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  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochimica et Biophysica Acta (BBA)/Biomembranes 550 (1979), S. 120-130 
    ISSN: 0005-2736
    Keywords: Intestinal absorption ; Michaelis constant ; Phenylalanine ; Unstirred layer
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Medicine , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 335 (1987), S. 97-102 
    ISSN: 1432-1912
    Keywords: Antipyrine ; Intestinal absorption ; Intestinal blood flow
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The appearance rate of antipyrine in intestinal venous blood was measured in anesthetized rats during perfusion (0.2 ml/min) of a buffered solution with 1 mmol/l labeled antipyrine through a jejunal, ileal, or colonic segment (length: 2–5 cm). When the blood flow rate was increased from 0.9–1.2 to 1.6–2.0 ml min−1 g−1 by raising the systemic blood pressure from 80 to 130 mm Hg, the absorption of antipyrine increased only in the colon. Stepwise reduction of the blood flow rate from 1.4–1.7 to 0.2–0.3 or stepwise raise from 0.2–0.3 to 1.4 ml min−1 g−1 by constriction or release of the mesenteric artery decreased or increased the absorption rate of antipyrine. The relation between absorption and flow rate can be described by curves which ascend at low and level off into a horizontal section at high flow rates. At the same blood flow rate the regional absorption rate decreased in the order jejunum, ileum, and colon with the largest step between ileum and colon. Model analysis yielded the following results for jejunum, ileum, and colon, respectively: permeability-surface area product 0.083, 0.074, and 0.037 ml min−1 g−1; fraction of absorptive site blood flow rate 0.24, 0.19, 0.08. The differences can be attributed mainly to the change of the surface area from jejunum to ileum and colon.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 304 (1978), S. 175-181 
    ISSN: 1432-1912
    Keywords: Small intestine ; Intestinal absorption ; Drug absorption ; Phenylalanine ; Intestinal unstirred layer
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The appearance rate of butanol, antipyrine, salicylic acid, and urea in the venous blood of rat jejunal loops perfused in vivo is increased up to 64%, if the intraluminal solution is mixed more efficiently by the simultaneous perfusion of air. The enhancement of the absorption can be attributed partly to the enlarged absorbing area but mainly to the reduction of the effective unstirred layer thickness by about 500 μm. The unstirred layer reduces the phenylalanine absorption at 0.1 mmol l−1 but not at 100 mmol l−1, since at high concentrations a full saturation of the transport system can be achieved in spite of the unstirred layer resistance. The interference of the unstirred layer increases with increasing absorbability of the substances.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 321 (1982), S. 149-156 
    ISSN: 1432-1912
    Keywords: Intestinal absorption ; Polyethylene glycol 4000 ; Osmolarity ; Laxatives ; Bile acids ; Net water flux
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In anaesthetized rats the appearance rate of 14C-polyethylene glycol 4000 (14C-PEG 4000) was measured in the intestinal venous blood after intraluminal administration into a jejunal, ileal, and colonic segment. The absorption rate was small, especially in the colon (0.5–4.2 % within 60 min in an intestinal segment of about 300 mg wet tissue weight depending on the batch of 14C-PEG 4000). The absorbed PEG in the plasma consisted mainly of molecules with lower molecular weight than 4000 which were included in the commercial batches of 14C-PEG 4000. The appearance rate of 14C-PEG decreased with time after single dose but remained constant, when a 14C-PEG solution was perfused continuously through the intestinal lumen. A hypotonic solution increased and a hypertonic one decreased slightly the absorption of PEG in the jejunum and ileum but not in the colon. The influence of bisacodyl (100 mg l−1) and ricinoleate (10 mmol l−1) on the absorption of PEG was small or absent, while deoxycholate (5 mmol l−1) raised the absorption rate considerably, predominantly of the high molecular weight fraction. If in intestinal absorption studies a batch of commercial 14C-PEG 4000 with a small low molecular weight fraction is used, the error in the determination of net water flux caused by the absorption of PEG can be neglected. The influence of osmolarity and laxatives is insignificant. Bile acids increase the intestinal permeability of PEG 4000, so that the net water flux determination can be biased considerably.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 329 (1985), S. 70-76 
    ISSN: 1432-1912
    Keywords: Intestinal absorption ; Serosal transfer ; Intestinal blood flow ; Distention of intestinal wall
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In anesthetized rats, the appearance rates of a series of labeled substances in jejunal venous blood (Φ B) and serosal bath (Φ S) were measured in vivo (intestinal blood flow rate 1.5 ml min−1g−1) after intraluminal administration of 0.5 ml buffer solution (initial concentration 1 mmol/l or 1 GBq/l tritiated water) into a closed jejunal segment (length 4–5cm). Between 32% (erythritol) and 93% (salicylic acid) of the administered activity (unchanged substance and possible metabolites) appeared in the intestinal venous blood within 60 min. The fraction recovered from the serosal bath after 15 (60) min was 11 (6) % for tritiated water, 7 (4) % for aniline, 3 (7)% for aminopyrine, 5 (4) % for butanol, 3 (3) % for benzyl alcohol, 2 (4) % for benzylamine, 1–2% for benzoic acid, theophyline, methyl-α-d-glucopyranoside,l-lysine, antipyrine, and urea, and less than 1% forl-phenylalanine,d-galactose, erythritol, and salicylic acid. During single pass perfusion of a jejunal segment (length 3–4 cm) the fraction of serosal transferΦ S/(Φ B+Φ S) was 19% for tritiated water, 4.9% for antipyrine, 0.5% for benzoic acid, and 0.08% for salicylic acid. Distension of the intestinal wall by administration of 1 ml buffer solution instead of 0.5 ml increased the appearance rate of benzoic acid and antipyrine in intestinal venous blood by a factor of 2 and serosal transfer by a factor of approximately 3. Reduction of blood flow rate from 1.26 to 0.91 ml min−1g−1 decreased the fraction of antipyrine recovered in the intestinal venous blood within 60 min from 84% to 72% and increased the fraction transferred into the serosal bath from 2.3% to 9.1%. A high mucosal-serosal transfer in rat small intestine with intact blood supply can be expected for substances with high epithelial permeability and low binding to plasma proteins.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 334 (1986), S. 514-524 
    ISSN: 1432-1912
    Keywords: Intestinal absorption ; Dietary fiber ; Diffusion coefficient ; Unstirred layer ; Intraluminal pressure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The appearance rates of antipyrine, benzoic acid, benzylamine, urea, andα-methyl-D-glucoside (MG) in jejunal venous blood of anesthetized rats were measured with and without dietary fibers methylcellulose, carboxymethylcellulose sodium, guaran, and sodium alginate in the luminal solution. Raising the concentration of methylcellulose from 0 to 17.5 g/l resulted in an exponential increase in the viscosity of the solution to 98 cSt, a linear decrease of the diffusion coefficient for antipyrine by 28%, and an increase in antipyrine absorption in the perfused jejunal segment by 23%. The simultaneous increase in intraluminal pressure and radius resulted in a linear relation between absorption rate and apparent mucosal surface area. Similar results were obtained by raising intraluminal pressure directly using a carbohydrate-free perfusion solution. In the perfused rat jejunum, the effect of increased pre-epithelial diffusion resistance (i.e. reduced diffusion coefficient and lengthened diffusion distance) induced by methylcellulose on absorption was overcome by the effect of the enlarged apparent mucosal surface area. Preperfusion of a substrate-free, guaran containing solution followed by perfusion with a guaran-free solution containing antipyrine and MG retarded the increase in the appearance rate of these substrates due to the additional viscous guaran layer left after preperfusion. Constant distension of the intestinal wall was achieved by injecting 0.5 ml of the solution into a closed jejunal segment. Addition of the carbohydrates to the injection solution (approx. 100 cSt viscosity) resulted in a 3% to 20% reduction in the diffusion coefficients and in the absorption of antipyrine, benzoic acid, and MG. Diffusion coefficients for urea and benzylamine were reduced by 5% to 12%; absorption varied in the range of the control (−22% to +43%). Model analysis revealed that, in the closed jejunal segment of the rat, the limiting step in the closed process of antipyrine, benzoic acid, and MG was pre-epithelial diffusion resistance; the reduction of absorption, therefore, corresponded roughly to that of the diffusion coefficient. In the case of urea and benzylamine, pre-epithelial diffusion resistance was only 20% of the total permeation resistance: the influence of the polymers on absorption, therefore, was not always significant.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 335 (1987), S. 204-215 
    ISSN: 1432-1912
    Keywords: Closed rat jejunum ; Intestinal absorption ; Pre-epithelial diffusion resistance ; Unstirred layer ; Model analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary After intraluminal injection of 0.5 ml buffer solution into closed jejunal segments (length, 3–5 cm) of anesthetized rats the appearance rates of a series of labeled substances in jejunal venous blood were measured for 30 min in situ (initial concentration, 0.02–10 mmol/1 or 1 GBq/1 tritiated water). The appearance rates quickly rose to a maximum and then declined almost exponentially. Model analysis of the descending of branch of the curves by two one-compartment models (perfect luminal mixing, radial diffusion without convection) revealed a relative pre-epithelial diffusion resistance of nearly 100% for benzoic acid, salicylic acid, l-lysine (0.02 and 1 mmol/1), α-methyl-d-glucoside, and l-phenylalanine; 80% to 95% for aniline and butanol; 50% to 80% for benzyl alcohol, theophylline, aminopyrine, antipyrine, dodecanol, and d-galactose; approximately 40% for tritiated water; approximately 30% for l-lysine (10 mmol/1); 10% to 20% for urea and benzylamine; and approximately 4% for erythritol. The shape of the curves was well described by a two-compartment model (intestinal lumen and “tissue”, radial luminal diffusion without convection); the variability of the data, however, prevented closer analysis of the parameters of this model. Since pre-epithelial diffusion (unstirred layer) in the closed jejunal segment without peristalsis is the rate limiting step in the absorption process of highly permeant substances, information on intestinal epithelium can be obtained only with poorly permeant substances.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 307 (1979), S. 265-274 
    ISSN: 1432-1912
    Keywords: Small intestine ; Intestinal absorption ; Perfusion rate ; Intestinal unstirred layer ; Intraluminal radius
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In anaesthetized rats a jejunal segment was perfused in situ varying the perfusion rate (0.1, 0.2, 0.5 ml/min) in a randomized order. The intraluminal radius of the segments was small (1.7 mm) or enlarged (3.1 mm) by increasing the intraluminal pressure. The appearance rate of butanol, antipyrine, salicylic acid, d-and l-phenylalanine but not of urea in the venous blood of the jejunal segments was increased up to 35 %, when the intraluminal perfusion rate was raised from 0.1 to 0.5 ml/min. Two factors contribute to this effect: the flattening of the concentration gradient down the segment and the reduction of the effective unstirred layer thickness. The length and the intraluminal radius of the perfused segments was not altered, when the perfusion rate was varied. Therefore, a change of the absorbing area did not contribute to the increase of the absorption rate induced by the increase of the perfusion rate. In the series with small intraluminal radius the experimental data corresponded to the theoretical predictions obtained for a laminar intraluminal flow. In the segments with enlarged intraluminal radius the increase of the absorption rate by raising the perfusion rate was less than expected for a laminar flow indicating that the flow might have been turbulent. The enlargement of the intraluminal radius from 1.7 to 3.1 mm increased the absorption rate up to 100%.
    Type of Medium: Electronic Resource
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