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Thursday, June 21, 2012

Most Beautifull Nature Photography Yellow




















The very first unit ...



 
It is with these devices has begun the development of various gadgets, without which our modern life difficult to manage ...
ANITA - the first electronic calculator (1961)



 
Sony CDP 101 CD player first CD (1982)
Motorola DynaTAC 8000X - first cell phone (1983) The dimensions are impressive ...
Pulsar - the first electronic watch (1970)
Ibm5100 - the first portable computer (1975)
Dycam Model I - the first commercial digital camera (1990)
NeXTcube - one of the first Web server (1990)
Regency TR1 - first transistor radio (1954)
Sony TPS-L2 - first audiokassetny Player Walkman (1979)
IBM SImon - the first smartphone (1993)
Saehan / Eiger Labs F10/F20 - is the first portable MP3 player (1998)
The Telcan - first VCR that could record live TV directly from your TV (1963)

Cannabis Catch-All?



Researchers in the U.K. are looking to breed marijuana to make medicines for metabolic disorders, epilepsy, and other diseases.

By Jef Akst |
GW Pharmaceuticals—the United Kingdom’s only legal cannabis production facility—is already developing Sativex, a drug consisting of two principal cannabinoids (THC and CBD). Sativex is currently in Phase III trials for treating muscle spasticity in multiple sclerosis patients. But GW’s researchers are also studying how marijuana derivatives could be used to treat a much wider range of diseases, including metabolic disorders, epilepsy, ulcerative colitis, psychosis, brain injury, and cancer pain.
“As rigorous modern research with cannabinoids comes to fruition, a new era of treatment options may have arrived,” David Potter, director of Botanical Research and Cultivation at GW Pharmaceuticals who wrote about the company’s efforts this month in The Biologist, said in a press release.
GW’s strategy is to breed cannabis plants that produce varying levels of natural cannabinoids. Among the plants the team has bred are those with high levels of THCV, a cannabinoid that is structurally similar to THC, but is normally present only in low quantities. There is evidence that THCV regulates a variety of metabolic functions, including lipid deposition, cellular energy expenditure, and insulin resistance, and company researchers are hopeful it will prove an effective treatment against type II diabetes.
Stay tuned for our July feature on alternative medicines to learn more about the potential uses of medical marijuana that are being investigated, as well as the legitimacy of other non-traditional treatments, including acupuncture, probiotics, and psychedelics.
Posted by
Robert Karl Stonjek

THE GALAPAGOS ISLANDS






















Scientists Identify Protein Required to Regrow Injured Nerves in Limbs



These are images of axon regeneration in mice two weeks after injury to the hind leg’s sciatic nerve. On the left, axons (green) of a normal mouse have regrown to their targets (red) in the muscle. On the right, a mouse lacking DLK shows no axons have regenerated, even after two weeks. (Credit: Jung Eun Shin)
ScienceDaily (June 20, 2012) — A protein required to regrow injured peripheral nerves has been identified by researchers at Washington University School of Medicine in St. Louis.
The finding, in mice, has implications for improving recovery after nerve injury in the extremities. It also opens new avenues of investigation toward triggering nerve regeneration in the central nervous system, notorious for its inability to heal.
Peripheral nerves provide the sense of touch and drive the muscles that move arms and legs, hands and feet. Unlike nerves of the central nervous system, peripheral nerves can regenerate after they are cut or crushed. But the mechanisms behind the regeneration are not well understood.
In the new study, published online June 20 in Neuron, the scientists show that a protein called dual leucine zipper kinase (DLK) regulates signals that tell the nerve cell it has been injured -- often communicating over distances of several feet. The protein governs whether the neuron turns on its regeneration program.
"DLK is a key molecule linking an injury to the nerve's response to that injury, allowing the nerve to regenerate," says Aaron DiAntonio, MD, PhD, professor of developmental biology. "How does an injured nerve know that it is injured? How does it take that information and turn on a regenerative program and regrow connections? And why does only the peripheral nervous system respond this way, while the central nervous system does not? We think DLK is part of the answer."
The nerve cell body containing the nucleus or "brain" of a peripheral nerve resides in the spinal cord. During early development, these nerves send long, thin, branching wires, called axons, out to the tips of the fingers and toes. Once the axons reach their targets (a muscle, for example), they stop extending and remain mostly unchanged for the life of the organism. Unless they're damaged.
If an axon is severed somewhere between the cell body in the spinal cord and the muscle, the piece of axon that is no longer connected to the cell body begins to disintegrate. Earlier work showed that DLK helps regulate this axonal degeneration. And in worms and flies, DLK also is known to govern the formation of an axon's growth cone, the structure responsible for extending the tip of a growing axon whether after injury or during development.
The formation of the growth cone is an important part of the early, local response of a nerve to injury. But a later response, traveling over greater distances, proves vital for relaying the signals that activate genes promoting regeneration. This late response can happen hours or even days after injury.
But in mice, unlike worms and flies, DiAntonio and his colleagues found that DLK is not involved in an axon's early response to injury. Even without DLK, the growth cone forms. But a lack of DLK means the nerve cell body, nestled in the spinal cord far from the injury, doesn't get the message that it's injured. Without the signals relaying the injury message, the cell body doesn't turn on its regeneration program and the growth cone's progress in extending the axon stalls.
In addition, it was shown many years ago that axons regrow faster after a second injury than axons injured only once. In other words, injury itself increases an axon's ability to regenerate. Furthering this work, first author Jung Eun Shin, graduate research assistant, and her colleagues found that DLK is required to promote this accelerated growth.
"A neuron that has seen a previous injury now has a different regenerative program than one that has never been damaged," Shin says. "We hope to be able to identify what is different between these two neurons -- specifically what factors lead to the improved regeneration after a second injury. We have found that activated DLK is one such factor. We would like to activate DLK in a newly injured neuron to see if it has improved regeneration."
In addition to speeding peripheral nerve recovery, DiAntonio and Shin see possible implications in the central nervous system. It is known for example, that some of the important factors regulated and ramped up by DLK are not activated in the central nervous system.
"Since this sort of signaling doesn't appear to happen in the central nervous system, it's possible these nerves don't 'know' when they are injured," DiAntonio says. "It's an exciting idea -- but not at all proven -- that activating DLK in the central nervous system could promote its regeneration."
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Shin JE, Cho Y, Beirowski B, Milbrandt J, Cavalli V, DiAntonio A. Dual leucine zipper kinase is required for retrograde injury signaling and axonal regeneration. Neuron. Online June 20, 2012.
This work was supported by the National Institutes of Health (NIH) Neuroscience Blueprint Center Core Grant (P30 NS057105) to Washington University, the HOPE Center for Neurological Disorders, the European Molecular Biology Organization (EMBO) long-term fellowship, the Edward Mallinckrodt Jr. Foundation, and NIH grants NS060709, AG13730, NS070053 and NS065053.
Washington University School of Medicine's 2,100 employed and volunteer faculty physicians also are the medical staff of Barnes-Jewish and St. Louis Children's hospitals. The School of Medicine is one of the leading medical research, teaching and patient care institutions in the nation, currently ranked sixth in the nation by U.S. News & World Report. Through its affiliations with Barnes-Jewish and St. Louis Children's hospitals, the School of Medicine is linked to BJC HealthCare.
 
Posted by
Robert Karl Stonjek