Effect of .ALPHA.-(3,5-di-tert-butyl-4-hydroxybenzylidene)-.GAMMA.-butyrolactone (KME-4), a new anti-inflammatory drug, on the established adjuvant arthritis in rats.
スポンサーリンク
概要
- 論文の詳細を見る
The effect of α-(3, 5-di-tert-butyl-4-hydroxybenzylidene)-γ-butyrolactone (KME-4), a new anti-inflammatory drug, on established adjuvant arthritis in rats was compared to that of indomethacin. When administered orally daily from days 14 to 27 starting on day 14 after the adjuvant (day 0), KME-4 (2 to 10 mg/kg) produced a dose-related reduction of the swelling of both injected and uninjected hindpaws, and it retarded body weight loss. The initiation of paw swelling after the cessation of therapy was not observed at either 5 mg/kg or 10 mg/kg of KME-4. On day 42 (15 days after discontinuation of dosing), KME-4 caused the recovery of organ weight, erythrocyte sedimentation rate (ESR) and serum albumin/globulin (A/G) ratio towards normal levels, and it also decreased radiographic bone damage scores in a dose-dependent manner. The results indicate that KME-4 produces the improvement of systemic symptoms in the established adjuvant arthritis. The results obtained with indomethacin were similiar to those with KME-4. However, the degree of the efficacy of indomethacin (2 mg/kg) was lower than that of KME-4 (10 mg/kg) as judged by the measured parameters (ESR, serum A/G ratio and bone damage).
- 公益社団法人 日本薬理学会の論文
著者
-
Watanabe Kiyoshi
Biochemical Research Laboratories Kanegafuchi Chemical Industry Co. Ltd.
-
Yamashita Toshiaki
Biochemical Research Laboratories Kanegafuchi Chemical Industry Co. Ltd.
-
HIDAKA Takayoshi
Biochemical Research Laboratories, Kanegafuchi Chemical Industry Co., Ltd.
-
HOSOE Kazunori
Biochemical Research Laboratories, Kanegafuchi Chemical Industry Co., Ltd.
関連論文
- Constitutive High-level Production of Human Lymphotoxin by CHO-K1 Cells Transformed with the Human Lymphotoxin Gene Controlled by a Human β-Actin Promoter(Biological Chemistry)
- Comparison of Human Lymphotoxin Gene Expression in CHO Cells Directed by Genomic DNA or cDNA Sequences(Biological Chemistry)
- Asymmetric Hydrolysis of (dl)-1-Acyloxy-2-halo-1-phenylethanes with Lipases(Organic Chemistry)
- Lipase-catalyzed Stereoselective Hydrolysis of 2-Acyl and 1-p-Tolylsulfonyl Substituted Propanediol and Butanediol
- Stereochemical Inversion of (R)-5-Hydroxymethyl-3-tert-butyl-2-oxazolidinone or (R)-5-Hydroxymethyl-3-isopropyl-2-oxazolidinone to the Corresponding (S)-Isomer
- Microbial Production of (R)-3-Halolactic Acid from(±)-3-Halo-1,2-Propanediol
- Stereospecific Hydrolysis of 2-Oxazolidinone Esters and Separation of Products with an Immobilized Lipase Column
- Production of D-β-Hydroxycarboxylic Acids from the Corresponding Carboxylic Acids by a Mutant of Candida rugosa : Studies of β-Hydroxycarboxylic Acids (V)
- Production of β-Hydroxypropionic Acid from Propionic Acid by a Candida rugosa Mutant Unable to Assimilate Propionic Acid : Studies on β-Hydroxycarboxylic Acids (IV)
- Production of d-β-Hydroxyisobutyric Acid from Isobutyric Acid by Candida rugosa and Its Mutant : Studies on β-Hydroxycarboxylic Acids (III)
- Produciton of β-Hydroxycarboxylic Acids from Aliphatic Carboxylic Acids by Microorganisms : Studies on β-Hydroxycarboxylic Acids (II)
- Stereoselective Conversion of Isobutyric Acid to β-Hydroxyisobutyric Acid by Microoganisms : Studies on β-Hydroxycarboxylic Acids (I)
- Enzymatic Resolution of 2-Oxazolidinone Estersf
- The Pharmacokinetic Pattern of Glycosylated Human Recombinant Lymphotoxin (LT) in Rats after Intravenous Administration
- Lipase-catalyzed Stereoselective Hydrolysis of 2-Acyloxy-3-chloropropyl p-toluenesulfonate
- Asymmetric Hydrolysis of (R, S)-5-Acetoxymethyl-3-terr-butyl-oxazolidin-2-one with Enzymes and Microorganisms
- Effect of .ALPHA.-(3,5-di-tert-butyl-4-hydroxybenzylidene)-.GAMMA.-butyrolactone (KME-4), a new anti-inflammatory drug, on the established adjuvant arthritis in rats.
- Pharmacological properties of a new anti-inflammatory compound, .ALPHA.-(3,5-di-tert-butyl-4-hydroxybenzylidene)-.GAMMA.-butyrolactone (KME-4), and its inhibitory effects on prostaglandin synthetase and 5-lipoxygenase.
- Inhibition of polymorphonuclear leukocyte 5-lipoxygenase and platelet cyclooxygenase by .ALPHA.-(3,5-di-tert-butyl-4-hydroxybenzylidene)-.GAMMA.-butyrolactone (KME-4), a new anti-inflammatory drug.
- Synthesis of (S)-β-Blockers from (S)-5-Hydroxymethyl-3-tert butyl-2-oxazolidinone or (S)-5-Hydroxymethyl-3-isopropyl-2-oxazolidinone