Literature DB >> 25714471

The Equine Movement Disorder "Shivers" Is Associated With Selective Cerebellar Purkinje Cell Axonal Degeneration.

S J Valberg1, S S Lewis2, J L Shivers3, N E Barnes2, J Konczak4, A C E Draper2, A G Armién5.   

Abstract

"Shivers" is a progressive equine movement disorder of unknown etiology. Clinically, horses with shivers show difficulty walking backward, assume hyperflexed limb postures, and have hind limb tremors during backward movement that resembles shivering. At least initially, forward movements are normal. Given that neither the neurophysiologic nor the pathologic mechanisms of the disease is known, nor has a neuroanatomic locus been identified, we undertook a detailed neuroanatomic and neuropathologic analysis of the complete sensorimotor system in horses with shivers and clinically normal control horses. No abnormalities were identified in the examined hind limb and forelimb skeletal muscles nor the associated peripheral nerves. Eosinophilic segmented axonal spheroids were a common lesion. Calretinin-positive axonal spheroids were present in many regions of the central nervous system, particularly the nucleus cuneatus lateralis; however, their numbers did not differ significantly from those of control horses. When compared to controls, calretinin-negative, calbindin-positive, and glutamic acid decarboxylase-positive spheroids were increased 80-fold in Purkinje cell axons within the deep cerebellar nuclei of horses with shivers. Unusual lamellar or membranous structures resembling marked myelin decompaction were present between myelin sheaths of presumed Purkinje cell axons in the deep cerebellar nuclei of shivers but not control horses. The immunohistochemical and ultrastructural characteristics of the lesions combined with their functional neuroanatomic distribution indicate, for the first time, that shivers is characterized by end-terminal neuroaxonal degeneration in the deep cerebellar nuclei, which results in context-specific hypermetria and myoclonus.
© The Author(s) 2015.

Entities:  

Keywords:  Purkinje cell; axonal degeneration; cerebellum; horse; myelin decompaction; myoclonus; shivering

Mesh:

Substances:

Year:  2015        PMID: 25714471     DOI: 10.1177/0300985815571668

Source DB:  PubMed          Journal:  Vet Pathol        ISSN: 0300-9858            Impact factor:   2.221


  4 in total

1.  Cerebellar hypoplasia and dysplasia in a juvenile raccoon with parvoviral infection.

Authors:  Arno Wünschmann; Robert Lopez-Astacio; Anibal G Armien; Colin R Parrish
Journal:  J Vet Diagn Invest       Date:  2020-05       Impact factor: 1.279

Review 2.  Dystonia and Paroxysmal Dyskinesias: Under-Recognized Movement Disorders in Domestic Animals? A Comparison with Human Dystonia/Paroxysmal Dyskinesias.

Authors:  Angelika Richter; Melanie Hamann; Jörg Wissel; Holger A Volk
Journal:  Front Vet Sci       Date:  2015-11-30

3.  A method to identify, dissect and stain equine neuromuscular junctions for morphological analysis.

Authors:  Stephen D Cahalan; Justin D Perkins; Ines Boehm; Ross A Jones; Thomas H Gillingwater; Richard J Piercy
Journal:  J Anat       Date:  2022-09-10       Impact factor: 2.921

4.  Commercial genetic testing for type 2 polysaccharide storage myopathy and myofibrillar myopathy does not correspond to a histopathological diagnosis.

Authors:  Stephanie J Valberg; Carrie J Finno; Marisa L Henry; Melissa Schott; Deborah Velez-Irizarry; Sichong Peng; Erica C McKenzie; Jessica L Petersen
Journal:  Equine Vet J       Date:  2020-10-29       Impact factor: 2.888

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.