Neuron
ArticleDifferential G protein-mediated coupling of D2 dopamine receptors to K+ and Ca2+ currents in rat anterior pituitary cells
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2015, European NeuropsychopharmacologyCitation Excerpt :Most probably, the D3 receptor mediates the Cl− influx of the bumetanide-insensitive and PTX-sensitive system (Skaaning Jensen et al., 1997). Furthermore Ca2+ channels, mostly involved in neurotransmitter release process (Nimmrich and Gross, 2012; Williams et al., 1992), are inhibited by all D2-like receptors (Fig. 4) (Lledo et al., 1992; Okada et al., 2003). Depression of P/Q-type Ca2+ channel inward currents could be mediated by D3 receptor agonists in a pertussis toxin-sensitive manner, suggesting a G-protein involvement (Kuzhikandathil and Oxford, 1999).
Activation of D<inf>2</inf> dopamine receptors inhibits estrogen response element-mediated estrogen receptor transactivation in rat pituitary lactotrophs
2013, Molecular and Cellular EndocrinologyCitation Excerpt :D2 receptor activation inhibits adenylate cyclase activity leading to decreased intracellular cAMP concentrations and the subsequent inhibition of protein kinase A (PKA) (De Camilli et al., 1979; Maurer, 1982b; Swennen and Denef, 1982). D2 receptor activation also inhibits intracellular Ca2+ concentrations (Ho et al., 1996; Malgaroli et al., 1987), which have been best illustrated to occur through inhibition of voltage-gated Ca2+ channels and/or activation of inward rectifier K+ channels (Einhorn et al., 1991; Lledo et al., 1992). In addition, D2 receptor activation leads to the inhibition of ERK1/2 in a PTX-dependent manner, (Liu et al., 2002).
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