How Do Excitotoxins Harm the Body

excitotoxins

How tissues are affected by excitotoxins

All excitotoxins harm the body. They cause a lot of ailments and diseases that may cause death.

What are excitotoxins?

Excitotoxins are substances, usually amino acids that react with receptors in the brain and destroy certain types of neurons. One of these excitotoxin is monosodium glutamate. It comes from natural glutamic acid.

Glutamic acid is one of the many amino acids that are building blocks of proteins. It is naturally found in tomatoes, milk, mushrooms, and in many food in varying concentrations. It is also found in  mother’s milk. Glutamic acid is found in the cells of the body and is involved in a variety of brain functions as a neurotransmitter. It is the most commonly used neurotransmitter by the brain, and the most important neurotransmitter in the hypothalamus. This natural glutamate in plants and animals is called L-glutamic acid. The digestive system breaks down this natural glutamic acid, and delivers this to the glutamate receptors in our body and brain. When broken this way, it is harmless. But when it undergoes processing with the use of strong chemicals, bacteria, and enzymes, it becomes “free” and harmful, and this is what is commonly known as MSG or monosodium glutamate. It is 78.2% glutamate, 12.2% sodium, and 9.6% water. Its chemical formulation has been altered, and is technically called as D-glutamic acid. It also contains L-glutamic acid, pyroglutamic acid, and contaminants. Take note that plant and animal proteins do not contain D-glutamic acid, pyroglutamic acid, nor contaminants.

Free glutamate or monosodium glutamate is the product of certain chemical processes such as hydrolysis, autolysis, and fermentation with the use of strong chemicals, bacteria, and enzymes. They come from  various raw materials mostly from corn.

How do excitotoxins harm the body?

Glutamate and other excitatory amino acids attach to special receptors such as NMDA, AMPA, kainate, and metabotropic. These in turn opens the calcium channel on the neuron cell membrane, allowing calcium to flood into the cell. This calcium will trigger various reactions including free radical generation, eicosanoid production, and lipid peroxidation which will destroy the cell. With this calcium-triggered stimulation, the neurons become very excited, firing its impulses repetitively up to the point of death. This activation of calcium channel also involves other membrane receptors like zinc, magnesium, phencyclidine, and glycine receptors.

Glutamate acts on its receptors via a nitric oxide mechanism. Over stimulation of glutamate receptor produces an accumulation of reactive nitrogen species which result in the generation of several species of dangerous free radicals including peroxynitrite. This is how excess glutamate damages the nerve cells. Many studies have demonstrated the link between free radical generation and excitotoxity.

Free radicals have been  shown to damage cellular proteins  (protein carbonyl product), and DNA. The most immediate DNA damage is the mitochondrial DNA, which controls protein expression within a particular cell and its progeny. Parkinson’s disease, a neurodegenerative disease is suspected to be affected in this way. Chronic free radical accumulation can result in an impaired functional reserve of antioxidants, vitamins, minerals, enzymes, and thiol which are needed in neural protection.

Monosodium glutamate penetrates the blood-brain barrier. This barrier is a system of specialized capillary structures designed to exclude toxic substances from the brain. But the brain has areas that normally do not have a barrier system. These unprotected areas are in the hypothalamus, the subfornical organ, organium vasculosum, area postrema, pineal gland, and the subcommisural organ. There is a most consistent finding that monosodium glutamate can penetrate the blood-brain barrier. It was found out that exposure to MSG damages the arcuate nucleus  of the hypothalamus. This area of the hypothalamus controls many neuroendocrine functions, and is intimately connected to several hypothalamic nuclei. It was demonstrated that high concentration of glutamate and aspartate can enter the blood-brain barrier by seeping through the unprotected areas, such as in the hypothalamus or in other circumventricular organs. This is the situation when individuals consume foods high in excitotoxins on a daily basis. Conditions associated with the seepage of toxic substances into the blood-brain barrier include hypertension, head trauma, diabetes, strokes, collage-vascular diseases, multiple sclerosis, AIDS, brain infections, Alzheimer’s disease, and premature aging.

Besides monosodiun glutamate,  a  growing list of excitotoxins are being discovered. One of  these is aspartame . It contains approximately 40% aspartic acid, 50% phenylalanine, and 10% of methyl ester. Aspartame, like monosodium glutamate can cause brain lesions,  brain tumors, and brain cancer.

Another excitotoxin is L-cysteine. It is a powerful excitotoxin that is added to certain bread dough, and is sold in health food store as a supplement. Also, hydrolyzed vegetable protein contains cysteic acid, another excitotoxin.

Harmful Effects of Caffeine

The harmful effects of caffeine are many. Among the harmful effects of caffeine are forgetfulness, nervousness, and addiction.

Caffeine is a psychoactive substance naturally found in coffee, tea, kola nuts,  and in lesser amount, in cocoa. It is also found in beans, leaves, and fruits of some plants that acts as a natural pesticide to ward off insects.

Caffeine is a common ingredient in soft drinks, such as cola which was originally prepared from kola nuts. Soft drinks usually  contain about 10 to 50 milligrams, and energy drinks, 80 milligrams of caffeine per servings. Guarana, a prime ingredient of energy drinks, contains large amounts of caffeine with small amounts of theobromine and theophylline. It is also found in tea, and in chocolates, in the form of cocoa, in small amount.

Caffeine is an excitotoxin that harms the brain. It stimulates the body in similar manner as cocaine and heroin, and its addiction is gradual and subtle. Like most excitotoxins, caffeine causes brain malfunctions. This substance, like alcohol and nicotine, can easily penetrate the blood-brain barrier and can over excite the brain neurons to death.

Busy people  who want to extend their working hours drink more coffee in order to stay awake all day. Caffeine blocks adenosine receptors in the central nervous system of our brain, and brings a temporary feeling of alertness and wakefulness. Adenosine is a neurotransmitter that is involved in the control of the sleep-wake cycle. It promotes drowsiness and sleep after long hours of work or mental activity.

Caffeine molecule is structurally similar to adenosine. It easily binds to adenosine  receptors on the cell surface without activating them, thus blocking and inhibiting their functions. Cells that are normally slowed down by adenosine are speeded up by caffeine. Sensing that the cells are not slowed down, and suspecting that an emergency has happened, the hypothalamus reacts by releasing a neuro-hormone called dopamine into the bloodstream which triggers the adrenal glands to start pumping. Dopamine  increases heart rate and blood pressure, thus the feeling of wakefulness and alertness when drinking coffee.

The temporary sensation of high energy and alertness after drinking coffee, soft drinks, and energy drinks could be due to the the effects of caffeine’s three by-products during its metabolism.   Paraxanthine increases the lipolysis process, which releases glycerol and fatty acids into the blood as a source of fuel for the muscles. Theobromine dilates the blood vessels to increase the amount of oxygen and the flow of nutrients to the brain and muscles. Theophylline relaxes the smooth muscle of the bronchioles;  changes the time of heart rate, and alters the force of  muscle contractions in the heart.

Caffeine is an excitetotoxin that destroys the brain. Its excitatory effects not only weaken the neurons in the brain but can even over excite them to death. Caffeine, by counteracting adenosine, has inhibitory effects on brain activity. It adversely affects the healthy functioning of the brain, and other learning skills.  Long-term consumption of caffeine even in small doses affects learning and memory by inhibiting the creation of neurons in the hippocampus of the brain.

Other harmful effects of caffeine are the following:

  • it causes nervousness, trembling, and abnormal muscle contractions
  • it causes dizziness and headaches
  • it causes indigestion
  • it slows down reaction to auditory and visual stimuli
  • it causes forgetfulness  and tip-of-the-tongue phenomenon
  • it increases the risk of myocardial infarction
  • it increases heart rate
  • it causes heart palpitation
  • it increases the risk of miscarriage in pregnant women
  • it causes lethargy, and irritability
  • it causes confusion and inability to focus
  • it causes visual hallucinations
  • it intensifies and prolongs the effects of psychostimulant drugs such as amphetamine, methamphetamine, and dextroamphetamine
  • it causes increased gastric acid secretion in the cells
  • it decreases broad-range thinking abilities

Some studies showed that caffeine is good for the heart, and increases mental performance related to focused thought. This may be true as in other contradicting results from studies done on the effects of caffeine. But these are all temporary and transitory. When the stimulating effects are gone, the harmful effects of caffeine appear in the form of illnesses and diseases.

Caffeine is a nerve irritant that does not nourish the system in any way. Its temporary effects of high energy, alertness, wakefulness, increased strength, vivid imagination, and mental arousal are only nervous excitements produce before caffeine is ever digested and assimilated by the body. When the effects of this stimulant are gone, these unnatural euphoric conditions disappear, and only results to debility and langor.