芦笋的抗糖尿病作用。在RIN-5F细胞,HepG2细胞和Wistar大鼠中

R. Sunday, E. Obuotor, Anil Kumar
{"title":"芦笋的抗糖尿病作用。在RIN-5F细胞,HepG2细胞和Wistar大鼠中","authors":"R. Sunday, E. Obuotor, Anil Kumar","doi":"10.24870/cjb.2019-000129","DOIUrl":null,"url":null,"abstract":"Background: The antidiabetic effect of Asparagus adscendens root ethanolic extract (AAE) was evaluated in this study using both in vivo and in vitro models. The effect of AAE on carbohydrate metabolizing enzymes (α-amylase and α-glucosidase) was determined. The safety of AAE was tested on Wistar rats and two different cell lines. Some mechanisms of action were also investigated with AAE’s dose-response. Methods: Glucose-loaded (10 g/kg) and streptozotocin-induced (60 mg/kg) diabetic Wistar rats were used in the in vivo model, whereas RIN-5F pancreatic cells and HepG2 liver cells were used in the in vitro model. Nontoxic mass value of AAE was used in the in vitro (from 0.625 to 2.5 μg/100 µl) and in vivo (up to 400 mg/kg) studies. The inhibitory activity of AAE on α-amylase and α-glucosidase was examined by spectrophotometric and microplate reader techniques. Results: The AAE inhibited α-amylase and α-glucosidase, two key enzymes of the carbohydrate metabolism, and stimulated the release of insulin in RIN-5F cells line and glucose uptake in HepG2 cells in a concomitant way. Lower mass values of the extract caused no significant change in the viability of the cells, whereas 5 μg caused a significant reduction in the viability of RIN-5F (59.78%) and HepG2 (56.87%) when compared to the control. The 2.5 μg extract stimulated 91% insulin release in RIN-5F cells when compared with the control. Also, 2.5 μg extract induced 86% and 83% glucose uptake in HepG2 cells in the presence and absence of insulin, respectively, when compared with the control. The median lethal dose of AAE was ≥5000 mg/kg in Wistar rats. AAE caused a decrease in fasting blood glucose level from 30 min in glucose-loaded Wistar rats and from the 4 th day in streptozotocin-induced diabetic rats when compared with the control. There was also an increase in serum insulin and serum α-amylase level in streptozotocin-induced diabetic rats, compared to the control, at the end of the study. Conclusion: A. adscendens root exerts its antidiabetic effect by inhibiting α-amylase and α-glucosidase enzymes, inducing insulin secretion in RIN-5F pancreatic cells, and enhancing glucose uptake in HepG2 liver cells.","PeriodicalId":166744,"journal":{"name":"Canadian Journal of Biotechnology","volume":"57 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2019-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Antidiabetic Effect of Asparagus adscendens Roxb. in RIN-5F Cells, HepG2 Cells, and Wistar Rats\",\"authors\":\"R. Sunday, E. Obuotor, Anil Kumar\",\"doi\":\"10.24870/cjb.2019-000129\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Background: The antidiabetic effect of Asparagus adscendens root ethanolic extract (AAE) was evaluated in this study using both in vivo and in vitro models. The effect of AAE on carbohydrate metabolizing enzymes (α-amylase and α-glucosidase) was determined. The safety of AAE was tested on Wistar rats and two different cell lines. Some mechanisms of action were also investigated with AAE’s dose-response. Methods: Glucose-loaded (10 g/kg) and streptozotocin-induced (60 mg/kg) diabetic Wistar rats were used in the in vivo model, whereas RIN-5F pancreatic cells and HepG2 liver cells were used in the in vitro model. Nontoxic mass value of AAE was used in the in vitro (from 0.625 to 2.5 μg/100 µl) and in vivo (up to 400 mg/kg) studies. The inhibitory activity of AAE on α-amylase and α-glucosidase was examined by spectrophotometric and microplate reader techniques. Results: The AAE inhibited α-amylase and α-glucosidase, two key enzymes of the carbohydrate metabolism, and stimulated the release of insulin in RIN-5F cells line and glucose uptake in HepG2 cells in a concomitant way. Lower mass values of the extract caused no significant change in the viability of the cells, whereas 5 μg caused a significant reduction in the viability of RIN-5F (59.78%) and HepG2 (56.87%) when compared to the control. The 2.5 μg extract stimulated 91% insulin release in RIN-5F cells when compared with the control. Also, 2.5 μg extract induced 86% and 83% glucose uptake in HepG2 cells in the presence and absence of insulin, respectively, when compared with the control. The median lethal dose of AAE was ≥5000 mg/kg in Wistar rats. AAE caused a decrease in fasting blood glucose level from 30 min in glucose-loaded Wistar rats and from the 4 th day in streptozotocin-induced diabetic rats when compared with the control. There was also an increase in serum insulin and serum α-amylase level in streptozotocin-induced diabetic rats, compared to the control, at the end of the study. Conclusion: A. adscendens root exerts its antidiabetic effect by inhibiting α-amylase and α-glucosidase enzymes, inducing insulin secretion in RIN-5F pancreatic cells, and enhancing glucose uptake in HepG2 liver cells.\",\"PeriodicalId\":166744,\"journal\":{\"name\":\"Canadian Journal of Biotechnology\",\"volume\":\"57 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-08-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Canadian Journal of Biotechnology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.24870/cjb.2019-000129\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Canadian Journal of Biotechnology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.24870/cjb.2019-000129","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

摘要

背景:本研究采用体内和体外模型对芦笋根乙醇提取物(AAE)的抗糖尿病作用进行了评价。测定了AAE对糖代谢酶(α-淀粉酶和α-葡萄糖苷酶)的影响。在Wistar大鼠和两种不同细胞系上测试了AAE的安全性。并结合AAE的剂量效应研究了其作用机制。方法:体内模型采用葡萄糖负荷(10 g/kg)和链脲佐菌素诱导(60 mg/kg)糖尿病Wistar大鼠,体外模型采用RIN-5F胰腺细胞和HepG2肝细胞。AAE在体外(0.625 ~ 2.5 μg/100 μ l)和体内(高达400 mg/kg)研究中均采用无毒质量值。采用分光光度法和酶标法检测AAE对α-淀粉酶和α-葡萄糖苷酶的抑制活性。结果:AAE抑制糖代谢关键酶α-淀粉酶和α-葡萄糖苷酶,同时刺激RIN-5F细胞株胰岛素释放和HepG2细胞葡萄糖摄取。较低质量的提取物对细胞活力无显著影响,而5 μg可使细胞的RIN-5F(59.78%)和HepG2(56.87%)活力较对照组显著降低。与对照组相比,2.5 μg提取物刺激RIN-5F细胞91%的胰岛素释放。与对照组相比,在胰岛素存在和不存在的情况下,2.5 μg提取物分别诱导HepG2细胞86%和83%的葡萄糖摄取。AAE对Wistar大鼠的中位致死剂量≥5000mg /kg。与对照组相比,AAE引起葡萄糖负荷Wistar大鼠从30分钟开始和链脲佐菌素诱导的糖尿病大鼠从第4天开始空腹血糖水平下降。在研究结束时,与对照组相比,链脲佐菌素诱导的糖尿病大鼠血清胰岛素和血清α-淀粉酶水平也有所增加。结论:附着木可能通过抑制α-淀粉酶和α-葡萄糖苷酶,诱导RIN-5F胰腺细胞分泌胰岛素,增强HepG2肝细胞的葡萄糖摄取来发挥其抗糖尿病作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Antidiabetic Effect of Asparagus adscendens Roxb. in RIN-5F Cells, HepG2 Cells, and Wistar Rats
Background: The antidiabetic effect of Asparagus adscendens root ethanolic extract (AAE) was evaluated in this study using both in vivo and in vitro models. The effect of AAE on carbohydrate metabolizing enzymes (α-amylase and α-glucosidase) was determined. The safety of AAE was tested on Wistar rats and two different cell lines. Some mechanisms of action were also investigated with AAE’s dose-response. Methods: Glucose-loaded (10 g/kg) and streptozotocin-induced (60 mg/kg) diabetic Wistar rats were used in the in vivo model, whereas RIN-5F pancreatic cells and HepG2 liver cells were used in the in vitro model. Nontoxic mass value of AAE was used in the in vitro (from 0.625 to 2.5 μg/100 µl) and in vivo (up to 400 mg/kg) studies. The inhibitory activity of AAE on α-amylase and α-glucosidase was examined by spectrophotometric and microplate reader techniques. Results: The AAE inhibited α-amylase and α-glucosidase, two key enzymes of the carbohydrate metabolism, and stimulated the release of insulin in RIN-5F cells line and glucose uptake in HepG2 cells in a concomitant way. Lower mass values of the extract caused no significant change in the viability of the cells, whereas 5 μg caused a significant reduction in the viability of RIN-5F (59.78%) and HepG2 (56.87%) when compared to the control. The 2.5 μg extract stimulated 91% insulin release in RIN-5F cells when compared with the control. Also, 2.5 μg extract induced 86% and 83% glucose uptake in HepG2 cells in the presence and absence of insulin, respectively, when compared with the control. The median lethal dose of AAE was ≥5000 mg/kg in Wistar rats. AAE caused a decrease in fasting blood glucose level from 30 min in glucose-loaded Wistar rats and from the 4 th day in streptozotocin-induced diabetic rats when compared with the control. There was also an increase in serum insulin and serum α-amylase level in streptozotocin-induced diabetic rats, compared to the control, at the end of the study. Conclusion: A. adscendens root exerts its antidiabetic effect by inhibiting α-amylase and α-glucosidase enzymes, inducing insulin secretion in RIN-5F pancreatic cells, and enhancing glucose uptake in HepG2 liver cells.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Antidiabetic Effect of Asparagus adscendens Roxb. in RIN-5F Cells, HepG2 Cells, and Wistar Rats Toxicogenetic Studies of Desplatsia dewevrei using Gene Expression of Blood, Pancreatic, and Intestinal Genes in Wistar rats Infusion of herbal plant extracts for insomnia and anxiety causes a dose-dependent increase of NO and has a protective effect on the renal cellular stress caused by hypoxia and reoxygenation Production of a xylanase by Trichoderma harzianum (Hypocrea lixii) in solid-state fermentation and its recovery by an aqueous two-phase system
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1