茄科糖生物碱:α-茄碱和α-查康碱可改变维拉帕米的心脏抑制活性。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Szymon Chowański, Magdalena Winkiel, Monika Szymczak-Cendlak, Paweł Marciniak, Dominika Mańczak, Karolina Walkowiak-Nowicka, Marta Spochacz, Sabino A Bufo, Laura Scrano, Zbigniew Adamski
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引用次数: 2

摘要

背景:茄科糖生物碱(SGAs)具有心脏调节活性。目的:研究维拉帕米与糖生物碱的潜在相互作用。材料与方法:采用微密度法测定维拉帕米和糖生物碱(α-龙葵碱和α-查康碱)在成虫心肌中的心脏活性。用维拉帕米和糖生物碱的纯物质和混合物治疗心肌9分钟,以生理盐水为对照。使用了两种实验变体:同时应用维拉帕米和糖生物碱或用其中一种化合物预孵育心肌,然后用维拉帕米溶液灌注。维拉帕米和糖生物碱的浓度分别为9 × 10-6-5 × 10-5 M和10-9-10-5 M。结果:维拉帕米、α-龙葵碱和α-查康碱的IC50值分别为1.69 × 10-5、1.88 × 10-7和7.48 × 10-7 M。当糖生物碱与维拉帕米同时应用时,观察到拮抗作用,最大抑制作用降低,t50和维拉帕米的恢复时间特征延长。我们还证实了编码l型钙通道α1亚基的基因在心肌和脑中的两种转录形式的表达,两种形式在心肌中的转录水平相等,并且在所测试的昆虫物种中,较短的形式在脑中显著占优势。讨论与结论:结果表明,在各种药物治疗期间,注意日常饮食的组成尤为重要。在后续的研究中,应该在分子水平上检查维拉帕米与SGAs相互作用的性质,以及这种相互作用是否会降低维拉帕米对人类心血管治疗的效率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Solanaceae glycoalkaloids: α-solanine and α-chaconine modify the cardioinhibitory activity of verapamil.

Solanaceae glycoalkaloids: α-solanine and α-chaconine modify the cardioinhibitory activity of verapamil.

Solanaceae glycoalkaloids: α-solanine and α-chaconine modify the cardioinhibitory activity of verapamil.

Solanaceae glycoalkaloids: α-solanine and α-chaconine modify the cardioinhibitory activity of verapamil.

Context: Solanaceae glycoalkaloids (SGAs) possess cardiomodulatory activity.

Objective: This study investigated the potential interaction between verapamil and glycoalkaloids.

Material and methods: The cardioactivity of verapamil and glycoalkaloids (α-solanine and α-chaconine) was tested in adult beetle (Tenebrio molitor) myocardium in vitro using microdensitometric methods. The myocardium was treated with pure substances and mixtures of verapamil and glycoalkaloids for 9 min with saline as a control. Two experimental variants were used: simultaneous application of verapamil and glycoalkaloids or preincubation of the myocardium with one of the compounds followed by perfusion with a verapamil solution. We used 9 × 10-6-5 × 10-5 M and 10-9-10-5 M concentration for verapamil and glycoalkaloids, respectively.

Results: Verapamil, α-solanine and α-chaconine showed cardioinhibitory activity with IC50 values equal to 1.69 × 10-5, 1.88 × 10-7 and 7.48 × 10-7 M, respectively. When the glycoalkaloids were applied simultaneously with verapamil, an antagonistic effect was observed with a decrease in the maximal inhibitory effect and prolongation of t50 and the recovery time characteristic of verapamil. We also confirmed the expression of two transcript forms of the gene that encodes the α1 subunit of L-type calcium channels in the myocardium and brain with equal transcription levels of both forms in the myocardium and significant domination of the shorter form in the brain of the insect species tested.

Discussion and conclusions: The results show that attention to the composition of the daily diet during therapy with various drugs is particularly important. In subsequent studies, the nature of interaction between verapamil and SGAs on the molecular level should be checked, and whether this interaction decreases the efficiency of cardiovascular therapy with verapamil in humans.

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CiteScore
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