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Transient heat release during induced mitochondrial proton uncoupling.


ABSTRACT: Non-shivering thermogenesis through mitochondrial proton uncoupling is one of the dominant thermoregulatory mechanisms crucial for normal cellular functions. The metabolic pathway for intracellular temperature rise has widely been considered as steady-state substrate oxidation. Here, we show that a transient proton motive force (pmf) dissipation is more dominant than steady-state substrate oxidation in stimulated thermogenesis. Using transient intracellular thermometry during stimulated proton uncoupling in neurons of Aplysia californica, we observe temperature spikes of ~7.5?K that decay over two time scales: a rapid decay of ~4.8?K over ~1?s followed by a slower decay over ~17?s. The rapid decay correlates well in time with transient electrical heating from proton transport across the mitochondrial inner membrane. Beyond ~33?s, we do not observe any heating from intracellular sources, including substrate oxidation and pmf dissipation. Our measurements demonstrate the utility of transient thermometry in better understanding the thermochemistry of mitochondrial metabolism.

SUBMITTER: Rajagopal MC 

PROVIDER: S-EPMC6659641 | biostudies-literature | 2019

REPOSITORIES: biostudies-literature

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Transient heat release during induced mitochondrial proton uncoupling.

Rajagopal Manjunath C MC   Brown Jeffrey W JW   Gelda Dhruv D   Valavala Krishna V KV   Wang Huan H   Llano Daniel A DA   Gillette Rhanor R   Sinha Sanjiv S  

Communications biology 20190726


Non-shivering thermogenesis through mitochondrial proton uncoupling is one of the dominant thermoregulatory mechanisms crucial for normal cellular functions. The metabolic pathway for intracellular temperature rise has widely been considered as steady-state substrate oxidation. Here, we show that a transient proton motive force (pmf) dissipation is more dominant than steady-state substrate oxidation in stimulated thermogenesis. Using transient intracellular thermometry during stimulated proton u  ...[more]

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