TY - JOUR
T1 - Activation of the Insulin Receptor by Sarcopoterium spinosum Extract and Identification of Sarcocyanidin A as a Novel Active Compound
AU - Wollman, Ayala
AU - Hasib Afana, Rania
AU - Carmeli, Shmuel
AU - Rosenzweig, Tovit
N1 - Publisher Copyright:
© 2025 The Authors. Published by American Chemical Society.
PY - 2025/4/22
Y1 - 2025/4/22
N2 - Sarcopoterium spinosum is a medicinal plant, presenting glucose-lowering properties. The study aimed to identify the active components and their mechanisms of action. Bioguided fractionation was utilized to isolate the active molecules, followed by NMR and HRESI MS for their identification and structural elucidation. Binding to the insulin receptor (IR) and activation of the receptor were measured in vitro. Glucose-lowering effects were validated in vivo. A novel procyanidin trimer, named sarcocyanidin A (1, catechin-(4α-8)-epicatechin-(4β-8)-epicatechin), was identified. Sarcocyanidin A (1) activated insulin signaling in CHO-IR and L6 myotubes, while the IR inhibitor abolished this effect. IR autofluorescence and cell-based thermal shift assays indicate a direct interaction of sarcocyanidin A (1) with IR. Sarcocyanidin A (1) also activated insulin signaling and reduced blood glucose in mice. Sarcocyanidin A, a novel procyanidin trimer, mediates at least part of the antidiabetic properties of SSE, through activation of IR.
AB - Sarcopoterium spinosum is a medicinal plant, presenting glucose-lowering properties. The study aimed to identify the active components and their mechanisms of action. Bioguided fractionation was utilized to isolate the active molecules, followed by NMR and HRESI MS for their identification and structural elucidation. Binding to the insulin receptor (IR) and activation of the receptor were measured in vitro. Glucose-lowering effects were validated in vivo. A novel procyanidin trimer, named sarcocyanidin A (1, catechin-(4α-8)-epicatechin-(4β-8)-epicatechin), was identified. Sarcocyanidin A (1) activated insulin signaling in CHO-IR and L6 myotubes, while the IR inhibitor abolished this effect. IR autofluorescence and cell-based thermal shift assays indicate a direct interaction of sarcocyanidin A (1) with IR. Sarcocyanidin A (1) also activated insulin signaling and reduced blood glucose in mice. Sarcocyanidin A, a novel procyanidin trimer, mediates at least part of the antidiabetic properties of SSE, through activation of IR.
UR - http://www.scopus.com/inward/record.url?scp=105003593385&partnerID=8YFLogxK
U2 - 10.1021/acsomega.5c00451
DO - 10.1021/acsomega.5c00451
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C2 - 40290999
AN - SCOPUS:105003593385
SN - 2470-1343
VL - 10
SP - 15511
EP - 15524
JO - ACS Omega
JF - ACS Omega
IS - 15
ER -