Gibson X A, Shartava A, McIntyre J, Monteiro C A, Zhang Y, Shah A, Campbell N F, Goodman S R
Department of Structural and Cellular Biology, University of South Alabama College of Medicine, Mobile, AL 36688, USA.
Blood. 1998 Jun 1;91(11):4373-8.
We show that N-acetylcysteine (NAC) has the ability to cause statistically significant diminishment in the in vitro formation of irreversibly sickled cells (ISCs) at concentrations greater than 250 micromol/L. Other antioxidants, approved for human use (cysteamine, succimer, dimercaprol), were not efficacious. NAC had the ability to cause statistically significant conversion of ISCs formed in vivo back to the biconcave shape. NAC was also shown to reduce the formation of dense cells and increase the available thiols in beta-actin. We showed that diminishing reduced glutathione (GSH), by treatment with 1-chloro-2,4-dinitrobenzene, resulted in increased dense cells. We conclude the NAC blocks dense cell formation and ISC formation by targeting channels involved in cellular dehydration and beta-actin, respectively. The efficacy of NAC is probably due to its combined antioxidant activity and ability to increase intracellular GSH.
我们发现,当浓度高于250微摩尔/升时,N-乙酰半胱氨酸(NAC)能够在体外使不可逆镰状细胞(ISC)的形成在统计学上显著减少。其他已获批准用于人类的抗氧化剂(半胱胺、二巯基丁二酸、二巯丙醇)则无效。NAC能够使体内形成的ISC在统计学上显著转化回双凹形。研究还表明,NAC可减少致密细胞的形成,并增加β-肌动蛋白中可利用的巯基。我们发现,用1-氯-2,4-二硝基苯处理以减少还原型谷胱甘肽(GSH)会导致致密细胞增加。我们得出结论,NAC分别通过靶向参与细胞脱水的通道和β-肌动蛋白来阻止致密细胞形成和ISC形成。NAC的功效可能归因于其抗氧化活性和增加细胞内GSH的能力。