The vertebrate brain is generally very sensitive to acidosis, so a hypoxia-induced decrease in pH is likely to have an effect on brain mitochondria (). Mitochondrial respiration (JO) is required to generate an electrical gradient (ΔΨm) and a pH gradient to power ATP synthesis, yet the impact of pH modulation on brain function remains largely unexplored. As intertidal fishes within rock pools routinely experience hypoxia and reoxygenation, they would most likely experience changes in cellular pH. We hence compared four New Zealand triplefin fish species ranging from intertidal hypoxia-tolerant species (HTS) to subtidal hypoxia-sensitive species (HSS). We predicted that HTS would tolerate acidosis better than HSS in terms of sustaining structure and function. Using respirometers coupled to fluorimeters and pH electrodes, we titrated lactic-acid to decrease the pH of the media, and simultaneously recorded JO, ΔΨm, and H buffering capacities within permeabilized brain and swelling of isolated from non-permeabilized brains. We then measured ATP synthesis rates in the most HTS () and the HSS () at pH 7.25 and 6.65. Mitochondria from HTS brain did have greater H buffering capacities than HSS (∼10 mU pH.mg ). HTS swelled by 40% when exposed to a decrease of 1.5 pH units, and JO was depressed by up to 15% in HTS. However, HTS were able to maintain ΔΨm near -120 mV. Estimates of work, in terms of charges moved across the inner-membrane, suggested that with acidosis, HTS may in part harness extra- H to maintain ΔΨm, and could therefore support ATP production. This was confirmed with elevated ATP synthesis rates and enhanced P:O ratios at pH 6.65 relative to pH 7.25. In contrast, volumes and ΔΨm decreased downward pH 6.9 in HSS and paradoxically, JO increased (∼25%) but ATP synthesis and P:O ratios were depressed at pH 6.65. This indicates a loss of coupling in the HSS with acidosis. Overall, the of these intertidal fish have adaptations that enhance ATP synthesis efficiency under acidic conditions such as those that occur in hypoxic or reoxygenated brain.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6346031PMC
http://dx.doi.org/10.3389/fphys.2018.01941DOI Listing

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