The ginsenosides Re, Rg1, Rg2, Rg3 and Rh2 (monomeric compounds identified by HPLC method, purity ≥98%; batch nos. DSTDR001401, DSTDR000901, DSTDR001001, DSTDR001101 and DSTDS003601) were all purchased from Chengdu Desite Biological Technology Co., Ltd. All drugs were dissolved in dimethyl sulfoxide (DMSO), and each experimental and control group contained ≤0.1%v/v DMSO.

SH-SY5Y cells were obtained from the American Type Culture Collection (cat. no. CRL-2266) and cultured in DMEM/F12 complete medium (supplemented with 10% fetal bovine serum and 1% penicillin-streptomycin; all from Hyclone; Cytiva) at 37°C in a 5% CO₂ atmosphere.

Cell viability was analyzed using a CCK-8 assay kit (Boster Biological Technology) according to the manufacturer's instructions. SH-SY5Y cells were seeded in 96-well plates (3×10³ cells/well) and incubated at 37°C for 24 h. The cells were then co-treated with 0.3 µM Rot (Dalian Meilun Biotechnology Co., Ltd.; cat. no. MB5842) and Re (1, 2.5, 5, or 10 µM), Rg1 (2.5 µM), Rg2 (5 µM), Rg3 (10 µM), Rh2 (10 µM), or L-dopamine (Beijing Solarbio Science & Technology Co., Ltd.; cat. no. ID0360; 5 or 10 µM) for 24 h. CCK-8 solution was added at 20 µl/well and the plates were incubated in the dark at 37°C for 30 min. The absorbance at 450 nm was measured with a microplate reader (Tecan Group, Ltd.).

LDH was measured using an LDH cytotoxicity assay kit (Nanjing Jiancheng Bioengineering Institute; cat. no. A020-2-2) according to the manufacturer's guidelines. Cells were seeded at 5×10⁴ cells/well and co-treated with Re (1, 2.5, 5, or 10 µM) and Rot (0.3 µM) at 37°C for 24 h. The absorbance at 490 nm was then measured with a microplate reader (Tecan Group, Ltd.) at room temperature.

Cells undergoing apoptosis were detected by flow cytometry after staining with Annexin V-FITC and PI (Becton Dickinson and Company). Cells were seeded at 5×10⁴ cells/well and co-treated with Rot (0.3 µM) and Re (5 µM) at 37°C for 24 h. The cells were collected, washed twice with phosphate-buffered saline (PBS), resuspended in 1X Binding Buffer, and mixed with Annexin V-FITC and PI staining solution. The cells were incubated at room temperature in the dark for 15 min and then analyzed using an flow cytometer (Amnis Corporation), and quantified using IDEAS software v6.1 (Amnis Corporation).

Cells were seeded at 5×10⁴ cells/well and co-treated with Rot (0.3 µM) and Re (5 µM) at 37°C for 24 h. The cells were then fixed in 4% paraformaldehyde (PFA) solution for 0.5 h at room temperature, washed twice with PBS, and incubated with Hoechst 33342 (Beyotime Institute of Biotechnology) staining solution at 1 ml/well. The plates were incubated at 37°C in the dark for 30 min, washed twice with PBS, and visualized using with an EVOS fluorescence microscope (Thermo Fisher Scientific, Inc.).

Caspase activities were measured using Caspase-3, Caspase-8 and Caspase-9 (cat nos. C1115, C1151; C1157; Beyotime Institute of Biotechnology) Activity assay kits according to the manufacturers' instructions. Cells were washed with PBS, centrifuged at 4°C (530 × g, 5 min) and 100 µl lysate was used per 2×10⁵ cells and incubated on ice for 15 min. Centrifugation at 4,246 × g at 4°C for 10 min. Protein concentration in supernatant was measured using a Bradford assay kit (Tiangen Biotech Co., Ltd.). Then 50 µl cell lysate supernatant and 10 µl AC-DevD-PNA (2 mM) for caspase-3, AC-IETD-PNA (2 mM) for caspase-8 and AC-LEHD -pNA (2 mM) for caspase-9 was mixed in a 40 µl detection buffer at 37°C for 4 h and then analyzed using a microplate reader (Tecan Group, Ltd.).

ATP was measured using a chemiluminescence ATP assay kit (Beyotime Institute of Biotechnology; cat. no. S0026). Following incubation of SH-SY5Y cells (5×10⁴ cells/well) with Rot (0.3 µM) and Re (5 µM) at 37°C for 24 h, the medium was discarded, 200 µl of ATP detection solution was added, and the plates were centrifuged at 4,246 × g for 5 min at 4°C. The supernatant was transferred to a new tube. A total of 100 µl of ATP detection buffer was added to each assay well and incubate at 37°C for 3 min to deplete background, followed by addition of 20 µl of supernatant to the assay wells. Optical density values were recorded using a microplate reader (Tecan Group, Ltd.) and ATP content was converted according to a standard curve.

Cells were seeded at 5×10⁴ cells/well and were incubated with Rot (0.3 µM) with or without Re (5 µM) at 37°C for 24 h, washed twice with PBS, mixed with 1 ml of JC-1 solution (Beijing Solarbio Science & Technology Co., Ltd.; cat. no. J8030) and incubated in the dark for 20 min (maintained at 37°C). The cells were washed twice with JC-1 staining buffer. The cells were then processed and examined with an EVOS fluorescence microscope (Thermo Fisher Scientific, Inc.).

Cells were seeded at 5×10⁴ cells/well and were incubated with Rot (0.3 µM) with or without Re (5 µM) at 37°C for 24 h, washed twice with PBS, mixed with Rhodamine 123 (2 µM) (Beijing Solarbio Science & Technology Co., Ltd.; cat. no. R8030), and incubated at 37°C for 30 min in the dark. The cells were then centrifuged at 530 × g for 5 min at room temperature, resuspended in PBS, and analyzed using a flow cytometer (Amnis Corporation), and quantified using IDEAS software v6.1 (Amnis Corporation).

Intracellular ROS levels were detected by flow cytometry (Amnis Corporation) and quantified using IDEAS software v6.1 (Amnis Corporation) or fluorescence microplate reader. Cells were seeded at 5×10⁴ cells/well and were incubated with Rot (0.3 µM) and Re (5 µM) at 37°C for 24 h, washed twice with PBS, mixed with 100 µl of 2,7-dichlorofluorescein diacetate (DCFH-DA; Beijing Solarbio Science & Technology Co., Ltd.; cat. no. CA1410) diluted in serum-free DMEM/F12 medium (final concentration, 10 µM), and incubated in the dark for 20 min at 37°C. The cells were then centrifuged at 530 × g for 5 min at room temperature, resuspended in PBS, and analyzed using an Amnis^® flow cytometer. Alternatively, cells were seeded at 3×10³ cells/well and incubated with Rot (0.3 µM) and Re (5 µM) at 37°C for 24 h, after being washed by PBS were inoculated into black 96-well plates, and a 10-µl probe was added before detection. The cells were incubated at 37°C for 20 min under dark conditions, and then detected using a fluorescence microplate reader. The excitation wavelength was 488 nm, and the emission wavelength was 530 nm.

Cells were seeded at 5×10⁴ cells/well and incubated with Rot (0.3 µM) in the presence or absence of Re (5 µM) at 37°C for 24 h. Glutathione (GSH), malondialdehyde (MDA), superoxide dismutase (SOD), and glutathione peroxidase (GSH-Px) were assayed using kits (Nanjing Jiancheng Bioengineering Institute; cat. no. A006-2-1, A003-4-1, A001-3-2, A005-1-2) according to the manufacturer's instructions and measured with a microplate reader (Tecan Group, Ltd.).

Experiments involving the following inhibitors included cell viability, ROS detection and western blotting: 15 µM PD98059 (ERK1/2 signal inhibitor, cat. no. HY-12028), 15 µM LY294002 (PI3K/AKT inhibitor, cat. no. HY-10108), 5 µM Akt inhibitor IV (cat. no. HY14971). 5 µM SB203580 [p38 mitogen-activated protein kinase (MAPK) inhibitor, cat. no. HY10256], 10 µM SP600125 [Jun N-terminal kinase (JNK) inhibitor, cat. no. HY12041], and 10 µM Compound C [CC; Adenosine 5′-monophosphate (AMP)-activated protein kinase (AMPK) inhibitor, cat. no. HY13418A], were only used in cell viability assays to determine which signalling pathways mediate Nrf2 activation. The inhibitors were added to cells before Re and/or Rot treatment for 1 h at 37°C and all inhibitors were purchased from Med Chem Express corporation. A customized siRNA reagent system (Guangzhou RiboBio Co., Ltd.) was used for cell viability or ROS assays as previously described (17). The target sequence of the negative control for RNA interference was 5′-CGUACGCGGAAUACUUCGA-3′ and the interference target sequences for Nrf2 were as follows: NRF2 siRNA-1, 5′-GAATGGTCCTAAAACACCA-3′; NRF2 siRNA-2; 5′-GAGAAAGAATTGCCTGTAA-3′; and NRF2 siRNA-3, 5′-GCTACGTGATGAAGATGGA-3′.

Cells were washed twice with PBS and centrifuged at 530 × g at 4°C to obtain cells pellet, cells were lysed with RIPA lysis buffer (Beyotime Institute of Biotechnology) and total protein was measured using a BCA kit (Beijing Solarbio Science & Technology Co., Ltd.; cat. no. P0012S). Subcellular fractions were produced using a Cell Mitochondria Isolation Kit (Beyotime Institute of Biotechnology; cat. no. C3601) for cytosolic and mitochondrial fractions and a Nuclear and Cytoplasmic Protein Extraction Kit (Beyotime Institute of Biotechnology; cat. no. P0027) for nuclear and cytosolic fractions. Proteins (20 µg/lane) were separated by SDS-PAGE and electron transfer onto a nitrocellulose membrane. Non-specific protein binding was blocked by incubation of the membranes with 5% (v/v) non-fat dried milk in PBS for 1 h at 25°C and the membranes were incubated overnight at 4°C with anti-B-cell lymphoma-2 (Bcl-2; 1:1,000; cat. no. BS1511), anti-Bcl-2 associated X protein (Bax; 1:1,000; cat. no. BS6420), anti-cleaved caspase-3 (1:1,000; cat. no. BS7004), anti-Nrf2 (1:1,000; cat. no. BS1258), anti-glutamate cysteine ligase modifier (GCLM; 1:1,000; cat. no. BS2927), anti-Akt (1:1,000; cat. no. BS90043), anti-PI3K (1:1,000; cat. no. BS9852M), anti-p-PI3K (1:1,000; cat. no. AP0153), anti-ERK (1:1,000; cat. no. BS1968), anti-p-ERK (1:1,000; cat. no. BS4759), anti-glyceraldehyde 3-phosphate dehydrogenase (GAPDH; 1:1,000; cat. no. AP0063), anti-cytochrome c oxidase IV (COX IV; 1:600; cat. no. AP0705), anti-histone 3 (H3; 1:1,000; cat. no. BS1161), and anti-β-actin (1:1,000; cat. no. AP0060), all from Bioworld Technology, Inc.. Anti-HO-1 (1:1,000; cat. no. 66743-1), anti-NAD(P)H:quinone oxidoreductase 1 (NQO1; 1:1,000; cat. no. 11451-1-AP), from Proteintech Group, Inc.. Anti-phosphorylated (p)-Akt (1:1,000; cat. no. #4060s; Cell Signaling Technology, Inc.), anti-cytochrome c (cyt-c, 1:600; cat. no. AF2047; Beyotime Institute of Biotechnology). Following washing with PBS containing 0.05% (v/v) Tween-20 (PBST), the membranes were incubated with horseradish peroxidase-conjugated anti-mouse IgG (1:0000; cat. no. #7076; Cell Signaling Technology Inc.) or horseradish peroxidase-conjugated anti-rabbit IgG (1:0000; cat. no. SA00001-2; ProteinTech Group, Inc.), and bands were visualized using Enhanced Chemiluminescence Reagent kit (Beyotime Institute of Biotechnology; cat. no. P0018S). Membranes were imaged using the iBright FL1000 Imaging System (Invitrogen; Thermo Fisher Scientific, Inc.). Image J software 1.53a (National Institutes of Health) was used to quantify the gray value of western blot bands and protein expression level was normalized as the gray value of the target protein/the loading control protein.

Total RNA was extracted using a Total RNA extraction kit (Tiangen Biotech Co., Ltd.) according to the manufacturer's instructions, and perform reverse transcribed according to Prime Script RT reagent kit instructions (Takara Biotechnology Co., Ltd.). Aliquots of cDNA were subjected to qPCR analysis with SYBR Green PCR Master Mix (Takara Biotechnology Co., Ltd.) and a Real-Time PCR system equipped with a CFX 96 Connect™ Optics Module (Bio-Rad Laboratories, Inc.). Reaction program [94°C pre-denaturation for 30 sec; 40 cycles (94°C denaturation for 5 sec, 60°C annealing for 1 min)]. Primer sets specific to GAPDH (reference gene) and NRF2 were as follows: GAPDH forward, 5′-ACCACAGTCCATGCCATCAC-3′ and reverse, 5′-TCCACCACCCTGTTGCTGTA-3′; NRF2 forward, 5′-CAGTCAGCGACGGAAAGAGT-3′ and reverse, 5′-ACGTAGCCGAAGAAACCTCA-3′. Data were analyzed according to the 2^−∆∆cq method as previously described (18).

Drosophila (including W⁻, UAS-CncC, UAS-CncC RNAi and da-Gal4) were obtained from Dr Yufeng Yang (Institute of Life Sciences, Fuzhou University, Fuzhou, China). UAS-CncC RNAi × da-Gal4 was obtained by mating UAS-CncC RNAi and da-Gal4. Flies were grown on sugar-yeast-agar medium with or without Re (final concentration 0.4 mM in DMSO) and Rot (final concentration 515 µM in DMSO), which was replenished daily and the number of deaths of flies was recorded. Flies were incubated in a humidified (50% relative humidity), temperature-controlled (29°C) incubator with a 12-h on/off light cycle. The significance of the survival curve was calculated using the Log-rank (Mantel-Cox) test.

On the day of the assay, flies were anesthetized with CO₂ and transferred into a glass pipette (height 22 cm, diameter 1.0 cm, capacity 25 ml) capped with a cotton plug. Following recovery, the flies were left for 15 min and the glass pipette was then placed vertically and flies were shaken down to the bottom of the tube. Data were recorded by taking photographs at 5 sec intervals for a total of 1 min. The climbing index was evaluated as follows. The fly movement area (18 cm from the bottom of the pipette to the lower end of the plug) was divided into 2-cm zones (1, 2, 3, 4, 5, 6, 7, 8, 9) from the bottom to the top. The climbing index was calculated as the total number of flies in each area multiplied by the number of regions.

To evaluate the HP level in Drosophila a hydrogen peroxide detection kit (cat. no. BC3590; Beijing Solarbio Science & Technology Co., Ltd.) Weigh about 0.1 g flies tissue and add 1 ml working solution for ice bath homogenization; centrifuged 8,000 × g at 4°C for 10 min, all supernatant was taken and placed on ice for testing. Add corresponding reagents according to the kit instructions, and use a microplate reader (Tecan Group, Ltd.) to detect at 415 nm.

ATP analysis and respiration measurement analysis methods were performed as previously described (19). Flies were homogenized in 500 µl PBS by a cell disruptor, centrifuged at 530 × g for 5 min at room temperature, and incubated in DCFH-DA (final concentration 20 µM; cat. no. CA1410; Beijing Solarbio Science & Technology Co., Ltd.) for 30 min at 37°C. ROS was measured with an Infinite^® 200 Pro microplate reader (Tecan Group, Ltd.) using excitation at 488 nm and emission at 530 nm (20).

Flies were anesthetized by CO₂ and next fixed in 4% paraformaldehyde at 25°C for 2.5 h, washed with PBST, and the brains were dissected and placed in blocking agent (PBS buffer; 0.1% Triton X-100; 10% heat-inactivated fetal bovine serum) at 25°C for 90 min. The blocking agent was removed and replaced with anti-tyrosine hydroxylase (TH) antibody (1:500; cat. no. AB152; Millipore corporation) overnight at 4°C in the dark. The brains were washed with pre-cooled PBST buffer, incubated with Rabbit anti-goat IgG antibody, FITC conjugate (1:200; cat. no. AP106F; Millipore corporation) for 2 h at 25°C in the dark, and washed again. Finally, the brains were mounted onto slides and imaged immediately with a laser confocal microscope.

Data are expressed as the mean ± standard deviation (SD). Data were evaluated using GraphPad Prism 6.0 software (GraphPad Software, Inc.). All experiments in the present study were repeated three times. Group means were compared using one-way analysis of variance (ANOVA) test followed by Tukey's post hoc tests. P≤0.05 was considered to indicate a statistically significant difference.

Rot has been shown to reproduce numerous features of PD in animal models (21); therefore, its effects in vitro were examined using the human neuroblastoma cell line SH-SY5Y. The results revealed that Rot alone significantly decreased cell viability (Fig. S1). The antioxidant and neuroprotective effects of ginseng are mediated by ginsenosides, the main active components of ginseng (22). To assess these compounds, the optimal nontoxic concentrations of five representative ginsenosides: Rg1, Rg2, Rg3 and Rh2 (Fig. S2), as well as Re (Figs. 1A and B, and S3A) were first determined using the CCK-8 cell viability assay. The protective effect of each monomer saponin on Rot-treated SH-SY5Y cells was then examined (Figs. S4, 1C and S3B). Among the ginsenosides assessed, Re had the most significant protective effect on Rot-induced SH-SY5Y cytotoxicity (Figs. 1D and S3C; Table SI). Re was protective at 2.5, 5, and 10 µM, with maximal protection observed at 5 µM Re (Figs. 1C and S3B). Moreover, there was no significant difference between the protective effects of Re at 5 µM and l-dopa at 5 or 10 µM (Figs. 1E and S3D). Re also displayed significant protection when Rot-induced cytotoxicity was measured using a LDH release assay (Fig. 1F).

To determine whether Rot-induced cell death was mediated by triggering of apoptosis, the cells were stained with Annexin V-FITC and propidium iodide (PI) and analyzed by flow cytometry. The results showed that exposure to Rot (0.3 µM) alone increased the abundance of cells in early [Annexin V-FITC⁺, PI^– (R4)] and late [Annexin V-FITC⁺, PI⁺ (R5)] apoptosis (total up to 33.97%), and that Re co-treatment significantly reduced the apoptotic rate (Fig. 2A and B). Similarly, microscopic analysis showed that SH-SY5Y cells treated with Rot exhibited the typical morphological characteristics of apoptosis, whereas Re co-treated cells exhibited a lower level of Hoechst 33342 staining and had uniformly stained chromatin, comparable to the untreated control cells (Fig. 2C). Cell apoptosis is regulated in part by a balance between the expression of the anti-apoptotic and pro-apoptotic regulatory proteins Bcl-2 and Bax (23). Therefore, the expression of these proteins in Rot and Re co-treated cells was examined by western blot analysis. Notably, the ratio of Bax to Bcl-2 protein was increased by Rot treatment and decreased by co-incubation of Rot-treated cells with Re (Fig. 2D).

Mitochondrial function was assessed in SH-SY5Y cells following Rot and/or Re treatment using several methods. First, the cells were labeled with JC-1, an MMP probe. In healthy cells, green-fluorescent JC-1 monomers accumulate in mitochondria and form red-fluorescent aggregates. Loss of MMP results in formation of JC-1 monomers; thus, the ratio of green/red fluorescence is a marker of MMP integrity and reflects mitochondrial health (24). Rot-treated cells exhibited an increase in green fluorescence compared with the red JC1 aggregates in control cells, which was reduced by co-treatment with Re (Fig. 3A). As a second method of MMP analysis, the cells were labeled with the fluorescent dye rhodamine 123. In healthy cells, rhodamine 123 selectively enters the mitochondrial matrix and emits bright yellow-green fluorescence; however, cells undergoing apoptosis or necrosis experience disruption of the MMP, which leads to opening of the mitochondrial permeability transition pore, release of rhodamine 123 from the mitochondria, and a reduction in mitochondrial fluorescence (25). Notably, the results obtained when MMP was assessed by rhodamine 123 labeling (Fig. 3B) were similar to those obtained using the JC-1 labeling method. Finally, ATP generation, as a third indicator of mitochondrial health in SH-SY5Y cells, was also detected. As expected, Rot-treated cells contained less ATP than the control cells, and Re significantly reversed these deleterious effects of Rot (Fig. 3C).

To determine whether the observed increase in SH-SY5Y cell apoptosis induced by Rot (Fig. 2) was mediated by the exogenous receptor-activated pathway or the endogenous mitochondrial pathway, the release of the mitochondrial enzyme cyt-c into the cytosol, a key feature of endogenous apoptosis (26), was examined, as well as the activity of caspases, which are the main effector enzymes of apoptosis (27). As expected, Rot treatment increased cyt-c release and stimulated the activities of caspase-3, −8, and −9; however, co-treatment with Re attenuated the effects of Rot on each of these parameters except activation of caspase-8 (Fig. 3D-F). Collectively, these results suggest that Re-mediated protection against Rot-induced cell injury involves attenuation of mitochondrial dysfunction and inhibition of the mitochondrial apoptotic pathway.

To determine whether Re affects Rot-induced oxidative stress in SH-SY5Y cells, several metabolites that undergo characteristic changes in expression upon cell exposure to oxidative stress were assessed. These included ROS, the fatty acid oxidation product, MDA, and the antioxidants GSH-Px, an enzyme that catalyzes reduction of lipid peroxides by GSH, and SOD, which catalyzes the dismutation of superoxide anions and is an important antioxidant enzyme (28). Rot treatment alone resulted in increased levels of ROS and MDA, decreased levels of GSH, and reduced SOD and GSH-Px activities (Fig. 4). Notably, each of these Rot-induced effects was reversed in cells co-treated with Re (Fig. 4), demonstrating that Re is able to counteract Rot-induced oxidative stress.

Nrf2 is a key component of the oxidative stress response and regulates the expression of antioxidant and cytoprotective genes (29). To determine whether Nrf2 is modulated by Rot and/or Re treatment, western blot analysis of SH-SY5Y subcellular fractions was performed. Compared with the untreated control cells, Rot treatment induced no significant change in the distribution of Nrf2 in the cytoplasm and nucleus, whereas Re-co-treated cells showed an increase in nuclear localization of Nrf2 (Fig. 5A). Nrf2 is generally cytosolic but translocates to the nucleus in response to oxidative stress, where it binds to antioxidant response elements and induces transcription of genes such as HO-1, GCLM, NQO1 (30). Consistent with this, Re treatment also significantly increased the expression of HO-1, GCLM, and NQO1 proteins (Fig. 5B).

To determine the importance of Nrf2 in Re-mediated protection against Rot, the cells were transfected with a control siRNA or Nrf2-targeting siRNA (Fig. 5C). The beneficial effects of Re on Rot-induced cytotoxicity (Fig. 5D) and ROS production (Fig. 5E and F) were reduced in siNrf2-transfected cells compared with control cells. Collectively, these results indicated that Nrf2 plays an essential role in Re-mediated neuroprotection against oxidative stress.

To determine which signaling pathways mediate Re-induced Nrf2 activation, SH-SY5Y cells were pretreated with inhibitors of PI3K/AKT (LY294002, 15 µM), JNK (SP600125, 10 µM), ERK (PD98059, 15 µM), AMPK (CC, 10 µM), and p38 MAPK (SB203580, 5 µM) and then the effects on Re activity were analyzed in cell viability assays. Compared with cells incubated under control conditions, LY294002 and PD98059 treatment significantly suppressed the protective effect of Re on Rot-induced cell viability (Fig. 6A) and ROS production (Fig. 6B; P<0.05), whereas the remaining inhibitors had no effect. The ERK and PI3K/AKT inhibitors prevented Re-stimulated nuclear localization of Nrf2 in SH-SY5Y cells (Fig. 6C). In addition, ROS levels, Nrf2 expression in the nucleus, and cell viability were all significantly altered by cell treatment with AKT inhibitor IV (Fig. S5). Confirming these associations, it was determined that Rot downregulated the expression of p-AKT (Fig. 6D and E), p-ERK (Fig. 6D and F) and phosphorylated (activated) PI3K (Fig. 6D and G), and these effects were significantly reversed by treatment with Re.

Exposure of Drosophila to Rot mimics numerous of the features of human PD and is widely used as a model for investigating the pathogenesis of PD (31). Consistent with the aforementioned study, it was determined that exposure of flies to 515 µM Rot for 7 days before analysis caused a loss of dopaminergic neurons, as measured by staining of Drosophila brains for the marker protein TH (Fig. 7A and B). However, flies that had been administered Rot plus Re (0.4 mM) showed partial reversal of neuron loss (Fig. 7C). Since Rot-induced dopaminergic neurotoxicity has been reported to cause locomotor deficits (32), the effects of Re treatment on fly movement were also examined. Exposure of flies to 515 µM Rot reduced their climbing ability to 39.3% compared with control flies, as measured by a quantitative climbing index (Fig. 7D). However, co-treatment of flies with Re (0.4 mM) significantly reversed the effect of Rot and increased the climbing index to 61.3% of that observed for the control flies (Fig. 7D).

Finally, whether reversal of Rot-induced oxidative stress and mitochondrial dysfunction contribute to the protective effects of Re were determined in the Drosophila PD model. Mitochondria are the predominant site of ATP production in cells, and changes in cellular ATP content can indicate impaired mitochondrial function (33). Accordingly, a reduction in ATP levels in Rot-treated flies was observed that was reversed by Re co-treatment (Fig. 8A). Consistent with a previous study, mitochondrial respiratory chain complex I (NADH oxidase) has been demonstrated to be related to the occurrence of PD (34). However, mitochondrial respiratory chain complex II (succinate dehydrogenase), which is the main element of electrons entering the mitochondrial electron transport chain (35), also exhibited a positive effect of Re in flies (Fig. 8B and C). Re also reduced the Rot-induced increase in ROS (Fig. 8D) and HP (Fig. 8E). However, Re had no significant effect on the survival curve of Rot-treated flies (UAS-CncC RNAi × da-Gal4) (Fig. 8F). Overall, these results indicated that the neuroprotective effect of Re in the Drosophila PD model was consistent with that detected using the SH-SY5Y cell model in vitro.