Platelet inhibitory effects of the nitric oxide donor drug MAHMA NONOate in vivo in rats


Autoria(s): Homer, Kerry L.; Wanstall, Janet C.
Contribuinte(s)

W. Gispen

F. Jijkamp

D. Versteeg

Data(s)

15/12/2003

Resumo

The platelet inhibitory effects of the nitric oxide (NO) donor drug MAHMA NONOate ((Z-1-{N-methyl-N-[6-(N-methylammoniohexyl)amino] diazen-1-ium-1,2-diolate) were examined in anaesthetised rats and compared with those of S-nitrosoglutathione (GSNO; an S-nitrosothiol). Bolus administration of the aggregating agent ADP dose-dependently reduced the number of circulating free platelets. Intravenous infusions of MAHMA NONOate (3-30 nmol/kg/min) dose-dependently inhibited the effect of 0.3 mumol/kg ADP. MAHMA NONOate was approximately 10-fold more potent than GSNO. MAHMA NONOate (0.3-10 nmol/kg/min) also reduced systemic artery pressure and was again 10-fold more potent than GSNO. Thus MAHMA NONOate has both platelet inhibitory and vasodepressor effects in vivo. The dose ranges for these two effects overlapped, although blood pressure was affected at slightly lower doses. The platelet inhibitory effects compared favourably with those of GSNO, even though NONOates generate free radical NO which, in theory, could have been scavenged by haemoglobin. Therefore platelet inhibition may be a useful therapeutic property of NONOates. (C) 2003 Elsevier B.V. All rights reserved.

Identificador

http://espace.library.uq.edu.au/view/UQ:65165

Idioma(s)

eng

Publicador

Elsevier

Palavras-Chave #Pharmacology & Pharmacy #Platelet Inhibition #In Vivo #Mahma Nonoate #Nitric Oxide (no) Donors #S-nitrosoglutathione #Vasodepression Systemic #S-nitroso-glutathione #Red-blood-cells #Aggregation #Activation #Plasma #Vitro #Mechanisms #Albumin #C1 #320503 Clinical Pharmacology and Therapeutics #730106 Cardiovascular system and diseases
Tipo

Journal Article