Neuroscience Letter 1985 Jun 24;57(3):251-6

Demonstration of regional blood-brain barrier permeability in human brain.

Landas S, Fischer J, Wilkin LD, Mitchell LD, Johnson AK, Turner JW, Theriac
M, Moore KC.

The brain of a 78-year-old woman with argyria was examined at autopsy.
Silver nitrate deposition was observed in circumventricular organs (CVO) and
in the paraventricular and supraoptic nuclei of the hypothalamus. These
findings parallel animal experiments of other investigators and are the best
demonstration so far of regional absence of the blood-brain barrier in
humans. These observations demonstrate similarities between humans and other
mammals of CVO anatomy, permeability to blood-borne agents, and perhaps
neural connections between CVOs and magnocellular nuclei.

PMID: 4034094

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: Microcirculation 2001 Apr;8(2):89-104


Regulation of blood-brain barrier permeability.

Mayhan WG.

Department of Physiology and Biophysics, University of Nebraska Medical
Center, Omaha 68198-4575, USA. [email protected]

The blood-brain barrier minimizes the entry of molecules into brain tissue.
This restriction arises by the presence of tight junctions (zonulae
occludens) between adjacent endothelial cells and a relative paucity of
pinocytotic vesicles within endothelium of cerebral arterioles, capillaries,
and venules. Many types of stimuli can alter the permeability
characteristics of the blood-brain barrier. Acute increases in arterial
blood pressure beyond the autoregulatory capacity of cerebral blood vessels,
application of hyperosmolar solutions, application of various inflammatory
mediators known to be elevated during brain injury, and/or activation of
blood-borne elements such as leukocytes can produce changes in permeability
of the blood-brain barrier. The second messenger systems that account for
increases in permeability of the blood-brain barrier during pathophysiologic
conditions, however, remain poorly defined. This review will summarize
studies that have examined factors that influence disruption of the
blood-brain barrier, and will discuss the contribution of various cellular
second messenger pathways in disruption of the blood-brain barrier during
pathophysiologic conditions.

PMID: 11379794

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1: Acta Neuropathol (Berl) 1983;60(1-2):92-8


Localization of exogenous silver in brain and spinal cord of silver exposed
rats.

Rungby J, Danscher G.

Exogenous silver in brain and spinal cord sections from rats treated with
Protargol, silver lactate or silver nitrate was visualized by physical
development. The silver penetrated the blood-brain barrier and accumulated
in neurones and glia. The distribution of silver in the CNS was
heterogeneous. Even with low doses and short survival periods, silver was
found to accumulate in large motoneurones in the brain stem and spinal cord
and neurones in the cerebellar nuclei. Silver was only found in di- and
telencephalic structures after extensive exposure. Silver distribution
following oral silver lactate and silver nitrate treatment differed in that
silver nitrate resulted in a relatively high content of silver in glia
whereas deposition occurred preferentially in neurones following silver
lactate treatment. Electron-microscopical studies showed that silver was
located intracellularly in the lysosomes and extracellularly in basement
membranes and elastic fibres of the vessels.

PMID: 6880627

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Acta Neuropathol (Berl) 1983;61(3-4):258-62


Neuronal accumulation of silver in brains of progeny from argyric rats.

Rungby J, Danscher G.

Using a photochemical method silver was demonstrated in the brains of 1-,
14-, and 45-day-old rats which had been exposed to silver on gestational
days 18 and 19. In the brain tissue of new-born rats, silver was found in
the lysosomes of neurons and astroglia. Minor changes in the anatomic
distribution of silver were observed between days 1 and 45. The pattern seen
at day 45 was identical to that observed in silver-exposed adults. At day 1,
the choroid plexus and meninges were heavily loaded with silver both intra-
and extracellularly. In particular, macrophage-like cells of the meningeal
spaces contained large amounts of silver. In these structures, the silver
had virtually disappeared by day 45. Silver was always seen in basement
membranes of the cerebral vessels.

PMID: 6650140


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