| Literature DB >> 29104343 |
Devante Horne1,2, Peter Jones2, Vasant Salgaonkar2, Matt Adams2,3, B Arda Ozilgen1,2, Peter Zahos2, Xinyan Tang3, Ellen Liebenburg3, Dezba Coughlin3, Jeffrey Lotz2,3, Chris Diederich1,2.
Abstract
Discogenic back pain presents a major public health issue, with current therapeutic interventions limited to short-term symptom relief without providing regenerative remedies for diseased intervertebral discs (IVD). Many of these interventions are invasive and can diminish the biomechanical integrity of the IVDs. Low intensity pulsed ultrasound (LIPUS) is a potential treatment option that is both non-invasive and regenerative. LIPUS has been shown to be a clinically effective method for the enhancement of wound and fracture healing. Recent in vitro studies have shown that LIPUS stimulation induces an upregulation functional matrix proteins and downregulation of inflammatory factors in cultured IVD cells. However, we do not know the effects of LIPUS on an in vivo model for intervertebral disc degeneration. The objective of this study was to show technical feasibility of building a LIPUS system that can target the rat tail IVD and apply this setup to a model for acute IVD degeneration. A LIPUS exposimetry system was built using a 1.0 MHz planar transducer and custom housing. Ex vivo intensity measurements demonstrated LIPUS delivery to the center of the rat tail IVD. Using an established stab-incision model for disc degeneration, LIPUS was applied for 20 minutes daily for five days. For rats that displayed a significant injury response, LIPUS treatment caused significant upregulation of Collagen II and downregulation of Tumor Necrosis Factor - α gene expression. Our preliminary studies indicate technical feasibility of targeted delivery of ultrasound to a rat tail IVD for studies of LIPUS biological effects.Entities:
Keywords: Aggrecan; Collagen; Interleukin; Low intensity pulsed ultrasound; TNF; disc degeneration; intervertebral disc; rat tail
Year: 2017 PMID: 29104343 PMCID: PMC5667559 DOI: 10.1117/12.2255761
Source DB: PubMed Journal: Proc SPIE Int Soc Opt Eng ISSN: 0277-786X