%0 Figure %A Yang, Dan %A Xie, Ping %A Liu, Zhihua %D 2013 %T SalA alleviates impairment of endothelial NO formation in response to IS/RP. %U https://plos.figshare.com/articles/figure/_SalA_alleviates_impairment_of_endothelial_NO_formation_in_response_to_IS_RP_/272478 %R 10.1371/journal.pone.0042076.g007 %2 https://ndownloader.figshare.com/files/601982 %K alleviates %K impairment %K endothelial %X

HUVECs were pretreated with SalA for 30 min in various concentrations, and then subjected to IS/RP treatment. (a) The MKP-3 and eNOS mRNA levels in each group were detected by quantitative RT-PCR (n = 5, means±SEM). *P<0.05 vs. control group; #P<0.05 vs. non-SalA-treated IS/RP group. (b) The protein levels of MKP-3, ERK1/2, eNOS, and GAPDH were detected by immunoblot analysis. A representative blot was shown (n = 4). (c) The NOS activity in the cell lysates was determined via examining the efficiency in conversion of [3H]L-arginine to [3H]L-citrulline (n = 4, means±SEM). *P<0.05 vs. control group; #P<0.05 vs. non-SalA-treated IS/RP group. (d) NO formation was detected as nitrite released into supernatant of confluent cultures of HUVECs (n = 3, means±SEM). *P<0.05 vs. control group; #P<0.05 vs. non-SalA-treated IS/RP group. (e) Cell apoptosis was determined by TUNEL assay. The number of TUNEL-positive cells was quantified, and at least 120 cells per dish were counted (n = 3, means ± SEM.). *P<0.05 vs. control group; #P<0.05 vs. non-SalA-treated IS/RP group.

%I PLOS ONE