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The arousal effect of hyperbaric oxygen through orexin/hypocretin an upregulation on ketamine/ethanol‐induced unconsciousness in male rats
Author(s) -
Bian* Hetao,
Huang* Lei,
Li Bo,
Hu Qin,
Liang Xiping,
Tang Jiping,
Zhang John H.
Publication year - 2020
Publication title -
journal of neuroscience research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.72
H-Index - 160
eISSN - 1097-4547
pISSN - 0360-4012
DOI - 10.1002/jnr.24414
Subject(s) - unconsciousness , ketamine , anesthesia , orexin a , intraperitoneal injection , arousal , medicine , pharmacology , orexin , psychology , neuroscience , neuropeptide , receptor
Approaches that facilitate the recovery from coma would have enormous impacts on patient outcomes and medical economics. Orexin‐producing neurons release orexins (also known as hypocretins) energy‐dependently to maintain arousal. Hyperbaric oxygen (HBO) could increase ATP levels by preserving mitochondrial function. We investigated, for the first time, the arousal effects of HBO and orexins mechanisms in a rat model of unconsciousness induced by ketamine or ethanol. A total of 120 Sprague‐Dawley male rats were used in this study. Unconsciousness was induced either by intraperitoneal injection of ketamine or ethanol. The HBO treatment (100% O2 at 3 ATA) was administered immediately after unconsciousness induction for 1 hr. SB334867, orexin‐1 receptor (OX1R) inhibitor, or JNJ10397049, orexin‐2 receptor (OX2R) inhibitor was administered 30 min intraperitoneally before unconsciousness induction. Loss of righting reflex test (LORR) and Garcia test were used to evaluate the unconsciousness duration and neurological deficits after recovering from unconsciousness, respectively. Enzyme‐linked immunosorbent assay was used to measure brain tissue ATP and orexin A levels. Ketamine or ethanol injection resulted in LORR immediately and neurological deficits 6 hr after unconsciousness induction. HBO treatment significantly reduced the LORR duration, improved Garcia scores and unregulated ATP and orexin A levels in the brain tissue. Administration of OX1R inhibitor or OX2 R inhibitor abolished arousal and neurological benefits of HBO. In conclusion, HBO exerted arousal‐promoting effects on unconscious rats induced by ketamine or ethanol. The underlying mechanism was via, at least in part, ATP/orexin A upregulation. HBO may be a practical clinical approach to accelerate unconsciousness recovery in patients.