Membrane properties of rat medial septum neurons

1992 ◽  
Vol 17 ◽  
pp. 61 ◽  
Author(s):  
Masashi Tsurusaki ◽  
Takashi Akasu ◽  
Joel P. Gallacher
Keyword(s):  
Medial Septum ◽  
Membrane Properties

scholarly journals Septohippocampal transmission from parvalbumin-positive neurons features rapid recovery from synaptic depression

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Feng Yi ◽  
Tavita Garrett ◽  
Karl Deisseroth ◽  
Heikki Haario ◽  
Emily Stone ◽  
...  
Keyword(s):  
Pyramidal Neurons ◽  
Synaptic Depression ◽  
Medial Septum ◽  
Membrane Properties ◽  
Projection Neurons ◽  
Calcium Dependent ◽  
Light Pulses ◽  
Diagonal Band ◽  
Initial Release ◽  
Intrinsic Membrane Properties

AbstractParvalbumin-containing projection neurons of the medial-septum-diagonal band of Broca ($$\hbox {PV}_{\text{MS-DBB}}$$ PV MS-DBB ) are essential for hippocampal rhythms and learning operations yet are poorly understood at cellular and synaptic levels. We combined electrophysiological, optogenetic, and modeling approaches to investigate $$\hbox {PV}_{\text{MS-DBB}}$$ PV MS-DBB neuronal properties. $$\hbox {PV}_{\text{MS-DBB}}$$ PV MS-DBB neurons had intrinsic membrane properties distinct from acetylcholine- and somatostatin-containing MS-DBB subtypes. Viral expression of the fast-kinetic channelrhodopsin ChETA-YFP elicited action potentials to brief (1–2 ms) 470 nm light pulses. To investigate $$\hbox {PV}_{\text{MS-DBB}}$$ PV MS-DBB transmission, light pulses at 5–50 Hz frequencies generated trains of inhibitory postsynaptic currents (IPSCs) in CA1 stratum oriens interneurons. Using a similar approach, optogenetic activation of local hippocampal PV ($$\hbox {PV}_{\text{HC}}$$ PV HC ) neurons generated trains of $$\hbox {PV}_{\text{HC}}$$ PV HC -mediated IPSCs in CA1 pyramidal neurons. Both synapse types exhibited short-term depression (STD) of IPSCs. However, relative to $$\hbox {PV}_{\text{HC}}$$ PV HC synapses, $$\hbox {PV}_{\text{MS-DBB}}$$ PV MS-DBB synapses possessed lower initial release probability, transiently resisted STD at gamma (20–50 Hz) frequencies, and recovered more rapidly from synaptic depression. Experimentally-constrained mathematical synapse models explored mechanistic differences. Relative to the $$\hbox {PV}_{\text{HC}}$$ PV HC model, the $$\hbox {PV}_{\text{MS-DBB}}$$ PV MS-DBB model exhibited higher sensitivity to calcium accumulation, permitting a faster rate of calcium-dependent recovery from STD. In conclusion, resistance of $$\hbox {PV}_{\text{MS-DBB}}$$ PV MS-DBB synapses to STD during short gamma bursts enables robust long-range GABAergic transmission from MS-DBB to hippocampus.

Membrane properties of cell types within guinea pig basal forebrain nuclei in vitro

1988 ◽  
Vol 59 (5) ◽  
pp. 1590-1612 ◽  
Author(s):  
W. H. Griffith
Keyword(s):  
Exponential Function ◽  
Cell Types ◽  
Medial Septum ◽  
Membrane Potentials ◽  
Membrane Properties ◽  
Cell Group ◽  
Double Labeling ◽  
Voltage Range ◽  
Cable Properties

1. Neurons in the nucleus of the diagonal band of Broca (nDBB) and ventral portion of the medial septum (MS) were studied using intracellular recording and single-electrode voltage clamp (SEVC) techniques in an in vitro brain slice preparation. Cell types could be operationally divided into three categories: cells with a slow postspike afterhyperpolarization (SAHP cell, 40%), neurons with a fast AHP (FAHP cells, 53%), and a third cell group recorded infrequently (7% of the cells) that fired in a burst pattern. Double-labeling techniques have shown that SAHP cells stain positively for acetylcholinesterase (AChE) and are presumably cholinergic (22). The present study provides a more detailed analysis of the passive and active membrane properties of SAHP and FAHP types within these forebrain nuclei. 2. SAHP cells were characterized by a postspike afterhyperpolarization (AHP) with an amplitude of 10-20 mV and duration of approximately 600 ms at -65 mV. In the voltage range of -60--70 mV, the AHP decayed as a single exponential function with a time constant of 170 +/- 53 ms (n = 10). However, many neurons at these membrane potentials exhibited an AHP decay that was a multiple exponential function lasting for seconds. The null potential of the SAHP was approximately -90 mV and shifted by 25 mV in 9 mM KCl, a value closely predicted for a potassium (K+) conductance. The SAHP was reversibly blocked by cadmium (Cd2+), suggesting the SAHP was mediated by a calcium (Ca2+)-activated K+ conductance. 3. FAHP cells displayed afterhyperpolarizations of smaller amplitude (5-10 mV) and duration (5-50 ms) that reversed at approximately -85 mV. Elevating extracellular K+ concentration [Ko] to 6 mM shifted the reversal 13 mV more positive. Cd2+ also reduced the AHP in these cells suggesting a second faster Ca2+-activated K+ conductance may be present. 4. Both SAHP and FAHP cells had similar input resistances and resting membrane potentials but markedly different action-potential characteristics. SAHP cells had a spike duration of 1.4 ms and a prominent shoulder on the falling phase of the SAHP cell action potentials that was reduced by Cd2+. In contrast, FAHP cells had an average spike duration of 0.63 ms that was unaffected by Cd2+. 5. The passive electrical cable properties of both cell types were characterized. Equivalent electrotonic length of the dendrites (L) and the dendritic-to-somatic conductance ratio (rho) were calculated for different cell groups. SAHP cells displayed average L values of 0.61, and the average rho was 2.13. Similar values of 0.69 and 2.14 were calculated for L and rho, respectively, in FAHP cells.(ABSTRACT TRUNCATED AT 400 WORDS)

Physicochemical study of basement membrane properties iii. diffusion of proline, glucose and insulin in krebs solution

1988 ◽  
Vol 85 ◽  
pp. 391-397
Author(s):  
Bo Tao Fan ◽  
Françoise Simonnet ◽  
Jean Schaeverbeke ◽  
Gérard Lapluye
Keyword(s):  
Basement Membrane ◽  
Membrane Properties ◽  
Physicochemical Study ◽  
Krebs Solution

scholarly journals Quantitative Analysis of the Membrane Affinity of Local Anesthetics Using a Model Cell Membrane

Membranes ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 579
Author(s):  
Wanjae Choi ◽  
Hyunil Ryu ◽  
Ahmed Fuwad ◽  
Seulmini Goh ◽  
Chaoge Zhou ◽  
...  
Keyword(s):  
Cell Membrane ◽  
Local Anesthetics ◽  
Electrophysiological Study ◽  
Local Area ◽  
Membrane Properties ◽  
Dominant Factor ◽  
Free Standing ◽  
Membrane Affinity ◽  
Conformational Effects ◽  
Model Protein

Local anesthesia is a drug that penetrates the nerve cell membrane and binds to the voltage gate sodium channel, inhibiting the membrane potential and neurotransmission. It is mainly used in clinical uses to address the pain of surgical procedures in the local area. Local anesthetics (LAs), however, can be incorporated into the membrane, reducing the thermal stability of the membrane as well as altering membrane properties such as fluidity, permeability, and lipid packing order. The effects of LAs on the membrane are not yet fully understood, despite a number of previous studies. In particular, it is necessary to analyze which is the more dominant factor, the membrane affinity or the structural perturbation of the membrane. To analyze the effects of LAs on the cell membrane and compare the results with those from model membranes, morphological analysis and 50% inhibitory concentration (IC50) measurement of CCD-1064sk (fibroblast, human skin) membranes were carried out for lidocaine (LDC) and tetracaine (TTC), the most popular LAs in clinical use. Furthermore, the membrane affinity of the LAs was quantitatively analyzed using a colorimetric polydiacetylene assay, where the color shift represents their distribution in the membrane. Further, to confirm the membrane affinity and structural effects of the membranes, we performed an electrophysiological study using a model protein (gramicidin A, gA) and measured the channel lifetime of the model protein on the free-standing lipid bilayer according to the concentration of each LA. Our results show that when LAs interact with cell membranes, membrane affinity is a more dominant factor than steric or conformational effects of the membrane.

scholarly journals Phenothiazines alter plasma membrane properties and sensitize cancer cells to injury by inhibiting annexin-mediated repair

2021 ◽  
pp. 101012
Author(s):  
Anne Sofie Busk Heitmann ◽  
Ali Asghar Hakami Zanjani ◽  
Martin Berg Klenow ◽  
Anna Mularski ◽  
Stine Lauritzen Sønder ◽  
...  
Keyword(s):  
Plasma Membrane ◽  
Cancer Cells ◽  
Membrane Properties

scholarly journals Quantitative linear dichroism imaging of molecular processes in living cells made simple by open software tools

2021 ◽  
Vol 4 (1) ◽  
Author(s):  
Alexey Bondar ◽  
Olga Rybakova ◽  
Josef Melcr ◽  
Jan Dohnálek ◽  
Petro Khoroshyy ◽  
...  
Keyword(s):  
Biological Systems ◽  
Linear Dichroism ◽  
Quantitative Information ◽  
Living Cells ◽  
Software Tools ◽  
Model Systems ◽  
Membrane Properties ◽  
Polarization Microscopy ◽  
Molecular Processes ◽  
Wide Range

AbstractFluorescence-detected linear dichroism microscopy allows observing various molecular processes in living cells, as well as obtaining quantitative information on orientation of fluorescent molecules associated with cellular features. Such information can provide insights into protein structure, aid in development of genetically encoded probes, and allow determinations of lipid membrane properties. However, quantitating and interpreting linear dichroism in biological systems has been laborious and unreliable. Here we present a set of open source ImageJ-based software tools that allow fast and easy linear dichroism visualization and quantitation, as well as extraction of quantitative information on molecular orientations, even in living systems. The tools were tested on model synthetic lipid vesicles and applied to a variety of biological systems, including observations of conformational changes during G-protein signaling in living cells, using fluorescent proteins. Our results show that our tools and model systems are applicable to a wide range of molecules and polarization-resolved microscopy techniques, and represent a significant step towards making polarization microscopy a mainstream tool of biological imaging.

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