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首页> 外文期刊>Japanese Journal of Pharmacology >Effects of Calcium Antagonists on the Nitrergic Nerve Function in Canine Corpus Cavernosum
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Effects of Calcium Antagonists on the Nitrergic Nerve Function in Canine Corpus Cavernosum

机译:钙拮抗剂对犬海绵体硝态神经功能的影响

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References(21) Cited-By(8) Effects of calcium antagonists on nitrergic nerve function were examined in the isolated canine corpus cavernosum. In the cavernous strips precontracted with phenylephrine, transmural electrical stimulation elicited frequency-dependent (2 – 5 Hz) relaxations that were abolished by NG-nitro-L-arginine (10−5 M), a nitric oxide (NO) synthase inhibitor; 1H[1,2,4]oxadiazole[4,3-a]quinoxalin-1-one (ODQ, 10−6 M), a soluble guanylate cyclase inhibitor; and tetrodotoxin (3 × 10−7 M). The relaxations were not affected by treatment with nifedipine or nicardipine (10−8 – 10 −6 M), L-type specific calcium channel inhibitors, but were significantly inhibited by amlodipine or cilnidipine, inhibitors of L- plus N-type calcium channels, in a concentration-related manner (10−7 – 10 −6 M). All of the inhibitors used did not affect the relaxations induced by exogenous NO (acidifed NaNO2). These findings suggest that N-type, but not L-type, calcium channels are responsible for increasing cytosolic free calcium, a prerequisite for the synthesis of NO, in the nitrergic dilator nerves innervating the corpus cavernosum.
机译:参考文献(21)By(8)研究了钙拮抗剂对离体犬海绵体中硝化神经功能的影响。在与去氧肾上腺素预收缩的海绵状带中,经壁电刺激引起频率依赖性(2 – 5 Hz)松弛,该松弛被一氧化氮(NO)合酶抑制剂NG-硝基-L-精氨酸(10-5 M)消除; 1H [1,2,4]恶二唑[4,3-a]喹喔啉-1-酮(ODQ,10-6 M),一种可溶性鸟苷酸环化酶抑制剂;和河豚毒素(3×10-7 M)。舒张不受L型特异性钙通道抑制剂硝苯地平或尼卡地平(10−8 – 10 -6 M)的治疗的影响,但氨氯地平或西尼地平是L + N型钙通道抑制剂的显着抑制,以浓度相关的方式(10-7 – 10 -6 M)。使用的所有抑制剂均不影响外源NO(酸化的NaNO2)引起的弛豫。这些发现表明,在支配海绵体的硝化扩张神经中,N型而不是L型钙通道负责增加胞质游离钙,这是合成NO的先决条件。

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