Retronasal smell

Retronasal smell, retronasal olfaction, is the ability to perceive flavor dimensions of foods and drinks. Retronasal smell is a sensory modality that produces flavor. It is best described as a combination of traditional smell (orthonasal smell) and taste modalities.[1] Retronasal smell creates flavor from smell molecules in foods or drinks shunting up through the nasal passages as one is chewing. When people use the term "smell", they are usually referring to "orthonasal smell", or the perception of smell molecules that enter directly through the nose and up the nasal passages. Retronasal smell is critical for experiencing the flavor of foods and drinks. Flavor should be contrasted with taste, which refers to five specific dimensions: (1) sweet, (2) salty, (3) bitter, (4) sour, and (5) umami. Perceiving anything beyond these five dimensions, such as distinguishing the flavor of an apple from a pear for example, requires the sense of retronasal smell.

History

Evolutionarily, smell has long been presumed to be a less-important sense for humans, especially compared to vision. Vision appears to dominate human stimuli perception, but researchers now argue that smell cues are highly informative to humans despite being less obviously so. Before his death in 1826, French gastronome Brillat-Savarin published his book, The Physiology of Taste; Or, Meditations on Transcendental Gastronomy: Theoretical, Historical, and Practical Work, in which he makes the first mention of the importance of smell in the “combined sense” of taste. He defines taste in terms of the five taste dimensions in addition to flavor created with the nasal apparatus.[1] Avery Gilbert, in his book The Nose Knows, reviews the work of Henry T. Finck, an American philosopher from the late 1800s who published a groundbreaking essay titled “The Gastronomic Value of Odours.” Flink called flavor a “second way of smelling,” and much subsequent scientific investigation in the early 1900s focused on attempting to break down smell dimensions into basic categories, a feat that has proven too complicated due to the vast number and complexity of odors.

Food connoisseurs and chefs are increasingly capitalizing on the newly ascertained understanding of the role smell plays in flavor. Food scientists Nicholas Kurti and Hervé This expanded upon the physiology of flavor and its importance in the culinary arts. In 2006, This published his book, Molecular Gastronomy: Exploring the Science of Flavor, in which he explores the physical mechanisms that bring about flavor perception. Kurti and This influenced others, such as Harold McGee, whose 1984 book, On Food and Cooking: The Science and Lore of the Kitchen, has been extensively revised in 2004 and remains a key reference on the scientific understanding of food preparation. His book has been described by television personality Alton Brown as “the Rosetta stone of the culinary world.” Such a breakthrough in the understanding of the mechanisms behind experiencing the flavor of different foods is likely to continue inspiring those in the culinary arts to create novel combinations and recipes.

Today, one of the most active food psychologists, Paul Rozin has been the first to successfully map the role of retronasal smell in flavor. In 1982, he explained that smell is a “dual-sense” and made the explicit differentiation between retronasal smell and orthonasal smell.[1] Rozin describes orthonasal smell as “breathing in” and retronasal smell as “breathing out.” In 1982, he devised an experiment in which he trained participants to accurately recognize smells orthonasally before introducing them to the back of the mouth, at which point the success rate fell drastically, demonstrating that smell operates through two distinct mechanisms.[2] His favored example of this duality is Limburger cheese, which is known for its repulsiveness to the nose yet pleasantness to the mouth.

Originally published in 2012, Neurogastronomy by Gordon M. Shepherd provides an overview of the way smell is perceived in humans. The book comprises a detailed review of how retronasal smell, in combination with taste, creates flavor. After a thorough account of the neural basis for identification, recognition, and preference for certain flavors, Shepherd explores potential political and social implications of a deeper understanding of flavor perception, such as causes of obesity and concerns of loss of smell sensitivity in old age.[1]

Overview of the smell pathway

To better understand this mechanism, a simple breakdown of smell pathway is provided below. When humans chew, volatile flavor compounds are pushed through the nasopharynx and smell receptors.

Human olfactory system. 1: Olfactory bulb 2: Mitral cells 3: Bone 4: Nasal epithelium 5: Glomerulus 6: Olfactory receptor neurons

Olfactory epithelium

The first stop in the olfactory system is the olfactory epithelium, or tissue resting on the roof of the nasal cavity which houses smell receptors. Smell receptors are bipolar neurons that bind odorants from the air and congregate at the olfactory nerve before passing axons to the dendrites of mitral cells in the olfactory bulb.[3] Sensory receptors in the mouth and nose are polarized at resting state, and they depolarize in response to some change in environment, such as coming in contact with odor molecules. Odor molecules, consisting of hydrocarbon chains with functional groups, bind to sensory receptors in the nose and mouth. Properties of functional groups include: (1) length of carbon chain, (2) terminal group, which concord with differences associated with different smells, (3) side group, (4) chirality, (5) shape, and (6) size. When odor molecules bind to sensory receptors, they do so in according to these properties. Each olfactory cell has a single type of receptor, but that receptor can be “broadly tuned” and odor molecules further interact at the receptor level, meaning that, in certain cases, an odor molecule alone may not bind to a receptor, but in the presence of another odor molecule, the original would bind and thus create a sensation of smell only in the presence of the second molecule.[4]

Olfactory bulb

In the olfactory bulb, smell molecules are mapped spatially. These spatial representations are known as “smell images."[1] Spatial representation permits lateral inhibition, or contrast enhancement and gain compression. Contrast enhancement is sensitive to change and highlights stimuli in the brain that are changing rather than at rest. Gain compression heightens sensitivity to low-intensity stimuli while lessening sensitivity to high-intensity stimuli. The olfactory bulb, while still in the primary stages of its understanding by researchers, distinguishes smell from other senses because it marks a deviation in the sensory pathway from what is characteristic of all other senses. Namely, all non-olfactory sensory information passes through the thalamus after the receptor level, but the fact that odor information instead enters its own specialized area could suggest the primitive history of smell and/or a distinct type of processing of odor information on its way to the cortex. The olfactory bulb houses glomeruli, or cell junctures, on which thousands of receptors of the same type, in addition to mitral cells, converge. This organization allows a vast amount of information to be concisely represented without requiring an equally large number of receptor types. The resulting combination of odor information is dubbed an odor image at the level of the olfactory bulb.[5]

Imaging in the olfactory bulb

2DG method

In 1977, biochemist Lou Sokoloff, Seymour Kety, and Floyd E. Bloom developed a way of mapping activity in the brain by tracking the rat brain's metabolization of oxygen. Nerve cells require oxygen and glucose for energy. 2-deoxyglucose (2DG) is a radioactive glucose isotope that can be tracked in the brain since it leaves a trace in the cell where it would normally be metabolized for energy if it were glucose. After stimulation of a certain region of cells, X-ray photographs can be sliced to reveal which cells were active, particularly at synaptic junctures.[6]

Functional magnetic resonance imaging (fMRI) can also be used to measure metabolism of an odor. This method is not terminal as is the 2-deoxyglucose method, so one animal can be measured with many odors, and the resulted images can be compared.

Green fluorescent protein method

Finally, the green fluorescent protein method genetically engineers mice to express a protein in active neurons, and a camera can then be placed inside the skull of the mouse to measure activity.[7]

Findings

These methods reveal, most notably, that the organization of smell information in the olfactory bulb is spatial. Similar molecular patterns result in similar activation patterns with regard to glomeruli, and glomeruli that are closer together encode similar features of smell information.[1][6][7]

Olfactory cortex

The three-layered olfactory cortex, containing pyramidal cells is the next benchmark on the smell pathway. One pyramidal cell receives information from a multiplicity of mitral cells from the olfactory bulb, making the previously organized glomerular pattern distributed in the olfactory cortex. This dispersion of mitral cell information allows for self-excitatory feedback connections, lateral excitation, and self- and lateral-inhibition. These processes contribute to Hebbian learning, named after Donald O. Hebb, and is often simplified by the saying “neurons that fire together wire together.” Long-term potentiation, the neural mechanism for Hebbian learning, allows for memory formation at the pyramidal cell level. Hebbian learning is thus essentially the phenomenon by which the olfactory cortex “remembers” the output of combinations of smell molecules and allows for recognition of previously sensed combinations faster than novel ones by matching them to stored input. The resulting smells that were previously called odor images are stored in the olfactory cortex for recognition are referred to now as odor objects.[5] Experience therefore strengthens signal-to-noise ratio in that a previously sensed odor object can be more easily distinguished against greater background noise.[8]

Orbitofrontal cortex

The orbitofrontal cortex (OFC) is the final destination of the odor information and is where conscious smell perception arises. Smell information enters directly after passing through the olfactory cortex, which marks the distinction from other sensory information that first pass through the thalamus. The OFC is located dorsal to the prefrontal cortex, allowing smell information direct input to the prefrontal cortex, or the major decision-making area of the brain. There are only three types of neurons that smell molecules pass before arriving at the OFC: the olfactory receptor cells in the olfactory epithelium, mitral cells, and olfactory pyramidal neurons.[1]

At the level of the OFC, associations with other brain areas are made, including input from the mouth (somatosensation), emotional input (amygdala), visual information, and evaluative information (prefrontal cortex). The OFC is responsible for selective odor tuning, fusing of sensory domains, and hedonic evaluations of smells.

At-home evidence of the role smell plays in flavor

The experience of eating favored foods with a cold often disappoints. This is because congestion blocks nasal passageways through which air and flavor molecules enter and exit, thus temporarily reducing retronasal smell capacity.

Another way to isolate the sense of retronasal smell is to use the “nose pinch test.” When eating while pinching the nostrils closed, the flavor of food appears to dissipate, namely because the pathway for air exiting the nose that creates the flavor image is blocked.

Speculative evolutionary significance

Deeper understanding of the role of retronasal smell in flavor has led many to rethink smell's evolutionary significance in humans. To dispel the notion that vision is wholly superior in humans and higher primates to olfaction, Gordon M. Shepherd contrasts the anatomy of the human nose to that of a canine.[1] In canines, smell receptors reside in the back of the nasal cavity. They have a unique cartridge-like organ that serves as an air filter. During quiet breathing, this cartridge directs the stream of air normally, but during active smelling, the rate of direction of information increases, allowing a canine to sniff as much as six to eight times faster than a human.[1]

This suggests that canines are adapted for stronger orthonasal smell capabilities. By contrast, humans seem to be selected to have superior retronasal smell capacities. The bipedal posture of humans reduces the need for a cartridge that functions in canines to mainly clean air entering. The short nasopharynx for retronasal smell in humans is what allows the volatiles from foods and drinks to travel from the mouth to the smell receptors in the nasal cavity. What remains less clear is the fact that canines still have a strong ability to discriminate foods.

Other speculations include the idea that the short route from the mouth to the nasal cavity resulted from selection from long-distance running when humans migrated out of Africa 2 million years ago.[9] The idea is that a shorter nasal apparatus would aid in balancing the head facilitate distance running. Lieberman cites other evolutionary changes that could have resulted from selection for running such as wider joint cartilages and longer bones in the legs.[10]

References

  1. 1 2 3 4 5 6 7 8 9 Shepherd, Gordon M. (2012). Neurogastronomy. New York: Columbia University Press. ISBN 9780231159104.
  2. ↑ Rozin, Paul (1982-07-01). ""Taste-smell confusions" and the duality of the olfactory sense". Perception & Psychophysics. 31 (4): 397–401. doi:10.3758/BF03202667. ISSN 0031-5117. PMID 7110896.
  3. ↑ Moran, D. T.; Rowley, J. C.; Jafek, B. W.; Lovell, M. A. (1982-10-01). "The fine structure of the olfactory mucosa in man". Journal of Neurocytology. 11 (5): 721–746. doi:10.1007/bf01153516. ISSN 0300-4864. PMID 7143026. S2CID 25263022.
  4. ↑ Duchamp-Viret, P.; Chaput, M. A.; Duchamp, A. (1999-06-25). "Odor Response Properties of Rat Olfactory Receptor Neurons". Science. 284 (5423): 2171–2174. doi:10.1126/science.284.5423.2171. ISSN 0036-8075. PMID 10381881.
  5. 1 2 Evolution of Nervous Systems. Academic Press. 2016-11-23. p. 17. ISBN 9780128040966.
  6. 1 2 Stewart, William B.; Kauer, John S.; Shepherd, Gordon M. (1979-06-15). "Functional organization of rat olfactory bulb analysed by the 2-deoxyglucose method". The Journal of Comparative Neurology. 185 (4): 715–734. doi:10.1002/cne.901850407. ISSN 1096-9861. PMID 447878. S2CID 41466291.
  7. 1 2 Brazelton, T. R.; Rossi, F. M.; Keshet, G. I.; Blau, H. M. (2000-12-01). "From marrow to brain: expression of neuronal phenotypes in adult mice". Science. 290 (5497): 1775–1779. doi:10.1126/science.290.5497.1775. ISSN 0036-8075. PMID 11099418. S2CID 16216476.
  8. ↑ Wilson, Donald A.; Stevenson, Richard J. (2006-05-11). Learning to Smell: Olfactory Perception from Neurobiology to Behavior. JHU Press. ISBN 9780801883682.
  9. ↑ Lieberman, Daniel E., and Dennis M. Bramble. 2007. The evolution of marathon running: Capabilities in humans. Sports Medicine 37(4-5): 288- 290.
  10. ↑ Lieberman, Daniel. The Evolution of the Human Head. Cambridge, MA: Belknap of Harvard UP, 2011. Print.
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