Catherine Heurteaux
DuPont
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Publication
Featured researches published by Catherine Heurteaux.
American Journal of Physiology-gastrointestinal and Liver Physiology | 2012
V. Gil; D. Gallego; H. Moha Ou Maati; Rémi Peyronnet; M. Martínez-Cutillas; Catherine Heurteaux; Marc Borsotto; M. Jiménez
Purinergic and nitrergic neurotransmission predominantly mediate inhibitory neuromuscular transmission in the rat colon. We studied the sensitivity of both purinergic and nitrergic pathways to spadin, a TWIK-related potassium channel 1 (TREK1) inhibitor, apamin, a small-conductance calcium-activated potassium channel blocker and 1H-[1,2,4]oxadiazolo[4,3-α]quinoxalin-1-one (ODQ), a specific inhibitor of soluble guanylate cyclase. TREK1 expression was detected by RT-PCR in the rat colon. Patch-clamp experiments were performed on cells expressing hTREK1 channels. Spadin (1 μM) reduced currents 1) in basal conditions 2) activated by stretch, and 3) with arachidonic acid (AA; 10 μM). l-Methionine (1 mM) or l-cysteine (1 mM) did not modify currents activated by AA. Microelectrode and muscle bath studies were performed on rat colon samples. l-Methionine (2 mM), apamin (1 μM), ODQ (10 μM), and N(ω)-nitro-l-arginine (l-NNA; 1 mM) depolarized smooth muscle cells and increased motility. These effects were not observed with spadin (1 μM). Purinergic and nitrergic inhibitory junction potentials (IJP) were studied by incubating the tissue with l-NNA (1 mM) or MRS2500 (1 μM). Both purinergic and nitrergic IJP were unaffected by spadin. Apamin reduced both IJP with a different potency and maximal effect for each. ODQ concentration dependently abolished nitrergic IJP without affecting purinergic IJP. Similar effects were observed in hyperpolarizations induced by sodium nitroprusside (1 μM) and nitrergic relaxations induced by electrical stimulation. We propose a pharmacological approach to characterize the pathways and function of purinergic and nitrergic neurotransmission. Nitrergic neurotransmission, which is mediated by cyclic guanosine monophosphate, is insensitive to spadin, an effective TREK1 channel inhibitor. Both purinergic and nitrergic neurotransmission are inhibited by apamin but with different relative sensitivity.
Journal of Vascular Surgery | 2000
Loïc Lang-Lazdunski; Catherine Heurteaux; Hervé Dupont; Catherine Widmann; Michel Lazdunski
Archive | 2010
Michel Lazdunski; Catherine Heurteaux; David Picard
Archive | 2013
Ou Maati Hamid Moha; Michel Lazdunski; Catherine Heurteaux; David Picard
Archive | 1999
Michel Lazdunski; Catherine Heurteaux
Archive | 2000
Michel Lazdunski; Loïc Lang-Lazdunski; Catherine Heurteaux
Archive | 2013
Hamid Moha ou Maati; Michel Lazdunski; Catherine Heurteaux; David Picard
Archive | 2001
Rainer Waldmann; Frederic Bassilana; Michel Lazdunski; Catherine Heurteaux; Eric Lingueglia; Guy Champigny
Archive | 2015
Georges Gaudriault; Catherine Heurteaux; Jean Mazella; Marc Borsotto; Ou Maati Hamid Moha; Julie Veyssiere
Archive | 2013
Georges Romey; Michel Lazdunski; Michel Fosset; Catherine Heurteaux; Miguel Salinas; Roberto Reyes