Test designed to screen resistance to cancer drug

(Reuters) – Researchers in Japan have designed a test to identify patients who are likely to be resistant to imatinib, the standard drug for treating leukemia or cancer of the blood cells.

Such a test is important as imatinib resistance occurs usually to relapse patients, who tend to deteriorate very rapidly if they are given the wrong treatment.

In a paper published in Clinical Cancer Research on Thursday, the scientists said they developed a test which will help doctors tell if a patient with chronic myeloid leukemia (CML) is resistant to imatinib.

Imatinib, known by the brand Gleevac, is sold by Novartis AG to treat CML and other cancers. It blocks the enzymes of cancer cells instead of killing all rapidly multiplying cells.

“Most patients are sensitive to imatinib when they are diagnosed with CML, but resistance can indeed be acquired during or after imatinib treatment,” said Yusuke Ohba, an associate professor at Hokkaido University Graduate School of Medicine.

“Even in cases where resistance develops or becomes apparent gradually, the most critical issue is what to switch over to. If the patient is switched to another (treatment) to which he/she is also resistant, the treatment will just be a waste of time and detrimental to the patient’s condition.”

“With our test, we can identify the most suitable drug, dose and/or drug combination, enabling therapy to be tailor-made for each individual patient. I believe this approach will make CML care more accurate and effective,” he said in an email reply to questions from Reuters.

New drugs being developed for treating CML claim to overcome imatinib resistance, but until now, it is difficult to tell who has that resistance.

Using this test developed by Ohba and his colleagues, blood samples are collected from patients and then cultured and tested to see if they are resistant to imatinib.

These tests should help doctors determine if the patient may require stronger doses, combination therapy, or other drugs, Ohba said.

(Reporting by Tan Ee Lyn; Editing by Sugita Katyal)

Study Shows Marked Neuroprotective Effects of Oxycyte(R) Perfluorocarbon Emulsion…

Study Shows Marked Neuroprotective Effects of Oxycyte(R) Perfluorocarbon
Emulsion in a Rat Model of Spinal Cord Injury

DURHAM, N.C., June 3, 2010 (GLOBE NEWSWIRE) — Oxygen Biotherapeutics, Inc.
(Nasdaq:OXBT) today reported on the results of two University of Miami Miller
School of Medicine studies involving the Company’s third-generation
perfluorocarbon, Oxycyte(R) perfluorocarbon emulsion. Both study reports showed
that Oxycyte(R) has a marked neuroprotective effect in a rat model of spinal
cord injury.

“Having proof-of-concept is a first step toward moving Oxycyte down the spinal
cord injury track. The positive results observed in both studies may warrant
efforts to pursue partnerships to conduct clinical studies of Oxycyte in spinal
cord injury in the future,” said Gerald Klein, Chief Medical Officer for Oxygen
Biotherapeutics.

The studies showed that histologically, Oxycyte improves the volume of preserved
neuronal tissue in the spinal cord following injury; a favorable improvement in
functional recovery, as assessed by footprint analysis six weeks post treatment,
has also been observed.

The study entitled “Possible Role of Hyperbaric Oxygen Therapy (HBO) and Oxycyte
After Spinal Cord Injury in Rats,” will be part of the poster sessions at the
National Neurotrauma Symposium on June 14-16, 2010 at the Paris Hotel in Las
Vegas. Results of the first study entitled “Evaluation of the Neuroprotective
and Behavioral Effects of the Perfluorocarbon Oxycyte After Spinal Cord Injury
(SCI) in the Rat” were presented in September 2009 at the annual
National-International Neurotrauma Symposium by Dr. Ross Bullock, University of
Miami Miller School of Medicine. Both studies received funding from Oxygen
Biotherapeutics.

Oxycyte emulsion is a proprietary therapeutic oxygen carrier. It is a
perfluorocarbon emulsified with water and a surfactant that is delivered
intravenously.

According to statistics from various studies compiled by the National Spinal
Cord Injury Statistical Center in Birmingham, AL, an estimated 12,000 new cases
of spinal cord injury occur each year in the United States; and the number of
people living in the United States with SCI is estimated to be approximately
259,000 people.

About the Company

Oxygen Biotherapeutics, Inc. is developing medical and cosmetic products that
efficiently deliver oxygen to tissues in the body. The company has developed a
proprietary perfluorocarbon (PFC) therapeutic oxygen carrier and liquid
ventilation product called Oxycyte(R) that is being formulated for both
intravenous and topical delivery. In April, the company launched its first
cosmetic product, Dermacyte(R) Oxygen Concentrate. In addition, the company is
focused on perfluorocarbon-based oxygen carriers for use in traumatic brain
injury, decompression sickness, personal care, and topical wound healing. More
information is available at www.oxybiomed.com or www.buydermacyte.com.

The Oxygen Biotherapeutics, Inc. logo is available at

http://www.globenewswire.com/newsroom/prs/?pkgid=7277

Caution Regarding Forward-Looking Statements

This news release contains certain forward-looking statements by the company
that involve risks and uncertainties and reflect the company’s judgment as of
the date of this release. These statements include those referring to the plans
for the expansion of development of the Oxycyte product line and the timing of
the introduction of those new products. The forward looking statements are
subject to a number of risks and uncertainties including matters beyond the
company’s control that could lead to delays in the new product introductions and
customer acceptance of these new products and other risks and uncertainties as
described in our filings with the Securities and Exchange Commission, including
in the current report on Form 8-K on May 4, 2010. Furthermore, there can be no
assurance that such plans will lead to meaningful sales of Dermacyte or generate
any revenue for the company. The company disclaims any intent or obligation to
update these forward-looking statements beyond the date of this release. This
caution is made under the safe harbor provisions of the Private Securities
Litigation Reform Act of 1995.

CONTACT: Oxygen Biotherapeutics, Inc.
Ellen Corliss, Vice President, Corporate Communications
& Investor Relations
(919) 806-4405

New gene therapy to effectively treat severe heart failure

Washington, June 4 (ANI): American researches have unveiled a new gene therapy that effectively treats severe heart failure.

The SERCA2a (produced as MYDICAR), developed by researchers at Mount Sinai School of Medicine, is designed to stimulate production of an enzyme that enables the failing heart to pump more effectively.

In a Phase II study, SERCA2a injection through a routine minimally invasive cardiac catheterization was safe and showed clinical benefit in treating this patient population and decreasing the severity of heart failure.

The data were recently presented at the Heart Failure Congress of the European Society of Cardiology in Berlin.

Trial investigator Jill Kalman, Associate Professor, Medicine, Cardiology, Director of the Cardiomyopathy Program, Mount Sinai School of Medicine, said: “SERCA2a met the primary endpoints and appears to be safe and effective in people with advanced heart failure.

“There is a significant unmet need for treatments in this patient population, and these data indicate that SERCA2a is a promising option for them.”

The CUPID (Calcium Up-regulation by Percutaneous administration of gene therapy In cardiac Disease) trial is a randomized, double-blind, placebo-controlled study, which enrolled 39 patients with advanced heart failure to study the safety and efficacy of SERCA2a.

Patients were randomized to receive SERCA2a gene delivery in one of three doses or placebo and were evaluated over six months.

The treatment is delivered directly to the patient”s heart during a routine outpatient catheterization procedure.

Patients in the SERCA2a group demonstrated improvement or stabilization in symptoms, heart function, and severity of heart failure.

They also saw an increase in time between cardiovascular events and a decrease in frequency of events.

SERCA2a was found to be safe, with no increases in adverse events, disease-related events, laboratory abnormalities, or arrhythmias compared to placebo. (ANI)

Study suggests possibilities for treatments for anxiety disorders

Washington, June 4 (ANI): A memory of safety can now be induced in rats” brain, mimicking the effect of training.

The study, which was carried out with support from the National Institute of Mental Health (NIMH), suggests possibilities for future treatment of anxiety disorders.

Rats normally freeze when they hear a tone they have been conditioned to associate with an electric shock.

The reaction can be extinguished by repeatedly exposing the rats to the tone with no shock. In this work, administering a protein directly into the brain of rats achieved the same effect as extinction training.

The protein, brain-derived neurotrophic factor or BDNF, is one of a class of proteins that support the growth and survival of neurons.

Prior work has shown that extinction training does not erase a previously conditioned fear memory, but creates a new memory associating the tone with safety.

Dr. Gregory Quirk at the University of Puerto Rico School of Medicine, who led the investigation, said: “The surprising finding here is that the drug substituted for extinction training, suggesting that it induced such a memory.”

Memory formation involves changes in the connections, or synapses, between neurons, a process known as synaptic plasticity.

One brain structure critical for extinction memory in rats is the infralimbic prefrontal cortex (ILC).

Drugs that block synaptic plasticity impair the formation of extinction memory when injected into the ILC, causing rats to continue freezing at high levels after extinction training.

BDNF, on the other hand, permits a learning experience to increase the size and strength of synaptic contacts between neurons.

Previous work from other groups has implicated BDNF in extinction learning.

In this study, after rats were conditioned to fear a tone by pairing it with a footshock, BDNF was infused directly into the ILC.

The next day, BDNF-infused rats showed little freezing to the tone, as if they had received extinction training.

Experiments showed that BDNF-induced extinction did not erase the original fear memory.

Training to reinstate the tone-shock association was just as effective with the rats receiving BDNF as those without.

Also, the effect of BDNF was specific to extinction. It did not reduce general anxiety or change the animals” tendency to move around.

The researchers also found that rats that were naturally deficient in BDNF were more likely to do poorly in extinction trials.

These rats were deficient in BDNF in the hippocampus, a brain structure that plays an important role in memory and extinction, and which has connections to the ILC.

Failure to extinguish fear is thought to contribute to anxiety disorders, such as post-traumatic stress disorder (PTSD). People with PTSD have a smaller than normal hippocampus and ILC.

NIMH Director Dr. Thomas Insel said: “Many lines of evidence implicate BDNF in mental disorders.

“This work supports the idea that medications could be developed to augment the effects of BDNF, providing opportunities for pharmaceutical treatment of post-traumatic stress disorder and other anxiety disorders.”

The study appears in the journal Science. (ANI)

Stem cells from embryo sac could heal damaged hearts

Washington, May 29 (IANS) Stem cells obtained from a new non-controversial source – the amniotic membrane discarded as medical waste after childbirth – can heal damaged hearts and form heart muscle cells, results of preliminary lab tests indicate.

Investigators in Japan used the membrane – the inner lining of the sac in which an embryo develops – to obtain stem cells called human amniotic membrane-derived mesenchymal (undifferentiated) cells (hAMCs).

‘The amniotic membrane is medical waste that could be collected and used after delivery,’ said Shunichiro Miyoshi, study co-author and assistant professor in cardiology at the Keio University School of Medicine, Tokyo.

In lab studies, the hAMCs transformed into heart muscle cells improved function of rat hearts 34 percent to 39 percent, when injected two weeks after a heart attack, while untreated hearts continued to decline in function.

They decreased the scarred area of damaged rat hearts 13 percent to 18 percent when injected after a heart attack.

The cells also survived for more than four weeks in the rat heart without being rejected by the recipient’s immune system, even without immunosuppressive medication.

The ability of hAMCs to convert into heart muscle cells was far greater than that from mesenchymal cells derived from bone marrow or fat, Miyoshi said.

That the implanted cells were not rejected is likely because the amniotic sac is a barrier between a woman and her developing foetus. To help prevent either of their immune systems from attacking the other as foreign tissue, the amniotic membrane between them does not produce the proteins that immune systems use to identify foreign tissue.

This means the usual tissue-type matching (HLA typing) needed prior to transplantation would not be needed if hAMCs were used. Drugs to suppress the immune system also might not be needed after transplant.

The findings also suggest that hAMCs can differentiate into cells of various organs, said a release of the American Heart Association (AHA).

Much work, however, remains to be done before testing hAMCs in humans, said the researchers, who are repeating their experiments in larger animals and working to boost the number of heart cells generated by the hAMCs.

The investigators ‘are to be congratulated for their careful work that has brought forward a cell type that may offer the real potential for off-the-shelf cardiac myocyte [muscle cell]-based therapy,’ wrote Marc S. Penn, and Maritza E. Mayorga of the Cleveland Clinic, in Circulation Research, which published these findings.

Sperm identification could improve male fertility

Washington, May 29 (IANS) Researchers have discovered a method to select sperm with the highest DNA integrity that is likely to improve male fertility.

The method is comparable to that of the egg’s natural selection abilities, says a new study.

‘Our results could help address the fact that approximately 40 percent of infertility cases can be traced to male infertility,’ said study co-author Gabor Huszar, senior research scientist in obstetrics, gynaecology and reproductive sciences at Yale School of Medicine.

Huszar said that past semen analysis focused on sperm concentration and motility (ability to move spontaneously and actively). It was assumed that if a man had a high sperm count and active sperm he was fertile.

But there was no information on the sperm’s fertility or its ability to attach to its mark, the female gamete.

In an ideal case, the egg naturally selects the optimal sperm, but during in-vitro (test tube) fertilisation treatment of men who had only a few sperm, clinicians did not know whether they were injecting the correct sperm into the egg for fertilisation.

‘We have now found a biochemical marker of sperm fertility so that we can select sperm with high genetic integrity,’ Huszar said.

Huszar and his colleagues tested the idea that binding sperm to hyaluronic acid selects sperm with high DNA integrity.

They studied semen samples from 50 men, and a part of the sperm in the semen was allowed to bind to hyaluronic acid. These sperm were isolated, and the DNA chain integrity was compared to the original sperm in semen.

The team used a reagent that stained sperm with high DNA integrity green, whereas sperm with fragmented DNA, and diminished DNA integrity were stained red.

‘The sperm with fragmented DNA work like scratched CDs,’ Huszar said. ‘They seem to be operational, but when you play them, some of the information is missing.’

‘These damaged sperm may also carry chromosomal aberrations that could be related to genetic diseases,’ Huszar added, according to an Yale release.

Other Yale authors included Artay Yagci, William Murk and Jill Stronk. These findings are slated for publication in the June/July issue of the Journal of Andrology.

First drug to demonstrate therapeutic effect in a type of autism identified

Washington, May 20 (ANI): American researchers have identified a drug that improves communication between nerve cells in a mouse model of Phelan-McDermid Syndrome (PMS).

Previous research has shown that a gene mutation in the brain called SHANK3 can cause absent or severely delayed language abilities, intellectual disability, and autism.

Researchers at Mount Sinai School of Medicine developed mice with a mutant SHANK3 gene and observed a lapse in communication between nerve cells in the brain, which can lead to learning problems. This communication breakdown indicated that the nerve cells were not maturing properly.

The scientists then injected the mice with a derivative of a compound called insulin-like growth factor-1 (IGF1), which is FDA-approved to treat growth failure in children.

After two weeks of treatment, nerve cell communication was normal and adaptation of nerve cells to stimulation, a key part of learning and memory, was restored.

Joseph Buxbaum, Director of the Seaver Autism Center for Research and Treatment at Mount Sinai School of Medicine, said: “The result of IGF1 treatment of these mice is an exciting development on the road to ultimate therapies for individuals with PMS.

“If these data are further verified in additional preclinical studies, individuals with a SHANK3 mutation may benefit from treatments with compounds like this one.” (ANI)

New role for zebrafish in human studies

Washington, May 20 (ANI): Zebrafish – an important animal model in disease and environmental studies – could eventually help scientists in revealing the function of a mysterious enzyme linked to the steroid cortisol, and found in the human brain, found a researcher at the University of California, San Diego School of Medicine.

In people and other vertebrates, steroids like cortisol perform a variety of diverse duties, including regulating immune response, bone formation and brain activity.

However, too much cortisol is unhealthy. High levels of the steroid have been linked to type 2 diabetes and may impair the brain”s ability to store memories.

The human body regulates cortisol by employing an enzyme called 11 beta-hydroxysteroid dehydrogenase-type 1 or 11beta-HSD1, which catalyzes the synthesis of cortisol in liver and fat cells.

A related enzyme known as 11 beta-HSD-type3 or 11 beta-HSD3 is expressed in the brain, though its utility remains unknown.

In new findings, Dr. Michael E. Baker has reported that 11 beta-HSD3 (but not 11 beta-HSD1) is present in zebrafish, where it appears to serve an important role in fish endocrine physiology.

This makes the fish a potentially useful analog for cortisol studies, including discovering the purpose and function of 11 beta-HSD3 in human brains, which may be an evolutionary precursor to 11 beta-HSD1.

Interestingly, Baker found that the genomes of mice and rats do not contain 11 beta-HSD3.

This means that inserting the appropriate gene for the enzyme in these animal models could provide additional avenues of investigation.

The study will be published in the latest issue of FEBS Letters. (ANI)

Progress made toward universal flu vaccine

Washington, May 20 (ANI): Scientists have come up with a novel influenza vaccine that could represent the next step towards a universal influenza vaccine eliminating the need for seasonal immunizations.

“Current influenza vaccines are effective against only a narrow range of influenza virus strains. It is for this reason that new vaccines must be generated and administered each year. We now report progress toward the goal of an influenza virus vaccine which would protect against multiple strains,” said study’s author Peter Palese, from Mt. Sinai School of Medicine.

The main reason the current seasonal vaccine is so strain-specific is that the antibodies it induces are targeted at the globular head of the hemaglutinin (HA) molecule on the surface of the influenza virus.

This globular head is highly variable and constantly changing from strain to strain.

In this study, the researchers constructed a vaccine using HA without its globular head. Mice immunized with the headless HA vaccine showed a broader, more robust immune response than mice immunized with full-length HA, and that immune response was enough to protect them against a lethal viral challenge.

“Our results suggest that the response induced by headless HA vaccines is sufficiently potent to warrant their further development toward a universal influenza virus vaccine. Through further development and testing, we predict that a single immunization with a headless HA vaccine will offer effective protection through several influenza epidemics,” said Palese.

The findings have been reported in the inaugural issue of mBio, the first online, open-access journal published by the American Society for Microbiology. (ANI)

Yogurt-like drink DanActive cuts rate of common infections in daycare kids

Washington, May 20 (ANI): The probiotic yoghurt-like drink DanActive can cut the rate of common sicknesses such as ear infections, sinusitis, the flu and diarrhoea in day-care children, according to researchers.

An additional finding, however, showed no reduction in the number school days missed.

Led by Daniel Merenstein of Georgetown University School of Medicine (GUSOM), the researchers studied the drink in the largest known probiotic clinical trial to be conducted in the United States.

Probiotic foods are continuing to increase in popularity and some are marketed for the potential benefits of probiotics such as Lactobacillus casei (L. casei) DN-114 001, the probiotic in DanActive.

Studies in other countries have found that probiotics, which are live micro-organisms, produce positive health benefits in children, including the reduction of school days missed due to infections.

However, most of the research was conducted outside the United States in structured conditions not comparable to normal everyday living.

“We were interested in a study that resembled how children in the U.S. consume drinks that are stored in home refrigerators and consumed without study personnel observation,” said the study”s lead author Dr. Daniel Merenstein, director of research in the Department of Family Medicine at GUSOM.

“…To our knowledge this is the largest probiotic clinical trial conducted in the U.S. and provides much needed data,” say the authors of the study. “We studied a functional food, not a medicinal product; parents will thus feed their children without any physician input and we felt it was best to assess [the drink] under similar conditions,” he added.

The study, titled DRINK (Decreasing the Rates of Illness in Kids), was a randomized, double-blind, placebo-controlled study – the gold standard in clinical research design.

It included 638 healthy children, aged three to six, who attended school five days a week.

Parents were asked to give their child a daily strawberry yogurt-like drink.

Some of the drinks were supplemented with the probiotic strain L. casei DN-114 001 (DanActive), while others had no probiotics (placebo).

Researchers found a 19 percent decrease of common infections among the children who drank the yogurt-like drink with L. casei DN-114 001 compared to those whose drink did not have the probiotic.

More specifically, those who drank DanActive had 24 percent fewer gastrointestinal infections (such as diarrhea, nausea, and vomiting), and 18 percent fewer upper respiratory tract infections (such as ear infections, sinusitis and strep).

However, the reduction in infections did not result in fewer missed school days or activities – also a primary outcome of the study.

“Our study had mixed results. Children in school or daycare are especially susceptible to these illnesses. We did find some differences in infection rates but this did not translate to fewer missed school days or change in daily activity. It is my hope that safe and tolerable ways to reduce illnesses could eventually result in fewer missed school days which means fewer work days missed by parents,” said Merenstein.

“It is important that more of these products are put under the microscope by independent academic researchers,” he concluded.

The study was published online in the European Journal of Clinical Nutrition. (ANI)

Bat fellatio study prompts sexual harassment row

London, May 18 (ANI): An academic at the University College Cork in Ireland found himself at the centre of a sexual harassment scandal after he discussed a scientific paper, titled ‘Fellatio in fruit bats prolongs copulation time’ with a female colleague.

Dylan Evans, a psychologist at the university”s school of medicine, has been saddled with a two-year period of intensive monitoring and counselling after discussing the paper with a colleague.

And now his university is coming under international pressure to lift the punishment meted out to Dylan.

As part of what he says was an ongoing discussion on human uniqueness, Evans showed a copy of the fellatio paper to a female colleague in the school of medicine.

“There was not a shred of a sign of offence taken at the time. She asked for a copy of the article,” New Scientist quoted Evans as saying.

A week later he got a letter informing him that he was being accused of sexual harassment.

Evans said that the whole case is “utterly bizarre”.

The complainant”s side of the argument is that she was “hurt and disgusted”, and asked Evans to leave a copy of the paper with her as way of cutting short the meeting.

Apparently, there was more to the grievance between Evans and the complainant than the fellatio paper incident, but an independent investigation found that Evans was not guilty of sexual harassment.

The investigation stated that it was reasonable for the colleague to have been offended and that showing the paper was a joke with a sexual innuendo, but that it was not Evans” intention to cause offence.

Nevertheless, the university”s president, Michael Murphy, imposed a censure, which Evans says has prevented him getting tenure.

An online petition calling on the university authorities to back down has been set up and has been signed by high-profile academics including philosopher Daniel Dennett of Tufts University in Medford, Massachusetts, and Steven Pinker of Harvard University.

Dennett called the punishment “an outrageous violation of academic freedom” and Pinker says the “absurd and shameful” judgment “runs contrary to the principle of intellectual freedom and freedom of speech, to say nothing of common sense”.

The paper, which was carried out by many popular journals, had a certain prurient interest, which was only heightened by an explicit video that went with itMovie Camera.

The Irish Federation of University Teachers has written to Murphy asking him to rescind the two-year period of monitoring. (ANI)

Wrinkles, not skin cancer risk, scare indoor tanners

Washington, May 18 (ANI): Young women were more likely to stay away from indoor tanning if they were warned that the practice could increase their risk of getting leathery, wrinkled skin, than being warned about risk of melanoma, the deadliest form of skin cancer, a study found.

The study found a 75 percent reduction in indoor tanning visits if girls were warned of skin deterioration and turning unattractive.

“They””re not worried about skin cancer, but they are worried about getting wrinkled and being unattractive,” said June Robinson, a professor of dermatology at Northwestern University Feinberg School of Medicine and senior author of the study.

The study examined the best strategy to wean college-age women who are considered addicted or pathological tanners from tanning salons.

“The fear of looking horrible trumped everything else. It was the most persuasive intervention, regardless of why they were going to tan,” said Robinson.

The research showed warning them about the effects on their appearance caused a 35 percent drop in their indoor tanning visits, which were measured at intervals up to six months after the intervention.

Joel Hillhouse, lead author of the paper, noted that some women in the study eventually stopped tanning.

“It was a progressive kind of thing. At first the women said they tried sunless tanning as an alternative, but over time they gave up tanning altogether,” he said.

Between 25 to 40 percent of older adolescent girls visit tanning salons, according to the study””s authors.

The study included 435 college women, ages 18 to 22, who visited tanning salons.

Within this population, researchers focused on women who visited salons up to four times a week – more than what is needed to maintain a tan – and who tanned for psychological reasons, not just for a special event.

These tanners included one group who strongly disliked the natural colour of their skin, which was related to a psychological condition called body dysmorphia.

“They thought their skin was disgusting when it was pale,” said Hillhouse.

The other group, who said tanning made them feel happier and more relaxed, showed symptoms of seasonal affective disorder (SAD) on a diagnostic psychological test.

“They were self medicating their own depression,” said Robinson, noting that lying in a tanning bed produces internal opioids.

The women received a 25-page booklet, authored by Hillhouse, that discussed the effect of tanning on appearance and explained how ultraviolet rays destroy collagen in the skin.

The booklet also offered many alternatives to meet the women””s needs for tanning, such as taking an exercise class for socializing and relaxation or getting a spray-on tan or self-tanning cream application at a spa.

After reading the booklet, the women reported their attitudes and behaviours twice a week in diaries.

The study results surprised researchers.

“The hypothesis was because this was an appearance intervention, it would have less of an effect on the people tanning for mood problems. We found the opposite. The intervention worked just as well for people with seasonal affective disorder as for people who didn””t like their skin color. That means it””s a really good intervention for everyone,” said Hillhouse.

Robinson stressed it was also important to offer women alternatives to tanning salons.

The study has been published in Archives of Dermatology. (ANI)

Recipe for making sensory hair cells from stem cells found

Washington, May 14 (ANI): A ten year long research has led scientists to discover the recipe for hearing— a way to coax embryonic stem cells as well as reprogrammed adult cells to develop into sensory cells that normally reside in the mammalian inner ear.

Those mechanosensitive sensory hair cells are the linchpin of hearing and balance.

Assuming their recipe can be further perfected to reliably generate hair cells in the millions, it opens the door to detailed molecular studies on the cells and new insight into the molecular basis for hearing, according to the researchers.

Stefan Heller of Stanford University School of Medicine said that is especially significant, because the “inner ear shelters the last of our senses for which the molecular basis is unknown.”

Such understanding could also set researchers on a path to discovering new ways to prevent or correct hearing loss by encouraging hair cells” regeneration.

After all, the researchers say, our inability to regenerate lost hair cells is the major reason for the permanence of hearing loss as well as certain balance disorders.

Scientists have been left in the dark on the molecular basis for hearing in large part because hair cells are relatively scarce by comparison to other sensory cells, explained Heller.

Our inner ears harbour about 30,000 sensory hair cells in total in two different types, few of which can be dissected out of the inner ear and kept alive for study.

Heller”s team long ago realized that one solution to this problem was to use stem cells as a source for generating new hair cells, and now they”ve got the recipe.

They have devised what they refer to as a stepwise guidance protocol for making the hearing cells, starting with either mouse embryonic stem cells or induced pluripotent stem (iPS) cells, which are stem cell-like cells derived from adult mouse cells.

The study was published in the latest issue of the journal Cell, a Cell Press publication. (ANI)

Music helps Alzheimer”s sufferers in remembering new information

Washington, May 13 (ANI): Patients with Alzheimer”s disease (AD) are better able to remember new verbal information when it is provided in the context of music even when compared to healthy, older adults, claim researchers from Boston University School of Medicine (BUSM).

The findings, which currently appear on-line in Neuropsychologia, offer possible applications in treating and caring for patients with AD.

AD, the most common form of dementia, is characterized by a general, progressive decline in cognitive function that typically presents first as impaired episodic memory. The onset and rate of this decline tends to vary across cognitive domains, and some functions may be preferentially spared in patients with AD.

To determine whether music can enhance new learning of information, AD patients and healthy controls were presented with either the words spoken, or the lyrics sung with full musical accompaniment along with the printed lyrics on a computer screen. The participants were presented visually with the lyrics to 40 songs. Twenty of the song lyrics were accompanied by their corresponding sung recording and 20 were accompanied by their spoken recording.

After each presentation, participants were asked to indicate whether or not they were previously familiar with the song they had just heard. The BUSM researchers found accuracy was greater in the sung condition than in the spoken condition for AD patients but not for healthy older controls.

“Our results confirmed our hypothesis that patients with AD performed better on a task of recognition memory for the lyrics of songs when those lyrics were accompanied by a sung recording than when they were accompanied by a spoken recording,” said senior author Brandon Ally, PhD, an assistant professor of neurology and director of Neuropsychology Research at the BUSM Center for Translational Cognitive Neuroscience. “However, contrary to our hypothesis, healthy older adults showed no such benefit of music, he added. (ANI)

Mum”s voice ”can spur recovery from a coma”

Washington, May 11 (ANI): Mother”s voice can spur recovery from a coma, suggests a new American study.

In January 2009, Ryan, 21, a college student from Huntley, Ill., was in a coma after he had been flung from his snowmobile into a tree during an ice storm.

He had a traumatic brain injury; the fibres of his brain had been twisted and stretched from the impact.

Recordings from Ryan”s mother, father or sister were played through headphones for him four times a day.

Ryan”s mother Karen Schroeder”s voice, recorded on a CD, reminded him of his 4-H project when he was 10 and decided to raise pigs.

She said: “You bid on three beautiful squealing black and white piglets at the auction.

“We took them home in the trunk of our Lincoln Town Car, because we didn”t have a truck.”

All the recordings were part of a new clinical trial investigating whether repeated stimulation with familiar voices can help repair a coma victim”s injured brain networks and spur his recovery.

Ryan regained consciousness after nearly one month in the trial and has made steady progress during the past year.

Researchers, however, won”t know for certain if the therapy helped his recovery until the study is over.

Theresa Pape, a research assistant professor of physical medicine and rehabilitation at Northwestern University Feinberg School of Medicine and a research health scientist at Hines VA Hospital, is leading the study.

The research may be useful to young people like Ryan as well as soldiers injured in combat, who have a high rate of traumatic brain injuries from roadside bombs.

Pape said: “Traumatic brain injury is a huge issue in our society.

“Every 21 seconds, we have a new head injury and about one-third of those will be severe.”

Pape hopes the study will provide an answer to the question that families are desperate to know when a loved one is in a coma: ”Can he hear me?”

She is especially eager to know if these family voices can facilitate repair of the brain to improve the subject”s ability to function and process and understand information.

Pape”s hypothesis is that repeated exposure to familiar voices could help repair the brain”s neural networks, some of which become sheared in traumatic brain injury.

In a previous small pilot study, Pape observed that subjects in a vegetative state responded more to the voices of people who are familiar to them compared with non-familiar voices.

When those subjects heard voices of their family members, an MRI scan showed that parts of their brain were activated, appearing as bright yellow and red blobs of light scattered in an unorganised pattern.

With unfamiliar voices, there was little activation.

Pape said: “The question became are the familiar voices therapeutic in some way?

“Will they spur an improvement in behavior?”

She added: “I was weaned on language processing, how the brain responds to different linguistic stimuli as well as familiar or non-familiar voices, different sounds.

“This is a very speech pathology-based study.” (ANI)

New study offers hope to colon cancer patients

London, May 10 (ANI): Suppressing activity of common intestinal bacteria reduces tumour growth, a new American study has found.

The study, led by researchers at the University of California, San Diego School of Medicine, has appeared in the journal Nature Medicine.

According to lead author Eyal Raz, a professor of medicine at UC San Diego, the research could portend an eventual new form of treatment for people with familial adenomatous polyposis or FAP, an inherited condition in which numerous initially benign polyps form in the large intestine, eventually transforming into malignant colon cancer.

Raz, with colleagues at the UC San Diego School of Medicine and Wonkwang University in the Republic of Korea, looked at interactions between the vast numbers of bacteria typically found in the gastrointestinal tract and the tract”s mucosal lining.

Ordinarily, the bacteria and tract establish a kind of homeostasis.

Raz said: “In a normal host, these bacteria actually serve important roles, such as supporting cell production.

“But in susceptible hosts, the presence of these bacteria turns out to be detrimental.”

Specifically, Raz and his co-authors found that mice with an engineered mutation that closely mimics FAP in humans leaves the mice notably vulnerable to inflammatory factors produced by ordinary bacterial activity.

The constant inflammation enhances expression of an oncogene called c-Myc.

Very quickly, the mice develop numerous tumours in their intestines and typically do not survive past six months of age.

In humans, FAP can be equally devastating.

It is a genetic condition in which patients at a young age begin to develop hundreds to thousands of polyps in their intestine.

By age 35, 95 percent of individuals with FAP have polyps.

The polyps start out benign, but ultimately become malignant without treatment. Current treatment essentially consists of prophylactic surgery — removal of the polyps before they turn cancerous.

Raz said: “Right now, people with FAP don”t have many options.

“They develop the cancer relatively early in life and the only treatment is surgery, often a total colectomy – the removal of the entire colon. And that still doesn”t preclude the possibility of developing tumors elsewhere in the body.”

That”s why the second part of the study was especially encouraging, Raz said.

When researchers administered a protein enzyme called extracellular signal-related kinase or ERK, it appeared to suppress intestinal turmorigenesis in the mice, causing cancer proteins to degrade more rapidly and increasing the survival time of the mice.

If the inhibiting enzyme, which is currently undergoing clinical trials elsewhere, proves to be safe and effective, researchers say it eventually could provide FAP patients with another option other than surgery.

Raz said: “This is a clear case of nature and nurture in molecular biology.

“Nature is the host, who in some cases is going to be genetically predisposed to develop certain diseases. Nurture is the environment, which in this case is bacterial activity and its effects. The mechanism for what”s happening here with these mice and tumor growth is very clear. We know what we want and need to do.” (ANI)

Too much driving may up skin cancer risk

Washington, May 8 (ANI): Too much driving may increase the risk of skin cancer, according to a new study.

Among a group of about 1,050 patients in Saint Louis, facial skin cancers were found to occur more often on the left-side — the side that”s next to the window while driving, reports Live Science.

What’s more, the findings were most significant for men.

“Drivers need to be aware of the amount of sun exposure they receive behind the wheel,” said study researcher Dr. Scott Fosko, chair of dermatology at Saint Louis University School of Medicine. “The cumulative effect of being exposed to the sun builds up over many years.”

“Professional drivers learn to wear proper safety equipment be it gloves, steel-toed boots or safety glasses when appropriate,” Fosko said. “Sunscreen should be added to the list. An ounce of sunscreen applied as prevention on the road can be worth a lot of time and expense parked in a doctor”s office later on.”

The study will be published in a forthcoming issue of the Journal of the American Academy of Dermatology. (ANI)

Endometrial stem cells could repair Parkinson”s related brain cell damage

Washington, May 7 (ANI): In a study on mice, researchers found that stem cells derived from the endometrium (uterine lining) could repair brain cells damaged by Parkinson”s disease, according to Yale School of Medicine researchers.

Although these are preliminary results, the findings increase the likelihood that endometrial tissue could be harvested from women with Parkinson”s disease and used to re-grow brain areas that have been damaged by the disease, according to lead author Dr. Hugh S. Taylor.

Because of their ability to divide into new cell types, stem cells could be the key to treating many different kinds of diseases, like Parkinson”s, in which the body”s own cells are damaged or depleted.

Parkinson”s is caused by a breakdown of dopamine-producing nerve cells in the brain stem. Dopamine is a neurotransmitter that stimulates the motor neurons that in turn control muscles.

When dopamine production is reduced, the nerves fail to control movement or maintain coordination.

In their study, the researchers collected and cultured endometrial tissue from nine women, and verified that they could be transformed into dopamine-producing nerve cells like those in the brain.

“The dopamine levels in the mice increased once we transferred the endometrial stem cells into their brains. This is encouraging because women have a ready supply of stem cells that are easily obtained, can differentiate into other cell types. They may have great potential for treating multiple diseases,” said Taylor.

Highlighting the benefits of using endometrial stem cells, Taylor said the ethical concerns surrounding the use of embryonic stem cells are eliminated when using adult stem cells.

Taylor also pointed out that endometrial stem cells are one of the best sources for generating neurons because they appear to be less likely to be rejected than stem cells from other sources.

“This is just the tip of the iceberg of what we will be able to do with these cells. We believe these neurons are only the first of many cell types derived from endometrium that will be used to treat a variety of diseases,” said Taylor.

The findings are published in the Journal of Cellular and Molecular Medicine. (ANI)

Brain may use clot-busting drug naturally to offer protection against stroke

Washington, May 6 (ANI): The clot-busting stroke drug tPA (tissue-type plasminogen activator) can act as a neuroprotectant and may form the keystone of an adaptive response to a reduction in blood flow, say scientists from Emory University School of Medicine.

In a new study, the boffins have shown that certain parts of the brains of mice lacking the gene for tPA are more vulnerable to stroke. In addition, tPA can protect neurons in the same part of the brain from the stress of hypoxia (low oxygen).

The results are published online in the Journal of Clinical Investigation.

“tPA is not only a drug, it is a natural protein produced in response to hypoxia,” says senior author Manuel Yepes, MD, associate professor of neurology at Emory University School of Medicine. “If you look at the parts of brain where the gene for tPA is turned on the most, one of these is the hippocampus. It is well known that the hippocampus is especially vulnerable to hypoxia compared with other regions of the brain. We believe there is a reason for this overlap.”

The hippocampus is a structure in the middle of the brain thought to be responsible for memory formation. In mice lacking the gene for tPA, neurons in the hippocampus are more vulnerable to dying after a short simulated stroke lasting 20 minutes, Yepes and his colleagues found. In the laboratory, pre-treatment with tPA protects hippocampal neurons in culture from hypoxia. In contrast, tPA has the opposite effect on neurons from the cortex.

tPA”s protective properties suggest that it may be playing a role in a process called “ischemic preconditioning,” where a less-than-lethal stroke can protect the brain against a later repeat, Yepes says. tPA”s effects on the blood-brain barrier can be seen as a way to get more blood to a deprived part of the brain. (ANI)

Caffeine ‘effective in preventing cataract formation’

Washington, May 6 (ANI): Caffeine may provide the lens protection against damage that could lead to the formation of cataracts, according to a new study.

The study has been presented at the 2010 Annual Meeting of the Association for Research in Vision and Ophthalmology.

Researchers from the University of Maryland School of Medicine in Baltimore, MD hypothesized that caffeine may inhibit the intraocular generation of reactive oxygen species in the lens and consequent damage to the tissue.

The team studied the oxyradical effects in vitro by incubating mice lenses in medium exposed UVA in the presence of kynurenine with and without caffeine. In vivo studies were conducted in rats by incorporating caffeine with galactose in their diet. In both cases, caffeine was found to be effective in protecting the lens against damage.

As reported in the abstract, “These effects of caffeine have not been reported before and are hence considered highly interesting in view of its relatively high content in widely consumed beverages.” (ANI)