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Comparative effects of several nitric oxide donors on intracellular cyclic GMP levels in bovine chromaffin cells: correlation with nitric oxide production
Author(s) -
Ferrero Rut,
RodríguezPascual Fernando,
MirasPortugal Ma Teresa,
Torres Magdalena
Publication year - 1999
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1038/sj.bjp.0702607
Subject(s) - snap , nitric oxide , sodium nitroprusside , chemistry , cyclic gmp , glutathione , intracellular , biophysics , biochemistry , medicine , endocrinology , biology , enzyme , computer graphics (images) , organic chemistry , computer science
Sodium nitroprusside, S‐nitroso‐N‐acetyl‐ D,L ‐penicillamine, Spermine NONOate and DEA NONOate raised cyclic GMP levels in bovine chromaffin cells in a time and concentration dependent manner with different potencies, the most potent being DEA/NO with an EC 50 value of 0.38±0.02 μ M . Measurements of NO released from these donors revealed that DEA/NO decomposed with a half‐life (t 1/2 ) of 3.9±0.2 min. The t 1/2 for SPER/NO was 37±3 min. SNAP decomposed more slowly (t 1/2 =37±4 h) and after 60 min the amount of NO produced corresponded to less than 2% of the total SNAP present. The rate of NO production from SNAP was increased by the presence of glutathione. For DEA/NO and SPER/NO there was a clear correlation between nitric oxide production and cyclic GMP increases. Their threshold concentrations were 0.05 μ M and maximal effective concentration between 2.5 and 5 μ M . For SNAP, threshold activation was seen at 1 μ M , whereas full activation required a higher concentration (500–750 μ M ). The dose‐response for SNAP increases in cyclic GMP was shifted nearly two orders of magnitude lower in the presence of glutathione. At higher concentrations an inhibition of cyclic GMP accumulation was found. This effect was not observed with either the nitric oxide‐deficient SNAP analogue or other NO donors. Although NO‐donors are likely to be valuable for studying NO functions, their effective concentrations and the amount of NO released by them are very different and should be assessed in each system to ensure that physiological concentrations of NO are used.British Journal of Pharmacology (1999) 127 , 779–787; doi: 10.1038/sj.bjp.0702607