Characterization of zymosan-induced arthritis in the rat: Effects on joint inflammation and cartilage metabolism

Life Sciences ◽  
1994 ◽  
Vol 55 (17) ◽  
pp. PL321-PL326 ◽  
Author(s):  
P. Gegout ◽  
P. Gillet ◽  
D. Chevrier ◽  
C. Guingamp ◽  
B. Terlain ◽  
...  
2020 ◽  
Vol 98 (Supplement_4) ◽  
pp. 41-41
Author(s):  
Amanda N Bradbery ◽  
Jessica L Leatherwood ◽  
Brittany L Silvers ◽  
Mattea L Much ◽  
Rafael E Martinez ◽  
...  

Abstract Intra-articular lipopolysaccharide is a common model to induce acute synovitis to investigate the effects of various therapeutic agents or nutraceuticals. The long-term effects of intra-articular lipopolysaccharide use in skeletally mature and immature horses has yet to be investigated; therefore, the objective of this study was to describe long-term effects of single-administration of intra-articular lipopolysaccharide on joint inflammation and cartilage metabolism. To test this objective, both radial carpal joints from 5 stock-type horses never exposed to lipopolysaccharide (CON; n = 10) were compared to radial carpal joints from 17 similar stock-type horses previously exposed to intra-articular lipopolysaccharide (INFL; n = 34). Joints within INFL were further categorized as the joint which received lipopolysaccharide (LPS; n = 17) and contralateral control which received iso-volumetric lactated Ringer’s solution (CONTRA; n = 17). A single synovial fluid sample from each joint was analyzed for prostaglandin E2 (PGE2), collagenase cleavage neopeptide (C2C), carboxypeptide of type II collagen (CPII), and chondroitin sulfate 846 (CS846). All data were analyzed using PROC MIXED of SAS with main effects of treatment (CON, INFL) and joint (CON, LPS, CONTRA). Time post-administration (1.5, 2, 6 yr) and age-at-administration (1, 3, 5, 7 yr) were included in the model within INFL joints (LPS, CONTRA). There was no influence of treatment on any biomarker (P > 0.40). Similarly, inflammation and cartilage metabolism were not different between CON, CONTRA, and LPS joints (P > 0.50). Within INFL, there was no influence of joint, age, or time post-administration for PGE2, CPII, or CS846 (P > 0.10). A joint x time interaction was observed for catabolic C2C (P < 0.01); however, where LPS was less than CONTRA 2 yr post-lipopolysaccharide administration and similarly when lipopolysaccharide was administered at 5 and 7 yr of age (P < 0.01). These data indicate no long-term negative effects for the use of intra-articular lipopolysaccharide as an acute inflammatory model in skeletally mature and immature horses.


2018 ◽  
Vol 96 (2) ◽  
pp. 579-590 ◽  
Author(s):  
Amanda N Bradbery ◽  
Josie A Coverdale ◽  
Kristine L Vernon ◽  
Jessica L Leatherwood ◽  
Carolyn E Arnold ◽  
...  

2015 ◽  
Vol 23 ◽  
pp. A86-A87
Author(s):  
A.C. Bay-Jensen ◽  
A. Valdes ◽  
I. Byrjalsen ◽  
M.A. Karsdal ◽  
N. Arden
Keyword(s):  

2011 ◽  
Vol 135 (4) ◽  
pp. 503-510
Author(s):  
Darcy A Kerr ◽  
Vincent A Memoli ◽  
Sara S Cathey ◽  
Brent T Harris

Abstract We report findings from an autopsy of a 45-year-old woman with the rare lysosomal storage disease mucolipidosis type III α/β. Her disease manifested most notably as multiple bone and cartilage problems with tracheal and bronchial malacia. Principal autopsy findings included gross abnormalities in bone and cartilage with corresponding microscopic cytoplasmic lysosomal granules. These cytoplasmic granules were also seen in histologic preparations of the brain, myocardium, heart valves, and fibroblasts of the liver and skin by light and electron microscopy. By electron microscopy there were scattered, diffuse vesicular cytoplasmic granules in neurons and glia and an increase in lysosomal structures with fine electron lucent granularity in the above tissue types. Our findings help elaborate current understanding of this disease and differentiate it from the mucopolysaccharidoses and related disorders. To our knowledge, this is the first report to document pathologic findings in a patient with mucolipidosis type III α/β by autopsy.


2002 ◽  
Vol 81 (10) ◽  
pp. 711-715 ◽  
Author(s):  
S. Yamada ◽  
S. Saeki ◽  
I. Takahashi ◽  
K. Igarashi ◽  
H. Shinoda ◽  
...  

Bone and cartilage metabolism is known to be more active during rest than during periods of activity. The purpose of this study was to examine the hypothesis that mandibular retractive force could be more effective when applied to rats during rest. Mandibular retractive force caused a considerable reduction in the condylar length in experimental groups, and the magnitude of this reduction was greater in the Light-period (08:00-20:00) group than in the Dark-period (20:00-08:00) group. The differentiation and proliferation of chondrocytes were inhibited in animals in the Light-period group, compared with those in the Dark-period group. These results suggest that the orthopedic effects of mandibular retractive force vary depending on the time of day the force is applied, and that such force may be more effective while animals are resting than while they are active.


Cartilage ◽  
2010 ◽  
Vol 2 (3) ◽  
pp. 265-278 ◽  
Author(s):  
Suzi Hoegh Madsen ◽  
Anne Sofie Goettrup ◽  
Gedske Thomsen ◽  
Søren Tvorup Christensen ◽  
Nikolaj Schultz ◽  
...  

1983 ◽  
Vol 5 (2) ◽  
pp. 93-99 ◽  
Author(s):  
A. Muhlrad ◽  
A. Setton ◽  
J. Sela ◽  
I. Bab ◽  
D. Deutsch

2014 ◽  
Vol 2014 ◽  
pp. 1-9 ◽  
Author(s):  
Jun Yamada ◽  
Kunikazu Tsuji ◽  
Kazumasa Miyatake ◽  
Yu Matsukura ◽  
Kahaer Abula ◽  
...  

Activins are proinflammatory cytokines which belong to the TGFβsuperfamily. Follistatin is an extracellular decoy receptor for activins. Since both activins and follistatin are expressed in articular cartilage, we hypothesized that activin-follistatin signaling participates in the process of joint inflammation and cartilage degeneration. To test this hypothesis, we examined the effects of follistatin in a carrageenan-induced mouse arthritis model. Synovitis induced by intra-articular injection of carrageenan was significantly alleviated by preinjection with follistatin. Macrophage infiltration into the synovial membrane was significantly reduced in the presence of follistatin. In addition, follistatin inhibited proteoglycan erosion induced by carrageenan in articular cartilage. These data indicate that activin-follistatin signaling is involved in joint inflammation and cartilage homeostasis. Our data suggest that follistatin can be a new therapeutic target for inflammation-induced articular cartilage degeneration.


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