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American journal of veterinary research2001; 62(9); 1387-1392; doi: 10.2460/ajvr.2001.62.1387

Pharmacokinetics and toxic effects of lithium chloride after intravenous adminstration in conscious horses.

Abstract: To determine the pharmacokinetics and toxic effects associated with IV administration of lithium chloride (LiCl) to conscious healthy horses. Methods: 6 healthy Standardbred horses. Methods: Twenty 3-mmol boluses of LiCl (0.15 mmol/L) were injected IV at 3-minute intervals (total dose, 60 mmol) during a 1-hour period. Blood samples for measurement of serum lithium concentrations were collected before injection and up to 24 hours after injection. Behavioral and systemic toxic effects of LiCl were also assessed. Results: Lithium elimination could best be described by a 3-compartment model for 5 of the 6 horses. Mean peak serum concentration was 0.561 mmol/L (range, 0.529 to 0.613 mmol/L), with actual measured mean serum value of 0.575 mmol/L (range, 0.52 to 0.67 mmol/L) at 2.5 minutes after administration of the last bolus. Half-life was 43.5 hours (range, 32 to 84 hours), and after 24 hours, mean serum lithium concentration was 0.13+/-0.05 mmol/L (range, 0.07 to 0.21 mmol/L). The 60-mmol dose of LiCl did not produce significant differences in any measured hematologic or biochemical variables, gastrointestinal motility, or ECG variables evaluated during the study period. Conclusions: Distribution of lithium best fit a 3-compartment model, and clearance of the electrolyte was slow. Healthy horses remained unaffected by LiCl at doses that exceeded those required for determination of cardiac output. Peak serum concentrations were less than steady-state serum concentrations that reportedly cause toxic effects in other species.
Publication Date: 2001-09-19 PubMed ID: 11560265DOI: 10.2460/ajvr.2001.62.1387Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research article discusses a study conducted on the effects of intravenous lithium chloride administration in conscious, healthy horses, especially its pharmacokinetics and potential toxicity.

Objective and Methodology

The main aim was to understand the pharmacokinetics – how the drug is absorbed, distributed, metabolized, and excreted in the body – and potential toxic effects of lithium chloride (LiCl) when administered intravenously in healthy horses. This involved:

  • Using a sample of six healthy Standardbred horses.
  • Administering twenty 3-mmol boluses of LiCl with a concentration of 0.15 mmol/liter at three-minute intervals, totaling 60 mmol over an hour.
  • Collecting blood samples pre-injection and up to 24 hours post-injection to measure serum lithium concentrations.
  • Evaluating behavioral and systemic toxic effects of LiCl.

Results

The study drew the following conclusions:

  • Lithium elimination best fit a tri-compartmental model in five of the six horses.
  • The mean peak serum concentration was 0.561 mmol/L, ranging between 0.529 to 0.613 mmol/L.
  • The mean serum lithium concentration was 0.575 mmol/L (ranging between 0.52 to 0.67 mmol/L) at 2.5 minutes after administering the last bolus.
  • The half-life of lithium was found to be approximately 43.5 hours, ranging between 32 to 84 hours.
  • 24 hours after administering the lithium, the mean serum lithium concentration was 0.13±0.05 mmol/L, with a range of 0.07 to 0.21 mmol/L.
  • Administering a 60-mmol dose of LiCl did not significantly impact any measured hematological or biochemical variables, gastrointestinal motility, or ECG variables across the study period.

Conclusion

Based on their findings, the researchers concluded that the distribution of lithium best fits a three-compartment model, and its clearance from the body is slow. Importantly, the healthy horses tolerated doses of LiCl that were higher than those required for determining cardiac output, with peak serum concentrations not reaching toxic levels as reported for other species. This suggests that LiCl could potentially be used safely in equine medical treatments, as long as the doses are controlled and monitored.

Cite This Article

APA
Hatfield CL, McDonell WN, Lemke KA, Black WD. (2001). Pharmacokinetics and toxic effects of lithium chloride after intravenous adminstration in conscious horses. Am J Vet Res, 62(9), 1387-1392. https://doi.org/10.2460/ajvr.2001.62.1387

Publication

ISSN: 0002-9645
NlmUniqueID: 0375011
Country: United States
Language: English
Volume: 62
Issue: 9
Pages: 1387-1392

Researcher Affiliations

Hatfield, C L
  • Department of Clinical Studies, Ontario Veterinary College, University of Guelph, Canada.
McDonell, W N
    Lemke, K A
      Black, W D

        MeSH Terms

        • Animals
        • Cardiac Output / drug effects
        • Electrocardiography / veterinary
        • Female
        • Gastrointestinal Motility / drug effects
        • Half-Life
        • Horses / metabolism
        • Injections, Intravenous / veterinary
        • Lithium Chloride / blood
        • Lithium Chloride / pharmacokinetics
        • Lithium Chloride / toxicity
        • Male

        Citations

        This article has been cited 3 times.
        1. Paranjape VV, Garcia-Pereira FL, Menciotti G, Saksena S, Henao-Guerrero N, Ricco-Pereira CH. Evaluation of Electrical Cardiometry for Measuring Cardiac Output and Derived Hemodynamic Variables in Comparison with Lithium Dilution in Anesthetized Dogs. Animals (Basel) 2023 Jul 20;13(14).
          doi: 10.3390/ani13142362pubmed: 37508139google scholar: lookup
        2. Wang L, Pawlak EA, Johnson PJ, Belknap JK, Eades S, Stack S, Cousin H, Black SJ. Impact of laminitis on the canonical Wnt signaling pathway in basal epithelial cells of the equine digital laminae. PLoS One 2013;8(2):e56025.
          doi: 10.1371/journal.pone.0056025pubmed: 23405249google scholar: lookup
        3. Pearse RM, Ikram K, Barry J. Equipment review: an appraisal of the LiDCO plus method of measuring cardiac output. Crit Care 2004 Jun;8(3):190-5.
          doi: 10.1186/cc2852pubmed: 15153237google scholar: lookup