首页> 外文期刊>Japanese Journal of Pharmacology >Different Modes of Potentiation by β-Eudesmol, a Main Compound from Atractylodes Lancea, Depending on Neuromuscular Blocking Actions of p-Phenylene-Polymethylene Bis-Ammonium Derivatives in Isolated Phrenic Nerve-Diaphragm Muscles of Normal and Alloxan-Diabetic Mice
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Different Modes of Potentiation by β-Eudesmol, a Main Compound from Atractylodes Lancea, Depending on Neuromuscular Blocking Actions of p-Phenylene-Polymethylene Bis-Ammonium Derivatives in Isolated Phrenic Nerve-Diaphragm Muscles of Normal and Alloxan-Diabetic Mice

机译:β-Eudesmol,一种来自白术的主要化合物,根据正常和四氧嘧啶-糖尿病小鼠孤立的ren神经-N肌中对苯撑-聚乙烯亚甲基双铵衍生物的神经肌肉阻滞作用,而具有不同的增效模式。

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References(10) Cited-By(1) The essential moieties in p-phenylene-polymethylene bis-ammonium (PMBA) derivatives, C6H4[X(CH2)nN+R3]2, on the potentiating effects by β-eudesmol, a main component of Atractylodes lancea, of their neuromuscular blockades were investigated in isolated phrenic nerve-diaphragm muscle preparations of normal and alloxan-diabetic mice. PMBA derivatives were separated into the following three groups based on the patterns of the potentiating effects: group I: PMBA-23 (n = 6, R = Me) and PMBA-24 (n = 6, R = Et); group II: PMBA-1 (n = 4, R = Me), PMBA-21 (n = 4, R = Et) and PMBA-2 (X = O, n = 3, R = Me); and group III: PMBA-31 (X = S, n = 3, R = Me), PMBA-3 (X = CO, n = 3, R = Me) and PMBA-4 (X = CHOH, n = 3, R = Me). The pretreatment with 80 μM β-eudesmol for 60 min did not affect group I-induced neuromuscular blocking action, and it potentiated group II and group III-induced ones. The potentiating effect of β-eudesmol on group III was greater in diabetic muscles than in normal ones and that on group II was to the same extent in both muscles. These results suggest that the four-methylene length of the side chains in normal muscles and the hydrophilic moieties adjacent to a phenylene ring in diabetic muscles are related to the potentiating effect by β-eudesmol on PMBA derivatives.
机译:参考文献(10)引用了(1)对-亚苯基-多亚甲基双铵(PMBA)衍生物C6H4 [X(CH2)nN + R3] 2的主要部分,对β-大麦芽酚的增效作用,在正常和四氧嘧啶糖尿病小鼠的分离的神经-肌制剂中,研究了白术的部分成分,其神经肌肉阻滞作用。根据增强作用的模式,将PMBA衍生物分为以下三组:第一组:PMBA-23(n = 6,R = Me)和PMBA-24(n = 6,R = Et);第二组:PMBA-1(n = 4,R = Me),PMBA-21(n = 4,R = Et)和PMBA-2(X = O,n = 3,R = Me);第三组:PMBA-31(X = S,n = 3,R = Me),PMBA-3(X = CO,n = 3,R = Me)和PMBA-4(X = CHOH,n = 3, R =我)。用80μMβ-艾地莫尔进行60分钟的预处理不影响I组诱导的神经肌肉阻滞作用,并且增强了II组和III组诱导的神经肌肉阻滞作用。 β-eudesmol对糖尿病组的增强作用要强于正常人,而对II组的增强作用在两个肌肉中都相同。这些结果表明,正常肌肉中的侧链的四亚甲基长度和糖尿病肌肉中与亚苯基环相邻的亲水部分与β-eudesmol对PMBA衍生物的增强作用有关。

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