Pharmacological investigation of the role of ion channels in salivary secretion.

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Pharmacological investigation of the role of ion channels in salivary secretion. / Stummann, Tina C; Poulsen, Jørgen H; Hay-Schmidt, Anders; Grunnet, Morten; Klaerke, Dan A; Rasmussen, Hanne B; Olesen, Søren-Peter; Jorgensen, Nanna K.

In: Pflügers Archiv: European Journal of Physiology, Vol. 446, No. 1, 2003, p. 78-87.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Stummann, TC, Poulsen, JH, Hay-Schmidt, A, Grunnet, M, Klaerke, DA, Rasmussen, HB, Olesen, S-P & Jorgensen, NK 2003, 'Pharmacological investigation of the role of ion channels in salivary secretion.', Pflügers Archiv: European Journal of Physiology, vol. 446, no. 1, pp. 78-87. https://doi.org/10.1007/s00424-002-0985-8

APA

Stummann, T. C., Poulsen, J. H., Hay-Schmidt, A., Grunnet, M., Klaerke, D. A., Rasmussen, H. B., ... Jorgensen, N. K. (2003). Pharmacological investigation of the role of ion channels in salivary secretion. Pflügers Archiv: European Journal of Physiology, 446(1), 78-87. https://doi.org/10.1007/s00424-002-0985-8

Vancouver

Stummann TC, Poulsen JH, Hay-Schmidt A, Grunnet M, Klaerke DA, Rasmussen HB et al. Pharmacological investigation of the role of ion channels in salivary secretion. Pflügers Archiv: European Journal of Physiology. 2003;446(1):78-87. https://doi.org/10.1007/s00424-002-0985-8

Author

Stummann, Tina C ; Poulsen, Jørgen H ; Hay-Schmidt, Anders ; Grunnet, Morten ; Klaerke, Dan A ; Rasmussen, Hanne B ; Olesen, Søren-Peter ; Jorgensen, Nanna K. / Pharmacological investigation of the role of ion channels in salivary secretion. In: Pflügers Archiv: European Journal of Physiology. 2003 ; Vol. 446, No. 1. pp. 78-87.

Bibtex

@article{92784bb0ab5511ddb5e9000ea68e967b,
title = "Pharmacological investigation of the role of ion channels in salivary secretion.",
abstract = "The role of K+ and Cl- channels in salivary secretion was investigated, with emphasis on the potential role of Ca2+ -activated K+ channels. Ligand saturation kinetic assays and autoradiography showed large-conductance (BK) K+ channels to be highly expressed in rat submandibular and parotid glands, whereas low-conductance (SK) K+ channels could not be detected. To investigate the role of K+ and Cl- channels in secretion, intact rabbit submandibular glands were vascularly perfused and secretion induced by 10 microM ACh. Secretion was inhibited by 34+/-3{\%} following perfusion with the general K+ channel inhibitor Ba2+ (5 mM), whereas organic inhibitors of BK (200 nM paxilline) or intermediate-conductance (IK) K+ channels (5 microM clotrimazole) had no effect. Secretion was strongly influenced by Cl- channel inhibitors, as 100 microM 5-nitro-2-(3-phenylpropylamino)benzoate (NPPB) completely abolished, while 10 microM NPPB, 20 microM NS1652 and 20 microM NS3623 reduced secretion by 34+/-3{\%}, 23+/-3{\%} and 59+/-4{\%}, respectively. In conclusion, although high expression levels of BK channels were demonstrated, pharmacological tools failed to demonstrate any role for BK, IK or SK channels in salivary secretion in the rabbit submandibular gland. Other types of K+ channel, however, and particularly Cl- channels, are essential for ACh-induced salivary secretion.",
author = "Stummann, {Tina C} and Poulsen, {J{\o}rgen H} and Anders Hay-Schmidt and Morten Grunnet and Klaerke, {Dan A} and Rasmussen, {Hanne B} and S{\o}ren-Peter Olesen and Jorgensen, {Nanna K}",
note = "Keywords: Acetylcholine; Animals; Autoradiography; Binding Sites; Chloride Channels; Female; Male; Parotid Gland; Peptides; Perfusion; Potassium Channel Blockers; Potassium Channels, Calcium-Activated; Rabbits; Rats; Rats, Wistar; Submandibular Gland",
year = "2003",
doi = "10.1007/s00424-002-0985-8",
language = "English",
volume = "446",
pages = "78--87",
journal = "Pfl{\"u}gers Archiv - European Journal of Physiology",
issn = "0031-6768",
publisher = "Springer",
number = "1",

}

RIS

TY - JOUR

T1 - Pharmacological investigation of the role of ion channels in salivary secretion.

AU - Stummann, Tina C

AU - Poulsen, Jørgen H

AU - Hay-Schmidt, Anders

AU - Grunnet, Morten

AU - Klaerke, Dan A

AU - Rasmussen, Hanne B

AU - Olesen, Søren-Peter

AU - Jorgensen, Nanna K

N1 - Keywords: Acetylcholine; Animals; Autoradiography; Binding Sites; Chloride Channels; Female; Male; Parotid Gland; Peptides; Perfusion; Potassium Channel Blockers; Potassium Channels, Calcium-Activated; Rabbits; Rats; Rats, Wistar; Submandibular Gland

PY - 2003

Y1 - 2003

N2 - The role of K+ and Cl- channels in salivary secretion was investigated, with emphasis on the potential role of Ca2+ -activated K+ channels. Ligand saturation kinetic assays and autoradiography showed large-conductance (BK) K+ channels to be highly expressed in rat submandibular and parotid glands, whereas low-conductance (SK) K+ channels could not be detected. To investigate the role of K+ and Cl- channels in secretion, intact rabbit submandibular glands were vascularly perfused and secretion induced by 10 microM ACh. Secretion was inhibited by 34+/-3% following perfusion with the general K+ channel inhibitor Ba2+ (5 mM), whereas organic inhibitors of BK (200 nM paxilline) or intermediate-conductance (IK) K+ channels (5 microM clotrimazole) had no effect. Secretion was strongly influenced by Cl- channel inhibitors, as 100 microM 5-nitro-2-(3-phenylpropylamino)benzoate (NPPB) completely abolished, while 10 microM NPPB, 20 microM NS1652 and 20 microM NS3623 reduced secretion by 34+/-3%, 23+/-3% and 59+/-4%, respectively. In conclusion, although high expression levels of BK channels were demonstrated, pharmacological tools failed to demonstrate any role for BK, IK or SK channels in salivary secretion in the rabbit submandibular gland. Other types of K+ channel, however, and particularly Cl- channels, are essential for ACh-induced salivary secretion.

AB - The role of K+ and Cl- channels in salivary secretion was investigated, with emphasis on the potential role of Ca2+ -activated K+ channels. Ligand saturation kinetic assays and autoradiography showed large-conductance (BK) K+ channels to be highly expressed in rat submandibular and parotid glands, whereas low-conductance (SK) K+ channels could not be detected. To investigate the role of K+ and Cl- channels in secretion, intact rabbit submandibular glands were vascularly perfused and secretion induced by 10 microM ACh. Secretion was inhibited by 34+/-3% following perfusion with the general K+ channel inhibitor Ba2+ (5 mM), whereas organic inhibitors of BK (200 nM paxilline) or intermediate-conductance (IK) K+ channels (5 microM clotrimazole) had no effect. Secretion was strongly influenced by Cl- channel inhibitors, as 100 microM 5-nitro-2-(3-phenylpropylamino)benzoate (NPPB) completely abolished, while 10 microM NPPB, 20 microM NS1652 and 20 microM NS3623 reduced secretion by 34+/-3%, 23+/-3% and 59+/-4%, respectively. In conclusion, although high expression levels of BK channels were demonstrated, pharmacological tools failed to demonstrate any role for BK, IK or SK channels in salivary secretion in the rabbit submandibular gland. Other types of K+ channel, however, and particularly Cl- channels, are essential for ACh-induced salivary secretion.

U2 - 10.1007/s00424-002-0985-8

DO - 10.1007/s00424-002-0985-8

M3 - Journal article

VL - 446

SP - 78

EP - 87

JO - Pflügers Archiv - European Journal of Physiology

JF - Pflügers Archiv - European Journal of Physiology

SN - 0031-6768

IS - 1

ER -

ID: 8419010