วันอาทิตย์ที่ 20 มิถุนายน พ.ศ. 2553

Our Body Uses Chemicals and Electrical Impulses For Communication

Introduction:

The central nervous system uses electric currents to communicate with the rest of the body. Sodium and potassium are responsible for causing the flow of the electric currents throughout the central nervous system. The flow of the electric current is a one-way process, terminating at a pre-synaptic neuron. Another chemical comes into play, namely calcium, which, with sodium and potassium, cause the release of further chemicals called neurotransmitters, which aid in the communication process.

The central nervous system (CNS) is composed of the brain and spinal cord. Signals from the CNS go, via a one-way system, to the motor neurons, which in turn communicate with the somatic (voluntary) muscles and the autonomic (involuntary) muscles to produce movement.

Sensory neurons, send signals to the CNS, via a one-way system, which interprets the information and acts accordingly. For example if person stands on a sharp nail, the information is communicated to the CNS, the brain then informs the foot, to move away from the source of the pain, all done within milliseconds.

But how is this achieved? It is all a question of chemical and electrical processes.

The cell body of the neuron initially receives the signal, or stimulus. This signal is transmitted down the neuron's axon, starting as an electrical impulse at the axon hillock.

Without any stimulus the neuron remains in a resting state. Even during this resting state there is a constant flow of chemical ions between the inside and outside of the neuron, due to the ion concentration gradient, which produces a difference in electric charge between the outside and inside of the neuron, which is called the resting membrane potential. During this stage the inside of the neuron is negative in relation to the outside which is positive. The resting electrical potential is approximately -60 mV.

The main chemical ions involved during the process of communication are Sodium ions (Na+), the main extracellular cations and Potassium ions (K+), the main intracellular cations. Within the cell there is concentration of 140 mM (millimoles per litre) of K+ ions and 15 mM of Na+ ions. Outside the cell the concentration is 5 mM of K+ ions and 150 mM of Na+ ions. This gives rise to two concentration gradients, where ions of a high concentration will try to pass through the plasma membrane of the axon to a low concentration of the same chemical ion. For example, the high concentration of K+ ions in the cell will attempt to pass to the outside of the cell where the concentration is less. This occurs continually via K+ channels, which are constantly open, allowing a constant flow of K+ ions through the channels in the membrane to the outside of the cell. There are voltage-gated Na+ channels (VGC), which are closed during the resting potential, thus preventing the Na+ ions from entering the cell. There are also chemically-gated K+ channels (CGCs), which are also closed during the resting potential. A chemically controlled gate is also called a Ligand gate. The channels are classed as passive transport, as no energy is required to power them, they rely on the concentration gradient to move ions from one area to another. Apart from ion channels there are sodium-potassium (Na+- K+ ) pumps which actively expel Na+ ions from the cell and exchanges them for K+ ions from the outside of the cell/plasma membrane. The Na+- K+ pump simultaneously transports 3 Na+ out of the cell and 2 K+ into the cell. The pump is classed as active transport as it works against the concentration gradient and requires energy in the form of ATP to power it.

K+ channels are the most common open channels in the plasma membrane of resting neurons, therefore resting neurons are more permeable to K+ ions than any other ion.

If neurons receive input signals from one or more cells, the neuron will generate an electrical signal or action potential which will travel down the length of the axon, starting at the axon hillock. On receiving the electrical stimulus, the VGCs will open, allowing Na+ ions to flood into the axon, which changes the charge from negative to positive. The CGC's will also open, allowing the K+ ions to flood out. This depolarising current then moves down the axon, opening up more VGCs and CGCs as it goes. However, as the electrical current moves forward, there is no current where the impulse started and so the VGCs and CGCs close, preventing more influx of Na+ ions and expulsion of K+ ions. The Na+- K+ pump then starts to expel the Na+ ions from the cell and exchanges them for K+ ions from the outside of the cell, thus re-instating a resting potential. There is also a refractory period of 1-2 milli seconds, where the VGCs cannot reopen, thus preventing (backup) of the current. It acts as a valve so that the current can only move in one direction. The current moves along the axon like a lit fuse, opening and closing channels as it progresses.

Eventually the current reaches the synaptic knobs, which are bounded by the presynaptic membranes. The synaptic knobs come into close contact with the dendrites and cell body of the post synaptic neuron, but do not touch the surfaces, there is a gap called a synaptic cleft.

The presynaptic neuron has now to communicate with the post synaptic neuron.

As the action potential arrives at the axon terminal, VGC's in the synaptic knob membrane open allowing Na+ ions to flow in to the knob. This depolarisation causes VGC's of Ca2+ ions to open. Ca2+ ions flow into the knob and trigger a fusion of vesicles, containing neurotransmitters, with the cell membrane. The neurotransmitter/s are released across the synaptic cleft and bind to ligand-gated receptor channels on the post-synaptic neuron. The receptors are activated into opening the ligand-gated channels of Na+, K+ and Ca2+ causing these ions to flow in to the post synaptic cell and depolarise it. The depolarisation spreads in the post synaptic membrane, firing an action potential within it.

There are different types of neurotransmitters, which are all chemically based. They include acetylcholine, monoamines, purines, amino acids, peptides and gas (nitric oxide). Each neurotransmitter can work alone or in combination with each other, depending on the required effect. For example, if the above action potential arrived at a muscle, the released neurotransmitter would be acetylcholine. The action potential firing in the post synaptic neuron (muscle) would cause movement in that muscle.

Conclusion

In order for muscles to move, voluntarily or involuntarily, the brain must communicate with the muscle in order for it to move. The brain does this by sending a signal to the muscle. The signal is the result of chemical and electrical processes passing along neurons, which in turn pass that information on to other neurons, for example, muscle neurons.

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วันเสาร์ที่ 19 มิถุนายน พ.ศ. 2553

Frequency Specific Microcurrent Offers New Hope For People With Chronic Pain and Fibromyalgia

Approximately 10 million Americans suffer from a condition known as fibromyalgia
syndrome. This condition is characterized by widespread muscle pain, extreme
fatigue and chronic non-restorative sleep disturbances for more than three months'
duration. Although pain and inflammation are among the symptoms, they are not
the cause of the disease. Therefore, treating the inflammation and pain of
fibromyalgia with anti-inflammatory drugs, pain medication or even natural
remedies is rarely effective.

There are four common traumas that can cause fibromyalgia. Most patients with
fibromyalgia have experienced one of the following events 4 to 12 months before
their symptoms appeared: (1) neck injuries or cervical spine trauma; (2) toxicity or
chemically induced trauma; (3) acute or prolonged severe emotional stress; and (4)
immune system trauma from unresolved viral or undiagnosed illness.

Although these traumatic events seem unrelated on the surface, each one can be
the precipitating cause of two systemic problems present in almost every
fibromylgia patient. The first effect is damage to the neuroendocrine system,
resulting in adrenal exhaustion and hormonal imbalance. The second effect is the
reduction of cellular energy in the mitochondria, which is the power-producing part
of the cell. Recovery from fibromyalgia requires that all causative factors and the
hormonal and cellular energy production problems be addressed and corrected.

Although this approach has been effective with all types of fibromyalgia, this article
will address the evaluation and treatment of fibromyalgia caused by cervical spine
trauma. Approximately 25 percent of patients with fibromyalgia report the onset of
pain following a cervical trauma. The most common injuries result from motor
vehicle accidents (whiplash), surgeries, trauma from falling down or injuries from
lifting or moving heavy objects.

The symptoms associated with cervical truma-induced fibromyalgia include: neck
pain; burning pain between the shoulder blades, shoulder, arm, hand, back, leg and
foot: headaches; fatigue; weakness; sleep disturbance; depression; and digestive
problems. Patients with this type of fibromyalgia complain of aching, burning,
sharp, shooting and/or stabbing pain.

A new treatment called frequency specific microcurrent (FSM) offers hope to patients
with fibromyalgia. A clinical trial of 160 patients with cervical trauma-induced
fibromyalgia treated from 1999 and 2003 was conducted using FSM. On a
subjective pain scale (1=no pain to 10=severe pain), these patients reported an
average pain reduction from 7.3 to 1.3 after their initial treatment with FSM.

The treatment involved the use of 200 to 600 microamperes of direct electrical
current to the spinal cord. Condition and tissue-specific frequencies are utilized to
effectively reduce the inflammation in the spinal cord and restore normal nerve
conduction. Most patients benefiting from this treatment were pain-free for the
first time in years. The initial pain relief lasted five to 48 hours and was the start of
recovery.

Follow-up FSM treatments were conducted twice a week and most patients required
daily use of a home FSM unit to control the pain. The average number of treatments
to remain pain-free was 10 treatments.

Recent studies have determined a biological mechanism for the result seen in
patients. FSM treatment affected the serum levels of several biochemical
constituents including IL-1, IL-6, TNF-a, Substance-P and LOX, which are
inflammation/pain-related biological chemicals. All were significantly reduced
when measured after the FSM treatment. There was also a dramatic increase in b-
endorphin, a naturally-occurring chemical which helps reduce pain, and a 500
percent increase in ATP, the body's fuel storage molecule used in cellular energy
production.

Dietary changes and nutritional supplements were combined with the FSM
treatments to address other contributing factors, such as the endocrine and cellular
energy weaknesses in all patients. Furthermore, depending on the individual needs
of the patient, the following imbalances were corrected before a lasting recovery
could be reached: neurotransmitter (serotonin and catecholamine) deficiencies,
digestive problems, liver, adrenal, and thyroid dysfunction, soft tissue and joint
problems, and unresolved mental/emotional issues.

Beyond alleviating the effects of fibromyalgia, FSM also has shown great promise in
the successful treatment of athletic injuries, chronic or acute joint pain/stiffness,
pain associated with gall stones and kidney stones, closed head injuries, shingles,
post herpetic neuralgia, infections, diabetic ulcers, wound healing, and other
conditions that are often unresponsive to conventional medical treatment.

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วันศุกร์ที่ 18 มิถุนายน พ.ศ. 2553

Indian Wells 2010 Baghdatis Tuesday Interview

Marcos Baghdatis hails the biggest win of his career after defeating World No. 1 Roger Federer on Tuesday evening in Indian Wells. <a href=" www.tennistv.comtarget="_blank">Watch Live Matches</a>. Video courtesy of <a href=" www.tennistv.com target="_blank">Tennis TV</a>, copyright ATP Media.



http://www.youtube.com/watch?v=Qg2vobyNklo&hl=en

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วันจันทร์ที่ 14 มิถุนายน พ.ศ. 2553

How the DP Exercise Bike Stacks Up Against Better Known Brands

The name DP exercise bike might not be as recognizable as other brands like Schwinn, Nautilus and ProForm, but this brand has been around for quite some time and is one of the most respected names in the physical fitness business. Currently, DP is better known for selling exercise bike parts and exercise equipment supplies.

Most DP indoor bikes are old models and are quite difficult to get hold of except in online stores and secondhand retailers. One of the models of DP that became quite popular was the DP Fit for Life Airgometer upright bike. This model costs around $1,000 to $1,200 and carries the basic features of an upright indoor bike.

Another model from the DP fitness brand is the Vita Master MBP2. It features various program settings and tension controls. It also has a heart-rate monitor and features battery operated controls. Aside from the Vita Master and the Airgometer, DP also offers DP Air Advantage, DP AirCisor, DP Prime Fit 6100, DP Sit for Life Aircizer and DP Vitamaster MD193.

DP has been overshadowed by more recognizable brands like Schwinn and ProForm. Schwinn, for one, has multiple models out in the market, including the 230 recumbent bike, the 130 upright and the Airdyne exercise bike. Scwhinn's products can cost from $350 to over $1,000. One of the brand's more expensive model, the Evolution, sells at more than $1,000 and has been highly rated by product reviewers. It features an inertia drive system, adjustable resistance and direct drive gearing.

ProForm, another brand competing with DP in the indoor bike market, offers machines that cost $150 to $1,200. One of its low end models is the SR30. The features of this machine are very basic and the model is geared at entry level market. It features magnetic resistance, pulse sensors and an LCD console. Other ProForm models targeting the low end and middle markets are the SR80, GL 35 and GL 105.

The DP brand might not be at the top of the market, but its machines still serve the basic operating functions of exercise bikes. They offer users the ability to tone and strengthen leg and thigh muscles and provide an effective cardiovascular exercise routine. Limited availability aside, DP exercise machines, including the secondhand models being sold in online auction sites, might still be worth consumers' time and investment.

The DP exercise bike is not exactly hogging the physical fitness equipment limelight, but there are still those who like the brand. For these loyal customers, auction sites and online stores are their best options of finding one these products.

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วันเสาร์ที่ 12 มิถุนายน พ.ศ. 2553

วันศุกร์ที่ 11 มิถุนายน พ.ศ. 2553

Stun Gun - Physiological Effects

Have ever watched the TV show Star Trek and heard of the Romulan disruptor stun weapon? Have you ever thought about what it disrupts? Does it disrupt all the molecules in the person on the receiving end of the ray gun? What about a real stun gun? What does a real stun gun disrupt?

In this article, I will attempt to explain to you what a stun gun does disrupt on the scientific level.

The basic premise of a stun gun is to disrupt the communication superhighway between the brain and the peripheral nerves.

In general, stun guns put out a high-voltage, low amperage charge. Simply put, the stun gun exhibits a lot of punches but lack of power behind those punches. It is kind of like a 3-year-old kid punching the heck out of his daddy's face but does not have enough force behind those punches to put his father in the hospital.

Upon depressing the stun gun's trigger, the electric charge passes into the perpetrator's body. Because it is high voltage (lots of punches), the electric charge will pass through thick clothing, fat under the skin, and subcutaneous soft tissue, particularly muscle. However, the low amperage (lack of power) does not have enough intensity to cause damage to the perpetrator's body unless the charge is applied over a period of time.

The electric charge of a real stun gun "disrupts" or interrupts the attacker's nervous system.

The following results could happen:


The charge of the stun gun can act synergistically with the electrical signals from the brain causing end tissue, such as a muscle, to contract continuously over short amount of time. The attacker will have a hard time telling is muscles to move in a different direction. This continuous contraction of the muscle will be hard to stop by the attacker due to the influx of an external charge provided by the stun gun. In laymen's terms, if he wanted to cease contracting his muscles, he couldn't because the charge provided by the stun gun is supplying the nerves that connect to his muscles.
The charge of the stun gun can exhibit a pulse frequency that imitates the body's own electrical signals. In this method, the charge from the stun gun will tell the attacker's muscles to do a ton of work, namely rapid repetitive contraction, in order to exhaust the attacker's adenosine triphosphate (ATP) in his muscle cells. ATP is the energy currency of all cells in the body. It is the energy of ATP that causes muscles to contract. The lack of ATP in the attacker's muscles will result in muscular weakness in the attacker. In other words, he will be too dazed and weak to get up after getting shocked.

The attacker has the same muscles and nerves throughout his entire body. Therefore, strategically placing the probes of the stun gun really does not matter in order to put down an attacker.

Note, however. Putting the probes of the stun gun in the attacker's stomach will not only cause severe muscular contraction in his abdominal (skeletal) muscles, but also cause the smooth muscles making up the digestive tract and the urinary bladder to contract as well. Simply put, you can cause your attacker to defecate AND urinate in his pants by the time he kisses the concrete!! YOU would have been a bad choice for this street punk.

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