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1
N-methylhydroxylamine inhibits and M&B 22948 potentiates relaxations of the mouse anococcygeus to non-adrenergic, non-cholinergic field stimulation and to nitrovasodilator drugs.N-甲基羟胺抑制而M&B 22948增强小鼠肛门尾骨肌对非肾上腺素能、非胆碱能场刺激以及对硝基血管扩张剂药物的舒张反应。
Br J Pharmacol. 1989 Mar;96(3):637-44. doi: 10.1111/j.1476-5381.1989.tb11863.x.
2
Cyclic nucleotide content of the rat anococcygeus during relaxations induced by drugs or by non-adrenergic, non-cholinergic field stimulation.药物或非肾上腺素能、非胆碱能场刺激诱导大鼠肛门尾骨肌松弛期间的环核苷酸含量
J Pharm Pharmacol. 1991 Apr;43(4):247-51. doi: 10.1111/j.2042-7158.1991.tb06677.x.
3
L-NG-monomethyl arginine and L-NG-nitro arginine inhibit non-adrenergic, non-cholinergic relaxation of the mouse anococcygeus muscle.L-NG-单甲基精氨酸和L-NG-硝基精氨酸抑制小鼠肛门尾骨肌的非肾上腺素能、非胆碱能舒张。
Br J Pharmacol. 1990 Mar;99(3):602-6. doi: 10.1111/j.1476-5381.1990.tb12976.x.
4
Differentiation by hydroquinone of relaxations induced by exogenous and endogenous nitrates in non-vascular smooth muscle: role of superoxide anions.对苯二酚对外源性和内源性硝酸盐在非血管平滑肌中诱导的舒张作用的分化:超氧阴离子的作用
Br J Pharmacol. 1991 Nov;104(3):645-50. doi: 10.1111/j.1476-5381.1991.tb12483.x.
5
An investigation of some S-nitrosothiols, and of hydroxy-arginine, on the mouse anococcygeus.对一些S-亚硝基硫醇和羟基精氨酸对小鼠肛门尾骨肌的研究。
Br J Pharmacol. 1992 Nov;107(3):715-21. doi: 10.1111/j.1476-5381.1992.tb14512.x.
6
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.
7
L-NG-nitro-arginine and its methyl ester are potent inhibitors of non-adrenergic, non-cholinergic transmission in the rat anococcygeus.L-NG-硝基精氨酸及其甲酯是大鼠肛尾肌中非肾上腺素能、非胆碱能传递的强效抑制剂。
Br J Pharmacol. 1990 Aug;100(4):749-52. doi: 10.1111/j.1476-5381.1990.tb14086.x.
8
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.
9
Effects of NG-substituted analogues of L-arginine on NANC relaxation of the rat anococcygeus and bovine retractor penis muscles and the bovine penile artery.L-精氨酸的N-取代类似物对大鼠肛门尾骨肌、牛阴茎退缩肌及牛阴茎动脉非肾上腺素能非胆碱能舒张的影响。
Br J Pharmacol. 1991 Sep;104(1):53-8. doi: 10.1111/j.1476-5381.1991.tb12384.x.
10
Involvement of nitric oxide in non-adrenergic non-cholinergic relaxation and action of vasoactive intestinal polypeptide in circular muscle strips of the rat gastric fundus.一氧化氮参与大鼠胃底环形肌条中非肾上腺素能非胆碱能舒张及血管活性肠肽的作用。
Pharmacol Res. 2001 Sep;44(3):221-8. doi: 10.1006/phrs.2001.0844.

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Adventures in vascular biology: a tale of two mediators.血管生物学奇遇:两种介质的故事
Philos Trans R Soc Lond B Biol Sci. 2006 May 29;361(1469):735-59. doi: 10.1098/rstb.2005.1775.
2
NO as a signalling molecule in the nervous system.一氧化氮作为神经系统中的信号分子。
Br J Pharmacol. 2002 Mar;135(5):1079-95. doi: 10.1038/sj.bjp.0704569.
3
Inhibition of capacitative calcium entry is not obligatory for relaxation of the mouse anococcygeus by the NO/cyclic GMP signalling pathway.对于通过NO/环鸟苷酸信号通路使小鼠肛门尾骨肌松弛而言,抑制储存式钙内流并非必要条件。
Br J Pharmacol. 2001 Feb;132(4):807-14. doi: 10.1038/sj.bjp.0703888.
4
Antioxidant protection of NO-induced relaxations of the mouse anococcygeus against inhibition by superoxide anions, hydroquinone and carboxy-PTIO.一氧化氮(NO)诱导的小鼠肛门尾骨肌舒张的抗氧化保护作用,以抵抗超氧阴离子、对苯二酚和羧基-PTIO的抑制。
Br J Pharmacol. 1996 Sep;119(2):432-8. doi: 10.1111/j.1476-5381.1996.tb16004.x.
5
Inhibition by sodium nitroprusside of a calcium store depletion-activated non-selective cation current in smooth muscle cells of the mouse anococcygeus.硝普钠对小鼠肛门尾骨肌平滑肌细胞中钙库耗竭激活的非选择性阳离子电流的抑制作用。
Br J Pharmacol. 1996 Aug;118(8):2001-8. doi: 10.1111/j.1476-5381.1996.tb15636.x.
6
Inhibition of relaxations to nitrergic stimulation of the mouse anococcygeus by duroquinone.杜罗醌对小鼠肛门尾骨肌硝化能刺激引起的舒张的抑制作用。
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Nitric oxide, an enteric nonadrenergic-noncholinergic relaxant transmitter: evidence using phosphodiesterase V and nitric oxide synthase inhibition.一氧化氮,一种肠道非肾上腺素能-非胆碱能舒张性递质:使用磷酸二酯酶V和一氧化氮合酶抑制的证据
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8
Variable potency of nitrergic-nitrovasodilator relaxations of the mouse anococcygeus against different forms of induced tone.小鼠肛门尾骨肌的一氧化氮能-硝基血管舒张对不同形式诱导张力的可变效力。
Br J Pharmacol. 1994 Dec;113(4):1494-500. doi: 10.1111/j.1476-5381.1994.tb17165.x.
9
Photon pharmacology of an iron-sulphur cluster nitrosyl compound acting on smooth muscle.一种作用于平滑肌的铁硫簇亚硝酰化合物的光药理学
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10
Evidence for the involvement of cGMP in neural bronchodilator responses in humal trachea.环磷酸鸟苷(cGMP)参与人体气管神经源性支气管扩张反应的证据。
J Physiol. 1995 Mar 1;483 ( Pt 2)(Pt 2):525-36. doi: 10.1113/jphysiol.1995.sp020603.

本文引用的文献

1
Responses of the isolated anococcygeus muscle of the mouse to drugs and to field stimulation.小鼠离体肛尾肌对药物和电场刺激的反应。
J Auton Pharmacol. 1981 Jun;1(3):225-33. doi: 10.1111/j.1474-8673.1981.tb00451.x.
2
The effects of vasoactive intestinal polypeptide and of adenosine 5'-triphosphate on the isolated anococcygeus muscle of the mouse.血管活性肠肽和5'-三磷酸腺苷对小鼠离体尾骨肌的作用。
Br J Pharmacol. 1982 Sep;77(1):97-103. doi: 10.1111/j.1476-5381.1982.tb09274.x.
3
Investigation of relaxations of the rabbit anococcygeus muscle by nerve stimulation and ATP using the ATP antagonist ANAPP3.使用ATP拮抗剂ANAPP3通过神经刺激和ATP对兔肛门尾骨肌松弛情况的研究。
Eur J Pharmacol. 1982 May 7;80(1):93-8. doi: 10.1016/0014-2999(82)90181-9.
4
Biphasic non-adrenergic, non-cholinergic relaxations of the mouse anococcygeus muscle.小鼠肛门尾骨肌的双相非肾上腺素能、非胆碱能舒张
Br J Pharmacol. 1983 Jun;79(2):611-5. doi: 10.1111/j.1476-5381.1983.tb11036.x.
5
Cyclic GMP mediates neurogenic relaxation in the bovine retractor penis muscle.环磷酸鸟苷介导牛阴茎退缩肌的神经源性舒张。
Br J Pharmacol. 1984 Apr;81(4):665-74. doi: 10.1111/j.1476-5381.1984.tb16133.x.
6
Block of some non-adrenergic inhibitory responses of smooth muscle by a substance from haemolysed erythrocytes.溶血红细胞中的一种物质对平滑肌某些非肾上腺素能抑制反应的阻断作用。
J Physiol. 1982 Jul;328:11-25. doi: 10.1113/jphysiol.1982.sp014250.
7
Evidence for vasoactive intestinal polypeptide as a neurotransmitter in smooth muscle of the urogenital tract.血管活性肠肽作为泌尿生殖道平滑肌神经递质的证据。
Brain Res. 1984 Jul 9;305(2):221-9. doi: 10.1016/0006-8993(84)90428-1.
8
A smooth muscle inhibitory material from the bovine retractor penis and rat anococcygeus muscles.一种来自牛阴茎退缩肌和大鼠肛门尾骨肌的平滑肌抑制物质。
J Physiol. 1980 Dec;309:55-64. doi: 10.1113/jphysiol.1980.sp013493.
9
The rat anococcygeus muscle and its response to nerve stimulation and to some drugs.大鼠肛门尾骨肌及其对神经刺激和某些药物的反应。
Br J Pharmacol. 1972 Jul;45(3):404-16. doi: 10.1111/j.1476-5381.1972.tb08097.x.
10
Synthesis and biochemical studies of various 8-substituted derivatives of guanosine 3',5'-cyclic phosphate, inosine 3',5'-cyclic phosphate, and xanthosine 3',5'-cyclic phosphate.鸟苷 3',5'-环磷酸酯、肌苷 3',5'-环磷酸酯和黄苷 3',5'-环磷酸酯的各种 8-取代衍生物的合成及生化研究。
Biochemistry. 1973 Dec 18;12(26):5310-9. doi: 10.1021/bi00750a014.

N-甲基羟胺抑制而M&B 22948增强小鼠肛门尾骨肌对非肾上腺素能、非胆碱能场刺激以及对硝基血管扩张剂药物的舒张反应。

N-methylhydroxylamine inhibits and M&B 22948 potentiates relaxations of the mouse anococcygeus to non-adrenergic, non-cholinergic field stimulation and to nitrovasodilator drugs.

作者信息

Gibson A, Mirzazadeh S

机构信息

Pharmacology Group, Biomedical Sciences Division, Kings College London.

出版信息

Br J Pharmacol. 1989 Mar;96(3):637-44. doi: 10.1111/j.1476-5381.1989.tb11863.x.

DOI:10.1111/j.1476-5381.1989.tb11863.x
PMID:2541847
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1854397/
Abstract
  1. The effects of N-methylhydroxylamine (NMH) and of M&B 22948 on relaxations of the mouse anococcygeus to non-adrenergic, non-cholinergic (NANC) field stimulation and to a number of smooth muscle relaxant drugs were investigated. 2. Relaxations to NANC field stimulation (10 Hz; 60 s train) were reversibly blocked by NMH (1-5 mM), which also caused weak, transient reductions of carbachol (50 microM)-induced tone. N,N-dimethylhydroxylamine (2 mM) and hydroxylamine (5 microM) reduced tone to the same extent as NMH, but neither produced any inhibition of NANC relaxations. 3. M&B 22948 10 microM, which by itself reduced tone by 12%, potentiated submaximal but not maximal relaxations to NANC field stimulation; overall the log frequency-response curve was displaced to the left by a factor of 2. 4. Sodium nitroprusside (0.01-1 microM), hydroxylamine (0.5-100 microM), and nitric oxide (2-200 microM) all relaxed carbachol-induced tone; relaxations to submaximal concentrations of these nitrovasodilators were reduced in the presence of 2 mM NMH, and potentiated in the presence of 10 microM M&B 22948. 5. Neither NMH (2 mM) nor M&B 22948 (10 microM) affected relaxations induced by submaximal concentrations of vasoactive intestinal peptide (VIP; 1 microM), papaverine (10 microM), 3-isobutyl-1-methyl-xanthine (10 microM), or 8-bromo-cyclic guanosine monophosphate (100 microM); relaxations to adenosine 5'-triphosphate (ATP, 2 mM) were unaffected by M&B 22948, but were potentiated by NMH. 6. The selective inhibition by NMH, and potentiation by M&B 22948, of NANC and nitrovasodilator-induced relaxations of the mouse anococcygeus suggests that the NANC transmitter is neither VIP nor ATP, but resembles the nitrovasodilator drugs in its mode of action. The NANC transmission system is therefore similar to that recently described in the bovine retractor penis.
摘要
  1. 研究了N-甲基羟胺(NMH)和M&B 22948对小鼠肛门尾骨肌对非肾上腺素能、非胆碱能(NANC)场刺激以及多种平滑肌松弛药物的松弛作用。2. NMH(1 - 5 mM)可可逆性阻断对NANC场刺激(10 Hz;60秒串刺激)的松弛反应,同时也会引起卡巴胆碱(50 microM)诱导的张力出现微弱、短暂的降低。N,N - 二甲基羟胺(2 mM)和羟胺(5 microM)降低张力的程度与NMH相同,但两者均未对NANC松弛产生任何抑制作用。3. 10 microM的M&B 22948本身可使张力降低12%,增强对NANC场刺激的亚最大但非最大松弛反应;总体而言,对数频率 - 反应曲线向左移动了2倍。4. 硝普钠(0.01 - 1 microM)、羟胺(0.5 - 100 microM)和一氧化氮(2 - 200 microM)均可使卡巴胆碱诱导的张力松弛;在存在2 mM NMH的情况下,对这些硝基血管扩张剂亚最大浓度的松弛反应减弱,而在存在10 microM M&B 22948的情况下则增强。5. 2 mM的NMH和10 microM的M&B 22948均未影响由亚最大浓度的血管活性肠肽(VIP;1 microM)、罂粟碱(10 microM)、3 - 异丁基 - 1 - 甲基黄嘌呤(10 microM)或8 - 溴环鸟苷单磷酸(100 microM)诱导的松弛反应;对三磷酸腺苷(ATP,2 mM)的松弛反应不受M&B 22948影响,但被NMH增强。6. NMH的选择性抑制以及M&B 22948对小鼠肛门尾骨肌NANC和硝基血管扩张剂诱导的松弛反应的增强作用表明,NANC递质既不是VIP也不是ATP,但其作用方式类似于硝基血管扩张剂药物。因此,NANC传递系统与最近在牛阴茎退缩肌中描述的系统相似。