Background. Patients on chronic hemodialysis (IID) are exposed to oxidative
stress. An I-ID session is used in this study as an in vivo model fur stud
ying the influence of heparin on oxidative stress caused partially by activ
ated peripheral blood polymorphonuclear leukocytes (PMNLs) during a I-ID se
ssion.
Methods. Each patient underwent HD once with and once without heparin. Oxid
ative stress was determined by evaluating both the rate of superoxide relea
se from phorbol 12-myristate: 13-acetate (PMA)-stimulated PMNLs and plasma
levels of oxidized glutathione (GSSG), both measured before and after the d
ialysis session.
Results. In vitro, heparin reduced the rate of superoxide release from sepa
rated PMA-stimulated PMNLs. In vivo, the rate of superoxide release from PM
NLs was always increased after the dialysis session, regardless of the pres
ence of heparin. However, in the presence of heparin, this increase was sig
nificantly smaller. The augmentation in the rate of superoxide release afte
r the dialysis session without heparin was accompanied by a significant ele
vation of GSSG, reflecting a preceding oxidation of plasma glutathione.
Conclusions. The increase in both parameters. the rate of superoxide releas
e, and the plasma GSSG concentration after HD treatment suggest that hepari
n in vivo alleviates the oxidative stress induced by the dialysis process.
Based on our results, heparin should be the anticoagulant of choice because
of its suppressant action on IID-induced oxidative stress.