Real-time monitoring of human blood-brain barrier disruption

PLoS One. 2017 Mar 20;12(3):e0174072. doi: 10.1371/journal.pone.0174072. eCollection 2017.

Abstract

Chemotherapy aided by opening of the blood-brain barrier with intra-arterial infusion of hyperosmolar mannitol improves the outcome in primary central nervous system lymphoma. Proper opening of the blood-brain barrier is crucial for the treatment, yet there are no means available for its real-time monitoring. The intact blood-brain barrier maintains a mV-level electrical potential difference between blood and brain tissue, giving rise to a measurable electrical signal at the scalp. Therefore, we used direct-current electroencephalography (DC-EEG) to characterize the spatiotemporal behavior of scalp-recorded slow electrical signals during blood-brain barrier opening. Nine anesthetized patients receiving chemotherapy were monitored continuously during 47 blood-brain barrier openings induced by carotid or vertebral artery mannitol infusion. Left or right carotid artery mannitol infusion generated a strongly lateralized DC-EEG response that began with a 2 min negative shift of up to 2000 μV followed by a positive shift lasting up to 20 min above the infused carotid artery territory, whereas contralateral responses were of opposite polarity. Vertebral artery mannitol infusion gave rise to a minimally lateralized and more uniformly distributed slow negative response with a posterior-frontal gradient. Simultaneously performed near-infrared spectroscopy detected a multiphasic response beginning with mannitol-bolus induced dilution of blood and ending in a prolonged increase in the oxy/deoxyhemoglobin ratio. The pronounced DC-EEG shifts are readily accounted for by opening and sealing of the blood-brain barrier. These data show that DC-EEG is a promising real-time monitoring tool for blood-brain barrier disruption augmented drug delivery.

MeSH terms

  • Adult
  • Aged
  • Anesthesia
  • Antineoplastic Agents / administration & dosage
  • Blood-Brain Barrier / diagnostic imaging
  • Blood-Brain Barrier / drug effects*
  • Blood-Brain Barrier / physiopathology*
  • Capillary Permeability / drug effects*
  • Capillary Permeability / physiology*
  • Carotid Arteries / diagnostic imaging
  • Carotid Arteries / drug effects
  • Carotid Arteries / physiopathology
  • Central Nervous System Neoplasms / diagnostic imaging
  • Central Nervous System Neoplasms / drug therapy
  • Central Nervous System Neoplasms / physiopathology
  • Electroencephalography* / methods
  • Female
  • Hemoglobins / metabolism
  • Humans
  • Infusions, Intra-Arterial
  • Lymphoma / diagnostic imaging
  • Lymphoma / drug therapy
  • Lymphoma / physiopathology
  • Male
  • Mannitol / administration & dosage
  • Middle Aged
  • Neurophysiological Monitoring / methods
  • Oxyhemoglobins / metabolism
  • Spectroscopy, Near-Infrared
  • Vertebral Artery / diagnostic imaging
  • Vertebral Artery / drug effects
  • Vertebral Artery / physiology
  • Young Adult

Substances

  • Antineoplastic Agents
  • Hemoglobins
  • Oxyhemoglobins
  • Mannitol
  • deoxyhemoglobin

Grants and funding

CSTI/SHOK Salwe WP302 grant (VKi), JAES grant (VKi), MRC Oulu DP-grant (VKo), Oulu University Scholarship Foundation (VKo), Tauno Tönning Foundation (VKo) and Academy of Finland grant # 275352 (VKi) is cordially acknowledged in this study.