Heme oxygenase-1 downregulate the activity of nuclear factor NF-κB and protect the damage of cardiocyte induced by lipopolysaccharide in rats. (12th October 2011)
- Record Type:
- Journal Article
- Title:
- Heme oxygenase-1 downregulate the activity of nuclear factor NF-κB and protect the damage of cardiocyte induced by lipopolysaccharide in rats. (12th October 2011)
- Main Title:
- Heme oxygenase-1 downregulate the activity of nuclear factor NF-κB and protect the damage of cardiocyte induced by lipopolysaccharide in rats
- Authors:
- Renqiang, Yang
Xiaoshu, Cheng
Kui, Hong
Yanqing, Wu
Jianxin, Hu
Juxiang, Li - Abstract:
- Abstract : Objective: To determine whether HO-1 played a important role in the protection of cardiocyte in the lipopolysaccharide-induced acute cardiocyte injury model. Method: Cardiocyte was isolated from SD neonate rat, and was enrolled into C group (normal culture), L group (with stimulation of LPS), L+H group (with stimulation of Hemin (inducer of HO-1), followed by LPS), and L+Z group (with stimulation of ZnPP (inhibitor of HO-1), followed by LPS). The levels of LDH, malondialdehyde (MDA), and superoxide dismutase (SOD) were measured. The cell heart rhythm, survival rate and the apoptosis rate were also examined. The expression of nuclear factor κB (NF-κB), HO-1, and tumour necrosis factor α (TNFα) were measured with RT-PCR, Western blotting and flow cytometry. Results: The level of LDH and MDA were significantly higher in L group than those in C group (113±15 vs 69±10 U/L, p<0.05, and 1.88±0.36 vs 0.87±0.25 mmol/l, p<0.05, respectively), and decreased in L+H groups (p<0.05). The level of SOD in L, L+H, and L+Z groups was significantly lower than that in control group (p<0.05). The level of SOD in L+H group is higher than that in L group (p<0.05). The rate of apoptosis and cardiocyte heart rhythm increased significantly and survival rate was significantly lower in L, L+H, and L+Z groups than those in C group (p<0.05). The level of HO-1 mRNA was higher in L, L+H, and L+Z groups than that in C group (p<0.01), among which L+H group was the highest. The level of HO-1, TNFαAbstract : Objective: To determine whether HO-1 played a important role in the protection of cardiocyte in the lipopolysaccharide-induced acute cardiocyte injury model. Method: Cardiocyte was isolated from SD neonate rat, and was enrolled into C group (normal culture), L group (with stimulation of LPS), L+H group (with stimulation of Hemin (inducer of HO-1), followed by LPS), and L+Z group (with stimulation of ZnPP (inhibitor of HO-1), followed by LPS). The levels of LDH, malondialdehyde (MDA), and superoxide dismutase (SOD) were measured. The cell heart rhythm, survival rate and the apoptosis rate were also examined. The expression of nuclear factor κB (NF-κB), HO-1, and tumour necrosis factor α (TNFα) were measured with RT-PCR, Western blotting and flow cytometry. Results: The level of LDH and MDA were significantly higher in L group than those in C group (113±15 vs 69±10 U/L, p<0.05, and 1.88±0.36 vs 0.87±0.25 mmol/l, p<0.05, respectively), and decreased in L+H groups (p<0.05). The level of SOD in L, L+H, and L+Z groups was significantly lower than that in control group (p<0.05). The level of SOD in L+H group is higher than that in L group (p<0.05). The rate of apoptosis and cardiocyte heart rhythm increased significantly and survival rate was significantly lower in L, L+H, and L+Z groups than those in C group (p<0.05). The level of HO-1 mRNA was higher in L, L+H, and L+Z groups than that in C group (p<0.01), among which L+H group was the highest. The level of HO-1, TNFα and NF-κB in L, L+H, and L+Z groups was also higher than those in C group (p<0.05), among which the level of HO-1 protein in L+H group was the highest, the level of TNFα and NF-κB was the highest in L+Z group. Conclusion: These data therefore suggested that HO-1 provide critical protection against LPS-induced cardiocyte injury. The protection seemed to be mediated through down-regulation of the activity of NF-κB. … (more)
- Is Part Of:
- Heart. Volume 97(2011)Supplement 3
- Journal:
- Heart
- Issue:
- Volume 97(2011)Supplement 3
- Issue Display:
- Volume 97, Issue 3 (2011)
- Year:
- 2011
- Volume:
- 97
- Issue:
- 3
- Issue Sort Value:
- 2011-0097-0003-0000
- Page Start:
- A10
- Page End:
- A10
- Publication Date:
- 2011-10-12
- Subjects:
- Heart -- Diseases -- Treatment -- Periodicals
Cardiology -- Periodicals
616.12 - Journal URLs:
- http://www.bmj.com/archive ↗
http://heart.bmj.com ↗
http://www.heartjnl.com ↗ - DOI:
- 10.1136/heartjnl-2011-300867.28 ↗
- Languages:
- English
- ISSNs:
- 1355-6037
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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- 18529.xml