Characterization of the inhibitory activity of natural tanshinones from Salvia miltiorrhiza roots on protein tyrosine phosphatase 1B

  • Chem Biol Interact. 2017 Dec 25;278:65-73. doi: 10.1016/j.cbi.2017.10.013.
Da Hye Kim  1 ,  Pradeep Paudel  1 ,  Ting Yu  1 ,  Thi Men Ngo  2 ,  Jeong Ah Kim  2 ,  Hyun Ah Jung  3 ,  Takako Yokozawa  4 ,  Jae Sue Choi  5
Affiliations
  • 1. Department of Nutrition and Food Science, Pukyong National University, Busan 48513, Republic of Korea.
  • 2. College of Pharmacy, Research Institute of Pharmaceutical Sciences, Kyungpook National University, Daegu 41566, Republic of Korea.
  • 3. Department of Food Science and Human Nutrition, Chonbuk National University, Jeonju 54896, Republic of Korea. Electronic address: [email protected].
  • 4. Graduate School Science and Engineering for Research, University of Toyama, Toyama 930-8555, Japan.
  • 5. Department of Nutrition and Food Science, Pukyong National University, Busan 48513, Republic of Korea. Electronic address: [email protected].
PMID: 29031618 DOI: 10.1016/j.cbi.2017.10.013
Abstract

Protein tyrosine Phosphatase 1B (PTP1B) is a negative regulator that plays an important role in many signaling pathways, especially those associated with Insulin resistance. In this study, we investigated the anti-diabetic potential of 12 natural tanshinones isolated from Salvia miltiorrhiza (S. miltiorrhiza) Bunge (Lamiaceae), deoxyneocryptotanshinone (1), grandifolia F (2), ferruginol (3), cryptotanshinone (4), tanshinone IIA (5), tanshinol B (6), tanshinone IIB (7), tanshinonal (8), methyl tanshinonate (9), 15,16-dihydrotanshinone I (10), tanshinone I (11), and dehydrodanshenol A (12) and evaluated their inhibitory activity against PTP1B. Tanshinones 4, 6 and 12 exhibited potent PTP1B inhibitory activity with IC50 values of 5.5 ± 0.9, 4.7 ± 0.4 and 8.5 ± 0.5 μM, respectively. In addition, tanshinones 1-3, 5 and 7-11 showed promising dose-dependent inhibition of PTP1B over IC50 values ranging from 18.6 to 254.8 μM. Enzyme kinetic analysis of PTP1B inhibition revealed that 4 and 6 were mixed -noncompetitive type inhibitors, whereas 12 was a classical-noncompetitive type inhibitor. Furthermore, 4, 6 and 12 were docked with the PTP1B enzyme using molecular docking simulations (AutoDock 4.2) and exhibited negative binding energy (-6.4 to -8.7 kcal/mol), indicating high binding affinity to PTP1B active site residues. Structure-activity relationships (SAR) analysis revealed that structural modifications of ring A and furan or dihydrofuran ring D on the basic structure of tanshinones influenced their activity. Overall, results indicated that tanshinones from S. miltiorrhiza are potential anti-diabetic candidates that should be explored in the development of preventive and therapeutic modalities for the treatment of diabetes as well as diabetes-associated complications.

Keywords
Anti-diabetes; Lamiaceae; Molecular docking; PTP1B; Salvia miltiorrhiza; Tanshinone.
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