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10.1590/1414-431X20165431

http://scihub22266oqcxt.onion/10.1590/1414-431X20165431
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suck abstract from ncbi


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pmid27599201      Braz+J+Med+Biol+Res 2016 ; 49 (10): ä
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  • Angiotensin-(1?7) inhibits inflammation and oxidative stress to relieve lung injury induced by chronic intermittent hypoxia in rats #MMPMID27599201
  • Lu W; Kang J; Hu K; Tang S; Zhou X; Yu S; Li Y; Xu L
  • Braz J Med Biol Res 2016[]; 49 (10): ä PMID27599201show ga
  • Obstructive sleep apnea is associated with inflammation and oxidative stress in lung tissues and can lead to metabolic abnormalities. We investigated the effects of angiotensin1?7 [Ang-(1?7)] on lung injury in rats induced by chronic intermittent hypoxia (CIH). We randomly assigned 32 male Sprague-Dawley rats (180?200 g) to normoxia control (NC), CIH-untreated (uCIH), Ang-(1?7)-treated normoxia control (N-A), and Ang-(1?7)-treated CIH (CIH-A) groups. Oxidative stress biomarkers were measured in lung tissues, and expression of NADPH oxidase 4 (Nox4) and Nox subunits (p22phox, and p47phox) was determined by Western blot and reverse transcription-polymerase chain reaction. Pulmonary pathological changes were more evident in the uCIH group than in the other groups. Enzyme-linked immunosorbent assays and immunohistochemical staining showed that inflammatory factor concentrations in serum and lung tissues in the uCIH group were significantly higher than those in the NC and N-A groups. Expression of inflammatory factors was significantly higher in the CIH-A group than in the NC and N-A groups, but was lower than in the uCIH group (P<0.01). Oxidative stress was markedly higher in the uCIH group than in the NC and N-A groups. Expression of Nox4 and its subunits was also increased in the uCIH group. These changes were attenuated upon Ang-(1?7) treatment. In summary, treatment with Ang-(1-7) reversed signs of CIH-induced lung injury via inhibition of inflammation and oxidative stress.
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