Bagchi Debasis, Swaroop Anand, Preuss Harry G, Bagchi Manashi
Department of Pharmacological and Pharmaceutical Sciences, University of Houston College of Pharmacy, Houston, TX, USA; Research & Development Division, Cepham Inc., Piscataway, NJ, USA.
Research & Development Division, Cepham Inc., Piscataway, NJ, USA.
Mutat Res. 2014 Oct;768:69-73. doi: 10.1016/j.mrfmmm.2014.04.004. Epub 2014 Apr 19.
A large number of investigations have demonstrated a broad spectrum of pharmacological and therapeutic benefits of grape seed proanthocyanidins (GSP) against oxidative stress and degenerative diseases including cardiovascular dysfunctions, acute and chronic stress, gastrointestinal distress, neurological disorders, pancreatitis, various stages of neoplastic processes and carcinogenesis including detoxification of carcinogenic metabolites. GSP exhibited potent free radical scavenging abilities in both in vitro and in vivo models. GSP exerted significant in vivo protection against structurally diverse drug and chemical-induced hepatotoxicity, cardiotoxicity, neurotoxicity, nephrotoxicity and spleentoxicity. GSP also protected against idarubicin and 4-hydroxyperoxy-cyclophosphamide-induced cytotoxicity toward human normal liver cells. GSP exhibited selective cytotoxicity toward selected human cancer cells, while enhancing the growth and viability of normal cells. GSP exhibited potent modulatory effects of pro-apoptotic and apoptotic regulatory bcl-XL, p53, c-myc, c-JUN, JNK-1 and CD36 genes. Long-term exposure to GSP may serve as a novel chemoprotectant against three stages of DMN-induced liver carcinogenesis and tumorigenesis including initiation, promotion and progression. GSP may selectively protect against oxidative stress, genomic integrity and cell death patterns in vivo. These results demonstrate that GSP may serve as a novel therapeutic intervention against carcinogenesis.
大量研究表明,葡萄籽原花青素(GSP)具有广泛的药理和治疗益处,可对抗氧化应激和退行性疾病,包括心血管功能障碍、急慢性应激、胃肠道不适、神经紊乱、胰腺炎、肿瘤发生的各个阶段以及致癌作用,包括致癌代谢物的解毒。在体外和体内模型中,GSP均表现出强大的自由基清除能力。GSP在体内对结构多样的药物和化学物质诱导的肝毒性、心脏毒性、神经毒性、肾毒性和脾毒性具有显著的保护作用。GSP还可保护人正常肝细胞免受伊达比星和4-羟基过氧环磷酰胺诱导的细胞毒性。GSP对选定的人类癌细胞表现出选择性细胞毒性,同时增强正常细胞的生长和活力。GSP对促凋亡和凋亡调节基因bcl-XL、p53、c-myc、c-JUN、JNK-1和CD36具有强大的调节作用。长期接触GSP可能作为一种新型化学保护剂,对抗二甲基亚硝胺诱导的肝癌发生和肿瘤发生的三个阶段,包括启动、促进和进展。GSP可能在体内选择性地保护免受氧化应激、基因组完整性和细胞死亡模式的影响。这些结果表明,GSP可能作为一种新型的抗癌发生治疗干预措施。