Oxidative Medicine and Cellular Longevity

Oxidative Medicine and Cellular Longevity / 2019 / Article
Special Issue

Natural Bioactive Products with Antioxidant Properties Useful in Neurodegenerative Diseases

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Research Article | Open Access

Volume 2019 |Article ID 5046280 | 13 pages | https://doi.org/10.1155/2019/5046280

Pasteurized Orange Juice Rich in Carotenoids Protects Caenorhabditis elegans against Oxidative Stress and β-Amyloid Toxicity through Direct and Indirect Mechanisms

Academic Editor: Luciana Scotti
Received04 Oct 2018
Revised28 Dec 2018
Accepted17 Jan 2019
Published18 Apr 2019


‘Cara Cara’ is a red orange (Citrus sinensis (L.) Osbeck) variety originally from Venezuela characterized by a significantly higher and diversified carotenoid content including higher-concentration lycopene, all-E-β-carotene, phytoene, and other carotenoids when compared with the carotenoid profile of its isogenic blond counterpart ‘Bahia’, also known as Washington navel. The exceptionally high carotenoid content of ‘Cara Cara’ is of special interest due to its neuroprotective potential. Here, we used the nematode Caenorhabditis elegans to analyze the antioxidant effect and the protection against β-amyloid-induced toxicity of pasteurized orange juice (POJ) obtained from ‘Cara Cara’ and compare to that from ‘Bahia’. POJ treatment reduced the endogenous ROS levels and increased the worm’s survival rate under normal and oxidative stress conditions. POJ treatment also upregulated the expression of antioxidant (gcs-1, gst-4, and sod-3) and chaperonin (hsp-16.2) genes. Remarkably, ROS reduction, gene expression activation, oxidative stress resistance, and longevity extension were significantly increased in the animals treated with ‘Cara Cara’ orange juice compared to animals treated with ‘Bahia’ orange juice. Furthermore, the body paralysis induced by β-amyloid peptide was delayed by both POJs but the mean paralysis time for the worms treated with ‘Cara Cara’ orange juice was significantly higher compared to ‘Bahia’ orange juice. Our mechanistic studies indicated that POJ-reduced ROS levels are primarily a result of the direct scavenging action of natural compounds available in the orange juice. Moreover, POJ-induced gst-4::GFP expression and –increased stress resistance was dependent of the SKN-1/Nrf2 transcription factor. Finally, the transcription factors SKN-1, DAF-16, and HSF-1 were required for the POJ-mediated protective effect against Aβ toxicity. Collectively, these results suggest that orange juice from ‘Cara Cara’ induced a stronger response against oxidative stress and β-amyloid toxicity compared to orange juice from ‘Bahia’ possibly due to its higher carotenoid content.

1. Introduction

Citrus sinensis L. Osbeck orange juice is considered an excellent dietary source of several bioactive compounds with beneficial properties for human health due to its high content of flavonoids, carotenoids, sugars, minerals, and fiber. Numerous epidemiological and intervention studies have provided substantial evidence to support an inverse correlation between orange juice intake and the occurrence of cardiovascular disease, cancer, and aging-related disorders [1, 2].

Among sweet oranges, there is increasing interest in C. sinensis Osbeck cv. ‘Cara Cara’, a bud mutation originated from ‘Bahia’ navel orange, also known as ‘Washington’ navel orange. ‘Cara Cara’ orange pulp is characterized by a bright red coloration due to a significantly higher and diversified carotenoid content compared to ‘Bahia’ juice, with a mixture of (Z)-isomers of lycopene, all-E-β-carotene, phytoene, and phytofluene isomers [3]. Total flavanone content as well as hesperidin levels are usually comparable in ‘Cara Cara’ and ‘Bahia’ pasteurized juice [1]. On the other hand, ‘Bahia’ presents a higher ascorbic acid content compared to ‘Cara Cara’ [1]. The exceptionally high carotenoid content of ‘Cara Cara’ may be of special interest due to recent nutritional studies that have demonstrated its association with the prevention and treatment of various diseases, including neurodegenerative diseases (ND) [4].

Carotenoids are the main pigments responsible for the color of the peel and pulp of citrus fruits. They have been indicated as important dietary nutrients having antioxidant, anti-inflammatory, antimutagenic, anticarcinogenic, and autophagy-modulatory activities [4, 5]. In addition to their direct antioxidant activities, carotenoids can protect cells from oxidative stress by activating the antioxidant network enzymes, including superoxide dismutase (SOD) and catalase (CAT) [4].

Given that oxidative damage and increased neuroinflammation are critically related with the pathogenesis of and neuronal loss in neurodegenerative diseases, the neuroprotective effect of carotenoids has been of specific interest in the search for effective treatments for these diseases. The beneficial effects of dietary carotenoids such as lycopene, astaxanthin, crocin, crocetin, and fucoxanthin on neurodegenerative diseases have been recently studied in animal and cell culture models for Alzheimer’s disease (AD) [4]. In a recent paper, Hwang et al. [6] showed that lycopene significantly inhibited intracellular β-amyloid accumulation and reduced mitochondrial ROS levels and apoptotic cell death in human neuronal SH-SY5Y cells. In the rodent models, administration of certain types of carotenoids, including lycopene, successfully attenuated not only cellular-level phenotypes such as mitochondrial oxidative damage and increased neuroinflammation but also organism-level phenotypes such as memory impairment and locomotive defects [7]. Despite these studies, there is a substantial lack of AD animal models to show the therapeutic potential of carotenoids against neurodegenerative disease [811].

The nematode worm Caenorhabditis elegans is an established model organism to study aging and age-related disorders [1214] and an attractive platform for rapidly screening drug safety and efficacy [15]. It has been demonstrated that lutein supplementation in C. elegans is able to suppress the ROS generation induced by the hepatotoxin microcystin-LR (MIC-LR) and restore the levels of the antioxidant enzyme CAT, as well as their survival rate [16]. Pons et al. [17] showed that transgenic β-carotene-enriched orange increases C. elegans survival under oxidative stress induced by hydrogen peroxide. Furthermore, a delay of paralysis in a β-amyloid peptide transgenic C. elegans strain was induced by lycopene [18], while fucoxanthin, but not β-carotene, provided positive effects on the C. elegans lifespan [19].

A number of genes and pathways have been identified to modulate lifespan, stress resistance, and proteostasis in C. elegans [20, 21]. These highly conserved pathways include the transcription factors heat shock factor 1 homologue HSF-1, the FOXO homologue DAF-16, and the Nrf-1/2 homologue SKN-1. HSF-1 controls the inducible transcription of a family of genes encoding heat shock proteins (HSPs), many of which are molecular chaperones. The DAF-16/FOXO target genes include specific hsps and other stress response/longevity genes. SKN-1 mediates the expression of genes involved in a wide range of detoxification processes, as well as in immunity, proteostasis, and metabolism. Collectively, these transcription factors orchestrate the expression of genes that contribute to longevity.

Up to date, there are no data demonstrating the antioxidant and neuroprotective capacity of pasteurized orange juice (POJ). Here in this work, we assessed and compared the antioxidant capacity and the protective effect against the β-amyloid peptide of pasteurized orange juice from ‘Cara Cara’ with respect to that from the ‘Bahia’ counterpart using the nematode C. elegans.

2. Materials and Methods

2.1. Chemicals, Reagents, and Strains

tert-Butyl hydroperoxide (TBHP), fluorodeoxyuridine (FUdR), and 2,7-dichlorodihydrofluorescein diacetate (H2DCFDA) were purchased from Sigma-Aldrich (St. Louis, MO, USA).

The following Caenorhabditis elegans strains were used: N2 (wild-type strain), EU40 (skn-1(zu129) IV/nT1 [unc-?(n754) let-?]) (IV;V), CF1038 (daf-16(mu86) I), PS3551 (hsf-1(sy441) I), CL2006 (dvIs2[pCL12(unc-54/human Abeta peptide 1-42 minigene) + pRF4]), CF1553 (muIs84 [pAD76(sod-3::GFP)]), CL2166 (dvls19[pAF15(gst-4::GFP::NLS)]), LD1171 (ldIs3[gcs-1p::GFP + rol-6(su1006)]), and TJ375 (gpls[hsp-16.2::GFP]).

2.2. Pasteurized Orange Juice (POJ) Preparation

Pasteurized orange juices obtained from C. sinensis L. Osbeck cv. ‘Cara Cara’ and cv. ‘Bahia’ were provided by Citrosuco (Matão, São Paulo, Brazil). Oranges from both cultivars were collected on June 7th 2016 in Araraquara (São Paulo, Brazil) located in southeastern São Paulo at 23°2319 S and 48°4322 W with an elevation of 600 m above sea level. Orange juices were obtained by cutting and squeezing, using an industrial extractor (model 391, JBT). The pasteurization process was achieved in an industrial pasteurizer (UHT/HTST Lab-25-DH, MicroThermics) at 92− 94°C for 17 s (750 mL/min). After processing, the juices were filled into 1 L plastic flasks and cooled to 1°C. All juices were immediately stored at −20°C.

2.3. POJ Characterization

Determination of °Brix/acidity ratio: juice acidity was determined by titration with phenolphthalein and 0.1 N NaOH and was expressed as mg citric acid per 100 g. The soluble solid content (°Brix) was estimated by refractometry, using an Atago® refractometer. The maturity index is expressed as the ratio of °Brix/acidity.

Determination of limonin and vitamin C: limonin extraction was performed by centrifugation of orange juice (50 mL) for 15 min at 5000 rpm. Subsequently, a volume of 2 mL of juice sample was passed through a C18 Sep-Pak cartridge (Waters), and water was added to the concentrated sample and eluted with vacuum using acetonitrile. Finally, the elution was filtered and prepared for HPLC analysis [22]. Vitamin C content was evaluated by the titration method described by Stevens [23].

Carotenoids were extracted as is described in Alquezar et al. [24]. UPLC analysis of individual carotenoids: the carotenoid composition of each sample was analyzed by UPLC with a Nexera X2 Shimadzu liquid chromatography system equipped with a LC-30AD pump and a SPD-M20A photodiode array detector, as well as LabSolutions software (version 5.57 SP1). An Acquity BEH C18 carotenoid column (, 1.8 μm) coupled to a C18 guard column () (Waters, USA) was used. Samples were prepared for UPLC by dissolving the dried carotenoid extracts in CHCl3 : MeOH : acetone (3 : 2 : 1, ). For carotenoid separation, a binary gradient elution was adapted from the ternary described by Alquezar et al. [24] by using the Gradient Method Calculator (Thermo Scientific). The initial solvent composition consisted of 100% MeOH : water (90 : 5, ) and 5% methyl tert-butyl ether (MTBE). The solvent composition changed in a linear fashion to 95% MeOH : water and 5% MTBE at 0.91 min. During the next minute, the solvent composition was changed to 86% MeOH : water and 14% MTBE. After reaching this concentration, the solvent was gradually changed to 75% MeOH : water and 25% MTBE at 2.28 min, 50% MeOH : water and 50% MTBE 50% at 3.8 min, and 25% MeOH : water and 75% MTBE at 5.32 min. The initial conditions were reached at 6 min, and the column was equilibrated for 2 min before the next injection. The flow rate was 0.5 mL min−1, column temperature was set to 27°C, and the injection volume was 3 μL. The photodiode array detector was set to scan from 250 to 800 nm, and for each elution a MaxPlot chromatogram was obtained, which plots each carotenoid peak at its corresponding maximum absorbance wavelength. Carotenoids were identified by their retention time, absorption, and fine spectra [2529]. The carotenoid peaks were integrated at their individual maxima wavelength, and their contents were calculated using calibration curves of β-carotene (Sigma) for α- and β-carotene; β-cryptoxanthin (Extrasynthese) for β-cryptoxanthin; zeaxanthin (Extrasynthese) for zeaxanthin; lutein (Sigma) for violaxanthin isomers, mutatoxanthin and antheraxanthin; lycopene (Sigma) for lycopene; and phytoene (Sigma) for phytoene and phytofluene.

2.4. C. elegans Culture Conditions

For all the experimental procedures, C. elegans were cultured at 20°C on Nematode Growth Medium (NGM) plates [30] seeded with Escherichia coli OP50. For treatment, worms were cultivated on NGM plates containing 1, 2, 5, or 10% POJ of either ‘Bahia’ or ‘Cara Cara’. The control group was prepared in the same manner but without POJ. Tests were also performed with heat-killed E. coli OP50 (OP50-HK). Heat-killed bacteria were prepared by incubating liquid cultures of E. coli OP50 to 75°C for 1 hour. Synchronized populations were obtained by either bleach treatment or egg-laying.

RNA interference (RNAi) was carried out using the feeding method described previously [31]. Briefly, RNAi clones were grown with 12.5 μg/mL tetracycline and 100 μg/mL ampicillin. On the following day, cultures were diluted in LB supplemented with 60 μg/mL ampicillin and grown to an OD600 of 1. This culture was used to seed plates containing ampicillin and 1 mM IPTG and left to dry for 2 days at room temperature. Synchronized L1 larvae were then placed at 20°C on E. coli HT115 that expressed target gene RNAi or control RNAi (empty vector pL4440) for 48 h, until they reached the L4 stage. skn-1 RNAi efficiency was verified by the absence of F1 larvae. For daf-16, RNAi efficiency was confirmed by the suppression of GFP emission on DAF-16::GFP transgenic line (TJ356). For hsf-1, RNAi efficiency was confirmed by the worms reduced survival at 35°C.

2.5. Quantification of Intracellular ROS

N2 wild-type animals synchronized at first-stage larvae (L1) were cultivated on NGM with different concentrations of POJ for 48 h. The experiments were performed under standard and stress conditions as described previously by de Freitas Bonomo et al. [32] with modification. For the stress condition, the animals were exposed to 10 mM tert-butyl hydroperoxide (TBHP) in M9 medium for 1 hour. Subsequently, 20 to 40 worms per group were collected in PBS+ 1% Tween-20, washed twice, and transferred to a 96-well microtiter plate, to which 50 μM H2DCF-DA was added. Measurements were performed in triplicate in a multilabel microplate reader GloMax®-Multi Detection System (Promega, Wisconsin, USA), with excitation at 490 nm and emission at 510-570 nm, and the mean values were calculated. Readings were performed every 30 min for 4 h.

2.6. Reporter Gene Analysis

Transgenic lines expressing gcs-1::GFP, gst-4::GFP, sod-3::GFP, and hsp-16.2::GFP were treated with 2% POJ for 48 h at 20°C since L1 until the L4 stage. The experiments were performed under standard and stress conditions. For gcs-1::GFP, gst-4::GFP, and sod-3::GFP animals, the stress condition was induced by incubating in 10 mM TBHP in M9 medium for 1 hour. For hsp-16.2::GFP, the stress condition was induced for 1 h at 35°C. Images of 25 worms from each group were acquired using the optic microscope Olympus BX51 (Tokyo, Japan) and fluorescent signals were measured with NIH ImageJ software.

2.7. Lifespan and Stress Resistance Assays

The lifespan assay was performed with synchronized N2 wild-type animals treated with 2% POJ starting at the L4 stage. We analyzed approximately 90 animals per group divided into 3 NGM plates containing FUdR to prevent progeny growth. The survival analysis consisted of scoring dead/alive animals every day beginning at the first day of adulthood () at 25°C. The animals were determined to be dead if no movement was shown with or without stimulation, and those animals with hatched eggs internally, extruded parts, or those who went missing, were excluded from analysis.

To evaluate the resistance to oxidative stress, L4 larval stage of wild-type animals and skn-1(zu129), daf-16(mu86), and hsf-1(sy441) mutants were treated with 2% POJ for 48 h on NGM plates containing FUdR seeded with either E. coli OP50 (OP50) or heat-killed E. coli OP50 (OP50-HK). After that, they were exposed to 10 mM TBHP. Approximately 50 animals were analyzed for each experimental group. Survival fractions were scored every three hours until all animals were considered dead, without pumping or pharyngeal movement. The oxidative stress resistance test was performed three times.

2.8. Bioassays for β-Amyloid-Induced Paralysis

CL2006 strains, which constitutively express Aβ1–42 peptide in the body wall muscle tissue, were treated since L1 until L4 stage on NGM plates with E. coli OP50 for 48 hours at 20°C. Animals were then transferred to new plates containing 2% POJ seeded with either E. coli OP50 or OP50-HK for another 48 hours at 20°C. The paralysis phenotype was accelerated by transferring the worms to 35°C. Paralysis was scored at 1 h intervals for up to 12 h. The worms were scored as “paralyzed” based on either the failure of the worms to move their body with the touch of a platinum loop or the formation of a halo on the bacterial lawn indicating a paralyzed condition. Each experiment was performed using at least 30 worms. The data represents mean of three different experiments.

2.9. Statistical Analyses

All experiments were performed three times. Statistical analyses were performed using GraphPad Prism (v. 5.0) software (CA, USA). Data were analyzed by Kolmogorov-Smirnov test for normality. For normally distributed data, Student’s test was used to compare pairs of groups, whereas a one-way ANOVA followed by Tukey’s posttest was used to compare three or more groups. Nonparametric data were analyzed using the Mann–Whitney test when comparing two groups and the Kruskal-Wallis test followed by Dunn’s posttest for comparing three or more groups. Survival curves were analyzed by the log-rank (Mantel-Cox) test. For all tests, statistical significance was determined as .

3. Results and Discussion

3.1. Quality and Phytochemical Characterization of Pasteurized Juice from ‘Cara Cara’ and ‘Bahia’ Oranges

After pasteurization, we compared some quality and phytochemical compounds of the ‘Bahia’ sweet orange juice and its spontaneous red-fleshed mutant ‘Cara Cara’, which contains large proportions of linear carotenes. Pasteurized ‘Bahia’ juice (PBJ) was more acidic than pasteurized ‘Cara Cara’ juice (PCJ) (Table 1). A higher content of ascorbic acid and limonin was recorded in PBJ compared to PCJ (Table 1). As expected, the total carotenoid content was significantly higher in ‘Cara Cara’ juice compared to ‘Bahia’, especially Z-violaxanthin, zeaxanthin, phytoene, phytofluene, lycopene, and β-carotene (Table 2). These results are comparable essentially to those of the previous studies by Brasili et al. [1] and Lee [3], which showed that lycopene and β-carotene accumulated at high levels in PCJ but their concentrations were very low or undetectable in PBJ.

ParametersBahiaCara Cara

Acidity (g/100 g)
Ratio °Brix/acidity
Vitamin C (mg/L)
Limonin (mg/L)

Carotenoid (ng/mL)BahiaCara Cara


n.d.: not detected. Tr.: traces. aIdentified tentatively, dtotal carotenoids calculated as the sum of all the carotenoids identified individually.
3.2. POJ Treatment Reduces Intracellular ROS Accumulation Primarily as a Result of Direct Scavenging

In order to determine the antioxidant capacity of POJ from ‘Bahia’ and ‘Cara Cara’ orange, we investigated the influence of the POJ treatment on the intracellular accumulation of ROS in C. elegans. Under standard condition, wild-type worms treated with 1, 2, 5, and 10% of either ‘Bahia’ or ‘Cara Cara’ juice displayed reduced ROS levels compared to the control group of untreated worms () (Figure 1(a)). Interestingly, ROS levels were significantly lower in the animals treated with 2% ‘Cara Cara’ juice compared to those from worms treated with 2% ‘Bahia’ juice () (Figure 1(a)). Similar results were also observed when the worms were treated with POJ and then subjected to stress conditions (Figure 1(b)). All concentrations tested of POJ were able to reduce ROS production under stress conditions to a level below to those observed in the animals subjected to standard condition () (Figure 1(b)). Under stress conditions, ‘Cara Cara’ juice reduced ROS production more efficiently than ‘Bahia’ juice did in all concentrations tested (). Since 2% ‘Cara Cara’ juice was the only concentration that showed better results than ‘Bahia’ juice under standard conditions, we performed all following assays using 2% POJ treatment.

Phytochemicals have the potential to modulate intracellular oxidative stress directly by scavenging free radicals. Besides that, they are also able to modulate oxidative stress indirectly by upregulating antioxidant and phase II detoxification enzymes which are the major enzymatic line of defense against electrophilic toxicants and oxidative stress. The induction of these adaptive systems by phytochemicals may be related to the fact that they function as xenobiotics in animals [33, 34]. The metabolism of xenobiotics/phytochemicals can produce reactive species, reactive intermediates, and metabolites that can act as prooxidants [35]. Therefore, phytonutrients would play a role as a mild stress trigger leading to the activation of defense mechanisms for their own detoxification, which in turn could induce organisms’ resistance to a more severe oxidative stress condition. In C. elegans, these defense mechanisms are at least partly a result of the activation of three transcription factors, DAF-16, SKN-1, and HSF-1 [36].

In order to elucidate whether ROS reduction was related to POJ direct or an indirect mechanism of action, we performed ROS quantification in animals submitted to RNAi for the SKN-1, DAF-16, and HSF-1 transcription factors. Under standard conditions, knockdown of skn-1, daf-16, and hsf-1 significantly reduced the ROS production in the worms treated with 2% of either ‘Bahia’ or ‘Cara Cara’ juices (Figure 2) suggesting that ROS reduction induced by POJ may be independent of these transcription factors. Interestingly, quantification of ROS levels showed that the lowest reduction was on skn-1(RNAi) animals (Figure 2). The ROS level diminished only by 6.75 and 8.18% on skn-1(RNAi) worms treated with 2% ‘Bahia’ and 2% ‘Cara Cara’ juices, respectively. Meanwhile, ROS reduction was 14.48% and 23.35% on daf-16(RNAi) animals and 33.88% and 66% on hsf-1(RNAi) animals treated with 2% ‘Bahia’ or ‘Cara Cara’ juices, respectively. This result suggests that ROS reduction promoted by POJ treatment was primarily a result of the direct scavenging action of the carotenoids and other phytonutrients present in the orange juice and secondly an outcome of the transcription factor SKN-1 indirect action.

3.3. POJ Treatment Induces the Expression of Antioxidant, Detoxification, and Chaperonin Genes

To better characterize the molecular responses associated with the direct and indirect antioxidant effects of POJ in C. elegans, we analyzed the gene expression of four reporter genes related to stress resistance, detoxification, and longevity. We selected γ-glutamyl cysteine synthetase (gcs-1) and glutathione-s-transferase-4 (gst-4), two SKN-1 target genes [37, 38], superoxide dismutase 3 (sod-3), a well-known DAF-16 target gene [39], and the chaperone hsp-16.2::GFP whose expression is regulated by DAF-16 and HSF-1 [40]. The fluorescence signals of gcs-1::GFP, gst-4::GFP, sod-3::GFP, and hsp-16.2::GFP animals were significantly increased after 2% POJ treatment with either ‘Bahia’ or ‘Cara Cara’ juices compared to untreated worms, both at standard and stress conditions (Figures 3(a)3(d)). Interestingly, the expression signal of gcs-1::GFP (Figure 3(a)), gst-4::GFP (Figure 3(b)), and hsf-16.2::GFP (Figure 3(d)) from the animals treated with 2% ‘Cara Cara’ juice were significantly higher than that of the animals treated with 2% ‘Bahia’ juice under standard conditions. Under stress conditions, the treatment with 2% ‘Cara Cara’ juice significantly increased the expression of gcs-1::GFP and sod-3::GFP.

The POJ induction, rather than an inhibition, of the antioxidant and detoxification genes indicates that the phytonutrients present in the POJ were not only directly scavenging ROS but also acting as prooxidants and inducing a mild cellular stress response [41, 42]. This phenomenon is also referred as hormesis since the phytochemicals are toxic and protect plants against insects and other harmful organisms and stresses. However, at the subtoxic doses, the phytochemicals involve kinases and transcription factors in order to induce the expression of genes that encode antioxidant enzymes, protein chaperones, phase-2 enzymes, neurotrophic factors, and other cytoprotective proteins [41, 42].

Since gst-4::GFP showed the strongest expression after POJ treatments, we assessed whether it was dependent on SKN-1, DAF-16, and HSF-1. RNAi of all three transcription factors reduced significantly gst-4::GFP expression induced by the POJ treatments suggesting that they all contribute to its activation (Figure 4). Moreover, knocking down of skn-1 caused the greatest reduction on gst-4::GFP expression induced by the POJ treatments. The fluorescent levels of gst-4::GFP in the worms treated with ‘Bahia’ juice were 3.26 times lower on skn-1(RNAi) animals compared to control(RNAi) animals while the reduction was 2.54 and 1.34 times lower on daf-16(RNAi) and hsf-1(RNAi) animals, respectively. This result suggests that SKN-1 seemed to play a more important role on gst-4 expression compared to DAF-16 or HSF-1.

3.4. POJ Treatment Increases Longevity and Oxidative Stress Resistance

To explore whether POJ antioxidant properties have a protective effect in vivo, we tested whether POJ could affect the lifespan of C. elegans under standard laboratory conditions. We determined the lifespan of N2 worms with and without 2% POJ treatment. The maximum and mean lifespan of N2 worms fed with either 2% pasteurized ‘Bahia’ or ‘Cara Cara’ juice was significantly increased compared to untreated worms (Figure 5(a), Table 3). Remarkably, animals treated with 2% ‘Cara Cara’ juice showed an increased lifespan compared to animals treated with 2% ‘Bahia’ juice () (Table 3).

ConditionMaximum survival ()Mean survival ()% mean survival time variation vs. untreated value (log rank) POJa vs. untreatedb value (log rank) PBJc vs. PCJb,de

Untreated243 (3)
2% Bahia22.0<0.0001255 (3)
2% Cara Cara29.5<0.00010.0003234 (3)

aPOJ, pasteurized orange juice, bcomparisons were performed using log-rank (Mantel-Cox) test. cPBJ, pasteurized ‘Bahia’ orange juice, dPCJ, pasteurized ‘Cara Cara’ orange juice, etotal number of animals analyzed. The number in parentheses indicates the number of independent trials.

Several studies have shown that lifespan extension is closely associated with enhanced resistance to various forms of environmental stressors [43]. Thus, we assessed the effects of the POJ treatments on C. elegans oxidative stress resistance. Oxidative stress assays were performed in wild-type animals treated with 2% POJ for 48 h and then submitted to stress conditions induced by tert-butyl hydroperoxide (TBHP). We observed that animals treated with either 2% ‘Bahia’ or ‘Cara Cara’ juice showed an increased maximum and mean lifespan, when compared to untreated controls (Figure 5(b), Table 4). Similar to the longevity assay, animals treated with 2% ‘Cara Cara’ juice showed increased oxidative stress resistance compared to animals treated with 2% ‘Bahia’ juice ().

Strains and conditionsMaximum survival ()% maximum survival time variation vs. untreatedMean survival ()% mean survival time variation vs. untreated value (log rank) POJa vs. untreatedb value (log rank) PBJc vs. PCJb,de

WT on E. coli OP50
 Untreated145 (3)
 2% Bahia57.068.0<0.0001144 (3)
 2% Cara Cara71.073.5<0.00010.0134149 (3)
WT on E. coli OP50-HK
 Untreated126 (3)
 2% Bahia14.011.0<0.0001134 (3)
 2% Cara Cara28.032.0<0.0001<0.0001131 (3)
skn-1(zu67) on E. coli OP50
 Control150 (3)
 2% Bahia0.0-2.00.2405150 (3)
 2% Cara Cara0.01.00.74410.1396150 (3)
daf-16(mu86) on E. coli OP50
 Control146 (3)
 2% Bahia21.024.0<0.0001147 (3)
 2% Cara Cara42.042.0<0.00010.0097148 (3)
hsf-1(sy441) on E. coli OP50
 Control141 (3)
 2% Bahia15.020.0<0.0001150 (3)
 2% Cara Cara30.035.0<0.0001<0.0001150 (3)

HK: heat killed. POJ, pasteurized orange juice, bcomparisons were performed using log-rank (Mantel-Cox) test. cPBJ, pasteurized ‘Bahia’ orange juice, dPCJ, pasteurized ‘Cara Cara’ orange juice, eTotal number of animals analyzed. The number in parentheses indicates the number of independent trials.

We also repeated the oxidative stress resistance assay in skn-1, daf-16, and hsf-1 knockout animals. POJ treatment with either 2% ‘Bahia’ or ‘Cara Cara’ juices significantly increased the maximum and mean survival time of daf-16 and hsf-1 mutants under stress conditions (Table 4). However, treatment with either 2% POJ ‘Bahia’ or ‘Cara Cara’ failed to increase skn-1 mutant survival under stress conditions (Table 4). These results suggest that the oxidative stress resistance induced by POJ could be mediated by the transcription factor SKN-1. In this work, POJ antioxidant capacity was positively related to an increase in survival under standard and oxidative stress conditions which would be in agreement with the free radical theory of aging.

Together, these results indicate that pasteurized juice treatment improves C. elegans antioxidant capacity, which is associated with the upregulation of antioxidant and chaperonin genes and increased lifespan and stress resistance. It is noteworthy that the treatment with ‘Cara Cara’ orange juice provided better results on all parameters analyzed here compared to ‘Bahia’ orange juice with the only exception for the expression of sod-3::GFP (Figure 3(c)) under standard conditions and for gst-4::GFP (Figure 3(b)) and hsp-16.2 (Figure 3(d)) under stress conditions. The beneficial effects of ‘Cara Cara’ orange juice could be related to its higher carotenoid content, especially Z-violaxanthin, phytoene, phytofluene, lycopene, and β-carotene, even though ‘Bahia’ juice has higher levels of vitamin C and limonin (Table 2). However, the additional effects of ‘Cara Cara’ orange juice compared to ‘Bahia’ orange juice are either moderate or small to be explained solely based on the total carotenoid difference between these two varieties.

3.5. POJ Treatment Delays Paralysis Induced by β-Amyloid (Aβ) Expression

The oxidative stress state has an important role in the development of neurodegenerative diseases such as Alzheimer’s disease (AD). Accumulation of ROS and deposition of toxic amyloid species have been proposed to exacerbate the symptoms observed in AD patients [44, 45]. The observation that POJ has antioxidant properties in vivo led us to ask whether POJ could protect against β-amyloid-induced toxicity in a C. elegans model for Alzheimer’s disease. The expression of human Aβ1–42 in the muscle of transgenic CL2006 strain promotes a paralysis that can be monitored over time. We observed that the onset of paralysis was significantly delayed in POJ-treated animals (Figure 6). The mean paralysis time for worms treated with 2% ‘Bahia’ and 2% ‘Cara Cara’ juices was increased by 25.0% and 46.0%, respectively, compared to untreated worms (Figure 6, Table 5).

Strain and conditionsMean paralysis time ()% mean paralysis time variation vs. control value (log rank) POJa vs. untreatedb value (log rank) PBJc vs. PCJb,de

CL2006 on E. coli OP50
 Untreated84 (3)
 2% Bahia25.0<0.000185 (3)
 2% Cara Cara46.0<0.0001<0.000184 (3)
CL2006 on E. coli OP50-HKa
 Untreated86 (3)
 2% Bahia23.0<0.000180 (3)
 2% Cara Cara48.0<0.0001<0.000182 (3)
CL2006 on control(RNAi)
 Untreated88 (3)
 2% Bahia14.0<0.000189 (3)
 2% Cara Cara15.0<0.00010.556289 (3)
CL2006 on skn-1(RNAi)
 Untreated87 (3)
 2% Bahia-6.00.019188 (3)
 2% Cara Cara-6.10.01510.855589 (3)
CL2006 on daf-16(RNAi)
 Untreated89 (3)
 2% Bahia0.90.601688 (3)
 2% Cara Cara1.90.40240.858289 (3)
CL2006 on hsf-1(RNAi)
 Untreated88 (3)
 2% Bahia7.20.006989 (3)
 2% Cara Cara-9.8<0.0001<0.000189 (3)

HK: heat killed, aPOJ, pasteurized orange juice, bcomparisons were performed using log-rank (Mantel-Cox) test. cPBJ, pasteurized ‘Bahia’ orange juice, dPCJ, pasteurized ‘Cara Cara’ orange juice, etotal number of animals analyzed. The number in parentheses indicates the number of independent trials.

Various studies have shown that the protective effect of flavonoids and carotenoids against amyloid-induced neurotoxicity is due to their antioxidant properties. Other possible mechanisms could be attenuation of Aβ aggregation in vivo by downregulating the expression level of β-amyloid precursor protein (APP) [18] and/or activation of protein degradation pathways [46]. In the present study, the POJ treatment delayed Aβ1–42-induced paralysis in worms suggesting that POJ may be able to attenuate the development of AD by altering Aβ aggregate states in vivo. Most importantly, our results indicate that ‘Cara Cara’ juice, with higher carotenoid contents, provides a superior protection against Aβ1–42-induced paralysis over that provided by Bahia.

We also evaluated the role of SKN-1, DAF-16, and HSF-1 in POJ-mediated protection against Aβ1-42 toxicity. To this end, we examined the effect of POJ on CL2006 worms using RNAi to knock down skn-1, daf-16, and hsf-1 expression. POJ treatment significantly delayed the paralysis rate of CL2006 worms with control(RNAi) (Table 5). In contrast, RNAi of skn-1 and daf-16 in CL2006 worms completely abolished POJ-mediated beneficial effects on delaying the progression of paralysis (Table 5). RNAi of hsf-1 in CL2006 worms only prevented the beneficial effect against β-amyloid paralysis for those animals treated with 2% ‘Cara Cara’ juice (Table 5). Together, these findings suggest that the transcription factors SKN-1, DAF-16, and HSF-1 are required for POJ-mediated protective effect against Aβ toxicity.

Taking these data together, our mechanistic studies indicated that POJ improves the antioxidant status of a whole organism by direct and indirect mechanisms. POJ-reduced ROS levels were primarily a result of the direct scavenging action of natural compounds available in the orange juice and secondly an outcome of the transcription factor SKN-1 indirect action. POJ promotes gst-4::GFP expression and oxidative stress resistance mainly through SKN-1 although DAF-16 and HSF-1 also contribute to a less extent to these effects. Finally, POJ delayed Aβ-induced onset paralysis on a SKN-1-, DAF-16-, and HSF-1-dependent manner. Previous studies in the nematode reported that DAF-16, SKN-1, and HSF-1 play pivotal roles in regulating longevity and ameliorating Aβ [12]. Since these transcription factors are key regulators of many important biological processes, including lifespan, stress responses, and proteostasis, we reasoned that POJ treatments might protect worms against Aβ1–42 toxicity by increasing antioxidant capacity and proteostasis.

3.6. POJ Protection against Oxidative Stress and Aβ Toxicity Is Partially Related to Antimicrobial Effect

Since E. coli has a pathogenic effect on C. elegans, which may alter its longevity, resistance to stress, and Aβ1–42-induced paralysis [47, 48], we investigated whether the POJ protective effects could be a secondary response of a possible POJ antimicrobial property. First, we repeated the oxidative stress resistance assay in animals treated with POJ on dead bacteria. We observed that wild-type animals treated with 2% POJ still showed increased survival on 10 mM TBHP compared to untreated controls () (Figure 7(a), Table 4). However, the mean survival variation observed for the POJ-treated animals on dead bacteria was considerably lower compared to the, respectively, POJ-treated animals on live bacteria (Table 4). The mean survival variation was 11 and 68% for the animals treated with 2% ‘Bahia’ juice on dead and live bacteria, respectively. Likewise, the mean survival variation was 32 and 73.5% for the animals treated with 2% ‘Cara Cara’ juice on dead and living bacteria, respectively (Table 4).

The role of bacterial in affecting longevity of aging C. elegans is well known [49]. Much experimental evidence supports bacterial infection and proliferation within the intestine of adults as a potential pathogen that triggers innate immune and stress host responses which may contribute as a double-edged effect to tissue damage and aging [47]. The conserved PMK1-p38 mitogen-activated protein kinase (MAPK) pathway is the major mediator of innate immunity in C. elegans. Interestingly, the PMK-1 pathway is also required for the activation of the transcription factor SKN-1 under stress conditions [50]. Thus, any intervention that attenuates bacterial pathogenicity and toxicity extends lifespan and stress resistance. The reduction of the variation survival time on stress when the POJ-treated animals were fed on bacterial previously killed by heat indicates that part of the survival extension observed on POJ-treated animals fed on live bacteria is due to its antimicrobial effect. It is also reasonable to suppose that this reduction of the variation survival time on stress could be a result of the animals acquiring less antioxidant buffer from their living bacterial food source [49]. Another possibility could be related to the fact that in the absence of pathogenic bacteria, the PMK-1-SKN-1 signaling pathway is also diminished and therefore the defense mechanisms activation is attenuated.

Next, we performed the Aβ1-42-induced paralysis assay also using bacteria killed by heat. Interestingly, the mean variation observed for the Aβ1-42-induced paralysis was not particularly different between the POJ treatments on dead or living bacteria (Figure 7(b), Table 5). The mean paralysis time variation for the animals treated with 2% ‘Bahia’ juice on dead bacteria was 23% compared to untreated animals while the variation for the same treatment on living bacteria was 25% (Table 5). For ‘Cara Cara’ juice treatment, the mean paralysis time variation was 48% compared to untreated animals on dead bacteria and 46% compared to untreated animals on living bacteria (Table 5).

Although the onset paralysis in the CL2006 animals grown on live OP50 was faster compared to those grown on dead OP50 as expected, we did not observe any significant difference of the paralysis time variation on the POJ-treated animals fed on dead bacteria compared to those fed on live bacteria (Table 5). This result suggests that the beneficial effect of POJ against Aβ toxicity is independent of the bacterial pathogenicity. This observation seems contradictory since many studies have shown a link between food source and proteotoxicity [48, 51]. Steinkraus et al. [51] showed that bacterial food deprivation suppresses proteotoxicity in Aβ worms through an hsf-1-dependent mechanism. It would be interesting for further studies to shed light on the possible relationship between POJ protection against Aβ in the absence of bacteria depends on HSF-1.

4. Conclusions

In this work, we investigated the in vivo effects of POJ from the ‘Bahia’ and ‘Cara Cara’ varieties using the C. elegans model. Treatment with POJ reduced the endogenous levels of ROS and increased the rate of survival of the worms under normal and stress conditions. Our mechanistic studies indicated that POJ promotes resistance to oxidative stress by acting through the transcription factor SKN-1. We observed that POJ treatments increased the expression of the antioxidant genes (gcs-1, gst-4, and sod-3) and chaperonin (hsp-16.2), which are known to be regulated by the transcription of SKN-1, DAF-16, and HSF-1 factors. In addition, POJ treatments delayed β-amyloid-induced paralysis in the transgenic model C. elegans in a manner requiring SKN-1, DAF-16, and HSF-1. Noteworthy, the treatment with the two juice types produced excellent results; however, ‘Cara Cara’ juice induced significantly better responses than ‘Bahia’ juice did in almost all experiments, possibly due to its higher content of carotenoids such as Z-violaxanthin, zeaxanthin, phytoene, phytofluene, lycopene, and β-carotene.

Data Availability

All data used to support the findings of this study are available from the corresponding author upon request.

Conflicts of Interest

The authors declare that there is no conflict of interests regarding the publication of this paper.


This study was supported by Fundecitrus, São Paulo, Brazil, and Universidade Federal do Rio Grande do Norte (UFRN). Research fellowships were sponsored by CNPq (Oliveira, R. P.). We thank the Caenorhabditis Genetics Center (CGC), which is funded by the NIH National Center for Research Resources (NCRR), and Dr. T. Keith Blackwell for supplying the C. elegans strains. We thank Citrosuco (Matão, São Paulo, Brazil) for providing access to their farms and processing the orange juices used in this study.


  1. E. Brasili, D. F. Seixas Chaves, A. A. O. Xavier, A. Z. Mercadante, N. M. A. Hassimotto, and F. M. Lajolo, “Effect of pasteurization on flavonoids and carotenoids in Citrus sinensis (L.) Osbeck cv. ‘Cara Cara’ and ‘Bahia’ juices,” Journal of Agricultural and Food Chemistry, vol. 65, no. 7, pp. 1371–1377, 2017. View at: Publisher Site | Google Scholar
  2. A. Milani, M. Basirnejad, S. Shahbazi, and A. Bolhassani, “Carotenoids: biochemistry, pharmacology and treatment,” British Journal of Pharmacology, vol. 174, no. 11, pp. 1290–1324, 2017. View at: Publisher Site | Google Scholar
  3. H. S. Lee, “Characterization of carotenoids in juice of red navel orange (Cara Cara),” Journal of Agricultural and Food Chemistry, vol. 49, no. 5, pp. 2563–2568, 2001. View at: Publisher Site | Google Scholar
  4. K. S. Cho, M. Shin, S. Kim, and S. B. Lee, “Recent advances in studies on the therapeutic potential of dietary carotenoids in neurodegenerative diseases,” Oxidative Medicine and Cellular Longevity, vol. 2018, Article ID 4120458, 13 pages, 2018. View at: Publisher Site | Google Scholar
  5. M. Obulesu, M. R. Dowlathabad, and P. V. Bramhachari, “Carotenoids and Alzheimer’s disease: an insight into therapeutic role of retinoids in animal models,” Neurochemistry International, vol. 59, no. 5, pp. 535–541, 2011. View at: Publisher Site | Google Scholar
  6. S. Hwang, J. Lim, and H. Kim, “Inhibitory effect of lycopene on amyloid-β-induced apoptosis in neuronal cells,” Nutrients, vol. 9, no. 8, p. 883, 2017. View at: Publisher Site | Google Scholar
  7. M. Qu, L. Li, C. Chen et al., “Protective effects of lycopene against amyloid β-induced neurotoxicity in cultured rat cortical neurons,” Neuroscience Letters, vol. 505, no. 3, pp. 286–290, 2011. View at: Publisher Site | Google Scholar
  8. Y. Ding, A. Qiao, Z. Wang et al., “Retinoic acid attenuates beta-amyloid deposition and rescues memory deficits in an Alzheimer’s disease transgenic mouse model,” The Journal of Neuroscience, vol. 28, no. 45, pp. 11622–11634, 2008. View at: Publisher Site | Google Scholar
  9. A. B. Goodman, “Retinoid receptors, transporters, and metabolizers as therapeutic targets in late onset Alzheimer disease,” Journal of Cellular Physiology, vol. 209, no. 3, pp. 598–603, 2006. View at: Publisher Site | Google Scholar
  10. A. B. Goodman and A. B. Pardee, “Evidence for defective retinoid transport and function in late onset Alzheimer’s disease,” Proceedings of the National Academy of Sciences, vol. 100, no. 5, pp. 2901–2905, 2003. View at: Publisher Site | Google Scholar
  11. M. Maden, “Retinoic acid in the development, regeneration and maintenance of the nervous system,” Nature Reviews Neuroscience, vol. 8, no. 10, pp. 755–765, 2007. View at: Publisher Site | Google Scholar
  12. A. Antebi, “Genetics of aging in Caenorhabditis elegans,” PLoS Genetics, vol. 3, no. 9, pp. 1565–1571, 2007. View at: Publisher Site | Google Scholar
  13. Y. Luo, “Long-lived worms and aging,” Redox Report, vol. 9, no. 2, pp. 65–69, 2004. View at: Publisher Site | Google Scholar
  14. C. A. Wolkow, K. D. Kimura, M. S. Lee, and G. Ruvkun, “Regulation of C. elegans life-span by insulin-like signaling in the nervous system,” Science, vol. 290, no. 5489, pp. 147–150, 2000. View at: Publisher Site | Google Scholar
  15. M. Artal-Sanz, L. de Jong, and N. Tavernarakis, “Caenorhabditis elegans: a versatile platform for drug discovery,” Biotechnology Journal, vol. 1, no. 12, pp. 1405–1418, 2006. View at: Publisher Site | Google Scholar
  16. P. R. Augusti, A. V. S. Brasil, C. Souto et al., “Microcystin-LR exposure induces oxidative damage in Caenorhabditis elegans: protective effect of lutein extracted from marigold flowers,” Food and Chemical Toxicology, vol. 109, Part 1, pp. 60–67, 2017. View at: Publisher Site | Google Scholar
  17. E. Pons, B. Alquezar, A. Rodriguez et al., “Metabolic engineering of β-carotene in orange fruit increases its in vivo antioxidant properties,” Plant Biotechnology Journal, vol. 12, no. 1, pp. 17–27, 2014. View at: Publisher Site | Google Scholar
  18. W. Chen, L. Mao, H. Xing et al., “Lycopene attenuates Aβ1–42 secretion and its toxicity in human cell and Caenorhabditis elegans models of Alzheimer disease,” Neuroscience Letters, vol. 608, pp. 28–33, 2015. View at: Publisher Site | Google Scholar
  19. E. Lashmanova, E. Proshkina, S. Zhikrivetskaya et al., “Fucoxanthin increases lifespan of Drosophila melanogaster and Caenorhabditis elegans,” Pharmacological Research, vol. 100, pp. 228–241, 2015. View at: Publisher Site | Google Scholar
  20. M. Dimitriadi and A. C. Hart, “Neurodegenerative disorders: insights from the nematode Caenorhabditis elegans,” Neurobiology of Disease, vol. 40, no. 1, pp. 4–11, 2010. View at: Publisher Site | Google Scholar
  21. J. Li and W. Le, “Modeling neurodegenerative diseases in Caenorhabditis elegans,” Experimental Neurology, vol. 250, pp. 94–103, 2013. View at: Publisher Site | Google Scholar
  22. Anon, FMC Food Tech. The Laboratory Manual. Procedures for Analysis of Citrus Products. Manual No. 054R11990, John Bean Technologies Corporation, Inc, Lakeland, FL, USA, 2000.
  23. J. W. Stevens, “Estimation of Ascorbic Acid in Citrus Juices,” Industrial & Engineering Chemistry Analytical Edition, vol. 10, no. 5, pp. 269–271, 1938. View at: Publisher Site | Google Scholar
  24. B. Alquezar, M. J. Rodrigo, and L. Zacarías, “Regulation of carotenoid biosynthesis during fruit maturation in the red-fleshed orange mutant Cara Cara,” Phytochemistry, vol. 69, no. 10, pp. 1997–2007, 2008. View at: Publisher Site | Google Scholar
  25. G. Britton, “Overview of carotenoid biosynthesis,” in Biosynthesis and Metabolism, G. Britton, S. Liaaen-Jensen, and H. Pfander, Eds., pp. 13–148, Birkhäuser Verlag, Basel, 1998. View at: Google Scholar
  26. L. Carmona, L. Zacarías, and M. J. Rodrigo, “Stimulation of coloration and carotenoid biosynthesis during postharvest storage of ‘Navelina’ orange fruit at 12 °C,” Postharvest Biology and Technology, vol. 74, pp. 108–117, 2012. View at: Publisher Site | Google Scholar
  27. M. J. Rodrigo, J. F. Marcos, F. Alferez, M. D. Mallent, and L. Zacarias, “Characterization of Pinalate, a novel Citrus sinensis mutant with a fruit-specific alteration that results in yellow pigmentation and decreased ABA content,” Journal of Experimental Botany, vol. 54, no. 383, pp. 727–738, 2003. View at: Publisher Site | Google Scholar
  28. M. J. Rodrigo, J. F. Marcos, and L. Zacarias, “Biochemical and molecular analysis of carotenoid biosynthesis in flavedo of orange (Citrus sinensis L.) during fruit development and maturation,” Journal of Agricultural and Food Chemistry, vol. 52, no. 22, pp. 6724–6731, 2004. View at: Publisher Site | Google Scholar
  29. R. L. Rouseff, L. Raley, and H. J. Hofsommer, “Application of diode array detection with a C-30 reversed phase column for the separation and identification of saponified orange juice carotenoids,” Journal of Agricultural and Food Chemistry, vol. 44, no. 8, pp. 2176–2181, 1996. View at: Publisher Site | Google Scholar
  30. S. Brenner, “The genetics of Caenorhabditis elegans,” Genetics, vol. 77, no. 1, pp. 71–94, 1974. View at: Google Scholar
  31. F. A. Paiva, L. de Freitas Bonomo, P. F. Boasquivis et al., “Carqueja (Baccharis trimera) protects against oxidative stress and beta-amyloid-induced toxicity in Caenorhabditis elegans,” Oxidative Medicine and Cellular Longevity, vol. 2015, Article ID 740162, 15 pages, 2015. View at: Publisher Site | Google Scholar
  32. L. de Freitas Bonomo, D. N. Silva, P. F. Boasquivis et al., “Açaí (Euterpe oleracea Mart.) modulates oxidative stress resistance in Caenorhabditis elegans by direct and indirect mechanisms,” PLoS One, vol. 9, no. 3, article e89933, 2014. View at: Publisher Site | Google Scholar
  33. A. M. Gonzalez-Paramas, B. Ayuda-Duran, S. Martinez, S. Gonzalez-Manzano, and C. Santos-Buelga, “The mechanisms behind the biological activity of flavonoids,” Current Medicinal Chemistry, vol. 25, 2018. View at: Publisher Site | Google Scholar
  34. A. Murakami, “Non-specific protein modifications may be novel mechanism underlying bioactive phytochemicals,” Journal of Clinical Biochemistry and Nutrition, vol. 62, no. 2, pp. 115–123, 2018. View at: Publisher Site | Google Scholar
  35. S. Y. Tang and B. Halliwell, “Medicinal plants and antioxidants: what do we learn from cell culture and Caenorhabditis elegans studies?” Biochemical and Biophysical Research Communications, vol. 394, no. 1, pp. 1–5, 2010. View at: Publisher Site | Google Scholar
  36. K. Koch, S. Havermann, C. Buchter, and W. Watjen, “Caenorhabditis elegansas model system in pharmacology and toxicology: effects of flavonoids on redox-sensitive signalling pathways and ageing,” Scientific World Journal, vol. 2014, article 920398, 15 pages, 2014. View at: Publisher Site | Google Scholar
  37. J. H. An and T. K. Blackwell, “SKN-1 links C. elegans mesendodermal specification to a conserved oxidative stress response,” Genes & Development, vol. 17, no. 15, pp. 1882–1893, 2003. View at: Publisher Site | Google Scholar
  38. L. A. Khan, T. Yamanaka, and N. Nukina, “Genetic impairment of autophagy intensifies expanded polyglutamine toxicity in Caenorhabditis elegans,” Biochemical and Biophysical Research Communications, vol. 368, no. 3, pp. 729–735, 2008. View at: Publisher Site | Google Scholar
  39. C. T. Murphy, S. A. McCarroll, C. I. Bargmann et al., “Genes that act downstream of DAF-16 to influence the lifespan of Caenorhabditis elegans,” Nature, vol. 424, no. 6946, pp. 277–283, 2003. View at: Publisher Site | Google Scholar
  40. E. Guisbert, D. M. Czyz, K. Richter, P. D. McMullen, and R. I. Morimoto, “Identification of a tissue-selective heat shock response regulatory network,” PLoS Genetics, vol. 9, no. 4, article e1003466, 2013. View at: Publisher Site | Google Scholar
  41. V. Murugaiyah and M. P. Mattson, “Neurohormetic phytochemicals: an evolutionary-bioenergetic perspective,” Neurochemistry International, vol. 89, pp. 271–280, 2015. View at: Publisher Site | Google Scholar
  42. T. G. Son, S. Camandola, and M. P. Mattson, “Hormetic dietary phytochemicals,” Neuromolecular Medicine, vol. 10, no. 4, pp. 236–246, 2008. View at: Publisher Site | Google Scholar
  43. K. I. Zhou, Z. Pincus, and F. J. Slack, “Longevity and stress in Caenorhabditis elegans,” Aging, vol. 3, no. 8, pp. 733–753, 2011. View at: Publisher Site | Google Scholar
  44. S. J. Choi, J. K. Kim, S. H. Suh et al., “Ligularia fischeri extract protects against oxidative-stress-induced neurotoxicity in mice and pc12 cells,” Journal of Medicinal Food, vol. 17, no. 11, pp. 1222–1231, 2014. View at: Publisher Site | Google Scholar
  45. H. R. Jeong, Y. N. Jo, J. H. Jeong, H. J. Kim, M.-J. Kim, and H. J. Heo, “Blueberry (Vaccinium virgatum) leaf extracts protect against Aβ-induced cytotoxicity and cognitive impairment,” Journal of Medicinal Food, vol. 16, no. 11, pp. 968–976, 2013. View at: Publisher Site | Google Scholar
  46. P. F. Boasquivis, G. M. M. Silva, F. A. Paiva, R. M. Cavalcanti, C. V. Nunez, and R. de Paula Oliveira, “Guarana (Paullinia cupana) extract protects Caenorhabditis elegans models for Alzheimer disease and Huntington disease through activation of antioxidant and protein degradation pathways,” Oxidative Medicine and Cellular Longevity, vol. 2018, Article ID 9241308, 16 pages, 2018. View at: Publisher Site | Google Scholar
  47. D. H. Kim, “Bacteria and the aging and longevity of Caenorhabditis elegans,” Annual Review of Genetics, vol. 47, no. 1, pp. 233–246, 2013. View at: Publisher Site | Google Scholar
  48. F. Munoz-Lobato, M. J. Rodriguez-Palero, F. J. Naranjo-Galindo et al., “Protective role of DNJ-27/ERdj5 in Caenorhabditis elegans models of human neurodegenerative diseases,” Antioxidants & Redox Signaling, vol. 20, no. 2, pp. 217–235, 2014. View at: Publisher Site | Google Scholar
  49. D. Garigan, A.-L. Hsu, A. G. Fraser, R. S. Kamath, J. Ahringer, and C. Kenyon, “Genetic analysis of tissue aging in Caenorhabditis elegans: a role for heat-shock factor and bacterial proliferation,” Genetics, vol. 161, no. 3, pp. 1101–1112, 2002. View at: Google Scholar
  50. H. Inoue, N. Hisamoto, J. H. An et al., “The C. elegans p38 MAPK pathway regulates nuclear localization of the transcription factor SKN-1 in oxidative stress response,” Genes & Development, vol. 19, no. 19, pp. 2278–2283, 2005. View at: Publisher Site | Google Scholar
  51. K. A. Steinkraus, E. D. Smith, C. Davis et al., “Dietary restriction suppresses proteotoxicity and enhances longevity by an hsf-1-dependent mechanism in Caenorhabditis elegans,” Aging Cell, vol. 7, no. 3, pp. 394–404, 2008. View at: Publisher Site | Google Scholar

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