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Paradoxes of Hymenoptera flight muscles, extreme machines

Journal

BIOPHYSICAL REVIEWS
Volume 14, Issue 1, Pages 403-412

Publisher

SPRINGERNATURE
DOI: 10.1007/s12551-022-00937-7

Keywords

Bees; Ants; Extreme contraction rate; Mitochondria; Creatine kinase; Adenylate diffusion

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Funding

  1. CAUL

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During the Carboniferous period, insects developed flight capabilities, with the evolution of specialized flight muscles called FMs. These FMs have unique adaptations for high frequency flight, but also present paradoxes and unanswered questions regarding their function and optimization.
In the Carboniferous, insects evolved flight. Intense selection drove for high performance and approximately 100 million years later, Hymenoptera (bees, wasps and ants) emerged. Some species had proportionately small wings, with apparently impossible aerodynamic challenges including a need for high frequency flight muscles (FMs), powered exclusively off aerobic pathways and resulting in extreme aerobic capacities. Modern insect FMs are the most refined and form large dense blocks that occupy 90% of the thorax. These can beat wings at 200 to 230 Hz, more than double that achieved by standard neuromuscular systems. To do so, rapid repolarisation was circumvented through evolution of asynchronous stimulation, stretch activation, elastic recoil and a paradoxically slow Ca2+ reuptake. While the latter conserves ATP, considerable ATP is demanded at the myofibrils. FMs have diminished sarcoplasmic volumes, and ATP is produced solely by mitochondria, which pack myocytes to maximal limits and have very dense cristae. Gaseous oxygen is supplied directly to mitochondria. While FMs appear to be optimised for function, several unusual paradoxes remain. FMs lack any significant equivalent to the creatine kinase shuttle, and myofibrils are twice as wide as those of within cardiomyocytes. The mitochondrial electron transport systems also release large amounts of reactive oxygen species (ROS) and respiratory complexes do not appear to be present at any exceptional level. Given that the loss of the creatine kinase shuttle and elevated ROS impairs heart function, we question how do FM shuttle adenylates at high rates and tolerate oxidative stress conditions that occur in diseased hearts?

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