multibarrel Search Results


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Carl Zeiss multibarrel perfusion apparatus
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Harvard Bioscience multibarrel pipette
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ALA Scientific Instruments multibarrelled local superfusion device
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MicroData Instrument Inc multibarreled glass capillary unit
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HEKA Electronics Incorporated multibarrel concentration-clamp device
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MicroData Instrument Inc multibarreled glass capillary unit microdata instruments
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Protech Technology Enterprise glass multibarrel recording pipette
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ALA Scientific Instruments multibarrel gravity-feed system
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Burleigh Instruments multibarrel flow pipe
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Sybron Corporation multibarrel micropipette
Transplantation of fetal mesencephalic tissue into the SN followed by KA bridging from the SN to the striatum restores the release and clearance of DA in the striatum 6–8 weeks after transplantation. A1, Local application of KCl (70 mm, 125 nl) (arrows) to the control nonlesioned striatum induces DA release. KCl is applied locally through a <t>multibarrel</t> pipette placed in the striatum of the rat. Extracellular DA concentration is recorded using Nafion-coated carbon fiber electrode. Upper trace, OX represents the extracellular signal from DA oxidation. The ratios of reduction (lower trace, RED) to oxidation currents are used to qualitatively identify the electroactive species as DA.A2, K+-induced DA overflow is abolished in the lesioned striatum and is restored in the lesioned striatum with a KA-bridged transplant (nigra to striatum) (A3). The peak of DA overflow (mean ± SEM) induced by K+stimulation is restored in the 6-OHDA-lesioned striatum from six transplanted animals. B1, Local application of DA (200 μm, 200 nl) (arrows) to the control nonlesioned striatum resulted in a retention of ∼6 μmDA overflow. B2, The extracellular DA concentration is increased after a 6-OHDA lesion (B2 vs B1) and is reduced in the lesioned striatum with a KA-bridged transplant (B3).C, A much broader area of DA release in the lesioned striatum is achieved by the KA-bridged transplant. A 2 × 3 × 3 mm striatal field is found responsible to K+ to release DA, with a higher release near the needle track.D, Restoration of DA clearance in transplanted animals.Open and filled bars represent peak extracellular DA concentrations in the lesioned and bridged striatum from six animals, respectively. The KA-bridged transplant diminishes the increase in DA overflow induced by local application of DA into the lesioned striatum (*p < 0.01, ttest).
Multibarrel Micropipette, supplied by Sybron Corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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SA Instruments multibarrel pipettes were advanced into the brain
Transplantation of fetal mesencephalic tissue into the SN followed by KA bridging from the SN to the striatum restores the release and clearance of DA in the striatum 6–8 weeks after transplantation. A1, Local application of KCl (70 mm, 125 nl) (arrows) to the control nonlesioned striatum induces DA release. KCl is applied locally through a <t>multibarrel</t> pipette placed in the striatum of the rat. Extracellular DA concentration is recorded using Nafion-coated carbon fiber electrode. Upper trace, OX represents the extracellular signal from DA oxidation. The ratios of reduction (lower trace, RED) to oxidation currents are used to qualitatively identify the electroactive species as DA.A2, K+-induced DA overflow is abolished in the lesioned striatum and is restored in the lesioned striatum with a KA-bridged transplant (nigra to striatum) (A3). The peak of DA overflow (mean ± SEM) induced by K+stimulation is restored in the 6-OHDA-lesioned striatum from six transplanted animals. B1, Local application of DA (200 μm, 200 nl) (arrows) to the control nonlesioned striatum resulted in a retention of ∼6 μmDA overflow. B2, The extracellular DA concentration is increased after a 6-OHDA lesion (B2 vs B1) and is reduced in the lesioned striatum with a KA-bridged transplant (B3).C, A much broader area of DA release in the lesioned striatum is achieved by the KA-bridged transplant. A 2 × 3 × 3 mm striatal field is found responsible to K+ to release DA, with a higher release near the needle track.D, Restoration of DA clearance in transplanted animals.Open and filled bars represent peak extracellular DA concentrations in the lesioned and bridged striatum from six animals, respectively. The KA-bridged transplant diminishes the increase in DA overflow induced by local application of DA into the lesioned striatum (*p < 0.01, ttest).
Multibarrel Pipettes Were Advanced Into The Brain, supplied by SA Instruments, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Transplantation of fetal mesencephalic tissue into the SN followed by KA bridging from the SN to the striatum restores the release and clearance of DA in the striatum 6–8 weeks after transplantation. A1, Local application of KCl (70 mm, 125 nl) (arrows) to the control nonlesioned striatum induces DA release. KCl is applied locally through a multibarrel pipette placed in the striatum of the rat. Extracellular DA concentration is recorded using Nafion-coated carbon fiber electrode. Upper trace, OX represents the extracellular signal from DA oxidation. The ratios of reduction (lower trace, RED) to oxidation currents are used to qualitatively identify the electroactive species as DA.A2, K+-induced DA overflow is abolished in the lesioned striatum and is restored in the lesioned striatum with a KA-bridged transplant (nigra to striatum) (A3). The peak of DA overflow (mean ± SEM) induced by K+stimulation is restored in the 6-OHDA-lesioned striatum from six transplanted animals. B1, Local application of DA (200 μm, 200 nl) (arrows) to the control nonlesioned striatum resulted in a retention of ∼6 μmDA overflow. B2, The extracellular DA concentration is increased after a 6-OHDA lesion (B2 vs B1) and is reduced in the lesioned striatum with a KA-bridged transplant (B3).C, A much broader area of DA release in the lesioned striatum is achieved by the KA-bridged transplant. A 2 × 3 × 3 mm striatal field is found responsible to K+ to release DA, with a higher release near the needle track.D, Restoration of DA clearance in transplanted animals.Open and filled bars represent peak extracellular DA concentrations in the lesioned and bridged striatum from six animals, respectively. The KA-bridged transplant diminishes the increase in DA overflow induced by local application of DA into the lesioned striatum (*p < 0.01, ttest).

Journal: The Journal of Neuroscience

Article Title: Constructing a New Nigrostriatal Pathway in the Parkinsonian Model with Bridged Neural Transplantation in Substantia Nigra

doi: 10.1523/JNEUROSCI.16-21-06965.1996

Figure Lengend Snippet: Transplantation of fetal mesencephalic tissue into the SN followed by KA bridging from the SN to the striatum restores the release and clearance of DA in the striatum 6–8 weeks after transplantation. A1, Local application of KCl (70 mm, 125 nl) (arrows) to the control nonlesioned striatum induces DA release. KCl is applied locally through a multibarrel pipette placed in the striatum of the rat. Extracellular DA concentration is recorded using Nafion-coated carbon fiber electrode. Upper trace, OX represents the extracellular signal from DA oxidation. The ratios of reduction (lower trace, RED) to oxidation currents are used to qualitatively identify the electroactive species as DA.A2, K+-induced DA overflow is abolished in the lesioned striatum and is restored in the lesioned striatum with a KA-bridged transplant (nigra to striatum) (A3). The peak of DA overflow (mean ± SEM) induced by K+stimulation is restored in the 6-OHDA-lesioned striatum from six transplanted animals. B1, Local application of DA (200 μm, 200 nl) (arrows) to the control nonlesioned striatum resulted in a retention of ∼6 μmDA overflow. B2, The extracellular DA concentration is increased after a 6-OHDA lesion (B2 vs B1) and is reduced in the lesioned striatum with a KA-bridged transplant (B3).C, A much broader area of DA release in the lesioned striatum is achieved by the KA-bridged transplant. A 2 × 3 × 3 mm striatal field is found responsible to K+ to release DA, with a higher release near the needle track.D, Restoration of DA clearance in transplanted animals.Open and filled bars represent peak extracellular DA concentrations in the lesioned and bridged striatum from six animals, respectively. The KA-bridged transplant diminishes the increase in DA overflow induced by local application of DA into the lesioned striatum (*p < 0.01, ttest).

Article Snippet: The working electrode and the multibarrel micropipette were mounted together with sticky wax (Kerr, Sybron, CA); the tips were separated by 200 μm.

Techniques: Transplantation Assay, Control, Transferring, Concentration Assay