Ion transport in rat antral mucosa in vitro: general characteristics. 1995

P Bakos, and D Jezová
Institute of Experimental Endocrinology, Slovak Academy of Sciences, Bratislava, Slovakia.

Although numerous studies have shown the existence of various types of ion conductance in antral part of gastric fundus mucosa epithelia of amphibian, practically no data are available on ion conductance in higher animal species. Present experiments were undertaken to check the possible existence of ion conductance in rat gastric antral mucosa and to investigate its general electrophysiological characteristics. Antral epithelia were isolated from adult Sprague Dawley rats. The tissues were mounted to a modified Ussing-type chamber and continually perfused with identical Krebs-Henseleit bicarbonate buffer on both sides. Antrum generated a transepithelial electrical potential difference (Vt = -10 +/- 2.6 mV) and short-circuit current (Isc = 76 +/- 15 microA.cm-2) with a transepithelial electrical resistance (Rt = 135 +/- 16.8 Ohm.cm2). Ion replacement experiments showed that it is mainly Na+ transport that contributes to Vt and Isc as evidenced by a) Na+ and/or Cl- removal, b) the effects of amiloride a sodium channel blocker, on the apical (secretory) surface, c) the effects of the Na(+)-K(+)-ATPase inhibitor ouabain on the basolateral (nutrient) side of the epithelium. Microelectrode experiments confirmed the existence of Na+ and/or Cl- conductance of the apical cell membrane. Antral mucosa also showed a gradual and time-dependent increase in sensitivity to amiloride (10(-5) mol/l). Maximum inhibition of Vt and Isc by amiloride in dose-dependent manner was detected after 1-2 h. This amiloride-sensitive sodium transport (maximal level 31.5 +/- 5.9 microA.cm-2) represented approximately 50% of the whole transepithelial ion conductance. Results of experiments with ouabain (10(-4 mol/l) suggest the presence of functional Na(+)-K(+)-ATPase and/or Na(+)-ATPase in the basolateral cell membranes. Which signals trigger this epithelial ion transport, which hormones are responsible for its regulation and what is the physiological significance of this ion conductance remains to be elucidated.

UI MeSH Term Description Entries
D007552 Isotonic Solutions Solutions having the same osmotic pressure as blood serum, or another solution with which they are compared. (From Grant & Hackh's Chemical Dictionary, 5th ed & Dorland, 28th ed) Solutions, Isotonic
D008297 Male Males
D008536 Meglumine 1-Deoxy-1-(methylamino)-D-glucitol. A derivative of sorbitol in which the hydroxyl group in position 1 is replaced by a methylamino group. Often used in conjunction with iodinated organic compounds as contrast medium. Methylglucamine
D008564 Membrane Potentials The voltage differences across a membrane. For cellular membranes they are computed by subtracting the voltage measured outside the membrane from the voltage measured inside the membrane. They result from differences of inside versus outside concentration of potassium, sodium, chloride, and other ions across cells' or ORGANELLES membranes. For excitable cells, the resting membrane potentials range between -30 and -100 millivolts. Physical, chemical, or electrical stimuli can make a membrane potential more negative (hyperpolarization), or less negative (depolarization). Resting Potentials,Transmembrane Potentials,Delta Psi,Resting Membrane Potential,Transmembrane Electrical Potential Difference,Transmembrane Potential Difference,Difference, Transmembrane Potential,Differences, Transmembrane Potential,Membrane Potential,Membrane Potential, Resting,Membrane Potentials, Resting,Potential Difference, Transmembrane,Potential Differences, Transmembrane,Potential, Membrane,Potential, Resting,Potential, Transmembrane,Potentials, Membrane,Potentials, Resting,Potentials, Transmembrane,Resting Membrane Potentials,Resting Potential,Transmembrane Potential,Transmembrane Potential Differences
D010042 Ouabain A cardioactive glycoside consisting of rhamnose and ouabagenin, obtained from the seeds of Strophanthus gratus and other plants of the Apocynaceae; used like DIGITALIS. It is commonly used in cell biological studies as an inhibitor of the NA(+)-K(+)-EXCHANGING ATPASE. Acocantherin,G-Strophanthin,Acolongifloroside K,G Strophanthin
D011706 Pyloric Antrum The region between the sharp indentation at the lower third of the STOMACH (incisura angularis) and the junction of the PYLORUS with the DUODENUM. Pyloric antral glands contain mucus-secreting cells and gastrin-secreting endocrine cells (G CELLS). Antrum, Pyloric,Gastric Antrum,Antrum, Gastric,Antrums, Gastric,Antrums, Pyloric,Gastric Antrums,Pyloric Antrums
D002712 Chlorides Inorganic compounds derived from hydrochloric acid that contain the Cl- ion. Chloride,Chloride Ion Level,Ion Level, Chloride,Level, Chloride Ion
D005260 Female Females
D005753 Gastric Mucosa Lining of the STOMACH, consisting of an inner EPITHELIUM, a middle LAMINA PROPRIA, and an outer MUSCULARIS MUCOSAE. The surface cells produce MUCUS that protects the stomach from attack by digestive acid and enzymes. When the epithelium invaginates into the LAMINA PROPRIA at various region of the stomach (CARDIA; GASTRIC FUNDUS; and PYLORUS), different tubular gastric glands are formed. These glands consist of cells that secrete mucus, enzymes, HYDROCHLORIC ACID, or hormones. Cardiac Glands,Gastric Glands,Pyloric Glands,Cardiac Gland,Gastric Gland,Gastric Mucosas,Gland, Cardiac,Gland, Gastric,Gland, Pyloric,Glands, Cardiac,Glands, Gastric,Glands, Pyloric,Mucosa, Gastric,Mucosas, Gastric,Pyloric Gland
D005947 Glucose A primary source of energy for living organisms. It is naturally occurring and is found in fruits and other parts of plants in its free state. It is used therapeutically in fluid and nutrient replacement. Dextrose,Anhydrous Dextrose,D-Glucose,Glucose Monohydrate,Glucose, (DL)-Isomer,Glucose, (alpha-D)-Isomer,Glucose, (beta-D)-Isomer,D Glucose,Dextrose, Anhydrous,Monohydrate, Glucose

Related Publications

P Bakos, and D Jezová
December 1976, The American journal of physiology,
P Bakos, and D Jezová
April 1975, The American journal of physiology,
P Bakos, and D Jezová
May 1993, The American journal of physiology,
P Bakos, and D Jezová
November 1976, Gastroenterology,
P Bakos, and D Jezová
June 2000, Comparative biochemistry and physiology. Part A, Molecular & integrative physiology,
P Bakos, and D Jezová
September 1996, The American journal of physiology,
P Bakos, and D Jezová
March 1985, The Journal of physiology,
P Bakos, and D Jezová
December 1987, Gastroenterology,
Copied contents to your clipboard!