Protective effect of bacterial lipase on lipopolysaccharide-induced toxicity in rat cardiomyocytes; H9C2 cell line.

Introduction: Cardiovascular system is highly sensitive to LPS-induced oxidative damage. This study aimed to show the inhibitory effect of bacterial Lipase on LPS-induced cardiomyoblasts toxicity. Methods: Rat cardiomyoblasts H9C2 were classified into Control, LPS (cells received 0.1, 1 and 10 μg/mL...

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Publicado en:Journal of Cardiovascular & Thoracic Research Vol. 12; no. 1; pp. 35 - 43
Autores principales: Mamipour, Mina, Yousefi, Mohammadreza, Dehnad, Alireza, Faridvand, Yousef, Zarezadeh, Reza, Khaksar, Majid, Pouyafar, Ayda, Rahbarghazi, Reza
Formato: research tables/charts Journal Article
Publicado: Tabriz University of Medical Sciences 2020
Acceso en línea:Ver este registro en EBSCOhost
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      dt: 2020
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      pub: Tabriz University of Medical Sciences
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        10.34172/jcvtr.2020.06
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        atl: Protective effect of bacterial lipase on lipopolysaccharide-induced toxicity in rat cardiomyocytes; H9C2 cell line.
      aug:
        au:
          Mamipour, Mina
          Yousefi, Mohammadreza
          Dehnad, Alireza
          Faridvand, Yousef
          Zarezadeh, Reza
          Khaksar, Majid
          Pouyafar, Ayda
          Rahbarghazi, Reza
        affil: Department of Biotechnology, Higher Education Institute of Rab-Rashid, Tabriz, Iran
      sug:
        subj:
          Bacteria
          Lipase Pharmacodynamics
          Myocytes, Cardiac Drug Effects
          Cell Line Drug Effects
          Oxidative Stress Drug Effects
          Animal Studies
          Rats
          Cell Viability
          Colorimetry
          Gene Expression
          Signal Transduction
          Toll-Like Receptors Metabolism
          Polymerase Chain Reaction
          Fatty Acids Analysis
          Chromatography, Gas
          Nitric Oxide Analysis
          NF-kappa B Drug Effects
      ab: Introduction: Cardiovascular system is highly sensitive to LPS-induced oxidative damage. This study aimed to show the inhibitory effect of bacterial Lipase on LPS-induced cardiomyoblasts toxicity. Methods: Rat cardiomyoblasts H9C2 were classified into Control, LPS (cells received 0.1, 1 and 10 μg/mL LPS) and LPS+ Lipase groups. In LPS+Lipase group, different concentrations of lipopolysaccharide were pre-incubated with 5 mg/mL bacterial lipase at 37˚C overnight prior to cell treatment. After 72 hours, cell viability was assessed by MTT assay. The expression of key genes related to toll-like receptor signaling pathways was assessed by real-time PCR assay. Percentage of fatty acids was evaluated in each group using gas chromatography assay. The levels of NO was also measured using the Griess reaction. Results: Data showed H9C2 cells viability was decreased after exposure to LPS in a dose-dependent manner (P < 0.05). Incubation of LPS with lipase increased cell survival rate and closed to near-to-control levels (P < 0.05). Lipase had the potential to blunt the increased expression of IRAK and NF-κB in cells after exposure to the LPS. Compared to the LPS group, lipase attenuated the increased level of NO-induced by LPS (P < 0.05). Gas chromatography analysis showed the reduction of saturated fatty acids in cells from LPS group while the activity of lipase prohibited impact of LPS on cell fatty acid composition. LPS decreased the ability of cardiomyoblasts to form colonies. Incubation of LPS with lipase enhanced clonogenic capacity. Conclusion: Reduction in lipopolysaccharide-induced cytotoxicity is possibly related to lipase activity and reduction of modified lipopolysaccharide with toll-like receptor.
      pubtype: Academic Journal
      doctype:
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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