DISSOCIATION OF TISSUE THIOLS CONTENT FROM NITROGLYCERIN-INDUCED CYCLIC-3',5'-GUANOSINE MONOPHOSPHATE AND THE STATE OF TOLERANCE - IN-VIVO EXPERIMENTS IN RATS

Citation
Ai. Hajyehia et Lz. Benet, DISSOCIATION OF TISSUE THIOLS CONTENT FROM NITROGLYCERIN-INDUCED CYCLIC-3',5'-GUANOSINE MONOPHOSPHATE AND THE STATE OF TOLERANCE - IN-VIVO EXPERIMENTS IN RATS, The Journal of pharmacology and experimental therapeutics, 273(1), 1995, pp. 94-100
Citations number
63
Categorie Soggetti
Pharmacology & Pharmacy
ISSN journal
00223565
Volume
273
Issue
1
Year of publication
1995
Pages
94 - 100
Database
ISI
SICI code
0022-3565(1995)273:1<94:DOTTCF>2.0.ZU;2-K
Abstract
The in vivo effects of nitroglycerin (GTN) on the biochemical response [cyclic-3',5'-guanosine monophosphate (cGMP) levels] of vascular (aor ta and inferior vena cava, IVC) and other tissues (heart and lung) wer e studied. GTN caused dose and time-dependent increases in cGMP conten t of aorta and IVC. Compared to base line, maximal concentrations of 3 - to 4-fold the basal levels of cGMP were measured in the aorta, IVC a nd lung of rats after 2 mg i.v. bolus doses of GTN. Tolerance to GTN, as assessed by the reduction in the cGMP increase in response to an i. v. GTN dose, developed 12 to 18 hr after continuous i.v. infusion (100 -200 mu g/hr) of the drug. Significant differences in the pattern of f ormation and degradation of cGMP were noted between tolerant and nonto lerant rats. Unlike the control IVC tissue, where elevated cGMP was me asured throughout the 5-min post GTN administration, in tolerant IVC, cGMP levels were not significantly different from the basal values at time points 3 and 5 min post GTN. These results suggest that IVC is mo re prone to (or less recoverable from) the state of tolerance than the aorta. Furthermore, when tissue thiols were measured in control and t olerant rats, a complete dissociation was observed between the state o f tolerance and the endogenous glutathione and cysteine concentrations . These data constitute strong evidence against an in vivo depletion o f tissue thiols as being the primary determinant underlying the develo pment of tolerance during nitrate therapy.