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A Series of Ferulic Acid Amides Reveals Unexpected Peroxiredoxin 1 Inhibitory Activity with in vivo Antidiabetic and Hypolipidemic Effects
Author(s) -
Yasmin Sabina,
Cerchia Carmen,
Badavath Vishnu Nayak,
Laghezza Antonio,
Dal Piaz Fabrizio,
Mondal Susanta K.,
Atlı Özlem,
Baysal Merve,
Vadivelan Sankaran,
Shankar S.,
Siddique Mohd Usman Mohd,
Pattnaik Ashok Kumar,
Singh Ravi Pratap,
Loiodice Fulvio,
Jayaprakash Venkatesan,
Lavecchia Antonio
Publication year - 2021
Publication title -
chemmedchem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.817
H-Index - 100
eISSN - 1860-7187
pISSN - 1860-7179
DOI - 10.1002/cmdc.202000564
Subject(s) - ferulic acid , insulin resistance , chemistry , in vivo , antioxidant , pharmacology , biochemistry , hyperlipidemia , rosiglitazone , insulin , diabetes mellitus , biology , endocrinology , receptor , microbiology and biotechnology
Insulin resistance is a major pathophysiological feature in the development of type 2 diabetes (T2DM). Ferulic acid is known for attenuating the insulin resistance and reducing the blood glucose in T2DM rats. In this work, we designed and synthesized a library of new ferulic acid amides (FAA), which could be considered as ring opening derivatives of the antidiabetic PPARγ agonists Thiazolidinediones (TZDs). However, since these compounds displayed weak PPAR transactivation capacity, we employed a proteomics approach to unravel their molecular target(s) and identified the peroxiredoxin 1 (PRDX1) as a direct binding target of FAAs. Interestingly, PRDX1, a protein with antioxidant and chaperone activity, has been implied in the development of T2DM by inducing hepatic insulin resistance. SPR, mass spectrometry‐based studies, docking experiments and in vitro inhibition assay confirmed that compounds VIe and VIf bound PRDX1 and induced a dose‐dependent inhibition. Furthermore, VIe and VIf significantly improved hyperglycemia and hyperlipidemia in streptozotocin‐nicotinamide (STZ‐NA)‐induced diabetic rats as confirmed by histopathological examinations. These results provide guidance for developing the current FAAs as new potential antidiabetic agents.