Literature DB >> 22744007

Mechanisms and roles of muscarinic activation in guinea-pig adrenal medullary cells.

Masumi Inoue1, Keita Harada, Hidetada Matsuoka, Jun Nakamura, Akira Warashina.   

Abstract

Muscarinic receptors are expressed in the adrenal medullary (AM) cells of various mammals, but their physiological roles are controversial. Therefore, the ionic mechanism for muscarinic receptor-mediated depolarization and the role of muscarinic receptors in neuronal transmission were investigated in dissociated guinea-pig AM cells and in the perfused guinea-pig adrenal gland. Bath application of muscarine induced an inward current at -60 mV. This inward current was partially suppressed by quinine with an IC(50) of 6.1 μM. The quinine-insensitive component of muscarine-induced currents changed the polarity at -78 mV and was inhibited by bupivacaine, a TWIK-related acid-sensitive K(+) (TASK) channel inhibitor. Conversely, the current-voltage relationship for the bupivacaine-insensitive component of muscarine currents showed a reversal potential of -5 mV and a negative slope below -40 mV. External application of La(3+) had a double action on muscarine currents of both enhancement and suppression. Immunoblotting and immunocytochemistry revealed expression of TASK1 channels and cononical transient receptor potential channels 1, 4, 5, and 7 in guinea-pig AM cells. Retrograde application of atropine reversibly suppressed transsynaptically evoked catecholamine secretion from the adrenal gland. The results indicate that muscarinic receptor stimulation in guinea-pig AM cells induces depolarization through inhibition of TASK channels and activation of nonselective cation channels and that muscarinic receptors are involved in neuronal transmission from the splanchnic nerve.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22744007      PMCID: PMC3774099          DOI: 10.1152/ajpcell.00147.2012

Source DB:  PubMed          Journal:  Am J Physiol Cell Physiol        ISSN: 0363-6143            Impact factor:   4.249


  57 in total

Review 1.  Molecular background of leak K+ currents: two-pore domain potassium channels.

Authors:  Péter Enyedi; Gábor Czirják
Journal:  Physiol Rev       Date:  2010-04       Impact factor: 37.312

2.  TRPC1 and TRPC5 form a novel cation channel in mammalian brain.

Authors:  C Strübing; G Krapivinsky; L Krapivinsky; D E Clapham
Journal:  Neuron       Date:  2001-03       Impact factor: 17.173

3.  Modes of secretagogue-induced [Ca(2+)](i) responses in individual chromaffin cells of the perfused rat adrenal medulla.

Authors:  A Warashina; Y Satoh
Journal:  Cell Calcium       Date:  2001-12       Impact factor: 6.817

4.  Histamine promotes excitability in bovine adrenal chromaffin cells by inhibiting an M-current.

Authors:  Damian J Wallace; Chen Chen; Philip D Marley
Journal:  J Physiol       Date:  2002-05-01       Impact factor: 5.182

5.  An oxygen-, acid- and anaesthetic-sensitive TASK-like background potassium channel in rat arterial chemoreceptor cells.

Authors:  K J Buckler; B A Williams; E Honore
Journal:  J Physiol       Date:  2000-05-15       Impact factor: 5.182

6.  Lanthanides potentiate TRPC5 currents by an action at extracellular sites close to the pore mouth.

Authors:  Silke Jung; Anja Mühle; Michael Schaefer; Rainer Strotmann; Gunter Schultz; Tim D Plant
Journal:  J Biol Chem       Date:  2002-11-26       Impact factor: 5.157

7.  Ca2+ imaging in perfused adrenal medullae.

Authors:  Akira Warashina; Masumi Inoue
Journal:  J UOEH       Date:  2012-06-01

8.  The transient receptor potential protein homologue TRP6 is the essential component of vascular alpha(1)-adrenoceptor-activated Ca(2+)-permeable cation channel.

Authors:  R Inoue; T Okada; H Onoue; Y Hara; S Shimizu; S Naitoh; Y Ito; Y Mori
Journal:  Circ Res       Date:  2001-02-16       Impact factor: 17.367

9.  Identification and role of muscarinic receptor subtypes expressed in rat adrenal medullary cells.

Authors:  Keita Harada; Hidetada Matsuoka; Takeyoshi Sata; Akira Warashina; Masumi Inoue
Journal:  J Pharmacol Sci       Date:  2011-11-18       Impact factor: 3.337

10.  Interactions of atropine with heterologously expressed and native alpha 3 subunit-containing nicotinic acetylcholine receptors.

Authors:  Julie C Parker; Deboshree Sarkar; Michael W Quick; Robin A J Lester
Journal:  Br J Pharmacol       Date:  2003-03       Impact factor: 8.739

View more
  6 in total

1.  Identification of muscarinic receptor subtypes involved in catecholamine secretion in adrenal medullary chromaffin cells by genetic deletion.

Authors:  Keita Harada; Hidetada Matsuoka; Hironori Miyata; Minoru Matsui; Masumi Inoue
Journal:  Br J Pharmacol       Date:  2015-01-08       Impact factor: 8.739

2.  Expression of p11 and Heteromeric TASK Channels in Rat Carotid Body Glomus Cells and Nerve Growth Factor-differentiated PC12 Cells.

Authors:  Hidetada Matsuoka; Mieczyslaw Pokorski; Keita Harada; Reiji Yoshimura; Masumi Inoue
Journal:  J Histochem Cytochem       Date:  2020-09-04       Impact factor: 2.479

Review 3.  Muscarinic receptors in adrenal chromaffin cells: physiological role and regulation of ion channels.

Authors:  Masumi Inoue; Hidetada Matsuoka; Keita Harada; Lung-Sen Kao
Journal:  Pflugers Arch       Date:  2017-07-31       Impact factor: 3.657

4.  Molecular mechanism for muscarinic M1 receptor-mediated endocytosis of TWIK-related acid-sensitive K+ 1 channels in rat adrenal medullary cells.

Authors:  Hidetada Matsuoka; Masumi Inoue
Journal:  J Physiol       Date:  2017-10-19       Impact factor: 5.182

5.  Nerve growth factor-induced endocytosis of TWIK-related acid-sensitive K⁺ 1 channels in adrenal medullary cells and PC12 cells.

Authors:  Hidetada Matsuoka; Keita Harada; Jun Nakamura; Masumi Inoue
Journal:  Pflugers Arch       Date:  2013-02-02       Impact factor: 3.657

Review 6.  Two-pore domain potassium channels in the adrenal cortex.

Authors:  Sascha Bandulik; Philipp Tauber; Enzo Lalli; Jacques Barhanin; Richard Warth
Journal:  Pflugers Arch       Date:  2014-10-23       Impact factor: 3.657

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.