Abstract
Myodural bridges have been described in various species as connective tissue structures “bridging” small cranio-cervical muscles to the dura. Myodural bridges are thought to stabilize the dural sac during head and neck movements and promote cerebrospinal fluid motion; however, their role in neurological diseases has not yet been established. We report ultrasonographic visualization, necropsy, histopathologic and ultrastructural findings of myodural bridges in horses with hereditary equine regional dermal asthenia (HERDA), an equine model of Ehlers-Danlos syndromes. Five HERDA and 5 control horses were studied. Post-mortem examination and ultrasonographic studies (3 HERDA and 4 controls) demonstrated that the atlanto-occipital and atlanto-axial myodural bridges are dynamic structures “moving” the dura. En block resection of the myodural bridges (4 HERDA and 5 controls) was accomplished and histopathology showed myofiber degeneration in 3 HERDA horses and 1 control. Ultrastructural examination revealed loosely packed collagen fibrils with abnormal orientation in all HERDA horses compared to mild abnormalities in 2 controls. Our study provides necropsy and ultrasonographic evidence of the dynamic aspect of the myodural bridges as dural sac stabilizers. Myodural bridges may be pathologically altered in connective tissue disease as evidenced by the ultrastructural morphology in the HERDA myodural bridge.
Highlights
Our main objective was to further describe MDBs in horses, and to demonstrate that they are abnormal in horses with connective tissue disease
Abnormalities were noted in 1 hereditary equine regional dermal asthenia (HERDA) horse, a 21-year-old Quarter Horse mare, that displayed mild truncal sway and a base-narrow, single-track gait in the hind limbs when blindfolded with the head elevated
It is conceivable that the function of the MDBs is impaired in HERDA horses, and we speculate in EDS patients as well
Summary
Our main objective was to further describe MDBs in horses, and to demonstrate that they are abnormal in horses with connective tissue disease. Hereditary equine regional dermal asthenia is an autosomal recessive disorder that occurs in Quarter Horses and is caused by a mutation in peptidyl-prolyl cis-trans isomerase B (PPIB) encoding for cyclophilin B www.nature.com/scientificreports/
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