Antiplatelet activity of β-carboline alkaloids from Perganum harmala : A possible mechanism through inhibiting PLCγ2 phosphorylation

• Published in: Vascular pharmacology Vol. 50; no. 5; pp. 147 - 152
• Main Authors: Im, Ji-Hyun, Jin, Yong-Ri, Lee, Jung-Jin, Yu, Ji-Yeon, Han, Xiang-Hua, Im, Se-Hyuk, Hong, Jin Tae, Yoo, Hwan-Soo, Pyo, Myoung-Yun, Yun, Yeo-Pyo
• Format: Journal Article
• Language: English
• Published: Elsevier Inc 01.05.2009
• Subjects: Antiplatelet activity; Cardiovascular; Collagen; PLCγ2; β-carboline alkaloids; β-carboline alkaloids; PLCγ2; Collagen; Antiplatelet activity
• ISSN: 1537-1891; 1879-3649
• DOI: 10.1016/j.vph.2008.11.008

Abstract Beta-carboline alkaloids including harmalol, harmaline, norharmane, harmol, harmine and harmane are important constituents of the medicinal plant, Perganum harmala L. (Zygophylaceae), which has been used in traditional medicine. In the present study, the antiplatelet activities of six β-carboline alkaloid compounds were investigated in vitro. At a concentration of 200 μM, these compounds have no effect on arachidonic acid (AA)-, thrombin- and U46619 (a thromboxane A2 mimic)-stimulated platelet aggregation. On the contrary, it was revealed that collagen-induced platelet aggregation could be inhibited by these compounds with different potencies (harmane and harmine were most potent, harmol had medium potency, and harmol, norharmane, harmalol and harmaline had a weak, non significant effect), indicating a selective inhibition on collagen-mediated platelet activation. Consistently, further study revealed that collagen-mediated phospholipase (PL) Cγ2 and protein tyrosine phosphorylation, cytosolic calcium mobilization and arachidonic acid liberation were completely inhibited by harmane and harmine in a concentration-dependent manner, while the other compounds were only partially or not effective at all. Taken together, these results indicate that three of these six β-carboline alkaloids can selectively affect collagen-induced platelet aggregation with different potencies; in particular, harmane and harmine were most potent, and their antiplatelet activities may be mediated by inhibiting PLCγ2 and protein tyrosine phosphorylation with sequential suppression of cytosolic calcium mobilization and arachidonic acid liberation, indicating that harmane and harmine have a potential to be developed as a novel agent for atherothrombotic diseases.