Category Archives: PATHWAYS/GRAY MATTER [ MESSENGERS ( THE NERVOUS SYSTEM ) ]

GOOD FEELINGS / PLEASURE CENTERS [ THE NERVOUS SYSTEM ]

GOOD FEELINGS / PLEASURE CENTERS [ NERVOUS SYSTEM ]

GOOD FEELINGS

Pleasure also has its centers In the brain. A Tulane University neurologist stumbled across one such center in the 1950s when he tried to electrically stimulate the brains of schizophrenics to break them out of their passivity. His patients told him their implanted electrodes created pleasant sensations. The neurologist, Robert G. Heath, seized upon the results, focused his attention on the brain’s pleasure centers, and published the 1964 book The Role of Pleasure in Behavior.

Together with the discovery of pain centers in the brain, research on the physical causes of the sense of pleasure seemed to prove the ancient wisdom that humans seek to act in ways that bring them pleasure and reduce or avoid pain. New paths of investigation have led to innovative treatments for addiction, which is a form of behavior based on compulsive forms of pleasure seeking. PET scans reveal how drugs such as cocaine and heroin activate the brain’s pleasure centers. Cocaine, for example, blocks a neuron’s reuptake mechanism, which causes dopamine to linger in the synaptic cleft.

PLEASURE CENTERS

Joy, happiness, pleasure-what-ever you want to call the positive feelings that bring rewarding sensations and make life worth living-arise from the sensations of security, warmth, and social well-being combined with an awareness of the rightness of such feelings. A healthy brain recognizes the conditions that give rise to pleasure and responds to them appropriately. An unhealthy brain, or one that has learned negative behaviors such as addiction, can miss out on experiencing life’s joys. Both are primarily a matter of chemistry.

GOOD FEELINGS / PLEASURE CENTERS [ THE NERVOUS SYSTEM ]

The sensation of pleasure registers in several brain regions, including significant centers in the hypothalamus and nucleus accumbens , which lies below a portion of the basal ganglia linked to movement. All such pleasure centers rely on the chemical work performed by endorphins and neurotransmitters, particularly dopamine, to create and sustain a happy mood. Experiments with rats have demonstrated the key role of dopamine. In the 1950s, scientists wired rats’ brains so that when they pressed a bar, they received a mild electric shock to the hypothalamus. This stimulation registered as pleasure; the rats would rather press the bar than eat. However, in later experiments, rats wired for self-stimulation first received injections of drugs that block the receptors where dopamine normally binds, denying its pleasure-giving action. The rats no longer felt a pleasant reward from pressing a lever to stimulate their brain, and they stopped doing so. When humans take a similar dopamine-lowering medication, often in order to ward off hallucinations and other psychotic behavior, the drug’s success comes at a price. Delusions may leave, but so do joy and motivation. Conversely, drugs like amphetamines that increase the activity of dopamine in the brain lower the threshold for the perception of pleasure. Too much of a drug-induced pleasant sensation, however, can lead to addiction and manic moods.

When the skin warms, the sympathetic division of the autonomic nervous system dilates blood vessels near the surface and activates the sweat glands. When body temperature cools, the autonomic nervous system narrows surface vessels to send blood to deeper, more vital organs.

“The greatest pleasure of life is love,” said the Greek playwright Euripides nearly 2,500 years ago. Like other forms of pleasure, love is processed by brain chemistry, specifically by heightened levels of neurotransmitters in the pleasure centers. MRI scans of the brain relate the feeling of lust to estrogen and androgens; attraction-more emotional than physical-appears to be associated with serotonin and dopamine. The brain chemistry that supports long-term relationships such as lifelong commitment has been harder to pin down.

Playing key roles in the sensation of pleasure are oxytocin, endorphins, and phenylethylamine , or PEA, sometimes called the love drug. These chemicals help foster the “high” felt in the first stages of love, as well as the euphoria some-times reported by long-distance runners. Even a small pleasure, such as finding your lost car keys, begins with a tiny rise of these and similar neurotransmitters in the brain’s pleasure centers.

DEGREES OF PAIN [ THE NERVOUS SYSTEM ]

DEGREES OF PAIN [ THE NERVOUS SYSTEM ]

Similar pains don’t always register with the same intensity. Although nearly all humans-besides the very few who lack the ability to feel pain recognize extreme heat or a deep cut as painful, they can react differently. Some tolerate pain more easily, whereas others feel it more intensely. Physical, cultural, and psychological variables may also influence a person’s individual degree of pain tolerance.

Cultural and psychological influences on an individual’s tolerance of pain are more ethereal and hard to measure than physiological influences. During World War II, British soldiers injured in the brutal fighting at Anzio, Italy, in 1943 routinely refused morphine to kill their pain, while civilians who suffered far less serious wounds demanded it to ease their pain. The surgeon who noted the difference came to the conclusion that certain kinds of pain could be a matter of mind, not of the body.

Ritual mortification of the flesh at the Hindu festival of Thaipusam in Malaysia demonstrates the power of brain over pain.
Ritual mortification of the flesh at the Hindu festival of Thaipusam in Malaysia demonstrates the power of brain over pain.

Long-term, intense pain can create a different perception in the brain. This chronic sensation may confuse the central nervous system and result in hyperalgesia, or pain amplification. Such pain registers on the same kind of synaptic receptors that are activated during certain kinds of learning. Under the worst- case scenarios, the chronic pain causes the spinal cord to “learn” hyperalgesia, and pain’s sensitivity increases. Examples include the lingering pain of phantom limbs-the sensation of pain from an amputated arm or leg.

Neural networks that process stimuli from a limb remain primed to respond to signals even after it’s gone. Random signals may get misinterpreted as tingling, itching, pain, or some other sensation. Neuroscientist Vilayanur Ramachandran found he could create sensations in phantom limbs by applying pressure to various skin surfaces. His conclusion: The cerebral cortex relocated sensation pathways associated with the old limb. These pathways may always have existed in a weak state, but loss of the limb amplified them. Unfortunately, neural networks that continue to recognize “pain” signals from a missing limb become more strongly primed to repeat the mistake. Treatments for phantom pain range from drug therapy to acupuncture and deep brain stimulation. Newer treatments, using mirrors or virtual reality goggles, trick the brain into thinking it can control the amputated limb.

PATHWAYS/GRAY MATTER [ MESSENGERS ( THE NERVOUS SYSTEM ) ]

PATHWAYS / GRAY MATTER [ MESSENGERS ( THE NERVOUS SYSTEM ) ]

PATHWAYS

Pain signals take rwo tracks on their way to the brain. The express line, like a nonstop train between cities, sends signals through the spinal cord and connects directly to the thalamus. While some pain signals are diverted along the way, those that reach the thalamus are relayed to the cerebral cortex, where they quickly get analyzed.

When you cut your finger while slicing an onion, the quick pathway of pain activates the cortex to figure out how much pain you feel and where you feel it. The brain’s quick recognition of the danger may stop you from bringing down the knife blade again and slicing your finger a second time.

The other, slower pathway travels through slow, narrow nerve fibers with frequent synaptic connections, lumbering like a commuter train that stops at every little burg. These sensations register in the brain stem and hypothalamus, as well as in other deep brain regions, before a portion of them reach the thalamus. Effects include longer-lasting aches as well as emotional reactions to pain, such as the sheepishness of realizing you injured yourself through either clumsiness or negligence (or both). These slow-action pains include the unremitting discomfort of chronic diseases such as cancer.

GRAY MATTER

But not all pain sensations terminate in the thalamus. Many halt at a portion of the brain stem known as the mesencephalic central gray matter. It’s a tiny spot that is difficult to locate. But as a conver gence zone for pain impulses, this area is highly sensitive. When lab animals have their mesencephalic gray matter stimulated by electricity, they can be operated on without painkillers. Yet they maintain their sensitivity to touch, heat, and other sensations in the pain- affected body parts.

PATHWAYS / GRAY MATTER [ MESSENGERS ( THE NERVOUS SYSTEM ) ]

CAPTAIN AHAB asked his ship’s carpenter for a special bit of work in the novel Moby-Dick. Ahab, who had lost a leg to the teeth of a white whale, hoped a replacement limb might expunge the feeling of “another leg in the same identical place with … my lost leg.” “Phantom” limbs, such as Ahab’s lost leg, have been reported since ancient times. American neurologist Silas Weir Mitchell cataloged many varieties in the Civil War. About 70 percent of phantom limbs proved excrUCiatingly and chronically painful. How could a missing leg create the illusion of existence, or even pain? The answer lies in the brain.