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Cat pheromone

From Wikipedia, the free encyclopedia
Cat attractants.
Chemical structure of nepetalactone Chemical structure of dihydronepetalactone
Nepetalactone Dihydronepetalactone
Chemical structure of epinepetalactone Chemical structure of neonepetalactone
Epinepetalactone Neonepetalactone
Chemical structure of isodihydronepetalactone
Isodihydronepetalactone
Chemical structure of (-)-mitsugashiwalactone Chemical structure of onikulactone
(-)-Mitsugashiwalactone Onikulactone
Chemical structure of iridomyrmecin Chemical structure of boschnialactone
Iridomyrmecin Boschnialactone
Chemical structure of actinidiolid Chemical structure of dihydroactinidiolide
Actinidiolide Dihydroactinidiolide
Chemical structure of actinidine Chemical structure of boschniakine
Actinidine Boschniakine

Cat pheromones are pheromones that are used by cats and other felids for cat communication.

Feline facial pheromone

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Feline facial pheromone is a hypothetical pheromone used by cats to mark places, objects, and persons as familiar by rubbing their face on surfaces. It is currently not known if there actually exists a "feline facial pheromone" and what its chemical structure is.

A preparation that claims to mimic the feline facial pheromone is commercially available under the name Feliway.[1] This product contains common fatty acids as active ingredients, mixed with Valeriana officinalis essential oil as attractant.[2] Valeriana officinalis is known for its behavioural effects on cats, similar to Nepeta (catnip).

"Cat attractants"

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A domestic cat demonstrating the effects of catnip such as rolling, pawing, and frisking

Cat attractants are odorants and constituents of essential oils that have an apparent effect on cat behavior. A cat presented with a cat attractant may roll in it, paw at it, or chew on the source of the smell. The effect is usually relatively short, lasting for only a few minutes after which the cats have a refractory period during which the response cannot be elicited. After 30 minutes to two hours, susceptible cats gain interest again. These compounds might mimic the feline facial pheromone.

The volatile chemicals that are currently known to cause these behavioral effects in cats are actinidine from Valeriana officinalis, nepetalactone from Nepeta (catnip), dihydronepetalactone, neonepetalactone, isodihydronepetalactone, epinepetalactone, boschnialactone, boschniakine, dihydroactinidiolide, actinidiolide, iridomyrmecin, (-)-mitsugashiwalactone, and onikulactone.[3][4]

Cat urine odorants

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Cat urine-like odorants
Chemical structure of 3-mercapto-3-methylbutan-1-ol
3-Mercapto-3-methylbutan-1-ol
Chemical structure of 4-methoxy-2-methylbutane-2-thiol
4-Methoxy-2-methylbutane-2-thiol
Chemical structure of 4-mercapto-4-methylpentan-2-one
4-Mercapto-4-methylpentan-2-one

Cat urine, especially that of male cats, contains the putative cat pheromone 3-mercapto-3-methylbutan-1-ol (MMB), a compound that gives cat urine its typical odor. The MMB precursor felinine is synthesized in the urine from 3-methylbutanol-cysteinylglycine (3-MBCG) by the excreted peptidase cauxin. Felinine then slowly degrades into the volatile MMB.[5]

Cat urine smell is highly aversive to rats and mice, but after infection with the parasite Toxoplasma gondii, they are attracted by it, highly increasing the likelihood of being preyed upon and of infecting the cat.[6]

Chemical structure of felinine Chemical structure of 3-mercapto-3-methylbutan-1-ol
Felinine MMB

See also

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References

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  1. ^ Feliway official web site Feliway official web site
  2. ^ Patent US5709863 Properties of cats' facial pheromones
  3. ^ Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  4. ^ Tucker AO, Tucker SS (1988). "Catnip and the catnip response". Economic Botany. 42 (2): 214–31. doi:10.1007/BF02858923.
  5. ^ Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  6. ^ M Berdoy, J P Webster, and D W Macdonald (2000). "Fatal attraction in rats infected with Toxoplasma gondii". Proc Biol Sci. 267 (1452): 1591–4. doi:10.1098/rspb.2000.1182. PMC 1690701. PMID 11007336.{{cite journal}}: CS1 maint: multiple names: authors list (link)
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