Deciphering In Vitro and In Vivo Pharmacological Properties of Seed and Fruit Extracts of Flacourtia jangomas (Lour.) Raeusch.

IF 2.1 Q3 PHARMACOLOGY & PHARMACY Advances in Pharmacological and Pharmaceutical Sciences Pub Date : 2024-07-26 eCollection Date: 2024-01-01 DOI:10.1155/2024/4035987
Farhana Alam Ripa, Fowzia Alam, Fahmida Haque Riya, Yesmin Begum, Sharmin Akter Eti, Nusratun Nahar, Zebunnesa Ahmed, Sabrina Sharmin
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Abstract

The objective of the study was to evaluate the pharmacological properties of the methanolic extract of Flacourtia jangomas (Lour.) Raeusch fruits (PFJM) and seeds (SFJM), along with their soluble fractions in ethyl acetate (fruit: PFJE; seed: SFJE) and chloroform (fruit: PFJC; seed: SFJC). Our phytochemical analysis of the examined extracts confirmed the presence of various therapeutically active phytoconstituents, including flavonoids, tannins, glycosides, and alkaloids. Employing the DPPH (2,2-diphenyl-1-picrylhydrazyl) radical quenching method, SFJC exhibited the highest antioxidative potential, with an IC50 of 48.84, compared to ascorbic acid (IC50 21.77). The thrombolytic activity was assessed through rapid clot analysis of human blood samples, revealing that SFJC demonstrated the highest thrombolytic activity (60.99 ± 2.28%) compared to streptokinase (72.89 ± 2.19%). In the protein denaturation antiarthritic test, the PFJE and SFJC extracts exhibited significant potency, achieving results of 74.28 ± 1.16% and 79.25 ± 0.83%, respectively, at a dose of 500 μg/mL. All samples displayed notable anthelmintic activity by reducing Pheretima posthuma paralysis and death time in a dose-dependent manner compared to albendazole. In both in vivo analgesic tests, SFJC demonstrated substantial (p < 0.01) pain inhibition percentages (tail immersion: 49.46%; acetic acid writhing: 66.43%) at a dose of 600 mg/kg. During neuropharmacological screening, all extracts significantly (p < 0.01;  p < 0.05) and dose-dependently decreased the mice's locomotion activity and motor balance. In the thiopental-induced sedation assay, SFJC significantly decreased the sleep latency time (4.18 ± 0.24 min) and increased the duration of sleep time (85.20 ± 2.39 min) at a higher dose. All samples notably reduced blood glucose levels in the oral glucose tolerance test in a dose-responsive manner, and SFJC exhibited a considerable hypoglycemic impact (7.38 ± 0.44 mmoles/L at 600 mg/kg). The frequency of diarrheal episodes in mice during the antidiarrhea assessment was significantly decreased by the tested plant samples. These findings can serve as a reference for future endeavors to isolate pure bioactive compounds from this plant for the development of novel phytomedicines.

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破译Flacourtia jangomas (Lour.) Raeusch种子和果实提取物的体外和体内药理特性
本研究的目的是评估罂粟果(Flacourtia jangomas (Lour.) Raeusch)果实(PFJM)和种子(SFJM)的甲醇提取物及其乙酸乙酯(果实:PFJE;种子:SFJE)和氯仿(果实:PFJC;种子:SFJC)中的可溶性馏分的药理特性。我们对所研究的提取物进行了植物化学分析,证实其中含有各种具有治疗活性的植物成分,包括黄酮类、单宁酸、苷类和生物碱。采用 DPPH(2,2-二苯基-1-苦基肼)自由基淬灭法,与抗坏血酸(IC50 21.77)相比,SFJC 的抗氧化潜力最高,IC50 为 48.84。通过对人体血液样本进行快速凝块分析来评估溶栓活性,结果显示,与链激酶(72.89 ± 2.19%)相比,SFJC 的溶栓活性最高(60.99 ± 2.28%)。在蛋白质变性抗关节炎试验中,PFJE 和 SFJC 提取物表现出显著的效力,在剂量为 500 μg/mL 时分别达到 74.28 ± 1.16% 和 79.25 ± 0.83%。与阿苯达唑相比,所有样品都具有显著的抗蠕虫活性,能以剂量依赖的方式减少Pheretima后麻痹和死亡时间。在两项体内镇痛试验中,SFJC 在剂量为 600 毫克/千克时,显示出显著的镇痛百分比(p < 0.01)(浸尾:49.46%;醋酸蠕动:66.43%)。在神经药理学筛选过程中,所有提取物都能显著(p < 0.01;p < 0.05)降低小鼠的运动活性和运动平衡能力,且其降低程度与剂量有关。在硫喷妥类诱导的镇静试验中,SFJC 在较高剂量下可明显降低睡眠潜伏时间(4.18 ± 0.24 分钟)并延长睡眠时间(85.20 ± 2.39 分钟)。在口服葡萄糖耐量试验中,所有样本都以剂量反应的方式明显降低了血糖水平,SFJC 表现出相当大的降血糖作用(600 毫克/千克时为 7.38 ± 0.44 毫摩尔/升)。在止泻评估过程中,受试植物样本显著降低了小鼠腹泻的频率。这些发现可为今后从该植物中分离纯生物活性化合物以开发新型植物药提供参考。
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CiteScore
4.30
自引率
3.60%
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0
审稿时长
17 weeks
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