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Theriogenology2019; 134; 83-89; doi: 10.1016/j.theriogenology.2019.05.009

Effects of lidocaine on equine ejaculated sperm and epididymal sperm post-castration.

Abstract: In equids, it is common to inject lidocaine into the testicles at the time of routine castration to provide analgesia. The effects of lidocaine on equine sperm have not been evaluated in vitro or on epididymal sperm collected following castration. The aims of this study were to determine effects of clinically relevant doses of lidocaine on equine spermatozoa in vitro using freshly collected semen and to compare the characteristics of epididymal spermatozoa after routine castration with or without intra-testicular lidocaine administration. We hypothesized that increasing concentrations of lidocaine would decrease total motility (TM), progressive motility (PM), velocity of the average path (VAP), velocity of the curved line (VCL), linearity (LIN), normal morphology (M) and membrane integrity (MI). We also hypothesized that injection of intra-testicular lidocaine would decrease TM, PM, VAP, VCL, LIN, M, and MI following routine castration, epididymal flushing and cryopreservation. In experiment 1, sperm was collected from four stallions and mixed with lidocaine at concentrations of 1 μg/ml, 10 μg/ml, 100 μg/ml, 1,000 μg/ml and 10,000 μg/ml. M and MI were compared to the control sample at 0 and 48 h. Motility parameters were analyzed at 0, 2, 4, 6, 24, and 48 h. In experiment 2, 12 stallions were castrated under general anesthesia. One testicle was removed without the use of intra-testicular lidocaine and the other testicle was removed 10 min after injection of 10 ml of 2% lidocaine. Results: In experiment 1, fresh sperm showed no significant difference (p < 0.05) compared to control at either 1 μg/ml or 10 μg/ml concentrations of lidocaine. There were significant decreases in PM, VAP, VCL, and LIN at concentrations of 100μg/ml-10,000 μg/ml and for TM at lidocaine concentrations of 1,000-10,000 μg/ml compared to control. Morphology did not change at any lidocaine concentration. Membrane integrity decreased significantly at 10,000 μg/ml lidocaine. In the second experiment 1.03 ± 0.42 μg/ml lidocaine was detected in the epididymal flush of stallions treated with lidocaine. There were no significant differences in any measured parameters between the control and the lidocaine treated testicles. Intra-testicular lidocaine injection at the time of castration did not affect any measured parameters after epididymal flush. Lidocaine concentrations higher than 100 μg/ml in-vitro resulted in decreased motility parameters of the spermatozoa independent of exposure time.
Publication Date: 2019-05-16 PubMed ID: 31153092DOI: 10.1016/j.theriogenology.2019.05.009Google Scholar: Lookup
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  • Journal Article

Summary

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This study explores the impact of lidocaine, a local anesthetic often used during routine castration in horses, on equine sperm physiology and characteristics of sperm found in the epididymis post-castration. Essentially, the researchers found that in concentrations higher than 100μg/ml, lidocaine reduced some sperm motility parameters, but did not significantly affect the sperm’s morphology or overall functioning following epididymal flush post-castration.

Research Methodology

The study was divided into two separate experiments.

  • In the first experiment, sperm was collected from four stallions and mixed with varying concentrations of lidocaine (ranging from 1 μg/ml to 10,000 μg/ml). Morphology and membrane integrity were assessed at the outset and 48 hours later. The researchers also studied sperm motility parameters such as total motility (TM), progressive motility (PM), velocity of average path (VAP), velocity of a curved line (VCL), and linearity (LIN) at multiple time points over a 48-hour period.
  • In the second experiment, 12 stallions were castrated under general anesthesia. One testicle was removed without using intra-testicular lidocaine, while the other was removed 10 minutes after injecting 10 ml of 2% lidocaine. The aim was to compare the characteristics of the epididymal spermatozoa under these two conditions.

Key Findings

In the first experiment, lidocaine concentrations of 1 μg/ml or 10 μg/ml showed no significant difference in sperm characteristics or motility compared to the control group. With much higher lidocaine concentrations (100-10,000 μg/ml), certain motility parameters like PM, VAP, VCL, and LIN decreased substantially, as did TM in concentrations of 1,000-10,000 μg/ml. However, the sperm morphology remained unchanged across all lidocaine concentrations. Membrane integrity was noticeably affected only at the highest concentration of 10,000 μg/ml lidocaine.

In the second experiment, the researchers found lidocaine present in the epididymal flush of stallions treated with the anesthetic. However, no significant differences were observed in any measured parameters between the control and lidocaine-treated testicles. This indicates that the administration of intra-testicular lidocaine at the time of castration did not noticeably affect sperm characteristics following epididymal flushing.

Research Significance

The results of this study provide important insights about the effects of lidocaine on equine spermatozoa, especially in a clinical, in-vitro setting. The findings suggest that while lidocaine can inhibit certain motility parameters of sperm at higher concentrations, it does not seem to significantly affect the functionality or morphology of the sperm, nor does it affect sperm characteristics following epididymal flushing post-castration. This implies that the use of lidocaine during castration does not have a detrimental effect on sperm recovered post-castration, which may have potential use in breeding programs.

Cite This Article

APA
Boye JK, Katzman SA, Kass PH, Dujovne GA. (2019). Effects of lidocaine on equine ejaculated sperm and epididymal sperm post-castration. Theriogenology, 134, 83-89. https://doi.org/10.1016/j.theriogenology.2019.05.009

Publication

ISSN: 1879-3231
NlmUniqueID: 0421510
Country: United States
Language: English
Volume: 134
Pages: 83-89

Researcher Affiliations

Boye, J K
  • William R. Pritchard Veterinary Medical Teaching Hospital, School of Veterinary Medicine, University of California, 1 Garrod Drive, Davis, CA, 95616, USA. Electronic address: jennykatrine@hotmail.com.
Katzman, S A
  • Department of Surgical and Radiological Sciences, School of Veterinary Medicine, University of California, 1 Garrod Drive, Davis, CA, 95616, USA. Electronic address: skatzman@vmth.ucdavis.edu.
Kass, P H
  • Department of Population Health and Reproduction, School of Veterinary Medicine, University of California, 1 Garrod Drive, Davis, CA, 95616, USA. Electronic address: phkass@ucdavis.edu.
Dujovne, G A
  • Department of Population Health and Reproduction, School of Veterinary Medicine, University of California, 1 Garrod Drive, Davis, CA, 95616, USA. Electronic address: gadujovne@ucdavis.edu.

MeSH Terms

  • Anesthetics, Local / adverse effects
  • Anesthetics, Local / therapeutic use
  • Animals
  • Cryopreservation / veterinary
  • Epididymis
  • Horses
  • Lidocaine / adverse effects
  • Lidocaine / therapeutic use
  • Male
  • Orchiectomy
  • Semen / drug effects
  • Semen Analysis / veterinary
  • Semen Preservation / veterinary
  • Sperm Motility / drug effects
  • Spermatozoa / drug effects
  • Spermatozoa / physiology
  • Testis / drug effects