Introduction
Humans have used traditional medicine (TM) ancestrally. Some people use it as the mainstay of healthcare delivery and others as complementary medicine (CM). 1 Nearly 80% of the world’s population relies on TM and plant-derived drug compounds to improve health, as opposed to licensed conventional medicines (40%). 2 Herbal medicine practices are usually not supported by studies on their effectiveness or safety, and there are concerns about the potential risks involved in their use. Reference Bernstein, Akram, Yaniv-Bachrach and Daniyal3 For this reason, the WHO Traditional Medicine Strategy 2014–2023 was created to set the course for TM and CM. 1 In Mexico, we have around 4,500 medicinal plant species, and many of them are recognized and used by ∼ 90% of the general population. Approximately 85% of healthcare professionals know about herbal medicines, and ∼ 75% recommend their use. Reference Cabada-Aguirre, López López, Mendoza, Garay Buenrostro, Luna-Vital and Mahady4
Pregnant women make use of TM for several reasons: lack of fetal turning, overdue delivery, breech pregnancy and false labor, morning sickness, abdominal pain, constipation, heartburn, dirty or air-filled uterus, sexually transmitted diseases, and high blood pressure. Reference Peprah, Agyemang-Duah and Arthur-Holmes5,Reference Peltzer6 Holst et al. Reference Holst, Wright, Haavik and Nordeng7 found that more than 50% of the pregnant women they studied used herbal remedies.
Bocconia frutescens L. is a plant native to tropical America, where it is commonly known as gordolobo, guauchilli, palo amarillo de México, llora sangre, mano de león, palo santo Reference Sánchez-Arreola, Hernández-Molina, Sánchez-Salas and Martínez-Espino8 , or boconnia, parrotweed, plume poppy, sea oxeye daisy, tree poppy, and tree celandine. The infusion of its leaves has been traditionally used in extensive parts of the American continent for the treatment of gastrointestinal disorders, skin ulcers, dermatitis, some respiratory tract infections, and tuberculosis. Reference Velázquez, Calzada, Torres, Gonzáles and Ceballos9,Reference Yu, Gao and Zhu10 Additionally, in rats, B. frutescens L. exhibited potent antidiarrheal activity9 and reduced peristalsis activity. Reference Calzada, Arista and Pérez11
Phytochemical analyses of B. frutescens L. have detected high levels of saponins and coumarins, as well as flavonoids, sesquiterpene lactones, alkaloids, Reference Yu, Gao and Zhu10 and cardiotonic in chloroformic, ketonic, and ethanolic extracts, whereas tannins and sterols were not detected. The effects of consuming some metabolites such as alkaloids during pregnancy must be evaluated since exposure to these compounds may cause defects in developing embryos and fetuses. Reference Green, Lee, Panter and Brown12-Reference Laines-Hidalgo, Muñoz-Sánchez, Loza-Müller and Vázquez-Flota16 In fact, in a previous study, we showed that orogastric consumption of B. frutescens L. at concentrations equivalent to those used for human consumption Reference Calzada, Arista and Pérez11 during the organogenesis period produces teratogenic effects, including external (umbilical hernia and growth retardation) and internal alterations (central rib ossification). Reference Lunagómez, Santiago-Roque, Gheno-Heredia, Corona-Morales and Bolado-García17
In addition, during gestation, external factors such as inadequate maternal diet and exposure to pollutants and toxins significantly affect the development of the fetal nervous system and may therefore increase the risk of neurodevelopmental/psychiatric disorders. Reference Marques, Bjørke-Monsen, Teixeira and Silverman18,Reference Naik, Patro and Patro19 It is unknown whether consumption of B. frutescens L. during pregnancy alters the neurodevelopment of the progeny. Given that maturation of neurological reflexes and motor coordination are hallmarks of nervous system development, Reference Altman and Sudarshan20 in the present study, we used a battery of noninvasive tests to quantify the sensory and motor function of rat pups; these tests included measurements of physical development, reflex testing, and locomotor maturation. Reference Cárdenas, García-García, Santiago-Roque, Martínez, Coria-Ávila and Corona-Morales21 The aim of this study was to investigate the possible association between the gestational consumption of B. frutescens L. at a dose equivalent to that consumed by humans and the neurological development of rat progeny.
Materials and method
Plant material
Leaves of B. frutescens L. (Papaveraceae family) were collected in Ixhuatlancillo, Veracruz-México (18° 53′ 32″ N, 97° 8′ 51″ W), in June 2017. Plant material was collected by S. Delgado Rodríguez no. 510, and the exsiccate was deposited at the herbarium of the Biological Research Institute, Universidad Veracruzana, under no. 25585UV. In this study, we used a wild plant collected from the ecotone between tropical and temperate zones, and our work posed no risk toward this species. During the collection, we carefully collected a small amount of leaves so as not to cause any damage to the plants.
Preparation of extract
Plant material was dried in an oven at 35°C–40°C for a period of 72 h and ground in a conventional mechanical mill until a fine powder was obtained. The powdered plant material (50 g) was then macerated for 72 h with 300 ml of reagent-grade hexane at room temperature and protected from light for a week. The solvent was removed at reduced pressure using a rotary evaporator (Heidolph Laborota 4001) at 35°C–40°C to obtain a green oily residue. This residue was dried in a vacuum oven (Thermo Scientific) to constant weight (0.4 g) with a yield of 0.8%, and the recovered plant material was macerated in 96% methanol (300 ml) for 72 h and protected from light at room temperature. The methanol was removed in a rotary evaporator (Heidolph Laborota 4001) at reduced pressure to obtain a green oily residue which was dried in a vacuum oven (Thermo Scientific) to constant weight (1.3 g) with a yield of 2.6%. Subsequently, the product was lyophilized (lyophilizer Labconco, USA) at −50°C, pressure 0.002 bar, to obtain the plant extract. For administration to the animals, the extract was diluted in canola oil (Capullo®) heated at 50°C as a vehicle.
Proton nuclear magnetic resonance (1H-NMR) spectroscopy
The 1H-NMR data was recorded on an Agilent Technologies Model DD2 nuclear magnetic resonance spectrometer at 25.0°C, operating at a proton NMR frequency of 500 MHz. For this process, 30 mg of the extract was dissolved in 0.6 ml methanol-d4 (99.8% D, Sigma-Aldrich Co., St Louis, MO, USA). The parameters consisted of 64 scans and relaxation time = 2 s. A pre-saturation sequence was used to suppress the residual H2O signal with low selective irradiation power at the H2O frequency during the recycling delay. Prior to the Fourier transform, a line broadening factor of 0.3 Hz was applied to the free induction decay data. Tetramethylsilane 0.00 parts per million was used as a reference, and NMR data were processed using MestReNova v12.0.4 software (MestreLab Research SL). The presence of alkaloids and flavonoids was detected by comparison with previously reported studies.
Animals and experimental design
The experiments were carried out with Wistar rats from the Animal Facility in the Health Sciences Unit, Universidad Veracruzana. All procedures described here fully complied with the National Guidelines for Production, Care, and Use of Laboratory Animals (Norma Oficial Mexicana NOM-062-ZOO-1999) and followed the ethical principles of animal care based on the international standards. 22
Virgin female Wistar rats, weighing 200 ± 10 g, were housed in polypropylene cages (32 × 47 × 20 cm), with a stainless-steel wire cover. The cages containing a bed of pine shaving and a maximum of five animals per cage were kept in a temperature-controlled room (22°C ± 2°C) with a 12/12-h light/dark cycle. The rats had free access to food (Rodent Lab Chow 5001®, Purina) and water.
After a two-week period of habituation to laboratory conditions, the rats were mated with sexually experienced males. We considered gestational day 0 the day that sperm cells appeared in a vaginal smear. Pregnant animals were housed individually and randomly assigned to the control group (Ctrl, n = 7) or the B. frutescens L. group (Bocf, n = 7). Bocf females were administered lyophilized extract of B. frutescens L. in a single orogastric dose of 300 mg/kg/day, using an adapted intravenous catheter of 16G × 47 mm. Given that no toxicity studies for rats have been reported with this extract, we decided on a dose of 300 mg/kg/day, which is closely equivalent to one cup of B. frutescens L. used by Mexican and Central American people in infusions or decoctions taken three times/day for the treatment of gastrointestinal disorders such as diarrhea. Reference Calzada, Arista and Pérez11 This dose also corresponds to that used in studies with animal models. Reference Velázquez, Calzada, Torres, Gonzáles and Ceballos9,Reference Calzada, Arista and Pérez11
Ctrl rats were administered only canola oil orogastrically. We administered B. frutescens L. extract or vehicle from day 7 to day 13 of gestation, which constitutes the period of organogenesis. The body weight of each mother was recorded on gestational days 0 and 21.
Assessment of pup development
Litter features and physical development
The weight of each litter was recorded at birth, as well as the number of pups per litter. The days each pup opened both eyes and their two incisors erupted were also recorded.
Sensorimotor maturation and reflex testing
One day after parturition, entire litters were removed from their does and one male and one female pup from each litter were randomly selected, marked, and individually tested in a different temperature-controlled room (32°C ± 2°C), with a very low level of ambient noise. At the end of the daily tests (3–5 min), the two selected pups per litter were returned to the litter and then simultaneously returned to the respective doe cage. Tests included auditory startle, grasp reflex, negative geotaxis, inclined board, and righting reflex; Reference Cárdenas, García-García, Santiago-Roque, Martínez, Coria-Ávila and Corona-Morales21 all tests were conducted blindly by the same researcher.
a) Auditory startle
A clicker was used at a distance of 30 cm above each pup, and we observed if the animal displayed a startle response immediately after the click. The day of appearance of this reflex was recorded.
b) Grasp reflex
Each pup was held in the air, and the forelimbs were gently stroked with a thin rod. The reflex was considered present when the animal closed the stimulated paw around the rod, and the first day of grasping was recorded.
c) Negative geotaxis
Each pup was placed on an inclined board with its head facing downward. The time taken for the pup to turn around 180° to put its head upward was recorded. If the pup took longer than 60 s, the test was stopped and recorded as 60 s. From postnatal day (PD) 1 to 10, the board had an inclination of 20° and from PD 11 to 17, an inclination of 50°.
d) Inclined board test
For this test, we used a wooden board with a previously graduated inclination scale. In the beginning, pups were placed on the inclined board with their head facing upward at an angle of 20°. Every 5 s, the board inclination was elevated by 5°, and the maximum angle the pup maintained its position on the board was recorded. The test was carried out daily from PD 10 to 21.
e) Righting reflex
Each pup was placed in the supine position, with the dorsum of its head and trunk in contact with the surface. The time taken for the pup to turn around its longitudinal axis and to put its four paws in contact with the surface was recorded. If the pup took longer than 120 s, the test was stopped and recorded as 120 s. This test was carried out daily from PD 1 to 10.
Statistical analysis
The body weight of each mother (difference between gestational day 0 and day 21) and the number of pups per dam were analyzed using Student’s t-tests. Temporal comparisons of pup weight, righting reflex, negative geotaxis, and inclined board between groups were analyzed using a generalized linear model with a design of a repeated measures factor (day) across testing sessions and comparison between treatment and sex. Since there was no difference in pup weight between females and males (F 1,24 = 0.67, p = 0.4), data of pups from the same litter were pooled, and the factor sex was excluded for statistical parsimony of the repeated measures models. Two-way Analysis of Variance (ANOVA) model analyses were applied for eye opening, incisor eruption, auditory startle, and grasp reflex, variables that only had a single record in the study subjects. In addition, we estimated Cohen’s d for the variables number of pups, eye opening, incisor eruption, auditory startle, and grasp reflex to measure the effect size. The data were tested previously for homogeneity and normality of variances and rank-transformed when necessary, Reference Conover and Iman23 and the results were expressed as mean ± standard error (SE). Differences between groups were considered statistically significant at α = 0.05. All statistical analyses were performed using JMP Pro 14.0.0 (SAS Institute, Inc. Cary, NC, USA, 1989–2014).
Results
Body weight gain during gestation of Ctrl and Bocf females was similar (Ctrl: 33.77 ± 5.31 SE, Bocf: 24.46 ± 5.31 SE, t-test = −1.24, p = 0.87). Also, days of gestation did not differ between Ctrl and Bocf groups (Ctrl: 22.71 ± 0.12 SE, Bocf: 22.71 ± 0.12 SE, t-test = 0.1, p = 0.5). However, Ctrl dams had more pups per litter than Bocf mothers (t-test = 3.63, p = 0.003; Fig. 1). Even so, Ctrl pups were heavier at birth than Bocf pups, and the difference increased during lactation (Table 1 and Fig. 2a). Differences in the physical development of the pups were also evident in eye opening and incisor eruption. In both variables, the offspring of the Bocf group showed a delay of more than 2 d with respect to the control group (Table 2 and Fig. 3a, b). In both cases, we found a very large Cohen’s d between the Ctrl and Bocf groups (Fig. 3).
Figure 1. Number of pups per dam. Independent student t-test was performed. Values represent the mean ± SE, and size of the effect is indicated with Cohen distance.
Figure 2. Pup weight, negative geotaxis, inclined board, and righting reflex. Pup weight between control (Ctrl) and B. frutescens L. (Bocf) groups (a). Effect of the Bocf treatment on daily performance in negative geotaxis 20° at PD 1 to 10 and 50° at PD 11 to 17. Latency refers to the time taken by the pup to turn around 180° to put its head upward (b). Effect of the Bocf treatment on daily pup performance in the inclined board test. The maximum angle of the position the pup maintained on the board is presented (c). Effect of the Bocf treatment on daily pup performance in the righting test. Latency refers to the time taken by the pup to turn around its longitudinal axis from a supine to a prone position (d). PD: postnatal day. The values represent the mean ± SE.
Figure 3. Appearance day of physical and sensory-motor development indexes of the control (Ctrl) and B. frutescens L. (Bocf) groups. Eye opening (a). Incisor eruption (b). Auditory startle (c). Grasp reflex (d). Values represent the mean ± SE, and the size of the effect is indicated with Cohen distance.
Table 1. Variation source of repeated measures ANOVA for pup weight and reflex tests
DF, Degrees of freedom; F, Fisher’s test in ANOVA. Values with asterisks represent *p < 0.05, **p < 0.01, ***p < 0.001.
Table 2. Variation source of two-way ANOVA for eye opening, incisor eruption, and reflex tests
DF, Degrees of freedom; F, Fisher’s test in ANOVA. Values with asterisks represent ***p < 0.001.
We tested pups for negative geotaxis with a board inclined 20° from PD 1 to 10 and from PD 11 to 17 with an inclination of 50°. We found significant differences between groups; the offspring of the Bocf group took longer to turn 180° (Table 1 and Fig. 2b).
In the inclined board test, there were significant differences between groups, showing that Bocf pups had less strength to maintain their position on the inclined board from PD 11 to 14 (Table 1 and Fig. 2c).
The righting reflex test showed a better ability of Ctrl pups to turn around their longitudinal axis since birth. During the first 3 PD, Bocf pups took more time to complete the test, and it was not until the fourth PD that both groups recorded similar latencies (Fig. 2d). The statistical analysis revealed a significant group effect (Table 1).
We also recorded the day of appearance of the auditory startle and grasp reflex. Like our findings with eye opening and incisor eruption, Bocf pups exhibited the appearance of the auditory and grasp reflexes 2 d later than Ctrl pups (Table 2 and Fig. 3c, d). For both reflexes, we found a large effect size between Ctrl vs Bocf animals when estimated by Cohen’s d.
Finally, 1H-NMR analysis showed signals for both flavonoids and alkaloids in the B. frutescens L. extract (Fig. 4).
Figure 4. 1H-NMR spectrum (500 MHz) of Bocconia frutescens L. extract δ 0.00–8.5 ppm. The amplified region corresponds to the aromatic region (δ 6.5–8.5 ppm).
Discussion
Previously, we reported the teratogenic effects of B. frutescens L. in rats. Reference Lunagómez, Santiago-Roque, Gheno-Heredia, Corona-Morales and Bolado-García17 Now, our results demonstrate that the orogastric consumption of its extract at concentrations equivalent to those of human consumption during pregnancy may compromise the neural development of the progeny.
B. frutescens L. administration decreased the number of pups per litter and the weight of the pups. The causes of these effects are not clear; however, there are other medicinal plants whose consumption during pregnancy causes similar effects; for example, the administration of St John’s wort (Hypericum perforatum L.) in experimental animals is associated with low birth weight. Reference Dugoua, Mills, Perri and Koren24
Eye opening and incisor eruption occurred 2 d later in Bocf pups. Accordingly, delayed eye opening and incisor eruption have been described in neurotoxicity studies. For example, in Sprague-Dawley rats exposed to inorganic arsenic. Reference Moore, Flanigan and Law25 Moreover, there are also reports of developmental delays in rat offspring when exposed to caffeine Reference Nehlig and Debry26 or alcohol Reference Thomas, Abou and Dominguez27 or fed a high-fat diet. Reference Giriko, Andreoli and Mennitti28 Furthermore, there are a few studies showing developmental delays associated with medicinal plants, for example, Mauritia flexuosa L. f., a palm tree native to the South American Amazon rainforest commercialized as medicine; Medeiros et al. Reference Medeiros, Aquino and Soares29 reported negative impacts on the growth and maturation of neonatal rats after its consumption and attributed it to essential fatty acids and vitamins present in the plant.
Phytochemical analyses of B. frutescens L. have detected the presence of alkaloids, and the exposure of a developing embryo or fetus to these alkaloids from plants, plant products, or plant-derived extracts has the potential to cause developmental alterations. Reference Green, Lee, Welch and Panter13 For example, swainsonine, an indolizidine alkaloid, is the principal toxic component of leguminous plants of the Astragalus genus. It stimulates neurologic symptoms inducing neuron apoptosis through a death receptor pathway and endoplasmic reticulum stress. Reference Lu, Ma, Zhang, Wang, Wu and Zhao30 Ibogaine, a psychoactive indole alkaloid characteristic of the shrub Tabernanthe iboga, may cause neurodegeneration in rats, probably mediated by stimulation of the inferior olive, Reference Litjens and Brunt31 which coordinates spinal cord signals to regulate motor coordination.
An 1H-NMR comparison of different samples of Mexican gordolobo showed characteristic signals for flavones gnaphaliin A, gnaphaliin B, araneol, and 3,5,7-Tri-O-methylgalangin. Reference Ontiveros-Rodríguez, Serrano-Contreras, Villagómez-Ibarra, García-Gutiérrez and Gerardo Zepeda-Vallejo32 Additionally, the extract produced signals related to those reported for flavonoids and phenolic compounds in the aromatic region (δ 6.5–8.5 ppm). It is important to note that the presence of benzophenanthridine alkaloids such as chelerythrine, sanguilutine, sanguirubine, chelirubine, chelilutine, sanguinarine, nitidine, and fagaronine have also been reported in the aromatic region. Reference Sečkářová, Marek, Dostál, Dommisse and Esmans33 In the present study, we observed signals for both flavonoids and alkaloids in the B. frutescens L. extract by 1H-NMR analysis. Benzophenanthridine alkaloids have been reported to possess cytotoxic effects by affecting DNA replication and cell cycle arrest. Specifically, sanguinarine, a quaternary benzophenanthridine alkaloid, can induce fragmentation of DNA, Reference Laines-Hidalgo, Muñoz-Sánchez, Loza-Müller and Vázquez-Flota16,Reference Singh and Sharma34 and there is evidence in vivo and in vitro that it may cause negative effects on mouse embryonic development, both pre- and postimplantation, via dietary intake. Reference Chan35
As we mentioned previously, B. frutescens L. also contains coumarins, which induce developmental delay in the offspring of female mice who received a toxic isocoumarin, ochratoxin A, which is derived from Aspergillus ochraceus and several Penicillium species. Reference Poppe, Stuckhardt and Szczech36
The potential danger of environmental factors during intrauterine development is of particular concern because of its irreversible nature. Although herbs are natural, not all are safe to be ingested during pregnancy. It is necessary to determine the chemical components and mechanism of action of traditional plants before recommendation.
Acknowledgments
We are grateful to María Elizabeth Márquez López from the School of Chemical Sciences in Orizaba (Universidad Veracruzana) for collecting Bocconia frutescens L. and obtaining the extract.
The authors thank Diane Fumiko Miyoshi for her assistance with English.
The authors are entirely responsible for the scientific content of the paper.
Financial support
This research was financed through grant PRODEP PTC-812 (VEBG). This funding source was not involved in the study design, data collection, analysis or interpretation, writing the manuscript, or the decision to submit it for publication.
Competing interests
None.
Ethical standard
The authors assert that all animal procedures contributing to this work were strictly in accordance with the ethical standards of the relevant national guidelines on the care and use of laboratory animals (Norma Oficial Mexicana NOM-062-ZOO-1999) and has been approved by the Animal Use Ethics Institutional Committee (Comité Interno para el Cuidado y Uso de Animales de Laboratorio del Instituto de Ciencias de la Salud CICUAL-ICS), under the number 2020-003. Furthermore, this study was conducted according to ARRIVE guidelines Reference du Sert, Hurst and Ahluwalia37 and international standards. 22
