Sensory Systems/Gustatory System
Introduction[edit | edit source]
The Gustatory System or sense of taste allows us to perceive different flavors from substances like food, drinks, medicine etc. Molecules that we taste or tastants are sensed by cells in our mouth, which send information to the brain. These specialized cells are called taste cells and can sense 5 main tastes: bitter, salty, sweet, sour and umami (savory). All the variety of flavors that we know are combinations of molecules which fall into these categories.
Measuring the degree by which a substance presents one of the basic tastes is done subjectively by comparing its taste to a taste of a reference substance according to relative indexes of different substances. For the bitter taste quinine (found in tonic water) is used to rate how bitter a substance is. Saltiness can be rated by comparing to a dilute salt solution. The sourness is compared to diluted hydrochloric acid (H+Cl-). Sweetness is measured relative to sucrose. The values of these reference substances are defined as 1.
Bitter[edit | edit source]
(Coffee, mate, beer, tonic water etc.)
It is considered by many as unpleasant. In general bitterness is very interesting because a large number of bitter compounds are known to be toxic so the bitter taste is considered to provide an important protective function. Plant leafs often contain toxic compounds. Herbivores have a tendency to prefer immature leaves, which have higher protein content and lower poison levels than mature leaves. It seems that even if the bitter taste is not very pleasant at first, there is a tendency to overcome this aversion because coffee and drinks containing rich amount of caffeine and are widely consumed. Sometimes bitter agents are added to substances to prevent accidental ingestion.
Salty[edit | edit source]
The salty taste is primarily produced by the presence of cations such as Li+ (lithium ions), K+ (potassium ions) and more commonly Na+ (sodium). The saltiness of substances is compared to sodium chloride, which is typically used as table salt (Na+Cl-). Potassium chloride K+Cl- is the principal ingredient used in salt substitutes and has an index of 0.6 (see bellow part 5) compared to 1 of Na+Cl-.
Sour[edit | edit source]
(Lemon, orange, wine, spoiled milk and candies containing citric acid)
Sour taste can be mildly pleasant and it is linked to salty flavor but more exacerbated. Typically sour are fruits, which are over-riped, spoiled milk, rotten meat, and other spoiled foods, which can be dangerous. It also tastes acids (H+ ions) which taken in large quantities can cause irreversible tissue damage. Sourness is rated compared to hydrochloric acid (H+Cl-), which has a sourness index of 1.
Sweet[edit | edit source]
(Sucrose (table sugar), cake, ice cream etc.)
Sweetness is regarded as a pleasant sensation and is produced by the presence of mostly sugars. Sweet substances are rated relative to sucrose, which has an index of 1. Nowadays there are many artificial sweeteners in the market, these include saccharin, aspartame and sucralose but it is still not clear how these substitutes activate the receptors.
Umami (savory or tasty)[edit | edit source]
(Cheese, soy sauce etc.)
Recently, umami has been added as the fifth taste. This taste signals the presence of L-glutamate and it is a very important for the Eastern cuisines. Monosodium glutamate is commonly used to bring umami to food, but various plants and meats are also sources of glutamates. Umami is further enhanced when glutamate is present with the nucleotides inosinate and guanylate.
Sensory Organs[edit | edit source]
Tongue and Taste Buds[edit | edit source]
Taste cells are epithelial and are clustered in taste buds located in the tongue, soft palate, epiglottis, pharynx and the esophagus the tongue being the primary organ of the Gustatory System.
Taste buds are located in papillae along the surface of the tongue. There are three types of papillae in human: fungiform located in the anterior part containing approximately five taste buds, circumvallate papillae which are bigger and more posterior than the previous ones and the foliate papillae that are in the posterior edge of the tongue. Circumvallate and foliate papillae contain hundreds of taste buds. In each taste bud there are different types of cells: basal, dark, intermediate and light cells. Basal cells are believed to be the stem cells that give rise to the other types. It is thought that the rest of the cells correspond to different stages of differentiation where the light cells are the most mature type of cells. An alternative idea is that dark, intermediate and light cells correspond to different cellular lineages. Taste cells are short lived and are continuously regenerated. They contain a taste pore at the surface of the epithelium where they extend microvilli, the site where sensory transduction takes place. Taste cells are innervated by fibers of primary gustatory neurons. They contact sensory fibers and these connections resemble chemical synapses, they are excitable with voltage-gated channels: K+, Na+ and Ca+ channels capable of generating action potentials. Although the reaction from different tastants varies, in general tastants interact with receptors or ion channels in the membrane of a taste cells. These interactions depolarize the cell directly or via second messengers and in this way the receptor potential generates action potentials within the taste cells, which lead to Ca2+ influx through Ca2+ voltage-gated channels followed by the release of neurotransmitters at the synapses with the sensory fibers.
Tongue map[edit | edit source]
The idea that the tongue is most sensitive to certain tastes in different regions was a long time misconception, which has now been proved to be wrong. All sensations come from all regions of the tongue.
Supertasters[edit | edit source]
An average person has about 5'000 taste buds. A "supertaster" is a person whose sense of taste is significantly more sensitive than average. The increase in the response is thought to be because they have more than 20’000 taste buds, or due to an increased number of fungiform papillae.
Transduction of Taste[edit | edit source]
As mentioned before we distinguish between 5 types of basic tastes: bitter, salty, sour, sweet and umami. There is one type of taste receptor for each flavor known and each type of taste stimulus is transduced by a different mechanisms. In general bitter, sweet and umami are detected by G protein-coupled receptors and salty and sour are detected via ion channels.
Bitter[edit | edit source]
Bitter compounds act through G protein coupled receptors (GPCR’s) also known as a seven-transmembrane domains, which are located in the walls of the taste cells. Taste receptors of type 2 (T2Rs) which is a group of GPCR’s is thought respond to bitter stimuli. When the bitter-tasting ligand binds to the GPCR it releases the G protein gustducin, its 3 subunits break apart and activate phosphodiesterase, which in turn converts a precursor within the cell into a secondary messenger, closing the K+ channels. This secondary messenger stimulates the release of Ca2+, contributing to depolarization followed by neurotransmitter release. It is possible that bitter substances that are permeable to the membrane are sensed by mechanisms not involving G proteins.
Salt[edit | edit source]
The amiloride-sensitive epithelial sodium channel (ENaC), a type of ion channel in the taste cell wall, allows Na+ ions to enter the cell down an electrochemical gradient, altering the membrane potential of the taste cells by depolarizing the cell. This leads to an opening of voltage-gated Ca2+ channels, followed by neurotransmitter release.
Sour[edit | edit source]
The sour taste signals the presence of acidic compounds (H+ ions) and there are three receptors: 1) The ENaC, (the same protein involved in salty taste). 2) There are also H+ gated channels; one is the K+ channel, which allows K+ outflux of the cell. H+ ions block these so the K+ stays inside the cell. 3) A third channel undergoes a configuration change when a H+ attaches to it leading to an opening of the channel and allowing an influx of Na+ down the concentration gradient into the cell, leading to the opening of a voltage gated Ca2+ channels. These three receptors work in parallel and lead to depolarization of the cell followed by neurotransmitter release.
Sweet[edit | edit source]
Sweet transduction is mediated by the binding of a sweet tastant to GPCR’s located in the apical membrane of the taste cell. Saccharide activates the GPCR, which releases gustducin and this in turn activates cAMP (cyclic adenylate monophosphate). cAMP will activate the cAMP kinase that will phosphorylate the K+ channels and eventually inactivate them, leading to depolarization of the cell and followed by neurotransmitter release.
Umami (Savory)[edit | edit source]
Umami receptors involve also GPCR’s, the same way as bitter and sweet receptors. Glutamate binds a type of the metabotropic glutamate receptor mGlurR4 causing a G-protein complex to activate a secondary receptor, which ultimately leads to neurotransmitter release. In particular how the intermediate steps work, is currently unknown.
Signal Processing[edit | edit source]
In humans, the sense of taste is transmitted to the brain via three cranial nerves. The VII facial nerve carries information from the anterior 2/3 part of the tongue and soft palate. The IX nerve or glossopharyngeal nerve carries taste sensations from the posterior 1/3 part of the tongue and the X nerve or vagus nerve carries information from the back of the oral cavity and the epiglottis.
The gustatory cortex is the brain structure responsible for the perception of taste. It consists of the anterior insula on the insular lobe and the frontal operculum on the inferior frontal gyrus of the frontal lobe. Neurons in the gustatory cortex respond to the five main tastes.
Taste cells synapse with primary sensory axons of the mentioned cranial nerves. The central axons of these neurons in the respective cranial nerve ganglia project to rostral and lateral regions of the nucleus of the solitary tract in the medulla. Axons from the rostral (gustatory) part of the solitary nucleus project to the ventral posterior complex of the thalamus, where they terminate in the medial half of the ventral posterior medial nucleus. This nucleus projects to several regions of the neocortex, which include the gustatory cortex.
Gustatory cortex neurons exhibit complex responses to changes in concentration of tastant. For one tastant, the same neuron might increase its firing and for an other tastant, it may only respond to an intermediate concentration.
Taste and Other Senses[edit | edit source]
In general the Gustatory Systems does not work alone. While eating, consistency and texture are sensed by the mechanoreceptors from the somatosensory system. The sense of taste is also correlated with the olfactory system because if we lack the sense of smell it makes it difficult to distinguish the flavor.
Spicy food[edit | edit source]
(black peppers, chili peppers, etc.)
It is not a basic taste because this sensation does not arise from taste buds. Capsaicin is the active ingredient in spicy food and causes “hotness” or “spiciness” when eaten. It stimulates temperature fibers and also nociceptors (pain) in the tongue. In the nociceptors it stimulates the release of substance P, which causes vasodilatation and release of histamine causing hiperalgesia (increased sensitivity to pain).
In general basic tastes can be appetitive or aversive depending on the effect that the food has on us but also essential to the taste experience are the presentation of food, color, texture, smell, previous experiences, expectations, temperature and satiety.
Taste disorders[edit | edit source]
Ageusia (complete loss of taste)[edit | edit source]
Ageusia is a partial or complete loss in the sense of taste and sometimes it can be accompanied by the loss of smell.
Dysgeusia (abnormal taste)[edit | edit source]
Is an alteration in the perception associated with the sense of taste. Tastes of food and drinks vary radically and sometimes the taste is perceived as repulsive. The causes of dysgeusia can be associated with neurologic disorders.