L-ARGININE REGULATES APOPTOSIS OF PULMONARY ARTERY SMOOTH MUSCLE
CELLS IN RATS WITH HYPOXIC PULMONARY VASCULAR STRUCTURAL REMODELING
Qi JG1, Du JB1, Guo ZL1, Zhao B2, Zhang
QY1
1 First Hospital of Peking University, Beijing,
China
2 Beijing Ji Shui Tan Hospital, Beijing, China
Objective: To
explore the impact of L-arginine on apoptosis of smooth muscle cells in
pulmonary arteries of the rats with hypoxic pulmonary vascular structural
remodeling.
Methods: Seventeen Wistar rats were randomly divided into
hypoxia group ( n=5 ), hypoxia with L-arginine group ( n=5 ) and control
group ( n=7 ). Hypoxic challenge was performed by putting the rats into a
normobaric hypoxic chamber with an oxygen concentration of 10%��0.5%
for two weeks. Pulmonary vascular microstructure was measured. Apoptotic
smooth muscle cells in pulmonary arteries were detected by TdT-mediated
dUTP-biotin nick end labeling, and the expression of Fas protein was
detected using immunohistochemistry technique.
Results: pulmonary vascular structural remodeling
developed after 2-week hypoxia. Meanwhile, the percentage of apoptotic
smooth muscle cells to smooth muscle cells in pulmonary arteries was
markedly decreased in hypoxic rats compared with normal controls. The
expression of Fas protein of hypoxic rats was inhibited obviously.
L-arginine ameliorated pulmonary vascular structural remodeling of hypoxic
rats in association with an increase in the percentage of apoptotic smooth
muscle cells to smooth muscle cells and a strengthened Fas expression by
pulmonary artery smooth muscle cells.
Conclusion: L-arginine plays an
important role in the regulation of development of hypoxic pulmonary
vascular structural remodeling through promoting Fas expression and thereby
strengthening apoptosis in pulmonary artery smooth muscle cells.