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G F Tseng

Publications and source records attributed to G F Tseng.

21 records · Page 2Linked to original sources

Deep neurons in piriform cortex. II. Membrane properties that underlie unusual synaptic responses.

1. Membrane properties of deep pyramidal and multipolar cells in layer III of the rat piriform cortex and multipolar cells in the underlying endopiriform nucleus (layer IV) were studied in a slice preparation with the primary goal of elucidating the origin of the unusual synaptic responses described in the companion paper. 2. Micropipettes containing either Lucifer yellow (LY) for combined morphological-physiological analysis or potassium acetate (KAc) were used for the analysis. Comparison of membrane properties of pyramidal cells measured with these two electrolytes revealed significant differences. With LY and other Li+ salts, resting membrane potentials were more depolarized, input resistances higher, spike amplitudes lower, and spike durations longer. 3. As measured with KAc-containing electrodes, membrane properties of deep pyramidal and multipolar cells were similar to each other, but differed from those of superficial pyramidal cells. Resting membrane potentials were more depolarized, thresholds lower, input resistances higher, membrane time constants slower, and spikes smaller and slower. 4. In response to depolarizing current pulses, both deep pyramidal and multipolar cells exhibited an initial depolarizing peak of graded amplitude that fell to a steady state within 150 ms. Current-voltage (I-V) relationships displayed a large increase in slope resistance during the depolarizing peak, but were relatively linear in the depolarizing direction at steady state. In cells with relatively hyperpolarized resting membrane potentials, threshold for the depolarizing peak could be -65 mV or below. Based on a reduction by steady depolarization, reduction by Co2+ and potentiation by Ba2+, it is postulated that the peak is generated in part by a low threshold inactivating Ca2+ current. A partial blockage of this peak by tetrodotoxin (TTX) suggests that a Na+ current also contributes. 5. In response to hyperpolarizing current pulses, especially at depolarized membrane potentials, there was usually a sag from an initial maximum and a depolarizing rebound after current offset in both deep pyramidal and multipolar cells. Based on the dependence on membrane potential (Vm), insensitivity to TTX and blockage by carbamylcholine chloride (carbachol), it is postulated that an M-current contributes to the sag and rebound. 6. The depolarizing rebound that followed offset of hyperpolarizing current pulses could trigger a Ba2+-potentiated local response that resembled the depolarizing peak triggered by depolarizing current, suggesting that the postulated low-threshold inactivating Ca2+ current contributes to its generation.(ABSTRACT TRUNCATED AT 400 WORDS)

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Characterization of synaptically mediated fast and slow inhibitory processes in piriform cortex in an in vitro slice preparation.

1. Intracellular recordings were obtained from anatomically verified layer II pyramidal cells in slices from rat piriform cortex cut perpendicular to the surface. 2. Responses to afferent and association fiber stimulation at resting membrane potential consisted of a depolarizing potential followed by a late hyperpolarizing potential (LHP). Membrane polarization by current injection revealed two components in the depolarizing potential: an initial excitatory postsynaptic potential (EPSP) followed at brief latency by an inhibitory postsynaptic potential (IPSP) that inverted with membrane depolarization and truncated the duration of the EPSP. 3. The early IPSP displayed the following characteristics suggesting mediation by gamma-aminobutyric acid (GABA) receptors linked to Cl- channels: associated conductance increase, sensitivity to increases in internal Cl- concentration, blockage by picrotoxin and bicuculline, and potentiation by pentobarbital sodium. The reversal potential was in the depolarizing direction with respect to resting membrane potential so that the inhibitory effect was exclusively via current shunting. 4. The LHP had an associated conductance increase and a reversal potential of -90 mV in normal bathing medium that shifted according to Nernst predictions for a K+ potential with changes in external K+ over the range 4.5-8 mM indicating mediation by the opening of K+ channels and ruling out an electrogenic pump origin. 5. Lack of effect of bath-applied 8-bromoadenosine 3',5'-cyclic monophosphate (8-Br-cAMP) or internally applied ethylene glycol-bis(beta-aminoethyl ether)-N,N,N',N'-tetraacetic acid (EGTA) on the LHP and failure of high amplitude, direct membrane depolarization to evoke a comparable potential, argue against endogenous mediation of the LHP by a Ca2+ activated K+ conductance [gK(Ca)]. However, an apparent endogenously mediated gK(Ca) with a duration much greater than the LHP was observed in a low percent of layer II pyramidal cells. Lack of effect of 8-Br-cAMP also indicates a lack of dependence of the LHP on cAMP. 6. Other characteristics of the LHP that were demonstrated include: a lack of blockage by GABAA receptor antagonists, a probable voltage sensitivity (decrease in amplitude in the depolarizing direction), and an apparent brief onset latency (less than 10 ms) when the early IPSP was blocked by picrotoxin. The LHP was unaffected by pentobarbital sodium when the early IPSP was blocked by picrotoxin. 7. Both the LHP and early IPSP were blocked by low Ca2+/high Mg2+, consistent with disynaptic mediation.(ABSTRACT TRUNCATED AT 400 WORDS)

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A Golgi and ultrastructural analysis of the centromedian nucleus of the cat.

The morphology of neurons in the centromedian nucleus (CM) was studied in rapid Golgi preparations of the adult cat. The ultrastructure of the nucleus, particularly its synaptic organization, was also studied with electron microscopy. The CM contains three types of neurons referred to as principal neurons, Golgi type II neurons, and bushy neurons. Principal neurons are the most numerous, have long dendrites, which branch infrequently, and are divided into two subgroups: principal-A neurons with dendrites that arborize radially, whereas principal-B neurons display horizontal orientations. Both subgroups show a frontal orientation in their dendritic organization and give rise to myelinated axons. Golgi type II neurons with their characteristic sinuous dendrites and unmyelinated axons are thought to be interneurons. The occurrence of bushy neurons in the cat's CM is a new finding. These bushy neurons resemble those of thalamic specific relay nuclei and give rise to myelinated axons. In addition to these three cell types, neurons with intermediate features between these three neuronal types are also described. The ultrastructure of CM neurons resembles, in general, typical central nervous system neurons. Presynaptic profiles are classified into four main categories. SR (small round) boutons are small in size, contain clear, round vesicles, and form asymmetrical synaptic contacts with predominantly small-diameter dendrites. LR (large round) boutons are relatively large and contain both clear and dense-cored vesicles. They interdigitate and form multiple, moderately asymmetrical synapses with their postsynaptic targets. Pale profiles are identified by their relatively electron-light appearance. They contain round vesicles and are thought to be dendritic in origin. The last category of presynaptic profiles is pleomorphic boutons. They contain vesicles of different shapes and are further subdivided into two subtypes: pleomorphic-I ends on soma and dendritic trunks, whereas pleomorphic-II contacts small-diameter dendrites. Both subtypes form symmetrical synapses. The glomeruli of specific thalamic relay nuclei generally contain dendrites, LR boutons, and pale profiles. In addition to these, pleomorphic-II boutons also participate in the formation of the glomerulus of the cat's CM.

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