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The veterinary quarterly2012; 32(2); 99-102; doi: 10.1080/01652176.2012.714089

Familial narcolepsy in the Lipizzaner horse: a report of three fillies born to the same sire.

Abstract: The occurrence of sleep disorder in three half sibling Lipizzaner is described. Sleepiness, swaying, stumbling, carpal joints buckling and falling down onto the carpal joints had been present since early foal age in all of them. Clinical signs had gradually reduced since the age of 2 years in cases 1 and 3. Sleepiness was induced by going out from the stable in adulthood. A physostigmine test was performed in all three affected horses and produced positive results in cases 1 and 3. The result of the test in case 2 was unclear due to the almost continuous sleepiness of the foal. Hypocretin-1 concentration in the cerebrospinal fluid was established using a standardised radioimmunoassay in case 1 (317.85 pg/mL), case 2 (303.43 pg/mL) and five adult control horses (275.2 ± 47.9 [SD] pg/mL) and was considered as normal in all horses. The sire of the affected horses has had 19 other registered offspring who did not show clinical signs of sleep disorder and also dams of all three cases produced healthy foals. Based on the demographic and clinical data together with the responses to the physostigmine challenges, the diagnosis of familial equine narcolepsy was made.
Publication Date: 2012-08-14 PubMed ID: 22889297DOI: 10.1080/01652176.2012.714089Google Scholar: Lookup
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Summary

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This study examines three Lipizzaner horses that displayed signs of narcolepsy, a sleep disorder typically characterized by excessive daytime sleepiness, hallucinations, and in some cases, sudden losses of muscle strength. Despite familial ties and showing symptoms since an early age, the horses’ conditions seemed to improve over time and their cerebrospinal fluid appeared normal.

Study Overview

  • The researchers observed three half-sibling Lipizzaner horses that exhibited symptoms of narcolepsy.
  • Signs such as excessive sleepiness, swaying, stumbling, and bouts of unsteadiness displayed by these horses were present early in their lives.
  • The clinical symptoms have lessened over time for two out of the three affected horses, otherwise, symptoms increase upon exiting their stables.

Testing and Evaluation

  • A physostigmine test, which is used to diagnose disorders causing muscle weakness, was performed on all three horses.
  • Two of the horses returned positive results, confirming the presence of a muscle-related disorder, possibly narcolepsy.
  • The third horse’s results were not clear due to its continual sleepiness.

Cerebrospinal Fluid Test

  • The level of Hypocretin-1, a neurotransmitter linked to narcolepsy, in the cerebrospinal fluid of the horses was measured.
  • These levels were found to be normal in all three horses.

Familial History

  • The sire, or father, of these three affected horses has had 19 other offspring that did not display any clinical signs of sleep disorders.
  • The dams, or mothers, of these three horses also gave birth to healthy foals indicating that the disorder may not be a result of genetic inheritance.

Conclusion

  • Based on the physostigmine test results, the horses’ symptoms, and the lacking presence of sleep disorders in their extended family, the researchers concluded that the three Lipizzaner horses are most likely affected by a familial form of equine narcolepsy.

Cite This Article

APA
Ludvikova E, Nishino S, Sakai N, Jahn P. (2012). Familial narcolepsy in the Lipizzaner horse: a report of three fillies born to the same sire. Vet Q, 32(2), 99-102. https://doi.org/10.1080/01652176.2012.714089

Publication

ISSN: 1875-5941
NlmUniqueID: 7909485
Country: England
Language: English
Volume: 32
Issue: 2
Pages: 99-102

Researcher Affiliations

Ludvikova, Eva
  • Equine Clinic, University of Veterinary and Pharmaceutical Sciences Brno, Palackeho 1-3, Brno 61242, Czech Republic. eludvikova@vfu.cz
Nishino, Seiji
    Sakai, Noriaki
      Jahn, Petr

        MeSH Terms

        • Animals
        • Female
        • Horse Diseases / diagnosis
        • Horse Diseases / genetics
        • Horses
        • Intracellular Signaling Peptides and Proteins / cerebrospinal fluid
        • Narcolepsy / diagnosis
        • Narcolepsy / genetics
        • Narcolepsy / veterinary
        • Neuropeptides / cerebrospinal fluid
        • Orexins
        • Physostigmine

        Citations

        This article has been cited 3 times.
        1. Almeneessier AS, Alballa NS, Alsalman BH, Aleissi S, Olaish AH, BaHammam AS. A 10-Year Longitudinal Observational Study Of Cataplexy In A Cohort Of Narcolepsy Type 1 Patients. Nat Sci Sleep 2019;11:231-239.
          doi: 10.2147/NSS.S229105pubmed: 31695532google scholar: lookup
        2. Black SW, Yamanaka A, Kilduff TS. Challenges in the development of therapeutics for narcolepsy. Prog Neurobiol 2017 May;152:89-113.
        3. Pizza F, Franceschini C, Peltola H, Vandi S, Finotti E, Ingravallo F, Nobili L, Bruni O, Lin L, Edwards MJ, Partinen M, Dauvilliers Y, Mignot E, Bhatia KP, Plazzi G. Clinical and polysomnographic course of childhood narcolepsy with cataplexy. Brain 2013 Dec;136(Pt 12):3787-95.
          doi: 10.1093/brain/awt277pubmed: 24142146google scholar: lookup