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Featured researches published by C. May.


Veterinary Record | 1998

Matrix metalloproteinases 2 and 9 in canine rheumatoid arthritis

A. R. Coughlan; Duncan H. L. Robertson; D. Bennett; C. May; Robert J. Beynon; S. D. Carter

Matrix metalloproteinases (MMPs) are considered important mediators of tissue damage in joint diseases. The levels of MMPs 2 and 9 were measured in samples of synovial fluid from 20 joints in seven dogs with rheumatoid arthritis by gelatin zymography. The results were compared with the actual gelatinolytic activity of the fluid measured in a gelatin-degradation ELISA. The gelatinolytic activity in synovial fluid from arthritic joints was markedly greater than that in fluid from disease-free joints. The zymographic activity attributable to MMP-9 (identified by Western blotting) was absent from synovial fluid from control joints but prominent in fluid from arthritic joints, and in these joints the presence of a 75 kDa form of MMP-9 was correlated with the gelatinolytic activity of the fluid measured by the ELISA (r=0.81, P<0.05). Synovial fluid from one dog with rheumatoid arthritis was examined before and after treatment with corticosteroids. After treatment its zymographic pattern had returned to normal.


Research in Veterinary Science | 1994

Measurement of glycosaminoglycans and keratan sulphate in canine arthropathies

M. Arican; S. D. Carter; D. Bennett; C. May

Glycosaminoglycans (GAG) and keratan sulphate (KS) were measured in sera and synovial fluids from dogs with either osteoarthritis (OA) or rupture of the cranial cruciate ligament (CCL) and normal dogs. The dogs with OA had higher synovial fluid GAG levels (P < 0.002) and serum KS (P < 0.03) compared to the normal dogs. No significant differences in serum GAG were found in either group. In both OA and rupture of the CCL, GAG levels were increased in the synovial fluid from the affected joint compared with the clinically normal (inactive) contralateral joint. Neither GAG nor KS measurements correlated with serum and synovial fluid antibodies to collagen type II, synovial fluid white cell count or age of dog. It is unlikely that the measurement of these cartilage breakdown products is of value for diagnostic or prognostic use in canine arthropathies.


Journal of Comparative Pathology | 1994

Hyaluronan in Canine Arthropathies

M. Arican; S. D. Carter; C. May; D. Bennett

Soluble hyaluronan (HA), which has been considered as a marker for joint disease in man, was measured in serum and synovial fluid (SF) from dogs with osteoarthritis (OA), rheumatoid arthritis (RA), and rupture of the cranial cruciate ligament (CCL) and from normal dogs (control). Dogs with OA and RA had significantly increased serum HA (P < 0.001) and decreased synovial fluid HA (P < 0.001), as did dogs with CCL rupture (serum, P < 0.05; synovial fluid, P < 0.005). In OA, HA was lower in the SF from the affected joint than in that from the clinically normal (inactive) contralateral joint; no such difference was seen in dogs with CCL rupture. Dogs with liver disease (portocaval shunts, viral infectious hepatitis, metastatic neoplasm and disease secondary to diabetes mellitus) had increased serum HA concentrations (P < 0.001). There was a significant overlap of HA values in the diseased and normal dogs. Therefore, it is unlikely that the measurement of this cartilage breakdown product would be of value for diagnosis or prognosis in canine arthropathies.


Veterinary Immunology and Immunopathology | 1992

Lymphocyte populations in the synovial membranes of dogs with rheumatoid arthritis

C. May; Dez Hughes; S. D. Carter; D. Bennett

Lymphocyte populations in the synovial membranes of dogs with canine rheumatoid arthritis (CRA) were investigated by immunohistochemical staining techniques. T-lymphocytes were the predominant cell type distributed throughout the supporting layer of the synovial membranes. B-lymphocytes expressing IgG were seen far more commonly than those expressing either IgA or IgM. Synovial membrane biopsies from normal and osteoarthritic joints did not have the marked cellular infiltrates seen in joints with CRA. The synovial immunohistopathological features in dogs with CRA are similar to those seen in human rheumatoid arthritis.


British Veterinary Journal | 1995

Antibodies to heat shock proteins in dogswith rheumatoid arthritis and systemic lupus erythematosus

S. C. Bell; S. D. Carter; C. May; D. Bennett

Antibodies to heat shock proteins of the 65 kDa group were demonstrated in canine sera and synovial fluid. This paper reports these antibody measurements in three groups of dogs with joint disease and compares them with those of a control population. Dogs with rheumatoid arthritis (RA) showed higher anti-heat shock proteins (HSP) antibody levels, in both their sera and synovial fluids, compared to the control dogs and these antibodies were predominantly of the IgG and IgM class; there was a significant correlation between IgM anti-HSP65 and IgM-rheumatoid factors. There was also a significant correlation between anti-HSP65 and antibodies to canine distemper virus, but only of the IgM class and the relevance of these antibodies to the overall pathogenesis of canine RA and, in particular, to the presence of canine distemper virus within the joint, are discussed.


Journal of Small Animal Practice | 1988

A reappraisal of anterior cruciate ligament disease in the dog

D. Bennett; B. J. Tennant; D. G. Lewis; J. Baughan; C. May; S. D. Carter


Journal of Small Animal Practice | 1991

Meniscal damage associated with cruciate disease in the dog

D. Bennett; C. May


Veterinary Record | 1993

Lameness associated with Borrelia burgdorferi infection in the horse.

A Browning; S. D. Carter; A. Barnes; C. May; D. Bennett


Journal of Small Animal Practice | 1998

Management of disc-associated wobbler syndrome with a partial slot fenestration and position screw technique.

J. P. Queen; A. R. Coughlan; C. May; D. Bennett; Jacques Penderis


Equine Veterinary Journal | 1994

Borrelia burgdorferi infection in UK horses.

S. D. Carter; C. May; A. Barnes; D. Bennett

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S. D. Carter

University of Liverpool

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A. Barnes

University of Liverpool

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S. C. Bell

University of Liverpool

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M. Arican

University of Liverpool

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A. Coutts

University of Liverpool

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C. McLean

University of Liverpool

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D. G. Lewis

University of Liverpool

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