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Journal of equine veterinary science2021; 107; 103774; doi: 10.1016/j.jevs.2021.103774

Efficacy and Side Effects of Low Single Doses of Cloprostenol Sodium or Dinoprost Tromethamine to Induce Luteolysis in Donkeys.

Abstract: Due to the limited literature available evaluating doses of Prostaglandin F2α in donkeys, doses for horses have been extrapolated and used as guidelines. This study aimed to assess the efficacy and side effects of four different cloprostenol sodium and dinoprost tromethamine doses to induce luteolysis in jennies. Sixty-three cycles of seven Jennies (nine cycles per jenny) were used in this study. Seven days after ovulation, jennies randomly received one of the treatments in a crossover design as follows: Control, no treatment was administered; C1, 250 µg of cloprostenol sodium (CS, Estrumate , Merck Animal Health, USA); C2, 125 µg of CS; C3, 65.5 µg of CS, C4, 37.5 µg of CS; DT1, 5 mg of dinoprost tromethamine (DT, Lutalyse, Zoetis, USA); DT2, 2.5 mg of DT; DT3, 1.25 mg of DT; DT4, 0.625 mg of DT. Jennies were monitored for 30 minutes following treatment, and adverse effects were recorded. The measurement of the corpus luteum (CL) and the length of the estrous cycle were recorded. All DT and CS treatment doses were effective (P < .0001) in reducing the estrous cycle length compared to jenny's Control cycle. The CL volume was decreased in all treated groups one day after treatment (P < .05). The adverse effects were reduced as the dose of both Prostaglandin F2α analogs were reduced. In conclusion, a single low dose of dinoprost tromethamine (0.625 mg) or cloprostenol sodium (37.5 µg) can induce luteolysis and shorten the estrous length in jennies producing fewer adverse effects.
Publication Date: 2021-09-20 PubMed ID: 34802629DOI: 10.1016/j.jevs.2021.103774Google Scholar: Lookup
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  • Journal Article
  • Randomized Controlled Trial
  • Veterinary
  • Research Support
  • Non-U.S. Gov't

Summary

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This research paper focuses on evaluating the efficiency and side effects of four different doses of cloprostenol sodium and dinoprost tromethamine in inducing luteolysis in donkeys, as the literature on this subject is limited. The study concludes that a single low dose of these drugs can shorten the estrous cycle and result in fewer side effects.

Study Design and Objectives

  • The study examined the impact of cloprostenol sodium and dinoprost tromethamine on donkeys. These two substances are analogs of the hormone Prostaglandin F2α.
  • Its main objective was to investigate the efficiency and adverse effects of different doses of these drugs to induce luteolysis — the degradation of the corpus luteum (a temporary endocrine structure in female animals) — in female donkeys, known as jennies.
  • The aim was to establish if a single low dose of these drugs could effectively induce luteolysis and shorten the estrous cycle — a physical cycle in mammals that results in ovulation and prepares females for pregnancy —with minimal side effects.

Methodology

  • For the purposes of the experiment, seven Jennies were used. Each Jenny had nine cycles, amounting to sixty-three cycles in total.
  • Seven days after ovulation, each Jenny was randomly given one of the treatments in a crossover design. The treatments included those using varying doses of cloprostenol sodium (CS) and dinoprost tromethamine (DT), and a control treatment with no administered drugs.
  • After treatment, the jennies were observed for 30 minutes, and any adverse effects were recorded. The size of the corpus luteum and the duration of the estrous cycle were also noted.

Findings

  • Results showed that all doses of cloprostenol sodium and dinoprost tromethamine were effective in reducing the estrous cycle length compared to the control cycle of the jennies.
  • The volume of the corpus luteum decreased the day after treatment in all groups administered with the drugs.
  • It was found that side effects were reduced as the doses of both Prostaglandin F2α analogs were lowered.
  • The study concluded that a single low dose of dinoprost tromethamine (0.625 mg) or cloprostenol sodium (37.5 µg) can induce luteolysis and shorten the estrous length in jennies while producing fewer adverse effects.

Cite This Article

APA
Segabinazzi LGTM, Landers M, Kent A, Peterson E, Gilbert R, French H. (2021). Efficacy and Side Effects of Low Single Doses of Cloprostenol Sodium or Dinoprost Tromethamine to Induce Luteolysis in Donkeys. J Equine Vet Sci, 107, 103774. https://doi.org/10.1016/j.jevs.2021.103774

Publication

ISSN: 0737-0806
NlmUniqueID: 8216840
Country: United States
Language: English
Volume: 107
Pages: 103774
PII: S0737-0806(21)00404-4

Researcher Affiliations

Segabinazzi, Lorenzo G T M
  • Ross University School of Veterinary Medicine, Basseterre, St. Kitts, West Indies.
Landers, McKinsey
  • Ross University School of Veterinary Medicine, Basseterre, St. Kitts, West Indies.
Kent, Ava
  • Ross University School of Veterinary Medicine, Basseterre, St. Kitts, West Indies.
Peterson, Erik
  • Ross University School of Veterinary Medicine, Basseterre, St. Kitts, West Indies.
Gilbert, Robert
  • Ross University School of Veterinary Medicine, Basseterre, St. Kitts, West Indies.
French, Hilari
  • Ross University School of Veterinary Medicine, Basseterre, St. Kitts, West Indies. Electronic address: HFrench@RossU.edu.

MeSH Terms

  • Animals
  • Cloprostenol
  • Dinoprost / analogs & derivatives
  • Equidae
  • Female
  • Horses
  • Luteolysis
  • Progesterone

Citations

This article has been cited 1 times.
  1. Segabinazzi LGTM, Gilbert RO, Ambrosia RL, Bergfelt DR, Samper JC, Peterson EW, French HM. Structural and Functional Dynamics of the Ovary and Uterus during the Estrous Cycle in Donkeys in the Eastern Caribbean. Animals (Basel) 2022 Dec 24;13(1).
    doi: 10.3390/ani13010074pubmed: 36611684google scholar: lookup