March 11th 2011 : Consequences of the Japanese Earthquakes: Radiation 1,000 times normal at Japanese Fukushima Daiichi nuclear plant

3 Responses to “March 11th 2011 : Consequences of the Japanese Earthquakes: Radiation 1,000 times normal at Japanese Fukushima Daiichi nuclear plant”

  1. […] March 11th 2011 : Consequences of the Japanese Earthquakes: Radiation 1,000 times normal at Japanese… ( […]

  2. I just want to say I am newbie to blogging and site-building and truly liked you’re web site. Likely I’m going to bookmark your blog . You surely have good articles. Thanks a lot for revealing your website page.

  3. David Spencer Says:

    I hope the nuclear authorities are aware of this technologies.
    Its not trial fully as yet but at least these brave soul will have a good chance of surviving.
    Bless you all.

    Radiation Sickness Cures and Anti-radiation Pills

    1. Dr. Andrei Gudkov has developed >medication that suppresses the “suicide mechanism” of cells hit by radiation, while enabling them to recover from the radiation-induced damages that prompted them to activate the suicide mechanism in the first place.

    The first series of tests included experiments on more than 650 monkeys. Each test featured two groups of monkeys exposed to radiation, but only one group was given the medication. The radiation dosage was equal to the highest dosage sustained by humans as result of the Chernobyl mishap.

    The experiment’s results were dramatic: 70% of the monkeys that did not receive the cure died, while the ones that survived suffered from the various maladies associated with lethal nuclear radiation. However, the group that did receive the anti-radiation shot saw almost all monkeys survive, most of them without any side-effects. The tests showed that injecting the medication between 24 hours before the exposure to 72 hours following the exposure achieves similar results.

    Another test on humans, who were given the drug without being exposed to radiation, showed that the medication does not have side-effects and is safe. Prof. Gudkov’s company now needs to expand the safety tests, a process expected to be completed by mid-2010 via a shortened test track approved for bio-defense drugs. Should experiments continue at the current rate, the medication is estimated to be approved for use by the FDA within a year or two.

    Technical information on the radiation sickness cure is here

    The drug CBLB502 switches on teh genes TLR5 and NF-kB but it did not cause an excessive response from the immune system. It was also far less toxic than raw flagellin and mice could tolerate double the dose. The drug activated a parade of protective proteins that greatly reduced the levels of apoptosis in the vulnerable intestines of irradiated mice, and protected the stem cells in both their guts and their bloodstreams.

    A single shot of CBLB502 at less than 1% of the maximum dose, 87% of mice managed to survive an otherwise lethal 13 Gray of radiation. The drug completely outclassed all known protective chemicals. Even the maximum possible dose of the second-best chemical – amifostine – only saved 54% of the irradiated mice.

    The drug could be given to cancer patients who are being treated with radiation, to protect healthy cells from dying off. She treated tumour-bearing mice with three daily radiation doses of 4 Gray to mimic the regular treatments that cancer patients often go through. When mice were injected with simple saline solution, the accumulated damage killed them all but when the doses were pre-empted by injections of CBLB502, every one of the mice survived.

    The celebrations would be short-lived however, if the drug defended tumour cells in a similar way. Fortunately, that wasn’t the case and the tumours in protected mice succumbed to the radiotherapy as per usual. If anything, the addition of CBLB502 killed slightly more cancer cells than usual, which may be due to small immune boosts triggered by the compound’s resemblance to flagellin.

    Burdelya also saw to a final worry. Apoptosis exists for a reason, and there is a risk that protected cells could survive the effects of radiation but live with damage that will lead to cancer in the long run. With this in mind, Burdelya tested the drug on a strain of cancer-prone mice and found that after a burst of radiation, they did not develop tumours any quicker or more frequently than they normally would.

    Abstract: An Agonist of Toll-Like Receptor 5 Has Radioprotective Activity in Mouse and Primate Models.

    The drug CBLB502 seems to be far ahead of the next two treatments in terms of proven effectiveness and in terms of deployment. However, the next two work on different mechanisms and appear to be complimentary to the drug CBLB502. (You might take both. One to reduce free radicals that cause damage and the CBLB502 to switch genes prevent cell death.)

If you wish you can Leave a Reply. We will publish it after moderation. Insults and Spam are automatically deleted. Thank you for visiting my blog today.

Fill in your details below or click an icon to log in: Logo

You are commenting using your account. Log Out / Change )

Twitter picture

You are commenting using your Twitter account. Log Out / Change )

Facebook photo

You are commenting using your Facebook account. Log Out / Change )

Google+ photo

You are commenting using your Google+ account. Log Out / Change )

Connecting to %s

%d bloggers like this: