Literature DB >> 1705906

The nature of noncholinergic membrane potential responses to transmural stimulation in guinea pig ileum.

J R Crist1, X D He, R K Goyal.   

Abstract

The effect of substance P antagonism on membrane potential responses to transmural nerve stimulation in the presence of atropine was examined in circular smooth muscle of the guinea pig ileum. Intracellular recordings of membrane potential responses recorded 3-5 mm oral to the transmural stimulus consisted of an inhibitory junction potential followed by two distinct depolarizations referred to as early and late excitatory junction potentials. Substance P antagonism was achieved by desensitization with high doses of substance P or use of the antagonist Spantide (Sigma Chemical Co., St. Louis, MO). Substance P antagonism had no effect on the amplitude of the inhibitory junction potential, caused an increase in the latter portion of the early excitatory junction potential, and abolished the late excitatory junction potential. The excitatory junction potential potentiated by substance P receptor antagonism was associated with a decrease in membrane resistance, increased in amplitude with conditioning hyperpolarizations to the estimated equilibrium potential for K+, and was blocked by the Cl-/HCO3- exchange inhibitor DIDS or prolonged perfusion with low-chloride solution. These studies suggest that a noncholinergic, non-substance P neurotransmitter is released from enteric motoneurons that produces excitation through an increase in smooth muscle chloride conductance.

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Year:  1991        PMID: 1705906     DOI: 10.1016/0016-5085(91)90276-q

Source DB:  PubMed          Journal:  Gastroenterology        ISSN: 0016-5085            Impact factor:   22.682


  7 in total

1.  CaMKII inhibition hyperpolarizes membrane and blocks nitrergic IJP by closing a Cl(-) conductance in intestinal smooth muscle.

Authors:  Xue-Dao He; Raj K Goyal
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2012-04-26       Impact factor: 4.052

2.  Both ATP and the peptide VIP are inhibitory neurotransmitters in guinea-pig ileum circular muscle.

Authors:  J R Crist; X D He; R K Goyal
Journal:  J Physiol       Date:  1992-02       Impact factor: 5.182

3.  β-Nicotinamide adenine dinucleotide acts at prejunctional adenosine A1 receptors to suppress inhibitory musculomotor neurotransmission in guinea pig colon and human jejunum.

Authors:  Guo-Du Wang; Xi-Yu Wang; Sumei Liu; Yun Xia; Fei Zou; Meihua Qu; Bradley J Needleman; Dean J Mikami; Jackie D Wood
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2015-03-26       Impact factor: 4.052

4.  Tachykinin NK1 and NK2 receptor antagonists and atropine-resistant ascending excitatory reflex to the circular muscle of the guinea-pig ileum.

Authors:  C A Maggi; R Patacchini; L Bartho; P Holzer; P Santicioli
Journal:  Br J Pharmacol       Date:  1994-05       Impact factor: 8.739

5.  Evidence that tachykinin NK1 and NK2 receptors mediate non-adrenergic non-cholinergic excitation and contraction in the circular muscle of guinea-pig duodenum.

Authors:  V Zagorodnyuk; P Santicioli; C A Maggi; A Giachetti
Journal:  Br J Pharmacol       Date:  1995-05       Impact factor: 8.739

6.  Nitric oxide involvement in the peptide VIP-associated inhibitory junction potential in the guinea-pig ileum.

Authors:  X D He; R K Goyal
Journal:  J Physiol       Date:  1993-02       Impact factor: 5.182

7.  Tachykinin NK1 but not NK2 receptors mediate non-cholinergic excitatory junction potentials in the circular muscle of guinea-pig colon.

Authors:  V Zagorodnyuk; P Santicioli; C A Maggi
Journal:  Br J Pharmacol       Date:  1993-10       Impact factor: 8.739

  7 in total

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