{"title":"6-氮脲对周围神经系统的影响[j]。对神经肌肉传递和横纹肌的作用","authors":"V. Bauer, R. Cˇapek","doi":"10.1016/0028-3908(69)90048-3","DOIUrl":null,"url":null,"abstract":"<div><p>The effects of 6-azauridine, a cancerostatic agent, on striated muscle and on neuromuscular transmission, were studied in the isolated phrenic nerve hemidiaphragm preparation of the rat. In the directly stimulated and curarized preparation, 6-azauridine in a concentration of 2 × 10<sup>−6</sup> to 2 × 10<sup>−4</sup> g/ml caused a late increase in contractions. Higher concentrations (2 × 10<sup>−3</sup> to 2 × 10<sup>−2</sup>) resulted in an initial increase in muscle contractions followed by inhibition of the contractions which developed gradually. The concentration of 6 × 10<sup>−2</sup> led to a decrease in muscle contractions only. In the indirectly stimulated preparation, low concentrations of the drug (2 × 10<sup>−6</sup> to 8 × 10<sup>−5</sup>) led to a slight increase in muscle contractions. The concentration from 8 × 10<sup>−4</sup> up to 6 × 10<sup>−2</sup> caused an inhibition or blockade of muscle contractions. It was possible to overcome this inhibition temporarily with physostigmine (1 × 10<sup>−5</sup>) or tetanic stimulation. The effects of 6-azauridine on the contractile mechanism of striated muscle correspond to the action on smooth muscle described previously, both being biphasic, depending on the dose. The action of 6-azauridine on neuromuscular transmission was inhibitory in the concentrations having an opposite effect on directly stimulated muscle. It is concluded that this curare-like action of 6-azauridine is non-depolarizing.</p></div>","PeriodicalId":14111,"journal":{"name":"International journal of neuropharmacology","volume":"8 3","pages":"Pages 271-272, IN7-IN8, 273-277"},"PeriodicalIF":0.0000,"publicationDate":"1969-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0028-3908(69)90048-3","citationCount":"0","resultStr":"{\"title\":\"The effects of 6-azauridine on the peripheral nervous system—II. The action on neuromuscular transmission and on striated muscle\",\"authors\":\"V. Bauer, R. Cˇapek\",\"doi\":\"10.1016/0028-3908(69)90048-3\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The effects of 6-azauridine, a cancerostatic agent, on striated muscle and on neuromuscular transmission, were studied in the isolated phrenic nerve hemidiaphragm preparation of the rat. In the directly stimulated and curarized preparation, 6-azauridine in a concentration of 2 × 10<sup>−6</sup> to 2 × 10<sup>−4</sup> g/ml caused a late increase in contractions. Higher concentrations (2 × 10<sup>−3</sup> to 2 × 10<sup>−2</sup>) resulted in an initial increase in muscle contractions followed by inhibition of the contractions which developed gradually. The concentration of 6 × 10<sup>−2</sup> led to a decrease in muscle contractions only. In the indirectly stimulated preparation, low concentrations of the drug (2 × 10<sup>−6</sup> to 8 × 10<sup>−5</sup>) led to a slight increase in muscle contractions. The concentration from 8 × 10<sup>−4</sup> up to 6 × 10<sup>−2</sup> caused an inhibition or blockade of muscle contractions. It was possible to overcome this inhibition temporarily with physostigmine (1 × 10<sup>−5</sup>) or tetanic stimulation. The effects of 6-azauridine on the contractile mechanism of striated muscle correspond to the action on smooth muscle described previously, both being biphasic, depending on the dose. The action of 6-azauridine on neuromuscular transmission was inhibitory in the concentrations having an opposite effect on directly stimulated muscle. It is concluded that this curare-like action of 6-azauridine is non-depolarizing.</p></div>\",\"PeriodicalId\":14111,\"journal\":{\"name\":\"International journal of neuropharmacology\",\"volume\":\"8 3\",\"pages\":\"Pages 271-272, IN7-IN8, 273-277\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1969-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/0028-3908(69)90048-3\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International journal of neuropharmacology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/0028390869900483\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International journal of neuropharmacology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0028390869900483","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
The effects of 6-azauridine on the peripheral nervous system—II. The action on neuromuscular transmission and on striated muscle
The effects of 6-azauridine, a cancerostatic agent, on striated muscle and on neuromuscular transmission, were studied in the isolated phrenic nerve hemidiaphragm preparation of the rat. In the directly stimulated and curarized preparation, 6-azauridine in a concentration of 2 × 10−6 to 2 × 10−4 g/ml caused a late increase in contractions. Higher concentrations (2 × 10−3 to 2 × 10−2) resulted in an initial increase in muscle contractions followed by inhibition of the contractions which developed gradually. The concentration of 6 × 10−2 led to a decrease in muscle contractions only. In the indirectly stimulated preparation, low concentrations of the drug (2 × 10−6 to 8 × 10−5) led to a slight increase in muscle contractions. The concentration from 8 × 10−4 up to 6 × 10−2 caused an inhibition or blockade of muscle contractions. It was possible to overcome this inhibition temporarily with physostigmine (1 × 10−5) or tetanic stimulation. The effects of 6-azauridine on the contractile mechanism of striated muscle correspond to the action on smooth muscle described previously, both being biphasic, depending on the dose. The action of 6-azauridine on neuromuscular transmission was inhibitory in the concentrations having an opposite effect on directly stimulated muscle. It is concluded that this curare-like action of 6-azauridine is non-depolarizing.