scholarly journals Ionic basis of receptor potential of frog taste cells induced by acid stimuli.

1988 ◽  
Vol 405 (1) ◽  
pp. 699-711 ◽  
Author(s):  
T Miyamoto ◽  
Y Okada ◽  
T Sato
1989 ◽  
Vol 94 (4) ◽  
pp. 591-595 ◽  
Author(s):  
Miyamoto Takenori ◽  
Okada Yukio ◽  
Sato Toshihide

Nature ◽  
1979 ◽  
Vol 281 (5733) ◽  
pp. 675-677 ◽  
Author(s):  
D. P. Corey ◽  
A. J. Hudspeth

1993 ◽  
Vol 174 (1) ◽  
pp. 1-17
Author(s):  
Y Okada ◽  
T Miyamoto ◽  
T Sato

The ionic mechanism underlying the receptor potential induced by a deionized water stimulus was studied in frog taste cells with conventional microelectrodes. The taste cells located in the proximal portion of the tongue generated a depolarizing receptor potential which averaged 10mV in response to stimulation with deionized water. The cell membrane of the water-sensitive taste cell could be divided into the taste-receptive (apical) and basolateral membranes and the cells were classified into two types: Cl(-)-dependent and Cl(-)-independent. In Cl(-)-dependent cells whose input resistance was decreased or unchanged by deionized water, the magnitude of the water-induced depolarization decreased with an increase in concentration of superficial Cl- in contact with the receptive membrane and with addition of blockers of anion channels (0.1 mmol l-1 SITS and 0.1 mmol l-1 DIDS) to deionized water. The reversal potential for the depolarization in this type shifted according to the concentration of superficial Cl-. These properties of the responses were consistent with those of the glossopharyngeal nerve which innervates the taste disc. In Cl(-)-independent cells whose input resistance was increased by deionized water, the reversal potential was approximately equal to the equilibrium potential for K+ at the basolateral membrane. The water-induced response of the glossopharyngeal nerve was decreased to about 60% of the control value by addition of interstitial 2 mmol l-1 Ba2+. It is concluded that the water-induced receptor potential is produced by Cl- secretion through the taste-receptive membrane in about 70% of water-sensitive frog taste cells, while it is generated by an inhibition of the resting K+ conductance of the basolateral membrane in the remaining 30% of the cells.


1973 ◽  
Vol 53 (2) ◽  
pp. 455-457 ◽  
Author(s):  
Toshihide Sato ◽  
Lloyd M. Beidler

1982 ◽  
Vol 32 (3) ◽  
pp. 459-462 ◽  
Author(s):  
Toshihide SATO ◽  
Kumiko SUGIMOTO ◽  
Yukio OKADA

1984 ◽  
Vol 34 (6) ◽  
pp. 973-983 ◽  
Author(s):  
Toshihide SATO ◽  
Kumiko SUGIMOTO ◽  
Yukio OKADA ◽  
Takenori MIYAMOTO

1978 ◽  
Vol 71 (6) ◽  
pp. 683-698 ◽  
Author(s):  
C C Hunt ◽  
R S Wilkinson ◽  
Y Fukami

The effect of changing the ionic composition of bathing fluid on the receptor potential of primary endings has been examined in isolated mammalian spindles whose capsule was removed in the sensory region. After impulse activity is blocked by tetrodotoxin, ramp-and-hold stretch evokes a characteristic pattern of potential change consisting of a greater dynamic depolarization during the ramp phase and a smaller static depolarization during the hold phase. After a high-velocity ramp there is a transient post-dynamic undershoot to below the static level. On release from hold stretch, the potential shows a postrelease undershoot relative to base line. The depolarization produced by stretch is rapidly decreased by the removal of Na+ and Ca2+. Addition of normal Ca2+ partly restores the response. Stretch appears to increase the conductance to Na+ and Ca2+ in the sensory terminals. The postdynamic undershoot is diminished by raising external K+ and blocked by tetraethylammonium (TEA). It apparently results from a voltage-dependent potassium conductance. The postrelease undershoot is decreased by raising external K+, but is not blocked by TEA. It is presumably caused by a relative increase in potassium conductance on release. Substitution of isethionate for Cl- or the addition of ouabain does not alter the postdynamic and postrelease undershoots.


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