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Biomedical subjects

U Hopfer

Publications and source records attributed to U Hopfer.

At least 91 records · Page 5Linked to original sources

Isolation of stable pancreatic zymogen granules.

Isolated pancreatic zymogen granules have been reported to lyse in common electrolyte solutions such as NaCl or KCl or at pH values above 5.5. A new method, based on an isosmotic Percoll density gradient, was developed for the isolation of zymogen granules and applied to rat pancreas. The granules are highly purified as judged by electron microscopic appearance and specific amylase activity. These granules exhibit a high degree of stability at physiological pH and in isotonic NaCl or KCl. Zymogen granule diameters, determined with a Coulter Counter, were 1.0 +/- 0.2 micron in either isotonic NaCl and KCl. These size values, obtained in physiological solutions, are comparable with granule sizes determined in intact cells by microscopy. Amylase activity averaged 0.66 microU per granule and protein content averaged 0.31 pg per granule; these values were not significantly influenced by different conditions of pH between 5.5 and 7.0 and ionic strength from near 0 to 0.15. The granule density estimated from the protein content was 1.13 g/ml, which agrees well with the behavior of granules in a density gradient. The properties of zymogen granules from the new preparation rectify the apparent discrepancy between their role as a storage organelle and their previously reported in vitro instability.

Animals↗

Purification of brush border membrane by thiocyanate treatment.

Rat small intestinal brush border membranes are purified from brush borders by homogenization in relatively high concentrations of thiocyanate salts (0.56 M LiSCN, 0.41 M NaSCN, or 0.52 M KSCN), removal of this salt, and differential centrifugation to separate cytoskeletal material from membranes. The marker enzyme, sucrase, is enriched 98-fold in the final membranes over the starting homogenate of intestinal scrapings at a yield of about 20%. The isolated membranes are capable of secondary active sodium-dependent glucose transport as demonstrated by sodium gradient-supported overshooting glucose uptake.

Animals↗

Inhibition of amiloride-sensitive sodium conductance by indoleamines.

To examine a possible role of indoleamines in the regulation of epithelial sodium absorption, the effect of serotonin (5-hydroxytryptamine) and several derivatives on electrolyte transport was measured in vitro in the baboon bronchus and in the trachea and colon of sodium-deficient rats. Serotonin, melatonin (N-acetyl-5-hydroxytryptamine), and harmaline (1-methyl-7-methoxy-3,4-dihydro-beta-carboline) inhibited sodium transport in all three preparations in a similar manner to the natriuretic agent amiloride. In all three epithelia, sodium absorption via the amiloride-sensitive pathway constitutes a substantial portion of total electrolyte transport, measured as the amiloride-sensitive short-circuit current. Thus 25 microM amiloride inhibited the short-circuit current 21% in the rat trachea, 63% in the baboon bronchus, and 90% in the rat colon. Serotonin, melatonin, and harmaline inhibited the amiloride-sensitive portion of the short-circuit current from the luminal side of the epithelium. The inhibition was rapid, requiring only seconds, and maximal inhibition by serotonin was identical to that by amiloride. When sodium was omitted from the luminal solution, the short-circuit current was reduced a similar amount, suggesting that sodium absorption was being inhibited by both amiloride and the indoles. The IC50 value for amiloride was 50 nM in the baboon bronchus and 500 nM in the rat colon. In contrast, the IC50 value for serotonin was 0.4 mM in the baboon bronchus and 8 mM in the rat colon. These results, together with the wide distribution of amine-precursor-uptake-and-decarboxylation (APUD) cells in the respiratory and intestinal tract, suggest that certain indoleamines could play a role as local regulators of fluid and electrolyte transport. For example, in the airways, indoleamines may be one of the factors involved in regulation of the depth of the periciliary fluid layer.

Amiloride↗

Mechanism of Cl- translocation across small intestinal brush-border membrane. I. Absence of Na+-Cl- cotransport.

Kinetic predictions from a putative Na+-Cl- cotransport system were tested in vesicles of isolated rat intestinal brush-border membranes. For the conditions of isotope exchange at equilibrium, the model predicts activation of the Na+ and Cl- exchange rates by increasing concentrations of the counterion, at least for concentrations well below the Km of the counterion. When Cl- was the test ion (150 mM), K+ plus monactin replaced Na+. When Na+ was the test ion (150 mM), SO42(-) replaced Cl-. Contrary to the predictions of the cotransport model, the velocities of Na+ and Cl- exchange were constant regardless of the concentration of the putative cosubstrates Cl- and Na+, respectively. Cl- transport in the isolated vesicles was carrier mediated as judged by the criterion of saturability of transport (Km = 255 mM), and the pathways involved in net NaCl movements accounted for minimally 70 and 40% of the Na+ and Cl- exchange rates, respectively. These findings exclude a significant contribution of a Na+-Cl- cotransport mechanism to NaCl uptake across the intestinal brush-border membranes in the concentration range tested, i.e., above 25 mM. The findings are, however, consistent with a double exchange of Na+ for H+ and of Cl- for OH- (HCO3(-). A Donnan potential of 10 mV (inside negative) can explain differences in the equilibrium uptake of Na+, anions, and glucose by intestinal brush-border membranes.

Animals↗

Mechanism of Cl- translocation across small intestinal brush-border membrane. II. Demonstration of Cl--OH- exchange and Cl- conductance.

The mechanisms of Cl- transport across the brush-border membrane from rat small intestine were investigated in vitro in isolated vesicles and in vivo in ileal and jejunal segments. A Cl--OH- exchange mechanism was demonstrated in isolated vesicles by observing concentrative Cl- uptake driven by a pH gradient (extravesicular pH less than intravesicular pH). A Cl- conductance pathway was demonstrated by concentrative Cl- uptake driven by a K+ diffusion potential. The K+ diffusion potential was generated by a K+ concentration gradient in the presence of valinomycin (extravesicular K+ concentration greater than intravesicular K+ concentration). Furosemide and stilbene 4-acetamido-4'-isothiocyanostilbene-2,2'-disulfonate (SITS) strongly inhibited the Cl--OH- exchange but did not affect the Cl- conductance pathway, Na+-dependent glucose transport, and Na+-Na+ exchange. Under isotope exchange conditions at equilibrium, SITS inhibited Cl- transport up to 63%, indicating that this portion of Cl- transport is mediated by the Cl--OH- exchange transporter, with the remainder presumably due to the Cl- conductance pathway. In perfused small intestinal segments, Na+, Cl-, HCO3(-), and water were absorbed from the lumen in the absence of SITS. The presence of 5 mM SITS inhibited NaCl absorption and decreased HCO3(-) and water absorption in both jejunum and ileum but did not affect glucose absorption. The inhibition of in vivo salt absorption by SITS suggests that the Cl--OH- exchange mechanism plays a major role in NaCl absorption in intact enterocytes.

4-Acetamido-4'-isothiocyanatostilbene-2,2'-disulfo↗

Kinetic features of cotransport mechanisms under isotope exchange conditions.

The mechanisms of carrier-mediated cotransport across biological membranes can be divided into those with ordered and those with random sequences of substrate binding to and debinding from the carrier. When the membrane is considered a symmetry plane, the sequence of substrate binding and debinding of ordered mechanisms can exhibited either of two symmetries: mirror or glide. The carrier-mediated cotransport of solutes is kinetically analyzed for equilibrium exchange in membrane vesicles to obtain criteria for distinguishing the different transport mechanisms. Three types of kinetic measurement are necessary to determine the type of cotransport mechanism: (1) isotope exchange of either substrate as a function of its concentration (Km determination); (2) isotope exchange of either substrate as a function of cosubstrate concentration (activation curves); and (3) ratios of mass exchange rates of both substrates as a function of various substrate concentration ratios. These criteria are applied to and discussed in terms of Na+-dependent D-glucose cotransport and putative Na+-Cl- cotransport.

Animals↗

The mechanism of Na+-dependent D-glucose transport.

The mechanism of Na+-dependent D-glucose transport was investigated by kinetic means in rabbit small intestinal and renal brush border membranes. The rate of glucose transport was measured under equilibrium exchange conditions as a function of its own concentration and of the Na+ concentration. Likewise, the rate of Na+ transport was measured as a function of the D-glucose concentration. Noteworthy characteristics of the Na+-dependent glucose transport system are: 1) linear dependence of the glucose transport rate on Na+ concentration up to 0.1 M (at constant ionic strength), indicating a 1:1 stoichiometry of Na+-D-glucose cotransport under net flux conditions; 2) virtual Na+ independence of the apparent affinity of the transport system for D-glucose; 3) a stimulation-inhibition pattern if the transport rate of either substrate (D-glucose, Na+) is measured as function of increasing concentrations of its co-substrate; 4) a varying flux ratio of D-glucose to Na+ which can be either above or below 1, depending on the concentration ratio of the two substrates; 5) a rate constant for translocation of the loaded carrier which is faster than that for the dissociation of Na+. Treating Na+-D glucose co-transport analogous to an enzyme reaction, these features are consistent with an iso-ordered-bi-bi kinetic model, whereby the first solute that binds to the transport system at one membrane interface is the one that is released first at the other interface (first-in-first-out characteristics). The kinetic model is explained by a gated pore mechanism, whereby the translocation of the transported solutes across the permeability barrier is achieved by a rocker-type conformational change of the transport system (presumed to be a protein) which moves the permeability barrier past the solutes.

Animals↗

Saliva from patients with cystic fibrosis inhibits amiloride-sensitive sodium transport.

A factor is present in the saliva and sweat from patients with cystic fibrosis (CF) which inhibits the reabsorption of sodium in the ducts of the salivary and sweat glands. Inasmuch as the physiology of sodium absorption is similar in salivary ducts and the distal colon, we have examined the sensitivity of the sodium absorption in the rat colon to saliva from CF patients. Sodium absorption by the rat colon, estimated as the shortcircuit current, was inhibited by saliva from both patients with CF and normal volunteers. However, only with CF saliva was the inhibition consistently proportional to the saliva concentration. Furthermore, the inhibitory activity of CF saliva was greater than the inhibition observed with saliva from age- and sex-matched controls (percentage of inhibition: CF = 20.1 +/- 2.2, and controls = 14.9 +/- 2.1; P < 0.02), and the inhibition of the colonic shortcircuit current was proportional to the activity measured by the ductal retrograde perfusion assay with the rat parotid gland (linear correlation coefficient = 0.634; P < 0.005). This latter assay is an accepted assay for CF factor activity. We conclude that the CF factor present in saliva probably interacts in a reversible manner with the amiloride-sensitive sodium transport system which is present in all sodium scavenging epithelia. The rat colon is a promising assay system for CF factor activity because the electrical measurements permit a rapid quantitative estimate of activity and a single piece of tissue can be used to measure the activity of several saliva samples.

Amiloride↗

Cytochemical localization of alkaline phosphatase and Na+-pump sites in adult rat colon.

The cellular and subcellular locialization of alkaline and K+-dependent phosphatase activities in the colonic mucosa of adult rats and rabbits was studied with the electron microscope. The 1-cysteine-sensitive alkaline phosphatase activity was observed in the brush border membrane of the chief cells. The contraluminal plasma membrane of chief cells was devoid of this enzyme activity. In contrast, the cardiac glycoside-sensitive K+-dependent phosphatase was predominantly localized in this region of the cheif cells.

Alkaline Phosphatase↗

Evidence against a specific effect of serum from patients with cystic fibrosis on sodium-dependent glucose transport in the rat jejunum.

Sera from patients with cystic fibrosis of the pancreas (CF) and normal human sera were assayed for the ability to inhibit sodium-dependent glucose transport in rat brush-border membrane vesicles. Fresh CF and age- and sex-matched control sera were both inhibitory when compared to physiologic saline. The inhibition by CF serum was 44 +/- 13% (mean +/- SD) at a final serum concentration of 6.7%, 67 +/- 34% at 10% serum, and 68 +/- 28% at 20% serum. The ratio of the inhibition of CF sera compared to that of control sera was 1.00, 0.78, and 0.93 at 6.7, 10, and 20% serum concentrations, respectively. Although a slightly greater inhibition by CF serum was observed at a concentration of 10%, this is probably not significant because no difference could be detected at a concentration of 20% serum. Glucose transport in the presence of serum was sensitive to phlorizin indicating that the residual glucose transport was proceeding by the sodium-dependent glucose transport system. These findings suggest that CF serum does not specifically inhibit the sodium-dependent glucose transport system. The intravesicular space accessible to glucose was reduced in the presence of CF or control serum. Fresh CF serum was 1.4 times more effective than fresh control serum (P less than 0.01). The presence of substantial vesicle-shrinking activity in control serum indicates that this activity cannot be considered specific for CF.

Animals↗

Transport in isolated plasma membranes.

Plasma membrane vesicles constitute a simpler experimental system for studying transport compared to cells or intact tissue. The principal advantages of the vesicle approach are the elimination of metabolism as a complicating factor and the ability to control the composition of the solutions on both sides of the membrane. The major disadvantage is vesicle heterogeneity. However, techniques are available to avoid the kinetic artifacts that are due to the heterogeneity. Results of transport studies using membrane vesicles have conclusively shown that D-glucose and amino acids are co-transported with Na+ and that transport against a concentration gradient is driven by an electrochemical Na+ gradient. As a result of coupling between Na+ and the nonelectrolytes, estimates of the kinetic parameters of transport, Km and Vmax, require that the load on the Na+ gradient be taken into account. This has rarely been done. Although electrolyte transport is a major function of the plasma membrane, knowledge of the mechanisms involved is limited. Future investigations employing specific ionophores should contribute much to our understanding of the mechanisms underlying ATP-independent ion transport. Examples of the application of membrane vesicles for studying transport-related aspects of diseases are discussed.

Biological Transport↗