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Stimulation of adenosine A1 and A2A receptors by AMP in the submucosal plexus of guinea pig small intestine.

Stimulation of adenosine A1 and A2A receptors by AMP in the submucosal plexus of guinea pig small intestine. Research Abstract Details 

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  • Stimulation of adenosine A1 and A2A receptors by AMP in the submucosal plexus of guinea pig small intestine. Abstract Text:

    na gaoNa Gao,hong-zhen huHong-Zhen Hu,sumei liuSumei Liu,chuanyun gaoChuanyun Gao,yun xiaYun Xia,jackie d woodJackie D Wood,

    Actions of adenosine 5'-monophosphate (AMP) on electrical and synaptic behavior of submucosal neurons in guinea pig small intestine were studied with "sharp" intracellular microelectrodes. Application of AMP (0.3-100 microM) evoked slowly activating depolarizing responses associated with increased excitability in 80.5% of the neurons. The responses were concentration dependent with an EC(50) of 3.5 +/- 0.5 microM. They were abolished by the adenosine A(2A) receptor antagonist ZM-241385 but not by pyridoxal-phosphate-6-azophenyl-2,4-disulfonic acid, trinitrophenyl-ATP, 8-cyclopentyl-1,3-dimethylxanthine, suramin, or MRS-12201220. The AMP-evoked responses were insensitive to AACOCF3 or ryanodine. They were reduced significantly by 1) U-73122, which is a phospholipase C inhibitor; 2) cyclopiazonic acid, which blocks the Ca(2+) pump in intraneuronal membranes; and 3) 2-aminoethoxy-diphenylborane, which is an inositol (1,4,5)-trisphosphate receptor antagonist. Inhibitors of PKC or calmodulin-dependent protein kinase also suppressed the AMP-evoked excitatory responses. Exposure to AMP suppressed fast nicotinic ionotropic postsynaptic potentials, slow metabotropic excitatory postsynaptic potentials, and slow noradrenergic inhibitory postsynaptic potentials in the submucosal plexus. Inhibition of each form of synaptic transmission reflected action at presynaptic inhibitory adenosine A(1) receptors. Slow excitatory postsynaptic potentials, which were mediated by the release of ATP and stimulation of P2Y(1) purinergic receptors in the submucosal plexus, were not suppressed by AMP. The results suggest an excitatory action of AMP at adenosine A(2A) receptors on neuronal cell bodies and presynaptic inhibitory actions mediated by adenosine A(1) receptors for most forms of neurotransmission in the submucosal plexus, with the exception of slow excitatory purinergic transmission mediated by the P2Y(1) receptor subtype.

    Stimulation of adenosine A1 and A2A receptors by AMP in the submucosal plexus of guinea pig small intestine. Publishing Authors By Initials

    n gaoN Gao,hz huHZ Hu,s liuS Liu,c gaoC Gao,y xiaY Xia,jd woodJD Wood,

    For similar heterocyclic compounds: heterocyclic compounds, 1-ring: azoles: triazoles research abstracts see: heterocyclic compounds: heterocyclic compounds, 1-ring: azoles: triazoles research

    PUBMED ID PMID:

    MEDLINE DATE:

    Stimulation of adenosine A1 and A2A receptors by AMP in the submucosal plexus of guinea pig small intestine. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: American journal of physiology. Gastrointestinal a

    VOLUME: 292

    Page Numbers: G492-500

    Journal Abbreviation: Am. J. Physiol. Gastrointest.

    ISSN: 0193-1857

    DAY: 5

    MONTH: 10

    YEAR: 2006

    Stimulation of adenosine A1 and A2A receptors by AMP in the submucosal plexus of guinea pig small intestine. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 100901227

    Stimulation of adenosine A1 and A2A receptors by AMP in the submucosal plexus of guinea pig small intestine. Keywords Mesh Terms:

    KEYWORDS: Triazoles

    MESH TERMS: pharmacology

    Chemical & Substance for Abstract: Stimulation of adenosine A1 and A2A receptors by AMP in the submucosal plexus of guinea pig small intestine. Information

    Substance Name: 1-(5-Isoquinolinesulfonyl)-2-Methylpiper

    Registry Number: 84477-87-2

    Grant and Affiliation Information for Stimulation of adenosine A1 and A2A receptors by AMP in the submucosal plexus of guinea pig small intestine.

    AFFILIATION: Dept of Physiology and Cell Biology, Columbus, OH 43210-1218, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NIDDK

    GRANT: R01 DK-57075

    ACRONYM: DK

    MEDLINETA: Am J Physiol Gastrointest Live

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

    Number Hits: 0

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