T. Jansson et al., NONELECTROLYTE SOLUTE PERMEABILITIES OF HUMAN PLACENTAL MICROVILLOUS AND BASAL MEMBRANES, Journal of physiology, 468, 1993, pp. 261-274
1. Permeability to non-electrolytes of isolated microvillous and basal
membranes from human term placenta was measured using stopped-flow li
ght-scattering techniques. The studied solutes were urea, ethylene gly
col, glycerol, creatinine, erythritol, arabitol and mannitol. 2. At 37
-degrees-C, permeability of the microvillous membrane to mannitol and
urea was 0.30 +/- 0.02 x 10(-6) cm/s (mean +/- S.E.M.) and 3.2 +/- 0.2
x 10(-6) cm/s, respectively. The corresponding permeabilities for the
basal membrane were 1.2 +/- 0.1 x 10(-6) cm/s (mannitol) and 4.4 +/-
0.3 x 10(-6) cm/s (urea). The basal membrane was substantially more pe
rmeable to hydrophilic solutes than the microvillous membrane. This is
probably due to differences in lipid composition, as illustrated by m
embrane cholesterol content, which was found to be approximately 50 %
lower in the basal as compared to the microvillous membrane. 3. Simila
rities between permeabilities in placental membranes and lipid bilayer
s and the linear relationship noted between solute hydrophobicity and
placental permeability suggested that solutes permeate both human sync
ytiotrophoblast membranes by a solubility/diffusion mechanism. In the
microvillous membrane this was supported by data obtained for activati
on energies (> 10 kcal/mol) and reflection coefficients (close to 1).
In the basal membrane, low activation energies for glycerol and urea a
nd a low reflection coefficient for urea indicated that these solutes
may, in part, share a common pathway with water. 4. It was estimated t
hat the placental permeability to molecules with a molecular weight un
der 200 observed in vivo can, to a great extent, be accounted for by t
ranscellular permeation.