Department of Pharmaceutical and Biomedical Sciences, Touro College of Pharmacy, New York, NY, USA.
Toxicology. 2010 Nov 28;278(1):6-16. doi: 10.1016/j.tox.2010.09.006. Epub 2010 Sep 24.
Fermented papaya preparation (FPP) (a product of yeast fermentation of Carica papaya Linn) is a food supplement. Studies in chronic and degenerative disease conditions (such as thalassemia, cirrhosis, diabetes and aging) and performance sports show that FPP favorably modulates immunological, hematological, inflammatory, vascular and oxidative stress damage parameters. Neuroprotective potential evaluated in an Alzheimer's disease cell model showed that the toxicity of the β-amyloid can be significantly modulated by FPP. Oxidative stress trigger apoptotic pathways such as the c-jun N-terminal kinase (JNK) and p38-mitogen activated protein kinase (MAPK) are preferentially activated by pro-inflammatory cytokines and oxidative stress resulting in cell differentiation and apoptosis. FPP modulated the H₂O₂-induced ERK, Akt and p38 activation with the reduction of p38 phosphorylation induced by H₂O₂. FPP reduces the extent of the H₂O₂-induced DNA damage, an outcome corroborated by similar effects obtained in the benzo[a]pyrene treated cells. No genotoxic effect was observed in experiments with FPP exposed to HepG2 cells nor was FPP toxic to the PC12 cells. Oxidative stress-induced cell damage and inflammation are implicated in a variety of cancers, diabetes, arthritis, cardiovascular dysfunctions, neurodegenerative disorders (such as stroke, Alzheimer's disease, and Parkinson's disease), exercise physiology (including performance sports) and aging. These conditions could potentially benefit from functional nutraceutical/food supplements (as illustrated here with fermented papaya preparation) exhibiting anti-inflammatory, antioxidant, immunostimulatory (at the level of the mucus membrane) and induction of antioxidant enzymes.
木瓜发酵制剂(FPP)(木瓜 Linn 的酵母发酵产物)是一种食品补充剂。在慢性和退行性疾病(如地中海贫血、肝硬化、糖尿病和衰老)以及竞技运动的研究中,FPP 有利于调节免疫、血液、炎症、血管和氧化应激损伤参数。在阿尔茨海默病细胞模型中评估的神经保护潜力表明,FPP 可显著调节β-淀粉样蛋白的毒性。氧化应激触发凋亡途径,如 c-jun N 末端激酶(JNK)和 p38-有丝分裂原激活蛋白激酶(MAPK),被促炎细胞因子和氧化应激优先激活,导致细胞分化和凋亡。FPP 调节 H₂O₂诱导的 ERK、Akt 和 p38 激活,减少 H₂O₂诱导的 p38 磷酸化。FPP 减少 H₂O₂诱导的 DNA 损伤程度,在苯并[a]芘处理的细胞中也获得了类似的效果。在暴露于 HepG2 细胞的 FPP 实验中未观察到遗传毒性作用,FPP 对 PC12 细胞也没有毒性。氧化应激诱导的细胞损伤和炎症与多种癌症、糖尿病、关节炎、心血管功能障碍、神经退行性疾病(如中风、阿尔茨海默病和帕金森病)、运动生理学(包括竞技运动)和衰老有关。这些疾病可能受益于具有抗炎、抗氧化、免疫刺激(在黏膜水平)和诱导抗氧化酶作用的功能性营养/食品补充剂(如这里所示的木瓜发酵制剂)。