Literature DB >> 8730594

Electrical properties of smooth muscle in the guinea-pig urinary bladder.

N J Bramich1, A F Brading.   

Abstract

1. The effects of transmural nerve stimulation were examined on preparations of detrusor smooth muscle from guinea-pig urinary bladder using intracellular recording techniques. Most recordings were made from preparations in which spontaneous and evoked action potentials had been inhibited by nifedipine (10 microM), a dihydropyridine that blocks L-type Ca2+ channels. 2. Supramaximal stimuli evoked excitatory junction potentials (EJPs) which could be divided into three basic types. Type 1 EJPs had short latencies (< 30 ms) and fast rise times (< 60 ms). Type 2 EJPs consisted of two components: a small depolarization that was followed by a second depolarization with a faster rise time. In a third type of cell, at high strengths of stimulation, EJPs resembled type 1 EJPs but at lower strengths of stimulation were similar in time course to type 2 EJPs. 3. All EJPs were abolished by tetrodotoxin (1 microM) and reduced by omega-conotoxin (0.1 microM), but were unaffected by hexamethonium (0.1 mM), suggesting that they result from the release of transmitter from post-ganglionic nerve fibres. All responses persisted in the presence of atropine (1 microM) but were abolished following the desensitization of P2-purinoceptors with alpha, beta-methylene ATP (m-ATP; 10 microM). 4. Spontaneous excitatory junction potentials (SEJPs) were also recorded from most cells. SEJPs were similar in appearance to fast single-component EJPs; however, in general they had a briefer time course. SEJPs persisted in the presence of tetrodotoxin (1 microM). 5. The electrical properties of urinary bladder smooth muscle were also examined. Voltage changes induced by point current injection into cells had fast rates of rise and decay (time constant, 5-20 ms). The input resistance of cells ranged between 12 and 108 M omega. When recordings were taken from cells near the point of current injection, resultant electrotonic potentials could be detected in only a small proportions of cells. 6. The results are discussed in relation to the idea that transmural nerve stimulation in the guinea-pig urinary bladder causes the activation of at least two different membrane conductances. Cells appear to be electrically coupled with one another. However, it is likely that coupling exists within discrete bundles of the smooth muscle.

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Year:  1996        PMID: 8730594      PMCID: PMC1158872          DOI: 10.1113/jphysiol.1996.sp021300

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


  8 in total

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3.  Some properties of the smooth muscle of mouse vas deferens.

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4.  The effect of omega conotoxin GVIA, a peptide modulator of the N-type voltage sensitive calcium channels, on motor responses produced by activation of efferent and sensory nerves in mammalian smooth muscle.

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5.  Atropine-resistant excitatory junction potentials in rabbit bladder are blocked by alpha,beta-methylene ATP.

Authors:  C H Hoyle; G Burnstock
Journal:  Eur J Pharmacol       Date:  1985-08-15       Impact factor: 4.432

6.  Action potentials and net membrane currents of isolated smooth muscle cells (urinary bladder of the guinea-pig).

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7.  Tetrodotoxin-sensitive action potentials in smooth muscle of mouse vas deferens.

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8.  Neuromuscular transmission and smooth muscle membrane properties in the guinea-pig ear artery.

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  8 in total
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Review 6.  Molecular mechanisms of detrusor and corporal myocyte contraction: identifying targets for pharmacotherapy of bladder and erectile dysfunction.

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7.  A molecular signature of tissues with pacemaker activity in the heart and upper urinary tract involves coexpressed hyperpolarization-activated cation and T-type Ca2+ channels.

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8.  The KV 7 channel activator retigabine suppresses mouse urinary bladder afferent nerve activity without affecting detrusor smooth muscle K+ channel currents.

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Review 9.  Electrophysiological properties of the bladder.

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10.  Spontaneous purinergic neurotransmission in the mouse urinary bladder.

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Journal:  J Physiol       Date:  2008-10-20       Impact factor: 5.182

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