Pharmaceutical Sciences Faculty Publications
Postsynaptic Dopamine (D2)-mediated Behavioural Effects of High Acute Doses of Artemisinin in Rodents
Document Type
Article
Publication Date
12-30-2003
Journal Title
Brain Research Bulletin
ISSN
0361-9230
Volume
62
Issue
3
First Page
255
Last Page
260
DOI
http://dx.doi.org/10.1016/j.brainresbull.2003.09.016
PubMed ID
14698358
Abstract
Artemisinin or qinghaosu is the active principle of quinghao (Artemisia annua L.) developed from Chinese traditional medicine, which is now widely used around the world against falciparum malaria. Behavioural effects of high acute doses of artemisinin were studied on spontaneous motor activity (SMA), exploratory behavior, apomorphine-induced stereotype behavior and pentobarbital sleeping time in mice and rats in order to provide additional evidence on its safety profile on the central nervous system (CNS). Effects of the drug on bromocriptine-induced hyperactivity in short term reserpinised mice were also evaluated. Intraperitoneal (i.p.) injection of artemisinin at doses of 50 and 100mg/kg, significantly (P<0.05) reduced the SMA in mice, prolonged the pentobarbital sleeping time in rats, and attenuated the apomorphine-induced stereotypy in mice. Mice pretreated with reserpine, showed a significant decrease in locomotor activity compared to the saline-treated group. Bromocriptine, a D2 receptor agonist, induced locomotor activity in mice pretreated with reserpine which was attenuated by artemisinin. The results suggest that artemisinin possesses sedative property, which may be mediated via postsynaptic dopamine (D2) receptor in the CNS.
Keywords
Artemisinin, apomorphine, bromocriptine, behavior, dopamine (D2) receptor, locomotor activity
Recommended Citation
Amos, Samson; Chindo, B. A.; Abbah, J.; Vongtau, H. O.; Edmond, I.; Binda, L.; Akah, P. A.; Wambebe, C.; and Gamaniel, K. S., "Postsynaptic Dopamine (D2)-mediated Behavioural Effects of High Acute Doses of Artemisinin in Rodents" (2003). Pharmaceutical Sciences Faculty Publications. 118.
https://digitalcommons.cedarville.edu/pharmaceutical_sciences_publications/118