Back to chapter

19.4:

Olfaction

JoVE Core
Biology
A subscription to JoVE is required to view this content.  Sign in or start your free trial.
JoVE Core Biology
Olfaction

Languages

Share

Olfaction, the chemical sense of smell, begins when airborne molecules enter the nasal cavities. At the top of the uppermost cavity sits the olfactory epithelium, a small patch of sensory receptor neurons.

When odorants reach this area, a molecule stimulates one of thousands of receptors on a neuron. It doesn't matter which, because each neuron only has one type. The same type of molecules, though, can stimulate several different neurons.

When enough receptors are stimulated, the neurons generate action potentials, passing on the smell information into the olfactory bulbs, which sit just above the nasal cavity below the brain. Here, neurites from similar olfactory neurons meet in a relay-like station called the glomeruli, where mitral cells collate the converging information.

Details about the types of receptors and the strength of stimulation are unique for each odor molecule. This combinatorial diversity allows us to distinguish between millions of different odors.

The mitral cells then pass the collated information on to the olfactory cortex. From there it splits into two destinations, the thalamus, where it integrates with other sensory information to create the perception of smell or flavor, and the hippocampus, where odor information is linked to memory formation.

19.4:

Olfaction

The sense of smell is achieved through the activities of the olfactory system. It starts when an airborne odorant enters the nasal cavity and reaches olfactory epithelium (OE). The OE is protected by a thin layer of mucus, which also serves the purpose of dissolving more complex compounds into simpler chemical odorants. The size of the OE and the density of sensory neurons varies among species; in humans, the OE is only about 9-10 cm2.

The olfactory receptors are embedded in the cilia of the olfactory sensory neurons. Each neuron expresses only one type of olfactory receptor. However, each type of olfactory receptor is broadly tuned and can bind to multiple different odorants. For example, if receptor A binds to odorants 1 and 2, receptor B may bind to odorants 2 and 3, while receptor C binds to odorants 1 and 3. Thus, the detection and identification of an odor depend on the combination of olfactory receptors that recognize the odor; this is called combinatorial diversity.

Olfactory sensory neurons are bipolar cells with a single long axon that sends olfactory information up to the olfactory bulb (OB). The OB is a part of the brain that is separated from the nasal cavity by the cribriform plate. Because of this convenient proximity between the nose and brain, the development of nasal drug applications is widely studied, especially in cases where direct access to the central nervous system is preferred.

Within the OB, axons from sensory neurons terminate in a specialized area called a glomerulus. Sensory neurons with the same olfactory receptor type send their axons to the same one or two glomeruli. As a result, there can be thousands of axons from similar sensory neurons converging within a single glomerulus. All of that sensory information is passed on to only 20-50 mitral and tufted cells per glomeruli, so there is a large convergence of information. Periglomerular and granular cells are inhibitory interneurons that mediate cross-talk between mitral/tufted cells before the olfactory information is sent to the cortex.

From the OB, the mitral/tufted cells project information to the olfactory cortex. The olfactory cortex is a complex of several cortical areas that process olfactory information. One olfactory area, the cortical amygdala, influences emotional responses to smell. The orbitofrontal cortex is involved in the identification of odors and the reward value of odors and tastes. The entorhinal cortex, another olfactory cortical area, projects to the hippocampus, which is implicated in olfactory memory.

The ability to detect and identify odors involves higher-order cortical areas. Such high-level integration may be linked to the impaired olfactory functioning observed in many neurodegenerative disorders, such as Parkinson’s and Alzheimer’s diseases. The reduced ability to smell—hyposmia—is an early symptom of both disorders.

Suggested Reading

Hayden, Sara, and Emma C. Teeling. “The Molecular Biology of Vertebrate Olfaction.” The Anatomical Record 297, no. 11 (2014): 2216–26. [Source]

Attems, Johannes, Lauren Walker, and Kurt A. Jellinger. “Olfaction and Aging: A Mini-Review.” Gerontology 61, no. 6 (2015): 485–90. [Source]