My friend at times can’t help but scratch her itchy skin and scalp furiously. She had a hemorrhagic stroke 10 years ago and is brain-injured. Now I know why.
“As most of us know, a good scratch can satisfy an itch. Yet the question of why we itch and scratch in the first place has confused researchers for years. Recently, however, science has begun to enlighten us to the mechanisms at work in the itch–scratch cycle.”
The itch sensation was thought to travel along the same nerve pathway used by pain signals. Itch was thought to be a lessened form of pain.
“Modern molecular, genetic, and anatomical studies now indicate that itch usually follows its own distinct course,” says Dr. Qiufu Ma, PhD, an HMS professor of neurobiology who has studied the phenomenon. Itch runs along the brain pathways and links the skin, the spinal cord, and the brain.
Itch and pain represent different sensations that evoke distinct behaviors. Place your hand on a hot burner and you instantly pull it away because the pain is intense. By contrast, when a piece of clothing brushes against your bare forearm, you scratch to quiet the irritation, giving little thought to the sensation and your reaction to it.
“These distinct behaviors likely developed to protect us against different types of threats,” says Anne Louise Oaklander, MD, PhD, an associate professor of neurology at HMS who studies chronic pain and itch.
“Pain is obvious and, without it, we wouldn’t live long. There would be nothing to prevent us from putting our hand into a fire or onto that hot burner. ” She adds that the itch–scratch cycle most likely evolved to protect us from small, clinging threats, insects or plants that can be avoided by withdrawal movements.
Studies focused on the neural mechanisms associated with itch, but several recently have succeeded in identifying a neural component to the itch sensation and its scratch response. In 2009, neuroscientists at the University of Minnesota identified part of the mechanism by which scratch relieves an itch. They showed that relief takes place deep within the spinal cord along the “spinothalamic” tract.
The STT transmits sensations, such as pain, temperature, touch and, it turns out, itch to the thalamus, deep within the brain. This process relays the information to the brain’s center for perceptual awareness, called the sensory cortex.
The scientists monitored spinal nerve activity in monkeys whose lower limbs had been exposed to itch-inducing histamine. With each exposure, the monkeys’ STT neurons went wild. But when the researchers used a device that mimics monkey fingers to scratch the itchy limbs, they saw a dramatic drop in STT neuronal activity. This sudden drop suggests that the act of scratching calmed the STT neurons.
In a recent study published in the journal Neuron, Ma identified a neural component necessary for the pain sensation and itch suppression that also may help answer “why do we itch?” question.
Ma knew this pain–itch came about unexpectedly, while monitoring the behavior of mice that had been genetically altered to lose the action of VGLUT2 (a protein, critical for normal brain function, and plays roles in pain perception, one of the causes for itchiness). He discovered VGLUT2-deficient mice developed itch disorders as severe as those found in humans with chronic itch disorders. Essentially, Ma’s research team had created a mouse model that mimics some types of chronic itch in human patients.
“Removing VGLUT2 from pain-related sensory neurons in these mice weakened their responses to acute and chronic pain and caused the sensitization of multiple itch pathways,” says Ma. “The mice began to scratch until they developed skin lesions.”
The VGLUT2 pathway, says Ma, likely quells excessive itching by activating certain inhibitory neurons in the spinal cord or brain.
Very common itches brought on by a chemical or mechanical stimulus—think mosquito bites and poison ivy—can be treated readily with agents that counteract histamine, a chemical the body produces to fight allergic reactions. A mosquito bite causes the body to release histamine in the area of the bite, turning the skin red and itchy. An antihistamine relieves the itch sensation by preventing histamine from binding to itch-instigating receptors in the skin.
Widespread itch, by contrast, is often caused by diseases of internal organs. More than 80 percent of chronic kidney disease patients have chronic, widespread itch, and some patients with liver disease and non-Hodgkin’s lymphoma also suffer from severe itch. Certain pain medications, such as opiates, can also trigger itching.
Neuropathic itch is a different kind of chronic itch caused by a malfunction of nerve cells.
Brain injuries can affect itchiness in several ways:
- Disrupting the normal neural pathways that regulate itch sensations
- Causing hypersensitivity in the nervous system similar to how chronic pain develops
- Creating phantom itch sensations where the brain perceives itching without an actual stimulus
It appears in many of the same conditions that can cause chronic neuropathic pain, including shingles, a very common viral infection. The complications of shingles are a focus of study for Dr. Anne Louise Oaklander in her laboratory at the Nerve Injury Unit of Massachusetts General Hospital. (Other conditions that can spur neuropathic itch include spinal cord lesions, brain tumors, and phantom limb syndrome).
“Neuropathic itch is ultimately caused by inappropriate firing of itch neurons in the central nervous system,” says Oaklander. “People with chronic itch often feel as if insects are crawling all over them.”
This treatment is based on paradoxical clinical observations. Morphine, which triggers a response in certain opioid receptors in the brain, suppresses pain but causes itch, while nalfurafine, which triggers action in another set of opioid receptors, suppresses itch. It is conceivable that a combination of morphine and nalfurafine might relieve pain without causing itch side effects.
And, if scientists manage to develop compounds that activate the inhibitory pathway discovered by Ma and his colleagues, “we would have a completely novel strategy to treat itch,” he says.
“Scratching,” said the sixteenth-century French essayist Montaigne, “is one of the sweetest gratifications of nature and as ready at hand as any. But repentance follows too annoyingly close at its heels.”
Now that the scientific community’s view of itch has evolved to the point where it’s considered a bona fide and potentially serious clinical condition, people who suffer as Montaigne did—his eczema caused him to scratch incessantly—may finally find some relief.
Itchiness in people with brain injuries is a recognized medical issue known as neuropathic itch. Unlike ordinary itch, which originates in the skin, a neuropathic itch is caused by damage to the nervous system itself, including the brain, spinal cord, or peripheral nerves:
- Lesions in the brain from conditions like stroke, tumors, or multiple sclerosis can interfere with the neural pathways that process itch signals, causing persistent itching.
- Neuropathic itch is considered a network disorder caused by an imbalance between the excitatory and inhibitory signaling of neurons.
- Brain damage can cause a miscommunication where internal nerve damage is perceived as an external itch. The brain knows something is wrong but misinterprets the signal.
- A stroke or traumatic brain injury (TBI) can result in sensory overload, where the brain becomes overwhelmed by stimulation. This can lead to various sensory issues, including pain, tingling, and itching.
- In some cases, a minor TBI or concussion can cause temporary symptoms like itching, similar to the sensation of stitches healing.
