Wong K K
Department of Pharmacology, National Yang Ming University, Taipei, Taiwan, Republic of China.
Planta Med. 1996 Jun;62(3):246-9. doi: 10.1055/s-2006-957869.
Dehydroevodiamine (DeHE) was reported to induce bradycardia and to have calcium-antagonizing activity besides other actions. The purpose of the present study was to investigate if DeHE could act as a calcium antagonist on the chronotropic and inotropic activities of mouse isolated atria. The data showed that DeHE induced bradycardia but did not decrease the contraction amplitude of the right atrium. Moreover, DeHE did not attenuate the contraction amplitude of the electrically driven left atrium and, in the presence of 1 x 10(-4) M DeHE, the contraction amplitude of left atrium was increased when the calcium concentration in Krebs solution was further increased. Since calcium antagonists are known to inhibit chronotropic and inotropic activities, it seems unlikely that DeHE acts as a calcium antagonist on the chronotropic and inotropic activities of mouse isolated atria.
据报道,除其他作用外,去氢吴茱萸碱(DeHE)可诱发心动过缓并具有钙拮抗活性。本研究的目的是调查DeHE是否可作为一种钙拮抗剂作用于小鼠离体心房的变时性和变力性活动。数据显示,DeHE可诱发心动过缓,但不降低右心房的收缩幅度。此外,DeHE不会减弱电驱动左心房的收缩幅度,并且在存在1×10⁻⁴ M DeHE的情况下,当Krebs溶液中的钙浓度进一步增加时,左心房的收缩幅度会增大。由于已知钙拮抗剂可抑制变时性和变力性活动,因此DeHE似乎不太可能作为一种钙拮抗剂作用于小鼠离体心房的变时性和变力性活动。