山菖蒲心材部分纯化Santalin A对四氧嘧啶诱导的糖尿病大鼠的抗糖尿病活性

Jyothi Chaitanya Pagadala, S. Yenugu, Padmaja Gudipalli
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摘要

越来越多地使用植物性药物作为疾病管理常规药物的替代品,需要对新化合物进行鉴定、分离和表征。尽管植物提取物具有减轻疾病发病率的潜力,但为了避免其他化合物的干扰,一些活性原理是首选的。在治疗糖尿病、心血管疾病、癌症和感染方面,已经描述了翼龙桃的提取物和分离化合物的有希望的健康益处。然而,这种对活性原理,即桑塔林的研究,并没有报道。本研究采用柱层析-制备层析-高效液相色谱法,从桑菖蒲心材中分离纯化桑菖蒲苷a和B。采用LC-MS、HR-MS和1h NMR对部分纯化的唐芦苷进行了表征。与心材粗提物相比,唐缕素组合体外总抗氧化活性和DPPH自由基清除活性更高。在四氧嘧啶诱导的糖尿病大鼠的肝脏、肾脏和胰腺中,桑他林A和B的混合物没有表现出任何降糖活性。然而,预处理大鼠1.0 mg/kg体重的桑他林混合物,可以防止四氧嘧啶诱导的糖尿病,血糖水平正常。在未发生四氧嘧啶诱导的糖尿病的santalin预处理大鼠中,高血糖相关的脂质过氧化被消除。此外,santalin预处理大鼠胰腺中过氧化氢酶、谷胱甘肽过氧化物酶和谷胱甘肽s -转移酶活性的改变可能是防止胰腺损伤的原因,因此不会在四氧嘧啶治疗后诱发糖尿病。因此,我们首次报道了分离santalins混合物的简化程序,包括它们在Wistar大鼠中预防诱导糖尿病的能力。我们的研究结果具有重要的临床意义,即补充桑他林可能潜在地避免或延迟高危人群糖尿病的发病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anti-diabetic Activity of Partially Purified Santalin A from the Heartwood of Pterocarpus santalinus L.f. in Alloxan-induced Diabetic Wistar Rat
The ever-increasing use of plant-based pharmaceuticals as alternatives to conventional drugs for disease management demands identification, isolation, and characterization of novel compounds. Despite the potential of plant extracts to mitigate the morbidity of diseases, several active principles are preferred to avoid the interference of other compounds. The promising health benefits of the extracts and isolated compounds of Pterocarpus santalinus in the treatment of diabetes, cardiovascular disease, cancer, and infections have been described. However, such studies on the active principle, namely, santalins, are not reported. In this study, we standardized the isolation of a mixture of santalins A and B from the heartwood of P. santalinus by column chromatography followed by preparative TLC and HPLC. The partially purified santalins were characterized by LC-MS, HR-MS, and 1 H NMR analyses. The isolated combination of santalins displayed higher total antioxidant and DPPH free radical scavenging activity in vitro than the crude heartwood extracts. Administration of the mixture of santalins A and B did not exhibit any antihyperglycemic activity in the liver, kidney, and pancreas of alloxan-induced diabetic rats. However, pretreatment of rats with a mixture of santalins at a dose of 1.0 mg/kg body weight prevented alloxan-induced diabetes as indicated by the normal blood glucose levels. Hyperglycemia-associated lipid peroxidation was abrogated in santalin-pretreated rats that did not develop alloxan-induced diabetes. Furthermore, the alterations in catalase, glutathione peroxidase, and glutathione-S-transferase activities in the pancreas of santalinpretreated rats could be responsible for preventing damage to the pancreas and thus non-induction of diabetes following alloxan treatment. Therefore, for the first time, we report the simplified procedure for isolating a mixture of santalins, including their ability to prevent the induction of diabetes in Wistar rats. The outcome of our study has significant clinical importance to the fact that supplementation of santalins may potentially avoid or delay the onset of diabetes in high-risk individuals.
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