Department of Pharmaceutical Biology, Institute of Pharmacy and Biochemistry, Johannes Gutenberg University, Mainz, Germany.
Division of Cancer Genome Research, German Cancer Research Center (DKFZ), German Cancer Consortium (DKTK), National Center for Tumor Diseases (NCT), Im Neuenheimer Feld 460, 69120 Heidelberg, Germany.
Phytomedicine. 2019 May;58:152743. doi: 10.1016/j.phymed.2018.11.004. Epub 2018 Nov 6.
Cancer chemotherapy-induced cognitive impairments are apparently associated with harmful effects on physiological functions of brain cells. Adaptogens, are known to exhibit neuroprotective effects and to increase cognitive functions in clinical studies. In our previous study (Seo et al., 2018), we demonstrated that selected adaptogenic extracts significantly attenuate cytostatic-induced regulation of more than 100 genes involved in the activation of neuronal death and inhibiting neurogenesis. Neuroprotective and cytoprotective activities of adaptogens rise the question about their possible impact on cytostatic effects of a chemotherapeutic combination of 5-fluorouracil, epirubicin and cyclophosphamide (FEC).
The aim of this study was to assess the effects of selected adaptogenic herbal extracts, namely of andrographolide (AND), Herba Andrographidis (AP), Radix Eleutherococci (ES) genuine extracts, their fixed combination (AE), and the combination of three adaptogenic herbs, Rhodiola Radix, Shisandra Fructus and Eleutherococci Radix (RSE) on the cytotoxicity of a fixed combination of 5-fluorouracil, epirubicin and cyclophosphamide (FEC) on neuroglia cells.
Cytotoxicity of FEC, adaptogenic extracts and their combination with FEC was tested on isolated T98G cells in a wide range of concentrations of all tested compounds.
FEC reproducibly inhibited the proliferation of T98G cells by 50% at concentrations of 5 × 10 µg/ml epirubicin, 500 × 10 µg/ml 5-fluorouracil and 20 × 10 µg/ml 4-hydroperoxycyclophosphamide after 24 h incubation of cells. These concentrations were subsequently used for experiments with adaptogenic extracts. The cytotoxic activity of FEC was not significantly changed in the presence of AND, ES and AE. Furthermore, it was potentiated by AP extract and RSE in concentrations of 0.06-6 µg/ml and 17.6-26.4 µg/ml.
The neuroprotective effect of adaptogens did not attenuate the cytotoxic activity of FEC. Application of cytostatic drugs in combination with adaptogenic plant extracts likely have no impact in cytotoxic effect of FEC. Furthermore, AP and RSE potentiated the cytotoxic effects of FEC.
癌症化疗引起的认知障碍显然与脑细胞生理功能的有害影响有关。适应原已知具有神经保护作用,并在临床研究中提高认知功能。在我们之前的研究中(Seo 等人,2018 年),我们证明了选定的适应原提取物可显著减轻细胞抑制剂引起的 100 多个与神经元死亡激活和抑制神经发生相关基因的调节。适应原的神经保护和细胞保护活性引发了一个问题,即它们是否可能对氟尿嘧啶、表阿霉素和环磷酰胺(FEC)联合化疗的细胞抑制作用产生影响。
本研究旨在评估选定的适应原草药提取物,即穿心莲内酯(AND)、穿心莲(AP)、刺五加(ES)正品提取物、它们的固定组合(AE)以及三种适应原草药,红景天、五味子和刺五加(RSE)对氟尿嘧啶、表阿霉素和环磷酰胺固定组合(FEC)对神经胶质细胞的细胞毒性的影响。
在广泛的浓度范围内,用 FEC、适应原提取物及其与 FEC 的组合测试对 T98G 细胞的细胞毒性。
FEC 在细胞孵育 24 小时后,以 5×10μg/ml 表阿霉素、500×10μg/ml 氟尿嘧啶和 20×10μg/ml 4-羟过氧环磷酰胺的浓度重现性地抑制 T98G 细胞的增殖 50%。随后将这些浓度用于适应原提取物的实验。AND、ES 和 AE 的存在并未显著改变 FEC 的细胞毒性活性。此外,AP 提取物和 RSE 在 0.06-6μg/ml 和 17.6-26.4μg/ml 的浓度下增强了 FEC 的细胞毒性。
适应原的神经保护作用并没有减轻 FEC 的细胞毒性活性。在细胞毒性药物联合应用适应原植物提取物的情况下,FEC 的细胞毒性作用可能没有影响。此外,AP 和 RSE 增强了 FEC 的细胞毒性作用。