Disulfiram like reaction medications or anti-seizure drugs, but the FDA and others have warned that their overuse can cause serious liver problems. The researchers believe that by targeting and selectively killing Bd Bz genes, they have found the key to treating Huntington's. "Our approach is novel in that it directly inhibits Bz in the liver of mice with Huntington's disease," says lead author Dr. Jeffrey D. Young. "Our results show that the drug can dramatically reduce liver burden of Bd and Bz, which is a very important step towards treating these deadly forms of the disease," writes Dr. Young in an article about the work published today in Journal of Neural Transmission. The study is first to directly target both a Bz gene and Bd in Huntington's disease, the first to show that Bz inhibitors can be safe and effective in human clinical trials. Scientists and doctors have studied ways to selectively kill the Bz genes or their messenger RNA for more than 20 years. In 2001 a team at the University of Washington developed a drug that specifically cleaves the Bz gene, but it was never approved by the government and is no longer available. Drug development has been hampered for almost 20 years because Bz proteins are too complex to target with a single drug. This is one reason why the United States does not currently have a drug to treat Huntington's. "This drug works in much the same way that antibodies Can you buy clomid over the counter in canada do in the clinic," explains Young, and in fact, it inhibits the protein production rather than killing it. Huntington's research showed that the messenger RNA gene is a crucial part of the disease, but no one was able to show that killing the messenger RNA gene alone could cure Huntington's. To prove Bz drugs could do the trick, Young and his colleagues studied mice that had a mutated form of the Bz gene called Bbq. disulfiram medication While normal, the Bbq mice do not show symptoms of Huntington's, and they are normal for most neurological diseases. They also develop an abnormal accumulation of the protein Bz in their livers -- an accumulation that is seen in both humans and mice when they develop Huntington's. But while normal mice develop their protein deposits in livers, the abnormal Bbq mice develop their deposits in disulfiram for cancer lungs. So Young's team started by taking four normal mice and breeding them with four Bbq mice. The normal mice were given anti-Bbq antibodies (like those used against malaria), while the Bbq mice were not. A third set of normal mice were given anti-Bz antibodies, while a fourth set of normal mice were given the drug as an injection. The researchers used drug every day for the next several months while normal mice were given no treatment. After the normal mice developed buildup of protein in their livers and lungs that is seen in Huntington's disease, they were then treated with drug trafficking from canada to the us Bbq anti-Bz antibodies to eliminate the buildup. The Bbq mice still developed some of their neurological symptoms, including an inability to walk normally and the inability to eat. But their muscle stiffness disappeared, atrophy decreased, and their cognitive function improved significantly. The authors write that results suggest Bz drugs can be safe for many patients with Huntington's, even though their condition may not necessarily be the same as what is seen in the early stages of disease. In addition, the mice treated with Bbq anti-Bz antibodies showed lower concentrations of Bbq protein in their livers than did the control mice. That indicates targeting both genes may be useful to treat a range of conditions. And the drugs could be even safer and more effective than the mnemonic for drugs causing disulfiram like reaction drugs used to fight malaria because the antimalarial drugs need to be injected, while both the Bbq and Bz proteins can be excreted through the kidneys. "This is a landmark discovery," says Dr. Daniel T. Schwartz, chairman of neurology at the University Pennsylvania's Perelman School of Medicine. "It's extremely exciting to see a single drug work in four different models of Huntington's."
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