16:00 - 18:00
Room: San Francisco
Poster session
Dual high-resolution α-glucosidase/PTP1B bioassays coupled with HPLC-HRMS-SPE-NMR for investigation of 'Insulin plants' (Myrcia sp.) as new medicines for type 2 diabetes
Lima Rita de Cassia Lemos 1, Kato Lucilia 2, Kongstad Kenneth T. 1, Jäger Anna K. 1, Staerk Dan 1
1 Department of Drug Design and Pharmacology, University of Copenhagen, Copenhagen, Denmark
2 Instituto de Química, Universidade Federal de Goiás, Goiânia, Brazil

Myrcia species or 'insulin plants' are used by indigenous communities in Brazil to treat type 2 diabetes [1]. Therapeutic targets for T2D include α-glucosidase- and protein tyrosine phosphatase 1B (PTP1B) inhibitors [2]. Herein, we report the screening of six Myrcia species for α-glucosidase and PTP1B inhibitory activity - M. guianensis (IC50AG=7.80 µg/mL; IC50PTP1B= 3.26 µg/mL), M. rubella (IC50AG=4.36 µg/mL; IC50PTP1B= 9.84 µg/mL), M. torta (IC50AG=5.80 µg/mL; IC50PTP1B= 27.00 µg/mL), M. variabilis (IC50AG=3.17 µg/mL; IC50PTP1B= 1.10 µg/mL), M. vestita (IC50AG=13.60 µg/mL; IC50PTP1B= 2.83 µg/mL), and M. virgata (IC50AG=6.30 µg/mL; IC50PTP1B= 3.00 µg/mL). M. rubella was chosen for further analyses, and the crude ethyl acetate extract was submitted to dual high-resolution α-glucosidase and PTP1B profiling for identification of bioactive constituents. Extensive analyses using HPLC-HRMS-SPE-NMR [3] led to the identification of 36 compounds including the α-glucosidase inhibitors – 4,5-dicaffeoylquinic acid (IC50AG= 1.98 µM), isoquercitrin (IC50AG= 22.4 µM), quercetin 3-O-β-D-glucuronide (IC50AG= 21.30 µM), and quercetin 3-O-(6''-malonylglucoside) (IC50AG= 6.60 µM). PTP1B inhibition was associated with triterpenes such as arjunolic acid and 3,4,3’-tri-O-methylellagic acid.

References:

[1] Cascaes MM, Guilhon GMSP, Andrade EHA, Zoghbi MGB, Santos LS. Constituents and pharmacological activities of Myrcia (Myrtaceae): A review of an aromatic and medicinal group of plants. Int J Mol Sci 2015; 16: 23881-23904.

[2] Zhang S, Zhang Z-Y. PTP1B as a drug target: recent developments in PTP1B inhibitor discovery. Drug Discov Today 2007; 12: 373-381.

[3] Wubshet SG, Tahtah Y, Heskes AM, Kongstad KT, Pateraki I, Hamberger B, Møller BL, Staerk D. Identification of PTP1B and α-glucosidase inhibitory serrulatanes from Eremophila spp. by combined use of dual high-resolution PTP1B and α-glucosidase inhibition profiling and HPLC-HRMS-SPE-NMR. J Nat Prod 2016; 79: 1063-1072.


Reference:
Mo-Poster Session 1-PO-202:
Session:
Poster Session 1
Presenter/s:
Rita de Cassia Lemos Lima
Presentation type:
Poster presentation
Room:
San Francisco
Date:
Monday, 4th September, 2017
Time:
16:00 - 18:00
Session times:
16:00 - 18:00