Tolerance to Sodium Nitroprusside: Studies in Cultured Porcine Vascular Smooth Muscle Cells

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Abstract

Background

Tolerance to nitrovasodilators, including sodium nitroprusside (SNP), is a clinical problem. SNP causes vasodilatation by releasing nitric oxide, which stimulates intracellular guanosine 3':5'-cyclic monophosphate (cGMP) accumulation in smooth muscle cells. This study examined tolerance to SNP in coronary smooth muscle cells by measuring intracellular cGMP formation.

Methods

Smooth muscle cells were isolated from pig coronary vessels. Intracellular cGMP formation in response to SNP, nitroglycerine, and atrial natriuretic peptide (ANP) was quantitated by radioimmunoassay before and after chronic pretreatment.

Results

The detection of tolerance of cells rechallenged with SNP required exposure to a minimum concentration of 1 μM for SNP for at least 60 min. In untreated cells, acutely applied 100 μM SNP increased the cGMP concentration to 300 ± 8.6 pmol/mg protein (mean ± SEM). The cGMP concentration in cells pretreated with 1 μM SNP for 60 min increased to 213 ± 11 pmol/mg in response to 100 μM SNP (P < 0.01, compared to untreated cells). The pretreatment of cells for 60 min with increasing concentrations of SNP caused a sequential reduction in the acute concentration-response curves of cGMP to SNP in cells pretreated with 100 μM nitroglycerine for 60 min was reduced significantly. Pretreatment with 100 μM SNP for 60 min did not change the response of cAMP accumulation to isoproterenol or forskolin. However, the respone of cGMP formation to ANP was potentiated after pretreatment. In addition, elevation of basal cAMP or cGMP concentrations, induced with isopoterenol or ANP, respectively, did not alter the response of cGMP formation to SNP.

Conclusion

The study yielded the following findings: (1) reversible tolerance to SNP was induced in cultured vascular smooth muscle cells; (2) chronic exposure to nitroglycerine induced cross-tolerance to SNP; (3) cells that were tolerant to SNP showed a potentiated response to ANP.

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