Arbault S, Edeas M, Legrand-Poels S, Sojic N, Amatore C, Piette J, Best-Belpomme M, Lindenbaum A, Vuillaume M
URA 1679 and UPR42 CNRS, Ecole Normale Supérieure, Paris, France.
Biomed Pharmacother. 1997;51(10):430-8. doi: 10.1016/s0753-3322(97)82321-9.
Phenylarsine oxide (PAO), which is described as an inhibitor of tyrosine phosphatase activity, inhibits H2O2 release from human peripheral blood mononuclear cells (PBMCs) as measured by electrochemistry. Since human immunodeficiency virus type 1 (HIV-1) replication is known to be favored under oxidative stress conditions, ex vivo experiments using uninfected PBMCs, primary monocytes or a latently infected promonocytic U1 cell line show that HIV-1 replication and reactivation, monitored by p24 antigen measurement, are inhibited by PAO in a time- and concentration-dependent manner. These observations can be linked with the inhibition of NF-kappa B activation when uninfected monocytes are induced by either tumor necrosis factor alpha (TNF-alpha) phorbol 12-myristate 13-acetate (PMA) or lipopolysaccharide (LPS).
苯胂化氧(PAO)被描述为酪氨酸磷酸酶活性的抑制剂,通过电化学方法测定,它能抑制人外周血单个核细胞(PBMC)释放过氧化氢。由于已知1型人类免疫缺陷病毒(HIV-1)在氧化应激条件下更易复制,使用未感染的PBMC、原代单核细胞或潜伏感染的原单核细胞U1细胞系进行的体外实验表明,通过p24抗原测量监测到的HIV-1复制和重新激活受到PAO的时间和浓度依赖性抑制。当未感染的单核细胞被肿瘤坏死因子α(TNF-α)、佛波酯12-肉豆蔻酸酯13-乙酸酯(PMA)或脂多糖(LPS)诱导时,这些观察结果可能与NF-κB激活的抑制有关。