Khlq. Sang et al., IN-VIVO SHEAR-FLOW AND ERYTHROCYTE-MEMBRANE FLUIDITY IN HYPERTENSIVE PATIENTS, British journal of clinical pharmacology, 36(5), 1993, pp. 437-443
1 To evaluate the response of red blood cells subjected to the shear f
low in hypertension, the relationships between wall shear phenomena de
termined in vivo in the brachial artery of hypertensive patients and t
he. modifications of the membrane dynamics measured in vitro in erythr
ocyte ghosts of 32 patients were investigated. 2 Two fluorescent probe
s, diphenylhexatriene (DPH) and its trimethylamino-derivative (TMA-DPH
), localized respectively in the lipid membrane core and at the lipid-
water interface, were used. 3 Shear rate, shear stress and blood veloc
ity were positively correlated with TMA-DPH anisotropy (P = 0.015, 0.0
05 and 0.026, respectively), but not with that of DPH. This indicates
that wall shear forces were associated with the microviscosity of the
outer part of the cell membrane. 4 The changes in wall shear forces an
d erythrocyte membrane microviscosity probed by TMA-DPH or DPH were ob
served to vary in parallel under nitrendipine therapy. 5 These results
suggest that in vivo shear forces participate in the control of eryth
rocyte membrane fluidity or that erythrocytes adapt their membrane pro
perties to blood flow conditions.