Abstract |
The antiarthritic potential of two different acyclic nucleotide analogs, i.e. 9-(2-phosphonomethoxyethyl)adenine (PMEA), its bis(pivaloyloxymethyl) ester ( Bis-POM-PMEA), and 1-(S)-(3-hydroxy-2-phosphonomethoxyethyl) cytosine ( HPMPC) was investigated in the rat model of mycobacterial adjuvant-induced arthritis. With dependence on the dose, timing and route of administration, as well as on the genetic constitution of the arthritis-prone animals, PMEA was able to delay the onset, and substantially reduce or nearly completely inhibit the development of arthritic paw swelling. HPMPC was less active in this model. As compared with PMEA, its prodrug, Bis-POM-PMEA, expressed much more pronounced beneficial effects after both oral and i.p. administration.
|
Authors | A Zídek, A Holý, D Franková, B Otová |
Journal | European journal of pharmacology
(Eur J Pharmacol)
Vol. 286
Issue 3
Pg. 307-10
(Nov 24 1995)
ISSN: 0014-2999 [Print] Netherlands |
PMID | 8608793
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
|
Chemical References |
- Organophosphonates
- Organophosphorus Compounds
- bis(pivaloyloxymethyl)-9-(2-phosphonylmethoxyethyl)adenine
- adefovir
- Cytosine
- Adenine
- Cidofovir
|
Topics |
- Adenine
(analogs & derivatives, therapeutic use)
- Animals
- Arthritis, Experimental
(prevention & control)
- Cidofovir
- Cytosine
(analogs & derivatives, therapeutic use)
- Female
- Organophosphonates
- Organophosphorus Compounds
(therapeutic use)
- Rats
- Rats, Inbred BN
- Rats, Inbred Lew
|