Non-selective Effects of Amiloride and Its Analogues on Ion Transport Systems and Their Cytotoxicities in Cardiac Myocytes
スポンサーリンク
概要
- 論文の詳細を見る
The effects of amiloride and its analogues (3, 4-dichlorobenzamil (DCB), 2, 4-dimethylbenzamil (DMB), 5-(<I>N</I>-ethyl-<I>N</I>-isopropyl)amiloride (EIPA) and 5-(<I>N</I>-methyl-<I>N</I>-isobutyl)amiloride (MIBA)) on cardiac ion transporters (Na<SUP>+</SUP>/Ca<SUP>2+</SUP> exchanger, Na<SUP>+</SUP>/H<SUP>+</SUP> exchanger, Na<SUP>+</SUP> pump and Ca<SUP>2+</SUP> pump) and their cytotoxicities were tested in cardiac myocytes. All the tested compounds showed concentration-dependent inhibitory effects on the ion transporters studied in canine cardiac sarcolemmal vesicles. The concentrations (μM) of amiloride, DCB, DMB, EIPA and MIBA required to produce 50% inhibition were > 1000, 19, 10, 83 and 84, respectively, for the Na<SUP>+</SUP>/Ca<SUP>2+</SUP> exchanger; 130, 73, 63, 16 and 14 for the Na<SUP>+</SUP>/H<SUP>+</SUP> exchanger; > 1000, 72, > 300, > 300 and > 300 for the Na<SUP>+</SUP> pump; and > 1000, 37, 93, 90 and 70 for the Ca<SUP>2+</SUP> pump, respectively. Furthermore, these agents induced cell death in isolated rat cardiac myocytes and the 50% lethal concentrations (μM) were > 1000, 9.2, 30, 16 and 17, respectively. These findings demonstrate that amiloride and its analogues have non-selective inhibitory effects on cardiac ion transporters and cytotoxicity in cardiomyocytes. When these drugs are employed as experimental tools to investigate the involvement of ion transporters in cell functions, the results must be interpreted with caution.
- 社団法人 日本薬理学会の論文
- 1995-07-01
著者
-
MURATA Yosuke
Department of Pharmacology, Faculty of Pharmaceutical Sciences, Osaka University
-
Murata Yosuke
Department Of Biology New Drug Research Laboratories Kanebo Ltd.
-
NAKAJIMA Fumio
Departments of Urology, National Defense Medical College
-
Nakajima Fumio
Department Of Biology New Drug Research Laboratories Kanebo Ltd.
-
Harada K
Roman Industries Co. Ltd.
-
MORITA Tomonari
Department of Pharmaceutics, Kyoritsu University of Pharmacy
-
Morita Tomonari
Department Of Pharmaceutics Kyoritsu University Of Pharmacy
-
Maruo Joji
New Drug Discovery Research Laboratory Kanebo Ltd.
-
HARADA Kengo
Department of Biology, New Drug Research Laboratories, Kanebo Ltd.
-
MARUO Joji
Department of Biology, New Drug Research Laboratories, Kanebo Ltd.
-
MORITA Tominori
Department of Biology, New Drug Research Laboratories, Kanebo Ltd.
関連論文
- Ouabain : Induced Cell Proliferation in Cultured Rat Astrocytes
- Simultaneous Presentation of Malignant Lymphoma of the Kidney and Multiple Myeloma of the Bone Marrow
- Synthesis and Evaluation of 1-Arylsulfony1-3-piperazinone Derivatives as Factor Xa Inhibitors^ IV. A Series of New Derivatives Containing a Spiro [5H-oxazolo [3, 2-a] pyrazine-2 (3H), 4'-piperidin] -5-one Skeleton
- Synthesis and Evaluation of 1-Arylsulfonyl-3-piperazinone Derivatives as a Factor Xa Inhibitor II. Substituent Effect on Biological Activities
- Clinical features of symptomatic primary biliary cirrhosis initially complicated with esophageal varices
- Clinical characteristics of autoimmune hepatitis in older aged patients
- Quantitative Structure-Activity Relationship Study of N-(3-Oxo-3,4-dihydro-2H-benzo[1,4]thiazine-6-carbonyl)guanidines as Potent Na/H Exchange Inhibitors
- Synthesis and Quantitative Structure-Activity Relationship of N-(3-Oxo-3,4-dihydro-2H-benzo[1,4]oxazine-5-carbonyl)guanidines as Na/H Exchange Inhibitors
- Design, Synthesis and Quantitative Structure-Activity Relationship Study of N-(3-Oxo-3,4-dihydro-2H-benzo[1,4]oxazine-7-carbonyl)guanidine Derivatives as Potent Na/H Exchange Inhibitors
- Structural Requirements for Potent Na/H Exchange Inhibitors Obtained from Quantitative Structure-Activity Relationships of Monocyclic and Bicyclic Aroylguanidines
- Conditionally Immortalized Syncytiotrophoblast Cell Lines as New Tools for Study of the Blood-Placenta Barrier
- Thrombosis in Inferior Vena Cava Due to Enlarged Renal Cysts in Autosomal Dominant Polycystic Kidney Disease
- Liver/spleen volume ratio as a predictor of prognosis in primary biliary cirrhosis
- Early biochemical response to ursodeoxycholic acid predicts symptom development in patients with asymptomatic primary biliary cirrhosis
- Ultimate boundedness of solutions for a generalized Lienard equation with forcing term
- Non-selective Effects of Amiloride and Its Analogues on Ion Transport Systems and Their Cytotoxicities in Cardiac Myocytes
- Oriental Medicinal Herb, Periploca sepium, Extract Inhibits Growth and IL-6 Production of Human Synovial Fibroblast-Like Cells(Pharmacognosy)
- Clinical Profile of Primary Biliary Cirrhosis that was Diagnosed as Symptomatic Primary Biliary Cirrhosis according to the Revised Diagnostic Criteria in Japan
- Value of the 13C-Urea Breath Test for Detection of Gastric Helicobacter spp. Infection in Dogs Undergoing Endoscopic Examination
- A Familial Case of Autoimmune Hepatitis
- Comparison of the cardiovascular and biochemical profiles of a new positive inotropic drug, AR-L 115 BS, with those of theophylline.
- Effects of KB-2796, a New Diphenylpiperazine Calcium Antagonist, on Renal Hemodynamics and Urine Formation in Anesthetized Dogs.
- Improvement of cardiac performance by AR-L 115 BS, a new cardiotonic drug, in the experimental failing dog heart.
- ALMOST PERIODIC GROSS-SUBSTITUTE DYNAMICAL SYSTEMS