Your browser doesn't support javascript.
loading
The Neural Circuits Underlying General Anesthesia and Sleep.
Moody, Olivia A; Zhang, Edlyn R; Vincent, Kathleen F; Kato, Risako; Melonakos, Eric D; Nehs, Christa J; Solt, Ken.
Afiliação
  • Moody OA; From the Department of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital, Boston, Massachusetts.
  • Zhang ER; Department of Anaesthesia, Harvard Medical School, Boston, Massachusetts.
  • Vincent KF; From the Department of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital, Boston, Massachusetts.
  • Kato R; From the Department of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital, Boston, Massachusetts.
  • Melonakos ED; Department of Anaesthesia, Harvard Medical School, Boston, Massachusetts.
  • Nehs CJ; From the Department of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital, Boston, Massachusetts.
  • Solt K; Department of Anaesthesia, Harvard Medical School, Boston, Massachusetts.
Anesth Analg ; 132(5): 1254-1264, 2021 05 01.
Article em En | MEDLINE | ID: mdl-33857967
General anesthesia is characterized by loss of consciousness, amnesia, analgesia, and immobility. Important molecular targets of general anesthetics have been identified, but the neural circuits underlying the discrete end points of general anesthesia remain incompletely understood. General anesthesia and natural sleep share the common feature of reversible unconsciousness, and recent developments in neuroscience have enabled elegant studies that investigate the brain nuclei and neural circuits underlying this important end point. A common approach to measure cortical activity across the brain is electroencephalogram (EEG), which can reflect local neuronal activity as well as connectivity among brain regions. The EEG oscillations observed during general anesthesia depend greatly on the anesthetic agent as well as dosing, and only some resemble those observed during sleep. For example, the EEG oscillations during dexmedetomidine sedation are similar to those of stage 2 nonrapid eye movement (NREM) sleep, but high doses of propofol and ether anesthetics produce burst suppression, a pattern that is never observed during natural sleep. Sleep is primarily driven by withdrawal of subcortical excitation to the cortex, but anesthetics can directly act at both subcortical and cortical targets. While some anesthetics appear to activate specific sleep-active regions to induce unconsciousness, not all sleep-active regions play a significant role in anesthesia. Anesthetics also inhibit cortical neurons, and it is likely that each class of anesthetic drugs produces a distinct combination of subcortical and cortical effects that lead to unconsciousness. Conversely, arousal circuits that promote wakefulness are involved in anesthetic emergence and activating them can induce emergence and accelerate recovery of consciousness. Modern neuroscience techniques that enable the manipulation of specific neural circuits have led to new insights into the neural circuitry underlying general anesthesia and sleep. In the coming years, we will continue to better understand the mechanisms that generate these distinct states of reversible unconsciousness.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sono / Encéfalo / Anestésicos Gerais / Estado de Consciência / Ondas Encefálicas / Anestesia Geral Limite: Animals / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sono / Encéfalo / Anestésicos Gerais / Estado de Consciência / Ondas Encefálicas / Anestesia Geral Limite: Animals / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article