Sensitization
Sensitization is an example of non-associative learning in which the progressive amplification of a response follows repeated administrations of a stimulus.[1] An everyday example of this mechanism is a warm sensation followed by pain caused by constantly rubbing an arm. The pain is the result of the progressively amplified response of the nerve endings. Sensitization is thought to underlie both adaptive as well as maladaptive learning processes in the organism.
Types of sensitization
Sensitization refers to the process by which a cellular receptor becomes more likely to respond to a stimulus (more efficient). There are a couple of different types of sensitization:
- Electrical or chemical stimulation of the rat hippocampus causes strengthening of synaptic signals, a process known as long-term potentiation or LTP.[2] LTP of AMPA receptors has been proposed as a potential mechanism underlying memory and learning in the human brain.
- A different type of sensitization is that of kindling, where repeated stimulation of hippocampal or amygdaloid neurons in the limbic system eventually leads to seizures in laboratory animals. Having been sensitized, very little stimulation is required to produce the 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.[3] Often, people suffering from temporal lobe epilepsy report symptoms of negative affect such as anxiety and depression that might result from limbic dysfunction.[4]
- A third type is central sensitization, where nociceptive neurons in the dorsal horns of the spinal cord become sensitized by peripheral tissue damage or inflammation.[5] This type of sensitization has been suggested as a possible causal mechanism for chronic pain conditions.
- Drug sensitization occurs in drug addiction, and is defined as an increased effect of drug following repeated doses (the opposite of drug tolerance). Addiction may also be related to increased (sensitized) drug craving when environmental stimuli associated with drug taking, or drug cues, are encountered. This process may contribute to the risk for relapse in addicts attempting to quit.[6] Such sensitization involves changes in brain mesolimbic dopamine transmission, as well as a molecule inside mesolimbic neurons called delta FosB.
These various types indicate that sensitization may underlie both pathological and adaptive functions in the organism.
Etiology
Sensitization has been implied as a causal or maintaining mechanism in a wide range of apparently unrelated pathologies including substance abuse and dependence, allergies, asthma, and some medically unexplained syndromes such as fibromyalgia and multiple chemical sensitivity. Sensitization has also been suggested in relation to psychological disorders such as post-traumatic stress disorder, panic anxiety and mood disorders.[7][8][9]
History
Eric Kandel was one of the first to study the neural basis of sensitization based on his experiments observing gill withdrawal of the seaslug Aplysia in the 1960s and 1970s. Kandel and his colleagues showed that after habituation from siphon touching (gill withdrawal response weakened), applying a paired noxious electrical stimulus to the tail and a touch to the siphon, gill withdrawal was once again noted. After this sensitization, applying a light touch to the siphon, absent of noxious stimulus to the tail, Aplysia produced a strong gill withdrawal response. When tested several days after the initial trials, this response was still manifest (After Squire and Kandel, 1999[10]). In 2000, Eric Kandel was awarded the Nobel Prize in Physiology or Medicine for his research in neuronal learning processes.
See also
References
- ^ Bell IR, Hardin EE, Baldwin CM, Schwartz GE (1995). "Increased limbic system symptomatology and sensitizability of young adults with chemical and noise sensitivities". Environ Res 70(2): 84–97, PMID 8674484, doi:10.1006/enrs.1995.1052.
- ^ Collingridge GL, Isaac JT, Wang YT (2004). "Receptor trafficking and synaptic plasticity". Nat Rev Neurosci 5(12): 952–962, PMID 15550950, doi:10.1038/nrn1556.
- ^ Morimoto K, Fahnestock M, Racine RJ (2004). "Kindling and status epilepticus models of epilepsy: Rewiring the brain". Prog Neurobiol 73(1): 1–60, PMID 15193778, doi:10.1016/j.pneurobio.2004.03.009.
- ^ Teicher MH, Glod CA, Surrey J, Swett C, Jr (1993). "Early childhood abuse and limbic system ratings in adult psychiatric outpatients". J Neuropsychiatry Clin Neurosci 5(3): 301–306, PMID 8369640.
- ^ Ji RR, Kohno T, Moore KA, Woolf CJ (2003). "Central sensitization and LTP: Do pain and memory share similar mechanisms?". Trends Neurosci 26(12): 696–705, PMID 14624855.
- ^ Robinson TE, Berridge KC (1993). "The neural basis of drug craving: An incentive-sensitization theory of addiction". Brain Res Brain Res Rev 18(3): 247–291, PMID 8401595.
- ^ Rosen JB, Schulkin J (1998). "From normal fear to pathological anxiety". Psychol Rev 105(2): 325–350, doi:10.1037/0033-295X.105.2.325 PMID 9577241.
- ^ Antelman SM (1988). "Time-dependent sensitization as the cornerstone for a new approach to pharmacotherapy: drugs as foreign/stressful stimuli". Drug Development Research 14: 1–30.
- ^ Post RM (1992). "Transduction of psychosocial stress into the neurobiology of recurrent affective disorder". Am J Psychiatry 149(8): 999–1010, PMID 1353322.
- ^ Squire LR, Kandel ER (1999). Memory: From Mind to Molecules. New York: Scientific American Library; New York: W.H. Freeman. ISBN 0716760371.