Kumai Toshio, Takeba Yuko, Matsumoto Naoki, Nakaya Sachiko, Tsuzuki Yoshimitsu, Yanagida Yohei, Hayashi Mikito, Kobayashi Shinichi
Department of Pharmacology, St. Marianna University School of Medicine, 2-16-1 Sugao, Miyamae-ku, Kawasaki 2168511, Japan.
Life Sci. 2007 Sep 22;81(15):1193-8. doi: 10.1016/j.lfs.2007.08.008. Epub 2007 Aug 17.
We investigated the effects of fasudil, a Rho kinase inhibitor, on hypertension in spontaneously hypertensive rats and on the catecholamine synthetic pathway. Ten-week-old male SHR and Wistar-Kyoto rats were administered fasudil (10 mg/kg/day s.c.) for 4 days. Systolic blood pressure was measured using the tail-cuff method. Catecholamine levels were measured with high-performance liquid chromatography-ECD methods. Tyrosine hydroxylase protein levels were measured in Western blot analysis. The tyrosine hydroxylase mRNA level was measured using real-time PCR methods. Fasudil significantly decreased systolic blood pressure in spontaneously hypertensive rats, but not in Wistar-Kyoto rats. Fasudil also significantly decreased catecholamine, tyrosine hydroxylase protein, and tyrosine hydroxylase mRNA levels in the adrenal medulla of spontaneously hypertensive rats. These results suggest that the depressor effects of fasudil on hypertension in spontaneously hypertensive rats may be related to inhibition of the catecholamine synthetic pathway.
我们研究了Rho激酶抑制剂法舒地尔对自发性高血压大鼠高血压及儿茶酚胺合成途径的影响。10周龄雄性自发性高血压大鼠(SHR)和Wistar-Kyoto大鼠连续4天皮下注射法舒地尔(10 mg/kg/天)。采用尾套法测量收缩压。用高效液相色谱-电化学检测法测定儿茶酚胺水平。通过蛋白质印迹分析测量酪氨酸羟化酶蛋白水平。使用实时聚合酶链反应法测量酪氨酸羟化酶mRNA水平。法舒地尔可显著降低自发性高血压大鼠的收缩压,但对Wistar-Kyoto大鼠无此作用。法舒地尔还可显著降低自发性高血压大鼠肾上腺髓质中的儿茶酚胺、酪氨酸羟化酶蛋白及酪氨酸羟化酶mRNA水平。这些结果表明,法舒地尔对自发性高血压大鼠高血压的降压作用可能与抑制儿茶酚胺合成途径有关。