Correlation of electrophysiology, neurochemistry and axonal projections of guinea‐pig sphincter of Oddi neurones

Sphincter of Oddi (SO) ganglia are comprised of two main types of neurones based either on their electrical or neurochemical properties. This study investigated whether any correlation exists between the electrical and neurochemical properties of these cells. SO neurones were characterized electrica...

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Veröffentlicht in:Neurogastroenterology and motility 1998-06, Vol.10 (3), p.235-244
Hauptverfasser: Hillsley, K., Mawe, G.M.
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Sprache:eng
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Zusammenfassung:Sphincter of Oddi (SO) ganglia are comprised of two main types of neurones based either on their electrical or neurochemical properties. This study investigated whether any correlation exists between the electrical and neurochemical properties of these cells. SO neurones were characterized electrically as either Tonic or Phasic cells, labelled with neurobiotin, fixed, and processed for β‐nicotinamide adenine dinucleotide phosphate diaphorase (NADPH‐DA) staining and choline acetyltransferase immunoreactivity to identify whether electrically characterized neurones were nitrergic or cholinergic. A total of 119 cells were analysed in this manner; 45% of cells were Tonic and 37% were Phasic. An equivalent number of Tonic (58.1%, 18/31) and Phasic cells (60%, 21/35) were choline acetyltransferase (ChAT) positive. Three of 34 Phasic cells were NADPH‐DA positive, whereas 11/33 Tonic cells were NADPH‐DA positive. In none of the preparations was ChAT immunoreactivity and NADPH‐DA reactivity ever observed in the same neurone. Calretinin immunoreactivity was present in a subpopulation of both Tonic and Phasic neurones. No correlation was observed between the direction of axon projections and the electrophysiological or neurochemical properties of the cell. These results suggest that there is a lack of correlation between the electrical properties and the neurochemical content of SO neurones. Various explanations for these findings are discussed.
ISSN:1350-1925
1365-2982
DOI:10.1046/j.1365-2982.1998.00101.x