K. Plaschke et al., Neuromodulatory effect of propentofylline on rat brain under acute and long-term hypoperfusion, BR J PHARM, 133(1), 2001, pp. 107-116
1 The effects of propentofylline (PPF, 25 mg kg(-1) body weight per day) on
rat cerebral energy state and cytokine expression as well as on behaviour
and histopathology were studied after acute and long-term permanent bilater
al common carotid artery occlusion (BCCAO).
2 In the absence of PPF, acute ischaemia led to a decrease in energy-rich p
hosphates in parietotemporal cortex and hippocampus which correlated with a
n increase in AMP and adenosine concentrations measured by high-performance
liquid chromatography technique. The concentrations of cortical cytokines
TNF alpha and IL1 beta were increased 12 and 19 fold, respectively.
3 PPF had a neuroprotective action after 20 min of BCCAO, reducing the dele
terious effect of acute ischaemia on rat brain energy state and microglial
reaction. Simultaneously, PPF treatment increased cyclic-AMP 3 fold.
4 Three weeks of permanent BCCAO did not significantly disturb brain energy
metabolism, microglial reaction or histopathology. However, a significant
reduction of 30-50% in rat memory capacities and a locomotor hyperactivity
were obtained.
5 Continuous PPF-application, however, led to a marked increase in rat work
ing memory and to reduced locomotor activity, which were returned nearly to
control levels by 1 week after permanent BCCAO.
6 In summary, PPF showed a clear neuroprotective effect on cerebral energy
state and proinflammatory cytokines under conditions of acute global ischae
mia. Continuous administration of PPF led to memory improvement during perm
anent BCCAO. These results underscore the benefit of treatment with PPF in
clinical practice, particularly during stroke, but also in cerebrovascular
and neurodegenerative disorders.