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La lettre de l'institut Upsa de la douleur - 9

La lettre de l'institut Upsa de la douleur - 9

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AINS et inhibiteurs sélectifs <strong>de</strong> <strong>la</strong> COXrofecoxib sont, par contre, une innovationen matière <strong>de</strong> développementdu médicament et offrent enfin <strong>la</strong> perspectived’une meilleure tolérance etsécurité digestive au prix d’une efficacitéconservée dans le traitementsymptomatique <strong>de</strong>s affections chroniquescomme l’arthrite rhumatoï<strong>de</strong> oul’arthrose invalidante. Leur caractéristiquespharmacocinétiques et le tempsn é c e s s a i re à l’obtention <strong>de</strong> l’état d’équili b re <strong>de</strong> quelques jours limitent en eff e tleur attrait dans <strong>la</strong> prise en charge <strong>de</strong><strong>douleur</strong>s aiguës ou subaiguës. Les nouvellesgénérations à courte <strong>de</strong>mi-vie<strong>de</strong>vraient combler cette <strong>la</strong>cune dans ledomaine <strong>de</strong> <strong>la</strong> <strong>douleur</strong> aiguë par excès<strong>de</strong> nociception.L’innocuité digestive apparente <strong>de</strong>sinhibiteurs COX-2 sélectifs suggère n tune utilisation accrue dans les annéesa v e n i r. Leur sélectivité <strong>de</strong>meurecependant re<strong>la</strong>tive et <strong>de</strong>s surd o s a g e s● Amin A.R., Attur M., Abramson S.B., Nitric oxi<strong>de</strong>synthase and cyclooxygenases : distribution, regu<strong>la</strong>tion,and intervention in arthritis. Curr Opin Rheumatol 11;2 0 2 - 9: 1999● Banwarth B., Demotes-Mainard F., Schauberle T. ,<strong>La</strong>bat L., Dehais J. Central analgesic effets of aspirinlike drugs. Fundam Clin Pharmacol. 9,1-7,1995● Barner A. Review of clinical trials and benefit/riskratio of meloxicam. Scand J Rheumatol Suppl 102;2 9 - 3 7 : 1996● Bateman DN. NSAID’s : Time to re-evaluate gutt o x i c i t y. <strong>La</strong>ncet 343; 1051-1052 : 1994● Battistini B., Botting R., Bakhle YS. Cox-1 andC o x - 2 : Toward the <strong>de</strong>veloppment of more selectiveN S A I D ’s. Drug News and perspective 7; 501-512 :1 9 9 4 .● Besson J.M., The neurobiology of pain. <strong>La</strong>ncet 353 ;1 6 1 0 - 1 6 1 5: 1999● Besson, J. M. et Chaouch, A.. Peripheral and spinalmechanisms of nociception. Physiol review6 7 : 67-186 : 1987● Bonnabry P., Leemann T., Dayer P., Role of humanliver microsomal CYP2C9 in the biotransformation oflornoxicam. Eur J Clin Pharmacol 49 : 305-8; 1996● Bradley Ed. 67-78, Plenum Press, New York, 1991● Bre<strong>de</strong>r C.D., Dewitt DL., Kraig RP. Characterizationof an inducible cyclooxygenase in rat brain. J CompNeurol. 355; 296-415 : 1995● Cashman JN The mechanisms of action of NSAIDsin analgesia Drugs 52; S 5 : 13-23 : 1996.● Cipollone C., Ganci A., Panara MR. Effects ofnabumetone on prostanoid biosynthesis in man.Clin Pharmacol Ther. 58 ; 335-341 : 1995● Comittee on Safety of Medicines : Nonsteroida<strong>la</strong>nti-inf<strong>la</strong>mmatory drugs and serious gastrointestina<strong>la</strong>dverse reactions. BMJ 292; 1191-1193 : 1986● Dinchuk JE., Car BD., Foch RJ. Renal abnormalitiesand an altered response in mice <strong>la</strong>ckingcyclooxygenase II. Nature 378 : 406-409 ; 1995● Dirig DM, Yaksh TL In vitro prostanoid release fromspinal cord following peripheral inf<strong>la</strong>mmation : effectsof substance P, NMDA and capsaicin. Br J Pharmacol1 2 6 : 1333-40 ; 1999● Do<strong>la</strong>n S., No<strong>la</strong>n A., NMDA induced mechanica<strong>la</strong>llodynia is blocked by nitric oxi<strong>de</strong> synthaseand cyclooxygenase-2 inhibitors.NeuroReport 10 : 449-452; 1999● Dunn M.J., Simpson M., Davidson EW., ScharschmidtLA., Sedor JR. Nonsteroidal anti-inf<strong>la</strong>mmatorydrugs and renal function. J Clin Pharmacol.2 8 : 524-520 ; 1988● Ehrich E.W., Dallob A., De Lepeleire I., Van Hecken A.,Rien<strong>de</strong>au D., Yuan W., Porras A., Wittreich J.,Seibold J.R., De Schepper P., Mehlisch D.R., Gertz B.J.,Characterization of rofecoxib as a cyclooxygenase-2isoform inhibitor and <strong>de</strong>monstration of analgesia inthe <strong>de</strong>ntal pain mo<strong>de</strong>l. Clin Pharmacol Ther6 5 : 336-47 ; 1999● Elseviers MM, De Broe ME. Analgesic nephropathy :Is it caused by multi-analgesic abuse or singlesubstance use. Drug Safety 20 : 15-24; 1999BIBLIOGRAPHIEpeuvent théoriquement conduireaux mêmes acci<strong>de</strong>nts digestifs. Parailleurs leur sécurité rénale semble qualitativementcomparable aux AINSc<strong>la</strong>ssiques et le risque <strong>de</strong> néphro p a-thies aiguës ou chroniques lors d’uneutilisation prolongée <strong>de</strong>vrait conduireà <strong>la</strong> pru<strong>de</strong>nce en particulier dans <strong>de</strong>ssituations à risques (co-médications ouco-morbidités rénales ou cardiovascu<strong>la</strong> i res). 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