A binary electrolyte model of a cylindrical alkaline cell

2000 ◽  
Vol 85 (2) ◽  
pp. 190-202 ◽  
Author(s):  
J.J. Kriegsmann ◽  
H.Y. Cheh
Keyword(s):  
1978 ◽  
Vol 125 (12) ◽  
pp. 1918-1923 ◽  
Author(s):  
Stuart M. Davis ◽  
Michael N. Hull
Keyword(s):  

1993 ◽  
Vol 48 (11-12) ◽  
pp. 946-951
Author(s):  
K. Tempel

Abstract Interactions of novobiocin (NB) and nalidixic acid (NA) with thiols were investigated in vitro in thymic (T-) and splenic (S-) cells of the rat, by determining nucleic acid synthesis as well as nucleoid sedimentation and viscosity of alkaline cell lysates. In T-cells NB, at concentrations of 0.35-1.4 mм, increased unscheduled D N A synthesis (UDS) and RNA synthesis (RNS), whereas S-cells underwent a dose-dependent inhibition of UDS and RNS following exposure to NB at concentrations > 0.7 mм. Combining NA and thiols (e.g., dithiothreitol) resulted in a slight stimulation of UDS in S-cells and in a highly significant increase of UDS in T-cells ascribed to a depletion of the cellular thymidine pool. In both cell types, neither NB nor NA exerted a significant effect on thiol-induced DNA damage. At a concentration of 1.4 mм, NB increased the viscosity of alkaline T-cell lysates; the opposite effect was observed in S-cells. From these results as well as from previous investigations we conclude that T-and S-cells differ in their state of chromatin conformation. This interpretation offers a simple model for the study of the influence of chromatin structure on cell-specific physico-and/or chemico-biologi-cal interactions.


1994 ◽  
Vol 48 (3) ◽  
pp. 361-370 ◽  
Author(s):  
Antonio Motori ◽  
Franco Sandrolini ◽  
Giovanni Davolio

1997 ◽  
Vol 272 (4) ◽  
pp. R1226-R1234 ◽  
Author(s):  
P. Bouyer ◽  
M. Cougnon ◽  
S. R. Thomas ◽  
P. Hulin ◽  
T. Anagnostopoulos ◽  
...  

This study measures the intrinsic buffering power (beta(i)) of giant fused cells from the proximal kidney tubule of the frog (Rana ridibunda) as a function of intracellular pH (pHi). We monitored pHi and transmembrane potential difference during acid or alkaline cell loading, achieved by removal of NH4Cl-containing solutions or CO2-HCO3(-)-equilibrated solutions, respectively, in the absence of extracellular Na+. Data were well fit by the equation for a single, monoprotic buffer with a maximum beta(i) at a pHi of 7.39 +/- 0.06 and a total buffer concentration of 30.7 +/- 1.6 mM (means +/- SD). From pHi measurements obtained during CO2-HCO3- exposure, we also calculated the buffering power afforded by the CO2-HCO3- pair, and we show its increasing contribution to total buffering power at increasing PCO2 and pHi. To our knowledge, this is the first report of a cell type in which intrinsic cell buffers can be adequately approximated as a single monoprotic buffer with a negative logarithm of apparent dissociation constant in the normal physiological range and essentially symmetric dependence on pHi in both acid and alkaline ranges.


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