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Tail Docking of Piglets 2: Effects of Meloxicam on the Stress Response to Tail Docking

SIMPLE SUMMARY: Previous research has shown that tail docking causes an acute stress response and tail docking using the cauterisation procedure may be less aversive than the clipper procedure. This experiment examined the efficacy of meloxicam in mitigating acute stress responses to tail docking. C...

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Autores principales: Morrison, Rebecca, Hemsworth, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7552786/
https://www.ncbi.nlm.nih.gov/pubmed/32962233
http://dx.doi.org/10.3390/ani10091699
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author Morrison, Rebecca
Hemsworth, Paul
author_facet Morrison, Rebecca
Hemsworth, Paul
author_sort Morrison, Rebecca
collection PubMed
description SIMPLE SUMMARY: Previous research has shown that tail docking causes an acute stress response and tail docking using the cauterisation procedure may be less aversive than the clipper procedure. This experiment examined the efficacy of meloxicam in mitigating acute stress responses to tail docking. Cauterisation was less aversive than the clipper procedure based on the stress response after docking. Meloxicam mitigated the cortisol response at 30 min after tail docking with the clipper and the behavioural response in the first 60 min after tail docking with the clipper. The commercial viability and implementation of meloxicam requires consideration before it is recommended for use compared to cauterisation alone, as it requires additional handling of piglets and higher costs. ABSTRACT: This experiment assessed the efficacy of the cauterisation procedure with or without pain relief (injectable meloxicam) in mitigating the acute stress response to tail docking. Male piglets (n = 432) were allocated to the following treatments at 2-d post-farrowing: (1) no handling, (2) sham handling, (3) tail docked using clippers, (4) tail docked using a cauteriser, (5) meloxicam + clipper, and (6) meloxicam + cauteriser. Meloxicam treatments used Metacam(®) at 5 mg/mL injected i.m. 1 h prior to tail docking. Blood samples were collected at 15 and 30 min post-treatment and analysed for total plasma cortisol. Behaviours indicative of pain such as escape attempts, vocalisations and standing with head lowered were measured. The duration of vocalisations and frequency of escape attempts during treatment were greater in all tail docking treatments compared to the sham treatment. Piglets in the clipper treatment had higher (p < 0.05) cortisol concentrations at 30 min but not 15 min after treatment and stood for longer (p < 0.001) with head lowered in the first 60 min after treatment than those in the cauterisation treatment. Meloxicam reduced (p < 0.05) both the cortisol response at 30 min after tail docking with the clipper as well as the behavioural response in the first 60 min after tail docking with the clipper. In comparison to the sham treatment, cortisol concentrations at 15 min were higher in the two tail docking treatments whereas the tail docking treatments with meloxicam were similar to the sham handling treatment. In comparison to the sham handling treatment, cortisol concentrations at 30 min post-docking were higher (p < 0.05) only in the clipper treatment. While cauterisation appears to be less aversive than the clipper procedure, the administration of meloxicam did not mitigate the behavioural response during tail docking using either procedure, but reduced standing with head lowered in the first hour after docking for both methods. The commercial viability of administration of meloxicam requires consideration before it is recommended for use compared to cauterisation alone, as it requires additional handling of piglets and costs.
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spelling pubmed-75527862020-10-19 Tail Docking of Piglets 2: Effects of Meloxicam on the Stress Response to Tail Docking Morrison, Rebecca Hemsworth, Paul Animals (Basel) Article SIMPLE SUMMARY: Previous research has shown that tail docking causes an acute stress response and tail docking using the cauterisation procedure may be less aversive than the clipper procedure. This experiment examined the efficacy of meloxicam in mitigating acute stress responses to tail docking. Cauterisation was less aversive than the clipper procedure based on the stress response after docking. Meloxicam mitigated the cortisol response at 30 min after tail docking with the clipper and the behavioural response in the first 60 min after tail docking with the clipper. The commercial viability and implementation of meloxicam requires consideration before it is recommended for use compared to cauterisation alone, as it requires additional handling of piglets and higher costs. ABSTRACT: This experiment assessed the efficacy of the cauterisation procedure with or without pain relief (injectable meloxicam) in mitigating the acute stress response to tail docking. Male piglets (n = 432) were allocated to the following treatments at 2-d post-farrowing: (1) no handling, (2) sham handling, (3) tail docked using clippers, (4) tail docked using a cauteriser, (5) meloxicam + clipper, and (6) meloxicam + cauteriser. Meloxicam treatments used Metacam(®) at 5 mg/mL injected i.m. 1 h prior to tail docking. Blood samples were collected at 15 and 30 min post-treatment and analysed for total plasma cortisol. Behaviours indicative of pain such as escape attempts, vocalisations and standing with head lowered were measured. The duration of vocalisations and frequency of escape attempts during treatment were greater in all tail docking treatments compared to the sham treatment. Piglets in the clipper treatment had higher (p < 0.05) cortisol concentrations at 30 min but not 15 min after treatment and stood for longer (p < 0.001) with head lowered in the first 60 min after treatment than those in the cauterisation treatment. Meloxicam reduced (p < 0.05) both the cortisol response at 30 min after tail docking with the clipper as well as the behavioural response in the first 60 min after tail docking with the clipper. In comparison to the sham treatment, cortisol concentrations at 15 min were higher in the two tail docking treatments whereas the tail docking treatments with meloxicam were similar to the sham handling treatment. In comparison to the sham handling treatment, cortisol concentrations at 30 min post-docking were higher (p < 0.05) only in the clipper treatment. While cauterisation appears to be less aversive than the clipper procedure, the administration of meloxicam did not mitigate the behavioural response during tail docking using either procedure, but reduced standing with head lowered in the first hour after docking for both methods. The commercial viability of administration of meloxicam requires consideration before it is recommended for use compared to cauterisation alone, as it requires additional handling of piglets and costs. MDPI 2020-09-20 /pmc/articles/PMC7552786/ /pubmed/32962233 http://dx.doi.org/10.3390/ani10091699 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Morrison, Rebecca
Hemsworth, Paul
Tail Docking of Piglets 2: Effects of Meloxicam on the Stress Response to Tail Docking
title Tail Docking of Piglets 2: Effects of Meloxicam on the Stress Response to Tail Docking
title_full Tail Docking of Piglets 2: Effects of Meloxicam on the Stress Response to Tail Docking
title_fullStr Tail Docking of Piglets 2: Effects of Meloxicam on the Stress Response to Tail Docking
title_full_unstemmed Tail Docking of Piglets 2: Effects of Meloxicam on the Stress Response to Tail Docking
title_short Tail Docking of Piglets 2: Effects of Meloxicam on the Stress Response to Tail Docking
title_sort tail docking of piglets 2: effects of meloxicam on the stress response to tail docking
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7552786/
https://www.ncbi.nlm.nih.gov/pubmed/32962233
http://dx.doi.org/10.3390/ani10091699
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