Literature DB >> 10523420

Quantal evoked depolarizations underlying the excitatory junction potential of the guinea-pig isolated vas deferens.

R Manchanda1, K Venkateswarlu.   

Abstract

1. The effects of a putative gap junction uncoupling agent, heptanol, on the intracellularly recorded junction potentials of the guinea-pig isolated vas deferens have been investigated. 2. After the stimulation-evoked excitatory junction potentials (EJPs) had been suppressed by heptanol (2.0 mM) to undetectable levels, a different pattern of evoked activity ensued. This consisted of transient depolarizations that were similar to EJPs in being stimulus locked and in occurring at a fixed latency, but differed from EJPs in that they occurred intermittently and had considerably briefer time courses. 3. Analysis of the amplitudes and temporal parameters of the rapid residual depolarizations revealed a close similarity with spontaneous EJPs (SEJPs). There was no statistically significant difference between the rise times, time constants of decay and durations of the rapid residual depolarizations and of SEJPs. 4. Selected evoked depolarizations were virtually identical to SEJPs occurring in the same cell. Evoked depolarizations of closely similar amplitude and time course also occurred, usually within a few stimuli of each other. 5. These depolarizations appear to represent the individual quantal depolarizations that normally underlie the EJP and are therefore termed 'quantal excitatory junction potentials' (QEJPs) to distinguish them from both EJPs and SEJPs. 6. We examined the possibility that heptanol revealed QEJPs by disrupting electrical coupling between cells in the smooth muscle syncytium. Heptanol (2.0 mM) had no effect on the amplitude distribution, time courses, or the frequency of occurrence of SEJPs. Intracellular input impedance (Rin) of smooth muscle cells was left unaltered by heptanol. 7. 'Cable' potentials of the vas deferens, recorded using the partition stimulation method, also remained unchanged in the presence of heptanol. Thus, heptanol appeared not to modify syncytial electrical properties of the smooth muscle in any significant way. 8. Our observations show directly that the quantal depolarizations underlying the EJP in syncytial smooth muscle are SEJP-like events. However, no unequivocal statement can be made about the mechanism by which heptanol unmasks QEJPs from EJPs.

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Year:  1999        PMID: 10523420      PMCID: PMC2269600          DOI: 10.1111/j.1469-7793.1999.00527.x

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


  31 in total

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Authors:  T Tomita
Journal:  J Physiol       Date:  1967-03       Impact factor: 5.182

2.  Electrical coupling between cells of the insect Aedes albopictus.

Authors:  F Bukauskas; C Kempf; R Weingart
Journal:  J Physiol       Date:  1992-03       Impact factor: 5.182

Review 3.  Gap junctions in vascular tissues. Evaluating the role of intercellular communication in the modulation of vasomotor tone.

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Journal:  Circ Res       Date:  1996-10       Impact factor: 17.367

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Authors:  R D Purves
Journal:  J Theor Biol       Date:  1976-07-21       Impact factor: 2.691

5.  Simultaneous intracellular and focal extracellular recording of junction potentials and currents, and the time course of quantal transmitter action in rodent vas deferens.

Authors:  T C Cunnane; R Manchanda
Journal:  Neuroscience       Date:  1989       Impact factor: 3.590

Review 6.  On the contribution of quantal secretion from close-contact and loose-contact varicosities to the synaptic potentials in the vas deferens.

Authors:  M R Bennett; W G Gibson
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  1995-01-30       Impact factor: 6.237

7.  Frequency dependent intermittency and ionic basis of impulse conduction in postganglionic sympathetic fibres of guinea-pig vas deferens.

Authors:  T C Cunnane; L Stjärne
Journal:  Neuroscience       Date:  1984-01       Impact factor: 3.590

8.  On the factors which determine the time-courses of junction potentials in the guinea-pig vas deferens.

Authors:  T C Cunnane; R Manchanda
Journal:  Neuroscience       Date:  1990       Impact factor: 3.590

9.  Rapid onset and calcium independence of the gap junction uncoupling induced by heptanol in cultured heart cells.

Authors:  B Bastide; J C Hervé; L Cronier; J Délèze
Journal:  Pflugers Arch       Date:  1995-01       Impact factor: 3.657

10.  CORRELATION OF FINE STRUCTURE AND PHYSIOLOGY OF THE INNERVATION OF SMOOTH MUSCLE IN THE GUINEA PIG VAS DEFERENS.

Authors:  N C MERRILLEES; G BURNSTOCK; M E HOLMAN
Journal:  J Cell Biol       Date:  1963-12       Impact factor: 10.539

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  6 in total

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2.  Effects of carbenoxolone on syncytial electrical properties and junction potentials of guinea-pig vas deferens.

Authors:  D Palani; P Ghildyal; Rohit Manchanda
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3.  The origin of the skewed amplitude distribution of spontaneous excitatory junction potentials in poorly coupled smooth muscle cells.

Authors:  J S Young; K L Brain; T C Cunnane
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4.  Prejunctional and postjunctional actions of heptanol and 18 beta-glycyrretinic acid in the rodent vas deferens.

Authors:  Faisal Rahman; Rohit Manchanda; Keith L Brain
Journal:  Auton Neurosci       Date:  2009-04-16       Impact factor: 3.145

5.  Electrical and optical study of nerve impulse-evoked ATP-induced, P2X-receptor-mediated sympathetic neurotransmission at single smooth muscle cells in mouse isolated VAS deferens.

Authors:  J S Young; K L Brain; T C Cunnane
Journal:  Neuroscience       Date:  2007-07-16       Impact factor: 3.590

6.  Physiological and pharmacological aspects of the vas deferens-an update.

Authors:  David S Koslov; Karl-Erik Andersson
Journal:  Front Pharmacol       Date:  2013-08-22       Impact factor: 5.810

  6 in total

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