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The Possible Link between Autism and Glyphosate Acting as Glycine Mimetic - A Review of Evidence from the Literature with Analysis | OMICS International
ISSN: 1747-0862
Journal of Molecular and Genetic Medicine
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The Possible Link between Autism and Glyphosate Acting as Glycine Mimetic - A Review of Evidence from the Literature with Analysis

Beecham JE and Stephanie Seneff *

Computer Science and Artificial Intelligence Laboratory, Massachusetts Institute of Technology, Cambridge MA 02139, USA

Corresponding Author:
Stephanie Seneff
Computer Science and Artificial Intelligence Laboratory
Massachusetts Institute of Technology
Cambridge MA 02139, USA
E-mail: [email protected]

Received Date: August 26, 2015 Accepted Date: October 06, 2015 Published Date: October 13, 2015

Citation:Beecham JE, Seneff S (2015) The Possible Link between Autism and Glyphosate Acting as Glycine Mimetic - A Review of Evidence from the Literature with Analysis. J Mol Genet Med 9:187. doi:10.4172/1747-0862.1000187

Copyright: ©2015 Beecham JE, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Abstract

The causes of autism spectrum disorder (ASD) are not well understood. Only a minority of cases are explainable by specific abnormalities in DNA sequence, whereas the majority are widely assumed to be linked to epigenetic effects, and/or likely impacted by environmental factors. Here, we postulate autism causation via environmental and/or dietary sourced toxin acting intermittently in utero on human fetuses to disrupt neurodevelopment in a nondose dependent manner. Our theory is informed by a mini-review and correlation of selected studies from the research literature related to autism, including radiologic, anatomic, metabolic, neurodevelopmental, pharmacologic and MRI studies. In reviewing and analyzing evidence, we focus on data supporting interaction of the theorized harmful glycine mimetic at one or more of the following calcium inflow regulatory factors for neurons: the N-methyl D-aspartate (NMDA) receptor, the glycine receptor (GlyR) and/or the glycine transporter protein 1 (GlyT1). We postulate this harmful glycine mimetic to act by exerting a direct molecular disruption to calcium regulatory factors for neurons. This disruption appears to occur in a time sensitive, rather than a strictly dose-dependent manner, leading to haphazard disorganizations of the normally carefully choreographed steps of early neuronal migration. Within this analysis, we find support for the contention that a strong candidate for the putative harmful glycine mimetic is glyphosate, the active ingredient in the pervasive herbicide Roundup®. In addition to glyphosate’s molecular similarity to glycine, glyphosate is known to have a propensity to avidly bind minerals such as manganese and magnesium, which minerals are implicated in the normal functioning of several neuronal calcium inflow regulatory factors. Our theory highlights areas deserving of further study.

Introduction

Since 1980, the number of children known to have autism spectrum disorder (ASD) has increased dramatically. However this increase is thought to be at least partly due to changes in diagnostic practices [1]. The risk of autism is known to be associated with advanced paternal age and with diabetes in the mother during pregnancy [2]. There is a well-known male preponderance in ASD cases [1]. Although autism is believed, by many experts, to be caused by inherited factors, no single specific DNA sequence alteration has been found to explain more than a minority of the cases.

A recent report by Yuen et al. [3] has raised questions about the subject of heritable gene defects in regard to autism causation. Because autism often runs in families, experts had assumed that siblings with the disorder were inheriting the same autism-predisposing genes from their parents. It now appears this may not be so. These researchers sequenced, from 85 families each having two children affected by autism, 340 whole genomes, including from 170 individuals with ASD. They found that the majority of autism sibling pairs (69 percent) had little to no overlap in abnormal genes. Sibling pairs shared the same autism-associated gene changes less than one third of the time (31 percent). The majority of autism-affected sibling pairs (69 percent) had little to no overlap in the gene variations thought to contribute to autism.

This raises the question whether children are developing autism from an environmental or dietary toxin for which the DNA alterations signal presence of the toxin, but wherein the genetic changes are not conferring all the autism-causing action. The possibility exists that the putative toxin is also, or perhaps principally, causing damage by interacting directly within the neurodevelopmental molecular structures and pathways of the developing brain. A candidate molecule, as will be discussed in more detail later, is glyphosate. It is noteworthy that, in a study by Koller et al. [4], human buccal epithelial cells from cell line TR146 were exposed to glyphosate alone in one test, and separately in another test using only the glyphosate-containing formulation known as Roundup®. Each test was at concentrations representing a 450-fold dilution of concentrations used in spraying crops in agriculture. Separately, in each of the two test exposures, DNA damage was found to occur in the exposed epithelial cells.

Experts, when ascribing causation in autism, often invoke epigenetic changes, citing unspecified reactions, or perhaps environmental influences [5]. Such epigenetic changes, while not modifying the DNA sequence code, are nevertheless thought to be heritable and causative, affecting early/fetal neurodevelopment [6]. Environmental causes thus have not been ruled out as causative or contributory in autism [7], and exposure to air pollution, especially particulates and heavy metals, are acknowledged to perhaps increase the risk of autism [8]. Furthermore, some cases of autism have been strongly associated with agents that cause birth defects [9], and these teratogens are widely believed to have their greatest effect within the first 8 weeks from conception.

Rzhetsky et al. [10] reported in 2014 on the results of their analysis of geographic spatial incidence patterns of ASD and Intellectual Disability (ID) as reflected in insurance claims datasets representing nearly 1/3 of the entire US population. They used “the rate of congenital malformations of the reproductive system as a surrogate for environmental exposure of parents to unmeasured developmental risk factors, including toxins” because “70 to 80% of male congenital malformations of the reproductive system have no clear genetic causes. Instead, they appear to be driven by specific environmental insults…” They found that, “Adjusted for gender, ethnic, socioeconomic, and geopolitical factors, the ASD incidence rates were strongly linked to population-normalized rates of congenital malformations of the reproductive system in males (an increase in ASD incidence by 283% for every percent increase in incidence of malformations, 95% CI: [91%, 576%], p<6×10-5)”. Their conclusions state that, in attempting to ascribe causation in cases of autism, in addition to evaluating possible chromosomal DNA sequence alterations, “detailed documentation of environmental factors should be recorded and used… and failure to do so risks omitting important information.”

To clarify theories of causation in autism, a review of selected studies was conducted and correlated, as described below.

Selected Magnetic Resonance Imaging (MRI) Studies Related to Autism

Haari et al. [11] reviewed structural MRI scans from 539 high functioning adults with autism and compared the images to structural MRI scans from 573 controls. These researchers concluded there was no evidence within their MRI images for significant between-group differences in any measures of gross anatomy or in specific brain regions, including several which had previously been implicated in anatomic studies of autism spectrum disorder (ASD), including the amygdala, hippocampus, most segments of the corpus callosum and the cerebellum.

By contrast, an MRI study by Shen et al. [12] reported it was possible to fairly reliably separate the MRI brain images of children who will go on to develop autism from controls (Figure 1). Fifty-five infants (33 'high-risk' infants having an older sibling with autism spectrum disorder and 22 'low-risk' infants having no relatives with autism spectrum disorder) were imaged at 6-9 months; 43 of these (27 high-risk and 16 low-risk) were imaged at 12-15 months; and 42 (26 high-risk and 16 low-risk) were imaged again at 18-24 months. The children were followed to determine which developed autism. The presence in the scans of increased brain volume and increased cerebrospinal fluid (CSF) accumulation was reported as predictive of subsequent development of autism, according to the researchers.

molecular-genetic-medicine-develop-autism-increased

Figure 1: Modified from Shen [12]: Illustration of MRI pattern from child (left) not destined to develop autism compared to same age child (right) destined to develop autism. Note increased brain size and CSF accumulation on the right side image.

Glial Cells in Autism

Background: The central nervous system is comprised of neurons and three basic types of glial cells: microglia, astrocytes, and oligodendrocytes. One primary function of glial cells is to support, protect, and nurture the neurons, a process that is essential for neural plasticity and stability. Microglia migrate to the central nervous system (CNS) during prenatal development and are the resident immune cells in both the brain and spinal cord. Microglia maintain vigilance for any type of toxic challenge to the CNS, including injury, infection, and ischemia. They respond with activation, into a pro-inflammatory state for example, in response to neuronal cell injury or death.

MRI study of pattern of glial cell activation in autism

Suzuki et al. [13] studied microglial activation using MRI images in a case-control study design with positron emission tomography and a radiotracer for microglia; [11C](R)-(1-[2-chrorophynyl]-N-methyl-N- [1-methylpropyl]-3 isoquinoline carboxamide) ([11C](R)-PK11195) (Figure 2). They recruited study participants from the area of Hamamatsu, Japan. Their study population consisted of Japanese citizens, twenty men with ASD (age range, 18-31 years; mean [SD] IQ, 95.9 [16.7]) and 20 age- and IQ-matched healthy men as controls.

molecular-genetic-medicine-autism-brain-microglia

Figure 2: Modified from Suzuki [13]: Illustration of MRI image pattern of control brain (left), and autism brain (right); both have same pattern of activated microglia, but degree varies, increased in autism brain.

Diagnosis of autism spectrum disorder (ASD) was made in accordance with the Autism Diagnostic Observation Schedule and the Autism Diagnostic Interview-Revised. The results focused on the amount of radiotracer activity discovered in various regions of the test subject brains as a representative measure of microglial activation in that subject. To their surprise, the pattern of brain region binding potential was essentially the same in the brains of control subjects as in the brains of autistic subjects; only the degree varied. In other words, in the autistic subjects the binding potential was higher, while maintaining the same general pattern of glial activation within brain regions as the age and IQ-matched healthy control subjects from the same area in Japan.

In Japan, glyphosate herbicides are widely used, including for weed control [14]. In addition, the country of Japan imports wheat from countries where glyphosate is sprayed onto wheat as a desiccant. Japan also imports rapeseed, for use as animal feed, from countries spraying glyphosate onto rapeseed as a desiccant. In the context of the theory herein advanced, these findings could fit the model of an environmental/dietary toxin.

Selected Microscopic Studies in Autistic Human Brains

Stoner et al. [15] examined post-mortem brain tissue from 22 children who died between the ages of 2 and 15. Half of the children studied had been diagnosed with autism, while the other half had not. The symptoms of those with autism varied from mild to severe. In 10 of the 11 autistic brains, they found patches of cortex in which the normal pattern of gene expression and cell organization was disrupted. These areas were only a few millimeters across (roughly a quarter to a half inch in size) across the wide expanse of otherwise histologically normal-appearing cortex.

In some of the abnormal patches, a specific layer was missing. In other patches, certain expected cells weren’t present. Similar changes were found in 1 of the 11 children without an autism diagnosis, a child who had suffered from seizures. All areas of cortex sampled from autistics demonstrated such patches, however the researchers indicated that the most affected areas of the brain were the prefrontal cortex and the temporal lobe cortex, while areas such as the optical cortex were relatively spared. The researchers speculated that the defects could have resulted from the brain cells in autistics undergoing some sort of disorganization event or events during the latter part of the first trimester or the early part of the second trimester of fetal development.

This study by Stoner et al. left the researchers speculating about causation of the observed disordered patches. They mentioned that their earlier studies had demonstrated that, between the ages of 2 and 16 years, brains from autistic children are heavier than non-autistic children brains and have a relative increase in prefrontal cortex neuron numbers of up to a startling 67%. Stoner et al. also discovered that a deficit of markers of excitatory neurons was the most robust indicator of such a patch of disorganization. Furthermore, they did not believe this was a result of downregulation of genes. Rather, they speculated that the patchy areas of disorganization somehow resulted from neurons ‘failing to reach their intended destination’ or from de novo changes in early neurodevelopment.

Lopez-Hurtado et al. [16] conducted a microscopic study of postmortem brains from 15 age-matched autistic and control subjects focusing on brain regions associated with the production and processing of speech. Of the brains studied, 8 were from autism patients and 7 were controls. They studied Wernicke’s area (Brodmann 22, speech recognition), Broca’s area (Brodmann 44, speech production) and the gyrus angularis (Brodmann 39, reading) from autistic subjects (7-44 years of age) and control subjects (8-56 years of age). These researchers found: “Striking differences in the density of glial cells, the density of neurons and the number of lipofuscincontaining neurons in the autistic group compared with the control group. The mean density of glial cells was greater in the autistic cohort than controls in area 22 (p<0.001), area 39 (p<0.01) and area 44 (p<0.05). The density of neurons was lesser in autism in area 22 (p<0.01) and area 39 (p<0.01). The autistic group exhibited significantly greater numbers of lipofuscin-containing cells in area 22 (p<0.001) and area 39 (p<0.01)”. They concluded that “the results are consistent with accelerated neuronal death in association with gliosis and lipofuscin accumulation in autism after age seven [17].”

Selected Studies of Neuron Structure in Autism, Link to Calcium-induced Reduction in Autophagy via mTOR Hyperactivation

Tang et al. [18] were able to discern differences in post-mortem brain samples from children with autism who had died from other causes (Figure 3). Thirteen brains came from children ages 2 to 9, and thirteen brains came from children ages 13 to 20. The controls were post-mortem brains from children without autism. Tang et al. measured synapse density in a small section of tissue in each brain, counting the number of tiny spines that branch from the cortical neurons. In the control brains, spine density had dropped by about half during childhood, but by comparison in the autistic brains the density had dropped by only 16 percent during childhood.

molecular-genetic-medicine-left-autism-neuronal-axon

Figure 3: Modified from Tang [18]: Normal neuronal axon illustrated on left – autism neuronal axon on right with extra spines, not well ‘pruned’.

The researchers then examined brains from mice, comparing autism-model mouse neurons versus non-autism normal mouse neurons. They studied Tsc2+/- ASD mice brains. These mice have alteration in the mammalian target of rapamycin (mTOR) such that the mTOR is constitutively overactive. mTOR is a serine/threonine kinase, which belongs to the phosphatidylinositol-3 kinase (PI3K) related kinase (PIKKs) family. It regulates cellular metabolism, growth, and proliferation. Tang et al.’s study of such autism-model mice with constitutively hyperactivated mTOR found signs of reduced autophagy. Autophagy is the process in neurons that, among other things, prunes neurons of excess spikes. Tang et al. [18] found that the autism-model mice, similar to the autistic children, had too numerous spikes on neurons. They deduced that this excess presence of spikes was due to a lack of adequate pruning, and postulated this was from a reduction or blockade of normal autophagy. These Tsc2+/- mice demonstrated ASD-like social behaviors.

Aberrant mTOR activation resulting in reduced autophagy is known to occur in human diseases on a genetic basis. For example, mutations in either of 2 genes (TSC1 or TSC2) have been determined to cause tuberous sclerosis complex. Among tuberous sclerosis patients, 20% to 60% are also diagnosed with autism [19,20]. It has been reported that, of all autism cases, approximately 1% to 4% are tuberous sclerosis patients [21]. Treatment of tuberous sclerosis patients with rapamycin can apparently partially correct their inherited defect of reduced autophagy.

The beneficial effect of rapamycin is thought to occur via rapamycin’s action to inhibit hyperactivated mTOR and thus induce an increase in autophagy [22]. Rapamycin has been used successfully in tuberous sclerosis patients to shrink angiomyolipomas [23] and astrocytomas [24]. Clinical trials are underway to assess the feasibility and safety of administering rapalogues sirolimus or everolimus in participants with Tuberous Sclerosis Complex (TSC). The assessment (Clinical Trial NCT01929642 USA) includes measuring any reduction in autistic symptoms, such as aggressive behaviors and/or any improvements in cognitive function.

Aberrant mTOR hyperactivation is thought to occur in a wide range of ASD patients with known genetic defects [25,26], such as those autistics found to have large head size (macrocephaly) early in life [27]. This finding of large head size is reminiscent of the increased brain volume and increased CSF accumulation found in the children destined to develop autism as studied by Shen et al. [12], as discussed above. Additionally, cases of genetic disease patients linked to mTOR hyperactivation who also relatively often have a diagnosis of autism include neurofibromatosis type I, Lhermitte-Duclos syndrome, and Fragile X syndrome [21,26].

It is conceivable however, that mTOR hyperactivation can occur in autistics for which a gene sequence alteration in DNA is not present. This type of mTOR hyperactivation is theorized to occur within neurons exposed intermittently to a toxin from diet and/or environment. Such a toxin is theorized herein to alter the influx of calcium into immature neurons in a haphazard and intermittent manner resulting in reduction of autophagy in such neurons so exposed, with effects dependent on their stage of development.

Such a haphazard hyperactivation of mTOR has been reproduced experimentally and linked to the presence of amino acids. Gulati et al. [28] studied HELA cells in culture and found that mTOR activation was in relation to the level of amino acids present in the cell culture. They found that increased amino acids in the cell culture medium resulted in an increase of HELA cell intracellular calcium, resulting in increased calcium binding with calmodulin within the cell, and subsequent increased activation through the mTOR pathway. Specifically, they state in their report “We demonstrate that the rise in [Ca(2+)] (i) increases the direct binding of Ca(2+)/calmodulin (CaM) to an evolutionarily conserved motif in hVps34 that is required for lipid kinase activity and increased mTOR Complex 1 signaling”. Glycine is an amino acid that is known to be present in and interact with human brain cells, in particular during neurodevelopment. A harmful glycine mimetic is herein theorized to be causative in at least some cases of autism, and to have an effect in human neurons similar to that effect of amino acids demonstrated in the cell culture studied by Guloti [28], i.e. an increased mTOR activation, thus reducing autophagy and leaving neuron spikes unpruned.

Human Post-mortem Selected Study of Autistic Brains Finds Markers of Increased Calcium in Autistic Brains versus Controls

Research on intracellular calcium in autism neurons offers a link to increased mTOR activation and reduced autophagy. Palmieri et al. [29] studied temporocortical gray matter from six matched patient-control pairs of normal and autistic brains to perform post-mortem biochemical and genetic studies of the mitochondrial aspartate/ glutamate carrier (AGC). The AGC participates in the aspartate/malate reduced nicotinamide adenine dinucleotide (NAD) shuttle and is physiologically activated by calcium (Ca(2+)). AGC transport rates were significantly higher in tissue homogenates from all six autism patients, including those with no history of seizures and with normal electroencephalograms prior to death. This increase was consistently blunted by the Ca(2+) chelator ethylene glycol tetraacetic acid. Neocortical Ca(2+) levels were significantly higher in all six autism patients compared to controls, according to these researchers. Furthermore, following removal of the Ca(2+)-containing postmitochondrial supernatant, these researchers reported they then observed no subsequent difference in AGC transport rates in isolated mitochondria from patients versus controls. This result clearly demonstrates that Ca(2+) entry provoked mTOR activation, leading to reduced autophagy in association with autism.

Calcium influx relates to action at neuron membranes of glycine-related factors

An article by Avila [30] reveals the link between calcium influx into neurons and the action of ligands at membrane-embedded protein structures of neurons. For example, Avila describes the glycine receptor’s (GlyR) action as follows: “GlyR activation during embryonic and early postnatal development most likely induces a depolarization of the cell membrane…which in turn may activate calcium influx”.

Thus, glycine binding at the GlyR appears capable of influencing the rate of calcium influx into neurons during early neurodevelopment. As will be further explored below, we theorize action of a harmful glycine mimetic in autism causation via its influence in causing harmful and haphazard influx of calcium into immature neurons during neurodevelopment. To further clarify this theory, we identified and reviewed known facts and selected published literature regarding a candidate molecule widely dispersed in the environment and present in certain foods, namely glyphosate.

Glyphosate, candidate glycine-mimetic molecule for comparison to requirements of theory

Glyphosate, a common herbicide, is known to be produced from the amino acid glycine via addition of a phosphonomethyl group (Figure 4). In 2007, according to the US EPA, glyphosate was the most used herbicide in the United States agricultural sector, with 180 to 185 million pounds (82,000 to 84,000 tons) applied, and the second-most used in the home and garden market, where users applied 5 to 8 million pounds (2,300 to 3,600 tons); in addition, industry, commerce, and government applied 13 to 15 million pounds (5,900 to 6,800 tons).

molecular-genetic-medicine-glycine-chemist-phosphonomethyl

Figure 4: To glycine, chemist adds a phosphonomethyl group to make glyphosate.

Glyphosate study, glyphosate from maternal diet found concentrated in piglet fetal brain

In a study by Kruger et al. [31] of 38 malformed piglets born to sows fed glyphosate-containing feed, brain tissue samples were obtained from euthanized 1 day old piglets’ brains. Following appropriate processing, these samples were tested for glyphosate using ELISA kits (Abraxis, USA). Glyphosate was found to be present in all piglet brain samples, at an average of 3.1 micrograms glyphosate per ml of sample. The authors commented that glyphosate was able to reach the fetal piglets from maternal feed, i.e. glyphosate from the feed eaten by the sow was able to pass the placental barrier. The feed, which contained 0.87 to 1.13 parts per million glyphosate, when consumed in the first 40 days of pregnancy, was associated with a rate of visible gross malformation in the piglets of 1 per 240 piglets. No microscopic evaluation of piglet brain tissue for autistic type changes was conducted.

Glyphosate usage on corn/soy crops versus rate of USA school children autism

Correlation is not proof of causation, but Swanson et al. [32] point out the near exact match in correlation between the rise of glyphosate usage on corn and soy crops in the USA, over the years 1992 to 2010, and the increase in autism rates over the same period as reported in the USA public school system (Figure 5). Among the most widely applied formulations of glyphosate is the pesticide known as Roundup®. We reviewed studies of glyphosate and Roundup® in relation to published research regarding brain tissue, including in relation to calcium influx into neurons.

molecular-genetic-medicine-glycine-glyphosate-children

Figure 5: From Swanson et al. [32], used by permission: Near exact match of tons of glyphosate applied to corn/soy versus number of children with autism as served under IDEA (US Department of Education, Individuals with Disabilities Education Act).

Glycine chelates, Glyphosate, manganese and the glutamate-glutamine cycle

Glycine, the simplest amino acid, has a molecular weight of 75, and naturally forms chelates with cations. The strength of glycine chelates is ideal for biologic processes, for example aiding mineral absorption from the intestine, while not overly avidly binding minerals which are needed for use in the body, such as for enzymatic reactions. When discussing a putative harmful glycine mimetic in the brain, it is useful to consider chelation in regard to the Glutamate-Glutamine cycle, and its apparent dysfunction in autism.

We begin with the synapse, the space between two neurons where chemical signals pass. Receiving the signal are receptors at the postsynaptic neuron membrane. Among these receptors are the NMDA receptors, which are neural membrane-embedded protein structures. When activated, the NMDA receptor opens to allow calcium to enter the neuron. The activation process, as will be discussed in detail below, includes the simultaneous binding to the NMDA receptor of both glutamate and glycine or a glycine mimetic [33].

Studies of autism and glutamate have documented that, in autism patients, glutamate activity is impaired [34], both in regard to actions at the synapse [35] where glutamate is released, and in the resultant calcium signaling, as it relates, for example, to dendritic growth [36]. A study by Page et al. [37] demonstrated that the ASD patients studied had a significantly higher concentration of glutamate in the amygdalahippocampal region of the brain than did normal controls. These findings suggest the Glutamate-Glutamine cycle is disrupted in autism.

The cycle can be viewed as starting with the step where glutamate is released into the synapse by the pre-synaptic neuron. The released glutamate can participate in binding the NMDA receptors of the postsynaptic neuron, thus transferring a signal. Such NMDA receptor activation is subject to other factors, as will be discussed below, but if the activation leads to excess calcium inflow into neurons, this can be problematic. The Glutamate-Glutamine cycle can be viewed as one of the natural controls to prevent such excess calcium inflow into neurons.

As the next step of the cycle, the free glutamate within the synapse space is normally quickly taken up for recycling by astrocytes. This removal of glutamate from the synapse helps prevent over-activation of the NMDA receptors. Within the astrocytes, the enzyme glutamine synthetase (GS) normally converts glutamate to glutamine. Glutamine is then returned from the astrocytes to the neuron. Within the presynaptic neuron, glutamine is converted back to glutamate for storage in internal vesicles. These vesicles will later move to the pre-synaptic neuron membrane and subsequently this glutamate will be released back into the synapse, where the cycle repeats [38].

In essence, GS can be viewed as helping protect neurons from excess glutamate activity/toxicity. However, GS activity depends on manganese as a cofactor, and this is where a putative harmful glycine mimetic could interfere. Glyphosate, as the candidate glycine mimetic, has a well-known action as an exceptionally avid chelator of cations, including manganese. Thus, glyphosate is viewed by some experts as having the potential to interfere with the free supply of manganese within astrocytes for use by GS within the Glutamate-Glutamine cycle [39]. This is theorized as one mechanism by which a putative harmful glycine mimetic, operating locally in patchy areas of the brain, might cause damage to neurons by increasing glutamate to toxic levels within the synapse, thus spiking calcium inflow haphazardly into neurons. This theory appears to correlate to the findings of Page et al. [37] regarding excess glutamate in autistic brains in the amygdalahippocampal area and the findings of Stoner et al. [15] regarding patchy areas of cortical disorganization found in brains of autistic patients.

As an example of its avidity in binding manganese and magnesium, glyphosate has been shown to deplete manganese and magnesium levels in young leaves of non-transgenic soybean plants exposed to glyphosate [40]. A recent study on dairy cows fed GMO Roundup- Ready feed showed dramatically reduced levels of serum manganese in association with glyphosate residues in the urine [41]. Autism has been linked to reduced manganese levels in the baby teeth of autistics [42]. Seizures, which have been associated with low serum manganese [43,44], are more prevalent among children with autism [45]. We will further explore these matters and related factors below.

Round-up’s effects on animal brain slices - calcium influx, apparently via NMDA receptor activation

Excess calcium entry into neurons is a well-known pathway to neuronal damage and/or disruption of neurodevelopment. In the study conducted by Hyrc et al. [46], increasing concentrations of calcium were applied to in vitro cultures of disassociated embryonic neurons from 15 to 18 day old mice embryos. Such concentrations of calcium were found to be predictive of neuronal death during NMDA stimulation. Cattani et al. [47] studied the effect of glyphosate on immature neurons of the hippocampus in rats. Maternal rat exposure to the pesticide involved treating dams orally with 1% Roundup® (0.38% glyphosate) during pregnancy and lactation (until 15 days old). Hippocampal slices from 15-day-old rats were acutely exposed to Roundup(® (0.00005-0.1%) during 30 min, and experiments were carried out to determine whether glyphosate affects (45)Ca(2+) influx and cell viability. In this preparation, these researchers investigated the pesticide’s effects on oxidative stress parameters, (14)C-α-methylamino- isobutyric acid ((14)C-MeAIB) accumulation, as well as glutamate uptake, release and metabolism. They found that acute exposure to Roundup(® (30 min) increases (45)Ca(2+) influx (apparently by activating NMDA receptors and voltage-dependent Ca(2+) channels), leading to oxidative stress and neuronal cell death. Signal transduction pathways involved in the Roundup®-induced 45Ca2 + uptake showed that either AP5 (a NMDA receptor antagonist) or KN-93 (a Ca2+/calmodulin-dependent protein kinase II selective inhibitor) prevented Roundup®-induced 45Ca2+ influx.

Cattani et al. [47] also found that such acute exposure of animal brain slices to glyphosate increased (3)H-glutamate release into the synaptic cleft, decreased glutathione (GSH) content and increased the lipoperoxidation, characterizing excitotoxicity and oxidative damage. They also observed that both acute and chronic exposure to Roundup(® decreased (3)H-glutamate uptake and metabolism, while inducing (45)Ca(2+) uptake and (14)C-MeAIB accumulation in immature rat hippocampus.

In view of the above suggestion that glyphosate has interaction at neural membrane-embedded receptors, a review was carried out regarding structure and function of neural membrane-embedded proteins, particularly as they relate to glycine, calcium influx and potential sites for interaction of glyphosate and/or glycine mimetics.

Neurotransmitters and membrane-embedded protein structures in neurons

Glycine is widely recognized as a neurotransmitter, i.e. glycine can, under specific circumstances, have an effect on the flow of ions across a neuron’s membrane. The neuron membrane is a lipid bilayer with embedded proteins. Some of these embedded proteins are pumps, such as the sodium-potassium ATPase pump, while many embedded proteins are ion channels. These ion channels are transmembrane proteins with a complex configuration that includes a pore through which ions can pass. Some channels permit passage of ions via opening of the pore as a result of membrane depolarization, and/or by the binding to the membrane-embedded protein of certain chemical ligands. Most channels have selectivity; i.e. when open they allow only certain ions to pass.

Neural membrane-embedded proteins/receptors: Sites for putative harmful glycine-mimetic action

Glycine receptor (GlyR)

GlyRs are formed by the assembly of five subunits which arrange symmetrically around a central pore. The beta subunit is the only one which interacts with the anchoring protein gephyrin, making it key to anchoring GlyRs at the area of the synapse. Of the alpha units, four types are known. Action of the GlyR, such as in terms of speed of opening kinetics, depends on which alpha units are present within a particular GlyR. While the alpha 1 beta combination displays the fastest kinetics, alpha 2 containing receptors are most abundant during neurodevelopment.

GlyR’s can be activated by glycine or by taurine or alanine. When open, chloride can traverse the pore, and flow is according to chloride gradient. In regard to autism, mutations in genes encoding the alpha 2 subunit have been found in patients who carry a diagnosis of autism [48].

The excellent article by Avila [30] reviews known facts about glycine receptor activity during neurodevelopment. The brain’s early cortical development includes formation of mini-columns via migrating neurons [49]. Interneurons make up only about 15% of neurons, but are important to establishment of these first brain circuits [50,51]. GlyRs have been demonstrated to have a role in controlling cortical interneuron development [30] and migration.

Figure 6 illustrates the GlyR ligand binding site. As mentioned, research has demonstrated that besides glycine, several other molecules can bind to the GlyR and alter the activation of GlyR. For example, strychnine is known to be an antagonist of the GlyR, as is caffeine. GlyR activation has an effect on clustering of receptors at post-synaptic sites [17].

molecular-genetic-medicine-Glycine-receptor-subunit

Figure 6: Glycine receptor (GlyR) viewed with 5th subunit (an alpha) removed.

A disruption of GlyR activation theoretically induces alterations in chloride outflow for immature neurons, and thus empowers haphazard disruptions for calcium inflow into immature neurons via the NMDA receptor channel (subject to occurrence of other coincident actions at the NMDA receptor as will be discussed below). This putative harmful glycine mimetic’s action at the GlyR, is envisioned to be via an exposure(s) from diet and/or environment, dosing the fetus or child in an intermittent variable-dose manner. The resulting haphazard calcium influxes theoretically enable a spectrum of severity in disrupted neuron migration, reflective of the spectrum of symptom severity in ASD cases clinically.

The mechanism by which outflow of chloride from an immature neuron affects calcium inflow into that immature neuron, has to do with the effect of chloride outflow on the electrical charge at the neuron’s membrane. A neural membrane usually retains a negative charge within the cell, and a positive charge on the exterior. However, at times, such as when chloride outflow through the GlyR is high, the charge of the membrane can change, leading to what is known as membrane depolarization. Membrane depolarization can then alter activity at other membrane-embedded protein structures, such as at the NMDA receptor. Because like charges repel each other, a depolarization of the membrane, which produces a temporary positive charge nearer the NMDA receptor, can dislodge the positively charged magnesium ion from its blocking position within the NMDA receptor, as illustrated in Figure 7.

molecular-genetic-medicine-magnesium-ion-depolarization

Figure 7: NMDA receptor, note the magnesium ion is dislodged from within the NMDA channel by the depolarization caused by chloride outflow at the GlyR when glycine binds there.

However, the NMDA receptor channel will not open to calcium inflow just because the magnesium ion exits the channel of the NMDA receptor. The two binding sites of the NMDA receptor must also be properly filled. A molecule capable of agonist binding at the so-called glycine binding site of the NMDA receptor must be in place. Also, a molecule of glutamate must be bound at the glutamate binding site of the NMDA receptor. Only when these three events occur at the same time, i.e. the magnesium ion’s exit from the NMDA channel, the binding of an activating molecule to the glycine site of the NMDA receptor, and the binding of glutamate to the glutamate site of the NMDA receptor, only then will the NMDA channel allow calcium to flow into the neuron.

From this complex set of requirements it is clear how carefully neurodevelopment guards against haphazard or excess entry of calcium into immature neurons. Conversely, as theorized herein, when a harmful glycine mimetic is able to disrupt this carefully choreographed system, the normal neurodevelopment sequence does not occur. Recall how calcium excess within a mouse brain model of autism was associated with reduced autophagy and malformed poorly ‘pruned’ neurons. It seems that proper neurodevelopment is critically dependent on the correct and beneficial control of calcium entry into immature neurons.

Taurine, an amino acid, is also capable of binding the GlyR. When taurine binds to the GlyR, such taurine binding, like the binding of glycine, opens the GlyR ion channel to gradient directed flow of chloride. However, taurine binding appears to induce only approximately half as much chloride flow as compared to glycine binding. In effect, taurine is a glycine mimetic which reduces chloride flow compared to glycine binding of the GlyR. This implies a reduced opportunity of chloride flow to spur depolarization of the immature neuron’s membrane. Thus, taurine is seen as a partial agonist of the GlyR.

Taurine tends to modulate the action of glycine at the GlyR, i.e. taurine’s presence can serve as a natural competition with glycine. This natural competition results in fewer membrane depolarization events. In effect, taurine’s binding at the GlyR during neurodevelopment is a partial interference with glycine’s ability to boost calcium inflow events for the neuron. This has profound potential to influence neuron migration during neurodevelopment.

Because taurine, as mentioned above, only permits approximately half the chloride flow at the GlyR when compared to glycine binding the GlyR, it is thus less likely that a membrane depolarization will occur with taurine bound to the GlyR (Figure 8). In fact, the amino acid taurine is reported [52-54] to serve to counteract glutamateinduced elevations in intracellular calcium ions within neurons, and thus taurine confers protection against neurodegeneration. The concentration of taurine compared to the concentration of glycine in the vicinity of the GlyR results in a choreographed competition. Taurine, in theory, will likely similarly compete for binding versus glyphosate, and therefore taurine likely would tend to protect from any theorized harm from glyphosate binding at the GlyR.

molecular-genetic-medicine-Taurine-binding-chloride

Figure 8: Taurine binding to GlyR reduces chloride flow by approximately 50% compared to flow from glycine binding of GlyR, so no depolarization occurs with taurine bound to GlyR, thus magnesium ion remains within NMDA receptor channel, continuing to block calcium from entering immature neuron.

Studies by Leon et al. [54] demonstrated a neuron-protective effect for taurine thought to operate via modulating the calcium influx to neurons which otherwise would occur due to glutamate at the NMDA receptor. Glutamate applied without taurine was able to drive apoptosis (neuron cell death) via release of cytochrome C. Taurine application along with glutamate was shown to prevent such apoptosis.

The level of taurine present in the brain is known to progressively increase during embryogenesis. At the same time, the different GlyR assemblies, from incorporation of different alpha subunits, means that another factor is present beyond taurine concentration. Different GlyRs vary in their sensitivity to taurine. Homomeric GlyRa2, for example, is 10 times less sensitive to taurine [30] compared to the most sensitive GlyR.

Thus the choreography of neurodevelopment is tuned to genetic distribution of different membrane-embedded receptors/proteins over time, and to effects of local concentrations of competing receptor agonists. In regard to the theory herein advanced, we theorize the harmful action of a putative glycine mimetic acting at the GlyR to disrupt such delicate choreography. This damaging effect on neurodevelopment is notably a local and time-sensitive effect, rather than dependent solely on overall dose of toxin to the fetus or mother.

Another balanced mechanism during neurodevelopment by which neurons and axons perform coordinated migration is the frequency of spontaneous waves within a neuronal circuit, i.e. waves of depolarizing or ‘bursting’ activity. The effects within the brain of a disruptive decrease of the local frequency of such spontaneous bursting activity via toxins that act at the GlyR was demonstrated by Hansen et al. [55,56].

They examined white leghorn chick embryos’ spinal neuron migration in ovo by cutting a square hole through the egg shell and placing a pipette via which they administered GlyR antagonists, strychnine or picrotoxin. By thereby decreasing calcium transient influxes locally, and thus decreasing the normal spontaneous rhythmic bursting activity (RBA) of developing neuron circuits, they noted migration abnormalities. Such GlyR antagonists, when administered at certain days during gestation, also altered gene expression locally of genes which normally code for neuron axon guidance/adhesion proteins.

Glycine as ligand, binding to NMDA receptor

As discussed above, the NMDA receptor has a binding site for both glutamate and glycine (D-serine also can bind the glycine site of the NMDA receptor). Only when both of these binding sites of the NMDA receptor, the glutamate site and the glycine site, are agonistically filled, and only if the magnesium ion is simultaneously displaced from the NMDA channel, only then will the NMDA channel allow calcium to enter the neuron. As mentioned, this tight control of calcium entry has import for neurodevelopment. The amount of calcium entering via the neuron’s NMDA receptors is known to be further modulated by pH and zinc.

If a molecule of the herein theorized putative harmful glycine mimetic binds more avidly than glycine at the glycine binding site of the NMDA receptor, then the chances of calcium inflow into immature neurons could theoretically be increased. This is because the theorized more avid binding of the putative harmful glycine mimetic to the NMDA receptor’s glycine site, would extend the time for the simultaneous occurrence of the other two events, i.e. for the simultaneous exit of the magnesium ion from the NMDA channel and the simultaneous binding of glutamate to the NMDA receptor’s glutamate binding site.

Glycine concentration at synapse, glycine transporter protein T1 (GlyT1)

Another mechanism by which a spectrum of severity of autism is envisioned to occur, from the action of the putative harmful glycine mimetic, relates to glycine transport proteins. Neurotransmitter glycine participates in a recycling mechanism of uptake of glycine from the synapse by cells in the brain. Storage of glycine in the pre-synaptic neurons occurs for a time, followed by re-release of the stored neurotransmitter back into the synapse (Figure 9).

molecular-genetic-medicine-Neurotransmitter-glycine

Figure 9: Neurotransmitter glycine is taken up from synapse by GlyT1 transporter protein (not shown), stored, then re-released into synapse to bind glycine receptor of post-synaptic neuron.

Glycine transporter proteins GlyT1 and GlyT2 are membraneembedded proteins specific for glycine handling. The primary role of GlyT1 is thought to be to maintain glycine concentrations below saturation level at postsynaptic NMDA receptors, thus modulating influx of calcium into neurons. GlyT1 is known to be subject to inhibition by glycine mimetics. For example, sarcosine, one of the naturally occurring N-methyl analogues of glycine, is a known inhibitor of GlyT1. Sarcosine is also one of the possible metabolic breakdown products of glyphosate.

We theorize that glyphosate directly, or sarcosine from glyphosate breakdown, act via GlyT1 inhibition to locally and intermittently inhibit the uptake of glycine from the synapse. We theorize that, during neurodevelopment, such inhibition of GlyT1 permits excess synaptic glycine to accumulate. Thus glycine could bind to saturation the NMDA receptor of an immature neuron, thus increasing calcium entry via the NMDA receptors into the immature neuron, damaging neurodevelopment.

In regard to GlyT1 inhibition and neurodevelopment, the work of Schmitz et al. [57] is of interest. They performed unilateral intrastriatal injection in mice of toxin 6-hydroxydopamine and studied the reenervation response with and without GlyT1 inhibition. In the studied mice whose glycine transporter protein1 function was inhibited pharmacologically for 4 weeks, the axon sprouting of the neurons responding to the denervation was, at 7 weeks, twice as dense as controls. This ‘over-sprouting’ occurred via action of the NMDA receptors, according to Schmitz et al.

If a re-enervation sequence can be conceptualized as similar to the original enervation sequences of neurodevelopment, then the study of Schmitz et al. might provide a relevant theoretical explanation. A spike of putative harmful glycine-mimetic molecules in a localized area of cortex in a developing human fetal brain might produce a disruptive effusion of neuron spikes due to local blockade of GlyT1 by the harmful glycine mimetic (or its metabolite). Such patches of putative over-exuberant neuron spikes are reminiscent of the findings of Tang et al. [18], and reminiscent of the increased neuron density found in patches in brains of autistic children by Stoner et al. [15].

In fascinating studies [56,58] by Hansen et al., these researchers administered the GlyT1 inhibitor sarcosine via in ovo method during neurodevelopment of white leghorn chick embryos. They documented that sarcosine caused an increase in the frequency of calcium transients, which translated into an increase of the frequency of spontaneous rhythmic neuronal bursting activity. They found this produced abnormalities in neuron/axon migration.

In summary, Hansen et al. confirmed that rhythmic bursting activity (RBA) of neuron circuits is key for early pathfinding decisions by neurons. Moderate slowing of the frequency of RBA causes “motoneurons to make dorsoventral (D-V) pathfinding errors and to alter the expression of molecules involved in that decision.” Conversely, moderate speeding up of RBA in neuron circuits strongly perturbs “the anteroposterior (A-P) pathfinding process by which motoneurons fasciculate into pool-specific fascicles at the limb base and then selectively grow to muscle targets.” In their studies, these researchers found that resumption of normal frequency of RBA sometimes allowed axons to correct the A-P pathfinding errors, perhaps leaving aberrant nerves.

Aberrant connectivity has, in fact, been documented in the brains of autistic children [59] using resting state functional magnetic resonance (MRI) imaging. Di Martino et al., studying autistic children using fMRI methods, concluded that their examination of functional connectivity (FC) of striatal networks in children with ASD revealed “abnormalities in circuits involving early developing areas, such as the brainstem and insula, with a pattern of increased FC in ectopic circuits that likely reflects developmental derangement rather than immaturity of functional circuits.” This pattern also fits our theory of a dietary/ environmental sourced toxin acting locally as a harmful glycine mimetic, having patchy effects in the CNS beyond the cortex.

Neuron migration has been visualized. Avila et al. [60] demonstrated in vivo, using cultured brain slices from mice embryos, that actomyosin contractions alter neuron migration. These researchers recorded an example of neuron migration in video format and have made the recording available for viewing online as movie S2 of their open access report [60].

In summary, this delicately choreographed neurodevelopmental process in humans, including the precise frequency of waves of depolarization in synchronized neurons within circuits, this pattern of neurons which alternately sprout, prune and migrate, this choreography can be locally disrupted, we theorize, by a relatively small number of molecules of a harmful glycine mimetic. From the available research literature, such disruption, for example via the GlyR and/or the GlyT1 and/or the NMDA receptor, can reasonably be theorized to produce neuronal/axonal migration defects reminiscent of those found in studies of brains of autistic patients.

Next, we will address the neuron membrane-embedded protein structures known as Na-K-Cl cotransporter 1 (NKCC1) and K-Cl cotransporter 2 (KCC2).

Glycine, NKCC1 versus KCC2 in neurons, brain weight

Within the brain during normal neurodevelopment, the types and numbers of membrane-embedded proteins will change as neurons mature. As illustrated in Figure 10, in immature neurons the membrane will typically have more NKCC1 proteins embedded, and fewer KCC2 proteins. One result is that immature neurons tend to keep internal chloride concentration higher.

molecular-genetic-medicine-normal-circumstances

Figure 10: In normal circumstances, the membranes of immature neurons include numerous NKCC1, fewer KCC2; intracellular chloride concentration tends to be higher in normal immature neurons as compared to mature neurons.

As neurons proceed through normal fetal development, they will begin to manufacture fewer of the NKCC1 proteins and instead manufacture more of the KCC2 proteins. Therefore, mature neurons will have more KCC2 proteins embedded in their membrane and fewer NKCC1 proteins embedded, as illustrated in Figure 11. The result, in normal circumstances, is that mature neurons tend to have a lower concentration of chloride internally.

molecular-genetic-medicine-mature-neurons-fewer

Figure 11: In normal circumstances, mature neurons have fewer NKCC1 and more KCC2; intracellular chloride concentration tends to be lower in normal mature neurons as compared to immature neurons.

In both the immature neuron and the mature neuron, the glycine receptors (GlyR) aid in keeping the internal chloride concentration within expected bounds (Figure 12). The programmed normal change of neuron membrane-embedded proteins predominance, from predominately NKCC1 (immature neurons) to predominately KCC2 (mature neurons), is commonly referred to as the ‘GABA switch.’ This reflects the fact that gamma amino butyric acid (GABA), in normal circumstances, acts to inhibit hyperactivity in mature neurons, such as during birth and post-natally [61]. The GABA switch is often found to be impaired in autism patients, a finding that we theorize might be related to action of a harmful glycine mimetic during neurodevelopment, as further described below.

molecular-genetic-medicine-chloride-flows-neuron

Figure 12: Under normal circumstances, chloride flows out of an immature neuron when GlyR is open. Under normal circumstances, chloride flows into a mature neuron when GlyR is open.

Interestingly, a partial agonist of the GlyR is caffeine. It is noteworthy that autistic children receiving a low dose of daily caffeine over weeks or months have been reported [62] to sometimes experience improvement of autism symptoms as a result of the caffeine.

As previously mentioned, it is well known that the brains of autistic children, in their early childhood years, are heavier than controls. We postulate that this weight increase is caused by increased water content of the brain, such as in neuropil, glial cells and/or neurons. We believe such water retention could be a response to excess cell-internal chloride, caused by impaired chloride e

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