Научная статья на тему 'Rodents and humans are able to discriminate the odour of L-lactate'

Rodents and humans are able to discriminate the odour of L-lactate Текст научной статьи по специальности «Биологические науки»

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Текст научной работы на тему «Rodents and humans are able to discriminate the odour of L-lactate»

Section MOLECULAR NEUROSCIENCE

Rodents and Humans are Able to Discriminate the Odour of L-Lactate

Valentina Mosienko*, Anja Teschemacher, Sergey Kasparov

University of Bristol, Biomedical Sciences, School of Physiology, Pharmacology and Neuroscience, UK. * Presenting e-mail: valentina.mosienko@bristol.ac.uk

Olfactory receptors (Olfrs) are seven transmembrane G-protein coupled receptors that are able to sense odorants. Rodents express over 1000 olfactory receptors while in humans only less than 400 of these genes are active. Some of the olfactory receptors are expressed not only in olfactory epithelium but in other tissues. One such receptor is mouse Olfr78 which has a rat and human orthologs (Orl59, OR51E2, correspondingly). Olfr78 has been implicated in various physiological processes due to its ectopic expression outside the olfactory system in other parts of the brain (brainstem, area postrema, nucleus tractus solitarius) and peripheral tissues (carotid body, prostate gland, kidney). It is activated by short chain fatty amino acids acetate and propionate, but also by L-lactate. Given that Olfr78 is specifically expressed in olfactory sensory neurons, we hypothesized that both rodents and humans should be able to smell lactate. To test this hypothesis we performed olfactory discrimination tasks with mice, rats and humans.

Our results show that adult male C57Bl/6 mice are able to distinguish L-lactate (1M, pH=7.4) in olfactory habitua-tion-dishabituation and discrimination tasks. Mice spend twice as much time sniffing L-lactate compared to water, and equal amounts of time sniffing peppermint extract. Upon multiple exposures, mice habituate to the smell of L-lactate, however, they clearly discriminate the next introduced odour as measured by increased sniffing time.

We also used an operant-conditioning task reinforced by food to test the ability of rats to distinguish L-lactate (1M, pH=7.4). Rats were kept to a diet to maintain 85% of their free body weight and trained to find a food reward guided by the smell of either almond (positive control) or L-lactate. Rats were offered three sponges in an arena, where only one was marked with an odorant and contained a food reward. Success in finding a food reward orienting on the smell was measured by the time elapsed until food retrieval. Both almond and L-lactate odour were equally effective as operant stimuli as rats spent the same amount of time to find and retrieve the food reward upon exposure and this latency to food retrieval decreased over trials for both odours. We observed no difference in accuracy (number of incorrect pokes into sponge probes) over all trials between almond and L-lactate.

In order to test whether humans can sense L-lactate we recruited young adult volunteers for an odorant discrimination task. Participants were asked to indicate a presence of smell in four jars containing liquids (1M acetate, propionate, pyruvate and L-lactate adjusted to pH 7.4). Distilled water served as a negative control. 99% of participants indicated the presence of smell for a solution containing propionate, 97% and 95% detected an odour in solutions of pyruvate or acetate, respectively. 93% of participants detected an odour in a solution containing L-lactate. All the participants were asked to rate all samples in dimensions of taste and odour. 34% of participants identified the smell of l-lactate as sweet and 19% described it as sour/acidic. Altogether, our data demonstrate that both rodents and humans are able to sense L-lactate, most likely via Olfr78 (or its ortholog). The biological significance of L-lactate detection by olfaction requires further investigation.

Calcineurin Inhibition Attenuates Function of the Neuronal Potassium-Chloride Cotransporter

Michael Zessin1, Christin Boldt1, Rudolf Deisz1, Ulf Strauß1, Sebastian Loyola1, Aljona Borschewski1, Jim McCormick2, and Kerim Mutig1*

1 Department of Anatomy, CharM-Universitätsmedizin Berlin, Germany;

2 Division of Nephrology and Hypertension, Oregon Health and Science University, Portland, Oregon, USA. * Presenting e-mail: kerim.mutig@charite.de

Aims

Calcineurin inhibitors, cyclosporine and tacrolimus, are broadly used for immunosuppression after organ transplantations but may cause serious neurologic side effects such as tremor, ataxia, or seizures suggesting that these drugs may induce hyperexdtability of neocortical neurons. Calcineurin has been implicated in the regulation of neuronal excitability and cellular chloride homeostasis. In this context, we tested the hypothesis that calcineurin inhibitors interfere with the function of major neuronal cation-chloride cotransporter KCC2.

OM&P

30 Opera Med Physiol 2016 Vol. 2 (S1)

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