Abstract
Dual excitation microfluorimetry (Fura-2) was used to measure changes in intracellular calcium ([Ca2+]i) in individual cultured guinea pig myenteric neurons. Bombesin (5-500 nM) induced concentration-dependent increases in [Ca2+]i responses, with a maximal effect at 500 nM (56% of neurons responding, mean peak Ca2+ response 244 +/- 25 nM vs. basal 65 +/- 7 nM). Removal of Ca2+ from the median did not affect the initial [Ca2+]i peak but eliminated the subsequent plateau phase. The [Ca2+]i responses to bombesin was abolished by preincubation with thapsigargin (1 microM), a Ca(2+)-ATPase inhibitor (91 +/- 7% inhibition). [Ca2+]i responses to bombesin were inhibited by U73122 (1 microM), an inhibitor of phospholipase C (84 +/- 6% inhibition).
MeSH terms
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Animals
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Animals, Newborn
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Bombesin / pharmacology*
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Calcium / metabolism*
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Calcium-Transporting ATPases / antagonists & inhibitors
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Cells, Cultured
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Dose-Response Relationship, Drug
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Enzyme Inhibitors / pharmacology*
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Estrenes / pharmacology
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Fluorometry
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Guinea Pigs
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Myenteric Plexus / cytology
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Myenteric Plexus / drug effects
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Myenteric Plexus / metabolism*
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Neurons / drug effects
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Neurons / metabolism*
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Phosphodiesterase Inhibitors / pharmacology
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Pyrrolidinones / pharmacology
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Signal Transduction
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Terpenes / pharmacology
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Thapsigargin
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Type C Phospholipases / antagonists & inhibitors
Substances
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Enzyme Inhibitors
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Estrenes
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Phosphodiesterase Inhibitors
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Pyrrolidinones
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Terpenes
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1-(6-((3-methoxyestra-1,3,5(10)-trien-17-yl)amino)hexyl)-1H-pyrrole-2,5-dione
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Thapsigargin
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Type C Phospholipases
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Calcium-Transporting ATPases
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Bombesin
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Calcium