Literature DB >> 20412326

Effect of chronic methylene blue administration on hypoxemia in rats with common bile duct ligation.

Akiko Miyamoto1, Yasumi Katsuta, Xue-Jun Zhang, Hong-Li Li, Masaru Ohsuga, Hirokazu Komeichi, Shuji Shimizu, Toshio Akimoto, Kyoichi Mizuno.   

Abstract

AIM: Acute administration of methylene blue (MB) can reverse hypoxemia in patients with hepatopulmonary syndrome (HPS). We evaluated the effect of chronic MB administration in common bile duct-ligated rats, which develop HPS by 5 weeks after surgery.
METHODS: A total of 96 Sprague-Dawley rats were used, including 63 rats with common bile duct ligation (CBDL), 22 sham-operated rats and 11 normal control rats. MB (6 mg/kg) was injected s.c. once a day for 4 weeks. Evaluation of hemodynamics and intrapulmonary vascular dilatation (IPVD), as well as blood sampling for arterial blood gas analysis, were done under conscious and unrestrained conditions. Hemodynamics were assessed by the reference sample method using (141)Ce-microspheres (15 microm in diameter), and IPVD was also determined by i.v. injection of these microspheres. Histological examination of the lungs was done with hematoxylin-eosin staining and immunohistochemical staining for von Willebrand factor or vascular endothelial growth factor.
RESULTS: Both the arterial oxygen tension and alveolar-arterial oxygen difference were significantly improved in MB-treated CBDL rats. The hyperdynamic circulation and splanchnic hyperemia seen in untreated CBDL rats were also alleviated by MB treatment. However, IPVD was not affected by MB. Histological examination of the lungs indicated that MB treatment reduced the proliferation of alveolar capillary vessels and angiogenesis, leading to improvement of arterial dysoxygenation. Hepatic synthetic and detoxification functions, as well as renal function, were not altered by MB treatment.
CONCLUSION: Methylene blue may be a candidate treatment for HPS that does not cause deterioration of hepatic or renal function.

Entities:  

Year:  2010        PMID: 20412326     DOI: 10.1111/j.1872-034X.2010.00640.x

Source DB:  PubMed          Journal:  Hepatol Res        ISSN: 1386-6346            Impact factor:   4.288


  8 in total

Review 1.  Hepatopulmonary syndrome: What we know and what we would like to know.

Authors:  Israel Grilo-Bensusan; Juan Manuel Pascasio-Acevedo
Journal:  World J Gastroenterol       Date:  2016-07-07       Impact factor: 5.742

Review 2.  Hepatopulmonary Syndrome.

Authors:  Yong Lv; Daiming Fan
Journal:  Dig Dis Sci       Date:  2015-03-03       Impact factor: 3.199

Review 3.  Hepatopulmonary syndrome: update on pathogenesis and clinical features.

Authors:  Junlan Zhang; Michael B Fallon
Journal:  Nat Rev Gastroenterol Hepatol       Date:  2012-07-03       Impact factor: 46.802

4.  The lung in liver disease: old problem, new concepts.

Authors:  Michael B Fallon; Junlan Zhang
Journal:  Trans Am Clin Climatol Assoc       Date:  2013

Review 5.  Review article: Update on current and emergent data on hepatopulmonary syndrome.

Authors:  Stergios Soulaidopoulos; Evangelos Cholongitas; George Giannakoulas; Maria Vlachou; Ioannis Goulis
Journal:  World J Gastroenterol       Date:  2018-03-28       Impact factor: 5.742

6.  MiR145-5p inhibits proliferation of PMVECs via PAI-1 in experimental hepatopulmonary syndrome rat pulmonary microvascular hyperplasia.

Authors:  Yang Chen; Congwen Yang; Yujie Li; Lin Chen; Yong Yang; Karine Belguise; Xiaobo Wang; Kaizhi Lu; Bin Yi
Journal:  Biol Open       Date:  2019-11-04       Impact factor: 2.422

Review 7.  Pharmacological treatment for hepatopulmonary syndrome.

Authors:  Ahad Eshraghian; Amir A'lam Kamyab; Seung Kew Yoon
Journal:  Biomed Res Int       Date:  2013-09-12       Impact factor: 3.411

Review 8.  Hepatopulmonary Syndrome and Liver Transplantation: A Recent Review of the Literature.

Authors:  Caglar Cosarderelioglu; Arif M Cosar; Merve Gurakar; Nabil N Dagher; Ahmet Gurakar
Journal:  J Clin Transl Hepatol       Date:  2016-03-15
  8 in total

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