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T Nakahari

Publications and source records attributed to T Nakahari.

At least 37 records · Page 2Linked to original sources

ADH-evoked [Cl-]i-dependent transient in whole cell current of distal nephron cell line A6.

The effect of antidiuretic hormone (ADH) on a distal nephron cell line (A6) was studied using the whole cell patch-clamp technique. A6 cells were cultured on a permeable support filter for 10-14 days in media containing 10% fetal bovine serum without supplemental aldosterone. In the unstimulated condition A6 cells had very small conductances of Na+,K+, and Cl-. Arginine vasotocin (AVT, 140 mU/ml, 280 nM) evoked a "transient" increase in whole cell currents as did dibutyryl-adenosine 3',5'-cyclic monophosphate (5 mM). These transients consisted of two components; one was the nonselective cation conductance, and the other was the Cl- conductance. Activation of these conductances was dependent on intracellular Cl- concentration ([Cl-]i). At low [Cl-]i (< or = 50 mM) both conductances were activated, whereas when [Cl-]i was 80 mM, only the Cl- conductance was activated. At high [Cl-]i (125 mM), both conductances were inhibited. It seems likely that the [Cl-]i maintained at a low level (< or = 50 mM) is an important requirement for A6 cells to respond to AVT.

Animals↗

Two types of exocytosis evoked by ACh in salivary acinar cells: a morphological observation in perfused submandibular gland of rats.

Exocytosis in the perfused rat submandibular gland was studied using electron microscopy. Stimulation with 1 microM acetylcholine (ACh) evoked exocytosis; i.e., the secretory granules fused with the luminal membrane and their contents were extruded into the luminal space, and watery vacuoles were observed in some acinar cells. Stimulation with 1 mM ACh also induced exocytosis, and led to a marked increase in the number of watery vacuoles. Some watery vacuoles were connected to the lumen and were thus suggested to be formed by the fusion of the granules. On the other hand, no watery vacuoles were observed in the acinar cells during 1 microM isoproterenol stimulation, while isoproterenol induced exocytosis and led to a marked decrease in the number of intracellular granules. Thus, the watery vacuolation is a characteristic response to the cholinergic stimulation, is dependent on the ACh dose in the submandibular acinar cells, and is regarded as a kind of exocytosis.

Acetylcholine↗

Antidiuretic hormone-responding nonselective cation channel in distal nephron epithelium (A6).

Arginine vasotocin (AVT, 70 mU/ml) added from the basolateral side transiently activated a nonselective cation (NSC) channel with a single-channel conductance of 28.5 pS and almost identical selectivity for Na+ and K+ in the apical membrane of distal nephron cells (A6) cultured on permeable supports for 10-12 days in media containing 10% fetal bovine serum without supplemental aldosterone. The open probability (Po) of the NSC channel at the apical resting membrane potential in cell-attached patches was approximately 0.09 and increased when the apical membrane depolarized. The Po of the NSC channel was decreased by a rise in cytosolic Ca2+ concentration within a range of 30 nM-1 microM but not affected by cytosolic pH within a range of 6-8. The channel was activated by the application of negative pressure (10-60 cmH2O) into the patch pipette. Gadolinium (2 microM), an inhibitor of stretch-activated channels, decreased the Po by 40%. This blocking action of gadolinium was more effective after the channel was activated by stretch, i.e., 2 microM gadolinium decreased the Po by 70% when a negative pressure (60 cmH2O) was applied into the patch pipette. Amiloride (10 and 100 microM) showed a blocking action on the channel only when the NSC channel was activated by stretch.

Amiloride↗

Cytosolic [Cl-] regulates Na+ absorption in fetal alveolar epithelium?: roles of cAMP and Cl- channels.

We studied the regulatory mechanism of Na+ absorption in fetal distal lung epithelium (FDLE), using patch clamp and single cell imaging techniques. A beta 2-agonist activated a 28 pS non-selective cation channel (NSCC) by: 1) producing a dependency of the NSCC activity on the cytosolic [Cl-] ([Cl-]c); 2) inducing a reduction in the [Cl-]c from 45 to 25 mM which directly activated the beta 2-treated NSCC. The beta 2-agonist-induced decrease in [Cl-]c was caused by activation of Ca(2+)-activated K+ channel and cAMP-activated Cl- channel. A development of the [Cl-]c-dependency and a reduction in [Cl-]c act as a second messenger of the beta 2 agonist signal transduction pathway in this Na+ transporting epithelium.

Action Potentials↗

Whole cell conductance regulated by cytosolic [Cl-] and ADH-activated Cl- channels in a distal nephron cell line (A6).

The effect of antidiuretic hormone (ADH) on a distal nephron cell line (A6) was studied using the whole cell patch clamp technique. Arginine vasotocin (AVT, 140mU/ml) evoked a "transient" increase in whole cell currents as did dibutyryl cyclic AMP (5 mM). These transients consisted of two components: one was the non-selective cation conductance and the other was the Cl- conductance. The transient was evoked by AVT in the lower cytosolic Cl- concentration ([Cl-]i) (< approximately 50 mM), and was suppressed by higher concentrations of [Cl-]i (125 mM) in A6 cells. It seems likely that the [Cl-]i maintained at a lower level is an important requirement for A6 cells to respond to AVT.

Animals↗

Exocytosis in the lingual mucus cells of Rana esculenta evoked by acetylcholine: observation of living cells by confocal laser scanning microscopy.

Exocytosis of a secretory cell is believed to occur when a part of the limiting membrane of the secretory granules fuses with the luminal plasma membrane to release their contents. Using a confocal laser scanning microscope, we have studied these events in living frog lingual gland cells. In a differential interference contrast (DIC) mode, secretory granules were found to be stable in general, but after stimulation with acetylcholine chloride (ACh) of more than 1 microM concentration, there were abrupt changes in the light intensity of granules as described in other cells. We found that with the same stimulation, two different types of secretion occurred. In the first type, a small vacuole was formed and granule contents were released from various regions of the cell. In the second type, a large vacuole was formed and granule contents were released all at once. Using two fluorescent dyes BCECF and Lucifer Yellow, we were able to perform positive and negative staining of the cell as well as its granules. Confocal images of the fluorescence mode clearly demonstrated the release process which corresponded to the DIC image observed simultaneously. The electron microscopic image also showed two different types of secretion.

Acetylcholine↗

Osmotically inactive space during hyperosmotic stress in the perfused submandibular gland of the rat.

Cell volume changes were measured by an impedance method during hyperosmotic stress in the perfused rat submandibular gland. When the perfusate osmolarity was raised to 484 mosmol, the cell volume decreased and remained at a plateau level (79%). The decrease was smaller than expected from the extracellular fluid osmolarity change. Furthermore, the potassium content of the gland increased by 7% during the hyperosmotic stress. These results suggest that the cell volume changes observed during hyperosmotic stress are affected by the existence of an osmotically inactive space and by an increase in the intracellular solute content.

Animals↗

Effect of alpha-tocopherol on oxidative hemolysis, as evaluated by impedance measurement.

Using a hypoxanthine-xanthine oxidase (HX-XOD) reaction system, the effect of vitamin E (VE) on oxidative membrane injury was studied by the impedance method. Both VE-sufficient and VE-deficient erythrocytes showed an elevation of low frequency permittivity in the early phase of reaction. In the later phase of reaction, VE-sufficient erythrocytes showed a sustained elevation in permittivity, while VE-deficient erythrocytes showed a decrease in permittivity with time. These changes consisted with the process of hemolysis in the HX-XOD system. The similarity of early phase change between VE-sufficient and VE-deficient erythrocytes indicates that the HX-XOD system exerted a similar effect on both erythrocytes in the early phase. The difference in changes of later phase between the two types of erythrocytes suggests that VE suppressed the reduction in permittivity. When the results were analyzed by the Pauly-Schwan's theory based on the assumption that erythrocytes are spherical, the product of VE-deficient or VE-sufficient erythrocyte size (R) and membrane capacity (Cm) showed a change similar to that in permittivity.

Algorithms↗

Dose effects of acetylcholine on the cell volume of rat mandibular salivary acini.

The effects of acetylcholine (ACh) on the cell volume of the isolated rat mandibular acini were studied stereologically using video-enhanced contrast optical microscopy. The lengths of major and minor axes of the acini were measured in the successive video images, from which the relative volume change was estimated. ACh induced a rapid shrinkage of the acinar cell to reach minimum volume within 1 min. Simultaneously, the acinus and acinar clump shrunk in the same proportion as the acinar cell. The initial volume decrease induced by ACh was dose dependent: 0.92 at 10(-8) M, 0.91 at 10(-6) M, 0.77 at 10(-5) M, 0.78 at 10(-4) M, and 0.75 at 10(-3) M (the relative volume compared with the resting control). During sustained stimulation by ACh for 3 min, the volume of acinar cell remained at the plateau level at concentrations lower than 10(-5) M ACh, whereas the volume increased by 0.1-0.15 at concentrations higher than 10(-4) M ACh. The dose-dependent manner of the cell volume coincided with the fluid secretion measured in the isolated perfused gland. The findings on the dose effects of ACh are discussed in connection with the intercellular communication and the movement of electrolytes.

Acetylcholine↗

Decrease in rat submandibular acinar cell volume during ACh stimulation.

Changes in acinar cell volume were measured in the perfused submandibular gland of the rat at 23 degrees C during salivary secretion induced by acetylcholine (ACh). Cellular volume was monitored by two methods: the impedance method and the morphometric method using video-enhanced contrast optical microscopy. Both measurements revealed a decrease in acinar cell volume in response to 1 microM ACh. Within the 1st min of stimulation, secretion increased to the initial maximum (initial secretion), and cell shrinkage occurred. During sustained stimulation, secretory rate and cell volume were maintained at the plateau level (steady secretion). The decrease in cell volume was 71.8 +/- 2.9% of resting volume (means +/- SE, n = 8) as measured by the impedance method and 76.1 +/- 2.0% (n = 20) as measured by the morphometric method. With the removal of ACh, cell volume increased to 111.6 +/- 2.7% (n = 8) of the prestimulation level as measured by the impedance method and 108.8 +/- 1.5% (n = 20) as measured by the morphometric method, and then recovered to the prestimulation level slowly. The weight of the gland decreased significantly during stimulation. These findings proved that volume decrease occurred during stimulation. The measurement of cell volume gave the net fluid flux of the acinar cell compartment. The net fluid flux and the rate of salivary secretion gave an estimation of the fluid influx across the basolateral membrane. These findings suggest that a transcellular route for fluid secretion exists in the salivary gland.

Acetylcholine↗

Shrinkage of rat mandibular acinar cell with acetylcholine detected by video-enhanced contrast microscopy.

Changes in acinar cell volume during secretion were observed in the perfused rat mandibular gland by the video-enhanced contrast (VEC) microscopy. The acinar cell shrank (81.3 +/- 4.9% (mean +/- S.D., n = 5] during acetylcholine stimulation and swelled (107.4 +/- 2.3% (n = 5] after cessation of the stimulation. These evidences suggested that a large amount of fluid is transported via transcellular route in the salivary gland.

Acetylcholine↗

Continuous measurements of tissue impedance during secretion in dog submandibular gland.

The electrical impedance of the dog submandibular gland, as an indicator of changes in extracellular fluid (ECF) volume, was measured at 5 kHz, 500 kHz, and 5 MHz at intervals of 10 s during secretory stimulation, because the conductivity calculated from impedance at low frequencies reflected the ECF volume. The decrease in conductivity occurred in the first minute of stimulation. Its decrease was more marked during stimulation after circulatory arrest. Salivary secretion under intact circulation consists of two phases: an initial secretion occurring in the first minute of stimulation with a high secretory rate and a steady secretion continuing during stimulation at a constant rate. A decrease in conductivity occurred in the initial secretion. Within a few minutes following the cessation of stimulation, the conductivity increased to a level higher than the resting one with an intact circulation, while the blood flow remained several times higher than in the resting state. The conductivity of the gland slowly recovered to the prestimulation level over a 30-min period. The histological examination revealed that the main compartment of the ECF change was the interlobular space. Impedance and histological studies showed that the ECF volume of salivary glands changes dynamically during secretion. On the other hand, the cellular volume also increased in the initial secretion of an isolated gland. Its increase suggested that the fluid was transported to the lumen via a cellular pathway as well as a paracellular pathway in the initial secretion.

Animals↗

Observation of electro-kinetic phenomena by imposing oscillating pressure and voltage gradients across some epithelial membranes.

When hydrostatic pressure across epithelia fixed between a Ussing-type chamber was oscillated mechanically, the membrane potential was found to oscillate synchronously. When the transepithelial potential was oscillated artificially, the hydrostatic pressure difference also oscillated synchronously. Under such oscillating gradient conditions, concentration changes in the unstirred layer can be minimized. Accordingly, the method using such oscillatory gradients seem to be appropriate for observation of the true streaming potential and electro-osmosis, respectively.

Animals↗

Measurement of extra-cellular fluid change in salivary gland using an impedance method.

The method of electrical impedance measurement was tested for its usefulness in monitoring of extra-cellular fluid (ECF) in the dog submandibular gland during salivary secretion. Measurements were performed during rest and stimulated state with or without blood supply. During stimulation with blood supply, the conductivities of the gland decreased to some extent. During stimulation without blood supply, the decrease in conductivities was markedly enhanced. The decrease of ECF compartment during stimulation without blood supply was ascertained by the stereological measurement. Coincidence of conductivity decrease and histologically observed decrease of ECF compartment supports the usefulness of impedance measurement for monitoring of ECF during secretory activity of gland tissue. The present study also shows that the interlobular space decreased mainly during stimulation when blood supply is absent. This indicates that, among ECF space, the interlobular space plays an important role as a fluid reservoir in the salivary gland.

Animals↗

Decrease of extracellular fluid in dog submandibular glands during secretion under arterial clamping conditions.

Microscopic observations were made of volume changes in ECF of the dog submandibular glands during resting state and stimulated state without blood supply. The interlobular space, one of the compartments of ECF, decreased significantly during stimulation when blood supply was absent. The results show that the interlobular space plays an important role as a reservoir of fluid in salivary secretion.

Animals↗

31P-NMR study of dog submandibular gland in vivo and in vitro using the topical magnetic resonance.

The topical magnetic resonance (TMR) was used to study the phosphorous metabolism of a dog's submandibular gland during acetylcholine stimulation. The experiments were carried out under two conditions. One was a normal blood supply (in vivo) and the other was vascular perfusion with the artificial perfusate (in vitro). The levels of phosphorous compounds in the gland were obtained for 31P-NMR spectra of the TMR. The saliva was secreted in the both conditions, though the salivary flow under the in vivo condition was higher than in vitro. During salivary secretion, only the levels of creatine phosphate decreased under in vivo condition, while the levels of creatine phosphate and ATP decreased and the levels of inorganic phosphate increased in in vitro cases. It was concluded that the decrement of creatine phosphate during the salivary secretion indicates the acceleration of the energy metabolism in the submandibular gland.

Acetylcholine↗

Intracellular K+ activity in canine submandibular gland cells in resting and its change during stimulation.

Intracellular K+ activity (alpha Ki) and transmembrane potential differences were simultaneously measured with double-barreled K+ selective microelectrodes in superfused canine submandibular glands at rest and during stimulation. Also intracellular K+ and N+ concentrations in the same gland were determined by chemical analyses for comparison with the intracellular K+ activity data. The activity coefficient for intracellular K+ thus obtained was 0.67, indicating that virtually all K+ ions in the cells are in diffusible and osmotically active form. Under control conditions, measured values of the resting membrane potential (Em), alpha Ki and K+ equilibrium potential (EK) were -40.2 +/- 0.6 mV (S.E., n = 163), -88.5 +/- 1.4 mM (S.E., n = 163), -83 mV respectively. Electrochemical potential differences for K+ across the basolateral membrane (delta micro K/F) were approximately +43 mV. Acetylcholine (ACh) induced an abrupt membrane hyperpolarization followed by a temporary fall of alpha Ki. The maximum rate of alpha Ki change in the cytoplasm during stimulated conditions was -35.5 +/- 0.9 mM/min on the average (n = 10). These results suggest that the membrane permeability increases to K+ upon stimulation. Possible changes in membrane permeabilities to Na+ and Cl- were also discussed.

Acetylcholine↗

Effects of Na+ depletion on fluid secretion and levels of phosphorus compounds as measured by 31P-NMR in perfused canine mandibular gland.

The dependency of fluid secretion on extracellular Na+ and the levels of phosphorus compounds were studied in the perfused canine mandibular gland (using 31P-NMR). During control perfusion, the resting levels of creatine phosphate (CP) and ATP were 0.62 +/- 0.05 mmol . kg-1 gland and 0.42 +/- 0.04 mmol . kg-1 (mean +/- S.E., n = 9), respectively. Acetylcholine (Ach; 1 mumol . l-1 for 3 min) induced a salivary secretion and decreased the CP level. When Na+ in the perfusate was completely replaced with Li+, Ach induced only a minimal salivary secretion and no change in the ATP and CP levels. Restitution of Na+ to the perfusion, even without added Ach, caused a decrease in ATP and CP, and a small increase in salivary secretion. These results suggest that the activity of Na+/K+ ATPase is increased inversely via a rise of the intracellular Na+ concentration and that the salivary secretion is induced not only by added secretagogues but by an increase in the Na+ entry without added secretagogues.

Adenosine Triphosphate↗