cyclic-gmp and endomorphin-2

cyclic-gmp has been researched along with endomorphin-2* in 1 studies

Other Studies

1 other study(ies) available for cyclic-gmp and endomorphin-2

Article	Year
Endomorphins restored the endothelium-dependent relaxation of the rabbit aorta rings exposed to high D-glucose condition via NO-cGMP pathway. Protein and peptide letters, 2006, Volume: 13, Issue:10 Rings of rabbit aorta that were both incubated in a high concentration of D-glucose and contracted submaximally by phenylephrine showed significantly decreased endothelium-dependent relaxations induced by acetylcholine. The cGMP production of aorta rings was also reduced. Treatment with endomorphins (1-1000 nmol/L) restored acetylcholine-induced relaxations of aorta rings incubated in high glucose concentrations and increased the cGMP synthesis. Moreover, this effect of endomorphins on endothelium was antagonized by naloxone, and the increase in the production of cGMP was also blocked. Topics: Animals; Aorta, Abdominal; Cyclic GMP; Endothelium, Vascular; Glucose; In Vitro Techniques; Muscle Relaxation; Nitric Oxide; Oligopeptides; Rabbits; Signal Transduction	2006

Article

Year

Endomorphins restored the endothelium-dependent relaxation of the rabbit aorta rings exposed to high D-glucose condition via NO-cGMP pathway.

Protein and peptide letters, 2006, Volume: 13, Issue:10

Rings of rabbit aorta that were both incubated in a high concentration of D-glucose and contracted submaximally by phenylephrine showed significantly decreased endothelium-dependent relaxations induced by acetylcholine. The cGMP production of aorta rings was also reduced. Treatment with endomorphins (1-1000 nmol/L) restored acetylcholine-induced relaxations of aorta rings incubated in high glucose concentrations and increased the cGMP synthesis. Moreover, this effect of endomorphins on endothelium was antagonized by naloxone, and the increase in the production of cGMP was also blocked.

Topics: Animals; Aorta, Abdominal; Cyclic GMP; Endothelium, Vascular; Glucose; In Vitro Techniques; Muscle Relaxation; Nitric Oxide; Oligopeptides; Rabbits; Signal Transduction

2006