AN IN-VIVO MODEL FOR SCREENING PEPTIDOMIMETIC INHIBITORS OF GELATINASE-A

• Published in: Journal of pharmaceutical sciences Vol. 84; no. 4; pp. 404 - 409
• Main Authors: CHANDER, SK, ANTONIW, P, BEELEY, NRA, BOYCE, B, CRABBE, T, DOCHERTY, AJP, LEONARD, J, MASON, B, MILLAR, K, MILLICAN, AT, MORPHY, R, MOUNTAIN, A, OCONNELL, J, PORTER, WILLMOTT, N
• Format: Journal Article
• Language: English
• Published: NEW YORK Elsevier 01.04.1995
• Subjects: Administration, Oral; Animals; Chemistry; Chemistry, Medicinal; Chemistry, Multidisciplinary; Dose-Response Relationship, Drug; Drug Evaluation, Preclinical; Female; Gelatinases - antagonists & inhibitors; Humans; Indicators and Reagents; Injections, Intraperitoneal; Kinetics; Life Sciences & Biomedicine; Male; Matrix Metalloproteinase 2; Metalloendopeptidases - antagonists & inhibitors; Mice; Peptides - administration & dosage; Peptides - chemistry; Peptides - pharmacology; Pharmacology & Pharmacy; Physical Sciences; Pleura - metabolism; Rats; Science & Technology; CELLS; INVASION; METASTASIS; EMBRYO; RECOMBINANT TISSUE INHIBITOR; C-TERMINAL DOMAIN; METALLOPROTEINASES; IV; PEPTIDE; TIMP
• ISSN: 0022-3549; 1520-6017
• DOI: 10.1002/jps.2600840405

Gelatinase A, a matrix metalloproteinase, is frequently associated with human solid tumors, and its secretion and activation in the tumor milieu is considered important in the process of angiogenesis, invasion, and metastasis. Consequently, metalloproteinase inhibitors may be of value in the therapy of cancer as well as other disease states involving tissue remodeling and release of biologically active peptide/protein by proteolytic cleavage, Here we describe the development of a rapid screening assay for in vivo activity of peptidomimetic inhibitors of gelatinase A that involves assessment of inhibition of an enzyme-substrate reaction in a circumscribed body compartment, the mouse pleural cavity. As examples of the utility of this assay, in vivo activity of the aryl sulfonamide, sulfamyl urea, morpholino and carboxylic acid functionality at the P-3' position of a series of hydroxamic acid inhibitors was examined after administration both intraperitoneally tip) (to approximate systemic administration) and orally. For up to 2 h after ip administration, all inhibitors tested showed marked activity (>90% inhibition) at 17 mu mol/kg (similar to 10 mg/kg). This activity declined in a dose-responsive manner to insignificant levels at 0.67 mu mol/kg (similar to 0.4 mg/kg). Aryl sulfonamides showed significant inhibition (>50%) for up to 7 h after administration. A higher dosage (136 mu mol/kg, similar to 80 mg/kg) was required to reveal oral activity, which was observed only with morpholino compounds (>50% inhibition). Thus, the model described may be of value in the identification of orally active gelatinase A inhibitors.