Dai Y, Chitaley K, Webb R C, Lewis R W, Mills T M
Department of Physiology, Medical College of Georgia, Augusta, Georgia 30912-3000, USA .
Int J Impot Res. 2004 Jun;16(3):294-8. doi: 10.1038/sj.ijir.3901171.
Studies from this laboratory have demonstrated that RhoA/Rho-kinase signaling mediates vasoconstriction in the penile circulation of the rat and that erection results from inhibition of this activity with Y-27632. In prior animal studies, Y-27632 was administered to the rats by intracavernous injection. To determine if topical application of the Rho-kinase inhibitor is an effective mode of delivery, Y-27632 was applied to the surface of the tunica albuginea or to the glans penis and surrounding skin in intact or castrated rats. Both sites of drug administration resulted in a marked increase in the erectile response both with and without stimulation of the autonomic innervation of the penile vasculature. Although high doses of the drug were found to reduce systemic blood pressure, topical administration of the Rho-kinase inhibitor, in appropriate doses, may have clinical value for the treatment erectile dysfunction.
该实验室的研究表明,RhoA/ Rho激酶信号传导介导大鼠阴茎循环中的血管收缩,而勃起是通过用Y-27632抑制这种活性而产生的。在先前的动物研究中,通过海绵体内注射将Y-27632给予大鼠。为了确定局部应用Rho激酶抑制剂是否是一种有效的给药方式,将Y-27632应用于完整或去势大鼠的白膜表面或阴茎头及周围皮肤。无论是否刺激阴茎血管系统的自主神经支配,两个给药部位均导致勃起反应显著增加。虽然发现高剂量的该药物会降低全身血压,但适当剂量的Rho激酶抑制剂局部给药可能对治疗勃起功能障碍具有临床价值。