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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2165860PMC
http://dx.doi.org/10.1136/bmj.1.5433.520-aDOI Listing

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Article Synopsis
  • A novel radiotracer, [C]SL25.1188, targets monoamine oxidase-B (MAO-B) enzyme primarily in astrocytes, linking its levels to altered astrocyte functions observed in schizophrenia.
  • A PET scan study involving 38 participants (14 with first-episode psychosis, 7 at clinical high risk, and 17 healthy volunteers) measured MAO-B concentration and found significantly lower levels in the high-risk group compared to healthy individuals.
  • The study also revealed that cannabis use impacted MAO-B levels, with a greater reduction in MAO-B concentration found in individuals using cannabis, emphasizing the potential role of astrocyte dysfunction in early psychosis and high-risk states.
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Data on medication interactions with psychedelics are limited. Here we present what may be the first published report of a hypertensive emergency following the combination of psilocybin mushrooms with a monoamine oxidase inhibitor (MAOI). A 42-year-old man with treatment-resistant major depressive disorder took 1 g of mushrooms, while prescribed tranylcypromine, extended-release dextroamphetamine-amphetamine, and other medications.

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The role of astrocytic γ-aminobutyric acid in the action of inhalational anesthetics.

Eur J Pharmacol

May 2024

Department of Anesthesiology and Pain Medicine, SMG-SNU Boramae Medical Center, Seoul, Republic of Korea; College of Medicine, Seoul National University, Seoul, Republic of Korea. Electronic address:

Background: Inhalational anesthetics target the inhibitory extrasynaptic γ-aminobutyric acid type A (GABA) receptors. Both neuronal and glial GABA mediate tonic inhibition of the extrasynaptic GABA receptors. However, the role of glial GABA during inhalational anesthesia remains unclear.

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Background: Perioperative neurocognitive disorders (PND), such as delirium and cognitive impairment, are commonly encountered complications in aged patients. The inhibitory neurotransmitter γ-aminobutyric acid (GABA) is aberrantly synthesized from reactive astrocytes following inflammatory stimulation and is implicated in the pathophysiology of neurodegenerative diseases. Additionally, the activation of NOD-like receptor protein 3 (NLRP3) inflammasome is involved in PND.

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