首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Novel Segmented Concentration Addition Method to Predict Mixture Hormesis of Chlortetracycline Hydrochloride and Oxytetracycline Hydrochloride to Aliivibrio fischeri
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Novel Segmented Concentration Addition Method to Predict Mixture Hormesis of Chlortetracycline Hydrochloride and Oxytetracycline Hydrochloride to Aliivibrio fischeri

机译:预测盐酸金霉素和盐酸土霉素对费氏疟原虫混合兴奋度的分段分段加香新方法

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摘要

Hormesis is a concentration-response phenomenon characterized by low-concentration stimulation and high-concentration inhibition, which typically has a nonmonotonic J-shaped concentration-response curve (J-CRC). The concentration addition (CA) model is the gold standard for studying mixture toxicity. However, the CA model had the predictive blind zone (PBZ) for mixture J-CRC. To solve the PBZ problem, we proposed a segmented concentration addition (SCA) method to predict mixture J-CRC, which was achieved through fitting the left and right segments of component J-CRC and performing CA prediction subsequently. We selected two model compounds including chlortetracycline hydrochloride (CTCC) and oxytetracycline hydrochloride (OTCC), both of which presented J-CRC to (AVF). The seven binary mixtures (M1–M7) of CTCC and OTCC were designed according to their molar ratios of 12:1, 10:3, 8:5, 1:1, 5:8, 3:10, and 1:12 referring to the direct equipartition ray design. These seven mixtures all presented J-CRC to AVF. Based on the SCA method, we obtained mixture maximum stimulatory effect concentration (EC ) and maximum stimulatory effect ( ) predicted by SCA, both of which were not available for the CA model. The toxicity interactions of these mixtures were systematically evaluated by using a comprehensive approach, including the co-toxicity coefficient integrated with confidence interval method (CTCICI), CRC, and isobole analysis. The results showed that the interaction types were additive and antagonistic action, without synergistic action. In addition, we proposed the cross point (CP) hypothesis for toxic interactive mixtures presenting J-CRC, that there was generally a CP between mixture observed J-CRC and CA predicted J-CRC; the relative positions of observed and predicted CRCs on either side of the CP would exchange, but the toxic interaction type of mixtures remained unchanged. The CP hypothesis needs to be verified by more mixtures, especially those with synergism. In conclusion, the SCA method is expected to have important theoretical and practical significance for mixture hormesis.
机译:兴奋是一种以低浓度刺激和高浓度抑制为特征的浓度响应现象,通常具有非单调的J形浓度响应曲线(J-CRC)。浓度增加(CA)模型是研究混合物毒性的金标准。但是,CA模型具有混合J-CRC的预测盲区(PBZ)。为了解决PBZ问题,我们提出了一种分段浓度相加(SCA)方法来预测混合物J-CRC,该方法是通过拟合分量J-CRC的左右段并随后进行CA预测来实现的。我们选择了两种模型化合物,包括盐酸金霉素(CTCC)和盐酸土霉素(OTCC),它们均将J-CRC呈现给(AVF)。根据它们的摩尔比为12:1、10:3、8:5、1:1、5:8、3:10和1:12设计了CTCC和OTCC的7种二元混合物(M1-M7)直接等分射线设计。这七种混合物均向AVF提供了J-CRC。基于SCA方法,我们获得了由SCA预测的最大刺激作用浓度(EC)和最大刺激作用()的混合物,这两种方法均不适用于CA模型。通过使用综合方法,包括与置信区间法(CTCICI),CRC和等密度分析相结合的共毒性系数,系统地评估了这些混合物的毒性相互作用。结果表明,相互作用类型为加和拮抗作用,无协同作用。此外,我们提出了呈现J-CRC的有毒相互作用混合物的交叉点(CP)假设,即观察到的J-CRC与CA预测的J-CRC之间通常存在CP。 CP两侧观察和预测的CRC的相对位置会交换,但是混合物的毒性相互作用类型保持不变。 CP假设需要更多的混合物来验证,尤其是具有协同作用的混合物。综上所述,SCA方法有望对混合荷尔蒙产生重要的理论和实践意义。

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