PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 16904088-6 2006 However, the anti-apoptotic effects of EPO were significantly decreased in wild-type cardiomyocytes treated with L-NAME, which inhibits nitric oxide synthase activity. NG-Nitroarginine Methyl Ester 113-119 erythropoietin Mus musculus 39-42 11849379-12 2002 The results of an in vivo mouse assay revealed that L-NAME inhibited the expression of Epo, but this inhibition of Epo expression by L-NAME was rescued by pretreatment with L-arginine. NG-Nitroarginine Methyl Ester 52-58 erythropoietin Mus musculus 87-90 12490547-6 2003 Compared with their wild-type littermates, aortic rings of Epo transgenic animals exhibited a marked reduction in vascular reactivity to ET-1 and big ET-1, but this effect was abrogated upon preincubation with the NO synthase inhibitor N-nitro-L-arginine methyl ester (L-NAME). NG-Nitroarginine Methyl Ester 269-275 erythropoietin Mus musculus 59-62 11849379-12 2002 The results of an in vivo mouse assay revealed that L-NAME inhibited the expression of Epo, but this inhibition of Epo expression by L-NAME was rescued by pretreatment with L-arginine. NG-Nitroarginine Methyl Ester 133-139 erythropoietin Mus musculus 115-118 10961869-4 2000 L-NAME (analogue of L-NMMA) also inhibited Epo production in anemic mice. NG-Nitroarginine Methyl Ester 0-6 erythropoietin Mus musculus 43-46 10678740-5 2000 Renal and hepatic EPO gene expression in wt+L-NAME appeared moderately increased relative to wt with a maximal 2.5-fold enhancement after CO exposure. NG-Nitroarginine Methyl Ester 44-50 erythropoietin Mus musculus 18-21 10678740-6 2000 EPO mRNA levels in eNOS-/- mirrored those of wt+L-NAME, but the effects were less prominent. NG-Nitroarginine Methyl Ester 48-54 erythropoietin Mus musculus 0-3 8397229-2 1993 Serum levels of EPO in ex-hypoxic polycythemic mice were significantly increased after injections of 200 micrograms/kg sodium nitroprusside for 4 d. One injection of NG-nitro-L-arginine methyl ester (L-NAME) produced a significant dose-related decrease in serum levels of EPO in ex-hypoxic polycythemic mice in response to hypoxia. NG-Nitroarginine Methyl Ester 166-198 erythropoietin Mus musculus 16-19 8397229-2 1993 Serum levels of EPO in ex-hypoxic polycythemic mice were significantly increased after injections of 200 micrograms/kg sodium nitroprusside for 4 d. One injection of NG-nitro-L-arginine methyl ester (L-NAME) produced a significant dose-related decrease in serum levels of EPO in ex-hypoxic polycythemic mice in response to hypoxia. NG-Nitroarginine Methyl Ester 166-198 erythropoietin Mus musculus 272-275 8397229-2 1993 Serum levels of EPO in ex-hypoxic polycythemic mice were significantly increased after injections of 200 micrograms/kg sodium nitroprusside for 4 d. One injection of NG-nitro-L-arginine methyl ester (L-NAME) produced a significant dose-related decrease in serum levels of EPO in ex-hypoxic polycythemic mice in response to hypoxia. NG-Nitroarginine Methyl Ester 200-206 erythropoietin Mus musculus 16-19 19901910-9 2010 In contrast, coadministration of L-Name abolished EPO-mediated tissue protection by abrogating the dilatory effect resulting in reduced FCD and tissue survival, without counteracting angiogenesis and apoptotic cell death, whereas additional administration of bevacizumab did not influence the beneficial effect of EPO on flap survival despite abrogating angiogenesis. NG-Nitroarginine Methyl Ester 33-39 erythropoietin Mus musculus 50-53 19901910-9 2010 In contrast, coadministration of L-Name abolished EPO-mediated tissue protection by abrogating the dilatory effect resulting in reduced FCD and tissue survival, without counteracting angiogenesis and apoptotic cell death, whereas additional administration of bevacizumab did not influence the beneficial effect of EPO on flap survival despite abrogating angiogenesis. NG-Nitroarginine Methyl Ester 33-39 erythropoietin Mus musculus 314-317