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United sued over pesticide in planes
and
Cabin crews sickened by pesticides

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I believe we should be objecting to the term "allergenic" reactions with regard to poison.  Allergic responses are adverse reactions to normally benign substances like roses or wheat. One cannot really be allergic to a poison since the adverse reaction is guaranteed by the incompatibility of a poison with our biochemistry.

I like to tell people that using the term "allergy" with regard to toxicants is similar to saying that Socrates died of an allergic reaction to hemlock.

Barbara

http://community.webtv.net/Raisyl/PHOENIXRISING

 


I've been saying this since I worked on the birth defects cases....
The critical portion of chlorpyrifos is NOT the OPO4... it is the tri-chlorinated part!!!!!!
Thanks for all your hard work.
Janette Sherman, MD


Hi Steve:

As long as Dow can keep the world looking for cholinergic effects, there will be no progress as to why Dursban (chlorpyrifos) is such a health hazard.

Rather than looking at ChE effects, researchers should note the similarity of chlorpyrifos to TCDD, 2,4-D and 2,4,5-T.  All of these contain phenyl or pyridyl groupings containing 2 or 3 chlorines.  In the case of TCDD, it is well established (A.  Brouwer et al.  from the Netherlands) that TCDD binds to transthyretin, the carrier protein that moves thyroid hormones and vitamin A from storage sites to the liver, where they are active.  If the protein is poisoned by reacting with dioxin (PCBs do the same thing) there will be a shortage of retinoic acid in the liver.  This shortage means protein synthesis will be decreased.  This means a shortage of enzymes to degrade the chemicals and a shortage of antibodies for antigens.  No wonder TCDD and the phenoxyacetic acid herbicides are carcinogens.

I am no longer in research but it seems obvious to me that chlorpyrifos, like its Dow-derived relatives, will react with transthyretin.  It is also likely that chlorpyrifos will poison the esterases that activate retinol, the vitamin precursor of retinoic acid, by inhibiting the process of turning storage retinyl esters to retinol.

These are the questions that need asking.  Working with PCBs and TCDD, the chemistry of 30 years ago, is simply not pertinent to the problems we face today.

What is the critical need today is the measurement of the interference of pesticides with the action of retinoic acid via either transthyretin binding or inhibition of the esterases.  Strange, isn't it, that no work in this area is never done in the U.S.?

Bill Plapp

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