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Mycolactone as Analgesic: Subcutaneous Bioavailability Parameters

Mycobacterium ulcerans is the bacillus responsible for Buruli ulcer, an infectious disease and the third most important mycobacterial disease worldwide, after tuberculosis and leprosy. M. ulcerans infection is a type of panniculitis beginning mostly with a nodule or an oedema, which can progress to...

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Autores principales: Babonneau, Jérémie, Bréard, Dimitri, Reynaert, Marie-Line, Marion, Estelle, Guilet, David, Saint André, Jean-Paul, Croué, Anne, Brodin, Priscille, Richomme, Pascal, Marsollier, Laurent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6473063/
https://www.ncbi.nlm.nih.gov/pubmed/31031626
http://dx.doi.org/10.3389/fphar.2019.00378
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author Babonneau, Jérémie
Bréard, Dimitri
Reynaert, Marie-Line
Marion, Estelle
Guilet, David
Saint André, Jean-Paul
Croué, Anne
Brodin, Priscille
Richomme, Pascal
Marsollier, Laurent
author_facet Babonneau, Jérémie
Bréard, Dimitri
Reynaert, Marie-Line
Marion, Estelle
Guilet, David
Saint André, Jean-Paul
Croué, Anne
Brodin, Priscille
Richomme, Pascal
Marsollier, Laurent
author_sort Babonneau, Jérémie
collection PubMed
description Mycobacterium ulcerans is the bacillus responsible for Buruli ulcer, an infectious disease and the third most important mycobacterial disease worldwide, after tuberculosis and leprosy. M. ulcerans infection is a type of panniculitis beginning mostly with a nodule or an oedema, which can progress to large ulcerative lesions. The lesions are caused by mycolactone, the polyketide toxin of M. ulcerans. Mycolactone plays a central role for host colonization as it has immunomodulatory and analgesic effects. On one hand, mycolactone induces analgesia by targeting type-2 angiotensin II receptors (AT(2)R), causing cellular hyperpolarization and neuron desensitization. Indeed, a single subcutaneous injection of mycolactone into the mouse footpad induces a long-lasting hypoesthesia up to 48 h. It was suggested that the long-lasting hypoesthesia may result from the persistence of a significant amount of mycolactone locally following its injection, which could be probably due to its slow elimination from tissues. To verify this hypothesis, we investigated the correlation between hypoesthesia and mycolactone bioavailability directly at the tissue level. Various quantities of mycolactone were then injected in mouse tissue and hypoesthesia was recorded with nociception assays over a period of 48 h. The hypoesthesia was maximal 6 h after the injection of 4 μg mycolactone. The basal state was reached 48 h after injection, which demonstrated the absence of nerve damage. Surprisingly, mycolactone levels decreased strongly during the first hours with a reduction of 70 and 90% after 4 and 10 h, respectively. Also, mycolactone did not diffuse in neighboring skin tissue and only poorly into the bloodstream upon direct injection. Nevertheless, the remaining amount was sufficient to induce hypoesthesia during 24 h. Our results thus demonstrate that intact mycolactone is rapidly eliminated and that very small amounts of mycolactone are sufficient to induce hypoesthesia. Taken together, our study points out that mycolactone ought to be considered as a promising analgesic.
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spelling pubmed-64730632019-04-26 Mycolactone as Analgesic: Subcutaneous Bioavailability Parameters Babonneau, Jérémie Bréard, Dimitri Reynaert, Marie-Line Marion, Estelle Guilet, David Saint André, Jean-Paul Croué, Anne Brodin, Priscille Richomme, Pascal Marsollier, Laurent Front Pharmacol Pharmacology Mycobacterium ulcerans is the bacillus responsible for Buruli ulcer, an infectious disease and the third most important mycobacterial disease worldwide, after tuberculosis and leprosy. M. ulcerans infection is a type of panniculitis beginning mostly with a nodule or an oedema, which can progress to large ulcerative lesions. The lesions are caused by mycolactone, the polyketide toxin of M. ulcerans. Mycolactone plays a central role for host colonization as it has immunomodulatory and analgesic effects. On one hand, mycolactone induces analgesia by targeting type-2 angiotensin II receptors (AT(2)R), causing cellular hyperpolarization and neuron desensitization. Indeed, a single subcutaneous injection of mycolactone into the mouse footpad induces a long-lasting hypoesthesia up to 48 h. It was suggested that the long-lasting hypoesthesia may result from the persistence of a significant amount of mycolactone locally following its injection, which could be probably due to its slow elimination from tissues. To verify this hypothesis, we investigated the correlation between hypoesthesia and mycolactone bioavailability directly at the tissue level. Various quantities of mycolactone were then injected in mouse tissue and hypoesthesia was recorded with nociception assays over a period of 48 h. The hypoesthesia was maximal 6 h after the injection of 4 μg mycolactone. The basal state was reached 48 h after injection, which demonstrated the absence of nerve damage. Surprisingly, mycolactone levels decreased strongly during the first hours with a reduction of 70 and 90% after 4 and 10 h, respectively. Also, mycolactone did not diffuse in neighboring skin tissue and only poorly into the bloodstream upon direct injection. Nevertheless, the remaining amount was sufficient to induce hypoesthesia during 24 h. Our results thus demonstrate that intact mycolactone is rapidly eliminated and that very small amounts of mycolactone are sufficient to induce hypoesthesia. Taken together, our study points out that mycolactone ought to be considered as a promising analgesic. Frontiers Media S.A. 2019-04-12 /pmc/articles/PMC6473063/ /pubmed/31031626 http://dx.doi.org/10.3389/fphar.2019.00378 Text en Copyright © 2019 Babonneau, Bréard, Reynaert, Marion, Guilet, Saint André, Croué, Brodin, Richomme and Marsollier. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Babonneau, Jérémie
Bréard, Dimitri
Reynaert, Marie-Line
Marion, Estelle
Guilet, David
Saint André, Jean-Paul
Croué, Anne
Brodin, Priscille
Richomme, Pascal
Marsollier, Laurent
Mycolactone as Analgesic: Subcutaneous Bioavailability Parameters
title Mycolactone as Analgesic: Subcutaneous Bioavailability Parameters
title_full Mycolactone as Analgesic: Subcutaneous Bioavailability Parameters
title_fullStr Mycolactone as Analgesic: Subcutaneous Bioavailability Parameters
title_full_unstemmed Mycolactone as Analgesic: Subcutaneous Bioavailability Parameters
title_short Mycolactone as Analgesic: Subcutaneous Bioavailability Parameters
title_sort mycolactone as analgesic: subcutaneous bioavailability parameters
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6473063/
https://www.ncbi.nlm.nih.gov/pubmed/31031626
http://dx.doi.org/10.3389/fphar.2019.00378
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