2/04/2009

Role of environmental factors in development of Parkinson's disease

The Parkinson's Institute today announced that new findings concerning the role of environmental factors in the development of Parkinson's disease will be reported at Asilomar (Pacific Grove, CA) as part of the final meeting of the Collaborative Centers for Parkinson's Disease Environmental Research...

The Parkinson's Institute today announced that new findings concerning the role of environmental factors in the development of Parkinson's disease will be reported at Asilomar (Pacific Grove, CA) as part of the final meeting of the Collaborative Centers for Parkinson's Disease Environmental Research (CCPDER). This collaborative research effort, sponsored by the National Institute of Environmental Health Sciences (NIEHS), brings together investigators from Emory University, the University of California Los Angeles and The Parkinson's Institute, which has served as the coordinating center for the study.


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Highlights of the research include:



* The role of pesticides (eg. Paraquat and Dieldrin) as potential risk factors for Parkinson's disease, a role suggested by both epidemiological statistics and laboratory evidence.



* The threat of toxic agents to damage neurons by causing the accumulation of harmful proteins.



* Intraneuronal protein aggregates as markers of Parkinson's pathology, based on work carried out at The Parkinson's Institute indicating that these aggregates could be formed as a consequence of toxic exposure.



* The importance of targeting a specific protein, alpha-synuclein, in order to achieve neuroprotection in Parkinson's



* The role of inflammation in the development of Parkinson's disease and the possibility that anti-inflammatory drugs could be beneficial to patients.



* The possibility that nicotine may act as a neuroprotective agent.



"Our collaboration with Emory University and UCLA has allowed us to make great strives in identifying environmental factors involved in the development of Parkinson's disease," said Donato A. Di Monte, M.D., director of basic research at The Parkinson's Institute. "The findings that will be discussed at Asilomar will help us better understand the disease process, intervene earlier with neuroprotective treatment and work on preventive measures against Parkinson's disease risk factors."



Source: The Parkinson's Institute


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Stem cells offer major step forward to develop new therapeutic approaches to hearing loss

Have you ever walked by someone listening to their i-Pod loud enough for you recognize the song? Studies have shown noise-induced hearing loss is going to become the next big epidemic affecting our younger generation though the effects wont show until it is too late to treat. In addition to loud noi...

Have you ever walked by someone listening to their i-Pod loud enough for you recognize the song? Studies have shown noise-induced hearing loss is going to become the next big epidemic affecting our younger generation though the effects won%26#8217;t show until it is too late to treat. In addition to loud noise, certain cancer drugs or genetic factors can cause hearing loss in humans due to loss or faulty development of the sensory %26#8216;microphones%26#8217; (hair cells) inside the ear %26#8211; the cochlea. Lost hair cells are not replaced and people exposed to these conditions face permanent hearing loss. Identification of the stem cells from the adult cochlea would be a major step forward to develop new therapeutic approaches to hearing loss.


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Members of the National Center for Regenerative Medicine research team, Dr. Robert Miller and Dr. Kumar Alagramam, both of Case Western Reserve University School of Medicine, recently published research findings in Developmental Neuroscience which suggest new ways of treating hearing loss. These researchers have isolated %26#8220;cochlear stem cells%26#8221; located in the inner ear and already primed for development into ear-related tissue due to their proximity to the ear and expression of certain genes necessary for the development of hearing. %26#8220;Previous work in our lab with young-adult mouse cochlear tissue showed expression of genes normally found in stem cells and neural progenitors. This led us to hypothesize that cochlea harbors stem cells and neural precursor cells. Our work in collaboration with Miller%26#8217;s lab supports our hypothesis%26#8221; Dr. Alagramam said. They say that in early life, these precursor cells may be able to regenerate hair cells, but their capacity to do so becomes limited as the ear develops and ages. The team's research is a major step in devising a therapy to reverse permanent hearing loss because it may lead to the activation of cochlear stem cells in the inner ear to regenerate new hair cells. %26#8220;Clearly we have miles to go before we reach our end goal, but the exciting part is now we can test compounds that could promote regeneration of hair cells from these precursor cells in vitro, we can study the genes expressed during the transition from stem cells to hair cells, and we can think of developing strategies for cell replacement, i.e. transplanting these cochlear stem cells into the adult cochlea to affect hair cell replacement in the mouse, by extension, in humans%26#8221; remarked Dr. Alagramam.



In this paper, Drs. Miller and Alagramam offer further evidence for the existence of cochlear stem cells in the mouse cochlea by confirming the ability to form %26#8216;stem cell%26#8217; spheres in culture and by characterizing these cells in terms of neural and hair cell development using a panel of stem cell development and hair cell markers. The formation of spheres from early postnatal cochlear tissues and their expression of a wide range of developmental markers unique to hair cells confirm the possibility that self-supporting hair cell precursors exist in or can be derived from the postnatal mammalian cochlea.



Currently there are no clinical treatments to repair these hair cells vital to normal hearing. In the United States, 30% of people over the age of 65 have a handicapping hearing loss and of those, one in 500 people become deaf before reaching adulthood. In most cases, the target is the highly specialized hair cells. Docked inside the spiral duct of the human cochlea are ~15,000 hair cells, which are highly specialized neuroepithelial cells that enable us to hear a violin or a whisper. These hair cells differ in length by minuscule amounts and are set in motion by specific frequencies of sound. We hear this sound because this motion induces the hair cell to release an electrical impulse which passes along the auditory nerve to the brain. If the sound is too loud, the hair cells are damaged and no longer send signals to the brain. Severely damaged hair cells do not repair themselves nor do they regenerate naturally.



While further research is necessary, the researchers believe these precursor cells have the potential to regenerate the damaged hair cells and restore normal hearing. The team has already begun animal studies to explore the use of cochlear stem cells in well-established hair cell ablation models and in deaf mouse mutants with predictable patterns of early hair cell loss. This line of research will evaluate the in vivo survival and differentiation of self-renewing cochlear cell populations and potentially lead to new therapies for the numerous individuals that are going to suffer from noise-induced hearing loss in the near future.



Source: Case Western Reserve University


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Better way to deliver drugs to tumors - Nanocylinders

Researchers at the University of Pennsylvania School of Medicine & School of Engineering and Applied Science have discovered a better way to deliver drugs to tumors. By using a cylindrical-shaped carrier they were able sustain delivery of the anticancer drug paclitaxel to an animal model of lung can...

Researchers at the University of Pennsylvania School of Medicine %26amp; School of Engineering and Applied Science have discovered a better way to deliver drugs to tumors. By using a cylindrical-shaped carrier they were able sustain delivery of the anticancer drug paclitaxel to an animal model of lung cancer ten times longer than that delivered on spherical-shaped carriers. These findings have implications for drug delivery as well as for better understanding cylinder-shaped viruses like Ebola and H5N1 influenza.


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This study appeared online in Nature Nanotechnology in advance of print publication in March 2007.



%26#8220;These are particles that go with the flow,%26#8221; says Dennis E. Discher, PhD, Professor of Chemical and Biomolecular Engineering at Penn%26#8217;s Institute for Medicine and Engineering. %26#8220;The blood stream is constantly pumping, and these cylindrical nanoparticles align with the flow and persist in circulation considerably longer than any known spherical particles.%26#8221;



In this study, the research team used skinny cylindrical nanoparticles composed of synthetic polymers to deliver the anticancer drug paclitaxel to a human lung tumor tissue implanted in mice. The cylinders have diameters as small as 20 nm and lengths approaching the size of blood cells. The paclitaxel shrunk the tumors and, because the cylinders remained in circulation for up to one week after injection, they delivered a more effective dose, killing more cancer cells and shrinking the tumors to a much greater extent. Spherical nanoparticles typically only stay in circulation for a few hours.



The research team used nanoparticles that contained one water-loving chain of a common polymer called polyethyleneglycol (PEG). PEGs are commonly found in everyday items like shampoo and some foods. Although synthetic, PEGs have already been approved as biocompatible to humans, making them ideal carriers, note the researchers.



While these findings could impact the way lung cancer is treated, this discovery of how to more effectively deliver drugs to the body could also improve the treatment of such other illnesses as cardiovascular disease as well as other types of cancers.



This discovery is also helping scientists understand why some viruses are so effective. %26#8220;Cylindrical delivery systems exist in nature, with two prime examples being the Ebola virus and the H5N1 Influenza virus,%26#8221; says Discher. %26#8220;These findings can help us understand how this shape evolved in nature and the advantages of using it for treating people.%26#8221;



Source: University of Pennsylvania


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Selfless and social behavior is genetic

A new study in Journal of Personality shows that selfless and social behavior is not purely a product of environment, specifically religious environment. After studying the behavior of adult twins, researchers found that, while altruistic behavior and religiousness tended to appear together, the cor...

A new study in Journal of Personality shows that selfless and social behavior is not purely a product of environment, specifically religious environment. After studying the behavior of adult twins, researchers found that, while altruistic behavior and religiousness tended to appear together, the correlation was due to both environmental and genetic factors.


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According to study author Laura Koenig, the popular idea that religious individuals are more social and giving because of the behavioral mandates set for them is incorrect. %26#8220;This study shows that religiousness occurs with these behaviors also because there are genes that predispose them to it.%26#8221;



%26#8220;There is, of course, no specific gene for religiousness, but individuals do have biological predispositions to behave in certain ways,%26#8221; says Koenig. %26#8220;The use of twins in the current study allowed for an investigation of the genetic and environmental influences on this type of behavior.%26#8221;



This research is another example of the way that genes have an impact on behavior. %26#8220;Society as a whole assumes that home environments have large impacts on behavior, but studies in behavior genetics are repeatedly showing that our behavior is also influenced by our genes,%26#8221; says Koenig.



Source: Journal of Personality


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Is breast feeding really best for babies?

Most new parents want to give their babies the very best start in life. They give careful thought to everything from nursery decorations to choice of family physician. Yet when it comes to their babies' nutrition, relatively few women in the United States heed the advice of the American Academy of P...

Most new parents want to give their babies the very best start in life. They give careful thought to everything from nursery decorations to choice of family physician. Yet when it comes to their babies' nutrition, relatively few women in the United States heed the advice of the American Academy of Pediatrics to breastfeed babies "for at least 12 months, and thereafter for as long as is mutually desired."



"With so much concern for what they put into their own bodies, it may be surprising to learn that almost one-third of all new mothers still don't breastfeed," said John Messmer, a physician with Penn State's Family and Community Medicine center in Hershey. "After five months, two-thirds of nursing mothers have stopped breastfeeding altogether."


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While there's nothing wrong with formula, said Messmer, even the companies that make it concede that breastfeeding is best. Why?



"Breast milk is designed specifically to feed human babies," he explained. "Breastfed babies digest their mother's milk more easily than formula and absorb more nutrients from it." In contrast to formula, babies are never allergic to their mother's milk.



Unlike formula, the composition of breast milk adapts to the growing baby's changing nutritional needs. Mother's milk contains more than 100 ingredients not found in formula, including crucial types of fatty acids such as RHA and DHA, thought to be responsible for healthy brain and eye functioning.



Judy Hopkinson, assistant professor at the Children's Nutrition Research Center at the Baylor College of Medicine, has observed, "Breast milk is really primarily an immune booster. We think of it as nutrition, but it is really integral to the immune system." Approximately 80 percent of the cells in breast milk are macrophages, cells that kill viruses, fungi and bacteria. Breastfed babies "receive maternal antibodies in the milk that reduce the risk of ear infections and diarrhea, as well as urinary and intestinal infections," commented Messmer.



Most crucially, the mother's body responds to whatever disease is present in the environment by making antibodies that are then passed in the milk to her baby, giving breastfed babies an immune-protective advantage over bottle-fed babies.



What's more, added Messmer, "Breastfed babies are less likely to be overweight or anemic and recent studies suggest that they may have an edge in brain development." Current research from the Centers for Disease Control links breastfeeding with lower rates of Sudden Infant Death Syndrome. While more research is needed to reach definitive conclusions, initial studies have found that babies who are not breastfed have higher rates of serious health conditions such as diabetes, lymphoma and bacterial meningitis.



With all these reasons for breastfeeding, asked Messmer, "Why are so many women using formula?" Some say formula is more convenient, "but is it?" he asked. "Formula involves mixing and heating it to the proper temperature and storing any unused portion in the refrigerator, not to mention carrying bottles everywhere and disposing of the cans properly."



In contrast to formula, breast milk is sterile and, straight from the breast, has no chance of becoming contaminated. Said Messmer, "Using formula sounds less convenient when you consider that mother's milk is always there and at the right temperature." In addition, Messmer added, breastfeeding may have psychological benefits since it "promotes the close physical contact important for developing babies."



Despite the clear evidence of breastfeeding's benefits, the number of nursing moms has been dropping since its peak in the mid-1980s. "In general, there's less support for extended breastfeeding in mainstream American culture than in some other societies," said Kay Hoover of the Penn State Breastfeeding Clinic. Women from countries with strong community support for breastfeeding (Norway, Sweden, Denmark, Poland and Romania top the list) come closer to achieving the World Health Organization's recommendation to breastfeed babies for a minimum of two years.



"When women feel unsupported in their decision to breastfeed, it can undermine their ability to nurse successfully," noted Hoover. "But seeking advice from a lactation consultant and organizations such as La Leche League can improve a new mom's chances of having a positive breastfeeding experience -- and that's what is in the best interest of babies."



Messmer agreed. "Ideally, all babies would be exclusively breastfed until 6 months of age." The undeniable benefits, he said, "make it worthwhile to continue to age 12 months and beyond."



Source: Penn State


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Plastic motor allows robotic medical devices to work with MRI machines

Engineers at the Johns Hopkins Urology Robotics Lab report the invention of a motor without metal or electricity that can safely power remote-controlled robotic medical devices used for cancer biopsies and therapies guided by magnetic resonance imaging. The motor that drives the devices can be so pr...

Engineers at the Johns Hopkins Urology Robotics Lab report the invention of a motor without metal or electricity that can safely power remote-controlled robotic medical devices used for cancer biopsies and therapies guided by magnetic resonance imaging. The motor that drives the devices can be so precisely controlled by computer that movements are steadier and more precise than a human hand.



"Lots of biopsies on organs such as the prostate are currently performed blind because the tumors are typically invisible to the imaging tools commonly used," says Dan Stoianovici, Ph.D., an associate professor of urology at Johns Hopkins and director of the robotics lab. "Our new MRI-safe motor and robot can target the tumors. This should increase accuracy in locating and collecting tissue samples, reduce diagnostic errors and also improve therapy."


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A description of the new motor, made entirely out of plastics, ceramics and rubber, and driven by light and air, was published in the February issue of the IEEE/ASME Transactions on Mechanotronics.



The challenge for his engineering team was to overcome MRI%26#8217;s dependence on strong magnetic interference. Metals are unsafe in MRIs because the machine relies on a strong magnet, and electric currents distort MR images, says Stoianovici. The team used six of the motors to power the first-ever MRI-compatible robot to access the prostate gland. The robot currently is undergoing preclinical testing.



"Prostate cancer is tricky because it only can be seen under MRI, and in early stages it can be quite small and easy to miss," says Stoianovici.



The new Johns Hopkins motor, dubbed PneuStep, consists of three pistons connected to a series of gears. The gears are turned by air flow, which is in turn controlled by a computer located in a room adjacent to the MRI machine. "We%26#8217;re able to achieve precise and smooth motion of the motor as fine as 50 micrometers, finer than a human hair," says Stoianovici.



The robot goes alongside the patient in the MRI scanner and is controlled remotely by observing the images on the MR. The motor is rigged with fiber optics, which feeds information back to the computer in real time, allowing for both guidance and readjustment.



"The robot moves slowly but precisely, and our experiments show that the needle always comes within a millimeter of the target," says Stoianovici. This type of precision control will allow physicians to use instruments in ways that currently are not possible, he says.



"This remarkable robot has a lot of promise - the wave of the future is image-guided surgery to better target, diagnose and treat cancers with minimally invasive techniques," says Li-Ming Su, M.D., an associate professor of urology and director of laparoscopic and robotic urologic surgery at the Brady Urological Institute at Hopkins.



Image: http://www.hopkinsmedicine.org/Press_releases/2007/images/robot.jpg



Source: Johns Hopkins Medical Institutions


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Flexible electronic membranes aid brain research

Flexible electronic membranes may overcome a longstanding dilemma faced by brain researchers: How to replicate injuries in the lab without destroying the electrodes that monitor how brain cells respond to physical trauma.Developed by a team of engineers at Princeton University, Columbia University a...

Flexible electronic membranes may overcome a longstanding dilemma faced by brain researchers: How to replicate injuries in the lab without destroying the electrodes that monitor how brain cells respond to physical trauma.



Developed by a team of engineers at Princeton University, Columbia University and the University of Cambridge, the membranes feature microelectrodes that are able to withstand the sudden stretching that is used to simulate severe head trauma. The systems could allow far more nuanced studies of brain injury than previously possible and may lead to better treatments in the minutes and hours immediately following the injury. The work also has implications for other areas of medicine, including next-generation prosthetics, as well as myriad industry and military applications.


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%26#8220;This is an immediate application of the electronics of the future,%26#8221; said Sigurd Wagner, a Princeton professor of electrical engineering. Wagner and former Princeton postdoctoral researcher Stephanie Lacour are part of a National Institutes of Health-funded project to develop flexible arrays of microelectrodes for brain research. Led by Barclay Morrison III, an assistant biomedical engineering professor at Columbia, members of the team will present their work at the April 9-13 conference of the Materials Research Society in San Francisco.



Existing techniques to study traumatic brain injury have been limited because it is almost impossible to insert an electrode into a cell to obtain a recording, remove the probe, injure the cell, and then reinsert the probe into the same cell, Morrison said. Because of this limitation, researchers rely on other surrogate markers of injury, such as cell death.



%26#8220;In terms of traumatic brain injury, there can be a lot of functional damage to the brain in other ways than just killing a cell,%26#8221; Morrison said. %26#8220;Neurons can still be alive, but not properly firing,%26#8221; which leads to problems ranging from comas to epilepsy.



These improperly functioning neurons can now be assessed by the electrodes in the stretchable membranes. After brain cells have been placed on the flexible surface and allowed to grow, the researchers measure their normal activity. The membrane is then suddenly stretched and returned to its original form. Having withstood the shock, the electrodes embedded in the membrane continue to monitor the cellular activity, providing a before and after picture of traumatic brain injury.



Future work will continue to refine these measurements and also attempt to obtain readings from cells during the injury events themselves, Morrison said. The flexible electrodes also can be used to provide electrical input to brain tissue and may one day be used to induce learning in brain cells damaged by trauma. This technology also has promising applications for the engineering of nervous, muscular and skeletal tissue. For instance, Morrison said, the electrodes could potentially be used to train heart tissue grown in the lab to contract appropriately when stimulated.



The new membranes build upon work done by Lacour during her time at Princeton in Wagner%26#8217;s lab. Lacour now is managing research in flexible electronics for neuroscience at the University of Cambridge in England. She has been recognized by Technology Review magazine, which named her to its 2006 list of 35 leading innovators under age 35.



Together, the engineers created the first working stretchable circuits by linking tiny pieces of traditional semiconductors mounted on a rubbery membrane with thin pieces of gold. Even when stretched, the circuits maintained their ability to conduct electricity.



Research on the flexible membranes also is likely to contribute to the longstanding challenge of connecting electronic devices to the human nervous system, Wagner said. Prosthetic devices, for example, could be coated with electronic %26#8220;skin%26#8221; that senses touch and temperature and sends that information back to the brain like any natural human limb.



%26#8220;A basic problem with the interface between electronics and living tissue is that electronics are hard and tissues are soft,%26#8221; he said, noting that nerve cells quickly become irritated when in contact with the hard electrodes of today. The hope is that the devices of the future will flex with living tissue, maintaining a connection without damaging the human cells.



Source: Princeton University


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Modified bone marrow cells can help recovery in an animal model of multiple sclerosis

A new study published in PLoS Medicine has shown that modified bone marrow cells can help recovery in an animal model of multiple sclerosis (MS). Harald Neumann and colleagues from the University of Bonn modified myeloid precursor cells to express a protein (triggering receptor expressed on myeloid ...

A new study published in PLoS Medicine has shown that modified bone marrow cells can help recovery in an animal model of multiple sclerosis (MS). Harald Neumann and colleagues from the University of Bonn modified myeloid precursor cells to express a protein (triggering receptor expressed on myeloid cells-2 (TREM2), which is normally made by microglia - a cell from the nervous system - and injected these TREM2-expressing cells into the veins of mice with experimental autoimmune encephalomyelitis (EAE, an animal model of MS).


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The researchers examined the migration of these cells into the spinal cord of the mice, their effect on the symptoms of EAE, and what effect there was on the clearance of cell debris and inflammatory responses in the spinal cord of the mice. They found that neither TREM2-expressing nor control myeloid precursor cells migrated into the spinal cord when injected into healthy mice or into animals just beginning to show the symptoms of EAE. However, both control and modified cells migrated into the spinal cord when injected into animals when EAE symptoms were at their peak. The injection of TREM2-expressing myeloid precursor cells (but not control myeloid precursor cells) at this time reduced EAE symptoms and nerve damage, and halted loss of myelin and also increased the clearance of cell debris and myelin fragments.



These findings will need to be repeated in further animal models before the implications for human disease are clear; however, they open up an avenue of further research.



http://medicine.plosjournals.org/perlserv/?request=get-document%26amp;doi=10.1371/journal.pmed.0040124




Source: PLOS


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Foods rich in cocoa appear to reduce blood pressure - Drinking tea may not

Foods rich in cocoa appear to reduce blood pressure but drinking tea may not, according to an analysis of previously published research in the April 9 issue of Archives of Internal Medicine, one of the JAMA/Archives journals.
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Current guidelines advise individuals with hypertension (high bloo...

Foods rich in cocoa appear to reduce blood pressure but drinking tea may not, according to an analysis of previously published research in the April 9 issue of Archives of Internal Medicine, one of the JAMA/Archives journals.


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Current guidelines advise individuals with hypertension (high blood pressure) to eat more fruits and vegetables, according to background information in the article. Compounds known as polyphenols or flavonoids in fruits and vegetables are thought to contribute to their beneficial effects on blood pressure and cardiovascular risk. "Tea and cocoa products account for the major proportion of total polyphenol intake in Western countries," the authors write. "However, cocoa and tea are currently not implemented in cardioprotective or anti-hypertensive dietary advice, although both have been associated with lower incidences of cardiovascular events."



Dirk Taubert, M.D., Ph.D., and colleagues at the University Hospital of Cologne, Germany, conducted a meta-analysis of 10 previously published trials, five of cocoa's effects on blood pressure and five involving tea. All results were published between 1966 and 2006, involved at least 10 adults and lasted a minimum of seven days. The studies were either randomized trials, in which some participants were randomly assigned to cocoa or tea groups and some to control groups, or used a crossover design, in which participants' blood pressure was assessed before and after consuming cocoa products or tea.



The five cocoa studies involved 173 participants, including 87 assigned to consume cocoa and 86 controls, 34 percent of whom had hypertension (high blood pressure). They were followed for a median (middle) duration of two weeks. Four of the five trials reported a reduction in both systolic (the top number, when the heart contracts) and diastolic (the bottom number, when the heart relaxes) blood pressure. Compared with those who were not consuming cocoa, systolic blood pressure was an average of 4.7 millimeters of mercury lower and diastolic blood pressure was an average of 2.8 millimeters of mercury lower.



The effects are comparable to those achieved with blood pressure-lowering medications, the authors note. "At the population level, a reduction of 4 to 5 millimeters of mercury in systolic blood pressure and 2 to 3 millimeters of mercury in diastolic blood pressure would be expected to substantially reduce the risk of stroke (by about 20 percent), coronary heart disease (by 10 percent) and all-cause mortality (by 8 percent)," they write.



Of the 343 individuals in the five tea studies, 171 drank tea and 172 served as controls, for a median duration of four weeks. Drinking tea was not associated with a reduction in blood pressure in any of the trials.



Tea and cocoa are both rich in polyphenols, but while black and green tea contain more compounds known as flavan-3-ols, cocoa contains more of another type of polyphenol, procyanids. "This suggests that the different plant phenols must be differentiated with respect to their blood pressure-lowering potential and thus cardiovascular disease prevention, supposing that the tea phenols are less active than cocoa phenols," the authors write.



The findings do not indicate a widespread recommendation for higher cocoa intake to decrease blood pressure, but it appears reasonable to substitute phenol-rich cocoa products such as dark chocolate for other high-calorie or high-fat desserts or dairy products, they continue. "We believe that any dietary advice must account for the high sugar, fat and calorie intake with most cocoa products," the authors conclude. "Rationally applied, cocoa products might be considered part of dietary approaches to lower hypertension risk."



Source: JAMA


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Nanotexture on implant material may prevent rejection by body

Biomedical engineers are constantly coming up with ways to repair the human body, replacing defective and worn out parts with plastic, titanium, and ceramic substitutesbut the body does not always accept such substitutes seamlessly. Engineers from Brown and Purdue universities have found that simply...

Biomedical engineers are constantly coming up with ways to repair the human body, replacing defective and worn out parts with plastic, titanium, and ceramic substitutes %26#8211; but the body does not always accept such substitutes seamlessly. Engineers from Brown and Purdue universities have found that simply changing the surface texture of implants can dramatically change the way cells colonize a wide variety of materials.


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Two recent experiments have focused on the materials used in stents %26#8211; those springy little cylinders that hold open once-clogged arteries %26#8211; and artificial blood vessels. Currently only about 30 percent of small diameter blood vessel grafts (less than 6 mm diameter) last more than five years, and up to 20 percent of stents need to be replaced because the artery walls thicken in and around them in a process known as restenosis. Drug-coated stents were introduced years ago as one way to combat this problem, but concerns have surfaced recently about increased clotting.



Instead of using chemistry to fight the body%26#8217;s response to such foreign materials, Thomas Webster, an associate professor of engineering, and Karen Haberstroh, an assistant professor of engineering, thought maybe they could use physical structure to allow the foreign materials to blend in better. %26#8220;What we%26#8217;re trying to do is fundamentally different,%26#8221; says Webster. %26#8220;We%26#8217;re trying to find materials that the body accepts, rather than develop drugs or develop materials that will kill a cell %26#8211; no matter if it kills a bad cell or a good cell. We%26#8217;re trying to find materials that accept good cells, as opposed to killing off bad cells.%26#8221;



Normal healthy blood vessels have a thin lining of specialized cells called the endothelium, surrounded by a thicker layer of smooth muscle cells that make up the arterial wall. The proteins collagen and elastin make up much of this lining and create a texture of fine nanoscale bumps on the inside of the blood vessel. This contrasts strongly with most of the materials used in implants, which have microscale texture, but are nearly smooth at the nanoscale.



When the researchers changed the surface texture of implant materials to better match the natural texture of the endothelium, they found that endothelial cells quickly colonized the foreign surfaces, effectively camouflaging them and preventing smooth muscle cells from overgrowing the implants. Once the endothelial cells form a single, solid layer, they stop piling on and switch to producing the proteins collagen and elastin.



In one experiment, published with Purdue University graduate student Saba Choudhary in the journal Tissue Engineering, Webster and Haberstroh pressed together titanium particles that were less than 1 micron in size to create titanium with nanoscale surface texture. When they compared samples of the nanostructured material to conventional titanium in mixed cell culture, they found that the nanoscale surface features encouraged endothelial cells to colonize the material and spread much faster than smooth muscle cells. Where endothelial cells established themselves, they formed a single thin layer that inhibited overgrowth of the smooth muscle cells that tends to narrow stented arteries.



In another experiment, published in the Journal of Biomedical Materials Research with Purdue graduate student Derick Miller, the team molded pieces of PLGA, a biodegradable polymer often used for blood vessel grafts, so they came out completely covered with bumps that were 100, 200 or 500 nanometers in diameter. The surface with 200-nanometer features strongly favored the adsorption and spreading of fibronectin, a protein that helps endothelial cells quickly coat the graft.



Webster and Haberstroh%26#8217;s next step will be to test such nanostructured implants in live animals. If the same behavior holds true for materials placed in the body, the rapid growth of endothelial cells would help the implants to integrate quickly into existing blood vessels, provoking less immune response and a longer-lasting repair.



Source: Brown University


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Stem cell transplantation helps patients with type 1 diabetes

A therapy that includes stem cell transplantation induced extended insulin independence in patients with type 1 diabetes mellitus, according to a preliminary study in the April 11 issue of JAMA.Type 1 diabetes mellitus (DM) results from a cell-mediated autoimmune attack against pancreatic beta cells...

A therapy that includes stem cell transplantation induced extended insulin independence in patients with type 1 diabetes mellitus, according to a preliminary study in the April 11 issue of JAMA.



Type 1 diabetes mellitus (DM) results from a cell-mediated autoimmune attack against pancreatic beta cells. At the time of clinical diagnosis, approximately 60 percent to 80 percent of the beta-cell mass has been destroyed, according to background information in the article. Beta-cell preservation has been shown to be an important target in the management of type 1 DM and in the prevention of its related complications.


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Julio C. Voltarelli, M.D., Ph.D., of the University of S%26#227;o Paulo, Ribeir%26#227;o Preto, Brazil, in collaboration with Richard Burt, M.D., of the Northwestern University Feinberg School of Medicine, Chicago, and colleagues conducted a study to examine the effect of high-dose immunosuppression followed by autologous nonmyeloablative hematopoietic stem cell transplantation (AHST) to preserve beta-cell function in 15 newly diagnosed patients with type 1 DM. AHST, which uses a patient's own blood stem cells, involves the removal and treatment of the stem cells, and their return to the patient by intravenous injection.



During a 7 to 36-month follow-up, 14 patients became insulin-free (one for 35 months, four for at least 21 months, seven for at least six months; and two with late response were insulin-free for one and five months, respectively). Among those, one patient resumed insulin use one year after AHST. The only severe adverse effects were pneumonia in one patient and endocrine dysfunction in two others.



"This is, to our knowledge, the first report of high-dose immunosuppression followed by autologous nonmyeloablative hematopoietic stem cell transplantation for human type 1 DM. Very encouraging results were obtained in a small number of patients with early-onset disease. Ninety-three percent of patients achieved different periods of insulin independence and treatment-related toxicity was low, with no mortality. Further follow-up is necessary to confirm the duration of insulin independence and the mechanisms of action of the procedure. In addition, randomized controlled trials and further biological studies are necessary to confirm the role of this treatment in changing the natural history of type 1 DM and to evaluate the contribution of hematopoietic stem cells to this change," the authors conclude.



Source: JAMA


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Flu vaccine made in insect cells just as safe as conventional vaccine

An experimental flu vaccine made in insect cellsnot in eggs, where flu vaccines currently available in the United States are grownis safe and as effective as conventional vaccines in protecting people against the flu, according to results published in the April 11 issue of the Journal of the America...

An experimental flu vaccine made in insect cells %26#8211; not in eggs, where flu vaccines currently available in the United States are grown %26#8211; is safe and as effective as conventional vaccines in protecting people against the flu, according to results published in the April 11 issue of the Journal of the American Medical Association.



Removing eggs from the flu vaccine manufacturing process is one option for health officials seeking to protect the population from seasonal flu as well as a potential bird-flu pandemic. Using eggs to grow vaccine takes time; a flu vaccine that relies on a different technology is capable of being produced in large amounts much more quickly, a key advantage if a bird flu pandemic were to occur.


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%26#8220;Eggs can be very cumbersome to work with,%26#8221; said John Treanor, M.D., the flu expert at the University of Rochester Medical Center who led the study of 460 people reported in JAMA. %26#8220;When you need hundreds of millions of fertilized eggs, you%26#8217;re dealing with a whole host of agricultural issues, as well as scientific concerns regarding the flu virus itself. Flu viruses can be temperamental, and it%26#8217;s not always an easy matter to get the virus to grow as you want in eggs.%26#8221;



The use of cell culture systems to grow vaccines %26#8211; using viruses as tiny factories to churn out mass amounts of vaccines %26#8211; is a growing business. A similar technology using human cell lines is used to produce the hepatitis B vaccine, while one form of a vaccine against human papilloma virus is made using the same insect cell line used in the JAMA study.



In the study conducted by Treanor, together with colleagues at Cincinnati Children%26#8217;s Hospital and the University of Virginia, scientists tested a vaccine called FluBlOk that is made by Protein Sciences Corp. of Meriden, Ct. FluBlOk relies on a virus known as baculovirus, which normally infects insects, to churn out the key components of the flu virus in a cell line drawn from caterpillars.



In the study funded by the company of 460 healthy people ages 18 to 49, one-third of the participants received a smaller dose of the vaccine (75 micrograms), one-third received a larger dose (135 micrograms), and one-third received a placebo shot that didn%26#8217;t include vaccine. Each of the %26#8220;real%26#8221; shots included vaccine designed to protect against the three strains of flu that had been predicted to be the greatest threat during the 2004-2005 winter, when the study was conducted.



As the scientists expected, both the smaller dose and the larger dose caused an immune reaction generally considered effective for fighting off the flu, with the larger dose creating a stronger immune response. The side effects of the vaccine were the same as those usually reported from a typical flu shot %26#8211; mainly mild arm pain.



Then, in the months that followed, there were seven cases of flu in the group that had not received the vaccine, compared to two cases in the group that received the smaller dose, and no cases in the group that received the larger dose. Together, the two vaccines reduced flu infection rate by 86 percent.



%26#8220;Even though the study was small, the results are very promising,%26#8221; said Treanor, who is professor of Medicine and of Microbiology and Immunology and director of the Vaccine and Treatment Evaluation Unit at the University of Rochester. %26#8220;While we certainly hoped and expected the vaccine to be protective, you don%26#8217;t know that until you actually test it. We%26#8217;ve shown that the vaccine does work in the real world.%26#8221;



Freedom from the egg brings implications important to a world facing the threat of pandemic bird flu.



For decades the nation%26#8217;s efforts to prevent flu have centered on growing flu virus in hundreds of millions of fertilized eggs, with each egg containing less than a teaspoonful of material that will ultimately become part of a vaccine. It%26#8217;s typically a six-month process to produce enough flu vaccine to protect the public.



Taking eggs out of the process would likely slice one or two months off the production process, Treanor said. In case of a bird-flu pandemic, that would allow manufacturers to ramp up vaccine production more quickly than if they had to wait for the production of millions of eggs. Not relying on chicken eggs might also be advisable in case a bird flu pandemic hits chicken flocks hard. The insect-cell technology also simplifies the manufacturing process in another way: A live flu virus is needed when growing vaccine in eggs, a danger when working with a potent bird-flu strain.



The technology would also help make it possible to boost the dose that patients receive, by increasing the nation%26#8217;s capacity to churn out vaccine. That%26#8217;s especially crucial in the fight against bird flu, as Treanor and other scientists have shown that an experimental vaccine appears to be effectively only at high doses.



The experimental vaccine differs from approved vaccines in another way as well. The experimental vaccine focuses on a portion of the flu virus known as the hemagglutinin, which the virus uses to attach to blood cells. Unlike conventional vaccines, FluBlOk does not also include neuraminidase, an enzyme that allows a flu virus to replicate and spread. While the hemagglutinin is the focus of most vaccines, scientists have been curious to measure how a vaccine without neuraminidase performs.



Source: University of Rochester


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