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The Arthus reaction in guinea-pig knee joints. A test for anti-inflammatory drugs

Identifieur interne : 003A30 ( Main/Exploration ); précédent : 003A29; suivant : 003A31

The Arthus reaction in guinea-pig knee joints. A test for anti-inflammatory drugs

Auteurs : Alan Blackham [Royaume-Uni] ; Henryk Radziwonik [Royaume-Uni] ; Ian H. Shaw [Royaume-Uni]

Source :

RBID : ISTEX:17B5D32353D1EFF4D5A022C6D36B14DA0AF6B3BD

English descriptors

Abstract

Abstract: A reversed passive Arthus reaction was produced in guinea-pig knee joints by intravenous injection of ovalbumin and intra-articular injection of homologous anti-ovalbumin antiserum or specific IgG2 antibody. The optimum response was obtained by varying the concentration of antigen while keeping the amount of antibody constant. Joint swelling, leucocyte infiltration in the synovial fluid and joint pathology were measured 4–6 hours and 24 hours after initiation of the reaction. The PRA lesions were almost completely inhibited by complement or polymorphonuclear leucocyte depletion. The effects of a range of drugs on the 4–6 hours response were investigated following intraperitoneal or oral administration. Cyproheptadine hydrochloride, Trasylol, indomethacin, aspirin, phenylbutazone, prednisolone sodium phosphate, chloroquine diphosphate, SKF36914 (gold triethyl phosphine), cyclophosphamide, ketoprofen, sudoxicam and naproxen all reduced one or more of the symptoms of inflammation. However, cyproheptadine was only active at high and probably non-specific dose levels. D(−)penicillamine hydrochloride and mepyramine maleate were inactive.

Url:
DOI: 10.1007/BF01972689


Affiliations:


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Le document en format XML

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<term>Arthus</term>
<term>Arthus reaction</term>
<term>Arthus reactions</term>
<term>Blood cells</term>
<term>Carrageenin foot oedema</term>
<term>Cell counts</term>
<term>Cell infiltration</term>
<term>Chloroquine diphosphate</term>
<term>Cohn fraction</term>
<term>Complement depletion</term>
<term>Complement titrations</term>
<term>Control animals</term>
<term>Control hahgg</term>
<term>Cyproheptadine</term>
<term>Dos</term>
<term>Dose levels</term>
<term>Exudate volume</term>
<term>French laboratories</term>
<term>Geigy pharmaceuticals</term>
<term>Gold triethyl phosphine</term>
<term>Heat aggregated</term>
<term>Human gamma globulin</term>
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<term>Important role</term>
<term>Indomethacin</term>
<term>Intraarticular injection</term>
<term>Intravenous</term>
<term>Intravenous injection</term>
<term>Joint macroscopy</term>
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<term>Leucocyte</term>
<term>Leucocyte counts</term>
<term>Leucocyte infiltration</term>
<term>Macroscopy</term>
<term>Macroscopy scores</term>
<term>Mustine</term>
<term>Mustine hydrochloride</term>
<term>Open columns</term>
<term>Oral administration</term>
<term>Ovalbumin</term>
<term>Passive arthus reaction</term>
<term>Periarticular tissues</term>
<term>Phenylbutazone</term>
<term>Phosphate buffer</term>
<term>Polymorphonuclear</term>
<term>Polymorphonuclear leucocyte depletion</term>
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<term>Prednisolone sodium phosphate</term>
<term>Prostaglandin</term>
<term>Prostaglandin synthetase inhibitors</term>
<term>Protein fraction</term>
<term>Rheumatoid arthritis</term>
<term>Serum complement levels</term>
<term>Significant reduction</term>
<term>Single experiment</term>
<term>Smith kline</term>
<term>Sudoxicam</term>
<term>Synovial</term>
<term>Synovial fluid</term>
<term>Synovial fluid leucocyte counts</term>
<term>Syntex pharmaceuticals</term>
<term>Total leucocyte counts</term>
<term>Trasylol</term>
<term>Unfractionated antiserum</term>
<term>Various doses</term>
<term>Ward blenkinsop</term>
<term>White blood cell counts</term>
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<div type="abstract" xml:lang="en">Abstract: A reversed passive Arthus reaction was produced in guinea-pig knee joints by intravenous injection of ovalbumin and intra-articular injection of homologous anti-ovalbumin antiserum or specific IgG2 antibody. The optimum response was obtained by varying the concentration of antigen while keeping the amount of antibody constant. Joint swelling, leucocyte infiltration in the synovial fluid and joint pathology were measured 4–6 hours and 24 hours after initiation of the reaction. The PRA lesions were almost completely inhibited by complement or polymorphonuclear leucocyte depletion. The effects of a range of drugs on the 4–6 hours response were investigated following intraperitoneal or oral administration. Cyproheptadine hydrochloride, Trasylol, indomethacin, aspirin, phenylbutazone, prednisolone sodium phosphate, chloroquine diphosphate, SKF36914 (gold triethyl phosphine), cyclophosphamide, ketoprofen, sudoxicam and naproxen all reduced one or more of the symptoms of inflammation. However, cyproheptadine was only active at high and probably non-specific dose levels. D(−)penicillamine hydrochloride and mepyramine maleate were inactive.</div>
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