scholarly journals Amino acids and carbohydrates absorption by Na+-dependent transporters in the pyloric ceca of Hoplias malabaricus (Erythrinidae)

2001 ◽  
Vol 31 (5) ◽  
pp. 793-797 ◽  
Author(s):  
Vania Lucia Pimentel Vieira ◽  
Bernardo Baldisserotto
Keyword(s):  
Amino Acids ◽  
Optimal Growth ◽  
Serosal Side ◽  
Carbohydrate Absorption ◽  
Hoplias Malabaricus ◽  
Main Site ◽  
Adequate Diet ◽  
Mucosal Side ◽  
Pyloric Ceca

Information about amino acids and carbohydrate absorption in fish is important to formulate an adequate diet to obtain optimal growth. Therefore, the objective of this study was to investigate if Na+-dependent transporters are involved on the absorption of glycine, L-glutamine, L-leucine, L-lysine, L-proline, L-alanine, and the carbohydrates fructose and glucose in the pyloric ceca of Hoplias malabaricus. The pyloric ceca were mounted in a system of continuous perfusion "in vitro". Amino acids and carbohydrates were placed on the mucosal side at concentrations of 10, 20, and 40mM. The serosal side of the pyloric ceca was positive in relation to the mucosal side. The addition of glycine, L-glutamine, L-leucine, L-lysine, L-proline (all tested concentrations), and glucose (at concentrations of 20 and 40mM) increased the positivity of the serosal side, indicating the presence of Na+-dependent transporters in the absorption of these substances. L-alanine and fructose did not change the positivity of the serosal side. The pyloric ceca seem to be the main site of nutrient absorption in the digestive tract of H. malabaricus.

scholarly journals Absorption and metabolism of volatile fatty acids by rumen and omasum

2012 ◽  
Vol 36 (1) ◽  
pp. 93-99 ◽  
Author(s):  
João Luiz Pratti Daniel ◽  
João Chrysostomo de Resende Júnior
Keyword(s):  
Fatty Acids ◽  
Mitotic Index ◽  
Volatile Fatty Acids ◽  
Diffusion Chamber ◽  
Serosal Side ◽  
Buffer Solution ◽  
Mucosal Side ◽  
Over Time ◽  
Fractional Absorption

Volatile fatty acids (VFA) absorption and metabolic capacity of rumen and omasum were compared, in vitro. Fragments of rumen wall and omasum laminae were taken from eight adult crossbred bovines. An isolated fragment of the mucosa was fitted in a tissue diffusion chamber. Valeric acid and CrEDTA were added to ruminal fluid and placed on the mucosal side and buffer solution was placed on the serosal side. Fractional absorption rates were measured by exponential VFA:Cr ratio decay over time. Metabolism rate was determined as the difference between VFA absorbed and VFA which appeared on the serosal side over time. Mitotic index was higher in omasum (0.52%) than in rumen epithelium (0.28%). VFA fractional absorption rate was higher in omasum (4.6%/h.cm²) than in rumen (0.4%/h.cm²). Acetate, propionate, butyrate, and valerate showed similar fractional absorption rates in both fragments. Percentage of metabolized acetate and propionate was lower than butyrate and valerate in both stomach compartments. In the rumen, individual VFA metabolism rates were similar (mean of 7.7 , but in the omasum, valerate (90.0 was more metabolized than butyrate (59.6 propionate (69.8 and acetate (51.7 . Correlation between VFA metabolism and mitotic index was positive in the rumen and in the omasum. In conclusion, VFA metabolism and absorption potential per surface of the omasum is higher than that of the rumen. Variations on rumen and omasum absorption capacities occur in the same way, and there are indications that factors capable of stimulating rumen wall proliferation are similarly capable of stimulating omasum walls.

Avian cecum: role of glucose and volatile fatty acids in transepithelial ion transport

1991 ◽  
Vol 260 (5) ◽  
pp. G703-G710 ◽  
Author(s):  
B. R. Grubb
Keyword(s):  
Fatty Acids ◽  
Ion Transport ◽  
Volatile Fatty Acids ◽  
Short Circuit ◽  
Short Circuit Current ◽  
Serosal Side ◽  
Na Transport ◽  
Cl Secretion ◽  
Mucosal Side

In the fowl cecum in vitro, the influence of glucose and the three most prevalent naturally occurring volatile fatty acids (acetate, propionate, butyrate) on short-circuit current (Isc), electrical resistance, and transport of Na and Cl was determined. When glucose, acetate, or butyrate was present, ion transport was characterized by electrogenic Na absorption, greater than 65% of which was amiloride inhibitable, and Cl secretion, which also was electrogenic. Isc could be completely accounted for by net fluxes of Na and Cl. When glucose, acetate, or butyrate (10 mM both sides) was included in the incubation medium, cecal tissue maintained its Isc and a constant rate of net Na absorption and Cl secretion for a 5-h period. When no substrate was present or propionate was included in the medium, a marked fall in Isc and net Na and Cl fluxes was seen. Glucose caused an increase in Isc when added only to the serosal side. As 3-O-methylglucose (not metabolized) was not effective in stimulating Isc of the cecum (serosal or mucosal addition), it appeared that glucose increased Isc by acting as an energy substrate for active Na transport. Acetate and butyrate appeared to be equally effective in stimulating Na transport and Isc when placed on either side of the membrane. When the preparation was supplied with glucose (serosal side) and acetate was added to the mucosal side, no further stimulation of Isc occurred. Thus it appeared that acetate and butyrate were acting as substrates for active Na transport rather than stimulating Na transport by some other mechanism such as a cotransport with Na.(ABSTRACT TRUNCATED AT 250 WORDS)

Fluid Movement Across the Wall of the Small Intestine in Vitro

1956 ◽  
Vol 187 (2) ◽  
pp. 244-246 ◽  
Author(s):  
T. Hastings Wilson
Keyword(s):  
Small Intestine ◽  
Sodium Chloride ◽  
Saline Solution ◽  
Isotonic Saline ◽  
Bicarbonate Secretion ◽  
Serosal Side ◽  
Fluid Movement ◽  
Mucosal Side

Small sacs of everted jejunum of the hamster were incubated in sugar free bicarbonate-saline solution in vitro. Both fluid and sodium chloride moved across the wall of the intestine from mucosal to serosal side. This movement of isotonic saline solution across the intestine was inhibited anaerobically. A small bicarbonate secretion was noted in the direction of serosal to mucosal side.

Effects of metabolic disturbances on potential difference across intestinal wall of rat

1963 ◽  
Vol 204 (1) ◽  
pp. 105-108 ◽  
Author(s):  
Masashi Sawada ◽  
Tomoaki Asano
Keyword(s):  
Small Intestine ◽  
Low Temperature ◽  
Intestinal Wall ◽  
Potential Difference ◽  
Rapid Decline ◽  
Serosal Side ◽  
Metabolic Disturbances ◽  
Temperature Dependent ◽  
Mucosal Side

The potential difference across the wall of the small intestine was determined in vitro under a variety of conditions using rats. When the normal Ringer's containing 200 mg/100 ml glucose was applied on both sides of the wall, the potential difference attained 5–9 mv, the serosal side being positive. The potential difference was temperature dependent, becoming reduced at low temperature, the temperature coefficient being 1.7 between 40 and 34 C. The potential difference was inhibited with 0.1 mm monoiodoacetic acid, 1 mm sodium azide, 0.1 mm dinitrophenol, and 50 µm ouabain applied on the mucosal side. Withdrawal and restitution of 200 mg/100 ml glucose on the mucosal side induced a rapid decline and recovery of the potential difference. The lowered potential difference was partially recovered by 200 mg/100 ml galactose but not by sorbitol.

Intestinal transport of l-tryptophan in vitro: inhibition by high concentrations

1960 ◽  
Vol 199 (6) ◽  
pp. 1033-1036 ◽  
Author(s):  
Richard P. Spencer ◽  
A. H. Samiy
Keyword(s):  
Amino Acids ◽  
Small Intestine ◽  
Aromatic Amino Acids ◽  
Intestinal Transport ◽  
Serosal Side ◽  
Mutual Inhibition ◽  
High Concentrations ◽  
Two Sides ◽  
Bathing Fluid

At a concentration of 5 x 10–3 m, everted hamster intestinal sacs showed net transport of l-tryptophan from the mucosal to the serosal side, when the concentration was initially equal on the two sides. Thus, l-tryptophan is not an exception to the generalization that such intestinal preparations transport monoamino-monocarboxylic amino acids against a concentration gradient. High concentrations of l-tryptophan inhibit such transport. This may account for previous failure by others to observe l-tryptophan transport against a gradient at an initial concentration of 20 x 10–3 m. Transport of l-tryptophan was greater by sacs from the middle of the small intestine than by those from the ends (this has been previously reported for l-phenylalanine and l-tyrosine). On the basis of this observation and those of mutual inhibition of transport, it is likely that the four aromatic amino acids share at least one common step in their intestinal absorption. Segments of hamster small intestine have been shown to accumulate l-tryptophan, developing a concentration greater than that of the bathing fluid.

Antimyotoxic Activity of Synthetic Peptides Derived from Bothrops atrox Snake Gamma Phospholipase A2 Inhibitor Selected by Virtual Screening

2019 ◽  
Vol 19 (22) ◽  
pp. 1952-1961 ◽  
Author(s):  
J.C. Sobrinho ◽  
A.F. Francisco ◽  
R. Simões-Silva ◽  
A.M. Kayano ◽  
J.J. Alfonso Ruiz Diaz ◽  
...  
Keyword(s):  
Amino Acids ◽  
Molecular Docking ◽  
Synthetic Peptides ◽  
Cell Damage ◽  
Neutralization Assay ◽  
Phospholipase Activity ◽  
Phospholipases A2 ◽  
Catalytically Active ◽  
Bothrops Atrox

Background: Several studies have aimed to identify molecules that inhibit the toxic actions of snake venom phospholipases A2 (PLA2s). Studies carried out with PLA2 inhibitors (PLIs) have been shown to be efficient in this assignment. Objective: This work aimed to analyze the interaction of peptides derived from Bothrops atrox PLIγ (atPLIγ) with a PLA2 and to evaluate the ability of these peptides to reduce phospholipase and myotoxic activities. Methods: Peptides were subjected to molecular docking with a homologous Lys49 PLA2 from B. atrox venom modeled by homology. Phospholipase activity neutralization assay was performed with BthTX-II and different ratios of the peptides. A catalytically active and an inactive PLA2 were purified from the B. atrox venom and used together in the in vitro myotoxic activity neutralization experiments with the peptides. Results: The peptides interacted with amino acids near the PLA2 hydrophobic channel and the loop that would be bound to calcium in Asp49 PLA2. They were able to reduce phospholipase activity and peptides DFCHNV and ATHEE reached the highest reduction levels, being these two peptides the best that also interacted in the in silico experiments. The peptides reduced the myotubes cell damage with a highlight for the DFCHNV peptide, which reduced by about 65%. It has been suggested that myotoxic activity reduction is related to the sites occupied in the PLA2 structure, which could corroborate the results observed in molecular docking. Conclusion: This study should contribute to the investigation of the potential of PLIs to inhibit the toxic effects of PLA2s.

The 1- and 2-Naphthylalanine Analogs of Oxytocin and Vasopressin

1995 ◽  
Vol 60 (12) ◽  
pp. 2170-2177 ◽  
Author(s):  
Zdenko Procházka ◽  
Jiřina Slaninová
Keyword(s):  
Amino Acids ◽  
Solid Phase ◽  
Pressor Test

Solid phase technique on p-methylbenzhydrylamine resin was used for the synthesis of four analogs of oxytocin and four analogs of vasopressin with the non-coded amino acids L- or D- and 1- or 2-naphthylalanine and D-homoarginine. [L-1-Nal2]oxytocin, [D-1-Nal2]oxytocin, [L-2-Nal2]oxytocin, [D-2-Nal2]oxytocin, [L-1-Nal2, D-Har8]vasopressin, [D-1-Nal2, D-Har8]vasopressin, [L-2-Nal2, D-Har8]vasopressin and [D-2-Nal2, D-Har8]vasopressin were synthesized. All eight analogs were found to be uterotonic inhibitors in vitro and in vivo. Analogs with 2-naphthylalanine are stronger inhibitors, particularly in the vasopressin series than the analogs with 1-naphthylalanine. Analogs with 1-naphthylalanine have no activity in the pressor test, analogs with 2-naphthylalanine are weak pressor inhibitors.

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