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异恶唑鎓阳离子对某些离体肌肉制剂的作用。

Effects of isoxazolium cations on some isolated muscle preparations.

作者信息

Mittag T W, Tormay A

出版信息

Br J Pharmacol. 1971 Nov;43(3):604-11. doi: 10.1111/j.1476-5381.1971.tb07190.x.

DOI:10.1111/j.1476-5381.1971.tb07190.x
PMID:4400529
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1665790/
Abstract
  1. The quaternary ammonium compound, N,t-butyl-5-methyl isoxazolium perchlorate (BIP), an anionic group reagent, initially causes contractions of the rat phrenic-nerve diaphragm, guinea-pig ileum and rabbit aortic strip preparations in vitro.2. In addition, the drug produces an irreversible block of indirectly elicited twitch responses in the diaphragm and of contractions induced by acetylcholine, methylfurmethide, dimethyl-phenylpiperazinium, 5-hydroxytryptamine (5-HT), histamine, angiotensin and pilocarpine in the ileum, while direct electrical stimulation of the diaphragm and contractions of the ileum to Ba and K ions are relatively unaffected.3. BIP is also an irreversible inhibitor of acetylcholinesterase but not of butyrylcholinesterase.4. On rabbit aortic strip preparations, responses to histamine, noradrenaline and 5-HT were differentially sensitive to irreversible blockade by BIP.5. Diphenhydramine, used in conditions which gave complete protection of the histamine response to irreversible block by dibenamine, did not protect against the blocking action of BIP but increased the blockade.6. These results suggest that BIP reacts covalently with anionic groups which mediate receptor initiated stimuli. The isoxazolium group may be useful in conferring irreversible properties by its substitution in drug molecules for the pyrrole or pyrrolidine group.
摘要
  1. 季铵化合物N,叔丁基-5-甲基异恶唑高氯酸盐(BIP)是一种阴离子基团试剂,最初可引起大鼠膈神经膈肌、豚鼠回肠和兔主动脉条离体标本的收缩。

  2. 此外,该药物可使膈肌中间接引发的抽搐反应以及回肠中由乙酰胆碱、甲基呋甲酯、二甲基苯基哌嗪鎓、5-羟色胺(5-HT)、组胺、血管紧张素和毛果芸香碱诱导的收缩产生不可逆阻滞,而对膈肌的直接电刺激以及回肠对钡离子和钾离子的收缩反应相对无影响。

  3. BIP还是乙酰胆碱酯酶的不可逆抑制剂,但不是丁酰胆碱酯酶的抑制剂。

  4. 在兔主动脉条标本上,对组胺、去甲肾上腺素和5-HT的反应对BIP的不可逆阻滞具有不同的敏感性。

  5. 在能完全保护组胺反应免受二苯那明不可逆阻滞的条件下使用的苯海拉明,不能防止BIP的阻滞作用,反而增强了这种阻滞。

  6. 这些结果表明,BIP与介导受体引发刺激的阴离子基团发生共价反应。异恶唑基团通过在药物分子中取代吡咯或吡咯烷基团,可能有助于赋予不可逆特性。

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1
Effects of isoxazolium cations on some isolated muscle preparations.异恶唑鎓阳离子对某些离体肌肉制剂的作用。
Br J Pharmacol. 1971 Nov;43(3):604-11. doi: 10.1111/j.1476-5381.1971.tb07190.x.
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Inhibitory effect of bassianolide, a cyclodepsipeptide, on drug-induced contractions of isolated smooth muscle preparations.环缩肽白僵菌素对药物诱导的离体平滑肌制剂收缩的抑制作用。
Jpn J Pharmacol. 1982 Feb;32(1):55-64. doi: 10.1254/jjp.32.55.
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Auton Autacoid Pharmacol. 2008 Jan;28(1):11-7. doi: 10.1111/j.1474-8673.2007.00415.x.
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Pharmacological evaluation of the histamine H1 and 5-HT blocking properties of 2-N-(carboxamidinonormianserin) (FCC5): in-vitro studies.2-N-(脒基去甲赛庚啶)(FCC5)组胺H1和5-羟色胺阻断特性的药理学评价:体外研究
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Acta Physiol Scand. 1977 Feb;99(2):190-207. doi: 10.1111/j.1748-1716.1977.tb10370.x.
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SOME PHARMACOLOGICAL PROPERTIES OF THE CIRCULAR AND LONGITUDINAL MUSCLE STRIPS FROM THE GUINEA-PIG ISOLATED ILEUM.豚鼠离体回肠环行肌条和纵行肌条的一些药理学特性
Br J Pharmacol Chemother. 1963 Dec;21(3):544-54. doi: 10.1111/j.1476-5381.1963.tb02022.x.
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Diisopropylammonium dichloroacetate (DIPA): reversible antagonism towards smooth muscle stimulants and inhibition of acetylcholinesterase in the isolated guinea pig ileum.二氯醋酸二异丙胺(DIPA):对离体豚鼠回肠中平滑肌兴奋剂具有可逆性拮抗作用,并抑制乙酰胆碱酯酶。
Res Commun Chem Pathol Pharmacol. 1971 Jul-Sep;2(4):439-46.

本文引用的文献

1
Spiral-cut strip of rabbit aorta for in vitro studies of responses of arterial smooth muscle.用于动脉平滑肌反应体外研究的兔主动脉螺旋切割条带。
Methods Med Res. 1960;8:177-86.
2
Studies on the noradrenaline alpha-receptor. II. Analysis of the "spare-receptor" hypothesis and estimation of the concentration of alpha-receptors in rabbit aorta.去甲肾上腺素α受体的研究。II. “备用受体”假说分析及兔主动脉中α受体浓度的估计。
Mol Pharmacol. 1967 Jan;3(1):28-36.
3
Studies on the noradrenaline alpha-receptor. I. Techniques of receptor isolation. The distribution and specificity of action of N-(2-bromoethyl)-N-ethyl-1-naphthylmethylamine, a competitive antagonist of noradrenaline.去甲肾上腺素α受体的研究。I. 受体分离技术。N-(2-溴乙基)-N-乙基-1-萘甲胺(一种去甲肾上腺素竞争性拮抗剂)的作用分布及特异性。
Mol Pharmacol. 1967 Jan;3(1):15-27.
4
An alkylating derivative of benzilylcholine with specific and long-lasting parasympatholytic activity.一种具有特异性和长效副交感神经阻滞活性的苄基胆碱烷基化衍生物。
Mol Pharmacol. 1966 Jul;2(4):284-97.
5
The nature of an "anionic" site in butyrylcholinesterase compared with that of a similar site in acetylcholinesterase.
Biochim Biophys Acta. 1966 Nov 15;128(2):351-62. doi: 10.1016/0926-6593(66)90182-2.
6
A novel irreversible inhibitor of acetylcholinesterase specifically directed at the anionic binding site: structure-activity relationships.一种专门针对阴离子结合位点的新型不可逆乙酰胆碱酯酶抑制剂:构效关系
Mol Pharmacol. 1966 Sep;2(5):411-22.
7
Acetylcholine receptor: covalent attachment of depolarizing groups at the active site.乙酰胆碱受体:去极化基团在活性位点的共价连接。
Science. 1969 Jun 20;164(3886):1420-1. doi: 10.1126/science.164.3886.1420.
8
Radiometric assay of cholinesterases in intact tissues in the nanomolar concentration range of acetylcholine.在乙酰胆碱纳摩尔浓度范围内对完整组织中的胆碱酯酶进行放射性测定。
Biochem Pharmacol. 1970 Jun;19(6):2165-9. doi: 10.1016/0006-2952(70)90316-3.
9
Affinity labeling of the acetylcholine-receptor.乙酰胆碱受体的亲和标记
Proc Natl Acad Sci U S A. 1967 Nov;58(5):2063-70. doi: 10.1073/pnas.58.5.2063.
10
The origin of acetylcholine released from guinea-pig intestine and longitudinal muscle strips.豚鼠肠道和纵肌条释放的乙酰胆碱的来源。
J Physiol. 1968 Jan;194(1):13-33. doi: 10.1113/jphysiol.1968.sp008392.