Literature DB >> 8887784

Glycosaminoglycan concentration in synovium and other tissues of rabbit knee in relation to synovial hydraulic resistance.

F M Price1, J R Levick, R M Mason.   

Abstract

1. The hydraulic resistance of the synovial lining of a joint, a key coupling coefficient in synovial fluid turnover, is thought to depend on the concentration of biopolymers (glycosaminoglycans (GAGs) and collagen) in the synovial intercellular spaces, because these polymers create hydraulic drag. The primary aim of this study was to obtain microscopically separated, milligram samples of the very thin synovium from eight rabbit knees, and to analyse these quantitatively for GAGs (chondroitin sulphate, heparan sulphate and hyaluronan) and collagen to allow comparison with published hydraulic resistance data. Synovial fluid and femoral cartilage were also studied. 2. Synovium comprised 73 +/- 3% water by weight (mean +/- S.E.M.). Of the 270 mg solid per gram of wet tissue, protein formed 136 mg (by automated amino acid analysis), and of this 94 mg was collagen by hydroxyproline analysis. From the collagen mass and fibril volume fraction (0.153 of tissue by morphometry), fibrillar specific volume was calculated to be 1.43 ml per gram of molecular collagen, and fibril water content 47% by volume. 3. The concentration of chondroitin 4-sulphate (C4S) plus chondroitin 6-sulphate (C6S), measured by capillary zone electrophoresis was 0.55 mg per gram of synovium--much greater than in synovial fluid (0.04 mg g-1) and much less than in cartilage (27.8 mg g-1). The C4S/C6S ratio in synovium (7.3) differed from that in cartilage (0.7), indicating that different proteoglycans predominated in synovium. The heparan sulphate concentration, assayed by radioactive Ruthenium Red binding, was 0.92 mg per gram of synovium (synovial fluid, 0.08 mg g-1; cartilage, 0.72 mg g-1). 4. In contrast to sulphated GAGs, the hyaluronan concentration was highest in synovial fluid (3.53 mg g-1; biotinylated G1 domain binding assay). The concentration in synovial interstitium was only 0.56 mg g-1 (corrected for interstitial volume fraction, 0.66), even though there is open contact between synovial interstitium and synovial fluid. This may be due to exclusion or washout. 5. Total GAG mass was approximately 4 mg per gram of synovial interstitium. A model of trans-synovial flow indicated that a uniform GAG concentration of 4 mg g-1 is less than 1/3rd of that required to explain the experimental estimate of synovial hydraulic resistance. Errors in the resistance estimate do not appear to be large enough to resolve the problem. It is possible, therefore, that additional polymeric material in the interstitium, such as glycoproteins and proteoglycan core protein, may contribute to the hydraulic resistance.

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Year:  1996        PMID: 8887784      PMCID: PMC1160783          DOI: 10.1113/jphysiol.1996.sp021634

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  40 in total

1.  A two-dimensional morphometry-based model of interstitial and transcapillary flow in rabbit synovium.

Authors:  J R Levick
Journal:  Exp Physiol       Date:  1991-11       Impact factor: 2.969

2.  Type III collagen: A major constituent of rheumatoid and normal human synovial membrane.

Authors:  D R Eyre; H Muir
Journal:  Connect Tissue Res       Date:  1975       Impact factor: 3.417

3.  Synovial fluid--its mass, macromolecular content and pressure in major limb joints of the rabbit.

Authors:  P Knox; J R Levick; J N McDonald
Journal:  Q J Exp Physiol       Date:  1988-01

4.  Type IV collagen and laminin in the synovial intimal layer: an immunohistochemical study.

Authors:  L E Pollock; P Lalor; P A Revell
Journal:  Rheumatol Int       Date:  1990       Impact factor: 2.631

5.  Microfibrillar meshwork of the synovial lining and associated broad banded collagen: a clue to identity.

Authors:  J R Levick; J N McDonald
Journal:  Ann Rheum Dis       Date:  1990-01       Impact factor: 19.103

6.  The connective tissue response to immobility: biochemical changes in periarticular connective tissue of the immobilized rabbit knee.

Authors:  W H Akeson; S L Woo; D Amiel; R D Coutts; D Daniel
Journal:  Clin Orthop Relat Res       Date:  1973-06       Impact factor: 4.176

Review 7.  Interstitial-lymphatic mechanisms in the control of extracellular fluid volume.

Authors:  K Aukland; R K Reed
Journal:  Physiol Rev       Date:  1993-01       Impact factor: 37.312

8.  Modulation of proteoglycan synthesis by bovine vascular smooth muscle cells during cellular proliferation and treatment with heparin.

Authors:  S P Williams; R M Mason
Journal:  Arch Biochem Biophys       Date:  1991-06       Impact factor: 4.013

9.  An immunohistochemical study of the collagens of rabbit synovial interstitium.

Authors:  D E Ashhurst; Y S Bland; J R Levick
Journal:  J Rheumatol       Date:  1991-11       Impact factor: 4.666

10.  Fluorometric determination of DNA in cartilage of various species.

Authors:  T R Oegema; B J Carpenter; R C Thompson
Journal:  J Orthop Res       Date:  1984       Impact factor: 3.494

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  21 in total

1.  Size selectivity of hyaluronan molecular sieving by extracellular matrix in rabbit synovial joints.

Authors:  S Sabaratnam; V Arunan; P J Coleman; R M Mason; J R Levick
Journal:  J Physiol       Date:  2005-06-16       Impact factor: 5.182

2.  Cyclic movement stimulates hyaluronan secretion into the synovial cavity of rabbit joints.

Authors:  K R Ingram; A K T Wann; C K Angel; P J Coleman; J R Levick
Journal:  J Physiol       Date:  2008-01-17       Impact factor: 5.182

3.  Characterization of the effect of high molecular weight hyaluronan on trans-synovial flow in rabbit knees.

Authors:  P J Coleman; D Scott; R M Mason; J R Levick
Journal:  J Physiol       Date:  1999-01-01       Impact factor: 5.182

4.  Fluid movement and joint capsule strains due to flexion in rabbit knees.

Authors:  William J McCarty; Koichi Masuda; Robert L Sah
Journal:  J Biomech       Date:  2011-09-25       Impact factor: 2.712

5.  Effect of depletion of interstitial hyaluronan on hydraulic conductance in rabbit knee synovium.

Authors:  P J Coleman; D Scott; A Abiona; D E Ashhurst; R M Mason; J R Levick
Journal:  J Physiol       Date:  1998-06-15       Impact factor: 5.182

6.  Hyaluronan secretion into the synovial cavity of rabbit knees and comparison with albumin turnover.

Authors:  P J Coleman; D Scott; J Ray; R M Mason; J R Levick
Journal:  J Physiol       Date:  1997-09-15       Impact factor: 5.182

7.  Changes in glycosaminoglycan concentration and synovial permeability at raised intra-articular pressure in rabbit knees.

Authors:  F M Price; J R Levick; R M Mason
Journal:  J Physiol       Date:  1996-09-15       Impact factor: 5.182

8.  Filtration rate dependence of hyaluronan reflection by joint-to-lymph barrier: evidence for concentration polarisation.

Authors:  S Sabaratnam; R M Mason; J R Levick
Journal:  J Physiol       Date:  2004-04-08       Impact factor: 5.182

9.  Effect of depletion of glycosaminoglycans and non-collagenous proteins on interstitial hydraulic permeability in rabbit synovium.

Authors:  D Scott; P J Coleman; A Abiona; D E Ashhurst; R M Mason; J R Levick
Journal:  J Physiol       Date:  1998-09-01       Impact factor: 5.182

10.  Ionic currents in intimal cultured synoviocytes from the rabbit.

Authors:  R J Large; M A Hollywood; G P Sergeant; K D Thornbury; S Bourke; J R Levick; N G McHale
Journal:  Am J Physiol Cell Physiol       Date:  2010-08-18       Impact factor: 4.249

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