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Updated: Aug 22, 2026

An In Vivo Duo-color Method for Imaging Vascular Dynamics Following Contusive Spinal Cord Injury
Published on: December 31, 2017
Arteriovenous glomeruli of the human spinal cord and their possible functional implications
1Robert E. Van Demark Institute of Anatomical Research, Division of Basic Medical Sciences, The University of South Dakota School of Medicine, Vermillion, South Dakota, USA. DrWParke@aol.com
Abstract:
A previous investigation of the radiculomedullary vascular distribution of the human spinal cord showed an immediate filling of the peripheral spinal veins during arterial injections. Because the perfused medium, a mixture of latex and India ink, had a sufficient viscosity to preclude capillary passage, an extensive system of arteriovenous anastomoses (AVA) was indicated. The injection of five additional anatomic cadaver spinal cords was undertaken to specifically determine the intraparenchymal position and structure of these AVA. It was found that only cleared and transilluminated longitudinal parasagittal sections adequately showed that the AVA were formed by an extensive array of intricately coiled arteriovenous glomeruli (AVG) that could pass substantial amounts of blood from third order arterial branches to equivalently sized veins, bypassing the capillary bed. The epithelioid structure of these AVG channel walls, coupled with their highly innervated adventitial tissue indicated a possible functional relationship to similar structures found in the ends (digital pads) of mammalian extremities. Stained serial sections of injected cords showed the vascular relations with nerve fibers derived from the intraspinal parenchyma as well as a possible extraparenchymal autonomic fiber source. The numbers and extent of these AVG complexes suggested they might be involved in the remarkable autoregulation of spinal cord blood flow (SCBF) that is impervious to middle range changes in systemic blood pressure. Future research may more accurately determine the functional role of these previously unreported human spinal AVG, particularly in their possible relation to SCBF autoregulation in normal and injured spines.
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