Kinetics of the sarcolemmal lactate carrier in single heart cells using BCECF to measure pHi

1994 ◽  
Vol 267 (5) ◽  
pp. H1759-H1769 ◽  
Author(s):  
X. Wang ◽  
A. J. Levi ◽  
A. P. Halestrap
Keyword(s):  
Guinea Pig ◽  
Specific Inhibitor ◽  
Limiting Factor ◽  
Heart Cells ◽  
Michaelis Constant ◽  
Hypoxic Conditions ◽  
Rapid Fall ◽  
Rat Myocytes ◽  
Rate Limiting ◽  
Kinetics Of

The pH-sensitive fluorescent indicator 2',7'-bis(carboxyethyl)-5(6)-carboxyfluorescein (BCECF) was used to measure lactate transport in single cardiac myocytes. Addition of lactate externally caused a rapid fall of intracellular pH (pHi), which was largely inhibited by 5 mM alpha-cyano-4-hydroxycinnamate (CHC), a specific inhibitor of the lactate carrier. Stilbene disulfonates such as 4,4'-dibenzamidostilbene-2,2'-disulfonate (DBDS) only partially inhibited the response, with inhibition being greater in guinea pig than rat myocytes. The data are consistent with two isoforms of the lactate carrier, one sensitive and one insensitive to DBDS, coexisting within a single myocyte and both having a stoichiometry of 1 lactate:1 proton. The initial rate of pHi fall was used to determine carrier kinetics. Rat myocytes had a Michaelis constant (Km) for external L-lactate of 2.74 mM and a Km for external pyruvate of 0.2 mM. Guinea pig cells had a Km for external L-lactate of 2.2 mM. Kinetics of lactate efflux were also evaluated using the rate of pHi recovery on removing external lactate. The Km and maximal rate values for efflux were both threefold higher than for influx and were related to each other and the transmembrane pH gradient as predicted by the Haldane relationship. It is suggested that under hypoxic conditions, the carrier may be the rate-limiting factor for lactate extrusion.

scholarly journals Dependence upon Bile Volume of the Biliary Excretion of Bromocresol Green and Amaranth in the Anaesthetized Rat

1975 ◽  
Vol 28 (4) ◽  
pp. 339 ◽  
Author(s):  
Alan G Clark ◽  
KarI M Rogers
Keyword(s):  
Biliary Excretion ◽  
Biliary Tree ◽  
Bulk Flow ◽  
Rate Equations ◽  
Bromocresol Green ◽  
Limiting Factor ◽  
Cumulative Volume ◽  
Rate Limiting ◽  
Kinetics Of ◽  
Anaesthetized Rat

The kinetics of the biliary excretion of both bromocresol green and amaranth are better described in terms of rate equations that are functions of the cumulative volume of bile excreted rather than of time. The rate of disappearance of bromocresol green from the liver also appears to depend on the volume of bile excreted rather than on time. It is proposed that bromocresol green, and probably also amaranth, rapidly equilibrates between the hepatic and biliary compartments as a result of reabsorption from the biliary tree and that the rate-limiting factor in the biliary excretion of these dyes is the removal of dye from the biliary tree by bulk flow.

Voltage-dependent kinetics of Na-Ca exchange current in Ca(2+)-loaded guinea pig heart cells

1993 ◽  
Vol 265 (5) ◽  
pp. C1258-C1265 ◽  
Author(s):  
K. Benndorf ◽  
C. Biskup ◽  
M. Friedrich
Keyword(s):  
Guinea Pig ◽  
Time Course ◽  
Exchange Current ◽  
Heart Cells ◽  
Current Component ◽  
Patch Clamp Technique ◽  
Initial Current ◽  
Current Increase ◽  
Voltage Dependent ◽  
Kinetics Of

Voltage-dependent properties of Na-Ca exchange current were revealed with the patch-clamp technique in Ca(2+)-overloaded guinea pig ventricular myocytes in the whole cell configuration. With the assumption that the transient inward current (Iti) is mediated by the Na-Ca exchanger, oscillations of internal Ca2+ concentration ([Ca2+]i) were used to investigate voltage-dependent kinetics of exchange current differences at two [Ca2+]i values. After Iti was elicited by clamping from -45 mV to basic pulses of +10 mV, pairs of equipotential short test pulses were applied during the basic pulse at both the phase of low [Ca2+]i (between two neighboring Iti values) and the phase of high [Ca2+]i (at the peak of Iti). The test pulses were short enough to leave the time course of Iti during the basic pulse approximately unchanged, which allowed study of the voltage dependence of the respective current differences without disturbing the underlying oscillation of [Ca2+]i. The current differences were inward at all potentials between -140 and +70 mV, started from an equal initial value, and obeyed characteristic voltage-dependent time courses: hyperpolarization to potentials negative to -70 mV caused an initial current increase, which was followed by a decay to very small amplitudes or zero with a decay time constant decreasing toward hyperpolarization e-fold per 45.6 mV. Depolarizing pulses caused a decay of the current differences to smaller levels. Respective current differences formed during a slowly decaying current component, following the Ca current spike, showed equal voltage-dependent properties. This indicates that the slowly decaying current component is preferentially also carried by the Na-Ca exchanger.(ABSTRACT TRUNCATED AT 250 WORDS)

scholarly journals Large Peptide Permeation Through a Membrane Channel: Understanding Protamine Translocation Through CymA from Klebsiella Oxytoca

2020 ◽  
Author(s):  
Sushil Pangeni ◽  
Jigneshkumar Dahyabhai Prajapati ◽  
Jayesh Arun Bafna ◽  
Nilam Mohamed ◽  
Werner M. Nau ◽  
...  
Keyword(s):  
Lipid Bilayers ◽  
Klebsiella Oxytoca ◽  
Limiting Factor ◽  
Membrane Channel ◽  
Voltage Dependent ◽  
Dynamics Simulations ◽  
Rate Limiting ◽  
Kinetics Of ◽  
Zero Voltage ◽  
Large Peptide

Quantifying the passage of the large peptide protamine (Ptm) across CymA, a passive channel for cyclodextrin uptake, is in the focus of this study. Using a reporter-pair based fluorescence membrane assay we detected the entry of Ptm into liposomes containing CymA. The kinetics of the Ptm entry was independent of its concentration suggesting that the permeation across CymA is the rate-limiting factor. Furthermore, we reconstituted single CymA channels into planar lipid bilayers and recorded the ion current fluctuations in the presence of Ptm. To this end, we were able to resolve the voltage-dependent entry of single Ptm peptide molecules into the channel. Extrapolation to zero voltage revealed about 1-2 events per second and long dwell times, in agreement with the liposome study. Applied-field and steered molecular dynamics simulations provided an atomistic view on the permeation. It can be concluded that a concentration gradient of 1 M Ptm leads to a translocation rate of about 1 molecule per second and per channel.

Kinetics of iron absorption in normal dogs

1961 ◽  
Vol 201 (1) ◽  
pp. 67-70 ◽  
Author(s):  
W. B. Stewart ◽  
S. R. Gambino
Keyword(s):  
Intestinal Tract ◽  
Iron Absorption ◽  
Radioactive Isotopes ◽  
High Rate ◽  
Intestinal Lumen ◽  
Inhibitory Mechanism ◽  
Rapid Fall ◽  
Rate Limiting ◽  
Kinetics Of ◽  
Very High

By means of the simultaneous use of two radioactive isotopes of iron, it has been possible to measure the rate of iron absorption from the gastrointestinal tract in normal dogs. One isotope was administered orally and another intravenously. By suitable calculation the rates of absorption at any given time were computed. Absorption begins at a very high rate, which varied from 22.8 µg/hr to 578 µg/hr in different dogs. The half-time of the absorption rate varied from 0.25 to 0.66 hr. The rapid fall in the rate of iron absorption is not caused entirely by the passage of the labeled material along the intestinal tract, but seems rather to be caused by the development of an inhibitory mechanism or the presence of a rate-limiting reaction in one of the steps in the passage of iron from the intestinal lumen to the plasma.

Michaelis-Menten kinetics of galactose elimination by the isolated perfused pig liver

1976 ◽  
Vol 230 (5) ◽  
pp. 1302-1313 ◽  
Author(s):  
S Keiding ◽  
S Johansen ◽  
K Winkler ◽  
K Tonnesen ◽  
N Tygstrup
Keyword(s):  
Irreversible Process ◽  
Experimental Uncertainty ◽  
Maximal Rate ◽  
Michaelis Constant ◽  
Pig Liver ◽  
Blood Concentrations ◽  
Saturation Kinetics ◽  
Rate Limiting ◽  
Kinetics Of ◽  
Galactose Elimination

The relation between galactose elimination rates and blood concentrations in the isolated perfused pig liver was analyzed by a mathematical kinetic model. It assumes that the substrate, under steady-state conditions, is removed from the blood that flows through the sinusoids by an irreversible process which follows Michaelis-Menten (i.e., saturation) kinetics. The experiments consisted of successive periods with constant infusions of galactose. The model fitted the data to within the experimental uncertainty. The estimated maximal rate (Vmax) ranged from 0.34 to 0.57 mmol-min(-1)-kg(-1) liver, and the Michaelis constant, Km, ranged from 0.12 to 0.30 mmol-liter(-1) plasma water in nine experiments. The ratio between the galactose concentration in hepatocyte water and plasma water was not significantly different from 1.0, indicating that membrane transport is not rate limiting for the elimination of galactose. In experiments with increasing concentrations of galactose in hepatocyte water and approximately saturated elimination rates, the concentrations of galactose 1-phosphate, UDPgalactose, and UDPglucose remained essentially constant. This indicates that the phosphorylation of galactose to galactose 1-phosphate is the rate-determining process.

Hydrolysis kinetics of dissolved polymer substrates

2002 ◽  
Vol 45 (10) ◽  
pp. 99-104 ◽  
Author(s):  
W.T.M. Sanders ◽  
G. Zeeman ◽  
G. Lettinga
Keyword(s):  
Enzyme Activity ◽  
Laboratory Experiments ◽  
Hydrolysis Rate ◽  
Limiting Factor ◽  
Hydrolysis Kinetics ◽  
Parent Molecule ◽  
Polymer Substrates ◽  
Rate Limiting ◽  
Kinetics Of ◽  
Hydrolysis Of

In this paper, the relation between the hydrolysis rate of dissolved polymer substrates and sludge concentration was investigated in two ways, viz. by laboratory experiments and by computer simulations. In the simulations, the hydrolysis of dissolved polymer components was regarded as a general depolymerisation process in which the bonds of the parent molecule break randomly until only monomer and dimer components remain. The results illustrate that for the hydrolysis of dissolved polymer substrates the enzyme activity is the rate-limiting factor. Moreover, a general depolymerisation process can describe the enzymatic hydrolysis of these components.

scholarly journals Large Peptide Permeation Through a Membrane Channel: Understanding Protamine Translocation Through CymA from Klebsiella Oxytoca

2020 ◽  
Author(s):  
Sushil Pangeni ◽  
Jigneshkumar Dahyabhai Prajapati ◽  
Jayesh Arun Bafna ◽  
Nilam Mohamed ◽  
Werner M. Nau ◽  
...  
Keyword(s):  
Lipid Bilayers ◽  
Klebsiella Oxytoca ◽  
Limiting Factor ◽  
Membrane Channel ◽  
Voltage Dependent ◽  
Dynamics Simulations ◽  
Rate Limiting ◽  
Kinetics Of ◽  
Zero Voltage ◽  
Large Peptide

Quantifying the passage of the large peptide protamine (Ptm) across CymA, a passive channel for cyclodextrin uptake, is in the focus of this study. Using a reporter-pair based fluorescence membrane assay we detected the entry of Ptm into liposomes containing CymA. The kinetics of the Ptm entry was independent of its concentration suggesting that the permeation across CymA is the rate-limiting factor. Furthermore, we reconstituted single CymA channels into planar lipid bilayers and recorded the ion current fluctuations in the presence of Ptm. To this end, we were able to resolve the voltage-dependent entry of single Ptm peptide molecules into the channel. Extrapolation to zero voltage revealed about 1-2 events per second and long dwell times, in agreement with the liposome study. Applied-field and steered molecular dynamics simulations provided an atomistic view on the permeation. It can be concluded that a concentration gradient of 1 M Ptm leads to a translocation rate of about 1 molecule per second and per channel.

Abnormal Platelet Serotonin Uptake and Binding Sites in Myeloproliferative Disorders

1984 ◽  
Vol 51 (03) ◽  
pp. 349-353 ◽  
Author(s):  
C Caranobe ◽  
P Sié ◽  
F Fernandez ◽  
J Pris ◽  
S Moatti ◽  
...  
Keyword(s):  
Binding Sites ◽  
High Capacity ◽  
Specific Inhibitor ◽  
Myeloproliferative Disorders ◽  
Normal Subjects ◽  
Binding Data ◽  
Full Explanation ◽  
Number Of Binding Sites ◽  
5 Ht Uptake ◽  
Kinetics Of

SummaryA simultaneous investigation of the kinetics of serotonin (5 HT) uptake and of binding sites was carried out in the platelets of normal subjects and of 10 patients affected with various types of myeloproliferative disorders (MD). The 5 HT uptake was analysed according to the Lineweaver-Burk and the Eadie-Hofstee methods. With the two methods, the patient’s platelets exhibited a dramatic reduction of the Vi max and of the Km; in some patients the Eadie-Hofstee analysis revealed that a passive diffusion phenomenon is superimposed on the active 5 HT uptake at least for the higher concentration used. The binding data were analysed with the Scatchard method. Two classes of binding sites (high affinity - low capacity, low affinity - high capacity) were found in normal subjects and patients. Pharmacological studies with imipramine, a specific inhibitor of 5 HT uptake, suggested that both the sites are involved in 5 HT uptake. The number of both binding sites was significantly decreased in patient’s platelets while the affinity constants of these binding sites were not significantly reduced in comparison with those of the control subjects. No correlations were found between Vi max, Km and the number of binding sites. These results suggest that a reduction in the number of platelet membrane acceptors for 5 HT commonly occurs in myeloproliferative disorders but does not provide a full explanation of the uptake defect.

Kinetics of cyclization of S-ethoxycarbonylmethylisothiouronium chloride to 2-imino-4-thiazolidone

1979 ◽  
Vol 44 (3) ◽  
pp. 912-917 ◽  
Author(s):  
Vladimír Macháček ◽  
Said A. El-bahai ◽  
Vojeslav Štěrba
Keyword(s):  
Hydrochloric Acid ◽  
Dilute Hydrochloric Acid ◽  
Base Catalysis ◽  
General Base ◽  
Rate Limiting Step ◽  
Limiting Step ◽  
Kinetics Of Formation ◽  
Acid Catalyzed ◽  
Rate Limiting ◽  
Kinetics Of

Kinetics of formation of 2-imino-4-thiazolidone from S-ethoxycarbonylmethylisothiouronium chloride has been studied in aqueous buffers and dilute hydrochloric acid. The reaction is subject to general base catalysis, the β value being 0.65. Its rate limiting step consists in acid-catalyzed splitting off of ethoxide ion from dipolar tetrahedral intermediate. At pH < 2 formation of this intermediate becomes rate-limiting; rate constant of its formation is 2 . 104 s-1.

Kinetics and mechanism of cyclization of N-(2-methoxycarbonylphenyl)-N’-methylsulphonamide to 3-methyl-(1H)-2,1,3-benzothiadiazin-4(3H)-one 2,2-dioxide

1991 ◽  
Vol 56 (8) ◽  
pp. 1701-1710 ◽  
Author(s):  
Jaromír Kaválek ◽  
Vladimír Macháček ◽  
Miloš Sedlák ◽  
Vojeslav Štěrba
Keyword(s):  
Potassium Hydroxide ◽  
Acid Catalysis ◽  
Potassium Hydroxide Solution ◽  
Hydroxide Solution ◽  
General Base ◽  
Rate Limiting Step ◽  
Limiting Step ◽  
Cyclization Kinetics ◽  
Rate Limiting ◽  
Kinetics Of

The cyclization kinetics of N-(2-methylcarbonylphenyl)-N’-methylsulfonamide (IIb) into 3-methyl-(1H)-2,1,3-benzothiadiazin-4(3H)-one 2,2-dioxide (Ib) has been studied in ethanolamine, morpholine, and butylamine buffers and in potassium hydroxide solution. The cyclization is subject to general base and general acid catalysis. The value of the Bronsted coefficient β is about 0.1, which indicates that splitting off of the proton from negatively charged tetrahedral intermediate represents the rate-limiting and thermodynamically favourable step. In the solutions of potassium hydroxide the cyclization of dianion of the starting ester IIb probably becomes the rate-limiting step.

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