Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
Add more filters










Database
Publication year range
1.
Neurosci Lett ; 636: 270-275, 2017 01 01.
Article in English | MEDLINE | ID: mdl-27984198

ABSTRACT

Pregabalin (PGB) is a chemical derivative of the inhibitory neurotransmitter γ-aminobutyric acid, and is successfully used for the treatment of neuropathic pain. Substantial evidence suggests that d-serine, an endogenous co-agonist at the strychnine-insensitive glycine site of the NMDA receptor, counteracts the antinociceptive actions of PGB at the level of the spinal cord. In the present study, we examined the impact of PGB treatment on spinal d-serine content and NMDA receptor-mediated synaptic transmission in the superficial dorsal horn of peripheral nerve-ligated neuropathic mice. Mechanical allodynia was assessed using von Frey filaments. On post-surgical day 9 (after 5days of treatment with PGB [50mg/kg] or saline vehicle), the lumbar spinal cord was removed, homogenized, and ultrafiltrated. Supernatant samples were treated with Marfey's reagent and analyzed with liquid chromatography-mass spectrometry to measure d-serine content. In the electrophysiological experiments, tight-seal whole-cell recording was performed on neurons in the superficial dorsal horn of spinal cord slices. Partial sciatic nerve ligation increased spinal d-serine content, increased the NMDA/non-NMDA ratio of EPSC amplitudes, and slowed the decay phase of the NMDA component of EPSCs (NMDA-EPSCs). PGB treatment attenuated mechanical allodynia and reduced spinal d-serine content, decreased the NMDA/non-NMDA ratio, and shortened the decay time of NMDA-EPSCs. Furthermore, bath-applied d-serine attenuated the effects of PGB treatment. Although the precise mechanism for the effect of PGB on d-serine metabolism and abundance is unknown, the antinociceptive action of PGB likely involves the reduction of spinal d-serine content and subsequent attenuation of NMDA receptor-mediated synaptic transmission in the superficial dorsal horn.


Subject(s)
Excitatory Postsynaptic Potentials/drug effects , Neuralgia/drug therapy , Neurons/drug effects , Pregabalin/pharmacology , Receptors, N-Methyl-D-Aspartate/drug effects , Synaptic Transmission/drug effects , Animals , Disease Models, Animal , Male , Mice , Neuralgia/metabolism , Neurons/metabolism , Serine/metabolism , gamma-Aminobutyric Acid/metabolism
2.
Neurosci Lett ; 558: 186-91, 2014 Jan 13.
Article in English | MEDLINE | ID: mdl-24269977

ABSTRACT

Pregabalin is widely used as an analgesic for the treatment of neuropathic pain. In the present experiments using mouse spinal slices, we recorded electrically evoked glutamatergic excitatory postsynaptic currents (eEPSCs) from superficial dorsal horn neurons. Pregabalin reduced the amplitude of eEPSCs, and increased the paired pulse ratio. Pregabalin also inhibited the frequency of spontaneously occurring miniature EPSCs without affecting their amplitude. Partial ligation of the sciatic nerve increased the expression of the calcium channel α2δ-1 subunit, and increased the presynaptic inhibitory action of pregabalin. Intrathecal injection of antisense oligodeoxynucleotide against the α2δ-1 subunit, decreased the expression of α2δ-1 mRNA in the spinal dorsal horn, and decreased pregabalin's action. These results provide further evidence that pregabalin exerts its presynaptic inhibitory action via binding with the α2δ subunit in a state-dependent manner. Furthermore, presynaptic actions of pregabalin were attenuated in knockout mice lacking the protein syntaxin 1A, a component of the synaptic vesicle release machinery, indicating that syntaxin 1A is required for pregabalin to exert its full presynaptic inhibitory action. These observations might suggest that direct and/or indirect interactions with the presynaptic proteins composing the release machinery underlie at least some part of pregabalin's presynaptic actions.


Subject(s)
Analgesics/pharmacology , Posterior Horn Cells/drug effects , Syntaxin 1/genetics , gamma-Aminobutyric Acid/analogs & derivatives , Animals , Calcium Channels/genetics , Calcium Channels/metabolism , Excitatory Postsynaptic Potentials/drug effects , In Vitro Techniques , Mice, Knockout , Miniature Postsynaptic Potentials/drug effects , Oligonucleotides, Antisense/pharmacology , Posterior Horn Cells/physiology , Pregabalin , Protein Subunits/genetics , Protein Subunits/metabolism , RNA, Messenger/metabolism , Sciatic Nerve/injuries , Synaptic Transmission/drug effects , gamma-Aminobutyric Acid/pharmacology
3.
Nihon Hoshasen Gijutsu Gakkai Zasshi ; 60(12): 1682-7, 2004 Dec.
Article in Japanese | MEDLINE | ID: mdl-15614219

ABSTRACT

To determine the effective lead thickness of the apron for radiation protective clothing, i.e., the lead equivalent, a method of performing the lead equivalent examination is provided in the Japanese Industrial Standards (JIS). We proposed a method of computation using an attenuation coefficient, and examined the measurement accuracy and optimal radiation quality using both methods. We were able to compute the lead equivalent with sufficient accuracy when using radiation quality of about 60 keV in the range of radiation quality examined. This technique was also examined in the measurement used for the marketing of radiation protective clothing.


Subject(s)
Protective Clothing/standards , Radiation Dosage , Radiation Protection/instrumentation , Lead
SELECTION OF CITATIONS
SEARCH DETAIL
...