Phytopharmacological Evaluation of Alcoholic Extract of Berberis aristata Leaf in the Treatment of Gastric Ulcer

R. Singh, Y. Trilochana
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Abstract

For over a century, peptic ulcer has been one of the most common gastrointestinal tract (GIT) disorder. There are number of drugs are now available for treatment. Drugs of herbal origin reduce the offensive factors and have proved to be safe, clinically effective, relatively less expensive, globally competitive, and with better patient tolerance.This study was performed to assess the anti-ulcer activity on different parts of B.aristata. Apart from that, acute toxicity, qualitative chemical analysis, total phenolic content (TPC), total flavonoid content(TFC) and in vitro antioxidant activities were evaluated. The potentially active plant part was selected for screening as gastro protective, in vivo antioxidant and antisecretory activities in ulcerated rats.The 50% ethanolic extract of B. aristata were subjected to preliminary phytochemical screening, estimation of TFC and TPC. The crude extract from the leaves of B. aristata gave best antiulcer activity among flower and stem. In acute toxicity studies, the administration of the crude extract of B. aristata leaves did not reveal any adverse effects or toxicity in rats at fourteen days observations.The results of these studies have shown that ethylexract of B.aristata leaf (EEBAL) produced a significant dose dependent ulcerprotective, antioxidant and antisecretory activity by blocking the activity of proton pump, protecting from antioxidants produced during stress induced ulcer and by enhancing glycoprotein levels. Abbreviation: TPC, total phenolic content; TFC, total flavonoid content; EEBAL, ethanolic extract of Berberis aristata leaf. Introduction: Peptic ulcer represents a major health problem, both in terms of morbidity and mortality. The aggressive acid-pepsin factors are responsible for the induction of ulcers. Berberis aristata DC var. aristata (Berberidaceae), are commonly known as Daruharidralocal to the Himalayas in India and in Nepal. It is also found in Nilgiri slopes in South India 1,2,3 .The plant is utilized customarily in irritation, wound mending, skin ailment, menorrhagia, looseness of the bowels, jaundice and fondness of eyes.Alcoholic extract of bark yielded berberine chloride, palmatine chloride and a mixture of both 4 . The chief constituent of the roots and stem bark of B. aristata is an alkaloid, berberine are responsible for hepatoprotective activity 5 . The crude extract of B.aristata fruits exhibit preventive and curative effects on paracetamol and chloroform induced hepatotoxicity 6 .Berberisaristata also exhibits anti-diarrhoeal, anti-fungal, anti-histaminic an anticholinergic activities 4 . Ratnaker Singh et al /International Journal of PharmTech Research, 2020,13(1): 01-05. DOI= http://dx.doi.org/10.20902/IJPTR.2019.130101 International Journal of PharmTech Research CODEN (USA): IJPRIF, ISSN: 0974-4304, ISSN(Online): 2455-9563 Vol.13, No.01, pp 01-05, 2020 Ratnaker Singh et al /International Journal of PharmTech Research, 2020,13(1): 01-05. 2 Material and Methods
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马兜铃叶醇提物治疗胃溃疡的植物药理学评价
一个多世纪以来,消化性溃疡一直是最常见的胃肠道疾病之一。现在有许多药物可用于治疗。草药来源的药物减少了令人不快的因素,并且已被证明是安全的,临床有效的,相对便宜的,具有全球竞争力的,并且具有更好的患者耐受性。本研究对马兜铃不同部位的抗溃疡活性进行了评价。此外,对其急性毒性、定性化学分析、总酚含量(TPC)、总黄酮含量(TFC)和体外抗氧化活性进行了评价。筛选出具有潜在活性的植物部分,对溃疡大鼠进行胃保护、体内抗氧化和抗分泌活性的筛选。对50%乙醇提取物进行初步的植物化学筛选、TFC和TPC的估算。马兜铃叶粗提物的抗溃疡活性在花和茎中最好。在急性毒性研究中,在14天的观察中,大鼠未发现任何不良反应或毒性。这些研究结果表明,马铃塔叶乙基提取物(EEBAL)通过阻断质子泵的活性,保护应激性溃疡产生的抗氧化剂,提高糖蛋白水平,具有显著的剂量依赖性的溃疡保护、抗氧化和抗分泌活性。简称:TPC,总酚含量;TFC:总黄酮含量;ebal,小檗叶乙醇提取物。简介:消化性溃疡代表了一个主要的健康问题,无论是在发病率和死亡率方面。侵袭性酸性胃蛋白酶因子是诱发溃疡的原因。小檗(Berberis aristata DC var. aristata,小檗科),通常被称为daruharidralal,原产于印度和尼泊尔的喜马拉雅山脉。它也生长在南印度的尼尔吉里山坡上。这种植物通常用于刺激、伤口愈合、皮肤疾病、月经过度、肠子松弛、黄疸和眼睛的喜爱。树皮的酒精提取物产生氯化小檗碱、氯化巴马汀和两者的混合物。马铃塔根和茎皮的主要成分是一种生物碱,小檗碱具有保护肝脏的作用。马里斯塔果粗提物对扑热息痛和氯仿引起的肝毒性具有预防和治疗作用。马里斯塔果还具有抗腹泻、抗真菌、抗组胺和抗胆碱能活性。[1]李建军,张建军,李建军,等。中国生物医学工程学报,2016,32(1):1- 5。DOI= http://dx.doi.org/10.20902/IJPTR.2019.130101 International Journal of PharmTech Research CODEN (USA): IJPRIF, ISSN: 0974-4304, ISSN(Online): 2455-9563 Vol.13, No.01, pp 01-05, 2020 Ratnaker Singh等/International Journal of PharmTech Research, 2020,13(1): 01-05。2材料与方法
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