Niflumic Acid Activates Additional Currents of the Human Glial L-Glutamate Transporter EAAT1 in a Substrate-Dependent Manner
スポンサーリンク
概要
- 論文の詳細を見る
The astrocytic <span style="font-variant: small-caps;">L</span>-glutamate (<span style="font-variant: small-caps;">L</span>-Glu) transporter EAAT1 participates in the removal of <span style="font-variant: small-caps;">L</span>-Glu from the synaptic cleft and maintenance of non-toxic concentrations in the extracellular fluid. We have shown that niflumic acid (NFA), a non-steroidal anti-inflammatory drug (NSAIDs), alters <span style="font-variant: small-caps;">L</span>-Glu-induced EAAT1 currents in a voltage-dependent manner using the two-electrode voltage clamp technique in Xenopus oocytes expressing EAAT1. In this study, we characterised the effects of NFA on each type of ion-flux through EAAT1. NFA modulated currents induced by both <span style="font-variant: small-caps;">L</span>-Glu and <span style="font-variant: small-caps;">L</span>-aspartate (<span style="font-variant: small-caps;">L</span>-Asp) in a voltage-dependent manner. Ion-substitution experiments revealed that the activation of additional H+ conductance was involved in the modulation of currents induced by <span style="font-variant: small-caps;">L</span>-Asp and <span style="font-variant: small-caps;">L</span>-Glu, but Cl− was involved only with the <span style="font-variant: small-caps;">L</span>-Asp currents. NFA activated additional currents of EAAT1 in a substrate-dependent manner.
- 公益社団法人 日本薬学会の論文
著者
-
Ishii-nozawa Reiko
Department Of Clinical Pharmacology Meiji Pharmaceutical University
-
Takeuchi Koichi
Department Of Anatomy
-
SEKINO Yuko
Laboratory of Neurochemistry, National Institiute for Physiological Sciences
-
Sekino Yuko
Laboratory of Neuropharmacology, Division of Pharmacology, National Institute of Health Sciences
-
Takahashi Kanako
Laboratory of Neuropharmacology, Division of Pharmacology, National Institute of Health Sciences
-
Nakazawa Ken
Laboratory of Neuropharmacology, Division of Pharmacology, National Institute of Health Sciences
-
Sato Kaoru
Laboratory of Neuropharmacology, Division of Pharmacology, National Institute of Health Sciences
関連論文
- PJ-379 Intracellular Signaling Pathways for an Anti-apoptotic Effect of Endothelin-1 in Cardiomyocytes(Apoptosis/Necrosis/Regeneration 1 (M) : PJ63)(Poster Session (Japanese))
- Effects of Dermatan and Dextran Sulfates on Arginine Amidase Activity Released from Isolated Rabbit Arteries
- OJ-196 AAV-mediated IL-10-gene Transfer into Apolipoprotein E-deficient Mice Inhibits Atherosclerosis through Anti-inflammatory and Cholesterol-lowering Effects(Atherosclerosis, Basic 2 (IHD) : OJ22)(Oral Presentation (Japanese))
- Involvement of c-Src-Bcl-xL Pathway in Anti-apoptotic Effects of Endothelin in Rat Cultured Cardiac Myocytes
- Interleukin-10 Prevents Atherogenesis through Inhibition of MCP-1 Expression and Correction of Lipoprotein Metabolism in Apo E-Deficient Mice
- Efficient Transduction of Primate Embryonic Stem Cell-Derived Cardiomyocytes Using a Simian Immunodeficiency Virus Vector
- Two Non-steroidal Anti-inflammatory Drugs, Niflumic Acid and Diclofenac, Inhibit the Human Glutamate Transporter EAAT1 Through Different Mechanisms
- Collection of Medical Drug Information in Pharmacies : Drug Event Monitoring (DEM) in Japan
- Effect of Dextran Derivatives on Arginine Amidase Activities Released from Isolated Rabbit Arteries
- Effect of Chondroitinase on Dermatan Sulfate-Facilitated Arginine Amidase Released from Rabbit Ear Artery
- Dysfunction of Neurotransmitter Modulation System on Adrenergic Nerves of Caudal Artery in Type 2 Diabetic Goto–Kakizaki Rats
- Stimulus-Transcription Coupling can be studied by in situ Hybridization of Brain Slice Preparation. Selective c-fos Expression in Hippocampal CA3 Pyramidal Cells.
- Detection of Arginine Amidases Released from Isolated Rabbit Arteries
- Niflumic Acid Activates Additional Currents of the Human Glial L-Glutamate Transporter EAAT1 in a Substrate-Dependent Manner
- Comparative gene expression analysis of the amygdala in autistic rat models produced by pre- and post-natal exposures to valproic acid