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1.
In. U.S. Central United States Earthquake Consortium (CUSEC). Hazard assessment preparedness, awareness, and public education emergency response and recovery socioeconomic and public policy impacts : Proceedings. Memphis, Tennessee, U.S. Central United States Earthquake Consortium (CUSEC), 1993. p.317-26, ilus.
Monography in En | Desastres -Disasters- | ID: des-6610

ABSTRACT

The unconsolidated sedimets (soils) underlying evanville, Indiana, are an important element contributing to the cities seismic risk. Knowledge of the shear - wave velocity of the unconsolidated sediment column is essential in predicting soil period, amplification potential, liquefaction risk, and other site responses to seismic shaking (AU)


Subject(s)
Earthquakes , Risk Assessment , 25686 , Soil Characteristics , Geology , Fluvial Erosion
2.
Am J Physiol ; 254(6 Pt 1): C829-38, 1988 Jun.
Article in English | MEDLINE | ID: mdl-3377070

ABSTRACT

Inhibitors of specific steps in the endocytosis of galactose-terminating glycoproteins (asialoglycoproteins) by cultured rat hepatocytes have been described (J. Cell Biol. 98: 375-381, 1984). In particular, substitution of K+ for Na+ in the culture medium results in reduced delivery of ligand to lysosomes; ligand-receptor internalization, dissociation, and segregation remain normal. We have now demonstrated by direct microelectrode measurement that incubation of hepatocytes in K+-substituted medium results in a reduction of intracellular pH by greater than or equal to 0.5 U. In addition, we have shown that reduced intracellular pH in these cells produced by either direct (CO2 diffusion) or indirect (K+ substitution) acidification inhibits ligand delivery to lysosomes. Return of internalized ligand-receptor complex to the cell surface (diacytosis) is also inhibited by these manipulations. These studies suggest that intracellular pH may modulate specific steps involving vesicle translocation and fusion in the receptor-mediated endocytosis of asialoglycoproteins. Similar effects of direct acidification of hepatocytes by CO2 diffusion and indirect acidification by K+ substitution for Na+, on diacytosis and ligand delivery to lysosomes, suggest that K+ substitution may influence these events by altering intracellular pH.


Subject(s)
Asialoglycoproteins , Cytosol/metabolism , Endocytosis , Liver/cytology , Orosomucoid/analogs & derivatives , Receptors, Immunologic/metabolism , Animals , Asialoglycoprotein Receptor , Cells, Cultured , Culture Media , Hydrogen-Ion Concentration , Ligands , Liver/metabolism , Lysosomes/metabolism , Microelectrodes , Orosomucoid/metabolism , Potassium/metabolism , Rats , Sodium/metabolism
3.
J Clin Invest ; 79(4): 1259-68, 1987 Apr.
Article in English | MEDLINE | ID: mdl-3031134

ABSTRACT

Transport of 35S-labeled sulfobromophthalein [35S]BSP was studied in short-term cultured rat hepatocytes incubated in bovine serum albumin. At 37 degrees C, initial uptake of [35S]BSP was 5-10-fold that at 4 degrees C, linear for at least 15 min, saturable, inhibited by bilirubin, and reduced by greater than 70% after ATP depletion or isosmotic substitution of sucrose for NaCl in medium. Replacement of Na+ by K+ or Li+ did not alter uptake, whereas replacement of Cl- by HCO-3 or gluconate- reduced uptake by approximately 40%. Substitution of Cl- by the more permeant NO-3 enhanced initial BSP uptake by 30%. Efflux of [35S]BSP from cells to media was inhibited by 40% after ATP depletion or sucrose substitution. To confirm these results in a more physiologic system, transport of [3H]bilirubin was studied in isolated livers perfused with control medium or medium in which Cl- was replaced by gluconate-. Perfusion data analyzed by the model of Goresky, revealed 40-50% reductions in influx and efflux with gluconate- substitution. These results are consistent with existence of a Cl-/organic anion-exchange mechanism similar to that described by others in renal tubules.


Subject(s)
Chlorides/pharmacology , Liver/drug effects , Adenosine Triphosphate/metabolism , Animals , Bilirubin/pharmacology , Biological Transport, Active/drug effects , Chlorides/metabolism , Lithium/metabolism , Lithium Chloride , Liver/metabolism , Male , Perfusion , Potassium Chloride/metabolism , Rats , Rats, Inbred Strains , Sodium Chloride/metabolism , Sulfobromophthalein/metabolism
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