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1
The local anaesthetic activity of a benzotriazinium salt.一种苯并三嗪鎓盐的局部麻醉活性。
Br J Pharmacol. 1978 Jul;63(3):475-9. doi: 10.1111/j.1476-5381.1978.tb07800.x.
2
Comparison of the effects of caffeine and a 2-alkyl-1,2,3-benzotriazinium iodide on frog rectus abdominis.咖啡因与一种2-烷基-1,2,3-苯并三嗪碘化物对青蛙腹直肌作用的比较。
Br J Pharmacol. 1977 Jul;60(3):375-8. doi: 10.1111/j.1476-5381.1977.tb07511.x.
3
Comparison of the effects of a benzotriazinium iodide and quinidine on guinea-pig heart.苯并三嗪碘化物和奎尼丁对豚鼠心脏作用的比较。
Br J Pharmacol. 1979 May;66(1):19-24. doi: 10.1111/j.1476-5381.1979.tb16092.x.
4
The effect of a benzotriazinium salt on in vitro and in vivo arrhythmias in guinea-pigs and mice.一种苯并三嗪盐对豚鼠和小鼠体外及体内心律失常的影响。
Arch Int Pharmacodyn Ther. 1980 Nov;248(1):154-65.
5
Screening of some basic amides for local anaesthetic and neuromuscular blocking activity.筛选某些碱性酰胺的局部麻醉和神经肌肉阻滞活性。
Indian J Physiol Pharmacol. 1973 Jan-Mar;17(1):55-62.
6
Effects of the sulphydryl inhibitor N-ethyl-maleimide on the phrenic nerve and diaphragm muscle of the rat.巯基抑制剂N-乙基马来酰亚胺对大鼠膈神经和膈肌的作用。
Neuropharmacology. 1989 Aug;28(8):765-73. doi: 10.1016/0028-3908(89)90165-2.
7
Physical and pharmacological properties of an irreversible local anesthetic.一种不可逆局部麻醉剂的物理和药理学特性。
J Med Chem. 1971 Jun;14(6):514-6. doi: 10.1021/jm00288a013.
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Differing potencies of muscle relaxants on rat and guinea-pig phrenic nerve diaphragm preparations.肌肉松弛剂对大鼠和豚鼠膈神经膈肌标本的不同效能。
J Pharm Pharmacol. 1986 Aug;38(8):623-4. doi: 10.1111/j.2042-7158.1986.tb03095.x.
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Arzneimittelforschung. 1975 Jan;25(1):52-5.
10
The action and interaction of diphenhydramine (Benadryl) hydrochloride at the neuromuscular junction.盐酸苯海拉明(苯那君)在神经肌肉接头处的作用与相互作用。
Eur J Pharmacol. 1973 May;22(2):169-74. doi: 10.1016/0014-2999(73)90008-3.

本文引用的文献

1
[Neutralization of the contractile effect of depolarized catelectronics by repolarization in anelectrotonus; the anode as antagonist of acetylcholine, choline, nicotine, coniine, veratrine, potassium and rubidium salts].[在电紧张状态下复极化对去极化阳离子收缩效应的中和作用;阳极作为乙酰胆碱、胆碱、尼古丁、毒芹碱、藜芦碱、钾盐和铷盐的拮抗剂]
Pflugers Arch Gesamte Physiol Menschen Tiere. 1951;253(3):264-82. doi: 10.1007/BF00363393.
2
A new method for measuring membrane potentials with external electrodes.一种使用外部电极测量膜电位的新方法。
Experientia. 1954 Dec 15;10(12):508-9. doi: 10.1007/BF02166189.
3
The action of quinine and quinidine on the contractions of striated muscle.奎宁和奎尼丁对横纹肌收缩的作用。
J Physiol. 1955 Aug 29;129(2):412-23. doi: 10.1113/jphysiol.1955.sp005364.
4
Structure-activity relationships in some series of 2-alkyl-1,2,3,-benzotriazinium compounds.某些系列的2-烷基-1,2,3-苯并三嗪鎓化合物的构效关系
Br J Pharmacol. 1973 Apr;47(4):819-26. doi: 10.1111/j.1476-5381.1973.tb08209.x.
5
Procaine, pentobarbital and halothane: effects on the mammalian myoneural junction.普鲁卡因、戊巴比妥和氟烷:对哺乳动物肌神经接头的影响。
J Pharmacol Exp Ther. 1971 May;177(2):360-8.
6
Alteration by xylocaine (lidocaine) and its derivatives of the time course of the end plate potential.利多卡因及其衍生物对终板电位时间进程的影响。
J Gen Physiol. 1968 Jul;52(1):144-61. doi: 10.1085/jgp.52.1.144.
7
A benzotriazinium salt as a potential antiarrhythmic agent [proceedings].一种作为潜在抗心律失常药物的苯并三嗪鎓盐[会议论文集]
Br J Pharmacol. 1977 Sep;61(1):131P-132P.
8
Comparison of the effects of caffeine and a 2-alkyl-1,2,3-benzotriazinium iodide on frog rectus abdominis.咖啡因与一种2-烷基-1,2,3-苯并三嗪碘化物对青蛙腹直肌作用的比较。
Br J Pharmacol. 1977 Jul;60(3):375-8. doi: 10.1111/j.1476-5381.1977.tb07511.x.

一种苯并三嗪鎓盐的局部麻醉活性。

The local anaesthetic activity of a benzotriazinium salt.

作者信息

French A M, Khan M T, Scott N C

出版信息

Br J Pharmacol. 1978 Jul;63(3):475-9. doi: 10.1111/j.1476-5381.1978.tb07800.x.

DOI:10.1111/j.1476-5381.1978.tb07800.x
PMID:307423
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1668102/
Abstract

1 The local anaesthetic properties of 2-n-propyl-4-p-tolylamino-1,2,3-benzotriazinium iodide (TnPBI) were compared with those of lignocaine hydrochloride on intact and desheathed sciatic nerves of the frog, on the phrenic nerve-hemidiaphragm preparation of the rat, and by the intradermal wheal test in the guinea-pig. 2 Both TnPBI and lignocaine were more potent on desheathed than on intact sciatic nerves. The potency of TnPBI was affected more than that of lignocaine by the presence of the sheath in intact nerves. 3 Both drugs inhibited conduction in the rat phrenic nerve, as shown by the reduction in twitch tension of the diaphragm elicited by nerve stimulation. TnPBI also caused an initial augmentation of the twitch tension of the diaphragm when applied directly to the muscle. 4 TnPBI was shown to be approximately twice as potent as lignocaine by the guinea-pig intradermal wheal test. 5 These results are discussed in view of the known effects of TnPBI on intracellular calcium storage.

摘要
  1. 将2-正丙基-4-对甲苯氨基-1,2,3-苯并三嗪碘化物(TnPBI)的局部麻醉特性与盐酸利多卡因在青蛙完整和去鞘坐骨神经、大鼠膈神经-半膈肌标本上以及通过豚鼠皮内风团试验进行了比较。2. TnPBI和利多卡因对去鞘坐骨神经的作用均比对完整坐骨神经更强。完整神经中鞘的存在对TnPBI效力的影响比对利多卡因的影响更大。3. 两种药物均抑制大鼠膈神经传导,如神经刺激引起的膈肌抽搐张力降低所示。直接应用于肌肉时,TnPBI还会使膈肌抽搐张力最初增强。4. 通过豚鼠皮内风团试验表明,TnPBI的效力约为利多卡因的两倍。5. 鉴于TnPBI对细胞内钙储存的已知作用,对这些结果进行了讨论。