The use of hyperosmotic saline for chondroprotection: implications for orthopaedic surgery and cartilage repair  N.M. Eltawil, S.E.M. Howie, A.H.R.W.

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The use of hyperosmotic saline for chondroprotection: implications for orthopaedic surgery and cartilage repair  N.M. Eltawil, S.E.M. Howie, A.H.R.W. Simpson, A.K. Amin, A.C. Hall  Osteoarthritis and Cartilage  Volume 23, Issue 3, Pages 469-477 (March 2015) DOI: 10.1016/j.joca.2014.12.004 Copyright © 2014 Osteoarthritis Research Society International Terms and Conditions

Fig. 1 Articular cartilage injury model in the rat knee joint. (A) H&E (left) toluidine blue (middle) and CMFDA with PI (right) staining of sham (lower panel) and injured (upper panel) rat articular cartilage. Arrows indicate the injury site. (B and C) Measurements of cartilage thickness, depth, width of the defect (B) and the percentage of injury depth to cartilage thickness under different irrigation strategies (C). Data are expressed as mean ± 95% CI; N = 10. Cartilage injury was induced by a single pass of a number 11 scalpel blade (see text for details) in the absence of irrigation solution (no irrigation; NI) or in the presence of normal saline (NS, 300 mOsm) or hyperosmolar saline (HS, 600 mOsm). Scale bar in (A) = 50 μm. Osteoarthritis and Cartilage 2015 23, 469-477DOI: (10.1016/j.joca.2014.12.004) Copyright © 2014 Osteoarthritis Research Society International Terms and Conditions

Fig. 2 In situ chondrocyte death after scalpel-induced injury. (A) A ROI was created in the axial CLSM image and live cells (marked in purple) and dead cells (marked in yellow) were identified and counted based on voxel intensity. (B) Axial CLSM projections of CMFDA and PI labelled injured chondrocytes within articular cartilage that was exposed to no irrigation (NI), normal saline (NS) or hyperosmolar saline (HS) at the indicated time points. (C and D) The PCD at day 0 (C) and at later time points (D) in injured and sham-operated joints exposed to different irrigation conditions. Data are expressed as mean ± 95% CI. P values are given in text. Scale bar in (B) = 100 μm. Osteoarthritis and Cartilage 2015 23, 469-477DOI: (10.1016/j.joca.2014.12.004) Copyright © 2014 Osteoarthritis Research Society International Terms and Conditions

Fig. 3 Histological assessment of the changes to articular cartilage following scalpel-induced injury. (A) H&E (left) and toluidine blue (right) staining of sections from injured and sham-operated rat knee joints at the indicated time points. Arrows indicate areas of hypo-cellularity. (B) Polarized light microscopy of sections from sham and injured joints 8 weeks after injury. Arrows identify the site of injury and asterisks indicate the area of poor collagen organization. (C) Wakitani repair score at the 8 week time point. Significantly improved repair score was observed in non-irrigated joints (NI) and joints irrigated with hyperosmolar saline (HS) as compared to joints irrigated with normal saline (NS). Data are expressed as mean ± 95% CI; N = 5, P values are given in text. Scale bar in (A) and (B) = 50 μm. Osteoarthritis and Cartilage 2015 23, 469-477DOI: (10.1016/j.joca.2014.12.004) Copyright © 2014 Osteoarthritis Research Society International Terms and Conditions

Fig. 4 Collagen and aggrecan immunoreactivity. Immunostaining for type II collagen (A) and aggrecan (B) in sham and injured articular cartilage 8 weeks after surgery. Injured articular cartilage was exposed to no irrigation (NI), normal saline (NS) or hyperosmolar saline (HS) before and after injury. Arrows identify the site of injury and asterisks indicate the area of reduced staining. (C and D) The area of reduced type II collagen (C) and aggrecan (D) in injured cartilage at 8 week time point. Data are expressed as mean ± 95% CI. P values are given in text. Scale bar in (A) and (B) = 50 μm. Osteoarthritis and Cartilage 2015 23, 469-477DOI: (10.1016/j.joca.2014.12.004) Copyright © 2014 Osteoarthritis Research Society International Terms and Conditions

Fig. 5 Quantitative measurements of the width of the injury in the axial view. (A) CLSM projections of CMFDA and PI labelled injured articular cartilage that was exposed to no irrigation (NI), normal saline (NS) or hyperosmolar saline (HS) at Day 0 and 8 weeks after injury. (B) The width of the defect at day 0 and week 8. Data are expressed as mean ± 95% CI. P values are given in text. Scale bar in (A) = 50 μm. Osteoarthritis and Cartilage 2015 23, 469-477DOI: (10.1016/j.joca.2014.12.004) Copyright © 2014 Osteoarthritis Research Society International Terms and Conditions

Fig. 6 Assessment of the inflammatory response following different irrigation conditions. (A) Representative H&E stained histological sections of the synovial membrane from injured knee joints exposed to no irrigation (NI), normal saline (NS) or hyperosmolar saline (HS) at 1 day, 1 week and 8 weeks after surgery. (B) Synovitis score in different irrigation conditions at 1 day, 1, 2 and 8 weeks post-surgery. (C) Cytokine array of serum samples obtained from control un-operated and experimental rats 1 day after injury. (D) IL-1α ELISA of serum samples from control and experimental rats at 1 day, 1, 2 and 8 weeks following cartilage injury. Data are expressed as mean ± 95% CI. N = 5. Scale bar in (A) = 200 μm. Osteoarthritis and Cartilage 2015 23, 469-477DOI: (10.1016/j.joca.2014.12.004) Copyright © 2014 Osteoarthritis Research Society International Terms and Conditions