Fukuda N, Honda M, Minato M, Soma M, Izumi Y, Hatano M
2nd Department of Internal Medicine, Nihon University School of Medicine, Tokyo, Japan.
Jpn Circ J. 1990 Jan;54(1):82-8. doi: 10.1253/jcj.54.82.
It has been demonstrated that the adenylate cyclase activity of vascular smooth muscle regulates its tonus. The present study was undertaken to examine adenylate cyclase activity in early and established deoxycorticosterone acetate (DOCA)/salt hypertensive rats. Early and established DOCA/salt hypertensive rats were prepared by injecting 30 mg of DOCA weekly for 3 and 10 weeks, respectively, into male Wistar rats given drinking water with 1% saline. The membrane protein fraction medium containing the protein, 50 microM isoproterenol, 100 microM GTP, 50 microM forskolin or 25 microM calmodulin was applied. The adenylate cyclase activity was determined by a modified method developed in our laboratory using double isotope counting. The adenylate cyclase activity in the early DOCA/salt hypertensive rats was significantly higher (p less than 0.05) than that in the control rats in the basal condition, which was unaffected by additions of isoproterenol, GTP or forskolin. There was no significant difference in basal adenylate cyclase activity between the established DOCA/salt hypertensive and control rats. The adenylate cyclase activities in the established DOCA/salt hypertensive rats were significantly lower with GTP (p less than 0.02) and forskolin (p less than 0.01) as compared with the control rats. Calmodulin elevated the adenylate cyclase activity significantly (p less than 0.05) in the established DOCA/salt hypertensive rats as well as in the control rats. However, enzyme activity with calmodulin in the established DOCA/salt hypertensive rats was significantly lower (p less than 0.05) than that in the control rats.(ABSTRACT TRUNCATED AT 250 WORDS)
业已证实,血管平滑肌的腺苷酸环化酶活性调节其张力。本研究旨在检测早期和已形成的醋酸脱氧皮质酮(DOCA)/盐性高血压大鼠的腺苷酸环化酶活性。通过分别每周给饮用含1%盐水的雄性Wistar大鼠注射30mg DOCA,持续3周和10周,制备早期和已形成的DOCA/盐性高血压大鼠。应用含有蛋白质、50μM异丙肾上腺素、100μM GTP、50μM福斯高林或25μM钙调蛋白的膜蛋白部分培养基。腺苷酸环化酶活性采用我们实验室开发的改良双同位素计数法测定。早期DOCA/盐性高血压大鼠在基础状态下的腺苷酸环化酶活性显著高于对照大鼠(p<0.05),添加异丙肾上腺素、GTP或福斯高林对此无影响。已形成的DOCA/盐性高血压大鼠与对照大鼠的基础腺苷酸环化酶活性无显著差异。与对照大鼠相比,已形成的DOCA/盐性高血压大鼠在添加GTP(p<0.02)和福斯高林(p<0.01)时,腺苷酸环化酶活性显著降低。钙调蛋白在已形成的DOCA/盐性高血压大鼠和对照大鼠中均显著提高了腺苷酸环化酶活性(p<0.05)。然而,已形成的DOCA/盐性高血压大鼠中钙调蛋白存在时的酶活性显著低于对照大鼠(p<0.05)。(摘要截短于250字)