Oscillations of apoplasmic K+ and H+ activities in Desmodium motorium (Houtt.) Merril. pulvini in relation to the membrane potential of motor cells and leaflet movements

Planta ◽  
1995 ◽  
Vol 196 (2) ◽  
Author(s):  
Bernd Antkowiak ◽  
Wolfgang Engelmann
Keyword(s):  
Membrane Potential ◽  
Motor Cells

Effects of vanadate, N2 and light on the membrane potential of motor cells and the lateral leaflet movements of Desmodium motorium

1992 ◽  
Vol 86 (4) ◽  
pp. 551-558 ◽  
Author(s):  
Bernd Antkowiak ◽  
Wolfgang Engelmann ◽  
Rut Herbjornsen ◽  
Anders Johnsson
Keyword(s):  
Membrane Potential ◽  
Lateral Leaflet ◽  
Motor Cells

Effects of vanadate, N2 and light on the membrane potential of motor cells and the lateral leaflet movements of Desmodium motorium

1992 ◽  
Vol 86 (4) ◽  
pp. 551-558 ◽  
Author(s):  
Bernd Antkowiak ◽  
Wolfgang Engelmann ◽  
Rut Herbjornsen ◽  
Anders Johnsson
Keyword(s):  
Membrane Potential ◽  
Lateral Leaflet ◽  
Motor Cells

Effects of Methylxanthines on Seismonastic Reaction, Proton Flux, Membrane Potential, Respiration and Calcium Uptake in Motor Cells of Mimosa pudica Pulvinus

1993 ◽  
Vol 142 (2) ◽  
pp. 197-202 ◽  
Author(s):  
Gabriel Roblin ◽  
Christelle Moyen ◽  
Pierrette Fleurat-Lessard ◽  
Janine Bonmort
Keyword(s):  
Membrane Potential ◽  
Calcium Uptake ◽  
Proton Flux ◽  
Mimosa Pudica ◽  
Motor Cells

Measurement of spontaneous neuronal membrane activity by time lapse confocal microscopy

1995 ◽  
Vol 53 ◽  
pp. 972-973
Author(s):  
R H. Selinfreund ◽  
A. H. Cornell-Bell
Keyword(s):  
Membrane Potential ◽  
Confocal Microscopy ◽  
Patch Clamp ◽  
Electrical Activity ◽  
Time Lapse ◽  
Neuronal Firing ◽  
Neuronal Membrane ◽  
Pituitary Cells ◽  
Patch Clamp Recording ◽  
Spontaneous Electrical Activity

Cellular electrophysiological properties are normally monitored by standard patch clamp techniques . The combination of membrane potential dyes with time-lapse laser confocal microscopy provides a more direct, least destructive rapid method for monitoring changes in neuronal electrical activity. Using membrane potential dyes we found that spontaneous action potential firing can be detected using time-lapse confocal microscopy. Initially, patch clamp recording techniques were used to verify spontaneous electrical activity in GH4\C1 pituitary cells. It was found that serum depleted cells had reduced spontaneous electrical activity. Brief exposure to the serum derived growth factor, IGF-1, reconstituted electrical activity. We have examined the possibility of developing a rapid fluorescent assay to measure neuronal activity using membrane potential dyes. This neuronal regeneration assay has been adapted to run on a confocal microscope. Quantitative fluorescence is then used to measure a compounds ability to regenerate neuronal firing.The membrane potential dye di-8-ANEPPS was selected for these experiments. Di-8- ANEPPS is internalized slowly, has a high signal to noise ratio (40:1), has a linear fluorescent response to change in voltage.

Fluorescent potentiometric dyes for membrane-potential imaging

1994 ◽  
Vol 52 ◽  
pp. 166-167
Author(s):  
Leslie M. Loew
Keyword(s):  
Membrane Potential ◽  
Single Cells ◽  
Quantitative Imaging ◽  
Optical Recording ◽  
Biological Processes ◽  
Major Focus ◽  
The Past ◽  
Excitable Systems ◽  
Major Application ◽  
The Impact

A major application of potentiometric dyes has been the multisite optical recording of electrical activity in excitable systems. After being championed by L.B. Cohen and his colleagues for the past 20 years, the impact of this technology is rapidly being felt and is spreading to an increasing number of neuroscience laboratories. A second class of experiments involves using dyes to image membrane potential distributions in single cells by digital imaging microscopy - a major focus of this lab. These studies usually do not require the temporal resolution of multisite optical recording, being primarily focussed on slow cell biological processes, and therefore can achieve much higher spatial resolution. We have developed 2 methods for quantitative imaging of membrane potential. One method uses dual wavelength imaging of membrane-staining dyes and the other uses quantitative 3D imaging of a fluorescent lipophilic cation; the dyes used in each case were synthesized for this purpose in this laboratory.

Sign in / Sign up

Export Citation Format

Share Document