Periovulatory administration of therapeutic and supratherapeutic doses of firocoxib does not impair induced ovulation or follicular dynamics in mares treated with a GnRH analogue.
Abstract: To evaluate the effects of therapeutic and supratherapeutic periovulatory doses of firocoxib on ovulation and follicular dynamics in mares. Methods: Seventy cycling mares were randomly assigned to receive firocoxib at 0.1 mg/kg (n = 27), firocoxib at 0.3 mg/kg (n = 22), or no treatment (control; n = 21). Treatments were initiated on Day 0, defined as the day of ovulation induction with a GnRH analogue administered intramuscularly, with firocoxib administered intravenously on Day 0 and Day 1 (24 h apart). Follicular diameter and ovulation timing were assessed by transrectal ultrasonography. Results: All mares ovulated within 72 h after ovulation induction, with no ovulatory failures or hemorrhagic anovulatory follicles. Time to ovulation did not differ among groups (P > 0.05). Dominant follicle diameter on Days -2 and -1 and percentage follicular growth between these days were similar across treatments (P > 0.05). Conclusions: Periovulatory administration of firocoxib, even at supratherapeutic doses, did not appear to impair induced ovulation or follicular development in mares under the conditions of this study.
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Research Overview
This study investigated whether giving mares therapeutic or higher-than-therapeutic doses of the drug firocoxib around the time of ovulation affects their ability to ovulate or the development of follicles when ovulation is induced by a GnRH analogue.
The findings showed that firocoxib did not interfere with ovulation or follicle growth under the tested conditions.
Ovulation induction using GnRH analogues is a common reproductive management tool in mares to control or synchronize timing of ovulation.
Since prostaglandins and inflammation are involved in follicle rupture and ovulation, NSAIDs like firocoxib could potentially impair this process.
The study aimed to test whether periovulatory administration (around the time of ovulation) of firocoxib at therapeutic or supratherapeutic doses would affect ovulation success or follicular dynamics in mares.
Methods
Seventy cycling mares were randomly divided into three groups:
27 mares received firocoxib at 0.1 mg/kg (therapeutic dose)
22 mares received firocoxib at 0.3 mg/kg (supratherapeutic dose, 3x the therapeutic dose)
21 mares received no treatment and served as controls
Day 0 was defined as the day of ovulation induction using a GnRH analogue administered intramuscularly.
Firocoxib was given intravenously twice: once on Day 0 and again 24 hours later on Day 1.
All mares, across all groups, ovulated successfully within 72 hours of ovulation induction.
No mares showed ovulatory failure or formation of hemorrhagic anovulatory follicles, indicating normal ovulatory responses.
Time elapsed to ovulation after induction was not significantly different among the three groups (no difference between treated and control mares).
Dominant follicle diameters measured two days and one day before ovulation induction were similar across all groups.
The percentage growth of follicles between these two pre-ovulation days was also similar, suggesting firocoxib did not affect follicular growth dynamics.
Conclusions and Implications
The periovulatory administration of firocoxib, even at doses three times higher than therapeutic levels, did not impair ovulation induction in mares treated with GnRH analogue.
Follicular development proceeded normally, with no negative impact on dominant follicle growth.
These findings suggest that firocoxib can be safely administered around ovulation in mares without compromising reproductive function related to induced ovulation.
Faria LG, Zutter BM, Freitas-Dell'Aqua CP, Camillo BL, Ávila-Júnior OS, Bassetti FS, Marcolino LC, Alvarenga MA.
(2026).
Periovulatory administration of therapeutic and supratherapeutic doses of firocoxib does not impair induced ovulation or follicular dynamics in mares treated with a GnRH analogue.
J Equine Vet Sci, 161, 105878.
https://doi.org/10.1016/j.jevs.2026.105878
Department of Veterinary Surgery and Animal Reproduction, School of Veterinary Medicine and Animal Science, São Paulo State University (UNESP), Botucatu, São Paulo, Brazil. Electronic address: gualberto.faria@unesp.br.
Zutter, B M
Department of Veterinary Surgery and Animal Reproduction, School of Veterinary Medicine and Animal Science, São Paulo State University (UNESP), Botucatu, São Paulo, Brazil.
Freitas-Dell'Aqua, C P
Department of Veterinary Surgery and Animal Reproduction, School of Veterinary Medicine and Animal Science, São Paulo State University (UNESP), Botucatu, São Paulo, Brazil.
Camillo, B L
Department of Veterinary Surgery and Animal Reproduction, School of Veterinary Medicine and Animal Science, São Paulo State University (UNESP), Botucatu, São Paulo, Brazil.
Ávila-Júnior, O S
Central Equina de Reprodução (CER), Boituva, São Paulo, Brazil.
Bassetti, F S
Central Equina de Reprodução (CER), Boituva, São Paulo, Brazil.
Marcolino, L C
Central Equina de Reprodução (CER), Boituva, São Paulo, Brazil.
Alvarenga, M A
Department of Veterinary Surgery and Animal Reproduction, School of Veterinary Medicine and Animal Science, São Paulo State University (UNESP), Botucatu, São Paulo, Brazil.
Declaration of competing interest Marco Antônio Alvarenga is a shareholder of Botupharma Animal Health, the manufacturer of the firocoxib formulation used in this study. The remaining authors declare no commercial or financial relationships that could be construed as a potential conflict of interest. Botupharma Animal Health had no role in the study design, data collection, data analysis, interpretation of the results, or preparation of the manuscript.