A Brainstem-Thalamic-Cortex Glutamatergic Neuron Pathway Modulates Propofol Anesthesia.
Обработка статьи · этапы, ошибки и управление
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
DuVall Adam S, McNeer Jennifer, Cheung Matthew C, Adrianzen-Herrera Diego A, Advani Anjali, Aljurf Mahmoud, Audino Anthony, Benitez Lydia, Deeter Anastasia, Dworkin Emily, Hiltbrand Olivia, Isenalumhe Leidy, Li Loretta, Miller-Chism Courtney, Mozessohn Lee, Ng Ashley P, Pu Jeffrey J, Shafer Danielle, Madueno Fernando Vargas, Viny Aaron, Wadhwa Aman, Yang Jay, Zarnegar-Lumley Sara, Mai Htun Ja, Kanaan Ghid, Sereda Yuliia, Saldanha Ian J, Balk Ethan M, Stock Wendy, Wolfson Julie A
Аннотация
METHODS: Anterograde and retrograde viral tracing techniques were employed to map the projections from the PB to the PVT and from the PVT to the mPFC. The activity within this pathway was monitored using fiber photometry during propofol anesthesia. The study further examined the role of this pathway during the induction and emergence phases of propofol anesthesia through optogenetic modulation in conjunction with cortical electroencephalography (EEG) recordings.
RESULTS: Glutamatergic neurons in the PB exhibit dense projections to the PVT, and in turn, PVT glutamatergic neurons project densely to the mPFC. Administration of propofol resulted in a reduction of calcium signals in the parabrachial glutamatergic nucleus to paraventricular thalamus (PBGlu-PVT) pathway. Moreover, it has been observed that optogenetic activation of the PBGlu-PVT pathway significantly enhances cortical activation during propofol anesthesia, whereas optogenetic inhibition of this pathway yields the opposite effect. Additionally, optogenetic stimulation of the PVTGlu-mPFC pathway accelerates the induction of propofol anesthesia but prolongs the emergence time. Conversely, inhibition of the PVTGlu-mPFC pathway facilitates cortical activation under propofol anesthesia.
CONCLUSION: Collectively, this study provides supportive evidence for the involvement of a brainstem-thalamic-cortical glutamatergic circuit in propofol anesthesia. The findings offer a preliminary perspective on how propofol may modulate consciousness and highlight potential pathways worthy of further investigation.