Analyze Diet
Veterinary anaesthesia and analgesia2003; 30(3); 138-146; doi: 10.1046/j.1467-2995.2003.00138.x

Changes in the EEG during castration in horses and ponies anaesthetized with halothane.

Abstract: To identify changes in the amplitude spectrum of the electroencephalogram (EEG) during a standardized surgical model of nociception in horses. Methods: Thirteen entire male horses and ponies referred to Division of Clinical Veterinary Science, Bristol (n = 9) and Department of Clinical Veterinary Medicine (n = 4) for castration. Methods: Following pre-anaesthetic medication with acepromazine, anaesthesia was induced with guaiphenesin and thiopental and maintained with halothane in oxygen. The EEG was recorded continuously using subcutaneous needle electrodes. Additional monitoring comprised ECG, arterial blood pressure, blood gas analysis, airway gases, and body temperature. All animals were castrated using a closed technique. The raw EEG was analysed after completion of each investigation and the EEG variables median frequency (F50), spectral edge frequency (SEF) 95% and total amplitude were derived from the spectra using standard techniques. The mean values of EEG variables recorded during a baseline time period (recorded before the start of surgery) and castration of each testicle were compared using analysis of variance for repeated measures. Results: Total amplitude (Atot) decreased and F50 increased during castration of each testicle compared to the baseline time period [(89.0 +/- 7.8% testicle 1, 87.0 +/- 7.8% testicle 2) and (110.0 +/- 15.0% testicle 1, 109.0 +/- 15.0% testicle 2), respectively]. Changes in SEF 95% were not significant. Conclusions: De-synchronization was identified in the EEG during the nociceptive stimulus of castration. The results suggest that an increase in F50 may be a specific marker for nociception in the horse. Conclusions: Studies investigating the efficacy of analgesic agents in horses are limited by difficulties in peri-operative pain assessment. This model, using EEG changes associated with nociceptive stimulation, can be used to investigate the anti-nociceptive efficacy of different anaesthetic agents in the horse.
Publication Date: 2003-09-23 PubMed ID: 14498845DOI: 10.1046/j.1467-2995.2003.00138.xGoogle Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

This research studied changes in the electroencephalogram (EEG) of horses during the pain-causing process of castration with the aim of identifying specific markers for pain detection in the horse.

Objective

The main goal of this research was to identify changes in the electrical activity of the horse brain (measured by EEG) during a standardized surgical model of pain induction in horses (castration). The investigation aimed to determine if there were specific markers that could indicate the presence of pain in horses, as determined during anaesthesia.

Methods

  • Thirteen male horses and ponies set for castration were involved in the study.
  • The horses were anaesthetized using acepromazine, guaiphenesin, thiopental, and then maintained on halothane throughout the procedure.
  • The EEG was recorded continuously using subcutaneous needle electrodes placed over their brains.
  • Other health indicators including ECG, arterial blood pressure, blood gases, airway gases, and temperature were also monitored.
  • Once the recording was over, the raw EEG data was analysed, with focus on median frequency (F50), spectral edge frequency (SEF) 95% and total amplitude as key variables.

Results

  • The researchers found that during castration, total EEG amplitude decreased while the F50 frequency increased as compared to baseline pre-operative readings.
  • Interestingly, there were no significant changes in the spectral edge frequency (SEF) 95% during the process.
  • These shifts in EEG readings indicated a clear EEG de-synchronization during the pain-causing stimulus of castration.

Conclusions

  • The outcomes suggest that an increase in F50 may be a reliable marker for pain detection in horses.
  • Due to the lack of techniques for assessing pain in horses, this research provides a promising method that uses EEG changes associated with pain-causing stimulus to measure the efficacy of different pain relieving (analgesic) agents in these animals.

Cite This Article

APA
Murrell JC, Johnson CB, White KL, Taylor PM, Haberham ZL, Waterman-Pearson AE. (2003). Changes in the EEG during castration in horses and ponies anaesthetized with halothane. Vet Anaesth Analg, 30(3), 138-146. https://doi.org/10.1046/j.1467-2995.2003.00138.x

Publication

ISSN: 1467-2987
NlmUniqueID: 100956422
Country: United States
Language: English
Volume: 30
Issue: 3
Pages: 138-146

Researcher Affiliations

Murrell, Joanna C
  • Department of Clinical Sciences of Companion Animals, University Utrecht, Faculty of Veterinary Medicine, PO Box 80154, NL-3508 TD, Utrecht. J.C.Murrell@vet.uu.nl
Johnson, Craig B
    White, Kate L
      Taylor, Polly M
        Haberham, Zainal L
          Waterman-Pearson, Avril E

            MeSH Terms

            • Anesthetics, Inhalation
            • Animals
            • Electroencephalography / veterinary
            • Halothane
            • Horses / physiology
            • Horses / surgery
            • Male
            • Orchiectomy / methods
            • Orchiectomy / veterinary
            • Pain Measurement / methods
            • Pain Measurement / veterinary

            Citations

            This article has been cited 19 times.
            1. Kumar P, Abubakar AA, Ahmed MA, Hayat MN, Ajat M, Kaka U, Goh YM, Sazili AQ. Electroencephalogram and Physiological Responses as Affected by Slaughter Empathy in Goats.. Animals (Basel) 2023 Mar 20;13(6).
              doi: 10.3390/ani13061100pubmed: 36978640google scholar: lookup
            2. Kumar P, Abubakar AA, Sazili AQ, Kaka U, Goh YM. Application of Electroencephalography in Preslaughter Management: A Review.. Animals (Basel) 2022 Oct 20;12(20).
              doi: 10.3390/ani12202857pubmed: 36290243google scholar: lookup
            3. Murillo C, Weng HY, Weil AB, Kreuzer M, Ko JC. Perioperative Brain Function Monitoring with Electroencephalography in Horses Anesthetized with Multimodal Balanced Anesthetic Protocol Subjected to Surgeries.. Animals (Basel) 2022 Oct 20;12(20).
              doi: 10.3390/ani12202851pubmed: 36290236google scholar: lookup
            4. Reiser J, Kreuzer M, Werner J, Saller AM, Fischer J, Senf S, Deffner P, Abendschön N, Groll T, Grott A, Miller R, Bergmann S, Erhard MH, Ritzmann M, Zöls S, Schneider G, Steiger K, Baumgartner C. Nociception-Induced Changes in Electroencephalographic Activity and FOS Protein Expression in Piglets Undergoing Castration under Isoflurane Anaesthesia.. Animals (Basel) 2022 Sep 6;12(18).
              doi: 10.3390/ani12182309pubmed: 36139169google scholar: lookup
            5. Raghazli R, Othman AH, Kaka U, Abubakar AA, Imlan JC, Hamzah H, Sazili AQ, Goh YM. Physiological and electroencephalogram responses in goats subjected to pre-and during slaughter stress.. Saudi J Biol Sci 2021 Nov;28(11):6396-6407.
              doi: 10.1016/j.sjbs.2021.07.013pubmed: 34764757google scholar: lookup
            6. Abubakar AA, Zulkifli I, Goh YM, Kaka U, Sabow AB, Awad EA, Imlan JC, Othman AH, Raghazli R, Mitin H, Sazili AQ. The Effects of Stocking Density and Distances on Electroencephalographic Changes and Cortisol as Welfare Indicators in Brahman Crossbred Cattle.. Animals (Basel) 2021 Oct 5;11(10).
              doi: 10.3390/ani11102895pubmed: 34679916google scholar: lookup
            7. Bergamasco L, Edwards-Callaway LN, Bello NM, Mijares S, Cull CA, Mosher RA, Coetzee JF. Unmitigated Surgical Castration in Calves of Different Ages: Electroencephalographic and Neurohormonal Findings.. Animals (Basel) 2021 Jun 15;11(6).
              doi: 10.3390/ani11061791pubmed: 34203947google scholar: lookup
            8. Stomp M, d'Ingeo S, Henry S, Lesimple C, Cousillas H, Hausberger M. EEG individual power profiles correlate with tension along spine in horses.. PLoS One 2020;15(12):e0243970.
              doi: 10.1371/journal.pone.0243970pubmed: 33315932google scholar: lookup
            9. Imlan JC, Kaka U, Goh YM, Idrus Z, Awad EA, Abubakar AA, Ahmad T, Nizamuddin HNQ, Sazili AQ. Effects of Slaughter Knife Sharpness on Blood Biochemical and Electroencephalogram Changes in Cattle.. Animals (Basel) 2020 Mar 30;10(4).
              doi: 10.3390/ani10040579pubmed: 32235510google scholar: lookup
            10. Mellor DJ. Mouth Pain in Horses: Physiological Foundations, Behavioural Indices, Welfare Implications, and a Suggested Solution.. Animals (Basel) 2020 Mar 29;10(4).
              doi: 10.3390/ani10040572pubmed: 32235343google scholar: lookup
            11. Harris C, White PJ, Mohler VL, Lomax S. Electroencephalography Can Distinguish between Pain and Anaesthetic Intervention in Conscious Lambs Undergoing Castration.. Animals (Basel) 2020 Mar 4;10(3).
              doi: 10.3390/ani10030428pubmed: 32143285google scholar: lookup
            12. Lacombe VA. Seizures in horses: diagnosis and classification.. Vet Med (Auckl) 2015;6:301-308.
              doi: 10.2147/VMRR.S62078pubmed: 30101115google scholar: lookup
            13. McIlhone AE, Beausoleil NJ, Kells NJ, Johnson CB, Mellor DJ. Effects of halothane on the electroencephalogram of the chicken.. Vet Med Sci 2018 May;4(2):98-105.
              doi: 10.1002/vms3.91pubmed: 29851306google scholar: lookup
            14. McIlhone AE, Beausoleil NJ, Kells NJ, Mellor DJ, Johnson CB. Effects of noxious stimuli on the electroencephalogram of anaesthetised chickens (Gallus gallus domesticus).. PLoS One 2018;13(4):e0196454.
              doi: 10.1371/journal.pone.0196454pubmed: 29698446google scholar: lookup
            15. Cousillas H, Oger M, Rochais C, Pettoello C, Ménoret M, Henry S, Hausberger M. An Ambulatory Electroencephalography System for Freely Moving Horses: An Innovating Approach.. Front Vet Sci 2017;4:57.
              doi: 10.3389/fvets.2017.00057pubmed: 28512633google scholar: lookup
            16. Tünsmeyer J, Hopster K, Kästner SB. Clinical Use of a Multivariate Electroencephalogram (Narcotrend) for Assessment of Anesthetic Depth in Horses during Isoflurane-Xylazine Anesthesia.. Front Vet Sci 2016;3:25.
              doi: 10.3389/fvets.2016.00025pubmed: 27014707google scholar: lookup
            17. Williams DC, Brosnan RJ, Fletcher DJ, Aleman M, Holliday TA, Tharp B, Kass PH, LeCouteur RA, Steffey EP. Qualitative and Quantitative Characteristics of the Electroencephalogram in Normal Horses during Administration of Inhaled Anesthesia.. J Vet Intern Med 2016 Jan-Feb;30(1):289-303.
              doi: 10.1111/jvim.13813pubmed: 26714626google scholar: lookup
            18. Kaka U, Hui Cheng C, Meng GY, Fakurazi S, Kaka A, Behan AA, Ebrahimi M. Electroencephalographic changes associated with antinociceptive actions of lidocaine, ketamine, meloxicam, and morphine administration in minimally anaesthetized dogs.. Biomed Res Int 2015;2015:305367.
              doi: 10.1155/2015/305367pubmed: 25695060google scholar: lookup
            19. Jang HS, Jang IS, Lee MG. The effects of tramadol on electroencephalographic spectral parameters and analgesia in rats.. Korean J Physiol Pharmacol 2010 Jun;14(3):191-8.
              doi: 10.4196/kjpp.2010.14.3.191pubmed: 20631893google scholar: lookup