Abstract
In the present study, we hypothesized that endotoxemia produces metalloendopeptidase (MEPD)-dependent generation of endothelin-1 (ET-1) and alters NOS expression correlating with p38-mitogen-activated protein kinase (MAPK) phosphorylation in thoracic aorta. Male Sprague-Dawley rats (350-400 g) were subjected to two groups randomly; sham-treated (N = 10) and lipopolysaccharide (LPS)-treated (N = 10) (E. coli LPS 2 mg/kg bolus + 2 mg/kg infusion for 30 min). The animals in each group were further subdivided into vehicle and MEPD inhibitor phosphoramidon (1 mg/kg bolus, PHOS)-treated groups. LPS produces a significant decrease in mean arterial pressure (MAP) at 2 h post endotoxemia that was blocked by PHOS. PHOS attenuated LPS-induced increase in tumor necrosis factor-alpha (TNF-α) concentration at 2- and 24 h post-LPS administration. LPS significantly elevated plasma concentrations of ET-1 at 2- and 24 h post endotoxemia. An upregulated preproET-1 expression following both LPS and MEPD inhibition was observed in thoracic aorta at 2 h post treatment. PHOS effectively blocked conversion of preproET-1 to ET-1 in thoracic aorta locally at 24 h post treatment in endotoxic rats. PHOS inhibited LPS-induced upregulation of inducible NOS (iNOS), downregulation of endothelial NOS (eNOS) and elevation of NO byproducts (NO x) in thoracic aorta. PHOS also blocked LPS-induced upregulated p38-MAPK phosphorylation in thoracic aorta at 24 h post endotoxemia. The data revealed that LPS induces MEPD-sensitive inflammatory response syndrome (SIRS) at 2- and 24 h post endotoxemia. We concluded that inhibition of MEPD not only decreases the levels of ET-1 but also simultaneously downregulates protein expression of iNOS and phosphorylated p38-MAPK while increasing eNOS in thoracic aorta during SIRS in endotoxemia. We suggest that MEPD-dependent ET-1 and NO mechanisms may be involved in endotoxemia-induced altered p38-MAPK phosphorylation. © 2004 Kluwer Academic Publishers.
Original language | American English |
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Journal | Molecular and cellular biochemistry |
Volume | 265 |
State | Published - Jan 1 2004 |
Keywords
- Animalia
- Animals
- Aorta
- Biological
- Cytokine
- Cytokines
- Endothelin
- Endothelin-1
- Glycopeptides
- Lipopolysaccharide
- Lipopolysaccharides
- Metalloendopeptidases
- Models
- Nitric Oxide Synthase Type II
- Nitric Oxide Synthase Type III
- Nos2 protein
- Nos3 protein
- Rats
- Signaling
- Sprague Dawley rat
- Sprague-Dawley
- Systemic hemodynamic
- TNF-α
- Thoracic
- Time Factors
- Up-Regulation
- animal
- animal tissue
- article
- biological model
- biosynthesis
- blood pressure
- chemistry
- clinical trial
- controlled clinical trial
- controlled study
- drug effect
- drug inhibition
- drug mechanism
- endothelial nitric oxide synthase
- endothelin 1
- endothelium cell
- endotoxemia
- enzyme activity
- enzyme phosphorylation
- enzymology
- glycopeptide
- hemodynamics
- immunoblotting
- inducible nitric oxide synthase
- inflammation
- male
- mean arterial pressure
- metabolism
- metalloproteinase
- metalloproteinase inhibitor
- mitogen activated protein kinase p38
- nitric oxide
- nitric oxide synthase
- nonhuman
- p38 Mitogen-Activated Protein Kinases
- pathology
- phosphoramidon
- phosphorylation
- protein expression
- protein synthesis
- randomized controlled trial
- rat
- regulatory mechanism
- signal transduction
- thoracic aorta
- time
- tumor necrosis factor alpha
- upregulation
Disciplines
- Life Sciences