Hossain Mohammad Shahadat, Reza A S M Ali, Rahaman Md Masudur, Nasrin Mst Samima, Rahat Mohammed Rasib Uddin, Islam Md Rabiul, Uddin Md Josim, Rahman Md Atiar
Department of Pharmacy, International Islamic University Chittagong, Chittagong, Bangladesh.
Department of Biochemistry and Molecular Biology, University of Chittagong, Chittagong, Bangladesh.
J Basic Clin Physiol Pharmacol. 2018 Jun 27;29(3):291-299. doi: 10.1515/jbcpp-2017-0042.
The present study was planned to investigate the phytochemical, antioxidant, antinociceptive, anticoagulant and cytotoxic activities of the Jacquemontia tamnifolia (L.) Griseb leaf methanol extract (MExJT) in the laboratory using both in vitro and in vivo methods.
Phytochemical values, namely, total phenolic and flavonoid contents, 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging effect and FeCl3 reducing power effects, were studied by established methods. In vivo antinociceptive activity was performed by acidic acid-induced writhing test and formalin-induced pain test on Swiss albino mice at doses of 125, 250 and 500 mg/kg body weight. The clot lysis and brine shrimp lethality bioassay in vitro were used to evaluate the thrombolytic and cytotoxic activities of the plant extract, respectively.
Phytochemical screening illustrates the presence of tannins, saponins, flavonoids, gums and carbohydrates, steroids, alkaloids and reducing sugars in the extract. The results showed the total phenolic content (146.33 g gallic acid equivalents/100 g extract) and total flavonoid content (133.33 g quercetin/100 g). Significant (p<0.05) IC50 values compared to respective standards were recorded in DPPH radical scavenging (289.5 μg/mL) and FeCl3 reduction (245.2 μg/mL). The antinociceptive effect was evaluated in the acetic acid-induced writhing test and formalin-induced pain models in Swiss albino mice with doses of 125, 250 and 500 mg/kg body weight. Significant (p<0.05) inhibition (72.87±2.73%) of writhing response compared to diclofenac sodium was achieved by 500 mg/kg body weight. The extract also significantly inhibited the licking response in both the early phase (51.59±1.57%, p<0.05) and the late phase (64.82±1.87%, p<0.05) in the formalin-induced writhing test. MExJT also showed (38.10±1.79%) clot lytic activity in the thrombolytic test and cytotoxicity with an LC50 value of 31.70 μg/mL in the brine shrimp lethality bioassay.
The plant is a potential source of antioxidants and might have one or more secondary metabolite(s) with central and peripheral analgesic activity. The results also demonstrate that MExJT has moderate thrombolytic and lower cytotoxic properties that may warrant further exploration.
本研究旨在通过体外和体内方法,在实验室中研究平卧银背藤(Jacquemontia tamnifolia (L.) Griseb)叶甲醇提取物(MExJT)的植物化学、抗氧化、抗伤害感受、抗凝血和细胞毒性活性。
采用既定方法研究植物化学值,即总酚和黄酮含量、1,1-二苯基-2-苦基肼(DPPH)自由基清除作用和FeCl3还原能力作用。对瑞士白化小鼠进行体内抗伤害感受活性实验,采用剂量为125、250和500mg/kg体重的乙酸诱导扭体试验和福尔马林诱导疼痛试验。体外凝块溶解和卤虫致死生物测定分别用于评估植物提取物的溶栓和细胞毒性活性。
植物化学筛选表明提取物中存在单宁、皂苷、黄酮、树胶和碳水化合物、类固醇、生物碱和还原糖。结果显示总酚含量(146.33g没食子酸当量/100g提取物)和总黄酮含量(133.33g槲皮素/100g)。与各自标准相比,DPPH自由基清除(289.5μg/mL)和FeCl3还原(245.2μg/mL)中记录到显著(p<0.05)的IC50值。在瑞士白化小鼠中,采用剂量为125、250和500mg/kg体重的乙酸诱导扭体试验和福尔马林诱导疼痛模型评估抗伤害感受作用。与双氯芬酸钠相比,500mg/kg体重的剂量实现了对扭体反应的显著(p<0.05)抑制(72.87±2.73%)。提取物在福尔马林诱导的扭体试验中还显著抑制了早期(51.59±1.57%,p<0.05)和晚期(64.82±1.87%,p<0.05)的舔舐反应。MExJT在溶栓试验中也显示出(38.10±1.79%)的凝块溶解活性,在卤虫致死生物测定中的LC50值为31.70μg/mL,具有细胞毒性。
该植物是抗氧化剂的潜在来源,可能含有一种或多种具有中枢和外周镇痛活性的次生代谢产物。结果还表明,MExJT具有适度的溶栓特性和较低的细胞毒性,可能值得进一步探索。