Tiwari Devkumar D, Thorat Vandana M, Pakale Prathamesh V, Patil Sarika J
Department of Pharmacology, Krishna Vishwa Vidyapeeth (Deemed to be University), Satara, IND.
Cureus. 2024 Jul 12;16(7):e64379. doi: 10.7759/cureus.64379. eCollection 2024 Jul.
Background and aim Diabetes is a chronic metabolic disorder characterized by elevated blood glucose levels. Although current antidiabetic drugs are highly effective, they are associated with various adverse drug reactions, including life-threatening hypoglycemia, skin rashes, and gastrointestinal intolerance, in addition to being costly. This animal-based experimental study aims to develop a herbal alternative or adjuvant to current antidiabetic drugs using () and (), which could potentially have fewer adverse drug reactions and reduce the required dose of existing antidiabetic medications. Material and methods Seventy-eight adult albino Wistar rats weighing between 150 and 250 g were used for the study. Diabetes mellitus (DM) was induced by intraperitoneal (i.p) injections of streptozotocin (STZ) (65 mg/kg) 15 minutes after nicotinamide (NIC) (110 mg/kg) administration. As the diabetes was confirmed (blood glucose level > 250 mg/dL), rats were divided into 13 different groups mentioned. The standard antidiabetic drugs (metformin [MET] and glimepiride [GLI]) and polyherbal combinations (PHC) ( + ) were administered orally, individually ( and ), and in combination ( + ). Blood samples were collected for biochemical analysis using the tail vein prick method. The study is based on a total of 13 groups, six rats in each group. Groups 1 and 2 (normal control [NC] and diabetic control [DC]) received distilled water at a dose of 10 mL/kg orally for 28 days. Groups 3-5 ( 250, 500, and 1000) received dried ethanolic root extract of at a dose of 250, 500, and 1000 mg/kg orally, respectively, for 28 days. Groups 6-8 ( 250, 500, and 1000) received dried ethanolic root extract of at a dose of 250, 500, and 1000 mg/kg orally, respectively, for 28 days. Groups 9-11 (PHC 250, 500, and 1000) received dried ethanolic root extract of + at a dose of 250, 500, and 1000 mg/kg orally, respectively, for 28 days. Groups 12 and 13 (MET and GLI) received standard drugs MET and GLI at a dose of 250 and 10 mg/kg orally, respectively, for 28 days. Results The dried ethanolic root extract of medicinal herbal plants and and their combination exhibited significant antidiabetic efficacy. PHC has been shown to have a superior antidiabetic effect than individuals. PHC 500 and 1000 showed blood glucose levels similar to those of the GLI group (P < 0.05). Additionally, PHC 1000 showed blood glucose levels similar to those of the MET group (P < 0.05). Conclusion Our results indicate that both and possess hypoglycemic activity, and their combination also has a synergistic antidiabetic effect compared to the individual extract. These findings are promising in developing new safe and cost-effective herbal combinations as alternatives or additives to currently used synthetic antidiabetic drugs.
背景与目的 糖尿病是一种以血糖水平升高为特征的慢性代谢紊乱疾病。尽管目前的抗糖尿病药物疗效显著,但它们会引发各种药物不良反应,包括危及生命的低血糖、皮疹和胃肠道不耐受,而且成本高昂。这项基于动物的实验研究旨在利用()和()开发一种草药替代品或辅助药物,以替代目前的抗糖尿病药物,这种替代品可能具有较少的药物不良反应,并减少现有抗糖尿病药物的所需剂量。
材料与方法 选用78只体重在150至250克之间的成年白化Wistar大鼠进行研究。在给予烟酰胺(NIC)(110毫克/千克)15分钟后,通过腹腔注射链脲佐菌素(STZ)(65毫克/千克)诱导糖尿病(DM)。糖尿病确诊后(血糖水平>250毫克/分升),将大鼠分为所述的13个不同组。标准抗糖尿病药物(二甲双胍[MET]和格列美脲[GLI])和多草药组合(PHC)(+)分别单独(和)以及联合(+)口服给药。使用尾静脉采血法采集血样进行生化分析。该研究共设13组,每组6只大鼠。第1组和第2组(正常对照[NC]和糖尿病对照[DC])口服给予剂量为10毫升/千克的蒸馏水,持续28天。第3 - 5组(250、500和1000)分别口服给予剂量为250、500和1000毫克/千克的干燥乙醇根提取物,持续28天。第6 - 8组(250、500和1000)分别口服给予剂量为250、500和1000毫克/千克的干燥乙醇根提取物,持续28天。第9 - 11组(PHC 250、500和1000)分别口服给予剂量为250、500和1000毫克/千克 的干燥乙醇根提取物+,持续28天。第12组和第13组(MET和GLI)分别口服给予剂量为250和10毫克/千克的标准药物MET和GLI,持续28天。
结果 药用植物的干燥乙醇根提取物及其组合表现出显著的抗糖尿病功效。已证明PHC比单独使用具有更优的抗糖尿病效果。PHC 500和1000组的血糖水平与GLI组相似(P<0.05)。此外,PHC 1000组的血糖水平与MET组相似(P<0.05)。
结论 我们的结果表明,()和()均具有降血糖活性,与单独提取物相比,它们的组合还具有协同抗糖尿病作用。这些发现对于开发新的安全且经济有效的草药组合作为目前使用的合成抗糖尿病药物的替代品或添加剂具有重要意义。