Jv. Greiner et al., EPIDERMAL AND DERMAL PHOSPHOLIPIDS OF THE HUMAN EYELID - A P-31 NUCLEAR-MAGNETIC-RESONANCE SPECTROSCOPY STUDY, Archives of dermatological research, 290(6), 1998, pp. 298-305
The phospholipids of the skin are difficult tea quantify because they
represent only a small fraction of the skin tissue. In this study, P-3
1 nuclear magnetic resonance, which permits precise profiling of these
phospholipids, was used to compare the phospholipids of upper eyelid
epidermal and dermal lipid extracts (n = 13 profiles). Phospholipid pr
ofiles included alkylacylphosphatidylcholine (AAPC), dihydrosphingomye
line (DHSM), diphosphatidylglycerol (cardiolipin), ethanolamine plasma
logen (EPLAS), lysophosphatidylcholine, phosphatidic acid, phosphatidy
lcholine (PC), phosphatidylethanolamine, phosphatidylinositol, phospha
tidylserine, sphingomyelin, and uncharacterized phospholipids (U1 and
U2, particularly enriched in the epidermis). The computed phospholipid
metabolic index (n = 86 indexes) findings can be summarized as follow
s: a lower content of the en-ol and ether phospholipids in the epiderm
is relative to the dermis, internal compensation among the component p
hospholipids so as to maintain the choline functional group ratio, and
a greater concentration of hydroxyl-containing functional groups in t
he epidermis. A membrane index (f(mem)) value of -0.37 for the epiderm
is deviated considerably from the value of -0.06 characteristic of liv
ing membranes and the dermis. The production of the reduced phosphatid
es, EPLAS and AAPC, indicates the use of alternative pathways between
the two tissues. Relative to the dermis, increased PC in the epidermis
coupled with decreased DHSM, EPLAS, and AAPC are factors enabling the
epidermis of eyelid tissue to be an effective water barrier.