Dale J. Benos
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Research Interests
Dale J. Benos has a total of 11 co-authors. Here are the top co-authors by number of shared publications:
Iskander I. Ismailov
Department of Physiology and Biophysics, University of Alabama, Birmingham, AL 35294, USA
3 shared publicationsBakhram K. Berdiev
Department of Physiology and Biophysics, University of Alabama at Birmingham, Birmingham, Alabama 35294-0005, USA
2 shared publicationsBiljana Jovov
§ Harvard Medical School, Renal Unit, Massachusetts General Hospital E, Boston, Massachusetts 02129
2 shared publicationsCatherine M. Fuller
§ Harvard Medical School, Renal Unit, Massachusetts General Hospital E, Boston, Massachusetts 02129
2 shared publicationsAdriana G. Prat
§ Harvard Medical School, Renal Unit, Massachusetts General Hospital E, Boston, Massachusetts 02129
1 shared publicationDennis A. Ausiello
§ Harvard Medical School, Renal Unit, Massachusetts General Hospital E, Boston, Massachusetts 02129
1 shared publication
Latest Publications
- 8 July 1997
- Published by National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 94 (14) , 7651-7654
Streaming potential measurements in αβγ-rat epithelial Na + channel in planar lipid bilayers
Streaming potentials across cloned epithelial Na+ channels (ENaC) incorporated into planar lipid bilayers were measured. We found that the establishment of an osmotic pressure gradient (Deltapi) across a channel-containing membrane mimicked the activation effects of a hydrostatic pressure differential (DeltaP) on alphabetagamma-rENaC, although with a quantitative difference in the magnitude of the driving forces. Moreover, the imposition of a Deltapi negates channel activation by DeltaP when the Deltapi was directed against DeltaP. A streaming potential of 2.0 +/- 0.7 mV was measured across alphabetagamma-rat ENaC (rENaC)-containing bilayers at 100 mM symmetrical [Na+] in the presence of a 2 Osmol/kg sucrose gradient. Assuming single file movement of ions and water within the conduction pathway, we conclude that between two and three water molecules are translocated together with a single Na+ ion. A minimal effective pore diameter of 3 A that could accommodate two water molecules even in single file is in contrast with the 2-A diameter predicted from the selectivity properties of alphabetagamma-rENaC. The fact that activation of alphabetagamma-rENaC by DeltaP can be reproduced by the imposition of Deltapi suggests that water movement through the channel is also an important determinant of channel activity.
- 8 July 1997
- Published by National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 94 (14) , 7651-7654
Streaming potential measurements in αβγ-rat epithelial Na + channel in planar lipid bilayers
Streaming potentials across cloned epithelial Na+ channels (ENaC) incorporated into planar lipid bilayers were measured. We found that the establishment of an osmotic pressure gradient (Deltapi) across a channel-containing membrane mimicked the activation effects of a hydrostatic pressure differential (DeltaP) on alphabetagamma-rENaC, although with a quantitative difference in the magnitude of the driving forces. Moreover, the imposition of a Deltapi negates channel activation by DeltaP when the Deltapi was directed against DeltaP. A streaming potential of 2.0 +/- 0.7 mV was measured across alphabetagamma-rat ENaC (rENaC)-containing bilayers at 100 mM symmetrical [Na+] in the presence of a 2 Osmol/kg sucrose gradient. Assuming single file movement of ions and water within the conduction pathway, we conclude that between two and three water molecules are translocated together with a single Na+ ion. A minimal effective pore diameter of 3 A that could accommodate two water molecules even in single file is in contrast with the 2-A diameter predicted from the selectivity properties of alphabetagamma-rENaC. The fact that activation of alphabetagamma-rENaC by DeltaP can be reproduced by the imposition of Deltapi suggests that water movement through the channel is also an important determinant of channel activity.
- 1 December 1996
- Published by American Physiological Society in Advances in Physiology Education
- Vol. 271 (6) , S2-9
Introduction to medical physiology: cellular membranes and transmembrane transport of solutes and water.
This article summarizes the comments made in the introductory session of the Medical Physiology course taught at the University of Alabama School of Medicine. The main thesis is that learning physiology is easier when fundamental principles are first delineated. Four general principles of physiology (mass balance, force-flow, capacitance, and equilibrium) are discussed. Clinical medicine becomes more comprehensible when these basic principles are understood. Cellular Physiology is taught first because it forms the conceptual basis for what follows in the course. The idea that the root of clinical medicine lies in the basic sciences is emphasized.
- 1 December 1996
- Published by American Physiological Society in Advances in Physiology Education
- Vol. 271 (6) , S2-9
Introduction to medical physiology: cellular membranes and transmembrane transport of solutes and water.
This article summarizes the comments made in the introductory session of the Medical Physiology course taught at the University of Alabama School of Medicine. The main thesis is that learning physiology is easier when fundamental principles are first delineated. Four general principles of physiology (mass balance, force-flow, capacitance, and equilibrium) are discussed. Clinical medicine becomes more comprehensible when these basic principles are understood. Cellular Physiology is taught first because it forms the conceptual basis for what follows in the course. The idea that the root of clinical medicine lies in the basic sciences is emphasized.
- Open Access
- 1 July 1996
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 271 (30) , 17704-17710
Regulation of Epithelial Sodium Channels by Short Actin Filaments
- 1 July 1996
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 271 (30) , 17704-17710
Open AccessRegulation of Epithelial Sodium Channels by Short Actin Filaments
- Open Access
- 1 March 1996
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 271 (9) , 4725-4732
Regulation of Epithelial Sodium Channels by the Cystic Fibrosis Transmembrane Conductance Regulator
- 1 March 1996
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 271 (9) , 4725-4732
Open AccessRegulation of Epithelial Sodium Channels by the Cystic Fibrosis Transmembrane Conductance Regulator