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Sensitization

Sensitization is a nonspecific phenomenon whereby repeated exposure to a stimulus results in the progressive enhancement of a response. The concept has been studied using the reflexes of animals such as Aplysia to better understand the underlying neural mechanisms. Research on sensitization includes a range of phenomena including drug sensitization and cross-sensitization, where a response is enhanced for a whole class of stimuli in addition to the original repeated stimulus. It has also been implicated in the pathologies of various health disorders.

History

Eric Kandel was one of the first researchers to study the neural basis of sensitization, conducting experiments in the 1960s and 1970s on the gill withdrawal reflex of the sea slug Aplysia. Kandel and his colleagues first habituated the reflex, weakening the response by repeatedly touching the animal's siphon. They then paired noxious electrical stimulus to the tail with a touch to the siphon, causing the gill withdrawal response to reappear. After this sensitization, a light touch to the siphon alone produced a strong gill withdrawal response, and this sensitization effect lasted for several days. (After Squire and Kandel, 1999). In 2000, Eric Kandel was awarded the Nobel Prize in Physiology or Medicine for his research in neuronal learning processes.

Neural substrates

The neural basis of behavioral sensitization is often unknown, but it typically results from a cellular receptor becoming more likely to respond to a stimulus. Several examples of neural sensitization include:

  • Electrical or chemical stimulation of the rat hippocampus causes strengthening of synaptic signals, a process known as long-term potentiation (LTP). The LTP of AMPA receptors is a potential mechanism underlying memory and learning in the brain.
  • In kindling, repeated stimulation of hippocampal or amygdaloid neurons in the limbic system eventually leads to seizures in laboratory animals. After sensitization, very little stimulation may be required to produce seizures. Thus, kindling has been suggested as a model for temporal lobe epilepsy in humans, where stimulation of a repetitive type (flickering lights for instance) can cause epileptic seizures. Often, people suffering from temporal lobe epilepsy report symptoms of negative effects such as anxiety and depression that might result from limbic dysfunction.
  • In central sensitization, nociceptive neurons in the dorsal horns of the spinal cord become sensitized by peripheral tissue damage or inflammation. This type of sensitization has been suggested as a possible causal mechanism for chronic pain conditions. The changes of central sensitization occur after repeated trials to pain. Research from animals has consistently shown that when a trial is repeatedly exposed to a painful stimulus, the animal’s pain threshold will decrease and result in a stronger pain response. Researchers believe that there are parallels that can be drawn between these animal trials and persistent pain in people. For example, after a back surgery that removed a herniated disc from causing a pinched nerve, the patient may still continue to feel pain. Also, newborns who are circumcised without anesthesia have shown stronger reactions to similar future procedures than those who were given anesthesia.
  • Drug sensitization (or reverse tolerance) occurs in substance use disorder, and is defined as an increased effect of drug following repeated doses (the opposite of drug tolerance). Such sensitization involves changes in brain mesolimbic dopamine transmission, as well as a protein inside mesolimbic neurons called delta FosB. An associative process may contribute to addiction, for environmental stimuli associated with drug taking may increase craving. This process may increase the risk for relapse in addicts attempting to quit.

Cross-sensitization

Cross-sensitization is a phenomenon in which sensitization to a stimulus is generalized to a related stimulus, resulting in the amplification of a particular response to both the original stimulus and the related stimulus. For example, types of cross-sensitization to the neural and behavioral effects of addictive drugs well characterized, such as sensitization to the locomotor response of a stimulant resulting in cross-sensitization to the motor-activating effects of other stimulants. Similarly, reward sensitization to a particular addictive drug often results in reward cross-sensitization, which entails sensitization to the rewarding property of other addictive drugs in the same drug class or even certain natural rewards.

In animals, cross-sensitization has been established between the consumption of many different types of drugs of abuse – in line with the gateway drug theory – and also between sugar consumption and the self-administration of drugs of abuse.

As a causal factor in pathology

Sensitization has been implied as a causal or maintaining mechanism in a wide range of apparently unrelated pathologies including addiction, allergies, asthma, overactive bladder, and potentially contribute to some medically unexplained syndromes such as fibromyalgia, as well as the controversial diagnosis multiple chemical sensitivity. Sensitization may also contribute to psychological disorders such as post-traumatic stress disorder, anxiety disorder or panic disorder, and mood disorders.

See also

References