拟对症治疗镰状细胞病的Drepanoalpha®乙醇提取物、天竺葵和辣木植物药物的体外生物活性研究

Benjamin Gbolo Zoawe, A. Nachtergael, D. Tshibangu, N. Misengabu, Victoire Nsabatien, P. Memvanga, D. Tshilanda, J. Ngbolua, P. Mpiana, P. Duez
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摘要

镰状细胞病(SCD)是一种常染色体隐性血液疾病,其特征是红细胞在低氧条件下呈异常的刚性镰状。这些镰状红细胞易于溶解、聚集并阻塞小血管,导致主要并发症。本研究的目的是研究drepanoalpha的活性特性,drepanoalpha是刚果民主共和国(DRC)开发的一种抗镰状细胞病的草药配方,用于镰状细胞病的预防和对症治疗。Drepanoalpha®乙醇提取物(DEE)是一种干提取物(药浸比,DER, 100/11),由2种食用植物Justicia secunda Vahl和Moringa oleifera Lam的1:1混合物的乙醇(96%,v/v)渗透制备。典型的镰状细胞计数方法是用光镜对从纯合子患者获得的稀释水洗红细胞进行测量;用2% Na2S2O5在DEE(悬浮在9‰NaCl中)、9‰NaCl(阴性对照)或cromoglycate二钠(DSCG,阳性对照)存在下处理红细胞。在所有测试条件下,用分光光度法测定镰状血红蛋白聚合、Fe2+/Fe3+比和中位红细胞脆性。DEE逆转镰状病变率为89.1%,与DSCG (87.7%;60.3µg/mL),抑制镰状细胞血红蛋白聚合率分别为77.8%和74.4%。DEE和DSCG的Fe2+/Fe3+比分别提高了18.0%和15.9%。NaCl 9‰、DSCG和DEE的中位脆性值分别为0.602、0.714和0.732。测定的体外参数验证了DEE有效的抗镰状细胞病作用,并证实了这一改进的传统草药配方对SCD治疗的价值。
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In Vitro Biological Activities of Drepanoalpha® Ethanolic Extract, A Justicia Secunda and Moringa Oleifera-Based Phytomedicine Proposed for The Symptomatic Treatment of Sickle Cell Disease
Sickle cell disease (SCD) is an autosomal recessive blood disorder characterized by red blood cells that assume an abnormal, rigid sickle shape under low-oxygen conditions. These sickle-shaped erythrocytes tend to lyse, aggregate, and obstruct small blood vessels, leading to major complications. The present study aims to investigate properties that may underlie the activity of Drepanoalphaâ, an antisickling herbal formulation developed in the Democratic Republic of Congo (DRC) for the prevention and symptomatic treatment of sickle cell disease crises. The Drepanoalpha® Ethanolic Extract (DEE) is a dry extract (drug-extract ratio, DER, 100/11) prepared from ethanol (96 %, v/v) percolation of a 1:1 mixture of 2 food plants, Justicia secunda Vahl and Moringa oleifera Lam. Sickling was classically measured by light microscopy on diluted washed erythrocytes obtained from homozygote patients; erythrocytes were treated with 2 % Na2S2O5 in the presence of DEE (suspension in 9 ‰ NaCl), 9 ‰ NaCl (negative control) or disodium cromoglycate (DSCG, positive control). For all tested conditions, the sickle hemoglobin polymerization, the Fe2+/Fe3+ ratio, and the median corpuscular fragility were measured by spectrophotometry. The DEE reversed sickling by 89.1 %, comparable to DSCG (87.7 %; 60.3 µg/mL), inhibiting sickle cell hemoglobin polymerization of 77.8 % and 74.4 %, respectively. The Fe2+/Fe3+ ratio was improved by 18.0 % for DEE and 15.9 % for DSCG. The median corpuscular fragility values were 0.602, 0.714, and 0.732 for NaCl 9 ‰, DSCG, and DEE, respectively. The measured in vitro parameters validate an effective antisickling effect of DEE and confirm the value of this improved traditional herbal formulation for the management of SCD.
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