Journals / Turkish Journal of Chemistry / 2019 / Cilt: 43 - Sayı: 5

Natural diterpenoid alysine A isolated from Teucrium alyssifolium exerts antidiabetic effect via enhanced glucose uptake and suppressed glucose absorption

Pages
1350–1364
Publication Date
2022-11-05
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Advanced in vivo studies are required to clarify the impact of this compound onglucose homeostasis completely.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Teucrium species have been used in folk medicine as antidiabetic, antiinflammatory, antiulcer, and antibacterial agents.
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Key Findings & Data:We have explored in vitro antidiabetic impacts of 2 natural diterpenoids, alysine A and alysine B, isolatedfrom Teucrium alyssifolium.
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Conclusion & Impact:Advanced in vivo studies are required to clarify the impact of this compound onglucose homeostasis completely.
🔬Design:Modeling & Simulation
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Teucrium species have been used in folk medicine as antidiabetic, antiinflammatory, antiulcer, and antibacterial agents. We have explored in vitro antidiabetic impacts of 2 natural diterpenoids, alysine A and alysine B, isolatedfrom Teucrium alyssifolium. The lactate dehydrogenase (LDH) cytotoxicity assay, glucose uptake test, glucose utilization(glycogen content) test, glucose transport test, glucose absorption (α-glucosidase activity) test, insulin secretion test,RNA isolation and cDNA synthesis assay, qPCR quantification assays, and statistical analyses were carried out in thepresent study. Alysine A exerted the following effects at non-cytotoxic doses:• Enhanced the glucose uptake, as much as the insulin in the C2C12, HepG2, and 3T3-L1 cells• Increased the glycogen content in the C2C12 and HepG2 liver cells, significantly higher than the insulin andmetformin• Suppressed the alpha-glucosidase and the GLUT2 expression levels in the Caco-2 cells• Suppressed the SGLT1 and GLUT1-5 expression levels in the Caco-2 cells• Induced the insulin receptor substrate (IRS)1 and GLUT2 expression levels of the BTC6 pancreatic cells• Induced the insulin receptor (INSR), IRS2, phosphoinositide 3-kinase (PI3K), GLUT4, and protein kinase (PK)expression levels of the 3T3-L1 and C2C12 cells• Increased glucose transport through the Caco-2 cell layer• Did not influence insulin secretion in the pancreatic BTC6 cellsConsequently, these data strongly emphasized the antidiabetic action of alysine A on the particularly critical modelmechanisms that assume a part in glucose homeostasis, such as glucose uptake, utilization, and storage. Moreover, theexpression level of the essential genes in glucose metabolism and insulin signaling was altered in a way that the resultswould be antihyperglycemic. A blend of in vitro and in situ tests affirmed the antihyperglycemic action of alysine A andits mechanism. Alysine A has exercised significant and positive results on the glucose homeostasis; thus, it is a naturaland pleiotropic antidiabetic agent. Advanced in vivo studies are required to clarify the impact of this compound onglucose homeostasis completely.

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Cite This Article

YILMAZ, A., ŞEN, A., AYAR, B., TURGUT, G. Ç., ACAR, Ö. Ö., TOPÇU, G. (2022). Natural diterpenoid alysine A isolated from Teucrium alyssifolium exerts antidiabetic effect via enhanced glucose uptake and suppressed glucose absorption. Turkish Journal of Chemistry, Cilt: 43 - Sayı: 5, 1350–1364. https://ajindex.com/articles/601731

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