Assuring that 1080 toxicosis in the red fox (Vulpes vulpes) is humane: fluoroacetic acid (1080) and drug combinations

Citation
Ca. Marks et al., Assuring that 1080 toxicosis in the red fox (Vulpes vulpes) is humane: fluoroacetic acid (1080) and drug combinations, WILDLIF RES, 27(5), 2000, pp. 483-494
Citations number
96
Categorie Soggetti
Animal Sciences
Journal title
WILDLIFE RESEARCH
ISSN journal
10353712 → ACNP
Volume
27
Issue
5
Year of publication
2000
Pages
483 - 494
Database
ISI
SICI code
1035-3712(2000)27:5<483:AT1TIT>2.0.ZU;2-H
Abstract
Fluoroacetic acid (1080) is frequently used to poison the introduced red fo x (Vulpes vulpes) in Australia. The symptoms of 1080 poisoning in dogs appe ar extremely distressing to observers as manic running, yelping and convuls ing are readily interpreted as being indicative of pain and distress. Asses sment of pain perceived by animals poisoned by 1080 is difficult, as severe CNS disruptions alter behaviour and EEG patterns that may otherwise be use ful in such assessments. This study compared three drug agents combined wit h 1080 to address the possibility of pain and distress that may be experien ced by foxes during 1080 toxicosis. A mixed-sex group of 15 foxes was used in the trial of each of the three drugs: an analgesic (carprofen; 10 mg kg( -1)), an anxiolytic/sedative (diazepam; 10 mg kg(-1)) or an analgesic/sedat ive (clonidine; 0.75 mg kg(-1)). Each group of 15 foxes was randomly alloca ted between three treatments of either 0.5 mg kg(-1) of 1080, 0.5 mg kg(-1) of 1080 and a dose of the trial drug, and a dose of the trial drug alone. A telemetry collar was used on each fox to monitor the duration and intensi ty of activity, and behaviour from dosage to death was recorded using dayli ght/infra-red video cameras. In foxes dosed with 1080 alone, a mean of 4.05 (+/- 0.86, P < 0.05) h was observed from dosage to symptoms and 1.57 (+/- 0.46, P < 0.05) h from symptoms to death. Diazepam reduced the overall inte nsity of activity from dosage to death (P < 0.002) and from first symptoms to death (P < 0.05). Diazepam also extended the time until death (P < 0.01) and time taken from dosage to first symptoms (P < 0.01). In the dosages us ed, clonidine was not as effective as diazepam in reducing activity associa ted with symptoms of poisoning, although it prolonged the time taken from d osing to first symptoms (P < 0.05). Carprofen did not significantly alter t he progression of 1080 toxicosis or the intensity of activity of foxes comp ared with the group that received 1080 alone. The initial symptoms of 1080 toxicosis include retching and manic running and foxes may be more capable of suffering at this stage than after collapse, where behaviour is likely t o be associated with CNS disruption. Diazepam may be effective in minimisin g any anxiety experienced by foxes especially during the first symptoms of 1080 toxicosis.