Many studies now show that zinc plays a critical and unique role in ce
ntral nervous system development and function. The cellular mechanisms
of zinc afflux and influx are largely unknown and few models exist th
at describe cellular zinc transport in the brain. This report provides
convincing evidence of a zinc transporter in plasma membrane vesicles
isolated from rat brain. Zinc uptake was saturable (K-m = 15 mu M; V-
max = 10 nmol/mg per 30 s), was seen in the absence of ATP, and was un
affected by gradients for other ions such as Na+ or K+. Increasing the
ionic strength of the extravesicular media with Na+, K+, or choline() reduced zinc uptake approximately 50%. Whereas, increasing extravesi
cular H+ concentration (pH = 5) resulted in near complete inhibition o
f zinc uptake. Intravesicular zinc was rapidly released upon lowering
extravesicular concentrations of zinc with the heavy metal chelator O-
phenanthroline (1 mM). The results are consistent with a freely-revers
ible transport of zinc across the plasma membrane of neurons. (C) 1998
Elsevier Science Ireland Ltd.