The goal of this research was to determine leukocyte rheology at baseline a
nd after chemotactic activation in type I and type II diabetics. In 19 norm
al subjects, 21 type I diabetics, and 16 type II diabetics at baseline and
after in vitro chemotactic activation (prolonged for 5 and 15 minutes) with
two stimulating agents (4-phorbol 12-myristate 13-acetate [PMA] and N-form
yl-methionyl-leucyl-phenylalanine [fMLP]), we evaluated polymorphonuclear (
PMN) filtration parameters (using a St. George filtrometer [Carri-Med, Dork
ing, UK] and considering the initial relative flow rate [IRFR] and the conc
entration of clogging particles [CPI) and PMN membrane fluidity (obtained b
y marking PMNs with the fluorescent probe 1-(4-[trimethylamino]phenyl)-6-ph
enyl-1,3,5-hexatriene (TMA-DPH), At baseline, there was a difference betwee
n normals and type I and II diabetics for PMN membrane fluidity only. After
activation in normals and diabetics of both types, a significant variation
was present in PMN filtration parameters (IRFR and CP) at both 5 and 15 mi
nutes. In normals, no variation was present in PMN membrane fluidity after
activation with PMA or fMLP, After PMN activation, only in type I diabetics
was a significant decrease in PMN membrane fluidity present at both 5 and
15 minutes. After PMN activation with either PMA or fMLP in comparison to b
asal values, only the mean variation (Delta%) of the IRFR was significantly
different between normals, type I diabetics, and type II diabetics at both
5 and 15 minutes. From the data obtained, it is evident that after activat
ion, the PMN filtration pattern shows a specific behavior in diabetics of b
oth types, while PMN membrane fluidity changes only in type I diabetics. Th
e latter finding may be the basis of a metabolic pattern present in PMNs of
this type, revealed after in vitro activation. Copyright (C) 1999 by W.B.
Saunders Company.