Literature DB >> 7462009

Kinetic characterization of unspecific alkaline phosphatase at different villus sites of rat jejunum. A quantitative histochemical study.

S Gutschmidt, U Lange, E O Riecken.   

Abstract

A quantitative histochemical method to determine the apparent Km and Vmax values of rat intestinal unspecific alkaline phosphatase at different sites of the villi is described. Naphthol-As-Bi-phosphate (0.025-1.5 mM) is employed as substrate and Fast Blue B as coupling reagent, and the resulting azo-dye in the brush border membrane has an absorbance maximum at lambda 550 nm. The ratio between the absorbance at lambda 550 and lambda 500 nm is constant as calculated from automatically recorded spectra at different intense dye deposits. Its absorbance is a linear function of incubation time up to 3 min and thickness of the slices up to 10 micrometers both with medium (0.5 mM) and high (1.5 mM) substrate concentrations. Using the histochemical assay under comparable conditions in test tube experiments with homogenates of intestinal mucosa an app. Km of 0.26 +/- 0.081 mM (weighted regression analysis) and 0.28-0.084 mM (direct linear plotting) is determined, demonstrating an affinity to the histochemical substrate, which is about 10 times higher than for p-Nitro-phenyl-phosphate with the purified enzyme. The results obtained by scanning the total dye deposits along jejunal villi show considerable differences in enzymatic activity between single villi and an increase from the villus base up to the transition between medium and apical villus third. As well in the apical region as at the villus base saturation curves are obtained by determining the relationship between the absorbance and the substrate concentration under standard conditions (slice thickness 10 micrometers, incubation time 3 min, 37 degrees C, pH 8.3). Calculated by weighted regression analysis and direct linear plotting from the absorbance data of six female rats the medium app. kinetic data +/- SD from the jejunal villi read as follows. Apical: Km = 0.81 +/- 0.43 mM, Vmax = 3.99 +/- 1.217 absorbance units (A) and Km = 0.87 +/- 0.428 mM, Vmax = 4.02 +/- 1.191 A, respectively. Basal: Km = 0.82 +/- 0.261 mM, Vmax = 3.26 +/- 0.719 A and Km = 0.77 +/- 0.184 mM, Vmax = 3.04 +/- 0.518 AU, respectively. As demonstrated by factorial analysis of variance only Vmax is influenced by the villus position.

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Year:  1980        PMID: 7462009     DOI: 10.1007/bf00533136

Source DB:  PubMed          Journal:  Histochemistry        ISSN: 0301-5564


  31 in total

1.  Statistical estimations in enzyme kinetics.

Authors:  G N WILKINSON
Journal:  Biochem J       Date:  1961-08       Impact factor: 3.857

2.  Anion-stimulated ATPase activity of brush border from rat small intestine.

Authors:  M H Humphreys; L Y Chou
Journal:  Am J Physiol       Date:  1979-01

3.  Theoretical and experimental aspects of enzyme determination in a cytochemical model system of polyacrylamide films containing alkaline phosphatase.

Authors:  P Van Duijn; E Pascoe; M Van der Ploeg
Journal:  J Histochem Cytochem       Date:  1967-08       Impact factor: 2.479

4.  The influence of various cell kinetic conditions on functional differentiation in the small intestine of the rat. A study of enzymes bound to subcellular organelles.

Authors:  N J de Both; J M van Dongen; B van Hofwegen; J Keulemann; W J Visser; H Galjaard
Journal:  Dev Biol       Date:  1974-05       Impact factor: 3.582

5.  The direct linear plot. A new graphical procedure for estimating enzyme kinetic parameters.

Authors:  R Eisenthal; A Cornish-Bowden
Journal:  Biochem J       Date:  1974-06       Impact factor: 3.857

6.  Purification and properties of alkaline phosphatase from the mucosa of rat small intestine.

Authors:  H Nakasaki; T Matsushima; S Sato; T Kawachi
Journal:  J Biochem       Date:  1979-11       Impact factor: 3.387

7.  The origin of the serum alkaline phosphatase in normal rats.

Authors:  A B Righetti; M M Kaplan
Journal:  Biochim Biophys Acta       Date:  1971

8.  Quantitative determination of enzymes in different parts of the villi and crypts of rat small intestine. Comparison of alkaline phosphatase, disaccharidases and dipepeptidases.

Authors:  C Nordström; A Dahlqvist; L Josefsson
Journal:  J Histochem Cytochem       Date:  1967-12       Impact factor: 2.479

9.  Submicroscopic localization of the alkaline phosphatase activity in the duodenum of the rat.

Authors:  J Hugon; M Borgers
Journal:  Exp Cell Res       Date:  1967-03       Impact factor: 3.905

10.  Developmental pattern of rat intestinal brush-border enzymic proteins along the villus--crypt axis.

Authors:  P M Simon; M Kedinger; F Raul; J F Grenier; K Haffen
Journal:  Biochem J       Date:  1979-02-15       Impact factor: 3.857

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  9 in total

1.  Automated histochemical analysis of cell populations in the intact follicle-associated epithelium of the mouse Peyer's patch.

Authors:  M W Smith; P S James; D R Tivey; D Brown
Journal:  Histochem J       Date:  1988-08

Review 2.  Analysis of enzyme reactions in situ.

Authors:  C J Van Noorden; G N Jonges
Journal:  Histochem J       Date:  1995-02

3.  Kinetic analysis of lactate dehydrogenase in situ in mouse liver determined with a quantitative histochemical technique.

Authors:  Y Nakae; P J Stoward
Journal:  Histochem J       Date:  1993-03

4.  Menadiol diphosphate, a new substrate for non-specific alkaline phosphatase in histochemistry and immunohistochemistry.

Authors:  A Dikow; R Gossrau; H G Frank
Journal:  Histochemistry       Date:  1990

5.  Identification of intestinal cells responsive to calcitriol (1,25-dihydroxycholecalciferol).

Authors:  M W Smith; M E Bruns; E D Lawson
Journal:  Biochem J       Date:  1985-01-01       Impact factor: 3.857

6.  "In situ"--measurements of protein contents in the brush border region along rat jejunal villi and their correlations with four enzyme activities.

Authors:  S Gutschmidt; U Lange; E O Riecken
Journal:  Histochemistry       Date:  1981

7.  Early changes in brush border disaccharidase kinetics in rat jejunum following subcutaneous administration of tetraiodothyronine: a quantitative histochemical study on villi revealing normal morphology.

Authors:  S Gutschmidt; C Emde
Journal:  Histochemistry       Date:  1981

8.  Adaptative response of alpha- and beta-glucosidase kinetics along the villi of rat self-filling jejunal blind loops.

Authors:  S Gutschmidt; F Sandforth; H Menge; E O Riecken
Journal:  Gut       Date:  1982-05       Impact factor: 23.059

9.  A quantitative histochemical study of dipeptidylpeptidase IV (DPP IV).

Authors:  S Gutschmidt; R Gossrau
Journal:  Histochemistry       Date:  1981
  9 in total

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