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Safety of an oral chondroprotective agent in horses.

Abstract: Six healthy, adult female horses were administered five times the minimum maintenance dose of an oral low-molecular-weight chondroitin sulfate, glucosamine HCl, and manganese ascorbate chondroprotective agent (Cosequin; Nutramax Laboratories, Inc., Edgewood, MD) daily for 35 days. Hematology, serum biochemistry, and synovial fluid parameters were assessed twice prior to administering the product and again at the end of the treatment period. Physical examinations performed daily throughout the study showed no abnormal clinical changes attributable to the product. All hematologic parameters measured were within normal reference ranges; however, hematocrit, hemoglobin, and white blood cell counts were significantly (P < .05) increased after treatment, as compared with values on Day 0. Mean serum urea nitrogen was mildly elevated above the reference range before and after treatments, and mean serum creatinine was significantly (P < .05) decreased after treatment. Several other biochemical parameters (calcium, phosphorus, potassium, total and indirect bilirubin, alkaline phosphatase, gamma-glutamyltransferase, lactic dehydrogenase, and sodium:potassium ratio) were significantly (P < .05) altered following administration of the chondroprotectant, but all remained within normal reference ranges. Mean creatine kinase levels were significantly higher after treatment than on Day 0 (429 U/L versus 310 U/L), but this represented only a mild elevation relative to the reference range (10 to 350 U/L). Synovial fluid total protein and specific gravity were unaffected. The minor shifts encountered in hematology and serum biochemistry parameters are not considered to have clinical significance. The results of this study suggest that the oral chondroprotective agent tested is safe for administration to horses at recommended dose rates.
Publication Date: 2001-10-01 PubMed ID: 19746657
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  • Clinical Trial
  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research article presents a study on the safety of an oral chondroprotective agent (an agent that supports joint health) in horses. The study found that the agent could be safely administered to horses as recommended, with no significant clinical effects observed.

Study Design and Procedure

  • The study involved six adult female horses, whom were given an oral chondroprotective agent containing low-molecular-weight chondroitin sulfate, glucosamine HCl, and manganese ascorbate at five times the minimum maintenance dose for 35 days.
  • The researchers conducted hematology, serum biochemistry, and synovial fluid parameters tests on the horses twice before administering the product and once again after the treatment period.
  • Apart from these tests, the horses also underwent daily physical examinations throughout the study to monitor for any abnormal clinical changes.

Results and Findings

  • There were no abnormal changes visible in the daily physical exams of the horses that could be linked to the product.
  • While the hematological parameters remained within the normal reference range, there was a significant increase in hematocrit, hemoglobin, and white blood cell counts when compared to the values on Day 0, which is considered non-negative.
  • Several biochemical parameters were also significantly altered after the administration of the chondroprotectant, but they all stayed within the normal reference ranges. This includes parameters like calcium, phosphorus, potassium, bilirubin, and some enzymes.
  • The level of creatine kinase, an enzyme found in muscles, was significantly higher after the treatment.
  • Synovial fluid total protein and specific gravity were not affected.
  • The researchers deemed that the minor shifts in hematology and serum biochemistry parameters were not of any clinical significance.

Conclusions

  • The results suggest that the oral chondroprotective agent tested is safe for administration to horses at the recommended dosage rates. It did not result in significant adverse effects on the horses’ health as per the clinical examination and laboratory results.

Cite This Article

APA
Kirker-Head CA, Kirker-Head RP. (2001). Safety of an oral chondroprotective agent in horses. Vet Ther, 2(4), 345-353.

Publication

ISSN: 1528-3593
NlmUniqueID: 100936368
Country: United States
Language: English
Volume: 2
Issue: 4
Pages: 345-353

Researcher Affiliations

Kirker-Head, C A
  • Tufts University, School of Veterinary Medicine, Department of Clinical Sciences, 200 Westborough Road, North Grafton, MA 01536, USA.
Kirker-Head, R P

    MeSH Terms

    • Administration, Oral
    • Animals
    • Chondroitin Sulfates / administration & dosage
    • Chondroitin Sulfates / adverse effects
    • Chondroitin Sulfates / pharmacology
    • Dose-Response Relationship, Drug
    • Drug Combinations
    • Female
    • Glucosamine / administration & dosage
    • Glucosamine / adverse effects
    • Glucosamine / pharmacology
    • Horses
    • Manganese / administration & dosage
    • Manganese / adverse effects
    • Manganese / pharmacology

    Citations

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