南非植物与血清素再摄取转运体和腺苷A1/A2A受体结合亲和力的初步筛选

IF 2.3 Q3 PHARMACOLOGY & PHARMACY Scientia Pharmaceutica Pub Date : 2023-08-22 DOI:10.3390/scipharm91030041
Scientia Pharmaceutica, Andisiwe Mnqika, A. Aremu, H. D. J. V. Rensburg, Makhotso Lekhooa
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引用次数: 0

摘要

在南非传统医学中,Gomphocarpus fruticosus (L.)w。t。艾顿。& C.A.好的。和Leonotis leonurus。(l)R.Br。已被记录在不同的民族是一个有价值的草药治疗抑郁症相关的条件。本研究研究了这三种植物对血清素再摄取转运体(SERT)和腺苷A1/A2受体的亲和力。选用六种溶剂(水、甲醇、丙酮、二氯甲烷、石油醚和己烷)对所选植物进行提取。通过体外应用结合实验,确定了8种提取物具有潜在的亲和力。Hypoxis hemocallidea的甲醇和丙酮提取物对[3H]西酞普兰的特异性结合率为60%,表明近40%的植物提取物与SERT结合。在腺苷受体结合实验中,益母草甲醇和己烷提取物的活性最高,rA1Ki值分别为0.038和0.176 mg/mL。二氯甲烷提取物的rA1Ki值为6.46 mg/mL。极性较强的溶剂甲醇和二氯甲烷提取物具有较高的结合亲和力。此外,这些植物提取物在腺苷A1受体上起拮抗剂作用。总的来说,目前的研究结果提供了一个潜在的抗抑郁作用的一些测试提取物基于它们与受体的结合评估的指示。然而,需要结合其他体外试验来确定可能的作用机制。此外,植物提取物的计算分析和分析对于鉴定与受体有较高亲和力的生物活性化合物至关重要。最终,体内研究仍然是必不可少的,以允许深入阐明作用机制。
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Preliminary Screening of South African Plants for Binding Affinity to the Serotonin Reuptake Transporter and Adenosine A1/A2A Receptors
In South African traditional medicine, Gomphocarpus fruticosus (L.) W.T. Aiton, Hypoxis hemerocallidea Fisch. & C.A. Mey., and Leonotis leonurus. (L.) R.Br. have been recorded among different ethnic groups to be a valuable herbal remedy for the management of depression-related conditions. The current study investigated the affinity of these three plants toward the serotonin reuptake transporter (SERT) and adenosine A1/A2 receptors. Six solvents (water, methanol, acetone, dichloromethane, petroleum ether, and hexane) were used to extract the selected plants. We established that eight extracts exerted potential affinity based on the applied in vitro binding experiment. The methanol and acetone extracts of Hypoxis hemerocallidea had 60% specific binding of [3H]citalopram, an indication that almost 40% of the plant extracts were bound to the SERT. For the adenosine receptor binding assays, methanol and hexane extracts of Leonotis leonurus were the most active, with rA1Ki values of 0.038 and 0.176 mg/mL, respectively. In addition, the dichloromethane extract of Gomphocarpus fruticosus had an rA1Ki value of 6.46 mg/mL. Extracts from the more polar solvents methanol and dichloromethane had higher binding affinity. Additionally, these plant extracts acted as antagonists at the adenosine A1 receptor. Overall, the current findings provide an indication of the potential antidepressant effects of some of the tested extracts based on their binding to the receptors evaluated. However, a combination of other in vitro assays is needed to establish possible mechanisms of action. In addition, computational analysis and profiling of plant extracts is crucial to identify the bioactive compounds with a higher affinity to the receptors. Ultimately, in vivo studies remain essential to allow for an in-depth elucidation of the mechanisms of action.
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来源期刊
Scientia Pharmaceutica
Scientia Pharmaceutica Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
4.60
自引率
4.00%
发文量
67
审稿时长
10 weeks
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