Somatostatin-related peptides isolated from the eel gut: effects on ion and water absorption across the intestine of the seawater eel.

1994 ◽  
Vol 188 (1) ◽  
pp. 205-216 ◽  
Author(s):  
T Uesaka ◽  
K Yano ◽  
M Yamasaki ◽  
K Nagashima ◽  
M Ando
Keyword(s):  
Amino Acid ◽  
Water Absorption ◽  
Short Circuit ◽  
Short Circuit Current ◽  
Neuronal Firing ◽  
European Eel ◽  
Amino Acid Residues ◽  
Stimulatory Action ◽  
Adrenergic Antagonist ◽  
Large Peptide

Four somatostatin-related peptides were isolated from eel guts. Two of them were the same as eel SS-25II (eSS-25II) and eel SS-25I (eSS-25I) isolated from European eel pancreas. The remaining two peptides were C-terminal tetradecapeptides (eSS-14II and eSS-14I) of eSS-25II and eSS-25I, respectively. These four peptides all enhanced the serosa-negative transepithelial potential difference and short-circuit current across the seawater eel intestine after pretreatment with isobutylmethylxanthine, serotonin (5-HT) and methacholine, an agonist of acetylcholine (ACh). Among these peptides, eSS-25II was the most potent enhancer, followed by eSS-25I and eSS-14II. Since the large peptide (eSS-25II) acts at a lower concentration than the small somatostatin (eSS-14II), the 11 N-terminal amino acid residues seem to potentiate somatostatin action in the eel intestine. In contrast, eSS-14II was more potent than mammalian SS-14, indicating that the three amino acid residues (Tyr18, Gly21, Pro22) in the C-terminal portion also contribute to the potency of somatostatin. Endogenous somatostatin (eSS-25II) activated net Na+, Cl- and water fluxes across the seawater eel intestine. This stimulatory action was not inhibited by tetrodotoxin or yohimbine, an adrenergic antagonist, indicating that eSS-25II does not act through neuronal firing or through catecholamine release. Thus, eel somatostatins may act directly on the enterocytes, but on a distinct receptor from that for adrenaline, to antagonize the inhibition of NaCl and water absorption by 5-HT and ACh in the seawater eel intestine.

An electrogenic amino acid transporter in the apical membrane of cultured human bronchial epithelial cells

1998 ◽  
Vol 275 (5) ◽  
pp. L917-L923 ◽  
Author(s):  
Luis J. V. Galietta ◽  
Luciana Musante ◽  
Leila Romio ◽  
Ubaldo Caruso ◽  
Annarita Fantasia ◽  
...  
Keyword(s):  
Nitric Oxide ◽  
Amino Acid ◽  
Epithelial Cells ◽  
Apical Membrane ◽  
Short Circuit ◽  
Short Circuit Current ◽  
Bronchial Epithelial Cells ◽  
Maximal Effect ◽  
Human Bronchial Epithelial Cells ◽  
Bronchial Epithelial

We performed Ussing chamber experiments on cultured human bronchial epithelial cells to look for the presence of electrogenic dibasic amino acid transport. Apical but not basolaterall-arginine (10–1,000 μM) increased the short-circuit current. Maximal effect and EC50were ∼3.5 μA/cm2and 80 μM, respectively, in cells from normal subjects and cystic fibrosis patients. The involvement of nitric oxide was ruled out because a nitric oxide synthase inhibitor ( NG-nitro-l-arginine methyl ester) did not decrease the arginine-dependent current. Apicall-lysine,l-alanine, andl-proline, but not aspartic acid, were also effective in increasing the short-circuit current, with EC50values ranging from 26 to 971 μM. Experiments performed with radiolabeled arginine demonstrated the presence of an Na+-dependent concentrative transporter on the apical membrane of bronchial cells. This transporter could be important in vivo to maintain a low amino acid concentration in the fluid covering the airway surface.

scholarly journals Tissue and salinity specific Na+/Cl− cotransporter (NCC) orthologues involved in the adaptive osmoregulation of sea lamprey (Petromyzon marinus)

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
A. Barany ◽  
C. A. Shaughnessy ◽  
R. M. Pelis ◽  
J. Fuentes ◽  
J. M. Mancera ◽  
...  
Keyword(s):  
Water Absorption ◽  
Salinity Tolerance ◽  
Ex Vivo ◽  
Short Circuit ◽  
Short Circuit Current ◽  
Sea Lamprey ◽  
Mrna Levels ◽  
Gene Encoding ◽  
Distal Intestine ◽  
Proximal Intestine

AbstractTwo orthologues of the gene encoding the Na+-Cl− cotransporter (NCC), termed ncca and nccb, were found in the sea lamprey genome. No gene encoding the Na+-K+-2Cl− cotransporter 2 (nkcc2) was identified. In a phylogenetic comparison among other vertebrate NCC and NKCC sequences, the sea lamprey NCCs occupied basal positions within the NCC clades. In freshwater, ncca mRNA was found only in the gill and nccb only in the intestine, whereas both were found in the kidney. Intestinal nccb mRNA levels increased during late metamorphosis coincident with salinity tolerance. Acclimation to seawater increased nccb mRNA levels in the intestine and kidney. Electrophysiological analysis of intestinal tissue ex vivo showed this tissue was anion absorptive. After seawater acclimation, the proximal intestine became less anion absorptive, whereas the distal intestine remained unchanged. Luminal application of indapamide (an NCC inhibitor) resulted in 73% and 30% inhibition of short-circuit current (Isc) in the proximal and distal intestine, respectively. Luminal application of bumetanide (an NKCC inhibitor) did not affect intestinal Isc. Indapamide also inhibited intestinal water absorption. Our results indicate that NCCb is likely the key ion cotransport protein for ion uptake by the lamprey intestine that facilitates water absorption in seawater. As such, the preparatory increases in intestinal nccb mRNA levels during metamorphosis of sea lamprey are likely critical to development of whole animal salinity tolerance.

Proline transport and oxidation in short-circuited locust rectum: effect of cAMP

1984 ◽  
Vol 62 (9) ◽  
pp. 1732-1736 ◽  
Author(s):  
J. Spring ◽  
J. E. Phillips
Keyword(s):  
Amino Acid ◽  
Active Transport ◽  
Energy Supply ◽  
Short Circuit ◽  
Flux Ratio ◽  
Short Circuit Current ◽  
Metabolic Substrate ◽  
Proline Transport

Proline absorption from the lumen is the main source of substrate supporting electrogenic Cl− transport and short-circuit current (Isc) in locust rectum. Since cAMP stimulates chloride-dependent Isc by up to 10-fold, we investigated whether this stimulant also increases active transport of the major metabolic substrate proline. A large 40:1 flux ratio of [14C]proline under short-circuited conditions confirmed that net absorption of this amino acid is by active transport. Unexpectedly, cAMP caused a 40% decrease in net transepithelial flux of proline. A 45% increase in the amount of proline oxidized to 14CO2 could account for only 10% of this decrease in proline flux, suggesting that increased Cl− transport after stimulation may competitively reduce the energy supply for proline transport.

Characterization of human uroguanylin: a member of the guanylin peptide family

1994 ◽  
Vol 266 (2) ◽  
pp. F342-F348 ◽  
Author(s):  
T. Kita ◽  
C. E. Smith ◽  
K. F. Fok ◽  
K. L. Duffin ◽  
W. M. Moore ◽  
...  
Keyword(s):  
Amino Acid ◽  
Amino Acid Sequence ◽  
Human Urine ◽  
Short Circuit ◽  
Short Circuit Current ◽  
T84 Cells ◽  
Heat Stable ◽  
Guanylate Cyclase C ◽  
Peptide Family

Guanylin, a peptide homologue of the bacterial heat-stable enterotoxins (ST), is an endogenous activator of guanylate cyclase C (GC-C). We have initiated a search for other members of the guanylin peptide family and in the current study describe a "guanylin-like peptide" from human urine. Bioactivity was monitored by determining the effect of urine extracts on T84 cell guanosine 3',5'-cyclic monophosphate (cGMP) levels. Purification yielded two bioactive peaks of peptides that, when sequenced by NH2-terminal analysis, possessed 15 and 16 amino acids. The sequence of the smaller peptide represented an NH2-terminal truncation of the larger peptide. We have termed the larger peptide human uroguanylin; it has the following amino acid sequence: NDDCELCVNVACTGCL. Human uroguanylin shares amino acid sequence homology with guanylin and ST. Synthetic uroguanylin increased cGMP levels in T84 cells, competed with 125I-labeled ST for receptors, and stimulated Cl- secretion as reflected by an increased short-circuit current. Thus we report the isolation from human urine of a unique peptide, uroguanylin, that behaves in a manner similar to guanylin and appears to be a new member of this peptide family.

Mode of activation of salt secretion by C-type natriuretic peptide in the shark rectal gland

1999 ◽  
Vol 277 (6) ◽  
pp. R1725-R1732 ◽  
Author(s):  
Patricio Silva ◽  
Richard J. Solomon ◽  
Franklin H. Epstein
Keyword(s):  
Short Circuit ◽  
Short Circuit Current ◽  
Chloride Secretion ◽  
Squalus Acanthias ◽  
Rectal Gland ◽  
Stimulatory Action ◽  
Kinase C ◽  
Shark Rectal Gland ◽  
Pkc Activation ◽  
Stimulation Of

We studied the modes of activation of the salt-secreting rectal gland of the spiny dogfish, Squalus acanthias, by the native cardiac peptide CNP. The stimulatory action of CNP in isolated perfused glands is inhibited by 10 mM procaine, presumably by blocking release of vasoactive intestinal peptide (VIP) from nerves. Procaine reduces the slope of the dose-response curve of human CNP and that of shark CNP (each P < 0.0001). CNP increases short-circuit current in cultured rectal gland cells from 4.8 ± 1.6 to 27.0 ± 7.8 μA/cm2. It also stimulates the secretion of chloride in isolated perfused glands in the presence of 10 mM procaine from 72 ± 31 to 652 ± 173 μeq ⋅ h−1 ⋅ g−1. These results suggest that CNP has a direct cellular action not mediated by the neural release of VIP. The residual stimulation of perfused glands in the presence of procaine was almost completely inhibited by staurosporine [10 nM; an inhibitor of protein kinase C (PKC)] from 652 ± 173 to 237 ± 61 μeq ⋅ h−1 ⋅ g−1. Although CNP stimulates guanylyl cyclase in shark rectal gland, chloride secretion of perfused glands was not elicited by 8-bromoadenosine-cGMP (8-BrcGMP) alone nor by the activator of PKC phorbol ester. The combination of PKC activation and 8-BrcGMP infusion, however, stimulated chloride secretion in perfused glands from 94 ± 30 to 506 ± 61 μeq ⋅ h−1 ⋅ g−1, a level comparable to that observed in glands blocked with procaine. Several parallel pathways appear to be synergistic in activating chloride secretion stimulated by CNP in the rectal gland.

Effect of sorbin on electrolyte transport in rat and human intestine

1999 ◽  
Vol 276 (1) ◽  
pp. G107-G114 ◽  
Author(s):  
Bruno Eto ◽  
Michel Boisset ◽  
Bertrand Griesmar ◽  
Jehan-François Desjeux
Keyword(s):  
Water Absorption ◽  
Short Circuit ◽  
Short Circuit Current ◽  
Electrolyte Transport ◽  
Secretory Diarrhea ◽  
Maximal Effect ◽  
Human Intestine ◽  
Ussing Chambers ◽  
Antisecretory Effect ◽  
Dose Dependent

Stimulating water absorption in the colon represents an important target to reduce stool output in secretory diarrhea. Recently, a 153-amino-acid peptide was isolated from porcine upper small intestine and purified, taking into account the increase of water absorption in guinea pig gallbladder. Accordingly, this peptide was named sorbin. The aim of the present study was to determine if the COOH-terminal heptapeptide of sorbin (C7-sorbin) participates in the regulation of electrolyte transport in the colon. Different regions (from duodenum to colon) of stripped intestinal mucosa from rats or humans were mounted in Ussing chambers to measure the changes in short-circuit current (Δ Isc) and net22Na and36Cl fluxes ([Formula: see text] and[Formula: see text]) after serosal exposure of 10−7to 10−3M C7-sorbin. In fasted rat intestine, C7-sorbin (10−4M) induced an immediate reduction in Iscin the distal ileum and proximal and distal colon but not in the duodenum and jejunum. In the colon, Iscreduction and[Formula: see text] and[Formula: see text] stimulation were dose dependent (EC50= 2 × 10−5M). At 10−3M, maximal effect was observed (Δ Isc= −1.14 ± 0.05, Δ[Formula: see text] = +4.97 ± 1.38, and Δ[Formula: see text] = +9.25 ± 1.44 μeq ⋅ h−1⋅ cm−2). C7-sorbin (10−3M) inhibited the increase in Iscinduced by a series of 10 secretory agents such as secretin, vasoactive intestinal peptide, PGE2, and serotonin. In HT-29-Cl19A cells, C7-sorbin induced an increase in Isc, with a maximal effect at 10−3M (Δ Isc= 0.29 ± 0.10 μeq ⋅ h−1⋅ cm−2). In human intestine, a dose-dependent decrease in Iscwas observed in right and sigmoid colons in basal and stimulated conditions (EC50≅ 10−5M; at 10−4M, Δ Isc= −2.66 ± 0.17 μeq ⋅ h−1⋅ cm−2) but not in the jejunum. The results indicate that C7-sorbin stimulated NaCl neutral absorption and inhibited electrogenic Cl−in rat and human intestinal epithelia. In addition, the antisecretory effect was essentially observed in the distal part of both rat and human intestine and the magnitude of the proabsorptive effect was directly related to the magnitude of the previously induced secretion.

scholarly journals Regulatory volume decrease in cultured kidney cells (A6): role of amino acids.

1995 ◽  
Vol 106 (3) ◽  
pp. 525-542 ◽  
Author(s):  
P De Smet ◽  
J Simaels ◽  
P E Declercq ◽  
W Van Driessche
Keyword(s):  
Amino Acids ◽  
Amino Acid ◽  
Acid Concentration ◽  
Short Circuit ◽  
Regulatory Volume Decrease ◽  
Short Circuit Current ◽  
Amino Acid Concentration ◽  
Cell Content ◽  
Volume Decrease

Volume regulation was studied in A6 epithelia grown on permeable supports by measuring cell thickness (Tc) while simultaneously recording short circuit current (ISC) and transepithelial conductance (Gt). Lowering the tonicity of the basolateral solution (pi b) from 250 or 215 to 140 mOsm/kg elicited a rapid rise in Tc followed by a regulation of the cell volume towards control. This decrease in Tc displays the characteristics of the regulatory volume decrease (RVD). Upon restoring the isoosmotic conditions, Tc decreased rapidly below its control value. A post RVD regulatory volume increase (RVI) as described for other cell types was not observed. The subsequent reduction of the basolateral osmolality increased Tc to the level recorded at the end of the first hypoosmotic pulse. Because cell content was not altered during the isoosmotic period the second hypoosmotic challenge was isotonic with the cell and did therefore not evoke an RVD. However, the cell did not lose its ability to volume regulate since an RVD could be elicited by further reduction of pi b from 140 to 100 mOsm/kg. The possibility of an involvement of amino acids in the RVD was tested. The amount of amino acids in the cell as well as excreted in the bath was determined by amino acid analysis. Millimolar concentrations of threonine, serine, alanine, glutamate, glycine and aspartate were found in the cell extract. The cellular amino acid concentration was 28.8 +/- 0.4 mM. The amounts of glycine, aspartate and glutamate excreted from the cell during the hypotonic treatment were significantly larger than in control conditions. The excretion of these amino acids during hypotonicity decreased the cellular amino acid concentration by 8.4 +/- 0.2 mM. This quantity cannot completely account for the RVD during the first hypotonic challenge. The addition of glycine, aspartate and glutamate to the bathing solutions, although used at concentrations higher than intracellularly, did not reduce RVD. On the contrary, this maneuver increased the amplitude of the RVD following both hypoosmotic pulses. This result suggests a stimulatory role of the amino acids on the processes responsible for the RVD.

Transport characteristics of isolated newborn rabbit ileum.

1978 ◽  
Vol 234 (3) ◽  
pp. E257 ◽  
Author(s):  
H J Cooke ◽  
D C Dawson
Keyword(s):  
Amino Acid ◽  
Amino Acid Transport ◽  
Short Circuit ◽  
Short Circuit Current ◽  
Acid Transport ◽  
Rabbit Ileum ◽  
Passive Permeability ◽  
Newborn Rabbit ◽  
Active Amino Acid ◽  
Potential Gradients

Segments of ileum from newborn rabbits were mounted as flat sheets in Lucite chambers and transmural fluxes of Na, Cl, and alanine were measured in the absence of electrochemical potential gradients. In the presence of 140 mM Na, the ileum of the newborn exhibited a serosa-positive electrical PD and a corresponding short-circuit current (Isc) which was markedly enhanced by the addition of D-glucose of L-alanine to the mucosal solution. Alanine-induced increments in Isc were a saturable function of the mucosal alanine concentration. In the presence of Na, alanine was actively absorbed, and the net alanine flux was a saturable function of alanine concentration. When the Na in the bathing solutions was completely replaced by choline, Isc declined to near zero, and the response of Isc to mucosal alanine was abolished. In addition, active amino acid transport was abolished in the absence of Na. In the absence of alanine, the isolated ileum of the newborn actively absorbed Na and Cl, and the algebraic sum of the net movements of these ions accounted for Isc. In the presence of alanine, active Cl transport was abolished and Isc was equal to the net Na absorption. These results indicate that the ileum of the newborn rabbit is similar to that of the adult in its ability to actively absorb Na, Cl, and alanine, but differs from the ileum of the adult by having a greater passive permeability to ions and amino acid, and differs particularly with regard to the effect of mucosal alanine on transmural ion transport.

Effects of amino acids on chloride transport in Aplysia intestine

1981 ◽  
Vol 240 (1) ◽  
pp. R61-R69 ◽  
Author(s):  
G. A. Gerencser
Keyword(s):  
Amino Acids ◽  
Amino Acid ◽  
Chloride Transport ◽  
Short Circuit ◽  
Short Circuit Current ◽  
Electrical Characteristics ◽  
Glucose Stimulation ◽  
Flux Measurements ◽  
Short Circuit Currents ◽  
Stimulation Of

This investigation was principally undertaken to examine the mechanism by which organic solutes (amino acids) stimulate chloride transport across the Aplysia californica intestine. Isolated intestine, mounted between identical oxygenated seawater solutions, maintained stable transmural potential differences (serosa negative) and short-circuit currents for several hours at 25 degrees C. The addition of glycine to the mucosal solution stimulated rapid sustained increases in these electrical characteristics. The change in short-circuit increased curvilinearly with increasing concentrations of mucosal glycine. Mucosal glycine stimulated transmural potential difference and short-circuit current after mucosal phlorizin had partially inhibited D-glucose stimulation of the electrical characteristics. Mucosal glycine enhanced the transmural electrical characteristics. Mucosal glycine enhanced the transmural electrical characteristics after serosal ouabain had abolished them. The major portion of the amino acid-induced short-circuit current was carried by a net, active, chloride transfer from mucosa to serosa as determined by flux measurements. These results suggest that the amino acid-induced effect on chloride transport is mediated by a common mucosal membrane carrier for both sodium and the amino acid.

scholarly journals Segment-specific effects of epinephrine on ion transport in the colon of the rat

1998 ◽  
Vol 275 (6) ◽  
pp. G1367-G1376 ◽  
Author(s):  
Silke Hörger ◽  
Gerhard Schultheiß ◽  
Martin Diener
Keyword(s):  
Ion Transport ◽  
Short Circuit ◽  
Ussing Chamber ◽  
Short Circuit Current ◽  
Distal Colon ◽  
Proximal Colon ◽  
Rat Colon ◽  
Second Phase ◽  
Stimulatory Action ◽  
Β Receptor

The effect of epinephrine on transport of K+, Na+, Cl−, and[Formula: see text] across the rat colon was studied using the Ussing chamber technique. Epinephrine (5 × 10−6mol/l) induced a biphasic change in short-circuit current ( Isc) in distal and proximal colon: a transient increase followed by a long-lasting decay. The first phase of the Iscresponse was abolished in Cl−-poor solution or after bumetanide administration, indicating a transient induction of Cl−secretion. The second phase of the response to epinephrine was suppressed by apical administration of the K+channel blocker, quinine, and was concomitant with an increase in serosal-to-mucosal Rb+flux, indicating that epinephrine induced K+secretion, although this response was much smaller than the change in Isc. In addition, the distal colon displayed a decrease in mucosal-to-serosal and serosal-to-mucosal Cl−fluxes when treated with epinephrine. In the distal colon, indomethacin abolished the first phase of the epinephrine effect, whereas the second phase was suppressed by TTX. In the proximal colon, indomethacin and TTX were ineffective. The neuronally mediated response to epinephrine in the distal colon was suppressed by the nonselective β-receptor blocker, propranolol, and by the β2-selective blocker, ICI-118551, whereas the epithelial response in the proximal colon was suppressed by the nonselective α-blocker, phentolamine, and by the selective α2-blocker, yohimbine. These results indicate a segment-specific action of epinephrine on ion transport: a direct stimulatory action on epithelial α2-receptors in the proximal colon and an indirect action on secretomotoneurons via β2-receptors in the distal colon.

Sign in / Sign up

Export Citation Format

Share Document