» Articles » PMID: 1357157

Evidence That S-nitrosothiols Are Responsible for the Smooth Muscle Relaxing Activity of the Bovine Retractor Penis Inhibitory Factor

Overview
Specialty Pharmacology
Date 1992 Oct 1
PMID 1357157
Citations 7
Authors
Affiliations
Soon will be listed here.
Abstract

Inhibitory factor (IF), an extract of the bovine retractor penis muscle, when treated with acid, becomes a vasodilator with properties similar to endothelium-derived relaxing factor (EDRF). EDRF has been proposed to be nitric oxide (NO), long known to be a potent vasodilator. Recently, biologically active IF was proposed to be NO, as well, generated by acid activation of inorganic nitrite. We compared acid-activated IF with acid-activated nitrite and found that NO formation was not sufficient to explain the properties of acid-activated IF. Endothelium-denuded rings of rabbit aorta were used to test the smooth muscle-relaxing properties of IF and nitrite. Although both IF (0.5 ml) and nitrite (1 microM) relaxed phenylephrine-contracted rabbit aorta to a similar extent after acid activation (approximately 30%), several significant differences were observed. IF was most active when acid activated by a 5-min, pH 2 step followed by neutralization; nitrite was relatively inactive when acid activated in this manner, and was most active when assayed immediately after acidification to pH 2. Purging with argon for 5 min reduced the smooth muscle-relaxing activity of 1.0 microM nitrite from 27 +/- 2 to 10 +/- 2% relaxation, whereas the activity of IF was not changed by argon purging (control, 31 +/- 2% relaxation; argon purged, 34 +/- 2% relaxation). When IF samples were assayed for nitrite content, the amount of nitrite found (0.5-5 nmol/0.5 ml sample) was not sufficient to explained the observed smooth muscle relaxing activity. Furthermore, acid-activated IF significantly stimulated cyclic GMP production by platelet-soluble guanylate cyclase from 3.2 +/- 0.2 to 12.4 +/- 0.4 pmol/min/mg protein.(ABSTRACT TRUNCATED AT 250 WORDS)

Citing Articles

Postprandial lipids accelerate and redirect nitric oxide consumption in plasma.

Vrancken K, Schroeder H, Longo L, Power G, Blood A Nitric Oxide. 2016; 55-56:70-81.

PMID: 27021272 PMC: 4890961. DOI: 10.1016/j.niox.2016.03.004.


Effect of thiol modulators and Cu/Zn superoxide dismutase inhibition on nitrergic relaxations in the rat gastric fundus.

DE Man J, DE Winter B, Boeckxstaens G, Herman A, Pelckmans P Br J Pharmacol. 1996; 119(5):1022-8.

PMID: 8922754 PMC: 1915936. DOI: 10.1111/j.1476-5381.1996.tb15773.x.


Effect of Cu2+ on relaxations to the nitrergic neurotransmitter, NO and S-nitrosothiols in the rat gastric fundus.

DE Man J, DE Winter B, Boeckxstaens G, Herman A, Pelckmans P Br J Pharmacol. 1996; 119(5):990-6.

PMID: 8922751 PMC: 1915940. DOI: 10.1111/j.1476-5381.1996.tb15769.x.


Non-adrenergic, non-cholinergic relaxation of the bovine retractor penis muscle: role of S-nitrosothiols.

Liu X, Gillespie J, Martin W Br J Pharmacol. 1994; 111(4):1287-95.

PMID: 8032616 PMC: 1910140. DOI: 10.1111/j.1476-5381.1994.tb14885.x.


Influence of S-nitrosothiols and nitrate tolerance in the rat gastric fundus.

Barbier A, Lefebvre R Br J Pharmacol. 1994; 111(4):1280-6.

PMID: 8032615 PMC: 1910166. DOI: 10.1111/j.1476-5381.1994.tb14884.x.