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. 2018 Jul 4;8(1):10128.
doi: 10.1038/s41598-018-28510-x.

Stimulating fermentation by the prolonged acceleration of gut transit protects against decompression sickness

Affiliations

Stimulating fermentation by the prolonged acceleration of gut transit protects against decompression sickness

Sébastien de Maistre et al. Sci Rep. .

Abstract

Massive bubble formation after diving can lead to decompression sickness (DCS). Gut fermentation at the time of a dive exacerbates DCS due to endogenous hydrogen production. We sought to investigate whether medium-term stimulation of fermentation as a result of polyethylene glycol (PEG)-induced acceleration of bowel transit before diving exacerbates DCS in rats. Seven days before an experimental dry dive, 60 rats were randomly divided in two groups: an experimental group treated with PEG (n = 30) and an untreated control group (n = 30). Exhaled hydrogen was measured before the dive. Following hyperbaric exposure, we assessed for signs of DCS. After anaesthetisation, arterial blood was drawn to assay inflammatory cytokines and markers of oxidative stress. PEG led to a significant increase in exhaled H2 (35 ppm [10-73] compared with control 7 ppm [2-15]; p = 0.001). The probability of death was reduced in PEG-treated rats (PEG: 17% [95% CI 4-41] vs control: 50% [95% CI 26-74]; p = 0.034). In addition, inflammatory markers were reduced, and the antioxidant activity of glutathione peroxidase was significantly increased (529.2 U.l-1 [485.4-569.0] versus 366.4 U.l-1 [317.6-414.8]; p = 0.004). Thus, gut fermentation might have a positive effect on DCS. The antioxidant and neuroprotective properties of the fermentation by-products H2 and butyrate may explain these results.

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Conflict of interest statement

The authors declare no competing interests.

Figures

Figure 1
Figure 1
Gut and fermentation activities in the at-risk population (Bu: butyrate, Pro: propionate, Ac: acetate, Va: valerate). *Denotes p < 0.05 between the groups.
Figure 2
Figure 2
Decompression sickness within 30 min after surfacing in the at-risk population. *Denotes p < 0.05 between the groups.
Figure 3
Figure 3
Gut and fermentation activities in the low-risk population (Bu: butyrate, Pro: propionate, Ac: acetate, Va: valerate). *Denotes p < 0.05 between the groups.
Figure 4
Figure 4
Relative variations of blood cell counts after hyperbaric exposure in the low-risk population. *Denotes p < 0.05 between paired groups and #denotes p = 0.066 between unpaired groups.
Figure 5
Figure 5
Pro inflammatory cytokines and markers of oxidative stress in the blood of the low-risk population. *Denotes p < 0,05 between the groups.
Figure 6
Figure 6
Summary of the effects of intestinal fermentation on the risk of decompression sickness.
Figure 7
Figure 7
Distribution of rats in experimental groups.

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