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Theriogenology2022; 197; 57-61; doi: 10.1016/j.theriogenology.2022.11.042

The effect of dexamethasone and flunixin-meglumine on ovulation, endometrial oedema, and inter-ovulatory interval length in the mare.

Abstract: The use of flunixin-meglumine (a potent non-steroidal anti-inflammatory drug) during the critical period of intrafollicular prostaglandin production before ovulation (24 and 36 h after hCG treatment) results in a high rate of ovulatory failure and formation of haemorrhagic anovulatory follicles (HAF) in the mare. Dexamethasone is commonly used to prevent persistent mating-induced endometritis in susceptible mares, but the effect on ovulation blockage within the pre-ovulatory critical window of intrafollicular prostaglandins production following hCG administration has not been determined. Six mares were followed during four consecutive cycles in a crossover design; once in oestrus with a follicle of >32 mm in diameter, mares were treated with hCG (Hour 0) and assigned to one of 4 groups randomly: 1) FM, mares received 1.7 mg/kg flunixin-meglumine at Hour 24 and 36; 2) CON, mares received no further treatment. 3) DEX1, mares received 0.1 mg/kg dexamethasone at Hour 24, and 4) DEX2, mares received 0.1 mg/kg dexamethasone at Hour 24 and 36. For all groups, ovulation and HAF rates, endometrial oedema profiles and the inter-ovulatory intervals (IOI) were determined and compared statistically. All CON and DEX mares ovulated normally and did not form any HAF. On the contrary, FM mares developed a HAF in 83% of cycles (P < 0.01). The endometrial oedema score was lower following DEX administration than FM (P < 0.05). The mean IOI was longer (P < 0.05) in DEX1 and DEX2 groups (26.5 and 26 days, respectively) than in CON and FM groups (21.5 and 22 days, respectively). In conclusion, dexamethasone treatment given either once or twice during the critical window of hCG-induced ovulation did not block or delay ovulation, but had a similar ovulation rate than untreated control mares. However, the inter-ovulatory intervals of dexamethasone treated mares was longer than control and FM treated mares. Finally, dexamethasone treatment was more effective in reducing endometrial oedema than FM.
Publication Date: 2022-11-28 PubMed ID: 36470110DOI: 10.1016/j.theriogenology.2022.11.042Google Scholar: Lookup
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  • Journal Article

Summary

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This research investigates the impact of the drugs dexamethasone and flunixin-meglumine on ovulation, endometrial oedema, and the interval between ovulations in mares. The study found that flunixin-meglumine can cause high rates of ovulation failure and anovulatory follicles, while dexamethasone did not block or delay ovulation, yet increased the interval between ovulations.

Objectives and Methodology

The study aimed to explore how the drugs flunixin-meglumine (a non-steroidal anti-inflammatory drug) and dexamethasone (used to prevent persistent mating-induced endometritis) affect ovulation, endometrial edema, and the length of the inter-ovulatory interval in mares. This involved monitoring six mares over four consecutive cycles using a crossover design.

  • The mares were treated with hCG, a hormonal trigger that stimulates ovulation, and then randomly assigned to one of four groups.
  • Group FM was treated with flunixin-meglumine 24 and 36 hours after hCG administration.
  • Groups DEX1 and DEX2 were treated with dexamethasone at the 24-hour mark, with DEX2 receiving an additional dose at the 36-hour mark.
  • Group CON received no further treatment as a control group.

Results and Key Findings

The research primarily focused on ovulation and HAF rates, endometrial oedema profiles, and the inter-ovulatory intervals (IOI).

  • It was found that all mares in both the control and dexamethasone groups ovulated normally without the formation of any haemorrhagic anovulatory follicles (HAF).
  • Mares in group FM, treated with flunixin-meglumine, however, showed a high rate of ovulatory failure, with 83% developing a HAF.
  • Endometrial oedema scores were lower when dexamethasone was administered, suggesting the drug was more effective at reducing endometrial oedema than flunixin-meglumine.
  • The inter-ovulatory intervals for mares treated with dexamethasone (both DEX1 and DEX2) were longer than those from the control and FM groups.

Conclusion

The research concluded that dexamethasone, whether administered once or twice during the critical window of hCG-induced ovulation, doesn’t block or delay ovulation. Instead, it results in similar ovulation rates as untreated control mares. However, it was noted that the inter-ovulatory intervals of dexamethasone-treated mares were longer than those untreated or treated with flunixin-meglumine. Dexamethasone proved more effective in reducing endometrial oedema than flunixin-meglumine.

Cite This Article

APA
Martínez-Boví R, Plaza-Dávila M, Cuervo-Arango J. (2022). The effect of dexamethasone and flunixin-meglumine on ovulation, endometrial oedema, and inter-ovulatory interval length in the mare. Theriogenology, 197, 57-61. https://doi.org/10.1016/j.theriogenology.2022.11.042

Publication

ISSN: 1879-3231
NlmUniqueID: 0421510
Country: United States
Language: English
Volume: 197
Pages: 57-61
PII: S0093-691X(22)00507-6

Researcher Affiliations

Martínez-Boví, Rebeca
  • Equine Fertility Group, Faculty of Veterinary Medicine, Universidad CEU Cardenal Herrera, CEU Universities, Alfara del Patriarca, Valencia, Spain.
Plaza-Dávila, María
  • Equine Fertility Group, Faculty of Veterinary Medicine, Universidad CEU Cardenal Herrera, CEU Universities, Alfara del Patriarca, Valencia, Spain.
Cuervo-Arango, Juan
  • Equine Fertility Group, Faculty of Veterinary Medicine, Universidad CEU Cardenal Herrera, CEU Universities, Alfara del Patriarca, Valencia, Spain. Electronic address: juan.cuervo@uchceu.es.

MeSH Terms

  • Female
  • Horses
  • Animals
  • Ovulation
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology
  • Anti-Inflammatory Agents, Non-Steroidal / therapeutic use
  • Anovulation / drug therapy
  • Anovulation / veterinary
  • Dexamethasone / pharmacology
  • Meglumine / pharmacology
  • Horse Diseases / drug therapy

Conflict of Interest Statement

Declaration of competing interest The authors declare no conflict of interest.

Citations

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