Comparative Analysis of Gastrointestinal and Bone Inflammation in Hindlimb Unloading Conference Paper uri icon

abstract

  • The hindlimb unloading (HU) rodent model is used to mimic changes incurred in spaceflight due to microgravity. Previously in 2weeks of rat HU, we found systemically impaired lymphatic transport. Recently we reported gastrointestinal (GI) inflammation and lymphatic immune cell alterations after 4weeks of HU in rats paralleling the GI pathology observed in inflammatory bowel disease (IBD) animal models. A known comorbidity of IBD is inflammationinduced bone loss; prior work in our lab with a 4week IBD rodent model documented bone loss as well as an increased prevalence of cancellous osteocytes positive for tumor necrosis factor (TNF), interleukin6 (IL6), and insulinlike growth factorI (IGFI) concurrent with GI inflammation. The implications of a potential inflammatory link between gut and bone in HU and spaceflight have not been reported. In this study we quantified TNF, IL6, and IGFI (via immunohistochemistry) in both bone and colon samples after 4weeks of HU in male Sprague Dawley rats (comparing HU and agematched controls). Proximal tibia cancellous bone volume, osteoid surface area, bone formation rate, and trabecular number were lower in HU versus controls, while osteoclast surface area and trabecular separation were higher. Measures of osteocytes in cancellous bone positive for IL6 and IGFI levels were lowered, but there was no change in TNF. Colon histopathology showed elevated structural damage in the mucosa region with a corresponding cellularity elevation in HU compared to controls. HU colons also had elevated TNF and IL6 expression across the mucosal and submucosal regions with IGFI a trending increase. Furthermore cytokine changes were dependent on the colon compartment. Fecal calprotectin (a clinical IBD marker of GI inflammation) was collected throughout the 4week time course; calprotectin was significantly increased at 2weeks of HU and trended towards elevation at 4weeks. After HU we did not find the same cytokine pattern in bone compared to what we have seen in an IBD model induced by the haptenizing agent TNBS, suggesting different inflammatory mechanisms. However there may be a time course impact of IBD development in the models.Support or Funding InformationStudy support received from NASA Grants: NNX15AG54G, NNX13AN33G, NNX13AQ87G. AN, JB, and SL were supported by the NASANSBRI Predoctoral Fellowship.

published proceedings

  • FASEB JOURNAL

author list (cited authors)

  • Narayanan, A., Metzger, C., Brezicha, J., Lenfest, S., Bloomfield, S., Hogan, H., & Zawieja, D.

citation count

  • 0

complete list of authors

  • Narayanan, Anand||Metzger, Corinne||Brezicha, Jessica||Lenfest, Scott||Bloomfield, Susan||Hogan, Harry||Zawieja, David

publication date

  • April 2016

publisher