Rodenticide

A wild rat

"Rat poison" redirects here. For the window manager, see ratpoison.

Rodenticides are a category of pest control chemicals intended to kill rodents.

Single feed baits are chemicals sufficiently dangerous that the first dose is sufficient to kill.

Rodents are difficult to kill with poisons because their feeding habits reflect their place as scavengers. They will eat a small bit of something and wait, and if they don't get sick, they continue. An effective rodenticide must be tasteless and odorless in lethal concentrations, and have a delayed effect.

Poisonous chemicals

Anticoagulants

A warning sign in a Chicago neighborhood advises that a dose of poison has recently been set out.

Anticoagulants are defined as chronic (death occurs after one to two weeks after ingestion of the lethal dose, rarely sooner), single-dose (second generation) or multiple-dose (first generation) rodenticides, acting by effective blocking of the vitamin K cycle, resulting in inability to produce essential blood-clotting factors — mainly coagulation factors II (prothrombin), VII (proconvertin), IX (Christmas factor) and X (Stuart factor).

In addition to this specific metabolic disruption, massive toxic doses of 4-hydroxycoumarin or 4-hydroxythiacoumarin and indandione anticoagulants cause damage to tiny blood vessels (capillaries), increasing their permeability, causing diffuse internal bleedings (haemorrhagias). These effects are gradual, developing over several days, but claims that they are painless are unfounded: in humans both warfarin poisoning and haemophilia commonly cause moderate to severe pain from bleeding into muscles and joints.^[1] In the final phase of the intoxication, the exhausted rodent collapses in hypovolemic circulatory shock or severe anemia and dies calmly. However, because of the duration of discomfort and pain before death it has been suggested that the use of rodenticides can be considered as inhumane.^[2]

The main benefit of anticoagulants over other poisons is that the time taken for the poison to induce death means that the rats do not associate the damage with their feeding habits.

• First generation rodenticidal anticoagulants generally have shorter elimination half-lives,^[3] require higher concentrations (usually between 0.005% and 0.1%) and consecutive intake over days in order to accumulate the lethal dose, and less toxic than second generation agents.

• Second generation agents are far more toxic than first generation. They are generally applied in lower concentrations in baits — usually on the order of 0.001% to 0.005% — are lethal after a single ingestion of bait and are also effective against strains of rodents that became resistant to first generation anticoagulants; thus, the second generation anticoagulants are sometimes referred to as "superwarfarins".^[4]

Class	Examples
Coumarins/4-hydroxycoumarins	First generation: warfarin, coumatetralyl Second generation: difenacoum, brodifacoum, [5] flocoumafen and bromadiolone.
1,3-indandiones	diphacinone, chlorophacinone, [6] pindone These are harder to group by generation. According to some sources, the indandiones are considered second generation.[7] However, according to the U.S. Environmental Protection Agency‎, examples of first generation agents include chlorophacinone and diphacinone.[5]
Other	Difethialone is considered a second generation anticoagulant rodenticide .[8]
Indirect	Sometimes, anticoagulant rodenticides are potentiated by an antibiotic or bacteriostatic agent, most commonly sulfaquinoxaline. The aim of this association is that the antibiotic suppresses intestinal symbiotic microflora, which are a source of vitamin K. Diminished production of vitamin K by the intestinal microflora contributes to the action of anticoagulants. Added vitamin D also has a synergistic effect with anticoagulants.

Vitamin K₁ has been suggested, and successfully used, as antidote for pets or humans accidentally or intentionally (poison assaults on pets, suicidal attempts) exposed to anticoagulant poisons. Some of these poisons act by inhibiting liver functions and in advanced stages of poisoning, several blood-clotting factors are absent, and the volume of circulating blood is diminished, so that a blood transfusion (optionally with the clotting factors present) can save a person who has been poisoned, an advantage over some older poisons.

Rodenticide in dogs

Rodenticide, also known as rat bait, is an anticoagulant used to kill rodents. This product is also lethal to many other species, specifically, dogs. Even in small doses this pest control substance can be fatal if not treated immediately.

Clinical signs for canine rodenticide toxicosis include lethargy, epistaxis, melena, bruising, acute blindness, seizures, dyspnea, depression, weakness, pallor, paresis or paralysis, gingival bleeding, profuse bleeding from wounds, hematemesis and hematuria. The vet may notice prolonged bleeding from venipuncture sites, hematomas and hemorrhaging into body cavities. If any of these signs are noticed and rodenticide ingestion is a probable cause, the pet should be taken to an animal hospital immediately.

This drug works by inhibiting an enzyme that uptakes and reuses vitamin K. Vitamin K is critical in the production of coagulation factors and thus when ceased it reduces the production of vitamin K dependent factors 2,7, 9 and 10. The body is then unable to activate vitamin K. Coagulation pathways are affected and can lead to coagulopathy. This is why external and internal bleeding are major signs that the patient has been exposed to rodenticide. It can take up to 5-7 days for signs to develop depending on the half-life of the active ingredient. The half-life of Warfarin is only 14.5 hours while others like second generation hydroxycoumarins and indanediones are between 4-6 days.

To diagnose rodenticide toxicosis, veterinarians use blood testing to find abnormal values to assess the patient’s clotting time and other related issues. Baseline testing includes pack cell volume (PVC), total protein (TP), complete blood count (CBC), platelet estimate and activated clotting time (ACT). From these values the veterinarian will be able to know if the patient is anemic, if the platelet count is within normal limits and if the clotting time is delayed. Further testing if time allows would include a coagulation screen (PT, PTT, fibrinogen, and FDP’s), PIVKA (proteins induced by vitamin K absence), complete serum biochemical profile, urinalysis, fecal exam, blood gas analysis and chemical analysis of heparinized plasma.

Treatment begins with identifying the specific toxic agent. This will significantly affect the depth and length of treatment needed for the patient and the prognosis. If the product was ingested within 1 hour upon presentation to the hospital then emesis will be utilized by administering an IV medication called apomorphine. If it has been between 2-4 hours of ingestion, gastric lavage will be performed. Activated charcoal should then be given by mouth every 3-4 hours and continued depending on the time of ingestion. Finally the antidote, vitamin K should be administered and repeated again depending on the time of exposure.

The prognosis of the patient all depends on what kind of rodenticide was ingested, the amount, the time lapse between ingestion and treatment, the severity of the symptoms, underlying diseases that may bring about further complications and the correct treatment and diagnosis. It is very important to bring your pet into a veterinarian as soon as you suspect ingestion and don’t wait for clinical signs. You will be saving their life the quicker you act upon it.

References

Plunkett, Signe J. (2001). Emergency Procedures for the Small Animal Veterinarian. Harcourt Publishers. pp. 289–292. ISBN 0-7020-2487-2. 

Gfeller, Roger W.; Shawn P. Messonnier (2004). Small Animal Toxicology and Poisonings. Mosby.. pp. 321–326. ISBN 0-323-01246-9. 

Metal phosphides

Rat poison vendor's stall at a market in Linxia City, China

Metal phosphides have been used as a means of killing rodents and are considered single-dose fast acting rodenticides (death occurs commonly within 1-3 days after single bait ingestion). A bait consisting of food and a phosphide (usually zinc phosphide) is left where the rodents can eat it. The acid in the digestive system of the rodent reacts with the phosphide to generate the toxic phosphine gas. This method of vermin control has possible use in places where rodents are resistant to some of the anticoagulants, particularly for control of house and field mice; zinc phosphide baits are also cheaper than most second-generation anticoagulants, so that sometimes, in the case of large infestation by rodents, their population is initially reduced by copious amounts of zinc phosphide bait applied, and the rest of population that survived the initial fast-acting poison is then eradicated by prolonged feeding on anticoagulant bait. Inversely, the individual rodents, that survived anticoagulant bait poisoning (rest population) can be eradicated by pre-baiting them with nontoxic bait for a week or two (this is important to overcome bait shyness, and to get rodents used to feeding in specific areas by specific food, especially in eradicating rats) and subsequently applying poisoned bait of the same sort as used for pre-baiting until all consumption of the bait ceases (usually within 2-4 days). These methods of alternating rodenticides with different modes of action gives actual or almost 100% eradications of the rodent population in the area, if the acceptance/palatability of baits are good (i.e., rodents feed on it readily).

Zinc phosphide is typically added to rodent baits in a concentration of 0.75% to 2.0%. The baits have strong, pungent garlic-like odor characteristic for phosphine liberated by hydrolysis. The odor attracts (or, at least, does not repulse) rodents, but has repulsive effect on other mammals. Birds, notably wild turkeys, are not sensitive to the smell, and will feed on the bait, and thus become collateral damage.

The tablets or pellets (usually aluminium, calcium or magnesium phosphide for fumigation/gassing) may also contain other chemicals which evolve ammonia, which helps to reduce the potential for spontaneous ignition or explosion of the phosphine gas.

Phosphides do not accumulate in the tissues of poisoned animals, so the risk of secondary poisoning is low.

Before the advent of anticoagulants, phosphides were the favored kind of rat poison. During World War II, they came into use in United States because of shortage of strychnine due to the Japanese occupation of the territories where strychnine-producing plants are grown (Strychnos nux-vomica, in southeast Asia). Phosphides are rather fast-acting rat poisons, resulting in the rats dying usually in open areas, instead of in the affected buildings.

Phosphides used as rodenticides are:

• aluminium phosphide (fumigant only)
• calcium phosphide (fumigant only)
• magnesium phosphide (fumigant only)
• zinc phosphide (in baits)

Hypercalcemia

Calciferols (vitamins D), cholecalciferol (vitamin D₃) and ergocalciferol (vitamin D₂) are used as rodenticides. They are toxic to rodents for the same reason they are important to humans: they affect calcium and phosphate homeostasis in the body. Vitamins D are essential in minute quantities (few IUs per kilogram body weight daily, only a fraction of a milligram), and like most fat soluble vitamins, they are toxic in larger doses, causing hypervitaminosis. If the poisoning is severe enough (that is, if the dose of the toxin is high enough), it leads to death. In rodents that consume the rodenticidal bait, it causes hypercalcemia, raising the calcium level, mainly by increasing calcium absorption from food, mobilising bone-matrix-fixed calcium into ionised form (mainly monohydrogencarbonate calcium cation, partially bound to plasma proteins, [CaHCO₃]⁺), which circulates dissolved in the blood plasma. After ingestion of a lethal dose, the free calcium levels are raised sufficiently that blood vessels, kidneys, the stomach wall and lungs are mineralised/calcificated (formation of calcificates, crystals of calcium salts/complexes in the tissues, damaging them), leading further to heart problems (myocardial tissue is sensitive to variations of free calcium levels, affecting both myocardial contractibility and excitation propagation between atrias and ventriculas), bleeding (due to capillary damage) and possibly kidney failure. It is considered to be single-dose, cumulative (depending on concentration used; the common 0.075% bait concentration is lethal to most rodents after a single intake of larger portions of the bait) or sub-chronic (death occurring usually within days to one week after ingestion of the bait). Applied concentrations are 0.075% cholecalciferol and 0.1% ergocalciferol when used alone.

There is an important feature of calciferols toxicology, that they are synergistic with anticoagulant toxicants, that means, that mixtures of anticoagulants and calciferols in same bait are more toxic than a sum of toxicities of the anticoagulant and the calciferol in the bait, so that a massive hypercalcemic effect can be achieved by a substantially lower calciferol content in the bait, and vice-versa, a more pronounced anticoagulant/hemorrhagic effects are observed if the calciferol is present. This synergism is mostly used in calciferol low concentration baits, because effective concentrations of calciferols are more expensive than effective concentrations of most anticoagulants.

The first application of a calciferol in rodenticidal bait was in the Sorex product Sorexa D (with a different formula than today's Sorexa D), back in early 1970s, which contained 0.025% warfarin and 0.1% ergocalciferol. Today, Sorexa CD contains a 0.0025% difenacoum and 0.075% cholecalciferol combination. Numerous other brand products containing either 0.075-0.1% calciferols (e.g. Quintox) alone or alongside an anticoagulant are marketed.

The Merck Veterinary Manual states the following:

Although this rodenticide [cholecalciferol] was introduced with claims that it was less toxic to nontarget species than to rodents, clinical experience has shown that rodenticides containing cholecalciferol are a significant health threat to dogs and cats. Cholecalciferol produces hypercalcemia, which results in systemic calcification of soft tissue, leading to renal failure, cardiac abnormalities, hypertension, CNS depression and GI upset. Signs generally develop within 18-36 hours of ingestion and can include depression, anorexia, polyuria and polydipsia. As serum calcium concentrations increase, clinical signs become more severe. ... GI smooth muscle excitability decreases and is manifest by anorexia, vomiting and constipation. ... Loss of renal concentrating ability is a direct result of hypercalcemia. As hypercalcemia persists, mineralization of the kidneys results in progressive renal insufficiency."^[9]

Additional anticoagulant renders the bait more toxic to pets as well as human. Upon single ingestion, solely calciferol-based baits are considered generally safer to birds than second generation anticoagulants or acute toxicants. A specific antidote for calciferol intoxication is calcitonin, a hormone that lowers the blood levels of calcium. The therapy with commercially available calcitonin preparations is, however, expensive.

Other

Civilian Public Service worker distributes rat poison for typhus control in Gulfport Mississippi, ca. 1945.

Other chemical poisons include:

• ANTU (α-naphthylthiourea; specific against Brown rat, Rattus norvegicus)
• Arsenic
• Barium (a toxic metal) compound
  • Barium carbonate
• Bromethalin (which affects the nervous system, no antidote)
• Chloralose (narcotic acting condensation product of chloral and glucose)
• Crimidine (2-chloro-N, N,6-trimethylpyrimidin-4-amine; a synthetic convulsant poison, antivitamin B₆)
• 1,3-Difluoro-2-propanol ("Gliftor" in the former USSR)
• Endrin (organochlorine cyclodiene insecticide, used in the past for extermination of voles in fields during winter by aircraft spraying)
• Fluoroacetamide ("1081")
• Phosacetim (a delayed-action organophosphorous rodenticide)
• White phosphorus
• Pyrinuron (an urea derivative)
• Scilliroside
• Sodium fluoroacetate ("1080")
• Strychnine
• Tetramethylenedisulfotetramine ("tetramine")
• Thallium (a toxic heavy metal) compounds
• Zyklon B (hydrogen cyanide absorbed in an inert carrier)

Combinations

In some countries, fixed three-component rodenticides, i.e., anticoagulant + antibiotic + vitamin D, are used. Associations of a second-generation anticoagulant with an antibiotic and/or vitamin D are considered to be effective even against most resistant strains of rodents, though some second generation anticoagulants (namely brodifacoum and difethialone), in bait concentrations of 0.0025% to 0.005% are so toxic that resistance is unknown, and even rodents resistant to other rodenticides are reliably exterminated by application of these most toxic anticoagulants.

List of rat eradications

• Campbell Island, New Zealand, largest ever.
• Rat Island (Alaska)
• Mokapu Island, Molokai
• Falkland Islands^{[citation needed]}
• San Jorge Islands, Mexico
• Canna, Scotland

References

1. ^ Choinière M, Melzack R (December 1987). "Acute and chronic pain in hemophilia". Pain 31 (3): 317–31. doi:10.1016/0304-3959(87)90161-8. PMID 3501097. 
2. ^ Meerburg BG, Brom FWA, Kijlstra A (2008). "The ethics of rodent control". Pest Manag Sci 64 (12): 1205–11. doi:10.1002/ps.1623. PMID 18642329. http://www3.interscience.wiley.com/journal/120746731/abstract. 
3. ^ Vandenbroucke V, Bousquet-Melou A, De Backer P, Croubels S (October 2008). "Pharmacokinetics of eight anticoagulant rodenticides in mice after single oral administration". J. Vet. Pharmacol. Ther. 31 (5): 437–45. doi:10.1111/j.1365-2885.2008.00979.x. PMID 19000263. http://www3.interscience.wiley.com/resolve/openurl?genre=article&sid=nlm:pubmed&issn=0140-7783&date=2008&volume=31&issue=5&spage=437. 
4. ^ Kotsaftis P, Girtovitis F, Boutou A, Ntaios G, Makris PE (September 2007). "Haemarthrosis after superwarfarin poisoning". Eur. J. Haematol. 79 (3): 255–7. doi:10.1111/j.1600-0609.2007.00904.x. PMID 17655702. http://www3.interscience.wiley.com/resolve/openurl?genre=article&sid=nlm:pubmed&issn=0902-4441&date=2007&volume=79&issue=3&spage=255. 
5. ^ ^{a b} "Final Risk Mitigation Decision for Ten Rodenticides | Pesticides | US EPA". http://www.epa.gov/pesticides/reregistration/rodenticides/finalriskdecision.htm. Retrieved 2008-12-24. 
6. ^ "LONG ACTING ANTICOAGULANT RODENTICIDES". http://www.addl.purdue.edu/newsletters/1995/rodent.shtml. Retrieved 2008-12-24. 
7. ^ "Anticoagulant Rodenticide Toxicosis in the Dog and Cat". http://www.vet.uga.edu/VPP/clerk/Harrell/index.php. Retrieved 2008-12-24. 
8. ^ Saravanan K, Kanakasabai R, Thiyagesan K (June 2003). "Field evaluation of difethialone, a new second generation anticoagulant rodenticide in the rice fields". Indian J. Exp. Biol. 41 (6): 655–8. PMID 15266918. 
9. ^ "Merck Veterinary Manual - Rodenticide Poisoning: Introduction". http://www.merckvetmanual.com/mvm/index.jsp?cfile=htm/bc/213000.htm. 

External links

• National Pesticide Information Center
• Fact Sheet on EPA's Proposed Risk Mitigation Decision for Nine Rodenticides
• EPA Rodenticide Cluster Reregistration Eligibility Decision Fact Sheet
• Wildcare Bay Area - Rodenticide Use Information