Role of nitric oxide on oxytocin-evoked contractions and prostaglandin synthesis in isolated pregnant rat uterus

1997 ◽  
Vol 57 (3) ◽  
pp. 323-329 ◽  
Author(s):  
M.A. Chaud ◽  
A.M. Franchi ◽  
M. Beron de Astrada ◽  
M.F. Gimeno
1998 ◽  
Vol 58 (6) ◽  
pp. 413-416 ◽  
Author(s):  
A Franchi ◽  
A Motta ◽  
M Farina ◽  
M.L Rivero ◽  
D Ogando ◽  
...  

2000 ◽  
Vol 182 (3) ◽  
pp. 612-619 ◽  
Author(s):  
Yuri P. Vedernikov ◽  
Ashu S. Syal ◽  
Toshiaki Okawa ◽  
Venu Jain ◽  
George R. Saade ◽  
...  

1997 ◽  
Vol 272 (6) ◽  
pp. E1008-E1015 ◽  
Author(s):  
R. K. Riemer ◽  
C. Buscher ◽  
R. K. Bansal ◽  
S. M. Black ◽  
Y. He ◽  
...  

Nitric oxide (NO) relaxes uterine smooth muscle and is produced by the pregnant uterus. Our previous studies revealed an increase in rat uterine NO synthase (NOS) activity in pregnancy and a decline at term. In the present study, we have examined the distribution of NOS isoform expression to determine whether their regulation is consistent with a role in the inhibition of uterine contractions before term. At day 17-18 of pregnancy, NOS immunohistochemistry revealed expression of two isoforms: endothelial constitutive form of NOS (ecNOS) in vascular endothelium and inducible form of NOS (iNOS) in myometrial and vascular smooth muscle and in decidual epithelium. Immunoblotting revealed that expression of iNOS declined nearly fivefold, whereas ecNOS declined twofold in laboring rats at term. We conclude that iNOS is expressed in myometrium of pregnant rat uterus but not the virgin rat and that iNOS expression declines at term when labor is present. The pattern of changes in myometrial iNOS expression with advancing gestation suggests that NO could act in an autocrine and/or paracrine manner to inhibit uterine contractions before term.


1998 ◽  
Vol 178 (4) ◽  
pp. 823-829 ◽  
Author(s):  
Gabriel Fiol ◽  
Francisco Machado ◽  
Isabel Hernandez ◽  
Andrés C. Inglés ◽  
Lorenzo Abad ◽  
...  

2000 ◽  
Vol 62 (4) ◽  
pp. 243-247 ◽  
Author(s):  
M. Farina ◽  
M.L. Ribeiro ◽  
D. Ogando ◽  
M. Gimeno ◽  
A.M. Franchi

1994 ◽  
Vol 77 (2) ◽  
pp. 590-596 ◽  
Author(s):  
J. Boczkowski ◽  
E. Vicaut ◽  
G. Danialou ◽  
M. Aubier

We evaluated by intravital microscopy in rats the relative importance of nitric oxide (NO) and prostaglandins in 1) the maintenance of basal diaphragmatic arteriolar tone and 2) the response of diaphragmatic arterioles to the endothelium-dependent vasodilator acetylcholine (ACh). One hundred two mechanically ventilated rats were studied. Separate applications of N omega-nitro-L-arginine (L-NNA) and mefenamic acid (MA), which are specific inhibitors of NO and prostaglandin synthesis, respectively, elicited a significant reduction in basal diaphragmatic arteriolar diameter. A dramatic potentiation of the effect of each inhibitor was observed when both agents were applied simultaneously. ACh application induced a significant and dose-dependent increase in arteriolar diameter that was not significantly modified by the separate application of L-NNA or MA. Conversely, the simultaneous administration of L-NNA and MA almost completely prevented ACh-induced arteriolar dilatation. Dilatation in response to sodium nitroprusside was not significantly modified in the presence of both inhibitors. These results suggest that NO and prostaglandins act in concert to regulate basal diaphragmatic arteriolar tone and to mediate diaphragmatic arteriolar response to ACh.


1995 ◽  
Vol 50 (4) ◽  
pp. 225-235 ◽  
Author(s):  
E. Gonzalez ◽  
A. Jawerbaum ◽  
V. Novaro ◽  
A. Faletti ◽  
M.A.F. Gimeno

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