the past 10 years, there has been more research and attention given to the very real PTSD and the stigma of mental illness and seeking treatment has also diminished somewhat.

So today, many of us are not only remembering where we were or what we were doing on that day, but those that perished, lost their lives trying to save lives and those still affected.

For more on PTSD, visit this past post: http://www.mentalhealthblog.com/2008/09/ptsd-victims-of-911.html

Our faded memories of 9-11

© www.mentalhealthblog.com

September 4, 2011

Sunday, September 04, 2011
New research suggests that infants can be trained to improve their concentration skills much earlier than once thought, which, unlike adults, can lead to improvements on unrelated tasks. Such abilities could lead to greater academic success, especially for those infants that may not be expected to thrive.
"Research suggests that differences in attentional control abilities emerge early in development and that children with better attentional control subsequently learn better in academic settings," said Sam Wass of the Centre for Brain and Cognitive Development at Birkbeck, University of London.
In other words, infants that can more readily concentrate on a specific object while ignoring other distractions are better equipped to learn. To test this theory, researchers observed 42 eleven-month-old infants on 5 occasions over 15 days. The cognitive abilities of each child were tested at the beginning and end of the 15 day period. Half of the babies watched TV, while the other half explored images on a computer screen. The latter half were tested to see how long they could watch a butterfly that flew only as long as they kept their eyes on it, meanwhile other distracting elements appeared on the screen.

Results showed that, “trained infants rapidly improved their ability to focus their attention for longer periods and to shift their attention from one point to another. They also showed improvements in their ability to spot patterns and small but significant changes in their spontaneous looking behavior while playing with toys”.

Consequently, the ability to stay focused on a task or to quickly shift attention can facilitate learning and social interactions, which can significantly impact abilities later in life.

Although the plasticity of the infant brain might allow training to occur at an earlier age, it remains a mystery whether infants might lose their novel skills just as quickly as they were learned.

Infants Trained to Concentrate Show Added Benefits

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August 7, 2011

Sunday, August 07, 2011
According to Larry D. Rosen, PhD, professor of psychology at California State University, Dominguez Hills, the effects of social media are becoming more and more visible.

Some of their findings suggest that the more time spent on Facebook is related to a greater tendency toward narcissistic behaviors among teenagers. Also, it has been discovered that young adults that spend excessive amounts of time on Facebook show more signs of other psychological disorders, including antisocial behaviors, mania and aggressive tendencies.

Additionally, studies have revealed that excessive daily use of social media can negatively affect the health of children, preteens and teenagers alike as they are more prone to anxiety, depression and other psychological disorders as well as more susceptible to future general health problems.

Furthermore, it is clear that school grades will suffer when spending too much time on Facebook as valuable study time is lost. “Studies found that middle school, high school and college students who checked Facebook at least once during a 15-minute study period achieved lower grades.”

Besides, some studies suggest that so-called teenage “hyper-social networkers” are more likely to engage in risky behaviors, such as smoking, drinking, drug use, fighting and promiscuity.

Consequently, Rosen claims that parents who secretly monitor their child’s social media usage are wasting their time. Instead he suggests that active, but overt, monitoring and open communication about appropriate usage is the key so that when questions or issues arise such as bullying, a child will feel comfortable communicating with their parents. This active role could prevent serious consequences such as depression, anxiety or even suicide. It is also important for parents to stay abreast with online trends and the latest technologies, websites and applications.

On the other hand, research has shown that, despite the numerous negative effects, Facebook can help young adults to express their virtual empathy and facilitate socialization among introverted teens. Also, “social networking can provide tools for teaching in compelling ways that engage young students.”

It seems, like most things in life, everything in moderation is best.

Social Networking's Good and Bad Impacts On Kids
Texting and Social Websites Associated With Risky Behaviors Among Teens

© www.mentalhealthblog.com

July 23, 2011

Saturday, July 23, 2011
In recent news, scientists have uncovered the molecular pathway involved in the onset of schizophrenia as well as a potential new treatment for the illness. By observing the effects of a cancer drug called MS-275 in mice, researchers discovered that symptoms of schizophrenia were successfully alleviated.

Schizophrenia is a mental disorder characterized by disintegration of thought processes and emotional responsiveness. It is most commonly manifested as auditory hallucinations, paranoid or bizarre delusions, or disorganized speech and thinking. The onset of symptoms typically occurs in young adulthood. Schizophrenia is accompanied by significant social or occupational dysfunction.

Additionally, the disease is said to be caused by a combination of genetic and environmental factors. Those with a diagnosis of schizophrenia have changes in both brain structure and chemistry. Studies using neuropsychological tests and brain imaging technologies such as fMRI and PET to examine functional differences in brain activity have shown that differences seem to most commonly occur in the frontal lobes, hippocampus and temporal lobes.

The greatest risk for developing schizophrenia is having a first-degree relative with the disease. Environmental factors associated with the development of schizophrenia include the living environment, drug use and prenatal stressors. Factors such as hypoxia and infection, or stress and malnutrition in the mother during fetal development, may result in a slight increase in the risk of schizophrenia later in life. A number of drugs have been associated with the development of schizophrenia including cannabis, cocaine and amphetamines.
“According to the World Health Organization, 90% of people with untreated schizophrenia are in developing countries. Current treatments for schizophrenia include both psychological treatments such as psychotherapy, counselling or cognitive behaviour therapy and/or medication. However, many of the antipsychotic drugs or major tranquillisers used to treat or manage the illness have very bad side-effects.”
Schizophrenia is said to affect about 24 million people worldwide.

Medications prescribed to treat schizophrenia include:
    • Chlorpromazine (Thorazine)
    • Haloperidol (Haldol)
    • Perphenazine (generic only)
    • Fluphenazine (generic only)
    • clozapine (Clozaril)
    • Risperidone (Risperdal)
    • Olanzapine (Zyprexa)
    • Quetiapine (Seroquel)
    • Ziprasidone (Geodon)
    • Aripiprazole (Abilify)
    • Aliperidone (Invega)
Typical side effects include:
    • Drowsiness
    • Dizziness when changing positions
    • Blurred vision
    • Rapid heartbeat
    • Sensitivity to the sun
    • Skin rashes
    • Menstrual problems for women
    • Rigidity
    • Persistent muscle spasms
    • Tremors
    • Restlessness
Professor Peter Giese at King's College London discovered that individuals with schizophrenia had a reduction in the enzyme activator called p35. By manipulating the level of this enzyme in mice, the researchers were able to mirror typical cognitive impairments found in those with schizophrenia. Consequently, human post-mortem brains revealed that schizophrenic patients had approximately 50% less p35 in their brains.

That being said, the brain requires, among other things, the activation of a protein call Cdk5 to assist in proper development and this protein can only be activated in the presence of the p35 enzyme.

Therefore, by manipulating the level of p35 enzyme in mice, researchers noted that “the mice showed a reduction in synaptic proteins -- important in maintaining neural connections -- and displayed symptoms associated with schizophrenia, including learning impairments and inability to react to sensory stimuli.”

Subsequently, Professor Giese and his research team noticed that the reduction of the p35 enzyme altered molecules in the brain that are targeted by the cancer drug MS-275. To their delight, the molecular changes were corrected and the schizophrenic symptoms were alleviated by this drug.

With any luck, more research will prove that this drug is more beneficial than current medications with intolerable side-effects.

Cancer Drugs May Help Treatment of Schizophrenia
Schizophrenia
Mental Health Medications

© www.mentalhealthblog.com

July 3, 2011

Sunday, July 03, 2011
Researchers of the CRASH-2 Intracranial Bleeding Study have uncovered the possibility that tranexamic acid may be able to prevent people from dying of head injuries. This hypothesis was derived from the examination of 270 adult trauma patients with traumatic brain injury and with, or at risk of, significant extracranial bleeding within 8 hours of injury. Results of the study were persuasive enough that a CRASH-3 study is needed to test the reliability of this drug among patients with head trauma.

Tranexamic acid, otherwise known as Lysteda or Cyklokapron in the U.S., is often prescribed for excessive bleeding. “It is an antifibrinolytic that competitively inhibits the activation of plasminogen to plasmin, a molecule responsible for the degradation of fibrin. Fibrin is the basic framework for the formation of a blood clot in hemostasis.” In addition to its value for treating trauma patients, it has been used to treat cases of excessive menstrual bleeding, to reduce blood loss during orthopedic surgery, as a mouthwash following dental surgery, as well as in obstetrics, cardiac surgery, hemophilia and hereditary angioedema.

If approved, tranexamic acid could be used immediately following trauma when bleeding typically progresses and causes more and more brain damage by reducing the breakdown of blood clots and decreasing the amount of bleeding into the brain thereby preventing brain damage and even death.
“Although the results are not definitive they provide hope about the potential effectiveness of this simple drug for head injury patients. If such an inexpensive and widely practicable treatment were found to improve patient outcomes after head injury this would have major implications for clinical care” Said Dr Pablo Perel.
Hopefully, CRASH-3 trials will unveil conclusive results so that such a simple treatment could be incorporated immediately following traumatic brain injuries to increase survival rates and reduce disability, not to mention avoiding extensive and challenging rehabilitation.

Potential of Simple Injection On Patients With Head Injury
Tranexamic acid

© www.mentalhealthblog.com

May 31, 2011

Tuesday, May 31, 2011
According to researchers of the Centre for Studies on Human Stress of Louis-H. Lafontaine Hospital at the University of Montreal, our brain loses its ability to associate negative emotions with painful memories while using the drug metyrapone.
“‘Metyrapone is a drug that significantly decreases the levels of cortisol, a stress hormone that is involved in memory recall,’ explained lead author Marie-France Marin. Manipulating cortisol close to the time of forming new memories can decrease the negative emotions that may be associated with them. "The results show that when we decrease stress hormone levels at the time of recall of a negative event, we can impair the memory for this negative event with a long-lasting effect," said Dr. Sonia Lupien, who directed the research.”
Researchers taught 33 men a story that consisted of neutral and negative events. They separated the men into different groups and observed them 3 days later. A third of the participants received a single dose of metyrapone, another third received a double dose and the final third received a placebo. Researchers asked the participants to recall the story while under the influence of the drug they were given. Their memory of the story was evaluated while using the drug and again 4 days later when the drug was no longer circulating in their bloodstream.
“‘We found that the men in the group who received two doses of metyrapone were impaired when retrieving the negative events of the story, while they showed no impairment recalling the neutral parts of the story,’ Marin explained. ‘We were surprised that the decreased memory of negative information was still present once cortisol levels had returned to normal.’”
Consequently, such research could be very useful in treating mental illness. Not only could this drug be successful in treating post-traumatic stress disorder (PTSD), but it could help many people with mental health issues resulting from traumatic experiences.

Unfortunately, metyrapone is no longer commercially produced; however research on the impact of certain compounds on cortisol levels can only lead to a better understanding of the way in which our brain processes negative emotions and memories. Additionally, this type of research may lead to the discovery of other medications that are currently available or potentially more successful in erasing our bad memories.

On the other hand, use of such a drug could lead to abuse as many of us could certainly pinpoint at least one painful memory that we would be willing to let go. Also, despite those whose lives have been seriously disrupted from past trauma, it is our experiences, both positive and negative, that molds us into the person we have become. Therefore, erasing our experience of negative emotions from certain memories may be toying with our personality and possibly creating havoc in our society.

Drug May Help Overwrite Bad Memories

© www.mentalhealthblog.com

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