The Effects of Propofol on a Human in vitro Blood-Brain Barrier Model

• Published in: Frontiers in cellular neuroscience Vol. 16; p. 835649
• Main Authors: Hughes, Jason M, Neese, Olivia R, Bieber, Dylan D, Lewis, Kirsten A, Ahmadi, Layla M, Parsons, Dustin W, Canfield, Scott G
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Research Foundation 11.05.2022; Frontiers Media S.A
• Subjects: Alzheimer's disease; Anesthesia; anesthesia toxicity; Anesthetics; Blood-brain barrier; brain microvascular-like endothelial cells; Dextran; Electrical resistivity; Endothelial cells; Localization; Matrix metalloproteinase; Metalloproteinase; Microvasculature; Neurodegenerative diseases; Neuroscience; Parenchyma; Permeability; Pluripotency; Propofol; Proteins; Sodium; Stem cells; tight junction dysfunction; St Louis Missouri; United States > US; blood-brain barrier; tight junction dysfunction; propofol; brain microvascular-like endothelial cells; anesthesia toxicity
• ISSN: 1662-5102; 1662-5102
• DOI: 10.3389/fncel.2022.835649

Recently, the safety of repeated and lengthy anesthesia administration has been called into question, a subset of these animal studies demonstrated that anesthetics induced blood-brain barrier (BBB) dysfunction. The BBB is critical in protecting the brain parenchyma from the surrounding micro-vasculature. BBB breakdown and dysfunction has been observed in several neurodegenerative diseases and may contribute to both the initiation and the progression of the disease. In this study we utilize a human induced pluripotent stem cell (iPSC) derived-BBB model, exhibiting near properties, to evaluate the effects of anesthetics on critical barrier properties. iPSC-derived brain microvascular endothelial cells (BMECs) expressed near barrier tightness assessed by endothelial electrical resistance and para-cellular permeability. Efflux transporter activity was determined by substrate transport in the presence of specific inhibitors. cellular transport was measured utilizing large fluorescently tagged dextran. Tight junction localization in BMECs was evaluated with fluorescent microscopy. The anesthetic, propofol was exposed to BMECs at varying durations and concentrations and BBB properties were monitored post-exposure. Following propofol exposure, BMECs displayed reduced resistance and increased permeability indicative of a leaky barrier. Reduced barrier tightness and the dysregulation of occludin, a tight junction protein, were partly the result of an elevation in matrix metalloproteinase (MMP) levels. Efflux transporter activity and cellular transport were unaffected by propofol exposure. Propofol induced barrier dysfunction was partially restored following matrix metalloproteinase inhibition. For the first time, we have demonstrated that propofol alters BBB integrity utilizing a human BBB model that displays key characteristics. A leaky BBB enables otherwise impermeable molecules such as pathogens and toxins the ability to reach vulnerable cell types of the brain parenchyma. A robust human BBB model will allow for the evaluation of several anesthetics at fluctuating clinical scenarios and to elucidate mechanisms with the goal of ultimately improving anesthesia safety.