Abstract

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 (mt). Mitochondrial respiration (JO2) is required to generate an electrical gradient (ΔΨm) and a pH gradient to power ATP synthesis, yet the impact of pH modulation on brain mt 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 mt 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 JO2, ΔΨm, and H+ buffering capacities within permeabilized brain and swelling of mt isolated from non-permeabilized brains. We then measured ATP synthesis rates in the most HTS (Bellapiscus medius) and the HSS (Forsterygion varium) at pH 7.25 and 6.65. Mitochondria from HTS brain did have greater H+ buffering capacities than HSS mt (∼10 mU pH.mgprotein-1). HTS mt swelled by 40% when exposed to a decrease of 1.5 pH units, and JO2 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 mt inner-membrane, suggested that with acidosis, HTS mt may in part harness extra-mt 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, mt volumes and ΔΨm decreased downward pH 6.9 in HSS mt and paradoxically, JO2 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 mt of these intertidal fish have adaptations that enhance ATP synthesis efficiency under acidic conditions such as those that occur in hypoxic or reoxygenated brain.

Highlights

  • In hypoxic or anoxic conditions, O2 becomes limiting and ATP production via mitochondrial oxidative phosphorylation (OXPHOS) is compromised

  • We assessed the mt function across a range of pH down to those experienced by hypoxic brain (Katsura et al, 1991, 1992a; Kraut and Madias, 2014; Witt et al, 2017)

  • It is the first study to explore these effects through pH titration and on a range of species with different tolerance to hypoxia, and it revealed significant differences among species that are consistent with species distribution

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Summary

Introduction

In hypoxic or anoxic conditions, O2 becomes limiting and ATP production via mitochondrial (mt) oxidative phosphorylation (OXPHOS) is compromised. To support ATP requirements, vertebrate cells increase anaerobic metabolism activities, which is ∼15-fold less efficient than the OXPHOS. Glycolysis may become substrate limited, and diminishing ATP production mediates rapid depletion of ATP stores (Pamenter, 2014). ATP hydrolysis mediates proton (H+) release (Wilson, 1988) alongside the accumulation of metabolic end-products (Azarias et al, 2011), which contributes to metabolic acidosis (Robergs et al, 2004). Lactate is possibly oxidized by neurons (Quistorff et al, 2008; Gallagher et al, 2009; Barros, 2013; Riske et al, 2017) this requires oxygen, and lactate accumulation contributes to intracellular acidosis (reviewed in Kraut and Madias, 2014). Up to 60% of glucose can be metabolized to lactate (Teixeira et al, 2008; Dienel, 2012), which the accumulation of has been shown to associate with hypercarbia and acidosis (Rehncrona, 1985a; Katsura et al, 1992b)

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