Excessive alcohol consumption induces methane production in humans and rats.

Various studies have established the possibility of non-bacterial methane (CH4) generation in oxido-reductive stress conditions in plants and animals. Increased ethanol input is leading to oxido-reductive imbalance in eukaryotes, thus our aim was to provide evidence for the possibility of ethanol-induced methanogenesis in non-CH4 producer humans, and to corroborate the in vivo relevance of this pathway in rodents. Healthy volunteers consumed 1.15 g/kg/day alcohol for 4 days and the amount of exhaled CH4 was recorded by high sensitivity photoacoustic spectroscopy. Additionally, Sprague-Dawley rats were allocated into control, 1.15 g/kg/day and 2.7 g/kg/day ethanol-consuming groups to detect the whole-body CH4 emissions and mitochondrial functions in liver and hippocampus samples with high-resolution respirometry. Mitochondria-targeted L-alpha-glycerylphosphorylcholine (GPC) can increase tolerance to liver injury, thus the effects of GPC supplementations were tested in further ethanol-fed groups. Alcohol consumption was accompanied by significant CH4 emissions in both human and rat series of experiments. 2.7 g/kg/day ethanol feeding reduced the oxidative phosphorylation capacity of rat liver mitochondria, while GPC significantly decreased the alcohol-induced CH4 formation and hepatic mitochondrial dysfunction as well. These data demonstrate a potential for ethanol to influence human methanogenesis, and suggest a biomarker role for exhaled CH4 in association with mitochondrial dysfunction.

Exhaled methane concentration profiles during exercise on an ergometer.

Exhaled methane concentration measurements are extensively used in medical investigation of certain gastrointestinal conditions. However, the dynamics of endogenous methane release is largely unknown. Breath methane profiles during ergometer tests were measured by means of a photoacoustic spectroscopy based sensor. Five methane-producing volunteers (with exhaled methane level being at least 1 ppm higher than room air) were measured. The experimental protocol consisted of 5 min rest--15 min pedalling (at a workload of 75 W)--5 min rest. In addition, hemodynamic and respiratory parameters were determined and compared to the estimated alveolar methane concentration. The alveolar breath methane level decreased considerably, by a factor of 3-4 within 1.5 min, while the estimated ventilation-perfusion ratio increased by a factor of 2-3. Mean pre-exercise and exercise methane concentrations were 11.4 ppm (SD:7.3) and 2.8 ppm (SD:1.9), respectively. The changes can be described by the high sensitivity of exhaled methane to ventilation-perfusion ratio and are in line with the Farhi equation.

Determination of endogenous methane formation by photoacoustic spectroscopy.

Aerobic methane generation was demonstrated earlier in plants and eukaryotes under various stress conditions. Our aims were to develop a real-time and noninvasive detection system for monitoring the methane production of small animals and humans with our without exposure to various treatments. A near-infrared diode laser technique was employed with photoacoustic spectroscopy to monitor a methane-containing atmosphere online. The whole-body methane generation of anesthetized mice and rats was determined under baseline conditions and following reduction of the intestinal methanogenic flora or after lipopolysaccharide administration. Single-breath methane analyses were also carried out in a cross-sectional clinical study in order to obtain comparative human data. The whole-body methane production of mice was significantly decreased after antibiotic treatment (M: 1.71 ppm cm(-2) 10(3); p25: 1.5 ppm cm(-2) 10(3); p75: 2.11 ppm cm(-2) 10(3)) and increased significantly in endotoxemia (M: 4.53 ppm cm(-2) 10(3); p25: 4.37 ppm cm(-2) 10(3); p75: 5.38 ppm cm(-2) 10(3)), while no difference was observed between the rat groups. The methane content of the exhaled breath in humans was found to be between 0 and 37 ppm. Photoacoustic spectroscopy is a reliable tool with which to monitor the in vivo dynamics of stress-induced methane production in laboratory animals, even in a very low concentration range.