Bromethalin

Bromethalin is a neurotoxic rodenticide that damages the central nervous system.

Bromethalin
Names
Preferred IUPAC name
N-Methyl-2,4-dinitro-N-(2,4,6-tribromophenyl)-6-(trifluoromethyl)aniline
Other names
2,4,6-Tribromo-N-[2,4-dinitro-6-(trifluoromethyl)phenyl]-N-methylaniline
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.109.042
KEGG
PubChem CID
UNII
Properties
Chemical formula
C14H7Br3F3N3O4
Molar mass 577.93 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Mechanism of action

Bromethalin works by uncoupling mitochondrial oxidative phosphorylation, which causes a decrease in adenosine triphosphate (ATP) synthesis. The decreased ATP inhibits the activity of the Na/K ATPase enzyme, thereby leading to a subsequent buildup of cerebral spinal fluid (CSF) and vacuolization of myelin. The excess CSF results in increased intracranial pressure, which in turn permanently damages neuronal axons. This damage to the central nervous system can cause paralysis, convulsions, and death.[1][2]

Risk of poisoning

No tests will diagnose bromethalin poisoning in pets, but signs to watch for include severe muscle tremors, hyperexcitability, fits, extreme sensitivity to being touched (hyperesthesia) and seizures that appear to be caused by light or noise. Signs can be delayed for several days.

No antidote for bromethalin is known; care is symptomatic and supportive. Owners of animals that have eaten it accidentally should seek immediate veterinary attention and be decontaminated. Contacting an animal poison control center can help ensure that timely and appropriate therapy is started.

The mechanism of bromethalin toxicity differs from that of popular rodent poisons, which are anticoagulants related to warfarin (Coumadin). These drugs, such as diphacinone and bromadiolone, eaten by the mouse as an overdose, inhibit vitamin K and lead to a loss of clotting activity over several days (clotting factors require vitamin K). The ultimate result is hemorrhage.

While bromethalin is labeled as a rodenticide, it is often used for other small mammals such as moles. It is often hidden inside a worm-like bait to attract moles.


References

  1. Bromethalin, Animal Disease Diagnostic Laboratory, Spring 1997 Newsletter
  2. "The Discovery and Development of Bromethalin, an Acute Rodenticide with a Unique Mode of Action". doi:10.1021/bk-1984-0255.ch004. Cite journal requires |journal= (help)
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