Literature DB >> 12804596

The regulating effect of heme oxygenase/carbon monoxide on hypoxic pulmonary vascular structural remodeling.

Shi Yun1, Du Junbao, Gong Limin, Zeng Chaomei, Tang Xiuying, Tang Chaoshu.   

Abstract

Hypoxic pulmonary vascular structural remodeling (HPVSR) is the important pathologic basis of hypoxic pulmonary hypertension (HPH). The discoveries of endogenous gaseous messenger molecules, nitric oxide (NO) and carbon monoxide (CO), have been moving the research of HPVSR to a very new phase. But the effect and significance of heme oxygenase (HO)/CO on the development of HPVSR have not been fully understood. In this study, we observed the alteration of endogenous HO/CO system in five time points during 14 days and found that the content of CO in lung homogenates in rats with HPVSR increased in a time-dependent double-peak manner. Exogenous supply of ZnPP-IX, an inhibitor of HO-1, decreased the content of CO in lung homogenate, decreased the expression of Fas and apoptotic cells in pulmonary artery smooth muscle cells (PASMCs), up-regulated the expression of PCNA in PASMCs, and worsened HPH and HPVSR of hypoxic rats. Meanwhile, exogenous supply of CO played an adverse action. The results showed that the up-regulation of HO/CO exerted a protective role in the development of HPVSR.

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Year:  2003        PMID: 12804596     DOI: 10.1016/s0006-291x(03)00998-7

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  3 in total

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Journal:  Adv Exp Med Biol       Date:  2021       Impact factor: 2.622

2.  DMF inhibits PDGF-BB induced airway smooth muscle cell proliferation through induction of heme-oxygenase-1.

Authors:  Petra Seidel; Stephanie Goulet; Katrin Hostettler; Michael Tamm; Michael Roth
Journal:  Respir Res       Date:  2010-10-20

3.  Cross talk between autophagy and apoptosis in pulmonary hypertension.

Authors:  Yang Jin; Augustine M K Choi
Journal:  Pulm Circ       Date:  2012-10       Impact factor: 3.017

  3 in total

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