Finite element models (FEMs) and analytical and experimental models based on poroelastic constitutive laws were developed for rhesus spinal motion segments (SMSs). Long-time creep, transient creep, and impact were studied for SMSs with normal and simulated degenerated discs. The results suggested that long-time creep observed in excised SMSs may be reduced in the in vivo SMS. The fluid phase included in these FEMs was shown to play a significant role in the mechanical response of SMSs. Relative fluid motion fields predicted in the SMS could be related to nutritional paths to the avascular interior of the disc and were found to be very sensitive to changes in discal stiffness. Reduced disc height, increased discal bulge, altered fluid motion, and stresses were quantified and may be related to mechanical failure, disc degeneration, and low-back pain.
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http://dx.doi.org/10.1097/00007632-198507000-00003 | DOI Listing |
Proc Natl Acad Sci U S A
January 2025
State Key Laboratory of Molecular Developmental Biology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100080, China.
Various mature tissue-resident cells exhibit progenitor characteristics following injury. However, the existence of endogenous stem cells with multiple lineage potentials in the adult spinal cord remains a compelling area of research. In this study, we present a cross-species investigation that extends from development to injury.
View Article and Find Full Text PDFSci Adv
December 2024
Department of Developmental Physiology, National Institute for Physiological Sciences, National Institute of Natural Sciences, Okazaki, Aichi 4448585, Japan.
Mammals can execute intended limb movements despite the fact that spinal reflexes involuntarily modulate muscle activity. To generate appropriate muscle activity, the cortical descending motor output must coordinate with spinal reflexes, yet the underlying neural mechanism remains unclear. We simultaneously recorded activities in motor-related cortical areas, afferent neurons, and forelimb muscles of monkeys performing reaching movements.
View Article and Find Full Text PDFJ Comp Neurol
December 2024
Department of Neuroscience, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Cell Rep
November 2024
Department of Neurobiology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA; Pittsburgh Center for Pain Research, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA; Department of Otolaryngology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA. Electronic address:
Key mechanisms underlying chronic pain occur within the dorsal horn. Genome-wide association studies (GWASs) have identified genetic variants predisposed to chronic pain. However, most of these variants lie within regulatory non-coding regions that have not been linked to spinal cord biology.
View Article and Find Full Text PDFNat Commun
October 2024
Rehab Neural Engineering Labs, University of Pittsburgh, Pittsburgh, PA, USA.
Cerebral white matter lesions prevent cortico-spinal descending inputs from effectively activating spinal motoneurons, leading to loss of motor control. However, in most cases, the damage to cortico-spinal axons is incomplete offering a potential target for therapies aimed at improving volitional muscle activation. Here we hypothesize that, by engaging direct excitatory connections to cortico-spinal motoneurons, stimulation of the motor thalamus could facilitate activation of surviving cortico-spinal fibers thereby immediately potentiating motor output.
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