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1
No evidence for a significant non-nitrergic, hyperpolarising factor contribution to field stimulation-induced relaxation of the mouse anococcygeus.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。
Br J Pharmacol. 1998 Jun;124(3):524-8. doi: 10.1038/sj.bjp.0701862.
2
Evidence that NO acts as a redundant NANC inhibitory neurotransmitter in the guinea-pig isolated taenia coli.一氧化氮作为豚鼠离体结肠带中一种多余的非肾上腺素能非胆碱能抑制性神经递质的证据。
Br J Pharmacol. 1997 Jun;121(3):604-11. doi: 10.1038/sj.bjp.0701113.
3
Evidence that both nitric oxide (NO) and a non-NO hyperpolarizing factor elicit NANC nerve-mediated relaxation in the rat isolated anocococcygeus.有证据表明,一氧化氮(NO)和一种非NO超极化因子均可引起大鼠离体肛门尾骨肌中神经介导的非肾上腺素能非胆碱能(NANC)神经舒张。
Br J Pharmacol. 1997 Feb;120(4):662-6. doi: 10.1038/sj.bjp.0700916.
4
Influence of a selective guanylate cyclase inhibitor, and of the contraction level, on nitrergic relaxations in the gastric fundus.选择性鸟苷酸环化酶抑制剂及收缩水平对胃底氮能舒张的影响。
Br J Pharmacol. 1998 Aug;124(7):1439-48. doi: 10.1038/sj.bjp.0701992.
5
P2 purinoceptor antagonists inhibit the non-adrenergic, non-cholinergic relaxation of the human colon in vitro.P2嘌呤受体拮抗剂在体外可抑制人结肠的非肾上腺素能、非胆碱能舒张作用。
Neuroscience. 2007 Jun 15;147(1):146-52. doi: 10.1016/j.neuroscience.2007.04.016. Epub 2007 May 23.
6
Characterization of the apamin- and L-nitroarginine-resistant NANC inhibitory transmission to the circular muscle of guinea-pig colon.蜂毒明肽和L-硝基精氨酸抗性非肾上腺素能非胆碱能抑制性神经传递对豚鼠结肠环行肌的作用特性研究
J Auton Pharmacol. 1996 Jun;16(3):131-45.
7
Nitrergic relaxation of the mouse gastric fundus is mediated by cyclic GMP-dependent and ryanodine-sensitive mechanisms.小鼠胃底的一氧化氮能舒张作用由环磷酸鸟苷依赖性和兰尼碱敏感机制介导。
Br J Pharmacol. 2000 Apr;129(7):1315-22. doi: 10.1038/sj.bjp.0703174.
8
Evidence for a role for nitric oxide in relation of the frog oesophageal body to electrical field stimulation.一氧化氮在青蛙食管体与电场刺激关系中作用的证据。
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9
Comparison of two soluble guanylyl cyclase inhibitors, methylene blue and ODQ, on sodium nitroprusside-induced relaxation in guinea-pig trachea.两种可溶性鸟苷酸环化酶抑制剂亚甲蓝和ODQ对硝普钠诱导的豚鼠气管舒张作用的比较。
Br J Pharmacol. 1998 Nov;125(6):1158-63. doi: 10.1038/sj.bjp.0702181.
10
Involvement of bradykinin B1 and B2 receptors in relaxation of mouse isolated trachea.缓激肽B1和B2受体在小鼠离体气管舒张中的作用
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引用本文的文献

1
Effect of the phosphodiesterase 5 inhibitors sildenafil, tadalafil and vardenafil on rat anococcygeus muscle: functional and biochemical aspects.磷酸二酯酶5抑制剂西地那非、他达拉非和伐地那非对大鼠肛尾肌的影响:功能和生化方面
Clin Exp Pharmacol Physiol. 2009 Apr;36(4):358-66. doi: 10.1111/j.1440-1681.2008.05071.x. Epub 2008 Oct 15.

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.

DOI:10.1038/sj.bjp.0701862
PMID:9647477
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1565417/
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。