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Medical Marijuana & Alzheimer’s Disease

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Alzheimer’s disease (AD) is a neurological disorder of unknown origin that is characterized by a progressive loss of memory and learned behavior. Patients with Alzheimer’s are also likely to experience depression, agitation and appetite loss, among other symptoms. Over 4.5 million Americans are estimated to be afflicted with the disease. No approved treatments or medications are available to stop the progression of AD, and few pharmaceuticals have been FDA-approved to treat symptoms of the disease.

A review of the recent scientific literature indicates that cannabinoid therapy may provide symptomatic relief to patients afflicted with AD while also moderating the progression of the disease.

Writing in the February 2005 issue of the Journal of Neuroscience, investigators at Madrid’s Complutense University and the Cajal Institute in Spain reported that the intracerebroventricular administration of the synthetic cannabinoid WIN 55,212-2 prevented cognitive impairment and decreased neurotoxicity in rats injected with amyloid-beta peptide (a protein believed to induce Alzheimer’s). Additional synthetic cannabinoids were also found to reduce the inflammation associated with Alzheimer’s disease in human brain tissue in culture. “Our results indicate that … cannabinoids succeed in preventing the neurodegenerative process occurring in the disease,” investigators concluded.[1] Follow up studies by investigators demonstrated that the administration of the nonpsychotropic plant cannabinoid cannabidiol (CBD) also mitigated memory loss in a mouse model of the disease.[2]

Investigators at The Scripps Research Institute in California in 2006 reported that THC inhibits the enzyme responsible for the aggregation of amyloid plaque — the primary marker for Alzheimer’s disease — in a manner “considerably superior” to approved Alzheimer’s drugs such as donepezil and tacrine. “Our results provide a mechanism whereby the THC molecule can directly impact Alzheimer’s disease pathology,” researchers concluded. “THC and its analogues may provide an improved therapeutic [option] for Alzheimer’s disease [by]… simultaneously treating both the symptoms and the progression of [the] disease.”[3]

More recently, investigators at Ohio State University, Department of Psychology and Neuroscience, reported that older rats administered daily doses of WIN 55,212-2 for a period of three weeks performed significantly better than non-treated controls on a water-maze memory test. Writing in the journal Neuroscience in 2007, researchers reported that rats treated with the compound experienced a 50 percent improvement in memory and a 40 to 50 percent reduction in inflammation compared to controls.[4]

Previous preclinical studies have demonstrated that cannabinoids can prevent cell death by anti-oxidation.[5] Some experts believe that cannabinoids’ neuroprotective properties could also play a role in moderating AD.[6] Writing in the September 2007 issue of the British Journal of Pharmacology, investigators at Ireland’s Trinity College Institute of Neuroscience concluded, “[C]annabinoids offer a multi-faceted approach for the treatment of Alzheimer’s disease by providing neuroprotection and reducing neuroinflammation, whilst simultaneously supporting the brain’s intrinsic repair mechanisms by augmenting neurotrophin expression and enhancing neurogenesis. … Manipulation of the cannabinoid pathway offers a pharmacological approach for the treatment of AD that may be efficacious than current treatment regimens.”[7]

In addition to potentially modifying the progression of AD, clinical trials also indicate that cannabinoid therapy can reduce agitation and stimulate weight gain in patients with the disease. Most recently, investigators at Berlin Germany’s Charite Universitatmedizin, Department of Psychiatry and Psychotherapy, reported that the daily administration of 2.5 mg of synthetic THC over a two-week period reduced nocturnal motor activity and agitation in AD patients in an open-label pilot study.[8]

Clinical data presented at the 2003 annual meeting of the International Psychogeriatric Association previously reported that the oral administration of up to 10 mg of synthetic THC reduced agitation and stimulated weight gain in late-stage Alzheimer’s patients in an open-label clinical trial.[9] Improved weight gain and a decrease in negative feelings among AD patients administered cannabinoids were previously reported by investigators in the International Journal of Geriatric Psychiatry in 1997.[10]

Additional study assessing the use of cannabinoids for Alzheimer’s would appear to be warranted.

REFERENCES

[1] Ramirez et al. 2005. Prevention of Alzheimer’s disease pathology by cannabinoids. The Journal of Neuroscience 25: 1904-1913.

[2] Israel National News. December 16, 2010. “Israeli research shows cannabidiol may slow Alzheimer’s disease.”

[3] Eubanks et al. 2006. A molecular link between the active component of marijuana and Alzheimer’s disease pathology. Molecular Pharmaceutics 3: 773-777.

[4] Marchalant et al. 2007. Anti-inflammatory property of the cannabinoid agonist WIN-55212-2 in a rodent model of chronic brain inflammation. Neuroscience 144: 1516-1522.

[5] Hampson et al. 1998. Cannabidiol and delta-9-tetrahydrocannabinol are neuroprotective antioxidants. Proceedings of the National Academy of Sciences 95: 8268-8273.

[6] Science News. June 11, 1998. ” Marijuana chemical tapped to fight strokes.

[7] Campbell and Gowran. 2007. Alzheimer’s disease; taking the edge off with cannabinoids? British Journal of Pharmacology 152: 655-662.

[8] Walther et al. 2006. Delta-9-tetrahydrocannabinol for nighttime agitation in severe dementia. Physcopharmacology 185: 524-528.

[9] BBC News. August 21, 2003. ” Cannabis lifts Alzheimer’s appetite.

[10] Volicer et al. 1997. Effects of dronabinol on anorexia and disturbed behavior in patients with Alzheimer’s disease. International Journal of Geriatric Psychiatry 12: 913-919.

This article originally available at http://www.norml.org/index.cfm?Group_ID=7003

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Confessions of an RX drug pusher – Gwen Olsen

Ex pharma Rep speaks out about Pharma and their real motivations and lack there of to cure , heal and care for you or your best interests. Only to cure the space in their pockets not yet filled with your cash.

If you, or someone you know is suffering from taking too many prescription medications and would like to try marijuana as an alternative for your chronic condition, please visit http://www.TheCannabisDoctors.com or call 626-344-7596 to schedule a confidential evalution today at our Pasadena location.

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National Cancer Institute Supports Medical Marijuana!

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Cannabis, also known as marijuana, originated in Central Asia but is grown worldwide today. In the United States, it is a controlled substance and is classified as a Schedule I agent (a drug with increased potential for abuse and no known medical use). The Cannabis plant produces a resin containing psychoactive compounds called cannabinoids. The highest concentration of cannabinoids is found in the female flowers of the plant.[1] Clinical trials conducted on medicinal Cannabis are limited. The U.S. Food and Drug Administration (FDA) has not approved the use of Cannabis as a treatment for any medical condition. To conduct clinical drug research in the United States, researchers must file an Investigational New Drug (IND) application with the FDA.

The potential benefits of medicinal Cannabis for people living with cancer include antiemetic effects, appetite stimulation, pain relief, and improved sleep. Although few relevant surveys of practice patterns exist, it appears that physicians caring for cancer patients in the United States who recommend medicinal Cannabis predominantly do so for symptom management.[2]

Cannabinoids are a group of terpenophenolic compounds found in Cannabis species (Cannabis sativa L. and Cannabis indica Lam.). This summary will review the role of Cannabis and the cannabinoids in the treatment of people with cancer and disease-related or treatment-related side effects.

References

  1. Adams IB, Martin BR: Cannabis: pharmacology and toxicology in animals and humans. Addiction 91 (11): 1585-614, 1996.  [PUBMED Abstract]
  2. Doblin RE, Kleiman MA: Marijuana as antiemetic medicine: a survey of oncologists’ experiences and attitudes. J Clin Oncol 9 (7): 1314-9, 1991.  [PUBMED Abstract]

If you or someone you know is suffering with symptoms from cancer and would like to learn more about using marijuana as medicine please call 626-344-7596 to schedule a confidential evaluation or visit http://www.TheCannabisDoctors.com

 

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Cannabis compound benefits blood vessels

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Smoking cannabis has long been associated with poor short term memory, but a study now suggests that the strain of cannabis makes all the difference. In a test of shor term memory skills, only users of “skunk” type strains exhibited impaired recall when intoxicated, whereas people who smoked hashish or herbal cannabis blends performed equally well whether they were stoned or sober.

The findings suggest that an ingredient more plentiful in some types of marijuana than in others may help to reduce the memory loss that some users suffer. The key difference between the types of cannabis is the ratio of two chemicals found in all strains. Tetrahydrocannabinol *THC) is the primary active ingredient, and is responsible for the effects associated with the classic “high”, including euphoria and giddiness but also anxiety and paranoia. The second chemical, cannabidiol has more calming effects, and brain imaging studies have shown that it can block the psychosis inducing effects of THC2. Skunk type strains of cannabis contain a higher ratio of THC to cannabidiol than do hashish or herbal types.

Valerie Curran, a Psycho-pharmacologist from University College London who led the latest study, says that if habitual users must partake they should be encouraged to use strains with higher levels of cannabidiol, rather than using skunk. She also argues that studying cannabidiol could provide insight into the mechanics of memory formation, and that it may have therapeutic benefits for disorders involving memory deficits. The findings are published in the British Journal of Psychiatry today.

Cannabis use has increased in recent years — almost as many 16-24 year olds in the UK have tried as haven’t according to the 2008 report Statistics on Drug Misuse by the National Health Service and concerns have been raised that increased levels of THC in skunk varieties owing to aggressive plant breeding over the past decade are responsible for a rise in the number of young users displaying mild to severe cognitive impairment.

Learn more at http://www.nature.com/news/2010/101001/full/news.2010.508.html

Heroin, prescription drug deaths still up

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2009, opiates, both legal and illegal, were named on the death certificates of more unintentional fatal overdose victims than they were absent from, according to data released by the state Tuesday.

Overall, non-suicide drug overdose deaths were down from 2008 to 2009, 1,473 to 1,393. Data for 2010 remains incomplete because of the lag time for toxicology testing and returns from residents who died outside of Ohio.

The Ohio Department of Health, which released the data to fulfill a public record request from CentralOhio.com, cautioned not to interpret the decrease as a break in the pattern of rising overdose deaths because the data might not be 100 percent complete for the same reasons that 2010 figures are not fit for analysis.

One trend clearly is unchallenged: The share of casualties attributed, at least in part, to heroin and other opiates continued upward.

Heroin and other opiates, a category which includes legal pain relievers such as OxyContin and Vicodin, contributed to 54.4 percent of all unintentional overdose deaths in 2009, up almost 8 percent from the year before, according to an analysis done by the health department’s Injury Prevention Program.

Data for the first decade of the century shows heroin’s ascendency closely tracks the year-over-year increases in the mentions of other opiates on the death certificates of Ohio overdose victims. This co-mingling of the two — closely related in chemistry — by users was detailed in CentralOhio.com’s 2009 series “Prescription to Addiction.”

Orman Hall, director of the Ohio Department of Alcohol and Drug Addiction Services, said the data reinforces only the widespread belief that heroin and prescription opiate addictions are coupled.

“Nobody starts on heroin, everybody starts are prescription opiates,” said Hall, the former executive director of the Fairfield County Alcohol, Drug Addiction and Mental Health board. “The big thing now is making sure everybody is connecting the dots.”

Hall, who is leading the state’s pushback against opiate addiction, said if we can limit the abuse of legal opiates, then obviously we’ll see reductions in deaths ascribed to those medications. He also thinks heroin deaths would plummet as result because fewer people will turn to that drug as a way of satisfying their opiate addiction created by misuse, or improper prescribing habits, of legal pain relievers.

The grouping other opiates is first in cause of death mentions for the second consecutive year in 2009.

Heroin was second and cocaine was third.

The 2009 figures show the continued decrease of cocaine, which was the top killer from 2002 to 2007.

Benzodiazepines, a family of depressants including brands such as Xanax or Klonopin, jumped from 154 mentions in 2008 to 212 in 2009, which was the biggest increase for any drug grouping.

Hall, who had not personally reviewed the data as of Tuesday, said he was encouraged by the apparent decrease, albeit a small step down.

“That’s certainly a sign that people are starting to pay attention,” he said. “I would have been encouraged by a smaller increase this year.”

Russ Zimmer can be reached at (740) 328-8830 or razimmer@centralohio.com.

Article from http://www.coshoctontribune.com/article/20110126/NEWS01/101260334/1014/OPINION/Heroin-prescription-drug-deaths-still-up?odyssey=nav|head

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Is the DEA legalizing THC?

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By Mike Riggs – The Daily Caller

In November of last year, the Drug Enforcement Administration (DEA) proposed a seemingly subtle change to its policy on marijuana. Citing recommendations from the assistant secretary for Health at the Department of Health and Human Services, the agency outlined its plan to reschedule pills containing organic dronabinol from schedule I to schedule III.

Dronabinol is short for tetrahydrocannabinol and long for THC. It’s more commonly known as the thing in marijuana that gets you high.

“This proposed action expands the schedule III listing to include formulations having naturally-derived dronabinol and products encapsulated in hard gelatin capsules,” reads the DEA’s proposed rule. “This would have the effect of transferring the FDA-approved versions of such generic Marinol [a synthetic THC drug] products from schedule I to schedule III.”

Paul Armentano of the National Organization for Reform of Marijuana Laws reads the proposal as a way of legalizing marijuana so just Big Pharma can make money from it.

“DEA is taking a shortcut by saying, well, we can reschedule organic THC because it mimics an existing drug on the market,” Armentano said. “Which is ironic given that they are saying the organic substance is derivative of the synthetic substance that is actually based on the organic substance.”

A spokesperson from the DEA told The Daily Caller that the rescheduling of pills containing organic dronabinol is not equivalent to legalizing THC. “Please note that DEA is not ‘rescheduling … organic THC,’” wrote the DEA’s Rusty Payne in an e-mail.

“THC, natural or synthetic, remains a schedule I controlled substance. Under the proposed rule, in those instances in the future where FDA might approve a generic version of Marinol, that version of the drug will be in the same schedule as the brand name version of the drug, regardless of whether the THC used in the generic version was synthesized by man or derived from the cannabis plant.”

In other words, THC in plant form or as an extract, will still be illegal. What won’t be illegal is if a pharmaceutical company buys THC from a government-licensed provider, puts it in a pill, receives the DEA’s stamp of approval, and sells it a price that will likely be far higher than the price of marijuana.

Armentano said such circular reasoning is a product of decades of hostility towards marijuana research.

“This is the insane rationale necessary for banning medical marijuana,” he said. “Take away the prohibition and the political elements, and you would never have the stretching of logic necessary to pass organic THC but only if it mimics Marinol.”

Payne protested the comparison. “Marinol is not the same thing as marijuana; nor is any generic version of Marinol that might be approved by the FDA in the future. Marijuana (the cannabis plant) contains approximately 500 different chemicals; and dronabinol (the form of THC found in Marinol) is just one of those numerous chemicals in the plant.”

The DEA’s proposed rule says that the agency will only entertain abbreviated new drug applications, the process by which most generics are approved when the patent expires on a branded drug. That means requiring an organic dronabinol drug to mimic Marinol may actually help get an organic pill on the market in record time.

Payne declined to say when the rules would pass. ”There is no timetable for the publication of the final rule. As with all proposed rules, DEA is required by law to give careful consideration to the public comments in deciding whether to finalize the rule.”

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A Closer Look: Weight-loss drugs

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Several have recently come before the FDA. Do they work? Are they safe?

By Jill U. Adams, Special to the Los Angeles Times

December 13, 2010

For many people who carry excess pounds, lifestyle changes don’t do enough or are too hard to maintain day in and day out.

The pharmaceutical industry has been trying to create weight-loss medicines — it is a huge market, after all — but the failures have outnumbered the successes. Dr. Kevin Niswender, an obesity expert at Vanderbilt University in Nashville, says every talk he gives begins with a slide that says: “Pharmacotherapy for obesity has a troubled past — and future.”

Part of the problem is that if there’s a drug they can take, people wrongly think they can stop the harder work of diet and exercise. Doctors who specialize in treating overweight and obese patients say that, at best, medications should be used as an adjunct to lifestyle change. “If you overeat, you’re going to overcome the drug,” says Dr. David Heber, who directs the UCLA Risk Factor Obesity Program.

The other problem for candidate drugs has been their safety profile, with cardiovascular side effects a particular issue, Niswender says. The medical rationale for losing weight is to prevent the development of obesity-related health conditions, such as heart disease and stroke. So a weight-loss drug that increases blood pressure is defeating part of its own purpose.

Here’s a closer look at the most recent weight-loss drugs to come before the Food and Drug Administration.

Contrave

What it is: It’s a combination of two drugs already used for other health conditions: bupropion (Wellbutrin, Zyban), an antidepressant that’s also used to help people quit smoking; and naltrexone (Revia), an antidote to heroin overdose that is also used to help curb alcoholic cravings.

Weight-loss results: A study published in the Lancet in August followed 1,453 overweight or obese patients — half of them for more than a year — and found that those on Contrave lost 5% (lower dose) and 6.1% (higher dose) of their initial body weight compared with a 1.3% loss in the placebo group. Another trial published online in June in the journal Obesity that also included training in diet and exercise found an average 9.3% weight loss with the higher dose compared with 5.1% with a placebo.

Safety profile: Some patients experienced a modest rise (1.5 mm Hg) in blood pressure. Headache, constipation and nausea were also reported.

FDA action: Approval recommended by an expert advisory panel on Dec. 7.

Qnexa

What it is: It’s a combination drug made up of phentermine, a well-known appetite suppressant, and topiramate, which is used to treat epilepsy and migraine headaches.

Weight-loss results: In 1,542 overweight and obese patients, those who took Qnexa for more than a year lost an average of 10.5% (lower dose) and 13.2% (higher dose) of their body weight compared with 2.4% of weight loss in the placebo group, according to company literature.

Safety profile: The main concerns of the advisory panel were the drug’s potential to cause birth defects in women of child-bearing age and an increase in heart rate in some patients. Other side effects were dry mouth, tingling and constipation.

FDA action: An advisory panel recommended against approval in October. The agency detailed what the company ( Vivus) would need to address in a subsequent application. These included managing potential serious side effects and submitting data from patients who had taken the drug for two years.

Lorcaserin (Lorqess)

What it is: The drug acts on one of many serotonin receptors in the brain to suppress appetite.

Weight-loss results: A study published in the New England Journal of Medicine in July followed 1,599 overweight or obese patients for a year and found that those on lorcaserin lost an average of 5.8% of their initial body weight compared with 2.2% in the placebo group. A second trial found an average 5.9% weight loss in the drug group compared with 2.8% in the placebo group in about 2,000 overweight or obese patients followed for a year.

Safety profile: The FDA advisory panel cited concerns about tumor growth in animal studies. Other side effects were headache, dizziness and nausea.

FDA action: The panel recommended against approval in October. The agency detailed what the company ( Arena Pharmaceuticals) would need to address in a subsequent application, such as more information about potential serious side effects.

Sibutramine (Meridia)

What it is: The drug acts to increase levels of two neurotransmitters in the brain, serotonin and norepinephrine,to reduce appetite.

Weight-loss results: Studies in the 1990s found that two-thirds of patients taking Meridia lost 5% or more of their body weight over a one-year period. However, subsequent studies after the drug was approved found a more modest effect, with the drug producing just 2.5% more weight loss than a placebo.

Safety profile: A study of about 10,000 overweight and obese people in Europe, Latin America and Australia after the drug was approved there found a 16% increased risk of cardiac events, such as heart attack and stroke, associated with the drug.

FDA action: The drug was approved in 1997, but this year the agency decided that the drug showed more risk than benefit, based on data from new studies. In October, the drug’s maker, Abbott, complied with the agency’s request to pull the drug from the market.

Rimonabant (Zimulti, Acomplia)

What it is: The drug blocks the cannabinoid receptor in the brain. Cannabinoids are naturally occurring chemicals in the body that are related to THC, the active ingredient in marijuana, which stimulates appetite.

Weight-loss results: A summary of four clinical trials published in the Lancet in 2007 found that patients on rimonabant for one year lost an average of 10 pounds more than patients on placebos. In one of them, a one-year North American study of 1,602 overweight or obese people, nearly half the subjects in a higher-dose group lost more than 5% of their body weight, whereas one-fifth lost that amount in the placebo group.

Safety profile: Patients taking rimonabant were more than twice as likely as the placebo-taking group to experience mental health symptoms, such as depression and anxiety.

FDA action: The agency considered the drug in 2006-2007 but never approved it. In 2007, the drug’s maker ( Sanofi-Aventis) withdrew its application in the U.S. and in 2008 discontinued its development efforts worldwide.

health@latimes.com

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