Skip to main content
PMC home page
Oxidative Medicine and Cellular Longevity logoLink to Oxidative Medicine and Cellular Longevity
. 2020 Oct 8;2020:1321354. doi: 10.1155/2020/1321354

Aqueous Bark Extract of Ceiba speciosa (A. St.-Hill) Ravenna Protects against Glucose Toxicity in Caenorhabditis elegans

Fabrine Bianchin dos Santos 1, Caroline Brandão Quines 1, Luiz Eduardo Ben Pilissão 1, Ana Helena de Castro Dal Forno 1, Cristiane Freitas Rodrigues 1, Cristiane Casagrande Denardin 1, Fabiane Moreira Farias 2, Daiana Silva Ávila 1,✉
PMCID: PMC7568133  PMID: 33101582

Abstract

Plants are widely used in folk medicine because of their pharmacological properties. Ceiba speciosa, popularly known as paineira-rosa or tree-of-wool, is a species found in the Northwest of Rio Grande do Sul, being native of the upper Uruguay River, Brazil. The tea obtained from the stem bark is employed in folk medicine to reduce cholesterol, triacylglycerides, and glucose levels. However, there are no studies in the literature proving its efficacy or the safety of its use. For this study, we used Caenorhabditis elegans as an animal model considering its advantages for risk assessment and pharmacological screenings. For the toxicological tests, C. elegans N2 (wild type) was treated with the aqueous extract of the stem bark of C. speciosa (ECE) at the first larval stage (L1) at concentrations of 5, 25, 50, and 250 μg/mL. To evaluate biological activities, we challenged the extract for oxidative stress resistance in the presence of paraquat (0.5 mM), H2O2 (1 mM), and against glucose-induced toxicity. Our results demonstrated that ECE did not alter survival rate, pharyngeal pumping, and reproduction of the nematodes. The extract was not able to protect the nematodes against the toxicity induced by prooxidants. Notably, ECE protected against glucotoxicity by increasing worms' life span and by reducing glucose levels. On the other hand, ECE treatment did not reduce lipid accumulation induced by exogenous glucose feeding, as observed in worms which lipid droplets were tagged with GFP. Based on our results, we believe that the extract is indeed promising for further studies focusing on carbohydrates metabolism; however, it needs to be carefully evaluated since the extract does not seem to modulate lipid accumulation.

1. Introduction

Glucose toxicity refers to the biological effects of its excessive levels in cells and tissues due to metabolic alterations and production of advanced glycation end products (AGEs) [1]. AGES interact with lipids, proteins, and other molecules causing cell damage by inducing oxidative stress and cell death [2]. With the growing interest in finding natural antioxidants and drugs with beneficial action on glucose metabolism, many extracts from different plants and their different parts have been tested [3, 4]. However, the indiscriminate use of natural products has led to cases of intoxication [5]. Therefore, a safety assessment of natural products should be performed previously to medicinal use [4].

The scientific literature describes some medicinal properties for several species of the genus Ceiba. A study conducted by Leal et al. [6] reported a considerable variety of secondary compounds in the bark extract and antimicrobial activity against strains of Staphylococcus aureus which may be related to the presence of phytochemicals such as tannins and phenols. In addition, Ceiba pentandra (L.) Gaertn, commonly known as silk cotton tree, has been used by practitioners of traditional medicine in Northern and Eastern Nigeria for diabetes control.

In this same pharmacological context, Ceiba speciosa (A. St.-Hil.) has been used by the southern Brazilian population [7]. The species is found in the Northwestern Rio Grande do Sul, Brazil, being native in the Upper Uruguay vegetation [8]. Regarding its use in folk medicine, there are records for the use of barks and flowers for the treatment of heart disease, hypertension, and diabetes [9]. With the increasing interest in the bioprospection of natural products, especially of vegetal material originating from the Pampa Biome, the validation and application of alternative models for the evaluation of these natural products becomes relevant.

Among the animal models that have been used to investigate the toxicology and pharmacology of medicinal plants is the nematode Caenorhabditis elegans. This worm has a number of characteristics that make it not only relevant but also quite powerful as a model for this type of research [10]. C. elegans is easy and cheap to maintain in the laboratory with an Escherichia coli diet, has a short reproductive cycle (3 days) and a large number of descendants (~200), which allow the large-scale production of animals within a short period of time. The transparent body allows a clear observation of all cells in these animals. Notably, C. elegans shows a strong conservation in molecular and cellular pathways with respect to mammals and humans [11], including those signaling related to glucose and lipid metabolism [12, 13].

Notably, this nematode does not have specialized storage tissues such as adipocytes, and the energetic excess is stored in lipid droplets in enterocytes, hypodermis, and gonads [14, 15]. On the other hand, the absence of adipocytes removes central components in the control of energetic metabolism in mammals, which may be advantageous by facilitating the interpretation of other conserved factors and mechanisms involved in energy homeostasis [16, 17]. Thus, this study is aimed at evaluating the safety of the aqueous bark extract from Ceiba speciosa (ECE) as well as at verifying the glucose-reducing levels action attributed to this plant using C. elegans as an animal model.

2. Materials and Methods

2.1. Extract Preparation

The stem bark of C. speciosa was collected in the municipality of Santo Antônio das Missões, Rio Grande do Sul, Brazil, on April 2012. The plant material was identified by a botanist, and an exsiccata or botanical voucher was deposited in the Zoobotanic Herbarium Augusto Ruschi at the University of Passo Fundo, under the code RSPF 12637. C. speciosa barks were ground, and the aqueous extract was prepared by decoction in distilled water according to Malheiros et al. [18]. Since we have used the exact same batch of lyophilized extract, the phytochemical composition has been already reported [18]. To expose worms, the lyophilized material was diluted in water to obtain a stock solution at 10 mg/mL that was subsequently used for further dilutions.

2.2. Caenorhabditis elegans Maintenance

The C. elegans strains used in this study were N2 (wild type) and VS29 (hjSi56 [vha-6p::3xFLAG::TEV::GFP::dgat-2::let-858 3′UTR]) [19] which were obtained from Caenorhabditis Genetics Center (CGC) and maintained in NGM (nematode growth medium) seeded with E. coli OP50 at 20°C [20]. First larval stage worms were obtained by a synchronization process, which consists of exposing pregnant worms to the lysis solution (0.45 N NaOH, 2% HOCl p/v) to separate the eggs from the worms. After 14 h, the eggs hatched and released the L1 larvae, used for exposures. All experiments were performed at 22°C in a controlled humidified environment.

2.3. Treatment Protocol and LC50 Determination

A total of 2,000 L1 nematodes were exposed to different concentrations of C. speciosa bark extract (ECE-5 μg/mL, 25 μg/mL, 50 μg/mL, and 250 μg/mL) for 30 min at 22°C, in a homogenizer. After treatment, the nematodes were washed with 85 mM NaCl solution for 3 times in order to terminate the exposure, and then, nematodes were plated on NGM seeded with E. coli OP50. Twenty-four hours after exposure, the number of surviving nematodes was counted, and a survival curve was drawn [21]. The experiments were performed in duplicates. The results were expressed as % of control.

2.4. Brood Size

The nematodes were treated as described above and were maintained on NGM/E. coli OP50 plates until they reached larval stage L4. To evaluate progeny size, one nematode from each ECE treatment was transferred to a new plate containing NGM medium, and the total number of progeny was counted during the whole reproductive period [22]. The experiments were performed in triplicates and independently repeated three times. The results were expressed as % of control.

2.5. Pharyngeal Pumping

This assay is used to verify the dietary intake of the nematodes. 24 h after the treatment described previously, 5 nematodes from each experiment were transferred to new plates without bacteria. The pharyngeal pumps were counted for 1 min at the stereomicroscope [23]. The experiments were repeated in three independent assays. The results were expressed as % of control.

2.6. Oxidative Stress-Resistance Assays

Nematodes were pretreated at the L1 stage as described previously. After the last wash, worms were posttreated with the prooxidants paraquat (0.5 mM) or hydrogen peroxide (1 mM) for 30 min. Subsequently, nematodes were washed four more times and then transferred to NGM/E. coli OP50 plates. The number of surviving nematodes on each plate 24 h postexposure was scored to determine stress resistance [10]. The experiments were performed in duplicates and repeated at least 3 times. The results were expressed as % of control.

2.7. Glucose Toxicity

In the pilot test, we have used 2 glucose concentrations (2 and 4%) to verify whether they would reduce worms' life span. Plates containing NGM medium were inoculated with E. coli OP50 which were UV-inactivated. Thereafter, glucose solution was added on top of the dried E.coli. Based on pilot results, we have chosen glucose 4% for the next assays. Worms were pretreated with different concentrations of the extract (ECE 5 μg/mL or 250 μg/mL) for 30 min, washed to remove the treatments, and then transferred to NGM/UV-inactivated E.coli plates containing glucose 4% or vehicle. Then, 20 live worms at the same developmental stage were collected at the late L4 stage and transferred daily to new plates NGM UV-inactivated E.coli + glucose 4% or vehicle in order to prevent contamination or progeny. Live animals were scored until all animals died. The experiments were performed in triplicates, and three independent experiments were conducted. The results were expressed as % of control.

2.8. Glucose Levels

The glucose content was quantified by glucose oxidase method. Worms (N2) were treated as described in Section 2.7 and kept in glucose 4% until they reached the L4 stage. After these 48 h, worms were washed off with M9 buffer from the plates and centrifuged at 2500 rpm for 2 min. Worms were washed until removing all existing bacteria. Then, worms were frozen and thawed 3 times, sonicated with lysis buffer, and centrifuged. The supernatant (50 μL) was transferred to a 96-well plate, and glucose levels were measured using a Labtest glucose colorimetric assay kit (Labtest Diagnostica S.A., Minas Gerais, Brasil). The optical density of each of the incubated samples (10 min at 37°C) was measured at 505 nm. For normalization of the data, protein was measured using Bradford colorimetric method and expressed as mg glucose/μg protein. The experiments were performed in duplicates and normalized as % of control.

2.9. Glucose-Induced Lipid Accumulation

N2 and VS29 nematodes were treated as described in Section 2.7, and worms were kept on NGM/UV-inactivated E.coli OP50 plates containing or not glucose 4% until reaching the larval stage L4. After these 48 hours of glucose exposure, worms were transferred to slides containing levamisole, and images were acquired in a fluorescent microscope to observe the effect of glucose exposure on lipid accumulation. VS29 has a transgene which DGAT2 (acyl CoA:diacylglycerol O-acyltransferase 2) is fused to GFP. This enzyme transfers acyl groups and is localized in the lipid particles; then, lipid droplets can be observed. N2 was used as control to verify lipofuscin or autofluorescence production caused by glucose treatment.

2.10. Statistical Analysis

Statistical analysis was carried out by one-way analysis of variance (ANOVA), followed by post hoc Tukey test when the overall p < 0.05. For life span assay, a repeated measure two-way analysis of variance (ANOVA) followed by post hoc Tukey test was applied.

3. Results

3.1. Toxicity Evaluation of C. speciosa Aqueous Bark Extract

Figure 1(a) shows that acute exposure to different concentrations of ECE did not alter C. elegans survival rate (up to 250 μg/mL), thus suggesting that no toxic effects occurred under the experimental conditions tested (acute). Based on that, we decided to use the concentrations of 5 μg/mL, 25 μg/mL, 50 μg/mL, and 250 μg/mL for further assays. In addition, we did not find any toxic effect of C. speciosa bark extract on worms' reproduction, as brood size did not change (Figure 1(b)). In order to verify whether ECE would affect food ingestion per se, we analyzed pharyngeal pumping, which was not changed as well (Figure 1(c)).

Figure 1.

Figure 1

Open in a new tab

Toxicological evaluation of different concentrations of C. speciosa aqueous extract in (a) nematodes survival, (b) brood size, and (c) pharyngeal pumping. Values are expressed as mean ± S.E.M. of four experiments. Data were analyzed by using one-way ANOVA following by the Tukey test.

3.2. Stress Resistance

To verify a possible stress resistance conferred by ECE, we exposed worms to different prooxidants: paraquat (a pesticide, Figure 2(a)) or hydrogen peroxide (H2O2, Figure 2(b)). Our results demonstrate that ECE did not protect against the damage induced by these prooxidants at any of the tested concentrations.

Figure 2.

Figure 2

Open in a new tab

Effect of different concentrations of ECE treatment in oxidative stress resistance. (a) Response to oxidative stress in paraquat posttreated nematodes (0.5 mM) and pretreated with ECE. Values are expressed as mean ± S.E.M. of six experiments. (b) Response to oxidative stress in post-H2O2 treated nematodes (1 mM) and pretreated with the ECE. Values are expressed as mean ± S.E.M. of three experiments. Data were analyzed by using one-way ANOVA following by the Tukey post hoc test. ∗ indicates p < 0.05; ∗∗ indicates p < 0.01; ∗∗∗ indicates p < 0.001 when compared to the control group.

3.3. ECE Treatment Protected against Glucose Toxicity

In order to verify the protection of ECE treatment against glucose toxicity, we analyzed life span. Post hoc analysis of the data depicted in Figure 3 has revealed that 4% glucose induced a reduction in worms' life span from day 5 until day 14. The treatment with ECE at both concentrations (5 and 250 μg/mL) was effective against the glucose-induced reduction in life span starting on day 6 until day 12. Two-way ANOVA demonstrated a significant interaction between treatment × days (F(54,162) = 4.418; p < 0.001), thus indicating a protection conferred by ECE throughout the life span. In addition, glucose 4% administration significantly increased glucose levels, and the treatment with ECE was effective by reducing this elevation (Figure 4(b)). Notably, ECE per se treatment did not alter glucose levels (Figure 4(a)).

Figure 3.

Figure 3

Open in a new tab

Effect of different concentration of ECE on glucose-induced toxicity in worms' life span. Values are expressed as mean ± S.E.M. of four experiments. Data were analyzed by using a repeated measures two-way ANOVA followed by the Tukey posttest. ∗ indicates p < 0.05; ∗∗ indicates p < 0.01; ∗∗∗ indicates p < 0.001 when compared to the control group. # indicates p < 0.05; ## indicates p < 0.01; ### indicates p < 0.001 when compared to the glucose group.

Figure 4.

Figure 4

Open in a new tab

Glucose levels in (a) following ECE treatment per se and (b) worms treated with ECE and exposed to glucose 4%. Values are expressed as mean ± S.E.M. of four experiments. Data were analyzed by using one-way ANOVA following by the Tukey post hoc test. ∗ indicates p < 0.05 when compared to the control group. # indicates p < 0.05; ### indicates p < 0.001 when compared to the glucose group.

Furthermore, we took advantage of a GFP-tagged strain and observed lipid accumulation induced by glucose vs. ECE pretreatment. In wild-type (N2) worms, no increase or decrease in fluorescence intensity caused by lipofuscin production was evidenced, even in those worms exposed to high glucose levels (Figures 5(a)–5(d)). On the other hand, in VS29 mutants, a stronger fluorescence around the gut following glucose 4% exposure was detected, therefore indicating an increase in lipid droplets accumulation (Figure 6(b)). However, ECE treatment did not reduce lipid accumulation at any of the concentrations tested since no significant reduction in GFP fluorescence was evidenced (Figures 6(c) and 6(d)).

Figure 5.

Figure 5

Open in a new tab

Representative images of N2 worms following glucose-induced lipid-accumulation and ECE treatment to observe autofluorescence: (a) untreated worms; (b) worms treated with glucose 4%; (c) worms treated with ECE 5 μg/mL+ 4% glucose; (d) worms treated with ECE 250 μg/mL+ 4% glucose.

Figure 6.

Figure 6

Open in a new tab

Representative images of VS29 worms following glucose-induced lipid-accumulation and ECE treated worms: (a) untreated worms; (b) worms exposed to glucose 4%; (c) worms treated with ECE 5 μg/mL+ 4% glucose; (d) worms treated with ECE 250 μg/mL+ 4% glucose.

4. Discussion

In the present work, the safety and pharmacological activity of C. speciosa aqueous bark extract were studied, since little scientific knowledge about its effects are described in the literature. The consumption of this plant occurs in the Northwestern region of the State of Rio Grande do Sul, Brazil, which consumes it as a tea due to its alleged beneficial effects in humans [9]. Our work verified that ECE is safe and protected against glucose-induced toxicity by reducing its levels and the associated consequences in C. elegans life span.

The antioxidant potential of the extract has been previously demonstrated in vitro through the DPPH radical scavenging capacity and demonstrated a good scavenging potential [18, 24]. The phytochemical analysis of the extract used in this study was published by Malheiros and cols and revealed that flavonoids (quercetin, rutin, and kaempferol) and phenolic acids (gallic, chlorogenic, ellagic, and caffeic) are present [18, 25].

In vivo, however, the extract did not show the same antioxidant performance. We challenged ECE against two powerful prooxidants, paraquat and H2O2, which have significantly increased nematodes mortality. Paraquat is an herbicide widely used in agriculture, but its biochemical mechanism responsible for its toxicity is not fully understood. It is known that paraquat is a superoxide radical generator (O2·), which can produce other reactive species such as hydrogen peroxide (H2O2) and hydroxyl radical (·OH), which are unstable and react quickly with fatty acids, causing lesions in the membranes, proteins, and DNA. H2O2 is one of the most versatile oxidants in existence, superior to chlorine, chlorine dioxide, and potassium permanganate; through catalysis, H2O2 can be converted to hydroxyl radical (·OH). It can easily pass through cell membranes [26, 27]. Our results demonstrated that despite the antioxidant action in vitro, the treatment with ECE was not able to reduce the toxicity induced by these prooxidants. In vivo, molecules can be transformed, sometimes losing activities presented in some in vitro assays, particularly those without tissue.

C. elegans contains many key metabolic-related components such as oxidative stress and insulin signaling pathways, making it a useful platform to improve our understanding of complex diseases such as metabolic syndrome [13]. Glucose is the main energy source and key regulator of animal metabolism; however, a chronic abundance of glucose will have deleterious effects on cellular and tissue functions [28]. Carbohydrate excess activates several lipogenic enzymes contributing to deregulation in lipid metabolism and insulin resistance development [29]. Furthermore, high levels of glucose induce cell injury of mammalian hepatocytes and pancreatic cells through molecular mechanisms of endoplasmic reticulum stress, oxidative stress, and mitochondrial impairment [29, 30]. Moreover, chronic hyperglycemia can deteriorate cognitive function and impair memory [31].

C. elegans is a suitable model organism to study glucose toxicity, once high glucose conditions impair their life span by increasing ROS formation and AGEs modification of mitochondrial proteins in a DAF-2 independent manner [32]. Furthermore, glucose-enriched diet significantly decreases worms' life span by inhibiting the translocation of DAF-16 and HSF-1 transcription factors that are involved in antioxidant response [33]. On the other hand, glucose restriction extends C. elegans life span by increasing the expression of proaging and antioxidant genes [34].

We have found promising results when we challenged ECE-treated worms against high glucose levels. The extract was able to protect from the reduced longevity and to diminish whole body glucose levels induced by high glucose exposure. A similar effect has been observed in the alloxan-induced diabetic rats treated with B. ceiba bark methanolic extract [35]. Furthermore, the alcoholic extract of C. pentandra, a species taxonomically related to C. speciosa which is commonly used in North Africa, has been used to control hyperglycemia in diabetic patients [36]. Notably, its alcoholic extract has been tested in rats, and it has been proven that besides safe, decreases plasma glucose levels following oral administration [37].

In relation to mechanism of action, the treatment with C. pentandra decreased glucose levels in diabetic rats through enhanced glucose utilization and regulation in insulin levels [38, 39]. Similar to C. pentandra, we believe that the treatment with ECE could enhance glucose utilization and stimulate another form of energy storage, like glycogen or trehalose. Notably, C. elegans can synthesize saturated and unsaturated fatty acids and is capable of storing energy as lipids (triglycerides, phospholipids, sphingolipids, etc.). Up to 35% of C. elegans dry body mass is lipids, being triacylglyceride fat deposits the major energy storage molecules, depending on diet and life stage [16]. To analyze that, we have used a transgenic strain which acyl CoA:diacylglycerol O-acyltransferase 2 is fused to GFP. This enzyme transfers the acyl groups and is localized in the lipid particles; then, lipid droplets can be observed in vivo. As expected, our results have shown that high glucose administration increased lipid accumulation in worms. However, ECE treatment failed to reduce this storage, therefore indicating that glucose levels reduced by the extract may have been converted to lipids.

Finally, we observed that acute exposure at different concentrations of ECE did not cause toxicological effects on worms, as analyzed by survival rate, brood size, and pharyngeal pumping. These findings confirm that worms were ingesting the extract and feeding normally, indicating that the use of these concentrations is safe, considering the experimental conditions tested. Previous in vitro data have also demonstrated that this same extract did not reduce leukocytes viability and did not cause genotoxicity [18]. C. speciosa is a plant widely used by southern Brazilians; therefore, the safety of its use by this population is germane. Thus, for the first time, it was demonstrated that the aqueous bark extract of C. speciosa has low toxicity and has potential against glucose toxicity, thus suggesting that ECE may be useful against hyperglycemia in mammals. Therefore, additional studies will be carried out by our group with the purpose of expanding the hypoglycemic effects of C. speciosa and its mechanisms.

Acknowledgments

The authors are thankful to PROPPI/Universidade Federal do Pampa (UNIPAMPA) for providing financial assistance. DSA is recipient of CNPq researcher scholarship and supported by FAPERGS/PqG # 18/2551-0000434-0. AHCDF and CFR were recipients of scholarships from Coordenação de Aperfeiçoamento de Pessoal de Nível Superior—Brasil (CAPES)—Finance Code 001. Some strains were provided by the CGC, which is funded by NIH Office of Research Infrastructure Programs (P40 OD010440).

Data Availability

All authors declare the availability of the use of data from this manuscript by the journal Antioxidants and Prooxidants: Effects on Health and Aging 2020.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Supplementary Materials

Supplementary Materials

The supplementary material includes the graphical abstract of the manuscript.

Click here for additional data file. (319.1KB, pdf)

References

  • 1.Luo X., Wu J., Jing S., Yan L. J. Hyperglycemic stress and carbon stress in diabetic glucotoxicity. Aging and Disease. 2016;7(1):90–110. doi: 10.14336/AD.2015.0702. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Pinkas A., Aschner M. Advanced glycation end-products and their receptors: related pathologies, recent therapeutic strategies, and a potential model for future neurodegeneration studies. Chemical Research in Toxicology. 2016;29(5):707–714. doi: 10.1021/acs.chemrestox.6b00034. [DOI] [PubMed] [Google Scholar]
  • 3.Surveswaran S., Cai Y. Z., Xing J., Corke H., Sun M. Antioxidant properties and principal phenolic phytochemicals of Indian medicinal plants from Asclepiadoideae and Periplocoideae. Natural Product Research. 2010;24(3):206–221. doi: 10.1080/14786410802228827. [DOI] [PubMed] [Google Scholar]
  • 4.Pisoschi A. M., Pop A., Cimpeanu C., Predoi G. Antioxidant capacity determination in plants and plant-derived products: a review. Oxidative Medicine and Cellular Longevity. 2016;2016:36. doi: 10.1155/2016/9130976.9130976 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Boubaker K., Ounissi M., Brahmi N., et al. Acute renal failure by ingestion of Euphorbia paralias. Saudi Journal of Kidney Diseases and Transplantation. 2013;24(3):571–575. doi: 10.4103/1319-2442.111069. [DOI] [PubMed] [Google Scholar]
  • 6.Leal I. C. R., dos Santos K. R. N., Júnior I. I., et al. Ceanothane and lupane type triterpenes from Zizyphus joazeiro– an anti-staphylococcal evaluation. Planta Medica. 2010;76(1):47–52. doi: 10.1055/s-0029-1185947. [DOI] [PubMed] [Google Scholar]
  • 7.Beleski-Carneiro E., Sugui J. A., Reicher F. Structural and biological features of a hydrogel from seed coats of Chorisia speciosa. Phytochemistry. 2002;61(2):157–163. doi: 10.1016/S0031-9422(02)00227-3. [DOI] [PubMed] [Google Scholar]
  • 8.Cappelatti L., Schmitt J. L. Caracterização da flora arbórea de um fragmento urbano de floresta estacional semidecidual no Rio Grande do Sul, Brasil, Pesquisas. Botânica. 2009;60:341–354. [Google Scholar]
  • 9.de Lucena R. F. P., do Nascimento V. T., de Lima Araújo E., de Albuquerque U. P. Local uses of native plants in an area of Caatinga vegetation (Pernambuco, NE Brazil) Ethnobotany Research and Applications. 2008;6:003–014. doi: 10.17348/era.6.0.3-14. [DOI] [Google Scholar]
  • 10.An J. H., Blackwell T. K. SKN-1 links C. elegans mesendodermal specification to a conserved oxidative stress response. Genes & Development. 2003;17(15):1882–1893. doi: 10.1101/gad.1107803. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Weinhouse C., Truong L., Meyer J. N., Allard P. Caenorhabditis elegans as an emerging model system in environmental epigenetics. Environmental and Molecular Mutagenesis. 2018;59(7):560–575. doi: 10.1002/em.22203. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Zheng J., Greenway F. L. Caenorhabditis elegans as a model for obesity research. International Journal of Obesity. 2012;36(2):186–194. doi: 10.1038/ijo.2011.93. [DOI] [PubMed] [Google Scholar]
  • 13.Watts J. L., Ristow M. Lipid and carbohydrate metabolism in Caenorhabditis elegans. Genetics. 2017;207(2):413–446. doi: 10.1534/genetics.117.300106. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Ashrafi K. Obesity and the regulation of fat metabolism. WormBook: The Online Review of C. Elegans Biology. 2007. pp. 1–20. [DOI] [PMC free article] [PubMed]
  • 15.Palikaras K., Mari M., Petanidou B., Pasparaki A., Filippidis G., Tavernarakis N. Ectopic fat deposition contributes to age-associated pathology in Caenorhabditis elegans. Journal of Lipid Research. 2017;58(1):72–80. doi: 10.1194/jlr.M069385. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Ashrafi K., Chang F. Y., Watts J. L., et al. Genome-wide RNAi analysis of Caenorhabditis elegans fat regulatory genes. Nature. 2003;421(6920):268–272. doi: 10.1038/nature01279. [DOI] [PubMed] [Google Scholar]
  • 17.Hashmi S., Wang Y., Parhar R. S., et al. A C. elegans model to study human metabolic regulation. Nutrition & Metabolism. 2013;10(1):p. 31. doi: 10.1186/1743-7075-10-31. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Malheiros C. K. C., Silva J. S. B., Hofmann T. C., et al. Preliminary in vitro assessment of the potential toxicity and antioxidant activity of Ceiba speciosa (A. St.-Hill) Ravenna (Paineira) Brazilian Journal of Pharmaceutical Sciences. 2017;53(2) doi: 10.1590/s2175-97902017000216098. [DOI] [Google Scholar]
  • 19.Xu N., Zhang S. O., Cole R. A., et al. The FATP1-DGAT2 complex facilitates lipid droplet expansion at the ER-lipid droplet interface. The Journal of Cell Biology. 2012;198(5):895–911. doi: 10.1083/jcb.201201139. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Brenner S. The genetics of Caenorhabditis elegans. Genetics. 1974;77(1):71–94. doi: 10.1093/genetics/77.1.71. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Avila D., Helmcke K., Aschner M. The Caenorhabiditis elegans model as a reliable tool in neurotoxicology. Human & Experimental Toxicology. 2012;31(3):236–243. doi: 10.1177/0960327110392084. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Guo Y., Yang Y., Wang D. Induction of reproductive deficits in nematode Caenorhabditis elegans exposed to metals at different developmental stages. Reproductive Toxicology. 2009;28(1):90–95. doi: 10.1016/j.reprotox.2009.03.007. [DOI] [PubMed] [Google Scholar]
  • 23.Raizen D., Song B.-m., Trojanowski N., You Y.-J. Methods for measuring pharyngeal behaviors. 2005. [DOI] [PMC free article] [PubMed]
  • 24.Yesmin M. N., Uddin S. N., Mubassara S., Akond M. A. Antioxidant and antibacterial activities of Calotropis procera Linn. American-Eurasian Journal of Agricultural & Environmental Sciences. 2008;4:550–553. [Google Scholar]
  • 25.Malheiros C. K. C. Avaliação Preliminar In Vitro do Potencial Antioxidante e da Toxicidade de Ceiba Speciosa (a. St.-hill) Ravenna (paineira) 2014.
  • 26.Azadmanesh J., Borgstahl G. E. O. A review of the catalytic mechanism of human manganese superoxide dismutase. Antioxidants. 2018;7(2):p. 25. doi: 10.3390/antiox7020025. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Younus H. Therapeutic potentials of superoxide dismutase. International Journal of Health Sciences. 2018;12(3):88–93. [PMC free article] [PubMed] [Google Scholar]
  • 28.Soto-Garcia M., Rosales-Castro M., Escalona-Cardoso G. N., Paniagua-Castro N. Evaluation of hypoglycemic and genotoxic effect of polyphenolic bark extract fromQuercus sideroxyla. Evidence-Based Complementary and Alternative Medicine. 2016;2016:7. doi: 10.1155/2016/4032618.4032618 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Mota M., Banini B. A., Cazanave S. C., Sanyal A. J. Molecular mechanisms of lipotoxicity and glucotoxicity in nonalcoholic fatty liver disease. Metabolism. 2016;65(8):1049–1061. doi: 10.1016/j.metabol.2016.02.014. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Liu C., Hao Y., Yin F., Zhang Y., Liu J. Geniposide protects pancreatic β cells from high glucose-mediated injury by activation of AMP-activated protein kinase. Cell Biology International. 2017;41(5):544–554. doi: 10.1002/cbin.10758. [DOI] [PubMed] [Google Scholar]
  • 31.Overman M. J., Pendleton N., O'Neill T. W., et al. Glycemia but not the metabolic syndrome is associated with cognitive decline: findings from the European Male Ageing Study. The American Journal of Geriatric Psychiatry. 2017;25(6):662–671. doi: 10.1016/j.jagp.2017.02.004. [DOI] [PubMed] [Google Scholar]
  • 32.Schlotterer A., Kukudov G., Bozorgmehr F., et al. C. elegans as model for the study of high glucose- mediated life span reduction. Diabetes. 2009;58(11):2450–2456. doi: 10.2337/db09-0567. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Lee S. J., Murphy C. T., Kenyon C. Glucose shortens the life span of C. elegans by downregulating DAF-16/FOXO activity and aquaporin gene expression. Cell Metabolism. 2009;10(5):379–391. doi: 10.1016/j.cmet.2009.10.003. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Schulz T. J., Zarse K., Voigt A., Urban N., Birringer M., Ristow M. Glucose restriction extends Caenorhabditis elegans life span by inducing mitochondrial respiration and increasing oxidative stress. Cell Metabolism. 2007;6(4):280–293. doi: 10.1016/j.cmet.2007.08.011. [DOI] [PubMed] [Google Scholar]
  • 35.Zahan R., Nahar L., Haque M., Nesa M. L., Alam Z. Antioxidant and antidiabetic activities of Alangium salvifolium and Bombax ceiba. Dhaka University Journal of Pharmaceutical Sciences. 2015;12(2):159–163. doi: 10.3329/dujps.v12i2.17617. [DOI] [Google Scholar]
  • 36.Majeed A., El-Sayed A. A., Khoja T., Alshamsan R., Millett C., Rawaf S. Diabetes in the Middle-East and North Africa: an update. Diabetes Research and Clinical Practice. 2014;103(2):218–222. doi: 10.1016/j.diabres.2013.11.008. [DOI] [PubMed] [Google Scholar]
  • 37.Fofie C. K., Nguelefack-Mbuyo E. P., Tsabang N., Kamanyi A., Nguelefack T. B. Hypoglycemic properties of the aqueous extract from the stem bark of Ceiba pentandra in dexamethasone-induced insulin resistant rats. Evidence-Based Complementary and Alternative Medicine. 2018;2018:11. doi: 10.1155/2018/4234981.4234981 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Satyaprakash R., Rajesh M., Bhanumathy M., et al. Hypoglycemic and antihyperglycemic effect of Ceiba pentandra l. gaertn in normal and streptozotocin-induced diabetic rats. Ghana Medical Journal. 2013;47(3):121–127. [PMC free article] [PubMed] [Google Scholar]
  • 39.Ladeji O., Omekarah I., Solomon M. Hypoglycemic properties of aqueous bark extract of Ceiba pentandra in streptozotocin-induced diabetic rats. Journal of Ethnopharmacology. 2003;84(2-3):139–142. doi: 10.1016/S0378-8741(02)00321-5. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Supplementary Materials

The supplementary material includes the graphical abstract of the manuscript.

Click here for additional data file. (319.1KB, pdf)

Data Availability Statement

All authors declare the availability of the use of data from this manuscript by the journal Antioxidants and Prooxidants: Effects on Health and Aging 2020.

Articles from Oxidative Medicine and Cellular Longevity are provided here courtesy of Wiley

RESOURCES