Formononetin‐Vitamin E Conjugate Synergistically Supports Adipogenesis, Attenuates Oxidative Stress, and Restores Insulin Sensitization in Differentiated Preadipocytes

Author:

Kumar Dhritlahre Rakesh12,Goel Abhishek32,Rana Rohit4,Maurya Sushil K.45,Padwad Yogendra32,Saneja Ankit12ORCID

Affiliation:

1. Formulation Laboratory, Dietetics & Nutrition Technology Division CSIR – Institute of Himalayan Bioresource Technology 176061 Palampur Himachal Pradesh India

2. Academy of Scientific and Innovative Research (AcSIR) 201002 Ghaziabad Uttar Pradesh India

3. Pharmacology and Toxicology Laboratory Dietetics & Nutrition Technology Division CSIR – Institute of Himalayan Bioresource Technology 176061 Palampur Himachal Pradesh India

4. CSIR – Institute of Himalayan Bioresource Technology 176061 Palampur Himachal Pradesh India

5. Department of Chemistry Faculty of Science University of Lucknow 226007 Lucknow Uttar Pradesh India

Abstract

AbstractIn this study, a hybrid conjugate of formononetin (FMN) and vitamin E (VESylated‐FMN) was synthesized through succinic acid linker and investigated for its synergistic effect in diabetes. The conjugate was characterized through Ultra Performance Liquid Chromatography – Mass Spectrometry (UPLC‐MS), High‐Resolution Mass Spectrometry (HRMS), Nuclear Magnetic Resonance (NMR), and Differential Scanning Calorimetry (DSC). The ability of VESylated‐FMN to promote adipogenesis and ameliorate insulin resistance brought on by oxidative stress was evaluated in differentiated preadipocytes. Interestingly, VESylated‐FMN promoted intracellular glucose absorption, which in turn increased lipid and triglyceride accumulation and thereby encouraged adipogenesis. VESylated‐FMN attenuated oxidative stress and promoted cell survival by reducing reactive oxygen species (ROS) generation and reversing apoptosis. Additionally, VESylated‐FMN improved insulin sensitization by upregulating the gene and protein expression of insulin‐sensitizing markers. Overall, FMN in conjugation with vitamin E can effectively augment prior insulin sensitivity by reducing oxidative stress for efficient glycemic control in hyperglycemia.

Funder

Science and Engineering Research Board

University Grants Commission of Bangladesh

Academy of Scientific and Innovative Research

Publisher

Wiley

Subject

General Chemistry

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