首页> 外文期刊>The Journal of Urology >Nitric oxide independent activation of guanylate cyclase by YC-1 causes erectile responses in the rat.
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Nitric oxide independent activation of guanylate cyclase by YC-1 causes erectile responses in the rat.

机译:YC-1对鸟苷酸环化酶的一氧化氮非依赖性激活会在大鼠中引起勃起反应。

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PURPOSE: Activation of soluble guanylate cyclase with a subsequent increase in intracellular levels of cyclic guanosine monophosphate is necessary for normal erection. In vascular tissue 3(5'-hydroxymethyl-2'-furyl-1-benzyl indazole (YC-1) (Abbott Laboratories, North Chicago, Illinois) has been shown to stimulate soluble guanylate cyclase independent of nitric oxide. We studied whether YC-1 modulates erectile responses in the rat. MATERIALS AND METHODS: The effects of YC-1 given intracavernously or intraperitoneally on intracavernous pressure were investigated in rats. Functional effects of YC-1 on neuronal and endothelial nitric oxide relaxations were studied in 3 x 10(-6) M. 1-noradrenaline contracted preparations of rat isolated corpus cavernosum. RESULTS: Intracavernous YC-1 (10 micromol. kg.-1) produced erectile responses with a mean intracavernous pressure plus or minus standard error of mean of 81 +/- 17 cm. water (p <0.001) and a mean duration of 7.1 +/- 3.3 minutes (p <0.001). YC-1 (10 micromol. kg.-1) given intraperitoneally also increased the amplitude and duration of erectile responses to cavernous nerve stimulation. Mean peak intracavernous pressure increased from 63 +/- 6 to 10(2) +/- 16 cm. water (p <0.05). Erections induced by a submaximal dose of 25 microg. kg.-1 apomorphine s.c. increased in number after 10 micromol. kg.-1 YC-1 intraperitoneally (p <0.05). In vitro nerve induced relaxant responses were enhanced by increasing concentrations of YC-1. Relaxations at 20 Hz. were increased from a mean of 9% +/- 5% to 52% +/- 5% at a YC-1 concentration of 10(-5) M. (p <0.001). At this concentration carbachol induced relaxations were enhanced from a mean of 19% +/- 3% to 40% +/- 9% (p <0.05). CONCLUSIONS: YC-1 can evoke erectile responses when given intracavernously and it enhances erections induced by cavernous nerve stimulation and apomorphine when given systemically. In vitro YC-1 enhances electrically evoked relaxations in rat corpus cavernosum. YC-1 represents an interesting pharmacological principle that may be useful for treating erectile dysfunction.
机译:目的:可溶性鸟苷酸环化酶的激活以及随后细胞内环鸟苷单磷酸水平的增加对于正常勃起是必要的。在血管组织中,3(5'-羟甲基-2'-呋喃基-1-苄基吲唑(YC-1)(伊利诺伊州北芝加哥的Abbott Laboratories)已显示可刺激可溶性鸟苷酸环化酶,而与一氧化氮无关。 -1调节大鼠的勃起反应材料和方法:研究了大鼠腔内或腹膜内给予YC-1对腔内压力的影响,并以3 x 10的剂量研究了YC-1对神经元和内皮一氧化氮松弛的作用。 (-6)大鼠去甲海绵体的M. 1-去甲肾上腺素收缩制剂结果:海绵体YC-1(10 micromol。kg.-1)产生勃起反应,平均海绵体内压力加或减标准平均值为81 + /-17厘米水(p <0.001)和平均持续时间7.1 +/- 3.3分钟(p <0.001)。腹腔注射YC-1(10 micromol。kg.-1)也增加了勃起的幅度和持续时间对海绵状神经刺激的反应。平均峰内腔压力从63 +/- 6厘米增加到10(2)+/- 16厘米。水(p <0.05)。亚最大剂量25微克诱发勃起。 kg.-1阿扑吗啡10 micromol后数量增加。腹膜内kg.-1 YC-1(p <0.05)。体外神经诱导的松弛反应通过增加YC-1的浓度而增强。 20 Hz时的弛豫。当YC-1浓度为10(-5)M时,平均浓度从9%+/- 5%的平均值增加到52%+/- 5%(p <0.001)。在该浓度下,卡巴胆碱引起的松弛从平均19%+/- 3%增强到40%+/- 9%(p <0.05)。结论:YC-1腔内给药可引起勃起反应,全身给药可增强海绵状神经刺激和阿扑吗啡诱导的勃起。体外YC-1可增强大鼠海绵体的电诱发弛豫。 YC-1代表了一种有趣的药理原理,可用于治疗勃起功能障碍。

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