Expression of nitric oxide synthase isoforms (NOS II and NOS III) in adult rat lung in hyperoxic pulmonary hypertension

1999 ◽  
Vol 295 (2) ◽  
pp. 317-329 ◽  
Author(s):  
Wolfgang Steudel ◽  
Masazumi Watanabe ◽  
Krikor Dikranian ◽  
Margaretha Jacobson ◽  
R. C. Jones
1995 ◽  
Vol 13 (2) ◽  
pp. 167-174 ◽  
Author(s):  
P W Shaul ◽  
A J North ◽  
T S Brannon ◽  
K Ujiie ◽  
L B Wells ◽  
...  

1998 ◽  
Vol 101 (4) ◽  
pp. 795-801 ◽  
Author(s):  
T D Le Cras ◽  
R C Tyler ◽  
M P Horan ◽  
K G Morris ◽  
R M Tuder ◽  
...  

CHEST Journal ◽  
1998 ◽  
Vol 114 (1) ◽  
pp. 35S-36S ◽  
Author(s):  
Timothy D. Le Cras ◽  
Robert C. Tyler ◽  
Marilee P. Horan ◽  
Ken G. Morris ◽  
Ivan F. McMurty ◽  
...  

2011 ◽  
Vol 41 (1) ◽  
pp. 25-31 ◽  
Author(s):  
Mehmet Fatih Gökçe ◽  
Süleyman Kaplan ◽  
Ayten Türkkani ◽  
Ramazan Kozan ◽  
Mustafa Ayyildiz ◽  
...  

1994 ◽  
Vol 266 (6) ◽  
pp. L635-L641 ◽  
Author(s):  
A. J. North ◽  
R. A. Star ◽  
T. S. Brannon ◽  
K. Ujiie ◽  
L. B. Wells ◽  
...  

The successful transition from fetal to neonatal life involves a marked decline in pulmonary vascular resistance which is modulated in part by endothelium-derived nitric oxide. To define the molecular processes which prepare the pulmonary circulation for nitric oxide mediation of vasodilatation at the time of birth, we determined the ontogeny of endothelial nitric oxide synthase (NOS-III) gene expression in lungs from fetal and newborn rats. Maturational changes in lung neuronal NOS (NOS-I) expression were also investigated; the latter isoform has been localized to rat bronchiolar epithelium. NOS proteins were examined by immunoblot analysis, and mRNA abundance was assessed in reverse transcription-polymerase chain reaction assays. Both NOS-III and NOS-I protein were detectable in 16-day fetal lung, they increased 3.8- and 3.1-fold, respectively, to maximal levels at 20 days of gestation (term = 22 day), and they fell postnatally (1-5 days). In parallel with the findings for NOS-III protein, NOS-III mRNA increased from 16 to 20 days gestation and fell after birth. In contrast, NOS-I mRNA abundance declined during late fetal life and rose postnatally. These findings were confirmed by Northern analyses. Thus NOS-III and NOS-I gene expression are developmentally regulated in rat lung, with maximal NOS-III and NOS-I protein present near term. The regulation of pulmonary NOS-III may primarily involve alterations in transcription or mRNA stability, whereas NOS-I expression in the maturing lung may also be mediated by additional posttranscriptional processes.


1997 ◽  
Vol 121 (7) ◽  
pp. 1241-1246 ◽  
Author(s):  
Shu Fang Liu ◽  
El-Bdaoui Haddad ◽  
Ian Adcock ◽  
Michael Salmon ◽  
Hiro Koto ◽  
...  

1994 ◽  
Vol 81 (SUPPLEMENT) ◽  
pp. A649
Author(s):  
R. A. Johns ◽  
C. Xue ◽  
A. Rengasmy ◽  
T. D. Le Cras ◽  
P. Koberna ◽  
...  

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