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2-Amino-5-phosphonovalerate (2 Amino 5 phosphonovalerate)

84  relevant articles (4 outcomes, 5 trials/studies) found for this Bio-Agent

Description: The D-enantiomer is a potent and specific antagonist of NMDA glutamate receptors (RECEPTORS, N-METHYL-D-ASPARTATE). The L form is inactive at NMDA receptors but may affect the AP4 (2-amino-4-phosphonobutyrate; APB) excitatory amino acid receptors.

Also Known As:
2 Amino 5 phosphonovalerate; 2 Amino 5 phosphonopentanoate; 2-APV; 2-Amino-5-phosphonopentanoate; 5-Phosphononorvaline; d-APV; dl-APV; 2 Amino 5 phosphonopentanoic Acid; 2 Amino 5 phosphonovaleric Acid; 5 Phosphononorvaline; 2-Amino-5-phosphonopentanoic Acid; 2-Amino-5-phosphonovaleric Acid; Norvaline, 5-phosphono-

Relationship Network

Bio-Agent Context: Research Results

Experts

1. Lu, Ying: 1 article (03/2003)
2. Vera-Portocarrero, Louis P: 1 article (03/2003)
3. Westlund, Karin N: 1 article (03/2003)

Related Diseases

1. Seizures (Seizure)
2. Pancreatitis
3. Anoxia (Hypoxia)
4. Ischemia
09/19/1994 - "The PIP was not affected by 2-amino-5-phosphonovalerate (APV) administered via microdialysis at 7 h post-ischemia"
08/04/1986 - "D-APV reduced the extracellular accumulation of all measured purine catabolites during ischemia/reflow and improved to some extent the recovery of the striatal electroencephalographic activity in the majority of the animals"
04/01/1991 - "Blockade of N-methyl-D-aspartate-sensitive excitatory amino acid receptors with 2-amino-5-phosphonovalerate reduces ischemia-evoked calcium redistribution in rabbit hippocampus."
04/01/1991 - "To evaluate the participation of excitatory amino acid receptors sensitive to N-methyl-D-aspartate (NMDA) in ischemia-evoked redistribution of Ca2+ ions from the extra- to the intracellular compartment of the hippocampus, 2-amino-5-phosphonovalerate (APV), a specific antagonist of NMDA receptors, was administered to the rabbit hippocampus through a dialysis probe before, during, and after complete reversible 15-min cerebral ischemia"
02/01/1994 - "The effects of the following drugs: nimodipine (1 mg/kg b.w., i.p.), 2-amino-5-phosphonovaleric acid (4 mg/kg b.w., i.p.) and propentofylline (25 mg/kg b.w., i.p.), administered (alone or in combination) at the end of 15 min bilateral ischemia in gerbils were evaluated on mitochondrial superoxide dismutase (SOD), glutathione reductase (GR), glucose-6 phosphate dehydrogenase (G6PD), monoamine oxidase (MAO) activities, and thiobarbituric acid reactive material (TBARM), and brain water content at 1 hour of reperfusion"
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5. Hyperalgesia
05/01/1997 - "Treatment with D-APV, but not saline, in the contralateral (but not ipsilateral) thalamus significantly reduced both the acute thermal and mechanical hyperalgesia in the injected paw; these same rats demonstrated significantly less thermal and mechanical hyperalgesia in the sub-acute phase than rats that had received saline or D-APV in the ipsilateral thalamus"
04/01/2003 - "There are four principle findings: 1) PDR as well as CCD and CCI induced thermal hyperalgesia; 2) PDR produced significantly less severe and shorter duration hyperalgesia than CCD and CCI; 3) intrathecal administration of NMDA receptor antagonists d-2-amino-5-phosphonovaleric acid (APV) and dizocilpine maleate (MK-801) inhibited thermal hyperalgesia in PDR, CCD, and CCI rats"
10/01/1996 - "The spinally-induced PGE2 hyperalgesia was antagonized by intrathecal injections (9 micrograms) of AP5 (2-amino-5-phosphonopentanoate/2-amino-5) a selective NMDA receptor antagonist"
11/01/2002 - "co-administration of the NMDA receptor antagonist D(-)-2-amino-5-phosphonovaleric acid (D-APV) with BDNF dose-dependently inhibits BDNF-induced hyperalgesia, suggesting that BDNF induces acute hyperalgesic responses and affects central sensitization in a process dependent on NMDA receptor activation."
05/01/1999 - "Furthermore, thermal hyperalgesia was significantly inhibited by the N-methyl-D-aspartate (NMDA) receptor antagonists, 2-amino-5-phosphonopentanoate (APV), dizocilpine and ifenprodil"
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Related Drugs and Biologics

1. N-Methylaspartate (NMDA)
2. Morphine (MS Contin)
3. 2-amino-7-phosphonoheptanoic acid
4. Aminophylline (Carine)
5. purine
6. Dizocilpine Maleate (Dizocilpine)
7. NG-Nitroarginine Methyl Ester (L-NAME)
8. Nitric Oxide Synthase (NO Synthase)
9. mu Opioid Receptors (mu Opioid Receptor)
10. Freund's Adjuvant

Related Therapies and Procedures

1. Electrodes (Electrode)
2. Electroacupuncture

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