scholarly journals Cartilage Interstitial Fluid Load Support in Unconfined Compression Following Enzymatic Digestion

2004 ◽  
Vol 126 (6) ◽  
pp. 779-786 ◽  
Author(s):  
Ines M. Basalo ◽  
Robert L. Mauck ◽  
Terri-Ann N. Kelly ◽  
Steven B. Nicoll ◽  
Faye H. Chen ◽  
...  

Interstitial fluid pressurization plays an important role in cartilage biomechanics and is believed to be a primary mechanism of load support in synovial joints. The objective of this study was to investigate the effects of enzymatic degradation on the interstitial fluid load support mechanism of articular cartilage in unconfined compression. Thirty-seven immature bovine cartilage plugs were tested in unconfined compression before and after enzymatic digestion. The peak fluid load support decreased significantly p<0.0001 from 84±10% to 53±19% and from 80±10% to 46±21% after 18-hours digestion with 1.0 u/mg-wet-weight and 0.7 u/mg-wet-weight of collagenase, respectively. Treatment with 0.1 u/ml of chondroitinase ABC for 24 hours also significantly reduced the peak fluid load support from 83±12% to 48±16%p<0.0001. The drop in interstitial fluid load support following enzymatic treatment is believed to result from a decrease in the ratio of tensile to compressive moduli of the solid matrix.

Author(s):  
Seonghun Park ◽  
Ramaswamy Krishnan ◽  
Steven B. Nicoll ◽  
Gerard A. Ateshian

Under physiological conditions of loading, articular cartilage is subjected to both compressive strains, normal to the articular surface, and tensile strains, tangential to the articular surface. Previous studies have shown that articular cartilage exhibits a much higher modulus in tension than compression. Theoretical analyses have suggested that this tension-compression nonlinearity enhances the magnitude of interstitial fluid pressurization during loading in unconfined compression, above a theoretical threshold of 33% of the average applied stress. The first hypothesis of this experimental study is that the peak fluid load support in unconfined compression is significantly greater than the 33% theoretical limit predicted for porous permeable tissues modeled with equal moduli in tension and compression [1]. The second hypothesis is that the peak fluid load support is higher at the articular surface side of the tissue samples than near the deep zone, because the disparity between the tensile and compressive moduli is greater at the surface zone.


2003 ◽  
Vol 36 (12) ◽  
pp. 1785-1796 ◽  
Author(s):  
Seonghun Park ◽  
Ramaswamy Krishnan ◽  
Steven B. Nicoll ◽  
Gerard A. Ateshian

1999 ◽  
Author(s):  
Anna Stankiewicz ◽  
Gerard A. Ateshian ◽  
Louis U. Bigliani ◽  
Van C. Mow

Abstract The nearly frictionless lubrication in diarthrodial joints and load support within articular cartilage depends on its mechanical properties. It has been shown that the majority of applied loads on cartilage are supported by interstitial fluid pressurization (Ateshian et al., 1994) which results from the frictional drag of flow through the porous permeable solid matrix. The duration and magnitude of this pressurization are a function of the permeability of cartilage (Lai et al., 1981).


Author(s):  
Ramaswamy Krishnan ◽  
Monika Kopacz ◽  
Michael J. Carter ◽  
Gerard A. Ateshian

This study investigates the hypothesis that the equilibrium friction coefficient of cartilage decreases with increasing compressive strain. Furthermore, when accounting for this strain-dependence, it is hypothesized that the temporal response of the friction coefficient correlates linearly with interstitial fluid load support, in the configuration of unconfined compression stress-relaxation. Both hypotheses were confirmed from theory and experiment.


2003 ◽  
Vol 125 (1) ◽  
pp. 84-93 ◽  
Author(s):  
Chun-Yuh Huang ◽  
Michael A. Soltz ◽  
Monika Kopacz ◽  
Van C. Mow ◽  
Gerard A. Ateshian

A biphasic-CLE-QLV model proposed in our recent study [2001, J. Biomech. Eng., 123, pp. 410–417] extended the biphasic theory of Mow et al. [1980, J. Biomech. Eng., 102, pp. 73–84] to include both tension-compression nonlinearity and intrinsic viscoelasticity of the cartilage solid matrix by incorporating it with the conewise linear elasticity (CLE) model [1995, J. Elasticity, 37, pp. 1–38] and the quasi-linear viscoelasticity (QLV) model [Biomechanics: Its foundations and objectives, Prentice Hall, Englewood Cliffs, 1972]. This model demonstrates that a simultaneous prediction of compression and tension experiments of articular cartilage, under stress-relaxation and dynamic loading, can be achieved when properly taking into account both flow-dependent and flow-independent viscoelastic effects, as well as tension-compression nonlinearity. The objective of this study is to directly test this biphasic-CLE-QLV model against experimental data from unconfined compression stress-relaxation tests at slow and fast strain rates as well as dynamic loading. Twelve full-thickness cartilage cylindrical plugs were harvested from six bovine glenohumeral joints and multiple confined and unconfined compression stress-relaxation tests were performed on each specimen. The material properties of specimens were determined by curve-fitting the experimental results from the confined and unconfined compression stress relaxation tests. The findings of this study demonstrate that the biphasic-CLE-QLV model is able to describe the strain-rate-dependent mechanical behaviors of articular cartilage in unconfined compression as attested by good agreements between experimental and theoretical curvefits (r2=0.966±0.032 for testing at slow strain rate; r2=0.998±0.002 for testing at fast strain rate) and predictions of the dynamic response r2=0.91±0.06. This experimental study also provides supporting evidence for the hypothesis that both tension-compression nonlinearity and intrinsic viscoelasticity of the solid matrix of cartilage are necessary for modeling the transient and equilibrium responses of this tissue in tension and compression. Furthermore, the biphasic-CLE-QLV model can produce better predictions of the dynamic modulus of cartilage in unconfined dynamic compression than the biphasic-CLE and biphasic poroviscoelastic models, indicating that intrinsic viscoelasticity and tension-compression nonlinearity of articular cartilage may play important roles in the load-support mechanism of cartilage under physiologic loading.


2018 ◽  
Vol 69 ◽  
pp. 113-120 ◽  
Author(s):  
Jocelyn N. Todd ◽  
Travis G. Maak ◽  
Gerard A. Ateshian ◽  
Steve A. Maas ◽  
Jeffrey A. Weiss

1984 ◽  
Vol 56 (3) ◽  
pp. 691-699 ◽  
Author(s):  
J. C. Parker ◽  
L. Campbell ◽  
S. Gilchrist ◽  
G. Longenecker ◽  
A. E. Taylor

Increased extravascular lung water has been reported following periods of myocardial ischemia. To determine whether increased pulmonary microvascular permeability was produced by ischemia, total protein lymph-to-plasma concentration ratios (CL/CP) were obtained at mechanically increased left atrial pressures (Pla) before and after ligation of the left anterior descending coronary artery in dogs. Pulmonary and systemic vascular pressures and cardiac output were monitored and lymph flow was measured from an afferent tracheobronchial lymphatic. Osmotic reflection coefficients (sigma) for total protein were estimated using CL/CP = 1-sigma at high filtration rates, and permeability-surface area (PSf) products were fit to the data. The postischemic lung lymph data best fit average values of sigma = 0.68 and PSf = 0.073 ml X min-1 X 100 g-1 wet weight. There were no significant differences in lymph protein or water clearances between the pre- and postischemic increased Pla states or for myocardial ischemia compared with control values for the experimental preparation. Levels of 6-ketoprostaglandin F1 alpha, a degradation product of prostacyclin, increased by 10- to 14-fold above preischemic values in pulmonary lymph, and there was a significant increase in pulmonary vascular resistance during ischemia. Extravascular lung water was not increased above that attributed to the increased Pla alone. These data indicate no significant increase in pulmonary microvascular permeability to plasma proteins during myocardial ischemia.


1986 ◽  
Vol 251 (6) ◽  
pp. H1232-H1243 ◽  
Author(s):  
L. P. Thompson ◽  
M. W. Gorman ◽  
H. V. Sparks

We tested the hypothesis that an increase in interstitial fluid (ISF) adenosine concentration contributes to vasodilation of high oxidative skeletal muscle during sustained free-flow exercise. Canine calf muscles were stimulated at 3 Hz for 10 min before and after the infusion of the adenosine receptor antagonist aminophylline (10 mg/kg). The vasodilation that occurred during aminophylline infusion was allowed to decay before the postaminophylline exercise period was begun. This dose of aminophylline shifted the response to infused adenosine 20-fold during rest and reduced the response to a standard dose by 90% during exercise. Aminophylline had no significant effect on blood flow or on O2 consumption at rest or during exercise. Adenosine release (venous minus arterial plasma concentration times plasma flow) increased during 3-Hz exercise both before and after aminophylline infusion, but venous plasma adenosine concentration did not increase in either case. We developed a mathematical model of adenosine movement between ISF and plasma to help us judge whether to use adenosine release or venous concentration as an index of ISF adenosine and decided that venous concentration should be used. We conclude that aminophylline has no effect on sustained 3-Hz exercise hyperemia because under these conditions ISF adenosine concentration does not increase.


1999 ◽  
Vol 66 (1) ◽  
pp. 137-145 ◽  
Author(s):  
R. Kelkar ◽  
G. A. Ateshian

Integral transform methods are used to solve the contact creep problem between two identical cylindrical biphasic cartilage layers bonded to rigid impermeable subchondral bone substrates. The biphasic model employed for cartilage consists of a binary mixture of an incompressible porous-permeable solid phase and an incompressible fluid phase. Solutions are obtained as a function of time, from the instantaneous to the equilibrium responses of the tissue. A significant result of this analysis is that under application of a step load, fluid pressurization may support upward of 96 percent of the total applied load for more congruent joints, shielding the solid collagen-proteoglycan matrix of the tissue from excessive stresses during physiological loading durations. The protection imparted by interstitial fluid pressurization to the solid collagen-proteoglycan matrix of cartilage is investigated, and the influence of material properties and osteoarthritic changes on the potential loss of this protective effect is discussed.


2000 ◽  
Vol 10 (3) ◽  
pp. 326-339 ◽  
Author(s):  
G. Gregory Haff ◽  
Alexander J. Koch ◽  
Jeffrey A. Potteiger ◽  
Karen E. Kuphal ◽  
Lawrence M. Magee ◽  
...  

The effects of carbohydrate (CHO) supplementation on muscle glycogen and resistance exercise performance were examined with eight highly resistance trained males (mean ± SEM, age: 24.3 ± 1.1 years, height: 171.9±2.0 cm, body mass: 85.7 ± 3.5 kg; experience 9.9 ± 2.0 years). Subjects participated in a randomized, double blind protocol with testing sessions separated by 7 days. Testing consisted of an initial isokinetic leg exercise before and after an isotonic resistance exercise (IRT) session consisting of 3 leg exercises lasting ~39 min. Subjects consumed a CHO (1.0 g CHO ·kg body mass−1) or placebo treatment (PLC), prior to and every 10-min (0.5 g CHO ·kg body mass−1) during the IRT. Muscle tissue was obtained from the m vastus lateralis after a supine rest (REST) immediately after the initial isokinetic test (POST-ISO) and immediately after the IRT (POST-IRT). The CHO treatment elicited significantly less muscle glycogen degradation from the POST-ISO to POST-IRT (126.9 ± 6.5 to 109.7 ± 7.1 mmol·kg wet weight−1) compared to PLC (121.4±8.1 to 88.3±6.0 mmol·kg wet weight−1). There were no differences in isokinetic performance between the treatments. The results of this investigation indicate that the consumption of a CHO beverage can attenuate the decrease in muscle glycogen associated with isotonic resistance exercise but does not enhance the performance of isokinetic leg exercise.


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