Suppr超能文献

没有证据表明存在一种重要的非一氧化氮能超极化因子对小鼠肛门尾骨肌的场刺激诱导舒张有贡献。

No evidence for a significant non-nitrergic, hyperpolarising factor contribution to field stimulation-induced relaxation of the mouse anococcygeus.

作者信息

Fonseca M, Uddin N, Gibson A

机构信息

Pharmacology Group, Biomedical Sciences Division, King's College London.

出版信息

Br J Pharmacol. 1998 Jun;124(3):524-8. doi: 10.1038/sj.bjp.0701862.

Abstract
  1. The aim of the study was to determine whether a nerve-derived hyperpolarizing factor (NDHF) might contribute to non-adrenergic, non-cholinergic (NANC) relaxations of the mouse anococcygeus when low concentrations of contractile agent are used to raise tone and low frequencies of field stimulation applied; such a non-nitrergic NDHF has been proposed to contribute to NANC relaxations of the rat anococcygeus and guinea-pig taenia coli. 2. Phenylephrine (0.1-100 microM) produced concentration-related contractions of the mouse isolated anococcygeus muscle; 0.2 microM phenylephrine (EC26) was used to raise tone in subsequent experiments. 3. Field stimulation (0.5, 1.0 and 5.0 Hz) produced frequency-dependent relaxations of phenylephrine-induced tone. In the presence of the nitric oxide synthase inhibitor L-NG-nitro-arginine (L-NOARG; 100 microM), the soluble guanylate cyclase inhibitor 1H-[1,2,4]oxodiazolo[4,3-a]quinoxalin-1-one (ODQ; 5 microM), or a combination of these two drugs, relaxations to field stimulation were abolished at all frequencies studied. Relaxations to sodium nitroprusside (0.01-5 microM) were unaffected by L-NOARG but strongly inhibited by ODQ; neither enzyme inhibitor affected relaxations to 8-Br-cyclic GMP (10 microM). 4. Nifedipine (1 microM) reduced the contractile response to 0.2 microM phenylephrine by 38%; however, it had no effect on NANC relaxations. 5. It is concluded that NANC relaxations of the mouse anococcygeus are purely nitrergic and that there is no significant contribution from a putative NDHF.
摘要
  1. 本研究的目的是确定当使用低浓度收缩剂提高张力并施加低频率场刺激时,神经源性超极化因子(NDHF)是否可能有助于小鼠肛门尾骨肌的非肾上腺素能、非胆碱能(NANC)舒张;有人提出这种非一氧化氮能的NDHF有助于大鼠肛门尾骨肌和豚鼠结肠带的NANC舒张。2. 去氧肾上腺素(0.1 - 100微摩尔)使小鼠离体肛门尾骨肌产生浓度依赖性收缩;在随后的实验中,使用0.2微摩尔去氧肾上腺素(EC26)提高张力。3. 场刺激(0.5、1.0和5.0赫兹)使去氧肾上腺素诱导的张力产生频率依赖性舒张。在一氧化氮合酶抑制剂L - NG - 硝基 - 精氨酸(L - NOARG;100微摩尔)、可溶性鸟苷酸环化酶抑制剂1H - [1,2,4]恶二唑并[4,3 - a]喹喔啉 - 1 - 酮(ODQ;5微摩尔)存在的情况下,或这两种药物联合使用时,在所研究的所有频率下,对场刺激的舒张均被消除。对硝普钠(0.01 - 5微摩尔)的舒张不受L - NOARG影响,但被ODQ强烈抑制;两种酶抑制剂均不影响对8 - 溴环鸟苷酸(10微摩尔)的舒张。4. 硝苯地平(1微摩尔)使对0.2微摩尔去氧肾上腺素的收缩反应降低38%;然而,它对NANC舒张没有影响。5. 得出的结论是,小鼠肛门尾骨肌的NANC舒张完全是一氧化氮能的,并且假定的NDHF没有显著贡献。

相似文献

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验