Vasorelaxant effect of isoquinoline derivatives from two species of Popowia perakensis and Phaeanthus crassipetalus on rat aortic artery

Five bisbenzyl isoquinolines (1-5), three benzyl isoquinolines (6-8), four isoquinoline alkaloids (9-12), and two unclassified compounds (13 and 14) from Popowia perakensis and Phaeanthus crassipetalus were evaluated for their vasorelaxant effect on rat aortic arteries. In aortic rings pre-contracte...

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Main Authors: Awang, K., Zaima, K., Takeyama, Y., Koga, I., Saito, A., Tamamoto, H., Syed Abd. Azziz, S.S., Mukhtar, M.R., Hadi, A.H., Morita, H.
Format: Article
Language:English
Published: Springer Verlag 2012
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Online Access:http://eprints.um.edu.my/10486/1/Vasorelaxant_effect_of_isoquinoline_derivatives_from_two_species_of_Popowia_perakensis_and_Phaeanthus_crassipetalus_on_rat_aortic_artery.pdf
http://eprints.um.edu.my/10486/
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Summary:Five bisbenzyl isoquinolines (1-5), three benzyl isoquinolines (6-8), four isoquinoline alkaloids (9-12), and two unclassified compounds (13 and 14) from Popowia perakensis and Phaeanthus crassipetalus were evaluated for their vasorelaxant effect on rat aortic arteries. In aortic rings pre-contracted with phenylephrine (PE, 0.3 μM), some of the bisbenzyl isoquinoline alkaloids, benzyl isoquinoline alkaloids, and isoquinoline alkaloids showed clearly vasorelaxant effects at 30 μM. The action of (-)-limacine (4) was deduced to be mediated through the increased release of NO from endothelial cells, and that of pecrassipine A (7) and backebergine (12) partly mediated by NO release. Further, the action of pecrassipine A (7) and backebergine (12) may be attributed to their inhibition of the voltage-dependent Ca(2+) channel and receptor-operated Ca(2+) channel.