JTE-607, an Inflammatory Cytokine Synthesis Inhibitor, Attenuates Ischemia/Reperfusion-Induced Renal Injury by Reducing Neutrophil Activation in Rats(GENETICS, MOLECULAR BIOLOGY, AND GENE ENGINEERING)
スポンサーリンク
概要
- 論文の詳細を見る
Renal ischemia/reperfusion (I/R) injury is one of the main causes of postoperative renal failure. Activated neutrophils are implicated in the development of I/R-induced renal failure. JTE-607 has been reported to be a potent inhibitor of the multiple inflammatory cytokines in the endotoxic shock mouse model and heart Langendorff perfusion model. In this study, we examined whether JTE-607 attenuates I/R-induced renal injury by reducing neutrophil activation. Male wistar rats were intravenously administered JTE-607 (JTE group, 30mg/kg) or 5% mannitol (control group) 30min before ischemia. JTE-607 reduced the I/R-induced increases in the serum concentrations of blood urea nitrogen and creatinine, and improved the histopathologic changes, including acute tubular necrosis. I/R-induced an increase in neutrophil activation, reflected by increases in renal cytokine-induced neutrophil chemoattractant (CINC)-1 and myeloperoxidase (MPO) concentrations which were significantly reduced by JTE-607. These findings indicate that JTE-607 attenuates I/R-induced acute renal injury, probably by inhibiting neutrophil activation. JTE-607 might be a novel therapeutic strategy for the protection of postoperative renal failure in surgery associated with renal ischemia as well as renal transplantation.
- 2008-07-25
著者
-
Chujo Kousuke
Department of Anesthesiology, Faculty of Medicine, Kagawa University
-
Asaga Takehiko
Department of Anesthesiology, Faculty of Medicine, Kagawa University
-
Ueki Masaaki
Department of Anesthesiology, Faculty of Medicine, Kagawa University
-
Ueki Masaaki
Department Of Pathology And Host Defense Faculty Of Medicine Kagawa University
-
Ueki Masaaki
Department Of Anesthesiology And Emergency Medicine Kagawa Medical University
-
Chujo Kousuke
Department Of Anesthesiology Faculty Of Medicine Kagawa University
-
Asaga Takehiko
Department Of Anesthesiology Faculty Of Medicine Kagawa University
-
Taie Satoshi
Department of Anesthesiology & Emergency Medicine, Faculty of Medicine, Kagawa University
-
Taie Satoshi
Department Of Anesthesiology And Emergency Medicine Kagawa University School Of Medicine
-
Ueki Masaaki
Department of Anesthesia, Nishiwaki Municipal Hospital:Department of Anesthesia and Perioperative Medicine, Kobe University
-
UEKI Masaaki
Department of Anesthesia, Nishiwaki Municipal Hospital
関連論文
- Atrial natriuretic peptide enhances recovery from ischemia/reperfusion-induced renal injury in rats(GENETICS, MOLECULAR BIOLOGY, AND GENE ENGINEERING)
- Protective Action of D-Ribose against Renal Injury Caused by Ischemia and Reperfusion in Rats with Transient Hyperglycemia
- D-Ribose Attenuated Ischemia/Reperfusion-Induced Renal Injury by Reducing Neutrophil Activation in Rats
- JTE-607, an Inflammatory Cytokine Synthesis Inhibitor, Attenuates Ischemia/Reperfusion-Induced Renal Injury by Reducing Neutrophil Activation in Rats(GENETICS, MOLECULAR BIOLOGY, AND GENE ENGINEERING)
- Atrial Natriuretic Peptide Attenuates Ischemia/Reperfusion-Induced Renal Injury by Reducing Neutrophil Activation in Rats
- D-Allose Protects Against Endotoxemic Acute Renal Injury(GENETICS, MOLECULAR BIOLOGY, AND GENE ENGINEERING)
- Antiadhesive Sites Present in the Fibronectin Type III-Like Repeats of Human Plasma Fibronectin(Molecular and Cell Biology)
- Polyglutamylation of Tubulin during Differentiation of Neural Precursor Cells
- Detection of Sulfated Peptides as Their Onium Salts in the Positive Mode by MALDI-TOF Mass Spectrometry
- N,N'-Dialkyldiamide-Type Phosphate Protecting Groups for Fmoc Synthesis of Phosphotyrosine-Containing Peptides: Optimization of the Alkyl Group^
- A New Efficient Method for S-CH_2-S Bond Formation and Its Application to a Djenkolic Acid-Containing Cyclic Enkephalin Analog
- Synthesis of Cyclic Peptides with S-CH_2-S Bridge Structure
- Amide-type Phosphate Protecting Group for Phosphopeptide Synthesis
- One-pot Deprotection and Coupling of Peptides by the Fmoc Strategy
- Biological Activities of YTIT/YTIY Analogous Sequences Present in Fibronectin-Like Type III Repeats
- Solid Phase Synthesis of α-N- and Side-Chain O-Fully Sulfated Homooligomers of Tyrosine
- Facile New Method for Preparation of Optically Active Protected Proline
- Urinary trypsin inhibitor ameliorates renal tissue oxygenation after ischemic reperfusion in rats
- Urinary Trypsin Inhibitor Reduces Inflammatory Response in Kidney Induced by Lipopolysaccharide(GENETICS, MOLECULAR BIOLOGY, AND GENE ENGINEERING)
- Inhibitory Effect of D-Allose on Neutrophil Activation after Rat Renal Ischemia/Reperfusion(GENETICS, MOLECULAR BIOLOGY, AND GENE ENGINEERING)
- Effects of ulinastatin (urinary trypsin inhibitor) on ATP, intracellular pH, and intracellular sodium transients during ischemia and reperfusion in the rat kidney in vivo
- Effexts of ulinastatin on rat renal energy metabolism and blood flow in hemorrhagic shock
- Direct Detection and Comparison of Non-covalent Complex Formation of Oligo(tyrosine sulfate)s with Synthetic Heparin-binding Peptides by MALDI-TOF-MS
- Analysis of Sulfo- and Phospho-Peptides as Quaternary Ammonium Salts by MALDI-TOF MS
- Solid Phase Synthesis, Characterization and Physical Properties of Oligo(tyrosine sulfate)s
- A Study on Interactions of Oligo(tyrosine sulfate)s with a Heparin-Binding Peptide by MALDI-TOF-MS
- Two New Opioid Delta-Receptor Ligands: A Highly Selective Agonist and a Potent Selective Antagonist in in Vitro Isolated Preparations
- Application of Fmoc-Phosphoarginine Bis(2, 2, 2-trichloroethyl) Ester to Solid Phase Synthesis of Arginine-Containing Peptides
- Solid Phase Synthesis Using N, N'-Isopropylidene-Dipeptides as Acyl Component
- Usefulness of Tetrabutylammonium Salt in Synthesis of Tyrosine Sulfate-Containing Peptides
- CHARACTERISTIC OF ANTINOCICEPTIVE EFFECT OF A TETRAPEPTIDE, Asn-Ala-Gly-Ala (NAGA)
- Identification of the Anti-Adhesive Site Buried within the Heparin-Binding Domain of Fibronectin
- Syntheses of Spacers with the Masked Pac Structure for Fmoc Solid Phase Synthesis
- Preparation of Fluorous-Tagged Active Ester for Rapid Peptide Synthesis
- Protection as Phosphate of Arginine Side-chain Guanidino Group
- A simple modification of the Trachlight for pediatric use
- Preparation of Optically Active L-Indospicine
- S-CH_2-S Bond Forming Intramolecular Cyclization of Penicillamine-containing Peptides
- SUT-8701, a Cholecystokinin Analog, Prevents the Cholinergic Degeneration in the Rat Cerebral Cortex Following Basal Forebrain Lesioning
- Curcumin ameliorates cisplatin-induced nephrotoxicity by inhibiting renal inflammation in mice(BREWING AND FOOD TECHNOLOGY)
- Peptide synthesis in alcohol solvents by the mixed anhydride method using dimethylphosphinothioyl chloride.
- D-Allose Ameliorates Cisplatin-Induced Nephrotoxicity in Mice
- Phosphinyl- and phosphinothioylamino acids and peptides. VIII. New practical removal conditions for the S-Mpt group and their application for the synthesis of bis(N,N-diallyl-(D-Ala2,L-Leu5)-enkephalyl)cystine.
- Phosphinyl- and phosphinothioylamino acids and peptides. IV. Further examples of use of the diphenylphosphinothioyl group for the protection of amino acids.
- Solid phase synthesis of crystalline protected penta-L-tryptophan methyl esters.
- Phosphinyl- and phosphinothioylamino acids and peptides. V. Preparation of dimethylphosphinothioylamino acids and solid phase peptide synthesis.