Literature DB >> 7441562

Electrophysiology of mouse parotid acini: effects of electrical field stimulation and ionophoresis of neurotransmitters.

D V Gallacher, O H Petersen.   

Abstract

1. Intracellular micro-electrode recordings of membrane potential and input resistance were made from surface acini of mouse parotid glands placed in a Perspex tissue bath through which oxygenated physiological saline solutions were circulated. The acinar cells were stimulated by microionophoresis of both acetylcholine (ACh) and adrenaline (Ad) from extracellular micropipettes, and by electrical field stimulation via a pair of platinum electrodes. 2. The acinar cells had a mean resting membrane potential of -64.9 mV +/- 0.6 S.E. The input resistance of the unstimulated cell was 4.63 M omega +/- 0.19 S.E. In a number of cells spontaneous miniature depolarizations were observed, associated with synchronous reductions in input resistance. 3. The responses to ionophoresis of both ACh and Ad and the response to supra-maximal field stimulation were identical. Stimulation always evoked a marked decrease in input resistance associated with an initial potential change, generally followed by a delayed hyperpolarization during which the input resistance returned to normal. 4. Field-stimulation responses could be evoked to single shock (1-2 msec) and to low frequency (1-4 Hz) stimulation. The latency for this response was 245 msec +/- 12 S.E. 5. The field-stimulation response was shown to be susceptible to blockade of nerve conduction in sodium-free or tetrodotoxin- (TTX-) containing media; and to blockade of neurotransmitter release in calcium-free media. 6. The field-stimulation and ACh responses were recorded at different levels of membrane potential within the same cells by applying either hyperpolarizing or depolarizing direct current through the recording electrode. The membrane potential at which the initial potential change undergoes reversal, i.e. changes from a depolarization to a hyperpolarization, is known as the equilibrium or reversal potential, EFS and EACh respectively. The field-stimulation (FS) and ACh responses underwent simultaneous reversal at about -60 mV, i.e. EFS = EACh. Equilibrium potentials were also determined indirectly by analysis of the responses evoked by each stimulus in the manner described by Trautwein & Dudel (1958). Using this technique the equilibrium potentials of the responses to all three stimuli, field stimulation, ACh and Ad, were again about -60mV, i.e. EFS = EACh = EAd. 7. Both the field-stimulation and ACh responses were abolished by atrophine (10(-6) M) while the response to Ad persisted. Atropine also abolished all spontaneous activity. The alpha-adrenergic blocker phentolamine (10(-5) M) abolished the response to Ad but left the field-stimulation response unaffected. 8. Electrical field stimulation of isolated segments of salivary gland evoked release of endogenous neurotransmitter as a consequence of neural excitation. The technique of field stimulation thus makes it possible to investigate the functional innervation of a gland using the in vitro preparation. In the mouse parotid gland the field stimulus response was mediated by ACh released from parasympathetic nerve endings.

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Year:  1980        PMID: 7441562      PMCID: PMC1282957          DOI: 10.1113/jphysiol.1980.sp013348

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  27 in total

1.  Electrophysiology of salivary glands.

Authors:  A LUNDBERG
Journal:  Physiol Rev       Date:  1958-01       Impact factor: 37.312

2.  Spontaneous subthreshold activity at motor nerve endings.

Authors:  P FATT; B KATZ
Journal:  J Physiol       Date:  1952-05       Impact factor: 5.182

3.  Effect of adrenergic agents on salivary composition.

Authors:  I D Mandel; A Zengo; R Katz; S Wotman
Journal:  J Dent Res       Date:  1975-06       Impact factor: 6.116

4.  Adrenergic and cholinergic nerve terminals in the rat parotid gland. Electron microscopic observations on permanganate-fixed glands.

Authors:  A R Hand
Journal:  Anat Rec       Date:  1972-06

5.  Membrane potential and input resistance in acinar cells from cat and rabbit submaxillary glands in vivo: effects of autonomic nerve stimulation.

Authors:  M Kagayama; A Nishiyama
Journal:  J Physiol       Date:  1974-10       Impact factor: 5.182

6.  Adrenergic innervation of the rat submandibular and parotid glands. An electron microscopic autoradiographic study of the uptake of tritiated norepinephrine.

Authors:  B I Bogart; C L De Lemos
Journal:  Anat Rec       Date:  1973-10

7.  Electron microscopy of the adrenergic and cholinergic nerve terminals in the mouse salivary glands.

Authors:  M Takeda
Journal:  Arch Oral Biol       Date:  1978       Impact factor: 2.633

8.  Packeted transmitter release in the mouse vas deferens; an electrophysiological study [proceedings].

Authors:  A G Blakeley; T C Cunnane
Journal:  J Physiol       Date:  1979-10       Impact factor: 5.182

9.  Pancreatic acinar cells: measurement of membrane potential and miniature depolarization potentials.

Authors:  P M Dean; E K Matthews
Journal:  J Physiol       Date:  1972-08       Impact factor: 5.182

10.  Parotid acinar cells: ionic dependence of acetylcholine-evoked membrane potential changes.

Authors:  M L Roberts; N Iwatsuki; O H Petersen
Journal:  Pflugers Arch       Date:  1978-09-06       Impact factor: 3.657

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  12 in total

Review 1.  Stimulus-secretion coupling: cytoplasmic calcium signals and the control of ion channels in exocrine acinar cells.

Authors:  O H Petersen
Journal:  J Physiol       Date:  1992-03       Impact factor: 5.182

2.  Effects of adrenergic neurotransmitter on K transport in superfused segments of rat submaxillary gland.

Authors:  K Katoh; K Kaneko; A Nishiyama
Journal:  Pflugers Arch       Date:  1986-01       Impact factor: 3.657

3.  Substance P: indirect and direct effects on parotid acinar cell membrane potential.

Authors:  D V Gallacher; O H Petersen
Journal:  Pflugers Arch       Date:  1981-01       Impact factor: 3.657

4.  Nervous control of membrane conductance in mouse lacrimal acinar cells.

Authors:  G T Pearson; O H Petersen
Journal:  Pflugers Arch       Date:  1984-01       Impact factor: 3.657

5.  Three types of calcium-dependent channel in rat lacrimal glands.

Authors:  A Marty; Y P Tan; A Trautmann
Journal:  J Physiol       Date:  1984-12       Impact factor: 5.182

6.  Beta-adrenergic receptor mechanisms in rat parotid glands: activation by nerve stimulation and 3-isobutyl-1-methylxanthine.

Authors:  C M Fuller; D V Gallacher
Journal:  J Physiol       Date:  1984-11       Impact factor: 5.182

7.  Electric current flow in a two-cell preparation from Chironomus salivary glands.

Authors:  P Metzger; R Weingart
Journal:  J Physiol       Date:  1984-01       Impact factor: 5.182

8.  Parotid acinar cells: ionic dependence of isoprenaline-evoked membrane potential changes.

Authors:  N Iwatsuki; A Nishiyama
Journal:  Pflugers Arch       Date:  1982-04       Impact factor: 3.657

9.  Substance P is a functional neurotransmitter in the rat parotid gland.

Authors:  D V Gallacher
Journal:  J Physiol       Date:  1983-09       Impact factor: 5.182

10.  Postnatal growth and differentiation of muscle fibres in the mouse. I. A histochemical and morphometrical investigation of normal muscle.

Authors:  P Wirtz; H M Loermans; P G Peer; A G Reintjes
Journal:  J Anat       Date:  1983-08       Impact factor: 2.610

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