New and Improved Deadly Snail Venom
SoyChemist writes "In 2004, the FDA approved the cone snail venom ziconotide (Prialt) for the treatment of chronic pain. It is only used for severe cases because it must be injected directly into the spinal column. This month, researchers from the University of Utah have reported the discovery of a new snail venom with a completely different amino acid sequence. Because it very selectively attaches to and blocks nerve signals by binding to a particular type of acetylcholine receptor without causing any collateral damage, the newly discovered venom could also become a fantastic medical tool."
You really should see these snails hunt and eat fish .
Some years ago, I spent a bit of time in Toto Olivera's lab (the guy who pioneered all of the conotoxin research) and it was amazing to watch these snails follow, track and eventually harpoon and eat fish in the aquarium. It turns out that the poison these snails use is a complex cocktail of peptides and small molecules that act on a variety of protein channels with implications for everything from the pain mentioned in the article to anesthesia to anti-convulsants.
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Something like 15 years ago I read a Michael Crichton novel (I suspect it was Sphere ) where a character claimed that the chemical reactions of cone snail venom "works faster than nerve conduction velocity", meaning that one is dead before one even feels the sting. Is there truth to this, or is it totally false?
"Of course, their insistence that ground rhino horn will bring back a man's impotent tallywhacker....the jury's still out."
No, the jury's not in any sense out. It doesn't work. And therein lies the problem with traditional medical "knowledge" - for every valid remedy there are four which are pure codswallop.
I am trolling
as antitoxins as well.
The most famous ACH receptor blocker is atropine (a poison itself derived originally from Atropa belladonna). This particular characteristic of atropine is why it is used to treat poisoning of several classes of poisons including Cholinesterase inhibitors (which include all current forms of chemical weapon nerve agents and a number of pesticides as well), muscarine (such as from certain forms of mushroom poisoning, f. ex. aminita muscaria) and the like.
Of course anything that touches the ACH cycle in the nerve is likely to be potentially deadly...
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I'm afraid you imagine wrong, at least in a theoretical sense. Side effects (and primary effects) are determined solely by the interaction of the chemical(s) with the human body, and there's no overarching difference between synthetic and naturally occurring chemicals - when you get down to it, it's all just a bunch of quarks and electrons. It tends to be possible to create more complex compounds naturally, however. So when we manufacture penicillin, we get some mould to secrete the basic ingredient, then substitute on different chemical groups to obtain different effects in the body - to produce a stronger, faster acting compound, with fewer or lesser side effects - hopefully. When it comes down to it though, lead compounds for drugs aren't really designed, they're discovered. Most of those compounds - like those that spawned aspirin, paracetamol, penicillin and the like - are naturally occurring. I suppose a few must have been discovered in synthetic compounds, but not many. The reason being that natural compounds, due to the way they are produced, can be much more complex. Drugs can have many chiral centres, and in classic syntheses, you'd obtain a mixture of all the different possible isomers - usually only one works. When an enzyme produces the feedstock, the compound is more likely to be a pure, or purer mixture, since the shape of the enzyme tends only to catalyse the production of one isomer. This restricts synthetic medicines to much simpler molecules until our synthetic procedures improve (which they are doing - designer molecules are becoming possible.) Even then, however, we have some way before we look at the shape of receptor sites and try and devise molecules to fit them. We are still at the stage where we notice a compound has a physiological effect, and then start looking closer.
im in ur
I live in constant, extreme pain 24 hours a day from a broken spine.
The break was repaired by spinal fusion and titanium hardware but I got ZERO pain relief from the surgery.
If anyone else had to live with the pain I live with, they would commit suicide before the end of the first day.
My surgeon told me to "just get over it".. I'm now at the point that I would gladly allow a doctor to severe the nerves so that I would lose all feeling from my neck down. Even if it left me paralyzed it would be worth it, just to stop hurting.
My problem is is that I can't work, don't have insurance, income, or anything else.
I don't qualify for assistance because I was self employed for too many years.
If some doctor would like to try this snail stuff out on me, I volunteer. I can't tolerate the pain anymore.