Molecular insight on ion hydration and association in aqueous choline chloride solutions

2020 ◽  
Vol 313 ◽  
pp. 113563
Author(s):  
Marina V. Fedotova ◽  
Sergey E. Kruchinin ◽  
Gennady N. Chuev
Cellulose ◽  
2021 ◽  
Vol 28 (16) ◽  
pp. 10127-10141
Author(s):  
Benkun Qi ◽  
Zhenwu Wang ◽  
Jianquan Luo ◽  
Yinhua Wan

1975 ◽  
Vol 228 (3) ◽  
pp. 839-844 ◽  
Author(s):  
F Garcia-Romeu ◽  
J Ehrenfeld

The relationship between the trans-epithelial Na+ and Cl minus absorptions from dilute external solutions and the H+ and base excretions were studied in Rana esculenta in vivo. The following results relate to transport from Na2SO4 solutions: 1) The Na+ absorbed is exchanged against endogenous H+. 2) Diamox injection (1.10-4 M-kg-1) simultaneously inhibits both Na+ absorption and H+ excretion. 3) The addition of amiloride to the external medium (final concn: 5-10-5 M) inhibits Na+ absorption and H+ excretion. Measurements of chloride movements from choline chloride solutions give the following results: 1) The chloride absorbed is exchanged against a base, probably HCO3-. 2) Diamox injection (1-10-4 M-kg-1)inhibits the net fluxes of both ions. When transport is measured in NaCl solutions, it is impossible to measure the HCO3-excreted when H+ is also being excreted (HCO3- plus H+ in equilibrium CO2 plus H2O). In these solutions, therefore, only the action of Diamox on the sodium and chloride fluxes was followed and was found to have similar effects on these fluxes as those described for choline chloride and sodium sulphate solutions. The results are discussed in relation to other studies on the action of inhibitors on sodium and chloride transport in the in vitro skin.


Author(s):  
Kazushige Hirosawa ◽  
Eichi Yamada

The pigment epithelium is located between the choriocapillary and the visual cells. The pigment epithelial cell is characterized by a large amount of the smooth endoplasmic reticulum (SER) in its cytoplasm. In addition, the pigment epithelial cell of some lower vertebrate has myeloid body as a specialized form of the SER. Generally, SER is supposed to work in the lipid metabolism. However, the functions of abundant SER and myeloid body in the pigment epithelial cell are still in question. This paper reports an attempt, to depict the functions of these organelles in the frog retina by administering one of phospholipid precursors.


1974 ◽  
Vol 31 (02) ◽  
pp. 309-318
Author(s):  
Phyllis S Roberts ◽  
Raphael M Ottenbrite ◽  
Patricia B Fleming ◽  
James Wigand

Summary1. Choline chloride, 0.1 M (in 0.25 M Tris. HCl buffer, pH 7.4 or 8.0, 37°), doubles the rate of hydrolysis of TAME by bovine thrombokinase but has no effect on the hydrolysis of this ester by either human or bovine thrombin. Only when 1.0 M or more choline chloride is present is the hydrolysis of BAME by thrombokinase or thrombin weakly inhibited. Evidence is presented that shows that these effects are due to the quaternary amine group.2. Tetramethyl ammonium bromide or chloride has about the same effects on the hydrolysis of esters by these enzymes as does choline chloride but tetra-ethyl, -n.propyl and -n.butyl ammonium bromides (0.1 M) are stronger accelerators of the thrombokinase-TAME reaction and they also accelerate, but to a lesser degree, the thrombin-TAME reaction. In addition, they inhibit the hydrolysis of BAME by both enzymes. Their effects on these reactions, however, do not follow any regular order. The tetraethyl compound is the strongest accelerator of the thrombokinase-TAME reaction but the tetra-ethyl and -butyl compounds are the strongest accelerators of the thrombin-TAME reaction. The ethyl and propyl compounds are the best (although weak) inhibitors of the thrombokinase-BAME and the propyl compound of the thrombin-BAME reactions.3. Tetra-methyl, -ethyl, -n.propyl and -n.butyl ammonium bromides (0.01 M) inhibit the clotting of fibrinogen by thrombin (bovine and human proteins) at pH 7.4, imidazole or pH 6.1, phosphate buffers and they also inhibit, but to a lesser degree, a modified one-stage prothrombin test. In all cases the inhibition increases regularly as the size of the alkyl group increases from methyl to butyl. Only the ethyl com pound (0.025 M but not 0.01 M), however, significantly inhibits the polymerization of bovine fibrin monomers. It was concluded that inhibition of the fibrinogen-thrombin and the one-stage tests by the quaternary amines is not due to any effect of the com pounds on the polymerization process but probably due to inhibition of thrombin’s action on fibrinogen by the quaternary amines.


1977 ◽  
Vol 86 (3) ◽  
pp. 552-560 ◽  
Author(s):  
Monica Söderberg ◽  
Inge-Bert Täljedal

ABSTRACT Effects of inorganic ions on the uptake of chloromercuribenzene-p-sulphonic acid (CMBS) were studied in microdissected pancreatic islets of non-inbred ob/ob-mice. Na2SO4 stimulated the total islet cell uptake of CMBS but decreased the amount of CMBS remaining in islets after brief washing with L-cysteine. CaCl2 stimulated both the total and the cysteine-non-displaceable uptake; the stimulatory effect of CaCl2 on the cysteine-non-displaceable CMBS uptake was counteracted by Na2SO4. NaCl, KCl or choline chloride had no significant effect on the total islet cell uptake of CMBS, whereas LiCl was stimulatory. It is concluded that β-cells resemble erythrocytes in having a permeation path for CMBS that is inhibited by SO42−. By analogy with existing models of the erythrocyte membrane, it is suggested that the SO42−-sensitive path leads to sulphydryl groups controlling monovalent cationic permeability in β-cells.


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