Guanosine diphosphate activates an adenosine 5'‐triphosphate‐sensitive K+ channel in the rabbit portal vein.

S. Kajioka, K. Kitamura, H. Kuriyama

Research output: Contribution to journalArticle

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Abstract

1. Properties of the pinacidil‐sensitive K+ channel in the smooth muscle of the rabbit portal vein were investigated using cell‐attached and inside‐ and outside‐out patch clamp techniques. 2. In the cell‐attached patch configuration, a K+ channel with a unitary conductance of 150 pS could be recorded when physiological salt solution (PSS) was in the pipette and high‐K+ solution was in the bath. Tetraethylammonium (TEA; less than 1 mM) and charybdotoxin (CTX; greater than 50 nM) inhibited the 150 pS K+ channel from the outside of the membrane. This channel was activated by an increase in the concentrations of intracellular Ca2+ but not by pinacidil (less than or equal to 500 microM). 3. In the cell‐attached patch configuration, bath application of pinacidil (greater than 3 microM) activated a K+ channel (ATP‐sensitive K+ channel) with a unitary conductance of 15 pS and the enhancing action of pinacidil was blocked by glibenclamide. However, in the cell‐free patch configuration, pinacidil (100 microM) failed to open the 15 pS K+ channel. With pinacidil in the pipette, the 15 pS K+ channel was completely inactivated within 5 s of the excision of the membrane. Opening of the 15 pS K+ channel also disappeared after saponin treatment (50 micrograms/ml). 4. In the cell‐free patch configuration, application of guanosine 5'‐diphosphate (GDP; greater than 100 microM) re‐activated the inactivated 15 pS K+ channel only when pinacidil was present either in the pipette or bath. GDP increased the mean open time and open probability of the 15 pS K+ channel in a concentration‐dependent manner. Simultaneous application of MgCl2 (less than or equal to 1 mM) with GDP did not modify the GDP‐induced activation. Neither GDP nor GTP (1 mM) had any effect on the 150 pS K+ channel. 5. Guanosine 5'‐triphosphate (GTP; 1 mM) activated the 15 pS K+ channel to a lesser extent that did GDP. Other guanine nucleotides (guanosine 5'‐monophosphate, GMP, 1 mM; guanosine 5'‐O‐(3‐thiotriphosphate), GTP gamma S, 100 microM; and guanosine 5'‐O‐(2‐thiodiphosphate), GDP beta S, 1 mM) failed to activate the 15 pS K+ channel. However, GDP beta S, but not GMP or GTP gamma S, inhibited this channel when it was activated by 1 mM‐GDP. 6. In the presence of pinacidil, adenosine 5'‐triphosphate (ATP; greater than or equal to 10 microM) inhibited the ATP‐sensitive K+ channel when it was activated by 1 mM‐GDP.(ABSTRACT TRUNCATED AT 400 WORDS)

Original languageEnglish
Pages (from-to)397-418
Number of pages22
JournalThe Journal of Physiology
Volume444
Issue number1
DOIs
Publication statusPublished - Dec 1 1991

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Pinacidil
Guanosine
Portal Vein
Adenosine Diphosphate
Rabbits
Guanosine Triphosphate
Baths
Guanosine Monophosphate
Guanosine 5'-O-(3-Thiotriphosphate)
Adenosine Triphosphate
Charybdotoxin
Magnesium Chloride
Tetraethylammonium
Guanine Nucleotides
Glyburide
Diphosphates
Saponins
Patch-Clamp Techniques
Ion Channels
Smooth Muscle

All Science Journal Classification (ASJC) codes

  • Physiology

Cite this

Guanosine diphosphate activates an adenosine 5'‐triphosphate‐sensitive K+ channel in the rabbit portal vein. / Kajioka, S.; Kitamura, K.; Kuriyama, H.

In: The Journal of Physiology, Vol. 444, No. 1, 01.12.1991, p. 397-418.

Research output: Contribution to journalArticle

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N2 - 1. Properties of the pinacidil‐sensitive K+ channel in the smooth muscle of the rabbit portal vein were investigated using cell‐attached and inside‐ and outside‐out patch clamp techniques. 2. In the cell‐attached patch configuration, a K+ channel with a unitary conductance of 150 pS could be recorded when physiological salt solution (PSS) was in the pipette and high‐K+ solution was in the bath. Tetraethylammonium (TEA; less than 1 mM) and charybdotoxin (CTX; greater than 50 nM) inhibited the 150 pS K+ channel from the outside of the membrane. This channel was activated by an increase in the concentrations of intracellular Ca2+ but not by pinacidil (less than or equal to 500 microM). 3. In the cell‐attached patch configuration, bath application of pinacidil (greater than 3 microM) activated a K+ channel (ATP‐sensitive K+ channel) with a unitary conductance of 15 pS and the enhancing action of pinacidil was blocked by glibenclamide. However, in the cell‐free patch configuration, pinacidil (100 microM) failed to open the 15 pS K+ channel. With pinacidil in the pipette, the 15 pS K+ channel was completely inactivated within 5 s of the excision of the membrane. Opening of the 15 pS K+ channel also disappeared after saponin treatment (50 micrograms/ml). 4. In the cell‐free patch configuration, application of guanosine 5'‐diphosphate (GDP; greater than 100 microM) re‐activated the inactivated 15 pS K+ channel only when pinacidil was present either in the pipette or bath. GDP increased the mean open time and open probability of the 15 pS K+ channel in a concentration‐dependent manner. Simultaneous application of MgCl2 (less than or equal to 1 mM) with GDP did not modify the GDP‐induced activation. Neither GDP nor GTP (1 mM) had any effect on the 150 pS K+ channel. 5. Guanosine 5'‐triphosphate (GTP; 1 mM) activated the 15 pS K+ channel to a lesser extent that did GDP. Other guanine nucleotides (guanosine 5'‐monophosphate, GMP, 1 mM; guanosine 5'‐O‐(3‐thiotriphosphate), GTP gamma S, 100 microM; and guanosine 5'‐O‐(2‐thiodiphosphate), GDP beta S, 1 mM) failed to activate the 15 pS K+ channel. However, GDP beta S, but not GMP or GTP gamma S, inhibited this channel when it was activated by 1 mM‐GDP. 6. In the presence of pinacidil, adenosine 5'‐triphosphate (ATP; greater than or equal to 10 microM) inhibited the ATP‐sensitive K+ channel when it was activated by 1 mM‐GDP.(ABSTRACT TRUNCATED AT 400 WORDS)

AB - 1. Properties of the pinacidil‐sensitive K+ channel in the smooth muscle of the rabbit portal vein were investigated using cell‐attached and inside‐ and outside‐out patch clamp techniques. 2. In the cell‐attached patch configuration, a K+ channel with a unitary conductance of 150 pS could be recorded when physiological salt solution (PSS) was in the pipette and high‐K+ solution was in the bath. Tetraethylammonium (TEA; less than 1 mM) and charybdotoxin (CTX; greater than 50 nM) inhibited the 150 pS K+ channel from the outside of the membrane. This channel was activated by an increase in the concentrations of intracellular Ca2+ but not by pinacidil (less than or equal to 500 microM). 3. In the cell‐attached patch configuration, bath application of pinacidil (greater than 3 microM) activated a K+ channel (ATP‐sensitive K+ channel) with a unitary conductance of 15 pS and the enhancing action of pinacidil was blocked by glibenclamide. However, in the cell‐free patch configuration, pinacidil (100 microM) failed to open the 15 pS K+ channel. With pinacidil in the pipette, the 15 pS K+ channel was completely inactivated within 5 s of the excision of the membrane. Opening of the 15 pS K+ channel also disappeared after saponin treatment (50 micrograms/ml). 4. In the cell‐free patch configuration, application of guanosine 5'‐diphosphate (GDP; greater than 100 microM) re‐activated the inactivated 15 pS K+ channel only when pinacidil was present either in the pipette or bath. GDP increased the mean open time and open probability of the 15 pS K+ channel in a concentration‐dependent manner. Simultaneous application of MgCl2 (less than or equal to 1 mM) with GDP did not modify the GDP‐induced activation. Neither GDP nor GTP (1 mM) had any effect on the 150 pS K+ channel. 5. Guanosine 5'‐triphosphate (GTP; 1 mM) activated the 15 pS K+ channel to a lesser extent that did GDP. Other guanine nucleotides (guanosine 5'‐monophosphate, GMP, 1 mM; guanosine 5'‐O‐(3‐thiotriphosphate), GTP gamma S, 100 microM; and guanosine 5'‐O‐(2‐thiodiphosphate), GDP beta S, 1 mM) failed to activate the 15 pS K+ channel. However, GDP beta S, but not GMP or GTP gamma S, inhibited this channel when it was activated by 1 mM‐GDP. 6. In the presence of pinacidil, adenosine 5'‐triphosphate (ATP; greater than or equal to 10 microM) inhibited the ATP‐sensitive K+ channel when it was activated by 1 mM‐GDP.(ABSTRACT TRUNCATED AT 400 WORDS)

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