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Sitagliptin protects rat kidneys from acute ischemia- reperfusion injury via upregulation of GLP-1 and GLP-1 receptors
by
Meng-wei CHANG Chih-hung CHEN Yi-ching CHEN Yin-chun WU Yen-yi ZHEN Steve LEU Tzu-hsien TSAI Sheung-fat KO Pei-hsun SUNG Chih-chau YANG Hsin-ju CHIANG Hsueh-wen CHANG Yen-ta CHEN Hon-kan YIP
in
angiogenesis
/ Animals
/ Biomedical and Life Sciences
/ Biomedicine
/ chronic
/ disease
/ GLP-1
/ Glucagon-Like Peptide 1 - metabolism
/ Glucagon-Like Peptide-1 Receptor
/ Immunology
/ inflammation
/ injury
/ Internal Medicine
/ ischemia
/ kidney
/ Kidney - drug effects
/ Kidney - metabolism
/ Male
/ Medical Microbiology
/ Original
/ original-article
/ oxidative
/ oxygen
/ Pharmacology/Toxicology
/ Pyrazines - pharmacology
/ Rats
/ Rats, Sprague-Dawley
/ reactive
/ Receptors, Glucagon - metabolism
/ reperfusion
/ Reperfusion Injury - drug therapy
/ Reperfusion Injury - metabolism
/ sitagliptin
/ Sitagliptin Phosphate
/ species;apoptosis
/ stress
/ Triazoles - pharmacology
/ Up-Regulation - drug effects
/ Vaccine
2015
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Sitagliptin protects rat kidneys from acute ischemia- reperfusion injury via upregulation of GLP-1 and GLP-1 receptors
by
Meng-wei CHANG Chih-hung CHEN Yi-ching CHEN Yin-chun WU Yen-yi ZHEN Steve LEU Tzu-hsien TSAI Sheung-fat KO Pei-hsun SUNG Chih-chau YANG Hsin-ju CHIANG Hsueh-wen CHANG Yen-ta CHEN Hon-kan YIP
in
angiogenesis
/ Animals
/ Biomedical and Life Sciences
/ Biomedicine
/ chronic
/ disease
/ GLP-1
/ Glucagon-Like Peptide 1 - metabolism
/ Glucagon-Like Peptide-1 Receptor
/ Immunology
/ inflammation
/ injury
/ Internal Medicine
/ ischemia
/ kidney
/ Kidney - drug effects
/ Kidney - metabolism
/ Male
/ Medical Microbiology
/ Original
/ original-article
/ oxidative
/ oxygen
/ Pharmacology/Toxicology
/ Pyrazines - pharmacology
/ Rats
/ Rats, Sprague-Dawley
/ reactive
/ Receptors, Glucagon - metabolism
/ reperfusion
/ Reperfusion Injury - drug therapy
/ Reperfusion Injury - metabolism
/ sitagliptin
/ Sitagliptin Phosphate
/ species;apoptosis
/ stress
/ Triazoles - pharmacology
/ Up-Regulation - drug effects
/ Vaccine
2015
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While trying to remove the title from your shelf something went wrong :( Kindly try again later!
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Sitagliptin protects rat kidneys from acute ischemia- reperfusion injury via upregulation of GLP-1 and GLP-1 receptors
by
Meng-wei CHANG Chih-hung CHEN Yi-ching CHEN Yin-chun WU Yen-yi ZHEN Steve LEU Tzu-hsien TSAI Sheung-fat KO Pei-hsun SUNG Chih-chau YANG Hsin-ju CHIANG Hsueh-wen CHANG Yen-ta CHEN Hon-kan YIP
in
angiogenesis
/ Animals
/ Biomedical and Life Sciences
/ Biomedicine
/ chronic
/ disease
/ GLP-1
/ Glucagon-Like Peptide 1 - metabolism
/ Glucagon-Like Peptide-1 Receptor
/ Immunology
/ inflammation
/ injury
/ Internal Medicine
/ ischemia
/ kidney
/ Kidney - drug effects
/ Kidney - metabolism
/ Male
/ Medical Microbiology
/ Original
/ original-article
/ oxidative
/ oxygen
/ Pharmacology/Toxicology
/ Pyrazines - pharmacology
/ Rats
/ Rats, Sprague-Dawley
/ reactive
/ Receptors, Glucagon - metabolism
/ reperfusion
/ Reperfusion Injury - drug therapy
/ Reperfusion Injury - metabolism
/ sitagliptin
/ Sitagliptin Phosphate
/ species;apoptosis
/ stress
/ Triazoles - pharmacology
/ Up-Regulation - drug effects
/ Vaccine
2015
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Sitagliptin protects rat kidneys from acute ischemia- reperfusion injury via upregulation of GLP-1 and GLP-1 receptors
Journal Article
Sitagliptin protects rat kidneys from acute ischemia- reperfusion injury via upregulation of GLP-1 and GLP-1 receptors
2015
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Overview
Aim: Sitagliptin, an oral glucose-lowering agent, has been found to produce cardiovascular protection possibly via anti-inflammatory and anti-atherosclerotic activities of glucagon-like peptide-1 receptor (GLP-1). The aim of this study was to investigate whether sitagliptin protected the kidney function from acute ischemia-reperfusion (IR) injury in rats. Methods: Adult male SD rats were categorized into 4 groups: sham control, IR injury, IR+sitagliptin (300 mg/kg) and IR+sitagliptin (600 mg/kg). Acute renal IR injury of both kidneys was induced by clamping the renal pedicles for I h. The drug was orally administered at 1, 24 and 48 h after acute IR. Blood samples and 24-h urine were collected before and at 72 h after acute IR. Then the rats were sacrificed, and the kidneys were harvested for biochemical and immunohistochemical studies.
Publisher
Nature Publishing Group UK,Nature Publishing Group
Subject
/ Animals
/ Biomedical and Life Sciences
/ chronic
/ disease
/ GLP-1
/ Glucagon-Like Peptide 1 - metabolism
/ Glucagon-Like Peptide-1 Receptor
/ injury
/ ischemia
/ kidney
/ Male
/ Original
/ oxygen
/ Rats
/ reactive
/ Receptors, Glucagon - metabolism
/ Reperfusion Injury - drug therapy
/ Reperfusion Injury - metabolism
/ stress
/ Up-Regulation - drug effects
/ Vaccine
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