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NG-单甲基-L-精氨酸(L-NMMA)和NG-硝基-L-精氨酸(L-NOARG)对人回肠环形肌非肾上腺素能非胆碱能舒张的影响。

Effect of NG-monomethyl L-arginine (L-NMMA) and NG-nitro L-arginine (L-NOARG) on non-adrenergic non-cholinergic relaxation in the circular muscle of the human ileum.

作者信息

Maggi C A, Barbanti G, Turini D, Giuliani S

机构信息

Pharmacology Department, A Menarini Pharmaceuticals, Italy.

出版信息

Br J Pharmacol. 1991 Aug;103(4):1970-2. doi: 10.1111/j.1476-5381.1991.tb12361.x.

DOI:10.1111/j.1476-5381.1991.tb12361.x
PMID:1912984
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1908194/
Abstract
  1. We have investigated the effect of the NO synthesis inhibitors, NG-monomethyl L-arginine (L-NMMA) and NG-nitro L-arginine (L-NOARG) on the non-adrenergic non-cholinergic (NANC) relaxation produced by electrical field stimulation in the circular muscle of the human ileum. 2. In the presence of atropine and guanethidine (1 and 3 microM, respectively), electrical field stimulation produced tetrodotoxin-sensitive relaxation of the strips. L-NMMA, starting from 100 microM, produced a concentration-dependent inhibition of the evoked relaxations (2Hz); maximal inhibition at 1 mM averaged about 35%. 3. The inhibitory effect of L-NMMA was unchanged by previous incubation with D-arginine while it was prevented by L-arginine (L-Arg). L-NMMA did not affect isoprenaline-induced relaxation. 4. L-NOARG (1-30 microM) concentration-dependently inhibited the evoked relaxations at 2 Hz, up to a maximum of 65% inhibition, although in some strips complete inhibition of the response was observed. The effect of L-NOARG was reversed by L-Arg. L-NOARG did not affect isoprenaline-induced relaxation. 5. These results suggest that NO may be involved in inhibitory NANC transmission in the circular muscle of the human ileum.
摘要
  1. 我们研究了一氧化氮(NO)合成抑制剂N-甲基-L-精氨酸(L-NMMA)和N-硝基-L-精氨酸(L-NOARG)对人回肠环形肌电场刺激所产生的非肾上腺素能非胆碱能(NANC)舒张作用的影响。2. 在阿托品和胍乙啶(分别为1和3微摩尔)存在的情况下,电场刺激使肠肌条产生对河豚毒素敏感的舒张。从100微摩尔开始,L-NMMA对诱发的舒张(2赫兹)产生浓度依赖性抑制;在1毫摩尔时最大抑制平均约为35%。3. 预先用D-精氨酸孵育后,L-NMMA的抑制作用不变,而L-精氨酸(L-Arg)可防止这种抑制。L-NMMA不影响异丙肾上腺素诱导的舒张。4. L-NOARG(1 - 30微摩尔)对2赫兹时诱发的舒张产生浓度依赖性抑制,最大抑制可达65%,尽管在一些肠肌条中观察到反应被完全抑制。L-Arg可逆转L-NOARG的作用。L-NOARG不影响异丙肾上腺素诱导的舒张。5. 这些结果表明,NO可能参与人回肠环形肌的抑制性NANC传递。

相似文献

1
Effect of NG-monomethyl L-arginine (L-NMMA) and NG-nitro L-arginine (L-NOARG) on non-adrenergic non-cholinergic relaxation in the circular muscle of the human ileum.NG-单甲基-L-精氨酸(L-NMMA)和NG-硝基-L-精氨酸(L-NOARG)对人回肠环形肌非肾上腺素能非胆碱能舒张的影响。
Br J Pharmacol. 1991 Aug;103(4):1970-2. doi: 10.1111/j.1476-5381.1991.tb12361.x.
2
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.
3
Actions and interactions of NG-substituted analogues of L-arginine on NANC neurotransmission in the bovine retractor penis and rat anococcygeus muscles.L-精氨酸的N-取代类似物对牛阴茎退缩肌和大鼠肛尾肌非肾上腺素能非胆碱能神经传递的作用及相互作用。
Br J Pharmacol. 1993 Jan;108(1):242-7. doi: 10.1111/j.1476-5381.1993.tb13469.x.
4
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。
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5
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6
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。
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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
L-NG-nitro arginine (L-NOARG), a novel, L-arginine-reversible inhibitor of endothelium-dependent vasodilatation in vitro.L-NG-硝基精氨酸(L-NOARG),一种新型的、体外可逆转内皮依赖性血管舒张的L-精氨酸抑制剂。
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Selective inhibition of basal but not agonist-stimulated activity of nitric oxide in rat aorta by NG-monomethyl-L-arginine.NG-单甲基-L-精氨酸对大鼠主动脉一氧化氮基础活性而非激动剂刺激活性的选择性抑制。
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Nitric oxide release accounts for the biological activity of endothelium-derived relaxing factor.一氧化氮的释放构成了内皮源性舒张因子的生物活性。
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L-arginine is the physiological precursor for the formation of nitric oxide in endothelium-dependent relaxation.L-精氨酸是内皮依赖性舒张中一氧化氮形成的生理前体。
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Apamin distinguishes two types of relaxation mediated by enteric nerves in the guinea-pig gastrointestinal tract.蜂毒明肽区分了豚鼠胃肠道中由肠神经介导的两种松弛类型。
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L-NG-nitro arginine (L-NOARG), a novel, L-arginine-reversible inhibitor of endothelium-dependent vasodilatation in vitro.L-NG-硝基精氨酸(L-NOARG),一种新型的、体外可逆转内皮依赖性血管舒张的L-精氨酸抑制剂。
Br J Pharmacol. 1990 Feb;99(2):408-12. doi: 10.1111/j.1476-5381.1990.tb14717.x.
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Essential role of nitric oxide in descending inhibition in the rat proximal colon.
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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.