NONELECTROLYTE SOLUTE PERMEABILITIES OF HUMAN PLACENTAL MICROVILLOUS AND BASAL MEMBRANES

Citation
T. Jansson et al., NONELECTROLYTE SOLUTE PERMEABILITIES OF HUMAN PLACENTAL MICROVILLOUS AND BASAL MEMBRANES, Journal of physiology, 468, 1993, pp. 261-274
Citations number
39
Categorie Soggetti
Physiology
Journal title
ISSN journal
00223751
Volume
468
Year of publication
1993
Pages
261 - 274
Database
ISI
SICI code
0022-3751(1993)468:<261:NSPOHP>2.0.ZU;2-P
Abstract
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.