Other studies show that l-arginine transport is mediated by the systems y+ and y+L (for l-arginine transport in exchange for l-leucine in the presence of Na+) [24] in endothelial cells from the microcirculation in the human placenta [26]. In the latter, mRNA for hCAT-1, hCAT-2A, hCAT-2B, and hCAT-4 was amplified, and only hCAT-1 protein was reported. Interestingly, A2AAR activation and high extracellular d-glucose concentration are apparently crucial playing a role in the abnormal phenotype

seen in HUVEC from GDM pregnancies [72, 91]. This cell type exhibits increased hCAT-1 expression and activity associated with increased NO synthesis check details and eNOS activation in GDM [91]. In a series of recent publications, we have proposed that hCAT-1 mediated l-arginine transport in HUVEC from GDM will depend on the regulation of SLC7A1 expression by other vasoactive molecules such as adenosine [81], insulin [37, 40, 39], or lipids [49]. In addition, SLC7A1 expression is now considered under modulation by other pathologies in pregnancy such as obesity or excessive gain of weight (i.e., supraphysiological) in pregnancy [50]. This phenomenon

implies not only an effect of GDM on the modulation of the existing APO866 order hCAT-1 protein but also a GDM effect at the gene level in human pregnancy. Nintedanib nmr Adenosine is a vasodilator in the placenta, coronary, cerebral, and muscular circulation, in several conditions including hypoxia and exercise [9, 15, 29, 98]. Extracellular adenosine activates P1 purinergic receptors

family, which is conformed by at least four subtypes, that is, A1 (A1AR), A2A (A2AAR), A2B (A2BAR), and A3 (A3AR) [15, 16, 34]. A1AR, A2AAR, and A3AR are activated by adenosine at nanomolar concentration, while A2BAR requires micromolar concentration for its activation [29, 34, 60, 74]. A1AR and A3AR are classically associated with inhibitory signaling receptors coupled to Gi/Go protein; however, A2AAR and A2BAR are associated with stimulatory signaling coupled to Gs protein [47]. Adenosine receptors activation depends on the adenosine extracellular level, which is mainly regulated by nucleoside membrane transporters [4, 15, 14, 81, 97]. In HUVEC and hPMEC, the extracellular adenosine is taken up primarily via the Na+-independent ENTs, where hENT1 and hENT2 isoforms play crucial roles in this phenomenon [71, 81, 97, 98]. In addition, Na+-dependent, CNTs have not been identified in these cell types. It has been shown that inhibition of hENT1 and hENT2 transport activity with NBTI [44] results in a higher extracellular concentration of adenosine and increased l-arginine transport and NO synthesis in HUVEC [91] and hPMEC [30].