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  2. Organophosphate poisoning - Wikipedia

    en.wikipedia.org/wiki/Organophosphate_poisoning

    Organophosphate poisoning is poisoning due to organophosphates (OPs). [4] Organophosphates are used as insecticides , medications, and nerve agents . [ 4 ] Symptoms include increased saliva and tear production, diarrhea , vomiting, small pupils , sweating, muscle tremors, and confusion. [ 2 ]

  3. Cholinesterase reactivator - Wikipedia

    en.wikipedia.org/wiki/Cholinesterase_reactivator

    In the treatment of organophosphate toxicity, cholinesterase reactivators such as Pralidoxime reactivate inhibited AChE at peripheral nicotinic receptors.Since AChE mediates effects on both nicotinic and muscarinic receptors, cholinesterase reactivators are co-administered with muscarinic antagonists, primarily atropine.

  4. Organophosphate - Wikipedia

    en.wikipedia.org/wiki/Organophosphate

    Organophosphate insecticides are acetylcholinesterase inhibitors, which disrupt the transmission of nerve signals in exposed organisms, with fatal results. The risk of human death through organophosphate poisoning [32] was obvious from the start and led to efforts to lower toxicity against mammals while not reducing efficacy against insects ...

  5. Sarin - Wikipedia

    en.wikipedia.org/wiki/Sarin

    The toxicity of sarin in humans is largely based on calculations from studies with animals. The lethal concentration of sarin in air is approximately 28–35 mg per cubic meter per minute for a two-minute exposure time by a healthy adult breathing normally (exchanging 15 liters of air per minute, lower 28 mg/m 3 value is for general population ...

  6. Carbamate poisoning - Wikipedia

    en.wikipedia.org/wiki/Carbamate_poisoning

    Pralidoxime, another antidote, can be considered to reactivate inhibited acetylcholinesterase enzymes, although this is often less important for carbamate poisoning than it is for organophosphate poisoning. [1] The most common cause of death following carbamate poisoning is respiratory failure. [3]

  7. Organothiophosphate - Wikipedia

    en.wikipedia.org/wiki/Organothiophosphate

    Variants with P=S double bonds were developed as insecticides because of their reduced mammalian toxicity. The phosphorothioate P=S bond is converted to the toxic P=O bond in the target insect. Similar oxidative conversion in mammals is slower, conferring lower toxicity in mammals.

  8. Suspect accused of trying to poison cats in Green mobile home ...

    www.aol.com/suspect-accused-trying-poison-cats...

    More: Fears that someone is trying to poison cats in Green spark concern, outrage. On Feb. 23, the Summit County Sheriff's Office said it received a report of an individual placing bowls of ...

  9. Cholinergic crisis - Wikipedia

    en.wikipedia.org/wiki/Cholinergic_crisis

    As a result of cholinergic crisis, the muscles stop responding to the high synaptic levels of acetylcholine, leading to flaccid paralysis, respiratory failure, and other signs and symptoms reminiscent of organophosphate poisoning. Other symptoms include increased sweating, salivation, bronchial secretions along with miosis (constricted pupils).