Sidenafil pre-treatment promotes decompression sickness in rats.

Vascular bubble formation after decompression contributes to endothelial injuries which form the basis for the development of decompression sickness (DCS). Nitric oxide (NO) is a powerful vasodilator that contributes to vessel homeostasis. It has been shown that NO-releasing agent may reduce bubble...

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Autores principales: Jean-Eric Blatteau, Alf O Brubakk, Emmanuel Gempp, Olivier Castagna, Jean-Jacques Risso, Nicolas Vallée
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Publicado: Public Library of Science (PLoS) 2013
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spelling oai:doaj.org-article:b856fe960beb4391a2f5470bb99c29492021-11-18T07:50:14ZSidenafil pre-treatment promotes decompression sickness in rats.1932-620310.1371/journal.pone.0060639https://doaj.org/article/b856fe960beb4391a2f5470bb99c29492013-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23580342/?tool=EBIhttps://doaj.org/toc/1932-6203Vascular bubble formation after decompression contributes to endothelial injuries which form the basis for the development of decompression sickness (DCS). Nitric oxide (NO) is a powerful vasodilator that contributes to vessel homeostasis. It has been shown that NO-releasing agent may reduce bubble formation and prevent serious decompression sickness. The use of sildenafil, a well-known, phosphodiesterase-5 blocker, which act by potentiating the vasodilatory effect on smooth muscle relaxation, has never been studied in DCS. The purpose of the present study was to evaluate the clinical effects of sildenafil pre-treatment on DCS in a rat model. 67 rats were subjected to a simulated dive at 90 msw for 45 min before staged decompression. The experimental group received 10 mg/kg of sildenafil one hour before exposure (n = 35) while controls were not treated (n = 32). Clinical assessment took place over a period of 30 min after surfacing. At the end, blood samples were collected for blood cells counts and the level of circulating bubbles in the right cavities was quantified. There were significantly more manifestations of DCS in the sildenafil group than in the controls (34.3% vs 6.25%, respectively, p = 0.012). Platelet count was more reduced in treated rats than in controls (-21.7% vs -7%, respectively, p = 0.029), whereas bubble grades did not differ between groups. We concluded that pre-treatment with sildenafil promotes the onset and severity of neurological DCS. When considering the use of phosphodiesterase-5 blockers in the context of diving, careful discussion with physician should be recommended.Jean-Eric BlatteauAlf O BrubakkEmmanuel GemppOlivier CastagnaJean-Jacques RissoNicolas ValléePublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 8, Iss 4, p e60639 (2013)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Jean-Eric Blatteau
Alf O Brubakk
Emmanuel Gempp
Olivier Castagna
Jean-Jacques Risso
Nicolas Vallée
Sidenafil pre-treatment promotes decompression sickness in rats.
description Vascular bubble formation after decompression contributes to endothelial injuries which form the basis for the development of decompression sickness (DCS). Nitric oxide (NO) is a powerful vasodilator that contributes to vessel homeostasis. It has been shown that NO-releasing agent may reduce bubble formation and prevent serious decompression sickness. The use of sildenafil, a well-known, phosphodiesterase-5 blocker, which act by potentiating the vasodilatory effect on smooth muscle relaxation, has never been studied in DCS. The purpose of the present study was to evaluate the clinical effects of sildenafil pre-treatment on DCS in a rat model. 67 rats were subjected to a simulated dive at 90 msw for 45 min before staged decompression. The experimental group received 10 mg/kg of sildenafil one hour before exposure (n = 35) while controls were not treated (n = 32). Clinical assessment took place over a period of 30 min after surfacing. At the end, blood samples were collected for blood cells counts and the level of circulating bubbles in the right cavities was quantified. There were significantly more manifestations of DCS in the sildenafil group than in the controls (34.3% vs 6.25%, respectively, p = 0.012). Platelet count was more reduced in treated rats than in controls (-21.7% vs -7%, respectively, p = 0.029), whereas bubble grades did not differ between groups. We concluded that pre-treatment with sildenafil promotes the onset and severity of neurological DCS. When considering the use of phosphodiesterase-5 blockers in the context of diving, careful discussion with physician should be recommended.
format article
author Jean-Eric Blatteau
Alf O Brubakk
Emmanuel Gempp
Olivier Castagna
Jean-Jacques Risso
Nicolas Vallée
author_facet Jean-Eric Blatteau
Alf O Brubakk
Emmanuel Gempp
Olivier Castagna
Jean-Jacques Risso
Nicolas Vallée
author_sort Jean-Eric Blatteau
title Sidenafil pre-treatment promotes decompression sickness in rats.
title_short Sidenafil pre-treatment promotes decompression sickness in rats.
title_full Sidenafil pre-treatment promotes decompression sickness in rats.
title_fullStr Sidenafil pre-treatment promotes decompression sickness in rats.
title_full_unstemmed Sidenafil pre-treatment promotes decompression sickness in rats.
title_sort sidenafil pre-treatment promotes decompression sickness in rats.
publisher Public Library of Science (PLoS)
publishDate 2013
url https://doaj.org/article/b856fe960beb4391a2f5470bb99c2949
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