Supplementation with Brush Border Enzyme Alkaline Phosphatase Slows Aging

2020 ◽  
Vol 23 (2) ◽  
pp. 171-175 ◽  
Author(s):  
James W. Larrick ◽  
Andrew R. Mendelsohn
Keyword(s):  
Alkaline Phosphatase ◽  
Brush Border ◽  
Brush Border Enzyme ◽  
Enzyme Alkaline Phosphatase

Presence of γ-glutamyltransferase in the renal microvascular compartment

1981 ◽  
Vol 59 (6) ◽  
pp. 383-386 ◽  
Author(s):  
P. D. Dass ◽  
R. P. Misra ◽  
T. C. Welbourne
Keyword(s):  
Alkaline Phosphatase ◽  
Phosphatase Activity ◽  
Density Gradient ◽  
Alkaline Phosphatase Activity ◽  
Brush Border ◽  
Sucrose Density Gradient ◽  
Isolated Glomeruli ◽  
Crude Homogenate ◽  
Brush Border Enzyme ◽  
Enzyme Alkaline Phosphatase

The association between the brush border enzyme alkaline phosphatase and γ-glutamyltransferase was determined by sucrose density gradient analysis of crude kidney homogenates, isolated glomeruli, and isolated microvessels. As previously established there is an overlap of these enzyme activities in the crude homogenate corresponding to a density of 1.17 g∙cm−3. In contrast, isolated glomeruli sedimented with a peak of 1.25 g∙cm−3 and exhibited γ-glutamyltransferase activity but little alkaline phosphatase activity; homogenizing isolated glomeruli shifted the fragments to a density coincident with that observed for the crude homogenate γ-glutamyltransferase peak. A second population of capillaries, isolated microvessels, were homogenized and analyzed on the sucrose density gradient. These fragments sedimented over the same range as crude homogenate γ-glutamyltransferase peak but were devoid of alkaline phosphatase activity and yet exhibited remarkable γ-glutamyltransferase activity. The results indicate homogenization of renal cortex results in a heterogenous collection of particles from both tubular and microvascular locations exhibiting γ-glutamyltransferase activity which overlap with the brush border alkaline phosphatase containing membranes. However, isolation of microvessels and glomeruli prior to homogenization allows separation of γ-glutamyltransferase from alkaline phosphatase activity; between 10 and 20% of the total homogenate γ-glutamyltransferase activity is estimated to be associated with the microvascular compartment.

Different diuresis-dependent excretions of urinary enzymes: N-acetyl-beta-D-glucosaminidase, alanine aminopeptidase, alkaline phosphatase, and gamma-glutamyltransferase.

1986 ◽  
Vol 32 (3) ◽  
pp. 529-532 ◽  
Author(s):  
K Jung ◽  
G Schulze ◽  
C Reinholdt
Keyword(s):  
Alkaline Phosphatase ◽  
Brush Border ◽  
Excretion Rate ◽  
Urine Flow ◽  
High Intake ◽  
Brush Border Enzymes ◽  
Urinary Creatinine ◽  
Gamma Glutamyltransferase ◽  
Alanine Aminopeptidase ◽  
Brush Border Enzyme

Abstract We studied how much of the lysosomal enzyme N-acetyl-beta-D-glucosaminidase (EC 3.2.1.30) and of the brush-border enzymes alanine aminopeptidase (EC 3.4.11.2), alkaline phosphatase (EC 3.1.3.1), and gamma-glutamyltransferase (EC 2.3.2.2) was excreted in urine over 8 h after a high intake of fluid (22 mL per kilogram of body weight). The hourly excretion of all four enzymes increased with the increasing urine flow rate. The excretion rate of the brush-border enzymes was more markedly influenced than that of N-acetyl-beta-D-glucosaminidase. By relating the enzyme excretion to urinary creatinine we could reduce the variability of brush-border enzyme output and could completely compensate for the effect of diuresis on the excretion of N-acetyl-beta-D-glucosaminidase.

Pattern of rat intestinal brush-border enzyme gene expression changes with epithelial growth state

1995 ◽  
Vol 269 (2) ◽  
pp. C385-C391 ◽  
Author(s):  
R. A. Hodin ◽  
S. M. Chamberlain ◽  
S. Meng
Keyword(s):  
Gene Expression ◽  
Alkaline Phosphatase ◽  
Brush Border ◽  
Longitudinal Axis ◽  
Mrna Levels ◽  
Intestinal Alkaline Phosphatase ◽  
Enzyme Gene ◽  
Growth State ◽  
Brush Border Enzyme ◽  
Epithelial Growth

Enterocyte growth and differentiation occur simultaneously within the epithelium, but little is known regarding any relationship between these two processes. Four rat models of small intestinal epithelial hypo- and hyperplasia (neonatal ontogeny, fasting/refeeding, hypo-/hyperthyroidism, and bombesin treatment) were used to study the regulation of enterocyte gene expression in relation to epithelial growth state. Mucosal scrapings, as well as crypt and villus cell populations, were subjected to Northern blot analyses using radiolabeled cDNA probes corresponding to lactase, intestinal alkaline phosphatase, villin, ornithine decarboxylase (ODC), and the actin control. In all four models, the hypoplastic (atrophic) condition is characterized by high levels of lactase and low levels of the 3.0-kb intestinal alkaline phosphatase mRNA, whereas under hyperplastic conditions this pattern is reversed. The changes in intestinal alkaline phosphatase and lactase are qualitatively similar along the longitudinal axis of the intestine and are proportional to the degree of hyperplasia, as verified by ODC mRNA levels. Furthermore, the crypt-villus axis of differentiation is maintained regardless of epithelial growth state. In conclusion, the pattern of brush-border enzyme gene expression changes as a function of epithelial growth state, indicating a previously unrecognized degree of plasticity to the state of enterocyte differentiation.

Effect of ethanol on disaccharidases of hamster jejunal brush border membrane.

1979 ◽  
Vol 237 (1) ◽  
pp. E68
Author(s):  
P K Dinda ◽  
R O Hurst ◽  
I T Beck
Keyword(s):  
Alkaline Phosphatase ◽  
Brush Border ◽  
Brush Border Membrane ◽  
Kinetic Studies ◽  
Time Dependent ◽  
Acute Exposure ◽  
Dependent Manner ◽  
Brush Border Enzyme ◽  
Dose Dependent

This study was undertaken to investigate the effect of alcohol on the activity of jejunal disaccharidases (DS). The activity of DS in a preparation of purified brush border membrane of hamster jejunum was measured in the absence and in the presence (0.8 to 6.4% wt/vol) of ethanol. To compare the effect of alcohol on DS with its action on a brush border enzyme of a different group, we also measured the activity of alkaline phosphatase (AP) under similar conditions. Ethanol depressed the activity of sucrase, maltase, and lactase in a dose-dependent and time-dependent manner, but it stimulated the activity of AP. The ethanol-induced inhibition of DS was completely reversible. Kinetic studies indicate that ethanol depressed the Vmax and increased the Km of sucrase and lactase. The Vmax of maltase also decreased, but the Km of this hydrolase was not affected by ethanol. From the results of this study it would appear that acute exposure of the jejunal brush border to ethanol depresses the DS activity of the membrane and that (because the AP was not depressed) the ethanol-induced inhibition of DS is not the result of a general inhibition of all enzymes of the brush border.

scholarly journals A combined microphysiological-computational omics approach in dietary protein evaluation

2020 ◽  
Vol 4 (1) ◽  
Author(s):  
Paulus G. M. Jochems ◽  
Willem R. Keusters ◽  
Antoine H. P. America ◽  
Pascale C. S. Rietveld ◽  
Shanna Bastiaan-Net ◽  
...  
Keyword(s):  
Enzyme Activity ◽  
Brush Border ◽  
Biological Effects ◽  
Whey Protein Concentrate ◽  
World Population ◽  
Biological Efficacy ◽  
Protein Sources ◽  
Immune Parameters ◽  
Peptide Composition ◽  
Brush Border Enzyme

AbstractFood security is under increased pressure due to the ever-growing world population. To tackle this, alternative protein sources need to be evaluated for nutritional value, which requires information on digesta peptide composition in comparison to established protein sources and coupling to biological parameters. Here, a combined experimental and computational approach is presented, which compared seventeen protein sources with cow’s whey protein concentrate (WPC) as the benchmark. In vitro digestion of proteins was followed by proteomics analysis and statistical model-based clustering. Information on digesta peptide composition resulted in 3 cluster groups, primarily driven by the peptide overlap with the benchmark protein WPC. Functional protein data was then incorporated in the computational model after evaluating the effects of eighteen protein digests on intestinal barrier integrity, viability, brush border enzyme activity, and immune parameters using a bioengineered intestine as microphysiological gut system. This resulted in 6 cluster groups. Biological clustering was driven by viability, brush border enzyme activity, and significant differences in immune parameters. Finally, a combination of proteomic and biological efficacy data resulted in 5 clusters groups, driven by a combination of digesta peptide composition and biological effects. The key finding of our holistic approach is that protein source (animal, plant or alternative derived) is not a driving force behind the delivery of bioactive peptides and their biological efficacy.

Alkaline phosphatase: A marker enzyme for brush border membrane

1972 ◽  
Vol 28 (4) ◽  
pp. 385-386 ◽  
Author(s):  
U. Schmidt ◽  
U. C. Dubach ◽  
I. Bieder ◽  
B. Funk
Keyword(s):  
Alkaline Phosphatase ◽  
Brush Border ◽  
Brush Border Membrane ◽  
Marker Enzyme

Membrane fluidity and enzyme activities in brush border and basolateral membranes of the dog kidney

1982 ◽  
Vol 242 (3) ◽  
pp. F246-F253 ◽  
Author(s):  
C. Le Grimellec ◽  
M. C. Giocondi ◽  
B. Carriere ◽  
S. Carriere ◽  
J. Cardinal
Keyword(s):  
Alkaline Phosphatase ◽  
Brush Border ◽  
Plasma Membranes ◽  
Physical State ◽  
Arrhenius Plot ◽  
Membrane Lipids ◽  
Basolateral Membranes ◽  
Brush Border Membranes ◽  
Dog Kidney ◽  
Additional Support

The physical state of membrane lipids and relationships with the activity of Na+-K+-ATPase and alkaline phosphatase were studied in basolateral and brush border membranes of the dog kidney. Fluorescence polarization and electron spin resonance experiments demonstrate that basolateral membranes are much more fluid than brush border membranes. This can be accounted for by a difference in fluidity of the lipid part of the membranes. Broad (43-17 degrees C) thermotropic transitions are observed in liposomes made from total lipid extracts of brush border and basolateral membranes. Fluorescence data strongly suggest that thermotropic transitions also occur in intact membranes and that a change in membrane physical state may take place around the physiological temperature. A nonlinear Arrhenius plot for the Na+-K+-ATPase activity in basolateral membranes (breakpoint 21 degrees C) provides additional support for the existence of a lipid liquid leads to gel transition in antiluminal plasma membranes. A break in the Arrhenius plot of alkaline phosphatase activity is also observed but at a temperature significantly higher (26 degrees C) than that of the end of the thermotropic transition. "Room temperature" appears as a critical zone for lipid physical state and activities of both enzymes.

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