TY - JOUR
T1 - Patch-clamp recordings of spiking and nonspiking interneurons from rabbit olfactory bulb slices
T2 - GABA- and other transmitter receptors
AU - Bufler, Johannes
AU - Zufall, Frank
AU - Franke, Christian
AU - Hatt, Hanns
PY - 1992/2
Y1 - 1992/2
N2 - Transmitter receptor ion channels from previously identified rabbit olfactory bulb neurons were studied by using a thin slice preparation in combination with patch-clamp measurements. PG cells, which closely resembled previously described periglomerular interneurons in their morphology, responded to microapplication of GABA, acetylcholine, norepinephrine and glycine with the activation of distinct ionic currents. JG cells, which belong either to the class of short axon cells or external tufted cells, never showed GABA responses. In mitral cells ionic currents activated by GABA, acetylcholine, norepinephrine and glutamate could be elicited. Further measurements of GABA-activated currents of PG cells were made and indicated that these cells expressed two different types of GABA receptors: one which showed fast desensitization with a decay time constant of about 5 s, and one which slowly desensitized with a decay time constant of about 20-30 s. Both types were completely inhibited by bicuculline methiodide (50 μM). GABA receptors were not blocked by Zn2+ (0.1 m M). From the dose-response relationship of the peak GABA-activated currents, an apparent dissociation constant of 50 μM was derived. From single channel measurements in excised outside-out patches, a single channel conductance of GABA-activated Cl- currents of 24 pS was obtained during continuous application of the agonist. Single channel events had a mean open time of 1.9 ms.
AB - Transmitter receptor ion channels from previously identified rabbit olfactory bulb neurons were studied by using a thin slice preparation in combination with patch-clamp measurements. PG cells, which closely resembled previously described periglomerular interneurons in their morphology, responded to microapplication of GABA, acetylcholine, norepinephrine and glycine with the activation of distinct ionic currents. JG cells, which belong either to the class of short axon cells or external tufted cells, never showed GABA responses. In mitral cells ionic currents activated by GABA, acetylcholine, norepinephrine and glutamate could be elicited. Further measurements of GABA-activated currents of PG cells were made and indicated that these cells expressed two different types of GABA receptors: one which showed fast desensitization with a decay time constant of about 5 s, and one which slowly desensitized with a decay time constant of about 20-30 s. Both types were completely inhibited by bicuculline methiodide (50 μM). GABA receptors were not blocked by Zn2+ (0.1 m M). From the dose-response relationship of the peak GABA-activated currents, an apparent dissociation constant of 50 μM was derived. From single channel measurements in excised outside-out patches, a single channel conductance of GABA-activated Cl- currents of 24 pS was obtained during continuous application of the agonist. Single channel events had a mean open time of 1.9 ms.
KW - GABA-activated ion channels
KW - Nonspiking interneuron
KW - Olfactory bulb slices
KW - Rabbit
KW - Transmitter receptors
UR - http://www.scopus.com/inward/record.url?scp=0026814722&partnerID=8YFLogxK
U2 - 10.1007/BF00196897
DO - 10.1007/BF00196897
M3 - Article
C2 - 1374799
AN - SCOPUS:0026814722
SN - 0340-7594
VL - 170
SP - 153
EP - 159
JO - Journal of Comparative Physiology A
JF - Journal of Comparative Physiology A
IS - 2
ER -