Developmental Changes in Prostacyclin Synthesis Are Conserved in Cultured Pulmonary Endothelium and Vascular Smooth Muscle

1999 ◽  
Vol 20 (1) ◽  
pp. 113-121 ◽  
Author(s):  
Philip W. Shaul ◽  
Margaret C. Pace ◽  
Zhong Chen ◽  
Timothy S. Brannon
1989 ◽  
Vol 257 (5) ◽  
pp. E617-E624
Author(s):  
M. B. Vallotton ◽  
C. Gerber-Wicht ◽  
W. Dolci ◽  
R. P. Wuthrich

The effect of angiotensin II (ANG II) and arginine vasopressin (AVP) on prostacyclin production by vascular smooth muscle cells (VSMC) has been examined. Cultured rat aortic VSMC were studied during either static incubation in multiwell plates or during dynamic incubation in superfusion columns. Prostacyclin synthesis was assessed by radioimmunoassaying one of its stable metabolites, 6-keto-prostaglandin F1 alpha (6-keto-PGF1 alpha). Both ANG II and AVP stimulated the biosynthesis of prostacyclin in a concentration-dependent manner (10(-10) to 10(-5) M). ANG II (ED50 = 3 nM) displayed a higher potency than AVP (ED50 = 10 nM). ANG II was 4.4 times more potent than AVP at 10(-8) M. The effect of both peptides was inhibited selectively by antagonists. In the case of AVP (10(-8) M), a pure V1 antagonist (dEt2AVP) and the V2 agonist dDAVP, both at 10(-6) M, completely blocked the production of prostacyclin induced by AVP, whereas a mixed V1-V2 antagonist [d(CH2)5-D-Leu-VAVP] at 10(-6) M displaced the concentration-response curve by approximately two orders of magnitude to the right. Superfusion with a calcium-free medium containing ethylene glycol-bis(beta-aminoethyl ether)-N,N,N',N'-tetraacetic acid inhibited 89 +/- 3% of the ANG II- and 70 +/- 8% of the AVP-induced prostacyclin production, whereas nifedipine (10(-6) M) had no effect. A potentiating effect was observed when the stimulation with either ANG II or AVP was repeated two or three times. An even more marked potentiation resulted when the stimulation by ANG II (10(-8) M) followed stimulation by AVP (10(-8) M).(ABSTRACT TRUNCATED AT 250 WORDS)


1991 ◽  
Vol 71 (3) ◽  
pp. 1129-1135 ◽  
Author(s):  
J. Belik ◽  
A. Halayko ◽  
K. Rao ◽  
N. Stephens

To evaluate the developmental changes in pulmonary vascular smooth muscle contractile protein content, mechanical properties, and their contribution to the high resistance characteristic of the fetal and immediate neonatal period, we studied pulmonary vessels of fetal, newborn, and adult sheep, as well as newborn and adult pigs. Strips of the second- through fifth-generation vessels were dissected, and their content of tissue total smooth muscle cell protein, myosin, and actin-to-myosin ratio were measured; the mechanical properties of the second-generation vascular strips were also studied. For all ages the smooth muscle protein and myosin content of the second-generation vessels were significantly greater than for the lower pulmonary vascular orders (P less than 0.05). The myosin content in fetal sheep (0.77 +/- 0.03 micrograms/mg wet tissue) was similar to that of the newborn (0.79 +/- 0.04) and adult (0.86 +/- 0.05). However, the smooth muscle protein content (7.94 +/- 0.21 micrograms/mg wet tissue) and the actin-to-myosin ratio of the pulmonary vascular tissue of the fetus (1.00 +/- 0.04) were lower (P less than 0.01) in the fetal than in the newborn (9.16 +/- 0.26 and 1.60 +/- 0.12) and adult (9.38 +/- 0.3 and 1.60 +/- 0.11, respectively). No differences were observed for these parameters between the newborn and adult pig. Stress (16.5 +/- 1.7 mN/mm2) and the maximum shortening capacity (13.0 +/- 1.5% of optimal length) in the newborn pulmonary vascular strips were significantly greater than for the fetus (6.8 +/- 1.4 and 5.9 +/- 1.0, respectively) but similar to those of the adult sheep.(ABSTRACT TRUNCATED AT 250 WORDS)


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