Clinicopathological aspects of imidocarb dipropionate toxicity in horses.
Abstract: Six groups of four adult horses were twice injected intramuscularly at a 24 hour interval with 0, 2, 4, 8, 16 or 32 mg/kg of imidocarb dipropionate (IMDP) and monitored for 21 days. The LD50 of IMDP for 21 days after injection was two doses of 15.99 +/- 1.49 mg/kg with mortalities occurring within six days following the first injection. Increasing levels of IMDP were correlated with increasing rates of morbidity, mortality, local and systemic reactions, increasing levels of blood urea nitrogen, serum aspartate amino transferase, serum sorbitol dehydrogenase, serum creatine phosphokinase, neutrophilia and increasing severity of renal, hepatic and pulmonary lesions. Mortalities were attributed to acute renal cortical tubular necrosis and acute periportal hepatic necrosis induced by two injections of 16 or 32 mg/kg of IMDP.
Publication Date: 1981-07-01 PubMed ID: 7313320
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- Comparative Study
- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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This research paper explores the detrimental effects of imidocarb dipropionate (IMDP) when administered in increasing doses to adult horses. Particularly, the paper highlights associations between high IMDP dosage and elevated morbidity, mortality, and a variety of significant systemic health complications.
Research Methods and Experimental Design
- A total of 24 adult horses were separated into six groups and each group was injected with varying doses (0, 2, 4, 8, 16, or 32 mg/kg) of IMDP twice in a 24-hour period. This allowed the researchers to analyse the effects of different IMDP dosages on overall horse health.
- The conditions of the horses were then monitored for a total of 21 days to track any potential long-term health effects caused by the IMDP injections.
Key Findings
- The lethal dose (LD50 – the dose lethal to 50% of the horses) of IMDP was found to be two injections of approximately 15.99 mg/kg each. Any horses that died during the study typically did so within the first six days after being injected with IMDP.
- The research also identified a correlation between increasing IMDP levels and a rise in the rates of morbidity (disease) and mortality amongst the horses. Essentially, the more IMDP a horse was injected with, the sicker it became, and the higher its risk of death became.
- High doses of IMDP were associated with a range of significant, detrimental health outcomes, including an increase in blood urea nitrogen, serum aspartate amino transferase, serum sorbitol dehydrogenase, serum creatine phosphokinase, neutrophilia (excess of neutrophilic white blood cells in the blood), and more severe renal (kidney-related), hepatic (liver-related) and pulmonary (lung-related) lesions.
- The cause of death in the horses that did not survive the study was attributed to acute renal cortical tubular necrosis (severe damage to the renal tubules in the kidneys) and acute periportal hepatic necrosis (serious damage to the liver) caused by the two injections of either 16 or 32 mg/kg of IMDP.
Implications and Conclusion
- The findings of this study show a clear link between high doses of IMDP and serious health issues in horses. Care must be taken when administering this substance to avoid causing adverse effects.
Cite This Article
APA
Adams LG.
(1981).
Clinicopathological aspects of imidocarb dipropionate toxicity in horses.
Res Vet Sci, 31(1), 54-61.
Publication
Researcher Affiliations
MeSH Terms
- Abortion, Veterinary / chemically induced
- Animals
- Aspartate Aminotransferases / blood
- Blood Urea Nitrogen
- Carbanilides / toxicity
- Creatine Kinase / blood
- Female
- Horse Diseases / blood
- Horse Diseases / chemically induced
- Horse Diseases / pathology
- Horses
- Imidocarb / toxicity
- Kidney / pathology
- L-Iditol 2-Dehydrogenase / blood
- Liver / pathology
- Male
- Pregnancy
Citations
This article has been cited 6 times.- Tuvshintulga B, Nugraha AB, Mizutani T, Liu M, Ishizaki T, Sivakumar T, Xuan X, Yokoyama N, Igarashi I. Development of a stable transgenic Theileria equi parasite expressing an enhanced green fluorescent protein/blasticidin S deaminase. Sci Rep 2021 Apr 27;11(1):9107.
- Sears K, Knowles D, Dinkel K, Mshelia PW, Onzere C, Silva M, Fry L. Imidocarb Dipropionate Lacks Efficacy against Theileria haneyi and Fails to Consistently Clear Theileria equi in Horses Co-Infected with T. haneyi. Pathogens 2020 Dec 10;9(12).
- Gimenez F, Hines SA, Evanoff R, Ojo KK, Van Voorhis WC, Maly DJ, Vidadala RSR, Mealey RH. In vitro growth inhibition of Theileria equi by bumped kinase inhibitors. Vet Parasitol 2018 Feb 15;251:90-94.
- Van Voorhis WC, Doggett JS, Parsons M, Hulverson MA, Choi R, Arnold SLM, Riggs MW, Hemphill A, Howe DK, Mealey RH, Lau AOT, Merritt EA, Maly DJ, Fan E, Ojo KK. Extended-spectrum antiprotozoal bumped kinase inhibitors: A review. Exp Parasitol 2017 Sep;180:71-83.
- Ueti MW, Mealey RH, Kappmeyer LS, White SN, Kumpula-McWhirter N, Pelzel AM, Grause JF, Bunn TO, Schwartz A, Traub-Dargatz JL, Hendrickson A, Espy B, Guthrie AJ, Fowler WK, Knowles DP. Re-emergence of the apicomplexan Theileria equi in the United States: elimination of persistent infection and transmission risk. PLoS One 2012;7(9):e44713.
- Schwint ON, Ueti MW, Palmer GH, Kappmeyer LS, Hines MT, Cordes RT, Knowles DP, Scoles GA. Imidocarb dipropionate clears persistent Babesia caballi infection with elimination of transmission potential. Antimicrob Agents Chemother 2009 Oct;53(10):4327-32.
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