Developmental lead (Pb)-induced deficits in hippocampal protein translation at the synapses are ameliorated by ascorbate supplementation.

BACKGROUND: Lead (Pb) is a persistent environmental neurotoxin and its exposure even in minute quantities has been known to induce neuronal defects. The immature brain is singularly sensitive to Pb neurotoxicity, and its exposure during development has permanent detrimental effects on the brain developmental trajectory and neuronal signaling and plasticity, culminating into compromises in the cognitive and behavioral attributes which persists even later in adulthood. Several molecular pathways have been implicated in the Pb-mediated disruption of neuronal signaling, including elevated oxidative stress, alterations in neurotransmitter biology, and mitochondrial dysfunction. Nevertheless, the neuronal targets and biochemical pathways underlying these Pb-mediated alterations in synaptic development and function have not been completely deduced. In this respect, recent studies have shown that synaptic signaling and its maintenance and plasticity are critically dependent on localized de novo protein translation at the synaptic terminals.
MATERIALS AND METHODS: The present study hence aimed to assess the alterations in the synapse-specific translation induced by developmental Pb exposure. To this end, in vitro protein translation rate was analyzed in the hippocampal synaptoneurosomal fractions of rat pups pre- and postnatally exposed to Pb using a puromycin incorporation assay. Moreover, we evaluated the therapeutic effects of ascorbic acid supplementation against Pb-induced deficits in synapse-localized protein translation.
RESULTS: We observed a significant loss in the rates of de novo protein translation in synaptoneurosomes of Pb-exposed pups compared to age-matched control pups. Interestingly, ascorbate supplementation lead to an appreciable recovery in Pb-induced translational deficits. Moreover, the deficit in activity-dependent synaptic protein translation was found to correlate significantly with the increase in the blood Pb levels.
CONCLUSION: Dysregulation of synapse-localized de novo protein translation is a potentially critical determinant of Pb-induced synaptic dysfunction and the consequent deficits in behavioral, social, and psychological attributes of the organisms. In addition, our study establishes ascorbate supplementation as a key ameliorative agent against Pb-induced neurotoxicity.

Introduction

Widespread industrial use of lead (Pb), a naturally occurring toxic heavy metal, has resulted in an elevated risk of its exposure in both animals and humans, making it a prominent environmental and occupational health hazard.1,2 In spite of measures to limit its use and contain its exposure, Pb remains a high-risk environmental toxin and a major threat to public health, particularly in developing countries.1 Several factors are responsible for this. First, Pb exposure can occur through contaminated air, water as well as food. Second, exposure of almost all forms of Pb (metallic, organic, and inorganic) is toxic.2

The nervous system constitutes as a prominent target of Pb toxicity which is evident by behavioral abnormalities, neuromuscular disabilities, and cognitive deficits in events of Pb exposure.2–4 Of note, exposure to even low levels of Pb, previously thought to be permissible, can be neurotoxic and have deleterious and irreversible cognitive and psychological outcomes.5–8 Brain functions including higher order sensory motor, cognitive and behavioral functions rely principally on the inter-neuronal communication at the synapses.9,10 Deleterious effects of Pb exposure on synapse function and their maintenance and plasticity have been confirmed by many studies7,11,12 and seem to involve alterations in several intricate interacting physiological processes including redox homeostasis, mitochondrial functions and dynamics, and signaling of calcium and other secondary messenger molecules, transcription and gene expression, membrane biophysics, neurotrophic signaling, neurotransmitter synthesis, and release and biology of their receptors.7,13

The developing nervous system is particularly vulnerable to early life lead exposure.14 Pb-induced changes in the synaptic functions during brain development have dire consequences on the function and plasticity of the brain,7,14,15 culminating into permanent alterations in higher order brain functions, including sensory motor, cognitive and social attributes as well as response to psychological stressors.5,16,17 Hence, a thorough assessment of the molecular and cellular players involved in synaptic dysfunction induced by developmental Pb exposure in the developing nervous system is warranted. Among several mechanisms implicated in maintenance and plasticity of proper synaptic signaling, the role of localized de novo protein translation is only beginning to be appreciated.18–21 In addition to the tightly controlled target mRNA transport to the synapses, presence of a functional translational machinery at the synaptic terminals empowers individual synapses to regulate the strengths of their signaling independently. Of note, changes in the synaptic proteome can be robustly induced by neuronal activity in part by alterations in the protein translation profiles.20,22 Consequently, localized protein translation at the synapses plays an important role in the proper re-configuration of neuronal circuitry in events of neuronal depolarization.18,20–23 In view of the critical roles of localized protein translation in the regulation of their function, maintenance and plasticity, alterations in synaptic protein translation are increasingly being perceived as major contributors to neuropathological outcomes in a wide variety of neurological disorders.20,24–28

In this study, we analyze the effects of early life Pb exposure on synapse-localized de novo protein translation in the rat hippocampus. The hippocampus is a limbic structure that is closely involved in learning and memory function. As such, neuronal circuitry of the hippocampi is particularly susceptible to activity-dependent alterations in synaptic strength. In fact, the best known mechanisms of activity-dependent neuronal plasticity, long-term potentiation, and long-term depression have been extensively characterized in the hippocampus and are implicated as potential mechanisms underlying the higher order brain functions, such as learning and memory, the formation and modification of cognitive maps, and the ability of organisms to react to stressful experiences.29 Of note, several recent studies have implicated dysfunction at the hippocampal circuitry as among the most critical mechanisms that govern brain deficits induced by Pb neurotoxicity.7,13,30–34

The present study also assesses the therapeutic effects of supplementation of ascorbic acid or vitamin C in preventing the Pb-induced alterations in the hippocampal synaptic protein translation. Ascorbic acid is a water soluble vitamin and has been shown to have tremendous neuromodulatory and neuroprotective properties in several neuropathologies, including ethanol-induced neuroinflammation, cerebral ischemia, oxidative damage, excitotoxicity, kainate-induced seizures as well as neuropsychiatric diseases.35–39 Neuroprotective effects of ascorbate supplementation in heavy metal toxicity are also well documented and stem from a multifaceted array of therapeutic mechanisms including metal chelation, antioxidant and anti-apoptotic actions, and modulation of neurotransmitter signaling.37,40,41 In particular, therapeutic effects of ascorbate in the events of Pb exposure and toxicity have been well-documented by a number of groups.42–47 Of note, our recent study has shown appreciable recovery of early life Pb-induced synapse-specific mitochondrial bioenergetic defects by ascorbate supplementation.48

Materials and methods

Chemicals, reagents, and antibodies

Puromycin dihydrochloride (CAS no. 58-58-2) and chloramphenicol (CAS no. 56-75-7) were procured from Millipore Merck (Billerica, MA, USA). Protease and phosphatase inhibitor cocktails were from Thermo Fisher Scientific (product no. 1861748; Waltham, MA, USA) and Sigma-Aldrich Co. (catalog no. P5726; St Louis, MO, USA). 100 µm and 10 µm nylon membrane filters were obtained from Merck Millipore (catalog nos. NY1H02500 and NY1002500, respectively). Antibodies against PSD-95 and α-tubulin were from Thermo Fisher Scientific (catalog nos. MA1046 and 322500, respectively). The antibody against puromycin was procured from Merck Millipore (catalog no. MABE341). The horse-radish peroxidase-linked secondary antibodies against rabbit (catalog no. 31460) and mouse immunoglobulin G (catalog no. 31430) were from Thermo Fisher Scientific. Clarity™ Western ECL substrate was obtained from Bio-Rad Laboratories Inc. (catalog no. 170-5061; Hercules, CA, USA). All other chemicals purchased were of analytical grade and from either Merck Millipore or Sigma-Aldrich Co.

Animals and experimental paradigms

All experiments involving animals were carried out in accordance with the institutional guidelines for animal care and use for scientific research and after approval by the institutional review board, Imam Abdulrahman Bin Faisal University, Dammam. The experimental paradigm of pre- and postnatal lead exposure and ascorbate supplementation employed has been previously reported by us.48 In brief, female Wistar rats were housed in cages with sexually mature males (2:1; male to female ratio) under a light/day 12/12 hours regime in rooms with a controlled temperature of 25°C. Food chow and drinking water were provided ad libitum. At gestation day 15 (GD15), the pregnant females were randomly divided into four groups: Ctrl (control), Pb (lead), Pb+Asc (lead and ascorbic acid) and Asc (ascorbic acid). Dams of the Ctrl and Asc groups were provided with normal drinking water and Pb and Pb+Asc groups received 0.2% lead acetate (2,000 ppm) in drinking water from GD15 until the day of weaning of pups at postnatal day 21 (P21). Mothers of Pb+Asc and Asc groups were provided with 500 mg/kg body weight of ascorbic acid using an oral gavage from GD15 until weaning of pups (P21). Treatment with ascorbic acid and/or lead acetate was stopped immediately after weaning of the pups. To abrogate the effects of gender-specific responses and outcomes to early life Pb exposure particularly in the hippocampus,49–52 only male pups were randomly selected from each group for the study and sacrificed at P30. This model of oral Pb administration in drinking water has been widely employed as it is thought to mimic the environmental exposure to this heavy metal.34,53–55

Measurement of blood Pb levels

Digestion of blood obtained immediately before sacrificing the rat pups was performed as described by Chaurasia et al with slight modifications.56 Briefly, blood (0.5 mL each sample) was digested in 5 mL of a nitric acid-perchloric acid solution (ratio of concentrated HNO3:HClO4 was 1:6) at 110°C for 1 hour. After filtering through a Whatman filter paper no. 41, the digested blood was analyzed for Pb levels by using an iCAP 6300 Duo inductively coupled plasma optical emission spectrometer (ICP-OES; Thermo Fisher Scientific).

Isolation of synaptoneurosomes

A protocol involving sequential filtration steps was employed for biochemical isolation of synaptoneurosomes. This method was chosen because it has been shown to be suitable for studying in vitro protein translation by us and others.24,27,57–59 Briefly, the hippocampi isolated from the pups were homogenized using a Potter-Elvehjem tissue grinder (Kimble, Rockwood, TN, USA) in 10× volume of ice-cold translation buffer (118 mM NaCl, 4.7 mM KCl, 1.2 mM MgSO4, 2.5 mM CaCl2, 1.53 mM KH2PO4, 212.7 mM glucose, 1 mM 1,4-dithiothreitol (DTT), pH 7.4) supplemented with protease inhibitor cocktail, phosphatase inhibitor cocktail, 30 U/mL RNAse inhibitor, and 200 µg⋅mL−1 chloramphenicol. The homogenate (denoted as Hgt) obtained was then sequentially passed through 100 µm (twice) and 10 µm nylon membrane filters. A small part of the filtrate obtained after passing through two 100 µm filters (designated filtrate 1 or F1) was saved to assess enrichment of post-synaptic density 95 (PSD-95), a synaptic marker protein58,59 for quality-control analysis of synaptoneurosomes. The final filtrate obtained after passing through the 10 µm filter was centrifuged at 1,500× g at 4°C for 10 minutes to obtain the supernatant (denoted Sup) and the synaptoneurosomal pellet (denoted as SN). The SN pellet was resuspended in translation buffer and processed immediately for in vitro protein translation assay. A part of the resuspended SN pellet was solubilized in SDS-PAGE sample buffer (62.5 mM Tris-HCl, pH 6.8, 2% SDS, 5% 2-mercaptoethanol, 20% glycerol, and 0.0006% bromophenol blue) and stored at −20°C for immunoblotting to assess PSD-95 levels.

Stimulation of synaptoneurosomes and puromycin incorporation assay

Subcellular preparations of synaptoneurosomes obtained using the sequential filtration protocol have been shown to be a robust in vitro system for assaying local synthesis of synaptic proteins.27,57–59 Because this protocol allows preservation of both the soluble factors and the energy sources (synaptic mitochondria) in their native form in the synaptoneurosomal fractions, their addition prior to in vitro protein translation assays is not required.60 We employed a puromycin-based nonradioactive surface sensing of translation, the SUnSET method,61 for the assessment of de novo protein synthesis in the synaptoneurosomal samples. The SUnSET protocol has been previously employed by us and others24,62,63 and was chosen because of its obvious advantage over the conventional radioactivity-based 35 S-methionine incorporation assay. In brief, synaptoneurosomes were diluted in translation buffer to a concentration of 1 mg⋅mL−1 protein and preincubated at 37°C for 5 minutes. Stimulation of synaptoneurosomes was performed in the presence of 50 mM KCl and 10 µg⋅mL−1 puromycin at 37°C for 15 minutes.24,27,57,64 Unstimulated samples were incubated with 10 µg⋅mL−1 puromycin alone. Chloramphenicol in the translation buffer ensured assay of protein translation in a synapse-specific manner by inhibiting any protein translation in the synaptic mitochondria present in the synaptoneurosomal fraction.24,57,60 Following puromycin incorporation into nascent peptide chains for 15 minutes, synaptoneurosomal samples were pelleted at high speed (14,300 rpm), resuspended in SDS-PAGE sample buffer, and stored at −20°C for immunoblotting.

Immunobloting

Synaptoneurosomal and other neuronal subcellular fractions were separated using 4%–15% gradient SDS-PAGE, electroblotted onto a polyvinylidene difluoride membrane, and immunostained using appropriate primary and secondary antibodies. Immunoreactive chemiluminescent signals were detected on a ChemiDoc™ MP Imaging System (Bio-Rad Laboratories Inc.) and quantified using Image Lab software (version 5.2; Bio-Rad Laboratories Inc.).

Statistical analysis

Results are represented as mean ± standard error of the mean (SEM), unless stated otherwise, and expressed as a multiple of the control unstimulated (Ctrl US) sample for each immunoblot. The multiple groups were compared using one-way ANOVA followed by post hoc tests with Newman–Keuls correction. The correlation between the ratio of stimulated to basal protein translation and blood Pb levels was calculated using Pearson’s correlation analysis. All analyses were performed using GraphPad Prism 5 software (GraphPad Software, Inc., La Jolla, CA, USA). Data were considered significant if P<0.05.

Results

Blood Pb levels are elevated upon pre-and postnatal delivery of lead acetate to rat pups

Although there were no significant differences in the volume of water consumed between the groups, the blood Pb levels in pups of the Pb group as assessed by ICP-OES were found to be around 50-folds in excess of those in the Ctrl pups. In addition, ascorbate supplementation significantly reduced the levels of blood Pb (Figure 1), as has been previously observed in both rodent and human subjects.47,65–71 However, it still remained higher than Ctrl values.

Figure 1

Ascorbate supplementation reduces the elevation in blood Pb levels induced by chronic Pb treatment through drinking.

Notes: Significant increase in blood Pb levels of pups of the Pb group (665.5±384.6; mean ± SD) was observed when compared to those of the Ctrl group (13.07±1.332; mean ± SD). Ascorbate supplementation reduced the blood Pb levels of Pb exposed pups to 131.8±39.53 (mean ± SD). Data are represented as mean ± SEM (n=6 rats per group). *,#Statistical significance when compared to Ctrl and Pb-Asc groups, respectively (P<0.0001; F=36.27; ANOVA with Newman–Keuls correction).

Abbreviations: Asc, ascorbic acid; SEM, standard error of the mean.

Hippocampal synaptoneurosomes are enriched in PSD-95

The protein levels of PSD-95 were measured using immunoblotting for various cellular fractions to assess the level of enrichment of the synaptoneurosomal preparations obtained by the filtration method. Protein expression of PSD-95 in the synaptoneurosomes was found to be more than fourfolds greater than the starting homogenate material, indicating a robust enrichment of synaptic components (Figure 2).

Figure 2

Hippocampal SNs isolated by the sequential filtration protocol are highly enriched in PSD-95 protein.

Notes: (A) Protein levels of PSD-95, a synaptic protein marker, were analyzed by immunoblotting to estimate the purity of the SN. (B) Immunoreactivity of PSD-95 in SN was increased by 4.731±1.150 (mean ± SD) fold when compared with the initial Hgt. Sup = supernatant obtained after the centrifugation step. F1 = filtrate 1 obtained after filtration using 100 µm filters. Data are represented as mean ± SEM (n=3 independent samples from three rats). *,&,#Statistical significance in the Sup, Hgt, and F1 groups (P<0.0001; F=36.27; ANOVA with Newman–Keuls correction).

Abbreviations: Hgt, homogenate; PSD-95, post-synaptic density 95; SEM, standard error of the mean; SN, synaptoneurosome.

Ascorbic acid supplementation rescues the Pb-induced alterations in localized protein translation in the synaptoneurosomes of rat pups

Appreciable increase in the rate of de novo protein synthesis, as assessed by puromycin incorporation, was observed when synaptoneurosomes isolated from Ctrl animals were stimulated with KCl (Figure 3), as previously reported.27,57,64 However, high K+-mediated depolarization did not stimulate a similar increase in protein translation in synaptoneurosomes of Pb-exposed pups. On the other hand, Pb induced a small decrease in the basal protein translation rate; the decrease however did not reach statistical significance when compared to Ctrl basal levels. Pb-induced decrease in both basal and K+-stimulated protein translation was recovered in Pb-Asc animals (Figure 3), indicating the ameliorative effects of ascorbate supplementation in Pb-induced protein translational deficits. However, ascorbate supplementation alone did not result in any changes in basal or activity driven synaptic translation when compared to control animals (Figure S1). Interestingly, the detrimental effects of Pb toxicity on protein translation were specific to synaptosomal preparations as no alterations were observed in global protein translation rates in the homogenate samples (Figure S2).

Figure 3

Ascorbate rescues the Pb-induced deficits in localized protein translation at hippocampal synapses.

Notes: (A) De novo protein translation rate under basal and KCl-stimulated conditions in the synaptoneurosomes was evaluated using the immunoblotting-based puromycin incorporation assay. (B) While depolarization in the presence of KCl significantly stimulated protein translation in synaptoneurosomes of the pups of the Ctrl (1.615±0.3992 for stimulated compared to 1.000±0.0 for unstimulated; mean ± SD) and Pb-Asc groups (1.443±0.3342 for stimulated compared to 1.026±0.3871 for unstimulated; mean ± SD), it was ineffective in increasing the rate of translation in Pb-exposed rats (0.6641±0.2668 for stimulated compared to 0.7546±0.1227 for unstimulated; mean ± SD). In addition, Pb treatment resulted in a small but insignificant reduction in the basal translation rates in the synaptoneurosomal samples when compared to both Ctrl and Pb-Asc pups. Data are represented as mean ± SEM (n=6 rats per group). *Statistical significance between the stimulated translation and the respective basal controls and #,&Statistical significance in the decrease of stimulated translation of Pb-exposed pups when compared to stimulated translation of Ctrl and Pb-Asc pups, respectively (P<0.0001; F=10.01; ANOVA with Newman–Keuls correction).

Abbreviations: Asc, ascorbic acid; SEM, standard error of the mean; US, unstimulated; St, stimulated.

Deficits in activity-dependent protein translation correlate with the blood Pb levels of the rat pups

Reduction in localized activity-dependent protein translation in synaptoneurosomes upon exposure of Pb was confirmed when analyzing the ratio of KCl-induced puromycin and the respective unstimulated basal puromycin incorporation rates for each of animals of the three groups (Figure 4A). Lastly, the correlation between activity-driven protein translation and blood Pb levels was also analyzed. Hippocampal Pb levels were not used as a correlative measure for the Pb-mediated neurotoxic effects because of the obvious advantage of evaluating the blood Pb levels as a diagnostic measure of Pb-mediated neurotoxicity. A strong and significant correlation was observed between the loss in K+-stimulated synaptoneurosomal translation (expressed as the ratio of stimulated to unstimulated translation) and increase in blood Pb levels (Figure 4B).

Figure 4

The decrease in the ratio of stimulated to basal protein translation in synaptoneurosomes is significantly correlated with increases in blood Pb levels.

Notes: (A) Pb induced a marked reduction in the ratio of the rates of depolarization-induced KCl-stimulated protein synthesis to those of the corresponding basal (unstimulated) samples (0.8836±0.3639; mean ± SD) when compared to control values (1.615±0.3992; mean ± SD). Pb-induced reduction in the ratio of the translation rates was rescued by ascorbate supplementation (1.570±0.5975; mean ± SD). (B) Significant correlation was observed between depletion in the ratio of KCl-stimulated to basal de novo protein translation at the synapse and the increase in the blood Pb levels of the pups. Data (n=6 rats per group) were analyzed using Pearson’s correlation analysis. Data are represented as mean ± SEM (n=6 rats per group). *,#Statistical significance when compared to the Ctrl and Pb-Asc groups, respectively (P=0.0267; F=4.656; ANOVA with Newman–Keuls correction).

Abbreviations: Asc, ascorbic acid; SEM, standard error of the mean.

Discussion

Because of the presence of a still-developing blood–brain barrier, the immature nervous system is particularly vulnerable to Pb exposure.14 Importantly, early life chronic Pb exposure has been shown to induce irreversible deleterious effects on the developmental trajectory and maintenance and function of the synapses, which in turn accounts for long-term deficits in sensory motor and cognitive skills as well vulnerability to neuropsychiatric stress.5,6,29

Pb neurotoxicity is most eminent in prefrontal cortex, hippocampus, and cerebellum3 where it results in morphological, structural, and pathological alterations in neuronal cells and their synaptic connections.29,75 Because of its interference with cellular processes which require divalent cations Ca2+ and Zn2+, mechanisms of lead neurotoxicity are both multifaceted and complex.76 Nevertheless, detrimental alterations in synaptic signaling and its maintenance and plasticity are among the prime factors underlying Pb neurotoxicity.7,11,12 Although changes in neurotransmitter (glutamate) release and N-methyl-d-aspartate receptor physiology are the best known pathways implicated in Pb-induced synaptic dysfunction, a complex interplay of several factors is probably at work in synchrony. Indeed, recent studies have shed light on some of the deleterious effects of Pb on redox and calcium homeostasis, cell signaling and death pathways, and membrane receptor trafficking and gene expression as candidate mechanisms of Pb-induced synaptic dysfunction.13,14

Recent studies have suggested that localized protein translation, and particularly activity-dependent protein translation, at the synapses play critical roles in the precise control of their function and plasticity.18,19,21–23 Indeed, synaptic plasticity and its long-term consolidation are critically dependent on both explicit and dynamic changes in the spatiotemporal regulation of localized protein translation, trafficking, and organization within the micro-domain of the synaptic contacts. Localized protein translation has significant effects on the expression and function of a wide variety of critical synaptic proteins, including neurotransmitter receptors, signaling proteins, and cytoskeletal and scaffold elements.23 Furthermore, any dysfunction of the synaptic machinery for protein translation could potentially lead to behavioral and cognitive deficits.23,77,78 Despite this, the role of the dysregulation of synapse-specific protein translation in neuropathological states is only being started to be acknowledged.24,27,57,59,79–81 In view of this, the present study aimed 1) to study the alterations of de novo synaptic protein translation induced by developmental Pb exposure, if any and 2) to evaluate the capacity of ascorbate supplementation as a beneficial therapeutic strategy in mitigation of this dysregulation. Our results suggest a significant breakdown of localized protein translation machinery at the hippocampal synapses in juvenile rats pre- and postnatally exposed to Pb. Local protein translation at the synapse is regulated by several signaling cascades, Akt/mTOR and Erk/MAP kinase pathways being the two most prominent among them.23,78,82 Interestingly, dysregulation of the signaling pathways of both the kinases has been observed in the brain, possibly by the induction of oxidative stress.73,83

Interestingly, the deficits in the KCl-stimulated protein translation observed in our study correlated significantly with blood Pb levels, indicating that synaptic protein translation is a critical molecular pathway linking developmental adversities, such as Pb exposure to their detrimental effects on neuronal communication at the pre- and post-synapse. It should be noted that early life Pb exposure paradigms through drinking water similar to that used in our study are also known to cause significant accumulation of Pb in hippocampal tissues34,72,73 and show a strong and significant correlation with blood Pb levels.74 Moreover, in support of previous studies in human subjects,1,6,8,17,32,84,85 our results suggest that blood Pb levels serve as a valuable diagnostic measure of Pb-mediated dysregulation of neurological functions. In addition, while our study implicates alterations in synapse-specific protein translation as a potential mechanism underlying Pb-induced alterations in synapse maintenance, plasticity; and consequently on memory and cognition as well as vulnerability to psychological stress, it also establishes ascorbic acid as an important therapeutic agent against Pb neurotoxicity,44,45,47,48 The mechanism of ascorbate-mediated neuroprotection in Pb toxicity seems to be multifactorial, stemming from both its antioxidant properties and its Pb chelating function. Being a lactone containing an enediol group, ascorbate can form a soluble complex with Pb, enhancing its urinary excretion while also preventing its gastrointestinal absorption, and eventually lowering its blood levels and reducing its bioavailability.70,86,87

Conclusion

Our results suggest that alteration in synaptic protein translation, particularly that induced by neuronal depolarization is observed upon exposure to Pb and potentially contributes to the neurotoxic effects of this environmental toxin in the developing brain with consequent long term effects on higher order brain functions of behavior and cognition. Moreover, the study proposes the utilization of ascorbate based therapeutic measures in mitigation of Pb-induced brain toxicity.

Ascorbate supplementation alone does not alter localized protein translation at hippocampal synapses.

Notes: (A) Basal and KCl-stimulated synaptosomal protein translation was evaluated in hippocampal samples of Ctrl and Asc pups. (B) Depolarization in the presence of KCl induced an increase in the protein translation in synaptoneurosomes of the pups of the Ctrl (1.555±0.6100 for stimulated compared to 1.000±0.0 for unstimulated; mean ± SD). A similar elevation in protein translation was observed in pups supplemented with ascorbate alone (1.720±0.4584 for stimulated compared to 1.126±0.2650 for unstimulated; mean ± SD). Data are represented as mean ± SEM (n=6 rats per group). *Statistical significance between the stimulated translation and the respective basal controls (P=0.0108; F=4.778; ANOVA with Newman–Keuls correction).

Abbreviations: Asc, ascorbic acid; NS, nonsignificant; SEM, standard error of the mean; US, unstimulated; St, stimulated.

Developmental Pb exposure does not influence global protein translation in the hippocampi of rat pups.

Notes: (A) De novo global protein translation rates were assessed in hippocampal homogenate samples from the pups of Ctrl, Pb, and Pb-Asc groups. (B) No alteration in global translation was observed upon developmental exposure of pups to Pb with (0.9294±0.5748 compared to the Ctrl; mean ± SD) or without ascorbate supplementation (0.9816±0.4963 compared to the Ctrl; mean ± SD). Data are represented as mean ± SEM (n=6 rats per group) (P=0.9616; F=0.03927; ANOVA with Newman–Keuls correction).