Prostaglandins are responsible for the inhibition of breathing observed with a placental extract in fetal sheep

2004 ◽  
Vol 144 (1) ◽  
pp. 35-44 ◽  
Author(s):  
Ruben E. Alvaro ◽  
Shabih U. Hasan ◽  
Sylvain Chemtob ◽  
Mansour Qurashi ◽  
Saif Al-Saif ◽  
...  
1996 ◽  
Vol 8 (3) ◽  
pp. 423 ◽  
Author(s):  
RE Alvaro ◽  
V Rehan ◽  
Almeida V de ◽  
Z Haider ◽  
M Robertson ◽  
...  

We have found previously that the infusion of a placental extract inhibits breathing induced by 100% O2 plus umbilical cord occlusion in the fetal sheep, suggesting that a placental factor is responsible for the inhibition of fetal breathing. To test whether this factor is specific to the placenta and whether it also inhibits spontaneous fetal breathing (occurring in the absence of cord occlusion), we administered extracts from the placenta, muscle and liver of the pregnant ewe, extracts of fetal liver, and Krebs solution to 16 chronically instrumented fetal sheep at 135 +/- 5 days of gestation. Infusions were made during low-voltage electrocortical activity, 5 to 15 min after a switch from high voltage, when breathing was well established. Within 90 s of the infusion of the placental extract in the carotid artery of the fetus, breathing decreased in 79% (33/42) of the experiments and was completely abolished in 71% (30/42) of them (P < 0.0001 compared with the other infusates). No apnoeas were observed with the Krebs solution (0/19) and the maternal muscle (0/20). Extracts of maternal and fetal liver abolished breathing in only 17% (4/23) and 21% (6/29) of the experiments respectively (NS compared with Krebs solution). There were no significant changes in blood gas tensions, pH, blood pressure and heart rate associated with the infusion of the extracts. The electrocortical activity (ECoG) switched from low to high voltage in 50% of the experiments using placental extract compared with 0% with Krebs solution and maternal muscle, and with 9% and 17% with maternal and fetal liver respectively (P < 0.005). Breathing output (integral of EMGdi x f) during and after the infusions significantly decreased only with the placental extract. These findings indicate the presence of a factor produced by the placenta which inhibits fetal breathing and may be responsible for the normal inhibition of breathing observed in fetal life.


1999 ◽  
Vol 45 (4, Part 2 of 2) ◽  
pp. 293A-293A ◽  
Author(s):  
R Alvaro ◽  
R Shiu ◽  
N Shepel ◽  
N Idiong ◽  
H Rigatto

1997 ◽  
Vol 9 (6) ◽  
pp. 641 ◽  
Author(s):  
Ruben E. Alvaro ◽  
May Robertson ◽  
Saad Al-Saedi ◽  
Robert P. Lemke ◽  
Don B. Cates ◽  
...  

Previous studies have revealed a placental extract that inhibits breathing in fetal sheep. In the present study of 29 chronically instrumented sheep at 132±1 days of gestation, infusion of the 1-10 kDa extract inhibited breathing in 76% of the experiments whereas Krebs’ solution inhibited it in 24%. It retained this activity after 6 months of freezing, after lyophilization, and upon lowering the pH during purication from 8·0 to 4·0, but it inhibited breathing in only 35% when the pH was lowered to 2·0. A signicant dose-dependent effect was observed from a 16-fold dilution to a 4-fold concentration. Treatment of the extract with proteinase K or boiling reduced the activity to 30% or 26% inhibition, respectively. The activity was not adsorbed to an ion-exchange column at pH 7·0 or 8· 0, but it was at pH 9· 0 and it eluted with increasing NaCl concentrations. On a polyacrylamide gel the activity was eluted at a Kav of 0· 66 (82% inhibition), corresponding to between 2·5 and 4·5 kDa. These ndings suggest that a peptide produced by the placenta, with a molecular mass between 2· 5 and 4·5 kDa, inhibits fetal breathing.


1997 ◽  
Vol 41 ◽  
pp. 300-300 ◽  
Author(s):  
Ruben Alvaro ◽  
May Robertson ◽  
Robert Lemke ◽  
Nnanake Idiong ◽  
Henrique Rigatto

1998 ◽  
Vol 5 (1) ◽  
pp. 156A-156A
Author(s):  
M SCHWAB ◽  
M ROEDEL ◽  
L BUCHWALDER ◽  
B WALTHER ◽  
P NATHANIELSZ
Keyword(s):  

Diabetes ◽  
1989 ◽  
Vol 38 (5) ◽  
pp. 597-603 ◽  
Author(s):  
J. R. Milley ◽  
J. S. Papacostas
Keyword(s):  

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