Sturgess Connie, Montgomery Hugh
Institute for Human Health and Performance, Department of Medicine, University College London, London, UK.
Exp Physiol. 2021 Nov;106(11):2155-2167. doi: 10.1113/EP089628. Epub 2021 Sep 28.
What is the topic of this review? Highland natives have undergone natural selection for genetic variants advantageous in adaptation to the hypobaric hypoxia experienced at high altitude. Why genes related to alcohol metabolism appear consistently selected for has not been greatly considered. We hypothesize that altitude-related changes in the gut microbiome offer one possible explanation. What advances does it highlight? Low intestinal oxygen tension might favour the production of ethanol through anaerobic fermentation by the gut microbiome. Subsequent increases in endogenous ethanol absorption could therefore provide a selection pressure for gene variants favouring its increased degradation, or perhaps reduced degradation if endogenously synthesized ethanol acts as a metabolic signalling molecule.
Reduced tissue availability of oxygen results from ascent to high altitude, where atmospheric pressure, and thus the partial pressure of inspired oxygen, fall (hypobaric hypoxia). In humans, adaptation to such hypoxia is necessary for survival. These functional changes remain incompletely characterized, although metabolic adaptation (rather than simple increases in convective oxygen delivery) appears to play a fundamental role. Those populations that have remained native to high altitude have undergone natural selection for genetic variants associated with advantageous phenotypic traits. Interestingly, a consistent genetic signal has implicated alcohol metabolism in the human adaptive response to hypobaric hypoxia. The reasons for this remain unclear. One possibility is that increased alcohol synthesis occurs through fermentation by gut bacteria in response to enteric hypoxia. There is growing evidence that anaerobes capable of producing ethanol become increasingly prevalent with high-altitude exposure. We hypothesize that: (1) ascent to high altitude renders the gut luminal environment increasingly hypoxic, favouring (2) an increase in the population of enteric fermenting anaerobes, hence (3) the synthesis of alcohol which, through systemic absorption, leads to (4) selection pressure on genes relating to alcohol metabolism. In theory, alcohol could be viewed as a toxic product, leading to selection of gene variants favouring its metabolism. On the contrary, alcohol is a metabolic substrate that might be beneficial. This mechanism could also account for some of the interindividual differences of lowlanders in acclimatization to altitude. Future research should be aimed at determining any shifts to favour ethanol-producing anaerobes after ascent to altitude.
本综述的主题是什么?高原原住民经历了自然选择,以获得有利于适应高海拔地区低氧低压环境的基因变异。但为何与酒精代谢相关的基因似乎一直被选择,这一点尚未得到充分探讨。我们推测,肠道微生物群与海拔相关的变化可能是一种解释。它突出了哪些进展?肠道内低氧张力可能有利于肠道微生物群通过无氧发酵产生乙醇。因此,内源性乙醇吸收的增加可能会为有利于其降解增加的基因变异提供选择压力,如果内源性合成的乙醇作为一种代谢信号分子,或许也会为有利于其降解减少的基因变异提供选择压力。
上升到高海拔地区会导致组织氧供应减少,因为那里的大气压力以及吸入氧气的分压会下降(低氧低压)。对人类来说,适应这种低氧环境是生存所必需的。尽管代谢适应(而非单纯的对流性氧气输送增加)似乎起着根本性作用,但这些功能变化仍未完全明确。那些一直生活在高海拔地区的人群已经经历了与有利表型特征相关的基因变异的自然选择。有趣的是,一个一致的遗传信号表明酒精代谢参与了人类对低氧低压的适应性反应。其原因尚不清楚。一种可能性是,肠道细菌在肠道缺氧时通过发酵增加酒精合成。越来越多的证据表明,能够产生乙醇的厌氧菌在高海拔暴露时变得越来越普遍。我们推测:(1)上升到高海拔会使肠道腔内环境越来越缺氧,有利于(2)肠道发酵厌氧菌数量增加,从而(3)合成酒精,酒精通过全身吸收导致(4)对与酒精代谢相关基因的选择压力。理论上,酒精可被视为一种有毒产物,从而导致有利于其代谢的基因变异被选择。相反,酒精是一种可能有益的代谢底物。这种机制也可以解释一些低地人在适应海拔高度方面的个体差异。未来的研究应旨在确定上升到海拔高度后有利于产生乙醇的厌氧菌的任何变化。