Alpha-chloralose poisoning in cats in three Nordic countries - the importance of secondary poisoning.
Alpha-chloralose
Cat
Chloralose
Feline
Metabolism
Mice
Poisoning
Secondary
Toxicosis
Journal
BMC veterinary research
ISSN: 1746-6148
Titre abrégé: BMC Vet Res
Pays: England
ID NLM: 101249759
Informations de publication
Date de publication:
05 Sep 2022
05 Sep 2022
Historique:
received:
01
05
2022
accepted:
27
06
2022
entrez:
5
9
2022
pubmed:
6
9
2022
medline:
8
9
2022
Statut:
epublish
Résumé
Alpha-chloralose (AC) is a compound known to be toxic to various animal species and humans. In 2018 and 2019 an increase in suspected cases of AC poisoning in cats related to the use of AC as a rodenticide was reported to national veterinary and chemical authorities in Finland, Norway and Sweden by veterinarians working in clinical practices in respective country. The aims of this study were to prospectively investigate AC poisoning in cats, including possible secondary poisoning by consuming poisoned mice, and to study metabolism and excretion of AC in cats through analysis of feline urine. Data on signalment, history and clinical findings were prospectively collected in Finland, Norway and Sweden from July 2020 until March of 2021 using a questionnaire which the attending veterinarian completed and submitted together with a serum sample collected from suspected feline cases of AC-poisoning. The diagnosis was confirmed by quantification of AC in serum samples. Content of AC was studied in four feline urine samples, including screening for AC metabolites by UHPLC-HRMS/MS. Bait intake and amount of AC consumed by mice was observed in wild mice during an extermination of a rodent infestation. In total, 59 of 70 collected questionnaires and accompanying serum samples were included, with 127 to 70 100 ng/mL AC detected in the serum. Several tentative AC-metabolites were detected in the analysed feline urine samples, including dechlorinated and oxidated AC, several sulfate conjugates, and one glucuronic acid conjugate of AC. The calculated amount of AC ingested by each mouse was 33 to 106 mg with a mean of 61 mg. Clinical recognition of symptoms of AC poisoning in otherwise healthy cats roaming free outdoors and known to be rodent hunters strongly correlated with confirmation of the diagnosis through toxicological analyses of serum samples. The collected feline exposure data regarding AC show together with the calculation of the intake of bait and subsequent AC concentrations in mice that secondary poisoning from ingestion of mice is possible. The results of the screening for AC metabolites in feline urine confirm that cats excrete AC both unchanged and metabolized through dechlorination, oxidation, glucuronidation and sulfatation pathways.
Sections du résumé
BACKGROUND
BACKGROUND
Alpha-chloralose (AC) is a compound known to be toxic to various animal species and humans. In 2018 and 2019 an increase in suspected cases of AC poisoning in cats related to the use of AC as a rodenticide was reported to national veterinary and chemical authorities in Finland, Norway and Sweden by veterinarians working in clinical practices in respective country. The aims of this study were to prospectively investigate AC poisoning in cats, including possible secondary poisoning by consuming poisoned mice, and to study metabolism and excretion of AC in cats through analysis of feline urine.
METHODS
METHODS
Data on signalment, history and clinical findings were prospectively collected in Finland, Norway and Sweden from July 2020 until March of 2021 using a questionnaire which the attending veterinarian completed and submitted together with a serum sample collected from suspected feline cases of AC-poisoning. The diagnosis was confirmed by quantification of AC in serum samples. Content of AC was studied in four feline urine samples, including screening for AC metabolites by UHPLC-HRMS/MS. Bait intake and amount of AC consumed by mice was observed in wild mice during an extermination of a rodent infestation.
RESULTS
RESULTS
In total, 59 of 70 collected questionnaires and accompanying serum samples were included, with 127 to 70 100 ng/mL AC detected in the serum. Several tentative AC-metabolites were detected in the analysed feline urine samples, including dechlorinated and oxidated AC, several sulfate conjugates, and one glucuronic acid conjugate of AC. The calculated amount of AC ingested by each mouse was 33 to 106 mg with a mean of 61 mg.
CONCLUSIONS
CONCLUSIONS
Clinical recognition of symptoms of AC poisoning in otherwise healthy cats roaming free outdoors and known to be rodent hunters strongly correlated with confirmation of the diagnosis through toxicological analyses of serum samples. The collected feline exposure data regarding AC show together with the calculation of the intake of bait and subsequent AC concentrations in mice that secondary poisoning from ingestion of mice is possible. The results of the screening for AC metabolites in feline urine confirm that cats excrete AC both unchanged and metabolized through dechlorination, oxidation, glucuronidation and sulfatation pathways.
Identifiants
pubmed: 36064401
doi: 10.1186/s12917-022-03370-w
pii: 10.1186/s12917-022-03370-w
pmc: PMC9446805
doi:
Substances chimiques
Chloralose
238BZ29MUE
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
334Subventions
Organisme : The Nordic Working Group for Chemicals, Environment and Health
ID : n/a
Organisme : The Nordic Working Group for Chemicals, Environment and Health
ID : n/a
Organisme : The Nordic Working Group for Chemicals, Environment and Health
ID : n/a
Informations de copyright
© 2022. The Author(s).
Références
Lab Anim Sci. 1993 Jun;43(3):210-6
pubmed: 8355479
PLoS One. 2013 Sep 09;8(9):e73771
pubmed: 24040064
J Vet Pharmacol Ther. 2014 Feb;37(1):18-24
pubmed: 23888985
Vet Rec. 1972 Sep 30;91(14):330-3
pubmed: 4562133
Psychopharmacologia. 1964 Jul 6;6(1):1-30
pubmed: 5318644
J Anal Toxicol. 2012 Jul;36(6):452-6
pubmed: 22572811
Vet Clin North Am Small Anim Pract. 2013 Sep;43(5):1039-54
pubmed: 23890237
Nat Commun. 2013;4:1396
pubmed: 23360987
Eur Neuropsychopharmacol. 2016 Mar;26(3):518-31
pubmed: 26796682
J Anal Toxicol. 2022 Jul 14;46(6):651-657
pubmed: 34313718
Anaesthesist. 2019 Dec;68(12):843-847
pubmed: 31701172
Hum Toxicol. 1988 May;7(3):285-7
pubmed: 3391628
Vet J. 2006 Jul;172(1):109-13
pubmed: 16772135
Br J Pharmacol. 2000 Feb;129(4):731-43
pubmed: 10683198
J Anal Toxicol. 2003 Apr;27(3):156-61
pubmed: 12731657
Int J Legal Med. 1996;108(4):191-3
pubmed: 8652423
Lab Anim Sci. 1987 Oct;37(5):587-95
pubmed: 3320515