Showing posts with label exposome. Show all posts
Showing posts with label exposome. Show all posts

Thursday, April 22, 2021

Odor Investigations

 

I do indoor air quality work with schools. Lots of schools are old, and suffer from indoor air quality problems. Odors are a common complaint, but they're a great diagnostic for bad ventilation. Here's a typical situation -- there's a classroom, and across the hall, a bathroom. The bathroom is supposed to have an exhaust fan running all the time, because a bathroom is a potent source of indoor contaminants (and not just from the obvious, but also for the powerful cleaning products used there). If this exhaust fan isn't working,  because maybe the rubber belt connecting the motor to the fan has deteriorated over time, then the air from the bathroom can get sucked into the classroom across the hall. 

This is a problem, obviously. But sometimes it's hard to convince those in charge that it needs fixing. Sometimes nobody knows how to fix it. (Because sometimes, just because you have a job doesn't mean you're good at it.)

When things get real crazy, the workers can convince their employer to get an "air test" in their classroom. This is usually not a good idea, because they will usually not find anything, whether it's there or not, and your problems will thenceforth be dismissed, regardless of their validity. There's other ways of diagnosing indoor air quality problems.

But sometimes it does work. I'm talking about a gas canister sample, sometimes called a TO-15. An environmental specialist will bring a metal canister into your room, twist off the top, and let it suck in the air in your room for a couple minutes. Then they close the canister, bring it back to a lab, release all the air that was sucked in from your room, and analyze it. Then they spit back a long list of the VOC's found, usually scary-sounding chemicals that are actually just your deodorant, hair gel, perfume, etc. But every once in a while, I get a hit on 1,4-Dichlorobenzene, and that's when I can say aha. The air from the bathroom is getting into your classroom. 

The VOC 1,4-Dichlorobenzene is the smell of a urinal cake, also described as "mothball-like." I don't know why it was chosen as THE smell of urinal cakes, but it is, and it doesn't belong in your classroom. 

Had we just fixed the exhaust fan in the first place, we could have skipped all the steps in between. But sometimes things have to be difficult. 

Thursday, September 3, 2020

Threat Detection, the Exposome and Olfactory Awareness


Global pandemics are real good for motivating exposure scientists to identify threats in the environment. Add to that the threat detection capabilities of chemosensation (smelling), and you've got some ingredients for a burgeoning field of study that overlaps with olfaction-inspired technologies.

 

Olfaction is for threat detection perhaps above all things, so it is fitting that we see this application become more common. One common use already being implemented by the company Aclima is the distributed air-quality sensor network for pollutants:

 

Early warning sensor sniffs out cities' harmful gas

May 2020, phys.org

 

The IGZO thin-film transistor acts as both an electronic component of the device and also as the NO2-sensing layer. The strongly electron-accepting NO2 molecule is drawn to the electrons on the transistor's surface. The more NO2 molecules that adhere to the IGZO, the more electrons are depleted from its surface, altering its electronic output and triggering an NO2 detection alert.

 

After a detection event, the sensor is reset by reviving the IGZO layer with the light from an integrated blue LED. Similar to a solar cell, the light generates negatively charged electrons and positively charged holes in the IGZO, which neutralizes the adsorbed NO2 and releases it from the surface. "This is the first study to achieve sensing and revival of a semiconducting metal oxide-based thin-film transistor sensor at room temperature," says Surya.

 

*Nitrous oxides (NO2) are a by-product of burning fuel, just like carbon monoxide, carbon dioxide, and sulfur oxides, and all of these are harmful to human health.

 

And here's another related report:

Aerosol-printed graphene unveiled as low cost, faster food toxin sensor

June 2020, phys.org

 

Researchers in the USA have developed a graphene-based electrochemical sensor capable of detecting histamines (allergens) and toxins in food much faster than standard laboratory tests.

 

The team created high-resolution interdigitated electrodes (IDEs) on flexible substrates, which they converted into histamine sensors by covalently linking monoclonal antibodies to oxygen moieties created on the graphene surface by a CO2 thermal annealing process.

 

As an additive manufacturing method that only deposits material where it is needed and therefore minimizes waste, aerosol-jet-printed sensors are low-cost, straightforward to make, and portable. This could potentially enable their use in places where continuous on-site monitoring of food samples is needed to determine and maintain the quality of products, as well as other applications.

 

-Aerosol-jet-printed graphene electrochemical histamine sensors for food safety monitoring, 2-D Materials, DOI: 10.1088/2053-1583/ab8919

 

And still further sensorific developments:

Paper-based device provides low-power, long-term method for analyzing sweat

June 2020, phys.org

 

Using a process known as capillary action, akin to water transport in plants, the device uses evaporation to wick fluid that mimics the features of human sweat to a sensor for up to 10 days or longer.

 

"We expected that the flow of the model sweat will be suppressed by the deposition of a salt layer inside the drying pad," Velev said. "By following the flow of model sweat, we found, quite surprisingly, that such a simple paper construct can achieve continuous sweat pumping and disposal for very long periods."

 

"The biological markers or drug metabolites that seep in the patient's sweat over a long period will be captured on the paper pad and preserved in a time-stamped manner to be analyzed later, similar to tree rings preserving the record of tree development," Dickey said.

 

-Principles of long-term fluids handling in paper-based wearables with capillary-evaporative transport, Biomicrofluidics (2020). aip.scitation.org/doi/10.1063/5.0010417

 

Post Script:

The exposome - When our environment drives health and disease

May 2020, phys.org

 

From this press article: The exposome is the sum of all the environmental drivers of health and diseases: a combination of external factors such as chemicals contained in the air, water or food, and of internal components produced by our organism in response to various stress factors.

 

Notes:

Aclima delivers hyperlocal air pollution and climate emissions intelligence at unprecedented block-by-block resolution.

 

 

 

Thursday, August 20, 2020

Neuroplasticity and Olfactory Existentialism

 

New study reveals how the brain organizes information about odors

Jul 2020, phy.org

 

A study by neurobiologists at Harvard Medical School now provides new insights into the mystery of scent. Reporting in Nature on July 1, the researchers describe for the first time how relationships between different odors are encoded in the olfactory cortex, the region of brain responsible for processing smell.

 

The sense of smell allows animals to identify the chemical nature of the world around them. Sensory neurons in the nose detect odor molecules and relay signals to the olfactory bulb, a structure in the forebrain where initial odor processing occurs. The olfactory bulb primarily transmits information to the piriform cortex, the main structure of the olfactory cortex, for more comprehensive processing. [But] Often, subtle chemical changes—a few carbon atoms here or oxygen atoms there—can lead to significant differences in smell perception.

 

They use a database of physical and chemical features of tons of molecules, probably from the Dragon dataset, which is a relatively new set of thousands of chemical identities based on molar mass, chemical formula, chirality, boiling point, etc.

 

Then they choose three different synthetic odors, each one made of a group of different molecules, and each group having either very diverse features, intermediate, or minimal diversity. The minimally-diverse "odor" group could be made of molecules differing by only one carbon atom, for example.

 

Another way to think about these chemical combinations -- some are grouped close together in chemospace and some are spread out, where chemospace is a map of all the features in the dataset. It's like facespace, made of thousands of faces and mapping all the features against each other; eventually you will find the "eignenface" right smack in the middle of the map. These are both examples of an n-dimensional information space, where n is the number of features listed in the dataset. If your understanding of dimensionality stops at the common physical world of three-, then you will need to stretch for this one.

 

Mice then get exposed to each of these "odors" while their neural activity is observed using multiphoton microscopy. They found that low-diversity molecule-groups, ones that were very similar to each other in their chemical characteristics, were associated with clustered neuron patterns. For the inverse, an odor made of very different chemicals would excite neurons all over the place (chemospace x neuronspace). They also found that in general, certain chemical features could be matched with recognizable neuron activity patterns.

 

This sounds as if there is some universal olfactory attributes in the chemical compendium.

 

BUT, they also found that if they repeatedly presented the mice with any two chemicals paired together, then the corresponding neural patterns would become more strongly correlated, and despite how different those two chemicals were.

 

"The brain can rearrange itself."

 

And again, and in other words, olfaction is confusing:

 

"Part of the reason why things like lemon and lime smell alike, he added, is likely because animals of the same species have similar genomes and therefore similarities in smell perception. But each individual has personalized perceptions as well.

 

"The plasticity of the cortex may help explain why smell is on one hand invariant between individuals, and yet customizable depending on our unique experiences."

-Sandeep Robert Datta, associate professor of neurobiology in the Blavatnik Institute at HMS

 

(He also says the phrase "virtual olfactory world" in reference to a future that sounds very exciting, although still very far away.)

 


There's another study here which looks pretty similar. They offer a reiteration of this new explanation for how smells are perceived, and it sounds like this -- we all share a similar smell-space due to our shared genome. This is manifest in the olfactory bulb, and in the way that it codes individual odor molecules based on their physical and chemical properties.

 

They ask "Can distant odours be grouped together if their context is learned to be the same?" And that answer, because of studies like these, is becoming clearer by the day -- yes.

 

In fact, this is the basis of how olfaction works, why it works, and what it's supposed to be doing for us. The common association between chemical properties and neural activity is just a given. It's in that second layer, and over the course of a lifetime of being exposed to different combinations of chemicals, that our brain generates the end results, olfactory perception, which by its nature must be subjective, and because of the transient, vacillating and boundless parameter space of our ontogenetic chemical exposome. (Chemosome?) They call this pairing of chemical milieu and existential moment an odor "contingency," and they say these contingencies are what rewrite the higher olfactive network space.

 

Random fact: "The mouse initiates the trial by touching the lickometer." Yes, the lickometer.

 

Both of these are true; Yes there is a static, predetermined program that senses chemicals in the air in mostly the same way for all people (excepting genetic variation, which can be up to 30%). But there is another network layer found in the olfactory cortex where we all diverge from each other, and this next layer is based on our autobiography, for lack of a better word. Who we are and the decisions we make are changing this second layer with every new encounter.

 

Back to the study, their statement "Our results indicate that representations of categories emerge dynamically by mitral cells in a way that fits not only task demands but also categorical logic" is another way of saying that we can train our nosebrain to interpret any smell in any way we want. And again, "Once learned, these tasks allowed us to assign the same odour stimuli to different category schemes. If mitral cells activity reflect the learning rules, odour representations would change in a way that follows categorical information."

 

The point here is that our olfactory perception network is constantly changing, and that's why it's so hard to pin it down. And that's what it's supposed to do -- it's supposed to help us respond to our environment; but our environment is constantly changing. Society and culture, for example, can cause major shifts in both the chemical soup that surrounds us and in the way we semi-autonomously assign meaning to odor objects. See mint and analgesics in the postwar population of England, or licorice for the same age group, or the smell of "new car" in the East vs West.

 

Body odor, and especially the odor of others who do not eat the same food as you, or follow the same culturally inculcated hygiene rituals as you, will definitely smell "foreign" to you. Until you become more acquainted, of course, at which point it slowly becomes part of your identity also. You do not begin to smell that way, but because your olfactory translation machine no longer flags a smell as "foreign" if it's been around your neighborhood for the past ten years, or if it's been in your own bed for example. The brain can rearrange itself. 

 


So, smells are both objective and subjective. There is a common denominator to the perception of odor molecules, but depending on the infinite variations of exposure that accumulate over a lifetime, that common denominator is shredded, stretched, skewed and refit to match your personal experience in the olfactory multiverse.

 

And so to answer an age old question in olfactory research -- "Do odors have their own universal identity, or is our nosebrain a blank slate?" -- the answer is, "Yes."

 

 

Notes:

Study 1 - Harvard Medical School

Stan L. Pashkovski et al, Structure and flexibility in cortical representations of odor space, Nature (2020). DOI: 10.1038/s41586-020-2451-1

http://dx.doi.org/10.1038/s41586-020-2451-1

[alt link]

https://www.newsbreak.com/news/1593236184136/structure-and-flexibility-in-cortical-representations-of-odour-space

 

Abstract: The cortex organizes sensory information to enable discrimination and generalization1,2,3,4. As systematic representations of chemical odour space have not yet been described in the olfactory cortex, it remains unclear how odour relationships are encoded to place chemically distinct but similar odours, such as lemon and orange, into perceptual categories, such as citrus5,6,7. Here, by combining chemoinformatics and multiphoton imaging in the mouse, we show that both the piriform cortex and its sensory inputs from the olfactory bulb represent chemical odour relationships through correlated patterns of activity. However, cortical odour codes differ from those in the bulb: cortex more strongly clusters together representations for related odours, selectively rewrites pairwise odour relationships, and better matches odour perception. The bulb-to-cortex transformation depends on the associative network originating within the piriform cortex, and can be reshaped by passive odour experience. Thus, cortex actively builds a structured representation of chemical odour space that highlights odour relationships; this representation is similar across individuals but remains plastic, suggesting a means through which the olfactory system can assign related odour cues to common and yet personalized percepts.

 

Study 2 - Hebrew University

Flexible Representations of Odour Categories in the Mouse Olfactory Bulb. Elena Kudryavitskaya, Eran Marom, David Pash, Adi Mizrahi. Hebrew University of Jerusalem. Mar 24 2020. BioRxiv. doi: https://doi.org/10.1101/2020.03.21.002006

https://www.biorxiv.org/content/10.1101/2020.03.21.002006v1.article-info

 

Summary: The ability to group sensory stimuli into categories is crucial for efficient interaction with a rich and ever-changing environment. In olfaction, basic features of categorical representation of odours were observed as early as in the olfactory bulb (OB). Categorical representation was described in mitral cells (MCs) as sudden transitions in responses to odours that were morphed along a continuum. However, it remains unclear to what extent such response dynamics actually reflects perceptual categories and decisions therein. Here, we tested the role of learning on category formation in the mouse OB, using in vivo two-photon calcium imaging and behaviour. We imaged MCs responses in naïve mice and in awake behaving mice as they learned two tasks with different classification logic. In one task, a 1-decision boundary task, animals learned to classify odour mixtures based on the dominant compound in the mixtures. As expected, categorical representation of close by odours, which was evident already in naïve animals, further increased following learning. In a second task, a multi-decision boundary task, animals learned to classify odours independent of their chemical similarity. BBBBBB Rather, odour discrimination was based on the meaning ascribed to them (either rewarding or not). Following the second task, odour representations by MCs reorganized according to the odour value in the new category. This functional reorganization was also reflected as a shift from predominantly excitatory odour responses to predominantly inhibitory odour responses. BBBBBB Our data shows that odour representations by MCs is flexible, shaped by task demands, and carry category-related information.

*In comparison to the above Harvard paper, for "mitral cells," read olfacotry bulb, and for "two-photon calcium imaging," read multiphoton microscopy.

 

 

Post Script:

Back to the "first layer" mentioned in the above studies, I need to mention what sounds to me like intensity being a big part of the universal "odor coder." It is certainly one of the chemical features in the corresponding dataset; odors tend to present to us in a known window of intensity, and each molecule has a detection threshold for humans measured in parts per million, billion or trillion. I'm not certain this is what's being implied and surely there's more complicated exclusions to it, but even prior research shows that intensity of an odor is a shortcut through a lot of these categorization and dimension-reduction attempts.

 

Next, this is nuts; pretty sure I've never seen this before -- "The general profile of excitatory vs. inhibitory responses by mitral cells changed with learning and task demands. In naive animals, most responsive cells (71%) responded by excitation to the odours (Fig. 6A,B). Following the learning of the 5-decision boundary task, the ratio of excitatory/inhibitory responses reversed. After learning, the majority (71.4%) of neurons now responded by inhibitory calcium transients to the odours (Fig. 6C,E). The ratio of inhibitory vs. excitatory responses reverted back to normal after retraining the mice on the 1-decision boundary task. Specifically, 73.3% of responsive neurons were again excitatory on day 18 (Fig. 6D,E). (The Hebrew U study)

 

So the "second layer," the one that adds the personal, subjective meaning to your odors, is all inhibition. It's dampening the neurons that were originally excited by this odor and based on universal chemical-genetic affinities, but now have to be quieted based on prior outcomes of interactions with it. It doesn't dampen everything, obviously, or else you wouldn't smell it at all (you mean like violets?), but it dampens enough that the overall pattern of the signal that finally does make it through can be dramatically different. You're literally evolving with every breath you take.

 

 

Compulsory Reference to the Greatest Work of Olfactory Philosophy Ever:

Hosek R J & Freeman W J (2001). Osmetic Ontogenesis, or Olfaction Becomes You: The Neurodynamic, Intentional Self and Its Affinities with the Foucaultian/Butlerian Subject. Configurations 9: 509–541.