The Mechanisms of Lipid Vesicle Fusion Inhibition by Extracts of Chaga and Buckthorn Leaves

IF 1.1 Q4 CELL BIOLOGY
S. S. Efimova, P. D. Zlodeeva, E. V. Shekunov, O. S. Ostroumova
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引用次数: 1

Abstract

The ability of extracts of grapefruit seeds (ESG), sea buckthorn leaves (ESBL), and chaga (EC) to inhibit membrane fusion was evaluated. It was found that ESBL and EC inhibited Ca2+-mediated fusion of phosphatidylglycerol-enriched lipid vesicles; the inhibition indexes were about 90 and 100%, respectively. ESG did not inhibit the fusion of negatively charged liposomes induced by calcium. In addition to calcium-mediated liposome fusion, EC inhibited the fusion of vesicles from a mixture of phosphatidylcholine and cholesterol under the action of polyethylene glycol with a molecular weight of 8000 Da (the inhibition index was 80%). The other two extracts had no effect on polymer-induced fusion of uncharged membranes. The effect of some major components of the tested extracts on the fusion of vesicles was evaluated. It has been shown that flavonols, quercetin and myricetin, which are major components of ESBL, inhibited the fusion of negatively charged membranes under the action of calcium (the inhibition indexes were about 85 and 60%, respectively). Another flavonol of ESBL, the glycoside of quercetin rutin, did not have such an effect. The data obtained made it possible to relate the ESBL suppression of calcium-induced fusion of lipid vesicles with the presence of quercetin and myricetin in its composition. These flavonols had virtually no effect on polyethylene glycol-induced vesicle fusion, which is consistent with the absence of ESBL action on liposome fusion under the action of polymer. The ability of quercetin and myricetin to reduce the melting temperature of phosphatidylglycerol with saturated hydrocarbon chains and to increase the half-width of the peak corresponding to melting has been demonstrated. The observed correlation between the parameters characterizing the thermotropic behavior of the lipid in the presence of quercetin and myricetin and the index of inhibition of calcium-mediated liposome fusion by these compounds may indicate a relationship between the ability of flavonols to influence the packaging of membrane lipids and inhibit vesicle fusion. Pentacyclic triterpenoids, betulin and lupeol, which are part of EC, did not inhibit the fusion of vesicles under the action of both calcium and polyethylene glycol, and their presence in EC cannot be responsible for the antifusogenic activity of EC.

Abstract Image

Chaga和鼠李叶提取物抑制脂质囊泡融合的机制
研究了葡萄柚籽(ESG)、沙棘叶(ESBL)和桦茸(EC)提取物对膜融合的抑制作用。结果发现,ESBL和EC抑制Ca2+介导的富含磷脂酰甘油的脂质囊泡融合;抑制率分别为90%和100%。ESG对钙诱导的带负电荷脂质体融合无抑制作用。除了钙介导的脂质体融合外,EC还能抑制磷脂酰胆碱和胆固醇混合物在分子量为8000 Da的聚乙二醇作用下的融合(抑制指数为80%)。另外两种提取物对聚合物诱导的不带电膜的融合没有影响。评价了所试提取物中主要成分对囊泡融合的影响。研究表明,ESBL的主要成分黄酮醇、槲皮素和杨梅素在钙的作用下抑制了带负电膜的融合(抑制指数分别为85%和60%)。另一种ESBL黄酮醇,槲皮素芦丁糖苷,没有这样的效果。所获得的数据使ESBL对钙诱导的脂质囊泡融合的抑制与其成分中槲皮素和杨梅素的存在有关。这些黄酮醇对聚乙二醇诱导的囊泡融合几乎没有影响,这与聚合物作用下ESBL对脂质体融合没有作用是一致的。槲皮素和杨梅素能够降低饱和烃链磷脂酰甘油的熔融温度,并增加与熔融相对应的峰的半宽度。槲皮素和杨梅素存在时表征脂质热致性行为的参数与这些化合物对钙介导的脂质体融合的抑制指数之间的相关性可能表明黄酮醇影响膜脂质包装和抑制囊泡融合的能力之间的关系。EC中的五环三萜、白桦脂素和鹿皮醇在钙和聚乙二醇的作用下都没有抑制囊泡的融合,它们在EC中的存在不可能是EC抗融合活性的原因。
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来源期刊
CiteScore
1.40
自引率
0.00%
发文量
28
期刊介绍: Biochemistry (Moscow), Supplement Series A: Membrane and Cell Biology   is an international peer reviewed journal that publishes original articles on physical, chemical, and molecular mechanisms that underlie basic properties of biological membranes and mediate membrane-related cellular functions. The primary topics of the journal are membrane structure, mechanisms of membrane transport, bioenergetics and photobiology, intracellular signaling as well as membrane aspects of cell biology, immunology, and medicine. The journal is multidisciplinary and gives preference to those articles that employ a variety of experimental approaches, basically in biophysics but also in biochemistry, cytology, and molecular biology. The journal publishes articles that strive for unveiling membrane and cellular functions through innovative theoretical models and computer simulations.
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