CHANGES OF THE NA K ATPASE ACTIVITY IN THE CEREBRAL CORTICAL MICROVESSELS OF RAT AFTER SINGLE INTRAPERITONEAL ADMINISTRATION OF MERCURIC-CHLORIDE - HISTOCHEMICAL-DEMONSTRATION WITH LIGHT AND ELECTRON-MICROSCOPY/
G. Szumanska et al., CHANGES OF THE NA K ATPASE ACTIVITY IN THE CEREBRAL CORTICAL MICROVESSELS OF RAT AFTER SINGLE INTRAPERITONEAL ADMINISTRATION OF MERCURIC-CHLORIDE - HISTOCHEMICAL-DEMONSTRATION WITH LIGHT AND ELECTRON-MICROSCOPY/, Acta Neuropathologica, 86(1), 1993, pp. 65-70
Since inorganic mercury salts only poorly penetrate the cerebral micro
vascular endothelial cells comprising the blood-brain barrier (BBB), t
heir neurotoxicity may be predicted to result from interference with B
BB transport enzymes. In the present study, we tested the effect of me
rcuric chloride (HgCl2) on Na+/K+ ATPase activity, a key enzyme involv
ed in the ion transport in and out of the brain. Routine histochemical
staining in conjunction with light and electron microscopy was used t
o evaluate the changes in the Na+/K+ ATPase activity in cerebral corti
cal microvessels of rats who received a single intraperitoneal injecti
on of 6 mg/kg HgCl2. At 1 h after HgCl2 administration, light microsco
py revealed uniform reduction of the Na+/K+ ATPase reaction in all cor
tical layers. Electron microscopy confirmed the enzyme reaction to be
very weak to completely absent in both the luminal and abluminal endot
helial cell membranes, and the luminal plasmalemma showed invagination
s and pinocytic vesicles indicative of changes in its transport functi
ons. The enzyme inhibition coincided with, and was likely to contribut
e to, profound perivascular swelling, involving mainly the astrocytic
endfeet. The enzyme activity showed a partial recovery 18 h after HgCl
2 treatment, mainly in cortical layers II and III. After 5 days, the r
ecovery of the enzyme activity appeared complete as observed by light
and electron microscopy.The recovery of the microvascular Na+/K+ ATPas
e coincided with the appearance of a strongly positive Na+/K+ ATPase r
eaction in the adjacent astrocytic processes and with the diminution o
f perivascular swelling.