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Nicole Gallo-Payet

Researcher at Université de Sherbrooke

Publications -  180
Citations -  6395

Nicole Gallo-Payet is an academic researcher from Université de Sherbrooke. The author has contributed to research in topics: Angiotensin II & Receptor. The author has an hindex of 46, co-authored 180 publications receiving 6111 citations. Previous affiliations of Nicole Gallo-Payet include King's College London & Faculté de médecine – Université de Sherbrooke.

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Design, synthesis, and biological evaluation of the first selective nonpeptide AT2 receptor agonist.

TL;DR: The first druglike selective angiotensin II AT(2) receptor agonist (21) with a K(i) value of 0.4 nM with a bioavailability of 20-30% after oral administration and a half-life estimated to 4 h in rat, induces outgrowth of neurite cells, stimulates p42/p44(mapk), and enhances in vivo duodenal alkaline secretion in Sprague-Dawley rats.
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Angiotensin II Induction of Neurite Outgrowth by AT2 Receptors in NG108-15 Cells: EFFECT COUNTERACTED BY THE AT1 RECEPTORS

TL;DR: The results demonstrate that the AT1 receptor inhibit the process of differentiation induced by dibutyryl cAMP, whereas the AT2 receptors potentiate this effect, illustrating negative cross-talk interaction between the two types of Ang II receptors.
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The Melanocortin System in Fugu: Determination of POMC/AGRP/MCR Gene Repertoire and Synteny, As Well As Pharmacology and Anatomical Distribution of the MCRs

TL;DR: The study shows that some parts of the MC system are highly conserved through vertebrate evolution, such as regions in POMC coding for ACTH, alpha- MSH, and beta-MSH, the C-terminal region of AGRP, key binding units within the MC1R, MC2R,MC4R, and MC5R, synteny blocks around the MCRs, and pharmacological properties of theMC2R.
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The angiotensin AT2 receptor modulates T-type calcium current in non-differentiated NG108-15 cells.

TL;DR: Angiotensin II and the AT2 receptor‐selective ligand, CGP 42112, modulate the T‐type calcium current in non‐differentiated NG108‐15 cells, which express only AT2 receptors, and it is suggested that the AT1 receptor mediates certain neurophysiological actions of this hormone.
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A G protein is involved in the angiotensin AT2 receptor inhibition of the T-type calcium current in non-differentiated NG108-15 cells.

TL;DR: The data suggest that phosphotyrosine phosphatase activation is proximal to receptor occupation, since sodium orthovanadate inhibits both GTPase activity and T-type current blockage induced by Ang II or CGP 42112, while GTPS inhibition of the T- type calcium current is not impaired.