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      Intracisternal or intrathecal glycine, taurine, or muscimol inhibit bicuculline-induced allodynia and thermal hyperalgesia in mice

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          Abstract

          Aim:

          To investigate the effects of GABA and glycine on analgesia in the central nervous system.

          Methods:

          Glycine, taurine, or muscimol was injected with bicuculline into the cistern magna or the lumbar subarachnoidal space in ICR mice. The effects on bicuculline-induced allodynia in a touch-evoked agitation test and on pain threshold index in a hot-plate test were assessed.

          Results:

          The dosages of the amino acids administered with bicuculline had no effect on motor behavior in conscious mice. Glycine or muscimol reduced bicuculline-induced allodynia regardless of the administration site, whereas intrathecal taurine reduced bicuculline-induced allodynia. Glycine, taurine, and muscimol all antagonized the effects induced by bicuculline in the hot-plate test, regardless of the administration site.

          Conclusion:

          Glycine, taurine, and muscimol were found to have anti-allodynic and anti-thermal hyperalgesic properties in vivo. These observations suggest an interaction between glycine and GABA receptors during the regulation of antinociception.

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          Most cited references26

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          Intrathecal morphine in mice: a new technique.

          A simple, rapid technique for intrathecal injections by lumbar puncture in unanesthetized mice is described. Intrathecal [3H]morphine base was not found in significant quantities in either the midbrain or forebrain. Submicrogram quantities of morphine sulfate induced Straub tail response and tail-flick analgesia. These effects were dose related and antagonized by subcutaneous naloxone.
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            Corelease of two fast neurotransmitters at a central synapse.

            It is widely accepted that individual neurons in the central nervous system release only a single fast transmitter. The possibility of corelease of fast neurotransmitters was examined by making paired recordings from synaptically connected neurons in spinal cord slices. Unitary inhibitory postsynaptic currents generated at interneuron-motoneuron synapses consisted of a strychnine-sensitive, glycine receptor-mediated component and a bicuculline-sensitive, gamma-aminobutyric acid (GABA)A receptor-mediated component. These results indicate that spinal interneurons release both glycine and GABA to activate functionally distinct receptors in their postsynaptic target cells. A subset of miniature synaptic currents also showed both components, consistent with corelease from individual synaptic vesicles.
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              • Record: found
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              • Article: not found

              The excitation and depression of spinal neurones by structurally related amino acids.

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                Author and article information

                Journal
                Acta Pharmacol Sin
                Acta Pharmacol. Sin
                Acta Pharmacologica Sinica
                Nature Publishing Group
                1671-4083
                1745-7254
                August 2010
                05 August 2010
                : 31
                : 8
                : 907-914
                Affiliations
                [1 ]Departments of Anesthesiology and Pain Medicine, College of Medicine, Korea University , Seoul, Republic of Korea
                [2 ]Anesthesiologist, Departments of Anesthesiology and Pain Medicine, College of Medicine, Korea University , Seoul, Republic of Korea
                Author notes
                Article
                aps201082
                10.1038/aps.2010.82
                4007821
                20686515
                0d461a37-28c7-4ae8-9ece-abd313d47b6e
                Copyright © 2010 CPS and SIMM
                History
                : 25 January 2010
                : 10 June 2010
                Categories
                Original Article

                Pharmacology & Pharmaceutical medicine
                allodynia,hyperalgesia,bicuculline,glycine,intracisternal,intrathecal drug delivery

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