» Articles » PMID: 7326329

Electrical Properties of Rabbit Corneal Endothelium As Determined from Impedance Measurements

Overview
Journal Biophys J
Publisher Cell Press
Specialty Biophysics
Date 1981 Dec 1
PMID 7326329
Citations 18
Authors
Affiliations
Soon will be listed here.
Abstract

Alternating- and direct-current electrical characteristics of rabbit corneal endothelium were studied under varying experimental conditions. The measurements were performed by sending a 10-microA current (AC or DC) across the tissue layer. Maximal values of transendothelial potential difference and resistance were 1.3 +/- 0.1 mV and 73 +/- 6 omega . cm2, respectively. The short-circuit current was estimated from the potential and resistance values. Impedance loci were obtained for the frequency range 0.5-100 kHz. A capacitive reactance (C = 0.63 +/- 0.02 microF/cm2) was observed in the 100 Hz-100 kHz range. To relate the impedance data to the electrical parameters of the cell membranes, the voltage-divider ratio was determined by sending square pulse across the tissue and measuring voltage responses across the apical and basal membranes with an intracellular microelectrode. The intracellular potential difference was on the average -61 +/- 1 mV, and the voltage-divider ratio was found to be between 0.33 and 4. Impedance data were fit by a computer to an equivalent circuit representing a "lumped" model, and the agreement between the model and the data was satisfactory. The results are discussed in terms of both the morphological characteristics and properties of the fluid transport mechanism across the preparation.

Citing Articles

Lumped-Element Circuit Modeling for Composite Scaffold with Nano-Hydroxyapatite and Wangi Rice Starch.

Tan X, Cheng E, Mohd Nasir N, Abdul Majid M, Jamir M, Khor S Polymers (Basel). 2023; 15(2).

PMID: 36679235 PMC: 9862369. DOI: 10.3390/polym15020354.


Models of the Blood-Brain Barrier: Tools in Translational Medicine.

Williams-Medina A, Deblock M, Janigro D Front Med Technol. 2022; 2:623950.

PMID: 35047899 PMC: 8757867. DOI: 10.3389/fmedt.2020.623950.


Electrical signaling in control of ocular cell behaviors.

Zhao M, Chalmers L, Cao L, Vieira A, Mannis M, Reid B Prog Retin Eye Res. 2011; 31(1):65-88.

PMID: 22020127 PMC: 3242826. DOI: 10.1016/j.preteyeres.2011.10.001.


Oxygen-deficient metabolism and corneal edema.

Leung B, Bonanno J, Radke C Prog Retin Eye Res. 2011; 30(6):471-92.

PMID: 21820076 PMC: 4101817. DOI: 10.1016/j.preteyeres.2011.07.001.


Comparative permeabilities of the paracellular and transcellular pathways of corneal endothelial layers.

Diecke F, Cacace V, Montalbetti N, Ma L, Kuang K, Iserovich P J Membr Biol. 2011; 242(1):41-51.

PMID: 21713417 DOI: 10.1007/s00232-011-9375-5.


References
1.
Lim J, Fischbarg J . Intra-cellular potential of rabbit corneal endothelial cells. Exp Eye Res. 1979; 28(6):619-26. DOI: 10.1016/0014-4835(79)90063-0. View

2.
Fischbarg J, Lim J . Determination of the impedance locus of rabbit corneal endothelium. Biophys J. 1973; 13(6):595-9. PMC: 1484284. DOI: 10.1016/S0006-3495(73)86009-6. View

3.
Fromter E . The route of passive ion movement through the epithelium of Necturus gallbladder. J Membr Biol. 1972; 8(3):259-301. DOI: 10.1007/BF01868106. View

4.
Fischbarg J, Warshavsky C, Lim J . Pathways for hydraulically and osmotically-induced water flows across epithelia. Nature. 1977; 266(5597):71-4. DOI: 10.1038/266071a0. View

5.
ANDERSON E, Fischbarg J, Spector A . Fluid transport, ATP level and ATPase activities in isolated rabbit corneal endothelium. Biochim Biophys Acta. 1973; 307(3):557-62. DOI: 10.1016/0005-2736(73)90300-3. View