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- Gordon, Amy R., et al.
(författare)
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Detection of Inflammation via Volatile Cues in Human Urine
- 2018
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Ingår i: Chemical Senses. - : Oxford University Press (OUP). - 0379-864X .- 1464-3553. ; 43:9, s. 711-719
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Tidskriftsartikel (refereegranskat)abstract
- Contagious disease is a major threat to survival, and the cost of relying on the immune system to defeat pathogens is high; therefore, behavioral avoidance of contagious individuals is arguably an adaptive strategy. Animal findings demonstrate the ability to detect and avoid sick individuals by the aid of olfactory cues, and a recent study indicated that human axillary odor also becomes more aversive as a function of immune activation. By injecting healthy human participants with lipopolysaccharide (0.6 ng/kg body weight) to experimentally induce inflammation, this study demonstrates that natural daily rhythms of urine odor-its perceived dimensions and volatile profile-are altered within hours of inflammation onset. Whereas healthy human urine decreases in averseness over the course of a single day, inflammation interrupts this process and results in an increased urine odor averseness and an altered volatile composition. These results support the notion that subtle and early cues of sickness may be detected and avoided, thereby complementing the immune system in its role of keeping us alive and healthy.
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| 2. |
- Gordon, Amy R., et al.
(författare)
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The scent of disease
- 2015
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Ingår i: Chemical Senses. - : Oxford University Press (OUP). - 0379-864X .- 1464-3553. ; 40:3, s. 254-254
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Tidskriftsartikel (refereegranskat)abstract
- Ability to detect diseases in conspecifics would be advantageous for the individual. In line with this, rodents avoid body odors of infected individuals. Two studies (Olsson et al. 20014; in prep.) indicated that this is possible by way of human smell and human observers. T-shirts from donors (worn for 4 hours) that had received an injection of endotoxin [0.8ng lipopolysaccharide (LPS) / kg body weight], which causes systemic inflammation, smelled more unpleasant, intense, and sick than shirts from donors that had received a placebo (Saline) injection. GC/MS analysis of the shirts suggested that the change of body odor was not due to a general increase of odorous compounds in the “sick shirts” compared to “placebo shirts” but rather to a qualitative change. Study 2 (ongoing) further investigated the nature of this perception. In a first experiment, we compared the body odor of 30 endotoxin (0.6ng LPS / kg body weight) and 21 placebo (Saline) donors. Again, body odors were sampled during 4 hours using T-shirts. Observers then smelled the shirts and rated intensity, pleasantness, and disgust. In a second experiment, urine from these donors were collected and was investigated in the same way with subjective ratings. Altogether the data suggest that systemic inflammation makes body odors more aversive within a few hours.
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| 3. |
- Sarolidou, Georgia, et al.
(författare)
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Disease detection : Volatile biomarkers in acute inflammation
- 2017
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Ingår i: Chemical Senses. - : Oxford University Press (OUP). - 0379-864X .- 1464-3553. ; 42:2
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Tidskriftsartikel (refereegranskat)abstract
- Through history, infectious bacteria and viruses have posed a threat to humanity. Being able to detect and avoid pathogens is, therefore, of crucial importance. It has been shown that body odor samples, such as urine, from immune-activated animals contain sickness cues and detection of which, results in avoidance behavior in conspecifics. Perceivable changes in body odor samples have also, recently, been shown in immune-activated human participants. The main aim of this study was to identify potential volatile biomarkers of the acute inflammatory response. Healthy volunteers were injected twice in a crossover design, once with the bacterial endotoxin lipopolysaccharide (LPS, 2ng/kg bw) and once with placebo (saline). LPS caused a transient systemic inflammatory response as shown by pro-inflammatory cytocines, tympanic temperature and subjective sickness ratings (significant interactions between condition and time with all ps<.001, and all ηρ2>.663). Axillary sweat and urine were collected both before and 2–4 hours after injection. Headspace from these samples were analyzed using gas chromatography-mass spectrometry (GC-MS). GC-MS data analyses assessed the differences in the profile of volatile compounds of urine and sweat from LPS and placebo donors. Results regarding possible differences between volatile biomarkers in LPS and placebo condition will be presented and discussed.
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