Murakami N, Sato Y, Tanase T, Nagai S, Ueda T, Sakakibara J, Ando H, Hotta Y, Takeya K, Asano M
Faculty of Pharmaceutical Sciences, Nagoya City University, Japan.
Yakugaku Zasshi. 1991 Aug;111(8):436-44. doi: 10.1248/yakushi1947.111.8_436.
To reduce the vascular contracting effect of the cardiac glycoside, proscillaridin (1), all kinds of its nitrates were prepared by utilizing effectively an isopropylidene function as a protective group. The pharmacological activities of proscillaridin nitrates were evaluated by the use of isolated guinea-pig papillary muscle preparations and Na+,K(+)-adenosine triphosphatase preparations from the dog kidney. Furthermore, the effect for smooth muscle using the helical strips isolated from 13-week old spontaneously hypertensive rat was examined. The positive inotropic effects and Na+, K(+)-adenosine triphosphatase inhibition activities of mononitrates (6, 9, 15) and dinitrates (3, 4, 5) were a little less potent than 1, but those of trinitrate (2) were much reduced. Every nitrate did not exhibited a vascular contracting effect but a relaxing effect. Among them, the vascular relaxing effects of 2',3'-dinitrate (3) and 2',4'-dinitrate (4) were more potent than those of the other nitrates.
为降低强心苷海葱次苷(1)的血管收缩作用,通过有效利用亚异丙基作为保护基制备了其各种硝酸盐。利用离体豚鼠乳头肌制剂和犬肾Na +,K(+) - 腺苷三磷酸酶制剂对海葱次苷硝酸盐的药理活性进行了评估。此外,还检查了使用从13周龄自发性高血压大鼠分离的螺旋条对平滑肌的作用。单硝酸盐(6、9、15)和二硝酸盐(3、4、5)的正性肌力作用和Na +,K(+) - 腺苷三磷酸酶抑制活性比1稍弱,但三硝酸盐(2)的活性则大大降低。每种硝酸盐均未表现出血管收缩作用,而是表现出舒张作用。其中,2',3'-二硝酸盐(3)和2',4'-二硝酸盐(4)的血管舒张作用比其他硝酸盐更强。